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Triterpenoids
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/cbdv.201300057openalex-snapshot
Limonoids with an Oxygen Bridge between C(1) and C(29) from the Seeds of a Krishna Mangrove, Xylocarpus granatum
inferredcites →https://doi.org/10.1002/cbdv.201300118openalex-snapshot
Simenoside A, a New Triterpenoid Saponin from Gypsophila simonii Hub.‐Mor.
inferredcites →https://doi.org/10.1002/cbdv.201300121openalex-snapshot
Oleanane‐Type Glycosides from Tremastelma palaestinum (L.) Janchen
inferredcites →https://doi.org/10.1002/cbdv.201300155openalex-snapshot
Triterpene Saponins from the Roots of Ilex asprella
inferredcites →https://doi.org/10.1002/cbdv.201300193openalex-snapshot
Inhibition of NO Production by Grindelia argentina and Isolation of Three New Cytotoxic Saponins
inferredcites →https://doi.org/10.1002/cbdv.201300266openalex-snapshot
Limonoids and Flavonoids from the Flowers of Azadirachta indica var. siamensis , and Their Melanogenesis‐Inhibitory and Cytotoxic Activities
inferredcites →https://doi.org/10.1002/cbdv.201300348openalex-snapshot
Cytotoxic and Melanogenesis‐Inhibitory Activities of Limonoids from the Leaves of Azadirachta indica (Neem)
inferredcites →https://doi.org/10.1002/cbdv.201300406openalex-snapshot
Limonoids from Azadirachta indica var. siamensis Extracts and Their Cytotoxic and Melanogenesis‐Inhibitory Activities
inferredcites →https://doi.org/10.1002/cbdv.201400004openalex-snapshot
New Triterpenoids from the Fruiting Bodies of Ganoderma lucidum and Their Bioactivities
inferredcites →https://doi.org/10.1002/cbdv.201400052openalex-snapshot
Three New and Other Limonoids from the Hexane Extract of Melia azedarach Fruits and Their Cytotoxic Activities
inferredcites →https://doi.org/10.1002/cbdv.201400190openalex-snapshot
Cytotoxic and Nitric Oxide Production‐Inhibitory Activities of Limonoids and Other Compounds from the Leaves and Bark ofMelia azedarach
inferredcites →https://doi.org/10.1002/cbic.201402261openalex-snapshot
Ribosylhopane, a Novel Bacterial Hopanoid, as Precursor of C 35 Bacteriohopanepolyols in Streptomyces coelicolor A3(2)
inferredcites →https://doi.org/10.1002/chem.201400226openalex-snapshot
Chemical and Toxicological Investigations of a Previously Unknown Poisonous European Mushroom Tricholoma terreum
inferredcites →https://doi.org/10.1002/cjoc.201400456openalex-snapshot
Two New Triterpenoids from Lycopodium japonicum Thunb.
inferredcites →https://doi.org/10.1002/ejoc.201402208openalex-snapshot
Roseic Acid and Roseolactones A and B, Furan‐Cucurbitane Triterpenes from Russula aurora and R. minutula (Basidiomycota)
inferredcites →https://doi.org/10.1002/hlca.201300008openalex-snapshot
Three New Triterpene Saponins from Bolbostemma paniculatum
inferredcites →https://doi.org/10.1002/hlca.201300147openalex-snapshot
Three New 24‐Nortriterpenoids from the Roots of Ilex asprella
inferredcites →https://doi.org/10.1002/hlca.201300155openalex-snapshot
New Dammarane‐Type Saponins from the Roots of Panax notoginseng
inferredcites →https://doi.org/10.1002/hlca.201300232openalex-snapshot
Floccosic Acid, a New Triterpenic Acid from Nepeta floccosa
inferredcites →https://doi.org/10.1002/hlca.201300292openalex-snapshot
Four New 13,28‐Epoxyoleanane Saponins from Lysimachia lobelioides
inferredcites →https://doi.org/10.1002/hlca.201300316openalex-snapshot
Irigermanone, a Noriridal with Unprecedented Methylketone Function, from Iris germanica
inferredcites →https://doi.org/10.1002/hlca.201300331openalex-snapshot
Two New Cycloartane Triterpenoids from Kleinhovia hospita
inferredcites →https://doi.org/10.1002/hlca.201300382openalex-snapshot
Three New Pentacyclic Triterpenoids from Centella asiatica
inferredcites →https://doi.org/10.1002/hlca.201300443openalex-snapshot
Aphagranols D – H: Five New Limonoids from the Fruits of Aphanamixis grandifolia
inferredcites →https://doi.org/10.1002/hlca.201300446openalex-snapshot
Two New Dammarane‐Type Triterpenoid Saponins from Gynostemma pentaphyllum
inferredcites →https://doi.org/10.1002/hlca.201400001openalex-snapshot
Sulfated Triterpenes from Lemon Balm
inferredcites →https://doi.org/10.1002/hlca.201400021openalex-snapshot
Tirucallane‐Type Triterpenoids from Celastrus stylosus Wall .
