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Plant-derived triterpenoids and analogues as antitumor and anti-HIV agents
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1 of the 200 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-04): 10.1002/mc.20442 (notice 2020-04-14).
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cbdv.200790037openalex-snapshot
A New Cytotoxic Lanostane‐Type Triterpene Glycoside from the Sea Cucumber Holothuria impatiens
inferredcites →https://doi.org/10.1002/cbdv.200890051openalex-snapshot
Bioactive Constituents of Myrrh and Frankincense, Two Simultaneously Prescribed Gum Resins in Chinese Traditional Medicine
inferredcites →https://doi.org/10.1002/cbdv.200890209openalex-snapshot
Study of Antimalarial Activity of Chemical Constituents from Diospyros quaesita
inferredcites →https://doi.org/10.1002/cber.19510840905openalex-snapshot
Crataegolsäure, ein neues Triterpenoid aus Crataegus oxyacantha. Ein Beitrag zur Konstitution der α‐Amyrine
inferredcites →https://doi.org/10.1002/hlca.200690271openalex-snapshot
Three New Triterpenoids from Dracocephalum forrestii
inferredcites →https://doi.org/10.1002/hlca.200790157openalex-snapshot
Isolation and Structure Elucidation of Nortriterpenoids from Schisandra rubriflora
inferredcites →https://doi.org/10.1002/hlca.200890200openalex-snapshot
Nortriterpenoids from Schisandra wilsoniana
inferredcites →https://doi.org/10.1002/ijc.21478openalex-snapshot
Signalling responses linked to betulinic acid‐induced apoptosis are antagonized by MEK inhibitor U0126 in adherent or 3D spheroid melanoma irrespective of p53 status
inferredcites →https://doi.org/10.1002/ijc.22174openalex-snapshot
Anticancer effects of amooranin in human colon carcinoma cell line in vitro and in nude mice xenografts
inferredcites →https://doi.org/10.1002/jps.2600650938openalex-snapshot
Tumor Inhibitory Agents from Vauquelinia corymbosa (Rosaceae)
inferredcites →https://doi.org/10.1002/mc.20442openalex-snapshot
Retracted: Prasad, S., Nigam, N., Kalra, N. and Shukla, Y. (2008), Regulation of signaling pathways involved in lupeol induced inhibition of proliferation and induction of apoptosis in human prostate cancer cells. Mol. Carcinog., 47: 916‐924. https://doi.org/10.1002/mc.20442
inferredcites →https://doi.org/10.1002/mc.20447openalex-snapshot
Betulinic acid suppresses constitutive and TNFα‐induced NF‐κB activation and induces apoptosis in human prostate carcinoma PC‐3 cells
inferredcites →https://doi.org/10.1002/med.10053openalex-snapshot
Chemistry, biological activity, and chemotherapeutic potential of betulinic acid for the prevention and treatment of cancer and HIV infection
inferredcites →https://doi.org/10.1002/med.20075openalex-snapshot
New developments in natural products‐based anti‐AIDS research
inferredcites →https://doi.org/10.1002/med.20138openalex-snapshot
HIV entry inhibitors and their potential in HIV therapy
inferredcites →https://doi.org/10.1002/mnfr.200700389openalex-snapshot
Ursolic acid: An anti‐ and pro‐inflammatory triterpenoid
inferredcites →https://doi.org/10.1002/ptr.2039openalex-snapshot
Antidermatophytic triterpenoids from Syzygium jambos (L.) Alston (Myrtaceae)
inferredcites →https://doi.org/10.1002/ptr.2058openalex-snapshot
Antiproliferative effect on human cancer cell lines after treatment with nimbolide extracted from an edible part of the neem tree ( Azadirachta indica )
inferredcites →https://doi.org/10.1002/ptr.2148openalex-snapshot
Anticancer activity of limonoid from Khaya senegalensis
inferredcites →https://doi.org/10.1002/ptr.2159openalex-snapshot
Gedunin, a limonoid from Xylocarpus granatum, inhibits the growth of CaCo‐2 colon cancer cell line In Vitro
inferredcites →https://doi.org/10.1002/ptr.2362openalex-snapshot
Review of Pharmacological Effects of Glycyrrhiza sp. and its Bioactive Compounds
inferredcites →https://doi.org/10.1002/qsar.19950140604openalex-snapshot
Application of Alternating Conditional Expectations Method to Quantitative Electronic Structure‐Activity Relationships (QESAR)
inferredcites →https://doi.org/10.1007/978-3-540-69297-3_19openalex-snapshot
Anti-angiogenic Activity of a Novel Class of Chemopreventive Compounds: Oleanic Acid Terpenoids
inferredcites →https://doi.org/10.1007/bf02969394openalex-snapshot
Cytotoxic terpenes and lignans from the roots ofAinsliaea acerifolia
inferredcites →https://doi.org/10.1007/bf02978831openalex-snapshot
Effects of triterpenoids and flavonoids isolated from alnus firma on HIV-1 viral enzymes
inferredcites →https://doi.org/10.1007/s00109-007-0251-9openalex-snapshot
Celastrol inhibits polyglutamine aggregation and toxicity though induction of the heat shock response
inferredcites →https://doi.org/10.1007/s00204-006-0072-6openalex-snapshot
Dual activity of triterpenoids: apoptotic versus antidifferentiation effects
inferredcites →https://doi.org/10.1007/s00210-006-0090-1openalex-snapshot
Betulinic acid decreases expression of bcl-2 and cyclin D1, inhibits proliferation, migration and induces apoptosis in cancer cells
inferredcites →https://doi.org/10.1007/s00280-006-0300-zopenalex-snapshot
In vitro anti-cancer activity and structure–activity relationships of natural products isolated from fruits of Panax ginseng
inferredcites →https://doi.org/10.1007/s00280-007-0676-4openalex-snapshot
Inhibition of P-glycoprotein and multidrug resistance protein 1 by dietary phytochemicals
inferredcites →https://doi.org/10.1007/s00405-008-0625-9openalex-snapshot
Inhibitory effects of cucurbitacin B on laryngeal squamous cell carcinoma
inferredcites →https://doi.org/10.1007/s00432-007-0255-4openalex-snapshot
Ursolic acid inhibits the formation of aberrant crypt foci and affects colonic sphingomyelin hydrolyzing enzymes in azoxymethane-treated rats
inferredcites →https://doi.org/10.1007/s10565-006-0104-2openalex-snapshot
Glioblastoma cell death induced by asiatic acid
inferredcites →https://doi.org/10.1007/s10616-007-9069-0openalex-snapshot
Differentiation-inducing activity of lupane triterpenes on a mouse melanoma cell line
inferredcites →https://doi.org/10.1007/s11094-008-0061-6openalex-snapshot
Synthesis and anti-HIV activity of triterpene conjugates of α-d-glucosamine
inferredcites →https://doi.org/10.1007/s12272-001-1137-yopenalex-snapshot
Selective toxicity of ginsenoside Rg3 on multidrug resistant cells by membrane fluidity modulation
inferredcites →https://doi.org/10.1016/j.bcp.2006.08.014openalex-snapshot
Inhibition of NF-κB activation through targeting IκB kinase by celastrol, a quinone methide triterpenoid
inferredcites →https://doi.org/10.1016/j.bcp.2006.10.007openalex-snapshot
Acylation with diangeloyl groups at C21–22 positions in triterpenoid saponins is essential for cytotoxcity towards tumor cells
inferredcites →https://doi.org/10.1016/j.bcp.2007.09.010openalex-snapshot
Identification and functional analysis of cyclooxygenase-1 as a molecular target of boswellic acids
inferredcites →https://doi.org/10.1016/j.bmc.2005.10.063openalex-snapshot
Activity of lupane triterpenoids from Maytenus species as inhibitors of nitric oxide and prostaglandin E2
inferredcites →https://doi.org/10.1016/j.bmc.2005.11.016openalex-snapshot
Synthesis and anti-HIV activity of bi-functional betulinic acid derivatives