inferredcites →https://doi.org/10.1002/hlca.201400027openalex-snapshot
Two New Limonoids from the Root Bark of Chinese Medicinal Plant Dictamnus dasycarpus
inferredcites →https://doi.org/10.1002/hlca.201400045openalex-snapshot
Two New C‐seco Limonoids from the Fruit of Melia azedarach
inferredcites →https://doi.org/10.1002/hlca.201400051openalex-snapshot
Four New Cucurbitacins from the Fruit of Momordica charantia
inferredcites →https://doi.org/10.1002/hlca.201400117openalex-snapshot
Velutinalide C, a New Polycyclic Phragmalin Limonoid from the Leaves of Chukrasia tabularis var. velutina
inferredcites →https://doi.org/10.1002/mrc.4023openalex-snapshot
Leptocarposide: a new triterpenoid glycoside from Ludwigia leptocarpa (Onagraceae)
inferredcites →https://doi.org/10.1007/s00044-013-0663-8openalex-snapshot
A novel saponin from Manilkara hexandra seeds and anti-inflammatory activity
inferredcites →https://doi.org/10.1007/s00217-014-2171-6openalex-snapshot
Analysis of saponins as bioactive zoochemicals from the marine functional food sea cucumber Bohadschia cousteaui
inferredcites →https://doi.org/10.1007/s00253-014-5801-9openalex-snapshot
Ginsenosides: prospective for sustainable biotechnological production
inferredcites →https://doi.org/10.1007/s10600-014-0874-3openalex-snapshot
A New Friedelane Triterpenoid Possessing Cytotoxicity from the Leaves and Stems OF Drypetes hainanensis
inferredcites →https://doi.org/10.1007/s10600-014-0876-1openalex-snapshot
Triterpenoid Saponins from the Carpophore of Xanthoceras sorbifolia
inferredcites →https://doi.org/10.1007/s10600-014-0935-7openalex-snapshot
Phytochemical Investigation of the Rhizomes of Acorus calamus
inferredcites →https://doi.org/10.1007/s10600-014-0936-6openalex-snapshot
Chemical Constituents of Aglaia abbreviata
inferredcites →https://doi.org/10.1007/s10600-014-0940-xopenalex-snapshot
A New Limonoid from Xylocarpus granatum
inferredcites →https://doi.org/10.1007/s10600-014-1051-4openalex-snapshot
A New Pentacyclic Triterpenoid from Lagerstroemia indica
inferredcites →https://doi.org/10.1007/s10600-014-1052-3openalex-snapshot
A New Dammarane Triterpene from Cleome arabica
inferredcites →https://doi.org/10.1007/s10600-014-1098-2openalex-snapshot
A New Taraxastane-Type Triterpene from the Flowers of Inula cappa
inferredcites →https://doi.org/10.1007/s10600-014-1149-8openalex-snapshot
Cycloartane Glycosides from Euphorbia boissierana
inferredcites →https://doi.org/10.1007/s11101-014-9337-5openalex-snapshot
Oleanane triterpenoids in the prevention and therapy of breast cancer: current evidence and future perspectives
inferredcites →https://doi.org/10.1007/s11418-013-0764-1openalex-snapshot
Opaciniols A–C, new terpenoids from Garcinia opaca
inferredcites →https://doi.org/10.1007/s11418-013-0808-6openalex-snapshot
New cytotoxic apotirucallanes from the leaves of Walsura trichostemon
inferredcites →https://doi.org/10.1007/s11418-014-0820-5openalex-snapshot
Cycloartane-type triterpene glycosides from Beesia calthaefolia and their anticomplement activity
inferredcites →https://doi.org/10.1007/s11418-014-0828-xopenalex-snapshot
3,4-seco-24-homo-28-nor-Cycloartane and drimane-type sesquiterpenes and their lactams from the EtOAc-soluble fraction of a leaf extract of Cinnamosma fragrans and their biological activity
inferredcites →https://doi.org/10.1007/s11655-013-1541-4openalex-snapshot
Research progress of ursolic acid’s anti-tumor actions
inferredcites →https://doi.org/10.1007/s12272-013-0133-3openalex-snapshot
Structure and bioactivity of triterpenoids from the stems of Schisandra sphenanthera
inferredcites →https://doi.org/10.1007/s12272-014-0428-zopenalex-snapshot
Cytotoxic triterpenoids from Saussurea phyllocephala
inferredcites →https://doi.org/10.1007/s13659-014-0019-1openalex-snapshot
Triterpenoids and Sterols from the Leaves and Twigs of Melia azedarach
inferredcites →https://doi.org/10.1007/s13659-014-0026-2openalex-snapshot
Highly Oxygenated Limonoids and Lignans from Phyllanthus flexuosus
inferredcites →https://doi.org/10.1007/s13659-014-0042-2openalex-snapshot
Limonoid and Steroidal Saponin from Azadirachta indica
inferredcites →https://doi.org/10.1016/b978-0-12-802215-3.00003-3openalex-snapshot
Ganoderic Acid and Lucidenic Acid (Triterpenoid)
inferredcites →https://doi.org/10.1016/b978-0-12-802215-3.00006-9openalex-snapshot
Research Progress on Natural Triterpenoid Saponins in the Chemoprevention and Chemotherapy of Cancer
inferredcites →https://doi.org/10.1016/b978-0-12-802215-3.00007-0openalex-snapshot
Neem Limonoids as Anticancer Agents
inferredcites →https://doi.org/10.1016/b978-0-444-63294-4.00001-2openalex-snapshot
Recent Insights into the Emerging Role of Triterpenoids in Cancer Therapy
inferredcites →https://doi.org/10.1016/b978-0-444-63294-4.00002-4openalex-snapshot
Highlights of Pentacyclic Triterpenoids in the Cancer Settings
inferredcites →https://doi.org/10.1016/b978-0-444-63294-4.00003-6openalex-snapshot
Immunomodulatory and Anticancer Activity of Sea Cucumber Triterpene Glycosides
inferredcites →https://doi.org/10.1016/j.bioorg.2014.04.003openalex-snapshot
Cytotoxic benzophenone and triterpene from Garcinia hombroniana
inferredcites →https://doi.org/10.1016/j.bmc.2013.11.002openalex-snapshot
Dammarane triterpenes from the leaves of Panax ginseng enhance cellular immunity
inferredcites →https://doi.org/10.1016/j.bmc.2014.06.051openalex-snapshot
Thiophenes, polyacetylenes and terpenes from the aerial parts of Eclipata prostrata
inferredcites →https://doi.org/10.1016/j.bmcl.2013.12.077openalex-snapshot
Limonoids from the leaves of Soymida febrifuga and their insect antifeedant activities
inferredcites →https://doi.org/10.1016/j.bmcl.2013.12.098openalex-snapshot
Rat intestinal sucrase inhibition of constituents from the roots of Rosa rugosa Thunb.