inferredcites →https://doi.org/10.1016/j.bmc.2006.04.021openalex-snapshot
Topical anti-inflammatory activity of 2α-hydroxy pentacyclic triterpene acids from the leaves of Ugni molinae
inferredcites →https://doi.org/10.1016/j.bmc.2006.05.075openalex-snapshot
Glycosidation of lupane-type triterpenoids as potent in vitro cytotoxic agents
inferredcites →https://doi.org/10.1016/j.bmc.2007.03.002openalex-snapshot
Selective inhibition of the interaction of C1q with immunoglobulins and the classical pathway of complement activation by steroids and triterpenoids sulfates
inferredcites →https://doi.org/10.1016/j.bmc.2007.05.057openalex-snapshot
The synthesis of 18β-glycyrrhetinic acid derivatives which have increased antiproliferative and apoptotic effects in leukemia cells
inferredcites →https://doi.org/10.1016/j.bmc.2007.06.033openalex-snapshot
Synthesis and structure–activity relationship study of cytotoxic germanicane- and lupane-type 3β-O-monodesmosidic saponins starting from betulin
inferredcites →https://doi.org/10.1016/j.bmc.2008.12.041openalex-snapshot
Solution- and solid-phase synthesis and anti-HIV activity of maslinic acid derivatives containing amino acids and peptides
inferredcites →https://doi.org/10.1016/j.bmcl.2007.02.051openalex-snapshot
Antitumor agents. 256. Conjugation of paclitaxel with other antitumor agents: Evaluation of novel conjugates as cytotoxic agents
inferredcites →https://doi.org/10.1016/j.bmcl.2007.04.034openalex-snapshot
Boswellic acids and glucosamine show synergistic effect in preclinical anti-inflammatory study in rats
inferredcites →https://doi.org/10.1016/j.bmcl.2007.09.081openalex-snapshot
Anti-AIDS agents 73: Structure–activity relationship study and asymmetric synthesis of 3-O-monomethylsuccinyl-betulinic acid derivatives
inferredcites →https://doi.org/10.1016/j.bmcl.2007.10.011openalex-snapshot
Cytotoxic and apoptotic activities of novel amino analogues of boswellic acids
inferredcites →https://doi.org/10.1016/j.bmcl.2007.12.016openalex-snapshot
Antimitotic quinoid triterpenes from Maytenus chuchuhuasca
inferredcites →https://doi.org/10.1016/j.bmcl.2008.03.031openalex-snapshot
Structure-dependent inhibition of bladder and pancreatic cancer cell growth by 2-substituted glycyrrhetinic and ursolic acid derivatives
inferredcites →https://doi.org/10.1016/j.bmcl.2008.08.003openalex-snapshot
Synthesis and cytotoxic activity of heterocyclic ring-substituted betulinic acid derivatives
inferredcites →https://doi.org/10.1016/j.bmcl.2008.10.098openalex-snapshot
Triterpene based compounds with potent anti-maturation activity against HIV-1
inferredcites →https://doi.org/10.1016/j.canlet.2006.11.003openalex-snapshot
Broad in vitro efficacy of plant-derived betulinic acid against cell lines derived from the most prevalent human cancer types
inferredcites →https://doi.org/10.1016/j.canlet.2007.06.018openalex-snapshot
23,24-Dihydrocucurbitacin B induces G2/M cell-cycle arrest and mitochondria-dependent apoptosis in human breast cancer cells (Bcap37)
inferredcites →https://doi.org/10.1016/j.canlet.2007.11.039openalex-snapshot
Induction of apoptosis accompanying with G1 phase arrest and microtubule disassembly in human hepatoma cells by jaspolide B, a new isomalabaricane-type triterpene
inferredcites →https://doi.org/10.1016/j.canlet.2007.12.026openalex-snapshot
Endogenous reverse transcriptase as a mediator of ursolic acid’s anti-proliferative and differentiating effects in human cancer cell lines
inferredcites →https://doi.org/10.1016/j.canlet.2008.01.043openalex-snapshot
Celastrol inhibits the growth of human glioma xenografts in nude mice through suppressing VEGFR expression
inferredcites →https://doi.org/10.1016/j.canlet.2008.01.047openalex-snapshot
Lupeol: Connotations for chemoprevention
inferredcites →https://doi.org/10.1016/j.carres.2008.02.011openalex-snapshot
Synthesis of lupane-type saponins bearing mannosyl and 3,6-branched trimannosyl residues and their evaluation as anticancer agents
inferredcites →https://doi.org/10.1016/j.ccr.2006.09.005openalex-snapshot
Gene expression signature-based chemical genomic prediction identifies a novel class of HSP90 pathway modulators
inferredcites →https://doi.org/10.1016/j.ejphar.2008.06.104openalex-snapshot
A quassinoid 6α-tigloyloxychaparrinone inhibits hypoxia-inducible factor-1 pathway by inhibition of eukaryotic translation initiation factor 4E phosphorylation
inferredcites →https://doi.org/10.1016/j.ejps.2006.04.006openalex-snapshot
Pharmacological properties of the ubiquitous natural product betulin
inferredcites →https://doi.org/10.1016/j.fct.2007.06.002openalex-snapshot
Preventive effects of lupeol on DMBA induced DNA alkylation damage in mouse skin
inferredcites →https://doi.org/10.1016/j.febslet.2007.09.031openalex-snapshot
Activation and inhibition of the proteasome by betulinic acid and its derivatives
inferredcites →https://doi.org/10.1016/j.febslet.2008.11.001openalex-snapshot
Methyl angolensate, a natural tetranortriterpenoid induces intrinsic apoptotic pathway in leukemic cells
inferredcites →https://doi.org/10.1016/j.jep.2007.05.031openalex-snapshot
Inhibition of Escherichia coli heat-labile enterotoxin-induced diarrhea by Chaenomeles speciosa
inferredcites →https://doi.org/10.1016/j.lfs.2005.05.066openalex-snapshot
Dehydrotrametenolic acid selectively inhibits the growth of H-ras transformed rat2 cells and induces apoptosis through caspase-3 pathway
inferredcites →https://doi.org/10.1016/j.lfs.2006.03.027openalex-snapshot
Ganoderiol F, a ganoderma triterpene, induces senescence in hepatoma HepG2 cells
inferredcites →https://doi.org/10.1016/j.mrfmmm.2006.03.008openalex-snapshot
Protective effects of ursolic acid and oleanolic acid in leukemic cells
inferredcites →https://doi.org/10.1016/j.phymed.2007.11.019openalex-snapshot
Boswellic acids: A leukotriene inhibitor also effective through topical application in inflammatory disorders
inferredcites →https://doi.org/10.1016/j.phymed.2008.02.017openalex-snapshot
The gastric ulcer protective effect of boswellic acids, a leukotriene inhibitor from Boswellia serrata, in rats
inferredcites →https://doi.org/10.1016/j.phytochem.2006.03.005openalex-snapshot
Pregnane, coumarin and lupane derivatives and cytotoxic constituents from Helicteres angustifolia
inferredcites →https://doi.org/10.1016/j.phytochem.2006.10.007openalex-snapshot
Oleanane-type triterpenes from the flowers, pith, leaves, and fruit of Tetrapanax papyriferus
inferredcites →https://doi.org/10.1016/j.phytochem.2006.12.007openalex-snapshot
Biotransformation of betulinic and betulonic acids by fungi
inferredcites →https://doi.org/10.1016/j.phytochem.2006.12.015openalex-snapshot
α-Glucosidase inhibitory pentacyclic triterpenes from the stem bark of Fagara tessmannii (Rutaceae)
inferredcites →https://doi.org/10.1016/j.phytochem.2007.02.020openalex-snapshot
α-Glucosidase inhibitory constituents from stem bark of Terminalia superba (Combretaceae)
inferredcites →https://doi.org/10.1016/j.phytochem.2007.10.020openalex-snapshot
Trinorcucurbitane and cucurbitane triterpenoids from the roots of Momordica charantia
inferredcites →https://doi.org/10.1016/j.phytochem.2007.11.019openalex-snapshot
Compounds from Kadsura heteroclita and related anti-HIV activity
inferredcites →https://doi.org/10.1016/j.phytochem.2008.03.004openalex-snapshot
Anti-HIV-1 protease triterpenoids from Stauntonia obovatifoliola Hayata subsp. intermedia
inferredcites →https://doi.org/10.1016/j.phytochem.2008.09.010openalex-snapshot
Nortriterpenoids and lignans from Schisandra sphenanthera
inferredcites →https://doi.org/10.1016/j.tet.2006.01.083openalex-snapshot
A structure–activity relationship study of brusatol, an antitumor quassinoid
inferredcites →https://doi.org/10.1016/j.tet.2006.02.067openalex-snapshot
Trypanocidal constituents of Dracocephalum komarovi
inferredcites →https://doi.org/10.1016/j.tet.2006.03.034openalex-snapshot
Novel 24-nor-, 24-nor-2,3-seco-, and 3,24-dinor-2,4-seco-ursane triterpenes from Diospyros decandra: evidences for ring A biosynthetic transformations
inferredcites →https://doi.org/10.1016/j.tet.2008.02.085openalex-snapshot
Isolation and characterization of miscellaneous terpenoids of Schisandra chinensis
inferredcites →https://doi.org/10.1016/j.tet.2008.05.054openalex-snapshot
The absolute stereostructures of three rare D:B-friedobaccharane skeleton triterpenes from the leaves of Salacia chinensis
inferredcites →https://doi.org/10.1016/j.tet.2008.10.035openalex-snapshot
Chemical modifications of natural triterpenes—glycyrrhetinic and boswellic acids: evaluation of their biological activity
inferredcites →https://doi.org/10.1016/j.tetlet.2006.03.006openalex-snapshot
Crassiflorone, a new naphthoquinone from Diospyros crassiflora (Hien)
inferredcites →https://doi.org/10.1016/j.tetlet.2007.05.152openalex-snapshot
Sphenalactones A–D, a new class of highly oxygenated trinortriterpenoids from Schisandra sphenanthera
inferredcites →https://doi.org/10.1016/j.tetlet.2007.09.171openalex-snapshot
Useful approach to access germanicanes from betulin
inferredcites →https://doi.org/10.1016/j.toxlet.2008.01.008openalex-snapshot
Comparison of the irritation potentials of Boswellia serrata gum resin and of acetyl-11-keto-β-boswellic acid by in vitro cytotoxicity tests on human skin-derived cell lines
inferredcites →https://doi.org/10.1016/j.vph.2006.09.008openalex-snapshot
Effect of acetyl 11-keto β-boswellic acid on metastatic growth factor responsible for angiogenesis
inferredcites →https://doi.org/10.1016/s0026-895x(24)12142-6openalex-snapshot
Acetyl-Boswellic Acids Are Novel Catalytic Inhibitors of Human Topoisomerases I and IIα
inferredcites →https://doi.org/10.1016/s0278-5846(01)00192-0openalex-snapshot
Celastrol, a potent antioxidant and anti-inflammatory drug, as a possible treatment for Alzheimer's disease
inferredcites →https://doi.org/10.1016/s0304-3835(01)00718-2openalex-snapshot
Selective cytotoxicity of betulinic acid on tumor cell lines, but not on normal cells
inferredcites →https://doi.org/10.1016/s0959-8049(97)00294-3openalex-snapshot
Betulinic acid induces apoptosis in human neuroblastoma cell lines
inferredcites →https://doi.org/10.1016/s0960-894x(02)00105-1openalex-snapshot
A novel dicyanotriterpenoid, 2-cyano-3,12-dioxooleana-1,9(11)-dien-28-onitrile, active at picomolar concentrations for inhibition of nitric oxide production
inferredcites →https://doi.org/10.1016/s0960-894x(98)00479-xopenalex-snapshot
Design and synthesis of 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid, a novel and highly active inhibitor of nitric oxide production in mouse macrophages
inferredcites →https://doi.org/10.1016/s1005-9040(08)60010-0openalex-snapshot
Synthesis and Anti-tumor Activity of Novel Amide Derivatives of Ursolic Acid
inferredcites →https://doi.org/10.1016/s1572-5995(06)80032-3openalex-snapshot
Quassinoids: Structural Diversity, Biological Activity and Synthetic Studies
inferredcites →https://doi.org/10.1017/s0007114508882979openalex-snapshot
Antiproliferative and apoptosis-inducing effects of maslinic and oleanolic acids, two pentacyclic triterpenes from olives, on HT-29 colon cancer cells
inferredcites →https://doi.org/10.1021/bk-2000-0758.ch001openalex-snapshot
Citrus Limonoid Research: An Overview
inferredcites →https://doi.org/10.1021/bk-2000-0758.ch002openalex-snapshot
Biochemistry of Limonoids in Citrus
inferredcites →https://doi.org/10.1021/jf052812qopenalex-snapshot
Antiproliferative Terpenoids from Almond Hulls (Prunus dulcis): Identification and Structure−Activity Relationships
inferredcites →https://doi.org/10.1021/jf063563oopenalex-snapshot
Triterpenoids Isolated from Apple Peels Have Potent Antiproliferative Activity and May Be Partially Responsible for Apple's Anticancer Activity
inferredcites →https://doi.org/10.1021/jf071797hopenalex-snapshot
Citrus Limonoids: Analysis, Bioactivity, and Biomedical Prospects
inferredcites →https://doi.org/10.1021/jm020069copenalex-snapshot
Anti-AIDS Agents 49. Synthesis, Anti-HIV, and Anti-Fusion Activities of IC9564 Analogues Based on Betulinic Acid
inferredcites →https://doi.org/10.1021/jm0601912openalex-snapshot
Anti-AIDS Agents 69. Moronic Acid and Other Triterpene Derivatives as Novel Potent Anti-HIV Agents
inferredcites →https://doi.org/10.1021/jm070295sopenalex-snapshot
Specific Plant Terpenoids and Lignoids Possess Potent Antiviral Activities against Severe Acute Respiratory Syndrome Coronavirus
inferredcites →https://doi.org/10.1021/jm8007486openalex-snapshot
Gedunin, a Novel Hsp90 Inhibitor: Semisynthesis of Derivatives and Preliminary Structure−Activity Relationships
inferredcites →https://doi.org/10.1021/jm950669uopenalex-snapshot
Betulinic Acid Derivatives: A New Class of Specific Inhibitors of Human Immunodeficiency Virus Type 1 Entry
inferredcites →https://doi.org/10.1021/jm950922qopenalex-snapshot
Betulinic Acid and Dihydrobetulinic Acid Derivatives as Potent Anti-HIV Agents
inferredcites →https://doi.org/10.1021/np010211xopenalex-snapshot
Anti-AIDS Agents. 48. Anti-HIV Activity of Moronic Acid Derivatives and the New Melliferone-Related Triterpenoid Isolated from Brazilian Propolis
inferredcites →https://doi.org/10.1021/np040142xopenalex-snapshot
Bioactive Constituents fromBoswelliapapyrifera
inferredcites →https://doi.org/10.1021/np0503303openalex-snapshot
Triterpenoids from Schisandra lancifolia with Anti-HIV-1 Activity
inferredcites →https://doi.org/10.1021/np058083qopenalex-snapshot
Cytotoxic Constituents from the Stem Bark of Dichapetalum gelonioides Collected in the Philippines,1
inferredcites →https://doi.org/10.1021/np060278qopenalex-snapshot
Sodwanone and Yardenone Triterpenes from a South African Species of the Marine Sponge Axinella Inhibit Hypoxia-Inducible Factor-1 (HIF-1) Activation in Both Breast and Prostate Tumor Cells
inferredcites →https://doi.org/10.1021/np060369nopenalex-snapshot
Cytotoxic Triterpenoids from the Leaves of Microtropis fokienensis
inferredcites →https://doi.org/10.1021/np060436dopenalex-snapshot
Triterpenoid Pyrazines and Benzopyrazines with Cytotoxic Activity
inferredcites →https://doi.org/10.1021/np060631sopenalex-snapshot
Triterpenoids from the Floral Spikes of Betula platyphylla var. japonica and Their Reversing Activity against Multidrug-Resistant Cancer Cells
inferredcites →https://doi.org/10.1021/np068010mopenalex-snapshot
Bisabolane-Type Sesquiterpenes from the Aerial Parts of Lippia dulcis
inferredcites →https://doi.org/10.1021/np068021fopenalex-snapshot
Hydroxylated Gedunin Derivatives from Cedrela sinensis