inferredcites →https://doi.org/10.1016/j.bmcl.2014.03.027openalex-snapshot
Three new cucurbitane triterpenoids from Hemsleya penxianensis and their cytotoxic activities
inferredcites →https://doi.org/10.1016/j.bmcl.2014.06.058openalex-snapshot
Five new quassinoids and cytotoxic constituents from the roots of Eurycoma longifolia
inferredcites →https://doi.org/10.1016/j.bmcl.2014.06.069openalex-snapshot
Phragmalin-type limonoids with NF-κB inhibition from Chukrasia tabularis var. velutina
inferredcites →https://doi.org/10.1016/j.bmcl.2014.07.042openalex-snapshot
Triterpene glycosides from red ginseng marc and their anti-inflammatory activities
inferredcites →https://doi.org/10.1016/j.bmcl.2014.08.059openalex-snapshot
Novel dammarane saponins from Gynostemma pentaphyllum and their cytotoxic activities against HepG2 cells
inferredcites →https://doi.org/10.1016/j.bmcl.2014.10.032openalex-snapshot
Cycloartane-type triterpenes from Euphorbia fischeriana stimulate human CYP3A4 promoter activity
inferredcites →https://doi.org/10.1016/j.bmcl.2014.10.036openalex-snapshot
Lithocarpic acids O–S, five homo-cycloartane derivatives from the cupules of Lithocarpus polystachyus
inferredcites →https://doi.org/10.1016/j.bmcl.2014.10.066openalex-snapshot
New 9,19-cycloartenol glycosides isolated from the roots of Cimicifuga simplex and their anti-inflammatory effects
inferredcites →https://doi.org/10.1016/j.bse.2014.01.001openalex-snapshot
Chemical constituents from Celastrus aculeatus Merr.
inferredcites →https://doi.org/10.1016/j.bse.2014.08.009openalex-snapshot
Cucumariosides F1 and F2, two new triterpene glycosides from the sea cucumber Eupentacta fraudatrix and their LC-ESI MS/MS identification in the starfish Patiria pectinifera, a predator of the sea cucumber
inferredcites →https://doi.org/10.1016/j.bse.2014.08.022openalex-snapshot
Chemical constituents from Cyclocarya paliurus (Batal.) Iljinsk
inferredcites →https://doi.org/10.1016/j.canlet.2014.01.016openalex-snapshot
Oleanolic acid and its synthetic derivatives for the prevention and therapy of cancer: Preclinical and clinical evidence
inferredcites →https://doi.org/10.1016/j.carres.2013.07.016openalex-snapshot
New triterpenoid saponins from the aerial parts of Schefflera kwangsiensis
inferredcites →https://doi.org/10.1016/j.drudis.2013.07.018openalex-snapshot
Triterpenoids as reversal agents for anticancer drug resistance treatment
inferredcites →https://doi.org/10.1016/j.fitote.2013.10.005openalex-snapshot
Cycloartane Triterpenes from Beesia calthaefolia (Maxim.)
inferredcites →https://doi.org/10.1016/j.fitote.2013.10.006openalex-snapshot
New ursane-type triterpenoid saponins from the stem bark of Schefflera heptaphylla
inferredcites →https://doi.org/10.1016/j.fitote.2013.10.009openalex-snapshot
Four new quassinoids from the roots of Eurycoma longifolia Jack
inferredcites →https://doi.org/10.1016/j.fitote.2013.10.018openalex-snapshot
Cycloartane glycosides from Astragalus plumosus var. krugianus and evaluation of their antioxidant potential
inferredcites →https://doi.org/10.1016/j.fitote.2013.11.004openalex-snapshot
Triterpenoids from the fruits of Azadirachta indica (Meliaceae)
inferredcites →https://doi.org/10.1016/j.fitote.2013.11.013openalex-snapshot
Oleanane type glycosides from Paronychia anatolica subsp. balansae
inferredcites →https://doi.org/10.1016/j.fitote.2013.12.021openalex-snapshot
Astershionones A–F, six new anti-HBV shionane-type triterpenes from Aster tataricus
inferredcites →https://doi.org/10.1016/j.fitote.2014.01.014openalex-snapshot
Cytotoxic cucurbitane triterpenoids isolated from the rhizomes of Hemsleya amabilis
inferredcites →https://doi.org/10.1016/j.fitote.2014.02.001openalex-snapshot
Absolute configurations of new limonoids from a Krishna mangrove, Xylocarpus granatum
inferredcites →https://doi.org/10.1016/j.fitote.2014.03.005openalex-snapshot
Cucurbitane-type triterpenoids from the stems and leaves of Momordica charantia