inferredcites →https://doi.org/10.1021/np0700927openalex-snapshot
Triterpenoids from Schisandra rubriflora
inferredcites →https://doi.org/10.1021/np0704396openalex-snapshot
Octanorcucurbitane and Cucurbitane Triterpenoids from the Tubers of Hemsleya endecaphylla with HIV-1 Inhibitory Activity
inferredcites →https://doi.org/10.1021/np070613qopenalex-snapshot
Antitumor Agents. 261. 20(S)-Protopanaxadiol and 20(S)-Protopanaxatriol as Antiangiogenic Agents and Total Assignment of 1H NMR Spectra
inferredcites →https://doi.org/10.1021/np0780001openalex-snapshot
Triterpene Acids from Poria cocos and Their Anti-Tumor-Promoting Effects
inferredcites →https://doi.org/10.1021/np50010a012openalex-snapshot
The Antineoplastic Quassinoids of Simaba cuspidata Spruce and Ailanthus grandis Prian
inferredcites →https://doi.org/10.1021/np50104a008openalex-snapshot
Anti-AIDS Agents, 11. Betulinic Acid and Platanic Acid as Anti-HIV Principles from Syzigium claviflorum, and the Anti-HIV Activity of Structurally Related Triterpenoids
inferredcites →https://doi.org/10.1021/np7007347openalex-snapshot
Dichapetalin-Type Triterpenoids and Lignans from the Aerial Parts of Phyllanthus acutissima
inferredcites →https://doi.org/10.1021/np800093aopenalex-snapshot
Lupane-Type Triterpenoids from Microtropis fokienensis and Perrottetia arisanensis and the Apoptotic Effect of 28-Hydroxy-3-oxo-lup-20(29)-en-30-al
inferredcites →https://doi.org/10.1021/np8001139openalex-snapshot
Anti-HIV-1 Protease Activity of Lanostane Triterpenes from the Vietnamese Mushroom Ganoderma colossum
inferredcites →https://doi.org/10.1021/np9800710openalex-snapshot
Anti-AIDS Agents. 30. Anti-HIV Activity of Oleanolic Acid, Pomolic Acid, and Structurally Related Triterpenoids
inferredcites →https://doi.org/10.1021/np990633vopenalex-snapshot
Anti-AIDS Agents 38. Anti-HIV Activity of 3-O-Acyl Ursolic Acid Derivatives
inferredcites →https://doi.org/10.1021/ol0473187openalex-snapshot
Lancifodilactone F: A Novel Nortriterpenoid Possessing a Unique Skeleton from Schisandra lancifolia and Its Anti-HIV Activity
inferredcites →https://doi.org/10.1021/ol050502nopenalex-snapshot
Lancifodilactone G: A Unique Nortriterpenoid Isolated from Schisandra lancifolia and Its Anti-HIV Activity
inferredcites →https://doi.org/10.1021/ol060062fopenalex-snapshot
Rubriflordilactones A and B, Two Novel Bisnortriterpenoids from Schisandra rubriflora and Their Biological Activities
inferredcites →https://doi.org/10.1021/ol060324dopenalex-snapshot
Sphenadilactones A and B, Two Novel Nortriterpenoids from Schisandra sphenanthera
inferredcites →https://doi.org/10.1021/ol061973sopenalex-snapshot
Iminium Salt Catalysts for Asymmetric Epoxidation: The First High Enantioselectivities
inferredcites →https://doi.org/10.1021/ol0620794openalex-snapshot
Sphenadilactones A and B, Two Novel Nortriterpenoids from Schisandra sphenanthera
inferredcites →https://doi.org/10.1021/ol701679nopenalex-snapshot
Structural Characterization of Schintrilactone, a New Class of Nortriterpenoids from Schisandra chinensis
inferredcites →https://doi.org/10.1038/nm1095-1046openalex-snapshot
Discovery of betulinic acid as a selective inhibitor of human melanoma that functions by induction of apoptosis
inferredcites →https://doi.org/10.1038/nrc2129openalex-snapshot
Triterpenoids and rexinoids as multifunctional agents for the prevention and treatment of cancer
inferredcites →https://doi.org/10.1038/sj.bjc.6604227openalex-snapshot
20(S)-25-methoxyl-dammarane-3β, 12β, 20-triol, a novel natural product for prostate cancer therapy: activity in vitro and in vivo and mechanisms of action
inferredcites →https://doi.org/10.1038/sj.onc.1207970openalex-snapshot
Cooperation of betulinic acid and TRAIL to induce apoptosis in tumor cells
inferredcites →https://doi.org/10.1039/b418841copenalex-snapshot
Cucurbitacins and cucurbitane glycosides: structures and biological activities
inferredcites →https://doi.org/10.1039/b501932jopenalex-snapshot
Structure and anti-HIV activity of micrandilactones B and C, new nortriterpenoids possessing a unique skeleton from Schisandra micrantha
inferredcites →https://doi.org/10.1055/s-2005-873187openalex-snapshot
Lupane Triterpenoids and a Diarylheptanoid fromClematoclethra actinidioides
inferredcites →https://doi.org/10.1055/s-2005-916178openalex-snapshot
Inhibition of Diacylglycerol Acyltransferase by Betulinic Acid fromAlnus hirsuta
inferredcites →https://doi.org/10.1055/s-2006-931575openalex-snapshot
Loading of Erythrocyte Membrane with Pentacyclic Triterpenes Inhibits Plasmodium falciparum Invasion
inferredcites →https://doi.org/10.1055/s-2006-947227openalex-snapshot
Boswellic Acids in Chronic Inflammatory Diseases
inferredcites →https://doi.org/10.1055/s-2006-951680openalex-snapshot
Characterization of 3α-Acetyl-11-keto-α-boswellic Acid, a Pentacyclic Triterpenoid Inducing Apoptosisin vitroandin vivo
inferredcites →https://doi.org/10.1055/s-2006-951723openalex-snapshot
Physical, Chemical and Pharmacological Characterization of a New Oleogel-Forming Triterpene Extract from the Outer Bark of Birch (Betulae Cortex)
inferredcites →https://doi.org/10.1055/s-2006-951725openalex-snapshot
Anti-HIV-1 Constituents from Leaves and Twigs of Cratoxylum arborescens
inferredcites →https://doi.org/10.1055/s-2006-951766openalex-snapshot
Phytochemical Investigation of Perovskia abrotanoides
inferredcites →https://doi.org/10.1055/s-2006-957666openalex-snapshot
Betulinic Acid: Isolation fromTriphyophyllum peltatumandAncistrocladus heyneanus, Antimalarial Activity, and Crystal Structure of the Benzyl Ester*
inferredcites →https://doi.org/10.1055/s-2007-967166openalex-snapshot
Triterpenoids from Gouania ulmifolia
inferredcites →https://doi.org/10.1055/s-2007-967188openalex-snapshot
Biocatalysis of the Anticancer Sipholane Triterpenoids
inferredcites →https://doi.org/10.1055/s-2007-993745openalex-snapshot
Effect of Triterpenoids Isolated from the Floral Spikes of Betula platyphylla var. japonica on P-Glycoprotein Function
inferredcites →https://doi.org/10.1055/s-2008-1034286openalex-snapshot
Growth Inhibition and G1 Cell Cycle Arrest Mediated by 25-Methoxyhispidol A, a Novel Triterpenoid, Isolated from the Fruit of Poncirus trifoliata in Human Hepatocellular Carcinoma Cells
inferredcites →https://doi.org/10.1073/pnas.2234683100openalex-snapshot
PA-457: A potent HIV inhibitor that disrupts core condensation by targeting a late step in Gag processing
inferredcites →https://doi.org/10.1073/pnas.91.9.3564openalex-snapshot
Triterpene derivatives that block entry of human immunodeficiency virus type 1 into cells.
inferredcites →https://doi.org/10.1074/mcp.m700259-mcp200openalex-snapshot
Proteomics Characterization of the Cytotoxicity Mechanism of Ganoderic Acid D and Computer-automated Estimation of the Possible Drug Target Network
inferredcites →https://doi.org/10.1080/01635580701613772openalex-snapshot
Induction of Apoptosis by Lupeol and Mango Extract in Mouse Prostate and LNCaP Cells
inferredcites →https://doi.org/10.1080/10286020500383742openalex-snapshot
Semi-synthetic modification of nimbolide to 6-homodesacetylnimbin and 6-desacetylnimbin and their cytotoxic studies
inferredcites →https://doi.org/10.1080/10286020600883419openalex-snapshot
A new anti-HIV lupane acid from Gleditsia sinensis Lam.
inferredcites →https://doi.org/10.1080/10426500601088838openalex-snapshot
Synthesis of Ursolic Phosphonate Derivatives as Potential Anti-HIV Agents
inferredcites →https://doi.org/10.1080/14756360701633187openalex-snapshot
Oleanolic acid and related derivatives as medicinally important compounds
inferredcites →https://doi.org/10.1080/14786410701614325openalex-snapshot
A new phenolic glycoside from the stems ofHydnocarpus hainanensis
inferredcites →https://doi.org/10.1080/87559129609541089openalex-snapshot
Biochemistry and biological functions of citrus limonoids
inferredcites →https://doi.org/10.1089/aid.2006.0137openalex-snapshot
Induction of a Nonproductive Conformational Change in gp120 by a Small Molecule HIV Type 1 Entry Inhibitor
inferredcites →https://doi.org/10.1093/carcin/bgm189openalex-snapshot
2-Cyano-lup-1-en-3-oxo-20-oic acid, a cyano derivative of betulinic acid, activates peroxisome proliferator-activated receptor in colon and pancreatic cancer cells
inferredcites →https://doi.org/10.1097/cmr.0b013e32830b3536openalex-snapshot
Research on the antitumor effect of ginsenoside Rg3 in B16 melanoma cells
inferredcites →https://doi.org/10.1111/j.1349-7006.2007.00554.xopenalex-snapshot
Sipholenol A, a marine‐derived sipholane triterpene, potently reverses P‐glycoprotein (ABCB1)‐mediated multidrug resistance in cancer cells
inferredcites →https://doi.org/10.1111/j.1742-7843.2006.pto_415.xopenalex-snapshot
Ginsenoside 20(S)‐Protopanaxadiol Inhibits the Proliferation and Invasion of Human Fibrosarcoma HT1080 Cells
inferredcites →https://doi.org/10.1111/j.1742-7843.2007.00115.xopenalex-snapshot
Effect of Betulinic Acid on Anticancer Drug‐Resistant Colon Cancer Cells
inferredcites →https://doi.org/10.1124/jpet.107.123356openalex-snapshot
Reciprocal Regulation of Endothelial Nitric-Oxide Synthase and NADPH Oxidase by Betulinic Acid in Human Endothelial Cells
inferredcites →https://doi.org/10.1124/mol.107.041285openalex-snapshot
Methyl 2-Cyano-3,11-dioxo-18β-olean-1,12-dien-30-oate Is a Peroxisome Proliferator-Activated Receptor-γ Agonist That Induces Receptor-Independent Apoptosis in LNCaP Prostate Cancer Cells
inferredcites →https://doi.org/10.1128/aac.00737-07openalex-snapshot
Betulinic Acid Derivatives That Target gp120 and Inhibit Multiple Genetic Subtypes of Human Immunodeficiency Virus Type 1
inferredcites →https://doi.org/10.1139/v81-385openalex-snapshot
Cytotoxic diterpenes triptolide, tripdiolide, and cytotoxic triterpenes from tissue cultures of Tripterygium wilfordii
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Inhibition of Hela Proliferation and Promotion of Apoptosis by Kuwanon C with an Isopentenyl Group: Disruption of Mitochondria and Endoplasmic Reticulum Normal Structure
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Antiproliferative Activity and Target Analysis of 18β-Glycyrrhetinic Acid Derivatives Modified with Α, Β-Unsaturated Carbonyl Groups
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Antiproliferative Activity and Target Analysis of 18β-Glycyrrhetinic Acid Derivatives Modified with Α, Β-Unsaturated Carbonyl Groups
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From Traditional to Modern Medicine: The Role of Herbs and Phytoconstituents in Pharmaceuticals, Nutraceuticals, and Cosmetics
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Isolation and Asymmetric Total Synthesis of Perforanoid A
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Fermentation and purification strategies for the production of betulinic acid and its lupane‐type precursors in Saccharomyces cerevisiae
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Platanic Acid‐Aryl Enones as Potential Anticancer Compounds: Synthesis and Biological Profiling against Breast, Prostate and Lung Cancer Cell Lines
inferred← citeshttps://doi.org/10.1002/cbic.201000618openalex-snapshot
Synthesis and Pro‐Apoptotic Activity of Novel Glycyrrhetinic Acid Derivatives
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ChemInform Abstract: Anitumor Agents. Part 267. Anti‐AIDS‐Agents. Part 77. Plant‐Derived Triterpenoids and Analogues as Antitumor and anti‐HIV Agents
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Pentacyclic triterpenic acids from Argania spinosa
inferred← citeshttps://doi.org/10.1002/ejoc.201001218openalex-snapshot
Synthesis of Limonoid Natural Products
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Synthesis of Lupane‐Type Saponins Containing an Unusual α‐ D ‐Idopyranoside Fragment as Potent Cytotoxic Agents
inferred← citeshttps://doi.org/10.1002/ejoc.201501147openalex-snapshot
Synthesis and Cytotoxicity of 28a‐Homothiolupanes and 28a‐Homothiolupane Saponins
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Antitumor activity of Lepidium latifolium and identification of the epithionitrile 1‐cyano‐2,3‐epithiopropane as its major active component
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Recent advances in natural anti‐HIV triterpenoids and analogs
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Effective Three‐Step Construction of Betulonic Acid Hybrids with Heterocycle‐Containing Peptidomimetic Fragments
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Production of Plant Bioactive Triterpenoid and Steroidal Saponins
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HIV and the Role of Various Medicinal Plants Against Infection in Humans, with Possible Mechanism of Action and Functions of Secondary Metabolites
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HIV and the Role of Various Medicinal Plants Against Infection in Humans, with Possible Mechanism of Action and Functions of Secondary Metabolites
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Quassinoids: Chemistry and Novel Detection Techniques
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Synthesis and evaluation of 29-norcycloartane triterpenoids as α-glucosidase inhibitors
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Synthesis and anticancer activity of aminopropoxytriterpenoids
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Synthesis of 2,11-dioxo-norolean A(1)-12,18(19)-dien-30-oic acid
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Synthesis and study of mutagenic properties of lupane triterpenoids containing 1,2,3-triazole fragments in the C-30 position
inferred← citeshttps://doi.org/10.1007/s10600-014-0938-4openalex-snapshot
Synthesis of 19-(2,6-Dimethylpyrid-4-yl)-20,29,30-trinorlupanes
inferred← citeshttps://doi.org/10.1007/s10600-019-02806-4openalex-snapshot
Synthesis of Stereoisomeric 2,3-Dihydroxy-11-Oxoolean-12-En-30-Oic Acids
inferred← citeshttps://doi.org/10.1007/s11101-010-9172-2openalex-snapshot
Anti-HIV activity of natural triterpenoids and hemisynthetic derivatives 2004–2009
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Triterpene-based plant defenses
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Fruit cuticular waxes as a source of biologically active triterpenoids
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Production of sapogenins (stigmasterol and hecogenin) from genetically transformed hairy root cultures of Chlorophytum borivilianum (Safed musli)
inferred← citeshttps://doi.org/10.1007/s11274-011-0870-8openalex-snapshot
Abiotic elicitation of gymnemic acid in the suspension cultures of Gymnema sylvestre
inferred← citeshttps://doi.org/10.1007/s11816-013-0290-3openalex-snapshot
Improved gymnemic acid production in the suspension cultures of Gymnema sylvestre through biotic elicitation
inferred← citeshttps://doi.org/10.1007/s12033-010-9257-6openalex-snapshot
Production of Plant Bioactive Triterpenoid Saponins: Elicitation Strategies and Target Genes to Improve Yields
inferred← citeshttps://doi.org/10.1016/b978-0-12-817907-9.00009-xopenalex-snapshot
Natural products from plants with prospective anti-HIV activity and relevant mechanisms of action
inferred← citeshttps://doi.org/10.1016/b978-0-12-819485-0.00014-1openalex-snapshot
Studies of pentacyclic triterpenoids structures and antidiabetic properties of Myrianthus genus
inferred← citeshttps://doi.org/10.1016/b978-0-444-63294-4.00002-4openalex-snapshot
Highlights of Pentacyclic Triterpenoids in the Cancer Settings
inferred← citeshttps://doi.org/10.1016/b978-1-63067-041-2.50013-6openalex-snapshot
Research and Innovative Approaches to Obtain Virgin Olive Oils with a Higher Level of Bioactive Constituents
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Modern drug discovery applications for the identification of novel candidates for COVID-19 infections
inferred← citeshttps://doi.org/10.1016/j.antiviral.2013.04.001openalex-snapshot
Development of a fluorescence-based HIV-1 integrase DNA binding assay for identification of novel HIV-1 integrase inhibitors
inferred← citeshttps://doi.org/10.1016/j.apjtb.2017.05.001openalex-snapshot
Phytochemistry and potential therapeutic actions of Boswellic acids: A mini-review
inferred← citeshttps://doi.org/10.1016/j.arabjc.2020.07.022openalex-snapshot
Phytochemical investigation and antioxidant activities of methanol extract, methanol fractions and essential oil of Dillenia suffruticosa leaves
inferred← citeshttps://doi.org/10.1016/j.bbamem.2014.05.027openalex-snapshot
Interactions of pentacyclic triterpene acids with cardiolipins and related phosphatidylglycerols in model systems
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2026.108992openalex-snapshot
Synthetic biomanufacturing of triterpenoids: From laboratory to industry
inferred← citeshttps://doi.org/10.1016/j.bjp.2018.10.006openalex-snapshot
Chemical diversity and activity profiles of HIV-1 reverse transcriptase inhibitors from plants
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.03.066openalex-snapshot
Cytotoxic heterocyclic triterpenoids derived from betulin and betulinic acid
inferred← citeshttps://doi.org/10.1016/j.bmc.2014.04.050openalex-snapshot
Preparation, anticholinesterase activity and molecular docking of new lupane derivatives
inferred← citeshttps://doi.org/10.1016/j.bmc.2015.02.034openalex-snapshot
Synthesis of novel 24-amino-25,26,27-trinorlanost-8-enes: Cytotoxic and apoptotic potential in U937 cells
inferred← citeshttps://doi.org/10.1016/j.bmc.2015.05.015openalex-snapshot
Simple structural modifications confer cytotoxicity to allobetulin
inferred← citeshttps://doi.org/10.1016/j.bmc.2021.116494openalex-snapshot
Microbial transformation of pentacyclic triterpenes for anti-inflammatory agents on the HMGB1 stimulated RAW 264.7 cells by Streptomyces olivaceus CICC 23628
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.10.041openalex-snapshot
Synthesis and biological evaluation of novel spin labeled 18β-glycyrrhetinic acid derivatives
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Cytotoxic triterpenoid glycosides (saikosaponins) from the roots of Bupleurum chinense
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Influence of intramolecular hydrogen bonds on regioselectivity of glycosylation. Synthesis of lupane-type saponins bearing the OSW-1 saponin disaccharide unit and its isomers
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Monodentately-coordinated bioactive moieties in multimodal half-sandwich organoruthenium anticancer agents
inferred← citeshttps://doi.org/10.1016/j.chroma.2012.03.094openalex-snapshot
Investigation of porous graphitic carbon for triterpenoids and natural resinous materials analysis by high performance liquid chromatography hyphenated to mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.chroma.2014.09.006openalex-snapshot
Expedient preparative isolation and tandem mass spectrometric characterization of C-seco triterpenoids from Neem oil
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2015.03.009openalex-snapshot
Grazing incidence diffraction studies of the interactions between ursane-type antimicrobial triterpenes and bacterial anionic phospholipids
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Influence of functional moiety in lupane-type triterpenoids in BACE1 inhibition
inferred← citeshttps://doi.org/10.1016/j.ejmech.2011.10.011openalex-snapshot
Maslinic acid derivatives induce significant apoptosis in b16f10 murine melanoma cells
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.03.035openalex-snapshot
Olean-18-ene triterpenoids from Celastraceae species inhibit HIV replication targeting NF-kB and Sp1 dependent transcription
inferred← citeshttps://doi.org/10.1016/j.ejmech.2013.06.043openalex-snapshot
Cytotoxic triterpenoids from Lysimachia parvifolia
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Semi-synthesis of acylated triterpenes from olive-oil industry wastes for the development of anticancer and anti-HIV agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.04.062openalex-snapshot
Synthesis of novel benzylidene analogues of betulinic acid as potent cytotoxic agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.01.020openalex-snapshot
Discovery and synthesis of novel beesioside I derivatives with potent anti-HIV activity
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Antitumor activity and transcriptome sequencing (RNA-seq) analyses of hepatocellular carcinoma cells in response to exposure triterpene-nucleoside conjugates
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105291openalex-snapshot
Synthesis and discovery of mitochondria-targeting oleanolic acid derivatives for potential PI3K inhibition
inferred← citeshttps://doi.org/10.1016/j.foodchem.2015.03.018openalex-snapshot
Semi-synthesis of new antimicrobial esters from the natural oleanolic and maslinic acids
inferred← citeshttps://doi.org/10.1016/j.heliyon.2021.e07232openalex-snapshot
In vitro inhibitory activity against HPV of the monoterpenoid zinc tetra-ascorbo-camphorate
inferred← citeshttps://doi.org/10.1016/j.jbc.2024.107839openalex-snapshot
Chemical genetic analysis of enoxolone inhibition of Clostridioides difficile toxin production reveals adenine deaminase and ATP synthase as antivirulence targets
inferred← citeshttps://doi.org/10.1016/j.jcis.2012.05.020openalex-snapshot
Investigation of the interactions of lupane type pentacyclic triterpenes with outer leaflet membrane phospholipids – Langmuir monolayer and synchrotron X-ray scattering study
inferred← citeshttps://doi.org/10.1016/j.jfluchem.2013.01.023openalex-snapshot
Study of addition of difluorocarbene on double bond of triterpenes
inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2018.02.004openalex-snapshot
Bioactive ruthenium(II)-arene complexes containing modified 18β-glycyrrhetinic acid ligands
inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.129433openalex-snapshot
Anti-COVID-19 terpenoid from marine sources: A docking, admet and molecular dynamics study
inferred← citeshttps://doi.org/10.1016/j.phytochem.2013.05.011openalex-snapshot
Biotransformation of oleanolic and maslinic acids by Rhizomucor miehei
inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.12.001openalex-snapshot
Polycyclic polyprenylated acylphloroglucinols and biphenyl derivatives from the roots of Garcinia nuntasaenii Ngerns. & Suddee
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113340openalex-snapshot
Selected plant triterpenoids and their amide derivatives in cancer treatment: A review
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114297openalex-snapshot
Triterpenoids from Frankincense and Boswellia: A focus on their pharmacology and 13C-NMR assignments
inferred← citeshttps://doi.org/10.1016/j.phytol.2012.12.003openalex-snapshot
Triterpenoids from Cassine xylocarpa and Celastrus vulcanicola (Celastraceae)
inferred← citeshttps://doi.org/10.1016/j.phytol.2021.06.027openalex-snapshot
A versatile tailoring tool for pentacyclic triterpenes of Penicillium griseofulvum CICC 40293
inferred← citeshttps://doi.org/10.1016/j.steroids.2015.04.005openalex-snapshot
Polyamine derivatives of betulinic acid and β-sitosterol: A comparative investigation
inferred← citeshttps://doi.org/10.1016/j.steroids.2016.07.007openalex-snapshot
Spectral and microscopic study of self-assembly of novel cationic spermine amides of betulinic acid
inferred← citeshttps://doi.org/10.1016/j.steroids.2016.08.002openalex-snapshot
Synthesis of novel lupane triterpenoid-indazolone hybrids with oxime ester linkage
inferred← citeshttps://doi.org/10.1016/j.steroids.2023.109332openalex-snapshot
Synthesis of methotrexate-betulonic acid hybrids and evaluation of their effect on artificial and Caco-2 cell membranes
inferred← citeshttps://doi.org/10.1016/j.tet.2009.11.114openalex-snapshot
Enantiospecific synthesis of ABC-ring system of A-nor and abeo 4(3→2) tetra and pentacyclic triterpenes
inferred← citeshttps://doi.org/10.1016/j.tet.2014.03.006openalex-snapshot
Synthesis and structure–activity relationship study of cytotoxic lupane-type 3β-O-monodesmosidic saponins with an extended C-28 side chain
inferred← citeshttps://doi.org/10.1016/j.tet.2015.03.057openalex-snapshot
Synthesis of lupane saponins from acetylated glycosyl donors by acetonitrile directed glycosylation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.12.047openalex-snapshot
Synthesis of triterpenoid-based 1,2,4-trioxolanes and 1,2,4-dioxazolidines by ozonolysis of allobetulin derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.04.015openalex-snapshot
Lipase mediated separation of triterpene structural isomers, α- and β-amyrin
inferred← citeshttps://doi.org/10.1016/j.ydbio.2023.09.010openalex-snapshot
Tenascin-C-EGFR activation induces functional human satellite cell proliferation and promotes wound-healing of skeletal muscles via oleanic acid
inferred← citeshttps://doi.org/10.1016/j.ymben.2018.10.001openalex-snapshot
Identification of a novel cytochrome P450 enzyme that catalyzes the C-2α hydroxylation of pentacyclic triterpenoids and its application in yeast cell factories
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00302openalex-snapshot
Alkaloids and Isoprenoids Modification by Copper(I)-Catalyzed Huisgen 1,3-Dipolar Cycloaddition (Click Chemistry): Toward New Functions and Molecular Architectures
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.0c01449openalex-snapshot
Development of Potential Antitumor Agents from the Scaffolds of Plant-Derived Terpenoid Lactones
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00271openalex-snapshot
Electrophilic Triterpenoid Enones: A Comparative Thiol-Trapping and Bioactivity Study
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00514openalex-snapshot
Triterpenoid Hydroxamates as HIF Prolyl Hydrolase Inhibitors
inferred← citeshttps://doi.org/10.1021/bk-2011-1067.ch011openalex-snapshot
Chemicals from Extractives
inferred← citeshttps://doi.org/10.1021/co500051zopenalex-snapshot
Solid-Phase Library Synthesis of Bi-Functional Derivatives of Oleanolic and Maslinic Acids and Their Cytotoxicity on Three Cancer Cell Lines
inferred← citeshttps://doi.org/10.1021/jacs.2c07198openalex-snapshot
Bioinspired Synthesis of Spirochensilide A from Lanosterol
inferred← citeshttps://doi.org/10.1021/jacs.3c04124openalex-snapshot
Total Synthesis and Structure Revision of (+)-Lancilactone C
inferred← citeshttps://doi.org/10.1021/jacs.7b07020openalex-snapshot
o -( p -Methoxyphenylethynyl)phenyl Glycosides: Versatile New Glycosylation Donors for the Highly Efficient Construction of Glycosidic Linkages
inferred← citeshttps://doi.org/10.1021/jf102039topenalex-snapshot
Pentacyclic Triterpenoids from Olive Fruit and Leaf
inferred← citeshttps://doi.org/10.1021/jf1039537openalex-snapshot
Determination of Triterpenic Acids in Human Serum by High-Performance Liquid Chromatography: Triterpenoid Interaction with Serum Protein
inferred← citeshttps://doi.org/10.1021/jm301652topenalex-snapshot
Discovery of a Potential Anti-Inflammatory Agent: 3-Oxo-29-noroleana-1,9(11),12-trien-2,20-dicarbonitrile
inferred← citeshttps://doi.org/10.1021/np5000796openalex-snapshot
New Horizons for Old Drugs and Drug Leads
inferred← citeshttps://doi.org/10.1021/ol300647kopenalex-snapshot
Synthesis of the Bridging Framework of Phragmalin-Type Limonoids
inferred← citeshttps://doi.org/10.1038/srep22627openalex-snapshot
Mevalonate-derived quinonemethide triterpenoid from in vitro roots of Peritassa laevigata and their localization in root tissue by MALDI imaging
inferred← citeshttps://doi.org/10.1039/c0np00025fopenalex-snapshot
Recent advances in anti-HIV natural products
inferred← citeshttps://doi.org/10.1039/c0np00069hopenalex-snapshot
Natural products and Chagas' disease: a review of plant compounds studied for activity against Trypanosoma cruzi
inferred← citeshttps://doi.org/10.1039/c1np00015bopenalex-snapshot
The saponins – polar isoprenoids with important and diverse biological activities
inferred← citeshttps://doi.org/10.1039/c2np20060kopenalex-snapshot
Ursane-type pentacyclic triterpenoids as useful platforms to discover anticancer drugs
inferred← citeshttps://doi.org/10.1039/c4md00344fopenalex-snapshot
3-(2,6-Dichloro-benzyloxy)-11-oxo-olean-12-ene-29-oic acid, a semisynthetic derivative of glycyrrhetic acid: synthesis, antiproliferative, apoptotic and anti-angiogenesis activity
inferred← citeshttps://doi.org/10.1039/c5np00015gopenalex-snapshot
Pentacyclic triterpenoids with nitrogen- and sulfur-containing heterocycles: synthesis and medicinal significance
inferred← citeshttps://doi.org/10.1039/c6nj01602bopenalex-snapshot
Concise synthesis of a new triterpenoid saponin from the roots of Gypsophila oldhamiana and its derivatives as α-glucosidase inhibitors
inferred← citeshttps://doi.org/10.1039/c6ra04597aopenalex-snapshot
Design, synthesis, and biological evaluation of novel asiatic acid derivatives as potential anticancer agents
inferred← citeshttps://doi.org/10.1039/c7ra01811hopenalex-snapshot
Site-selective biotransformation of ursane triterpenes by Streptomyces griseus ATCC 13273
inferred← citeshttps://doi.org/10.1039/d0qo00203hopenalex-snapshot
Recent progress in the synthesis of limonoids and limonoid-like natural products
inferred← citeshttps://doi.org/10.1039/d1sc05772copenalex-snapshot
Hydrogen bond activated glycosylation under mild conditions
inferred← citeshttps://doi.org/10.1055/a-0832-2383openalex-snapshot
Natural Product Triterpenoids and Their Semi-Synthetic Derivatives with Potential Anticancer Activity
inferred← citeshttps://doi.org/10.1055/a-1576-4080openalex-snapshot
Biological Activities of Extracts from Ageratum fastigiatum: Phytochemical Study and In Silico Target Fishing Approach
inferred← citeshttps://doi.org/10.1063/5.0018484openalex-snapshot
SAR analysis and bioactive potential of C(3) alkylated triterpenoids
inferred← citeshttps://doi.org/10.1080/00914037.2017.1342251openalex-snapshot
Novel olygomeric C-3 esters of betulin derivatives
inferred← citeshttps://doi.org/10.1080/10426507.2016.1165679openalex-snapshot
Synthesis of S-(28a-homobetulin-28a-yl) thiophosphate, thiophosphonate, and thiophosphinate
inferred← citeshttps://doi.org/10.1080/10826076.2015.1116092openalex-snapshot
Simultaneous determination of five triterpenic acids in fourCorydalisherb medicines by reversed-phase high performance liquid chromatography–fluorescence-mass spectrometer (RP-HPLC–FLD-MS) based on pre-column derivatization
inferred← citeshttps://doi.org/10.1080/14786419.2016.1146887openalex-snapshot
A new cytotoxic diterpenoid glycoside from the leaves of Blumea lacera and its effects on apoptosis and cell cycle
inferred← citeshttps://doi.org/10.1080/15376516.2021.1941463openalex-snapshot
Curcumin reverses hepatic epithelial mesenchymal transition induced by trichloroethylene by inhibiting IL-6R/STAT3
inferred← citeshttps://doi.org/10.1080/17460441.2021.1956901openalex-snapshot
Glycyrrhetinic acid: a promising scaffold for the discovery of anticancer agents
inferred← citeshttps://doi.org/10.1093/jac/dkaf190openalex-snapshot
Oleanolic acid derivative bardoxolone combats multidrug-resistant Staphylococcus aureus by destroying cell membrane and pyruvate metabolism pathway
inferred← citeshttps://doi.org/10.1101/2022.04.20.488993openalex-snapshot
The licorice metabolite enoxolone attenuates Clostridioides difficile pathophysiology by corrupting its metabolic and toxin production networks
inferred← citeshttps://doi.org/10.1111/cbdd.12543openalex-snapshot
Synthesis and Biological Evaluation of Oxygen‐containing Heterocyclic Ring‐fused 23‐Hydroxybetulinic Acid Derivatives as Antitumor Agents
inferred← citeshttps://doi.org/10.1111/cbdd.70190openalex-snapshot
Antiproliferative Activity and Target Analysis of 18β‐Glycyrrhetinic Acid Derivatives Modified With α, β‐Unsaturated Carbonyl Groups
inferred← citeshttps://doi.org/10.1126/science.adf1017openalex-snapshot
Complex scaffold remodeling in plant triterpene biosynthesis
inferred← citeshttps://doi.org/10.1134/s1068162013020027openalex-snapshot
Synthetic transformations of higher triterpenoids. XXX. Synthesis and cytotoxic activity of betulonic acid amides with fragments of nitroxyl radicals
inferred← citeshttps://doi.org/10.1134/s1068162013060083openalex-snapshot
Hepatoprotective activity of betulonic acid amides containing piperidine or pyrrolidine nitroxide moieties
inferred← citeshttps://doi.org/10.11609/jott.2682.8.11.9384-9390openalex-snapshot
A note on the taxonomy, field status and threats to three endemic species of Syzygium (Myrtaceae) from the southern Western Ghats, India
inferred← citeshttps://doi.org/10.1177/1934578x1601100315openalex-snapshot
Synthesis of 5,19-(2,6-Dimethylpyridin-4-yl)-trisnorlupane and Oleanane
inferred← citeshttps://doi.org/10.1177/1934578x1701200508openalex-snapshot
Pentacyclic Triterpenoids from Maytenus cuzcoina
inferred← citeshttps://doi.org/10.1177/2040206614566580openalex-snapshot
Identification of a dibenzocyclooctadiene lignan as a HIV-1 non-nucleoside reverse transcriptase inhibitor
inferred← citeshttps://doi.org/10.1186/s13765-019-0435-3openalex-snapshot
Nuclear magnetic resonance assignment strategy for pentacyclic triterpenes, using lup-20(29)-ene from Pilotrichella flexilis as model system, combining spectrally filtered proton-to-carbon schemes and DFT–GIAO approach
inferred← citeshttps://doi.org/10.1201/b11196-7openalex-snapshot
Natural Products as Treatments for and Leads to Active Compounds in Viral Diseases
inferred← citeshttps://doi.org/10.1248/cpb.59.767openalex-snapshot
Composite Constituent: Lactucenyl Acetate, a Novel Migrated Lupane Triterpenoid from Lactuca indica Revision of Structure of Tarolupenyl Acetate
inferred← citeshttps://doi.org/10.1517/13543776.2015.1038239openalex-snapshot
Dammarane triterpenoids for pharmaceutical use: a patent review (2005 – 2014)
inferred← citeshttps://doi.org/10.1590/0074-02760220396openalex-snapshot
Natural compounds based chemotherapeutic against Chagas disease and leishmaniasis: mitochondrion as a strategic target
inferred← citeshttps://doi.org/10.17816/maj13215-32openalex-snapshot
BETULENOL DERIVATIVES AS POTENTIAL ANTI-HIV AGENTS
inferred← citeshttps://doi.org/10.18097/bmcrm00127openalex-snapshot
Anticoronaviral activity of triterpenoids
inferred← citeshttps://doi.org/10.18632/oncotarget.27085openalex-snapshot
Deep insights into the response of human cervical carcinoma cells to a new cyano enone-bearing triterpenoid soloxolone methyl: a transcriptome analysis
inferred← citeshttps://doi.org/10.18805/ijare.a-5408openalex-snapshot
Isolation and Identification of Insect Antifeedant Compound from Ethanol Extract of Hemidesmus indicus Root
inferred← citeshttps://doi.org/10.19261/cjm.2013.08(2).12openalex-snapshot
Molecular Rearrangements of Highly Functionalized Terpenes. An Unique Reactivity of Bicyclic Framework and Polienic Chain Inhibition under Superacidic Treatment
inferred← citeshttps://doi.org/10.2174/092986713805219118openalex-snapshot
Marine Natural Products with Anti-HIV Activities in the Last Decade
inferred← citeshttps://doi.org/10.2174/138945012804545498openalex-snapshot
Bioavailability Challenges Associated with Development of Saponins As Therapeutic and Chemopreventive Agents
inferred← citeshttps://doi.org/10.22146/ijc.25052openalex-snapshot
Cytotoxic Triterpenoids from the Stembark of Aglaia argentea (Meliaceae)
inferred← citeshttps://doi.org/10.24966/fsn-1076/100024openalex-snapshot
Comparison of Cytotoxicity and the Chemical Composition in Disporopsis pernyi and its Confused Variety
inferred← citeshttps://doi.org/10.3389/fcell.2020.555359openalex-snapshot
Modulation of Lipid Transport and Adipose Tissue Deposition by Small Lipophilic Compounds
inferred← citeshttps://doi.org/10.3390/agriculture12122142openalex-snapshot
Application and Development of Natural Plant Metabolite Oleanolic Acid in the Nano Era
inferred← citeshttps://doi.org/10.3390/cosmetics9060119openalex-snapshot
Biochemical Properties and Cosmetic Uses of Commiphora myrrha and Boswellia serrata
inferred← citeshttps://doi.org/10.3390/ijms14059424openalex-snapshot
Synthesis, Cytotoxicity, DNA Binding and Apoptosis of Rhein-Phosphonate Derivatives as Antitumor Agents
inferred← citeshttps://doi.org/10.3390/ijms25136989openalex-snapshot
Oleanolic Acid Dimers with Potential Application in Medicine—Design, Synthesis, Physico-Chemical Characteristics, Cytotoxic and Antioxidant Activity
inferred← citeshttps://doi.org/10.3390/ijms25158293openalex-snapshot
Kuwanon C Inhibits Tumor Cell Proliferation and Induces Apoptosis by Targeting Mitochondria and Endoplasmic Reticulum
inferred← citeshttps://doi.org/10.3390/metabo11040239openalex-snapshot
Specialized Metabolites from Ribosome Engineered Strains of Streptomyces clavuligerus
inferred← citeshttps://doi.org/10.3390/microorganisms9050969openalex-snapshot
Limonin Enhances the Antifungal Activity of Eugenol Nanoemulsion against Penicillium Italicum In Vitro and In Vivo Tests
inferred← citeshttps://doi.org/10.3390/molecules25092070openalex-snapshot
Structure-Activity-Relationship and Mechanistic Insights for Anti-HIV Natural Products
inferred← citeshttps://doi.org/10.3390/molecules25214878openalex-snapshot
Bioactive Natural Antivirals: An Updated Review of the Available Plants and Isolated Molecules
inferred← citeshttps://doi.org/10.3390/molecules28124655openalex-snapshot
Novel Oleanolic Acid-Phtalimidines Tethered 1,2,3 Triazole Hybrids as Promising Antibacterial Agents: Design, Synthesis, In Vitro Experiments and In Silico Docking Studies
inferred← citeshttps://doi.org/10.3390/nu14030623openalex-snapshot
Oleanolic Acid: Extraction, Characterization and Biological Activity
inferred← citeshttps://doi.org/10.3390/ph18111639openalex-snapshot
Valorization of Olive Leaf Extract via Tailored Liposomal Carriers: Comparative Analysis of Physicochemical Features, Antioxidant Capacity, and Stability
inferred← citeshttps://doi.org/10.3746/jkfn.2025.54.12.1030openalex-snapshot
Inhibitory Effects of Tetrapanax papyriferus Extract on Filaggrin Downregulation and Inflammation of Atopic Dermatitis
inferred← citeshttps://doi.org/10.4103/0974-8490.102260openalex-snapshot
Modulation of genotoxicity of oxidative mutagens by glycyrrhizic acid from Glycyrrhiza glabra L.
inferred← citeshttps://doi.org/10.5897/jmpr.9001035openalex-snapshot
Potential role of natural molecules in health and disease: importance of boswellic acid.
inferred← citeshttps://doi.org/10.7282/t30z71b9openalex-snapshot
The potential effect of triterpenoids in triple negative breast cancer
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