inferredcites →https://doi.org/10.1016/j.fitote.2014.04.004openalex-snapshot
New triterpenic acids from Uncaria rhynchophylla: Chemistry, NO-inhibitory activity, and tandem mass spectrometric analysis
inferredcites →https://doi.org/10.1016/j.fitote.2014.04.006openalex-snapshot
Carapanolides C–I from the seeds of andiroba (Carapa guianensis, Meliaceae)
inferredcites →https://doi.org/10.1016/j.fitote.2014.04.012openalex-snapshot
Lycojaponicuminol A–F: Cytotoxic serratene triterpenoids from Lycopodium japonicum
inferredcites →https://doi.org/10.1016/j.fitote.2014.05.006openalex-snapshot
Cytotoxic effect of triterpenoids from the root bark of Hibiscus syriacus
inferredcites →https://doi.org/10.1016/j.fitote.2014.05.019openalex-snapshot
Cytotoxic 9,19-cycloartane triterpenes from the aerial parts of Cimicifuga yunnanensis
inferredcites →https://doi.org/10.1016/j.fitote.2014.05.020openalex-snapshot
Triterpene saponins from the roots of Ilex pubescens
inferredcites →https://doi.org/10.1016/j.fitote.2014.06.009openalex-snapshot
Apotirucallane protolimonoids from the Chinese mangrove Xylocarpus granatum Koenig
inferredcites →https://doi.org/10.1016/j.fitote.2014.06.010openalex-snapshot
Triterpenoids with anti-tobacco mosaic virus activities from Melia Toosendan
inferredcites →https://doi.org/10.1016/j.fitote.2014.06.015openalex-snapshot
Triterpenoid saponins from the roots of Clematis argentilucida
inferredcites →https://doi.org/10.1016/j.fitote.2014.07.014openalex-snapshot
Bioactivity-guided chemical analysis of Melia azedarach L. (Meliaceae), displaying antidiabetic activity
inferredcites →https://doi.org/10.1016/j.fitote.2014.07.016openalex-snapshot
Triterpenoids and α-glucosidase inhibitory constituents from Salacia hainanensis
inferredcites →https://doi.org/10.1016/j.fitote.2014.07.020openalex-snapshot
Triterpenoids of sour jujube show pronounced inhibitory effect on human tumor cells and antioxidant activity
inferredcites →https://doi.org/10.1016/j.fitote.2014.08.004openalex-snapshot
Triterpenoids of Ganoderma theaecolum and their hepatoprotective activities
inferredcites →https://doi.org/10.1016/j.fitote.2014.08.016openalex-snapshot
Five new triterpenoidal saponins from the roots of Ilex cornuta and their protective effects against H2O2-induced cardiomyocytes injury
inferredcites →https://doi.org/10.1016/j.fitote.2014.09.004openalex-snapshot
New terpenoid glycosides obtained from Rosmarinus officinalis L. aerial parts
inferredcites →https://doi.org/10.1016/j.fitote.2014.09.010openalex-snapshot
Cytotoxic and anti–inflammatory tirucallane triterpenoids from Dysoxylum binectariferum
inferredcites →https://doi.org/10.1016/j.foodchem.2013.11.030openalex-snapshot
Two new noroleanane-type triterpene saponins from the methanol extract of Salicornia herbacea
inferredcites →https://doi.org/10.1016/j.jgr.2013.11.013openalex-snapshot
New dammarane-type triterpenoids from the leaves of Panax notoginseng and their protein tyrosine phosphatase 1B inhibitory activity
inferredcites →https://doi.org/10.1016/j.jpba.2013.11.021openalex-snapshot
New triterpene saponins from the roots of Glycyrrhiza yunnanensis and their rapid screening by LC/MS/MS
inferredcites →https://doi.org/10.1016/j.jscs.2011.11.003openalex-snapshot
New manglanostenoic acids from the stem bark of Mangifera indica var. “Fazli”
inferredcites →https://doi.org/10.1016/j.phytochem.2012.08.020openalex-snapshot
Friedolanostanes and xanthones from the twigs of Garcinia hombroniana
inferredcites →https://doi.org/10.1016/j.phytochem.2013.10.013openalex-snapshot
Saponins with highly hydroxylated oleanane-type aglycones from Silphium asteriscus L.
inferredcites →https://doi.org/10.1016/j.phytochem.2013.11.003openalex-snapshot
Acylated oleanane-type saponins from Ganophyllum giganteum
inferredcites →https://doi.org/10.1016/j.phytochem.2013.11.006openalex-snapshot
Methyl angolensate and mexicanolide-type limonoids from the seeds of Cipadessa baccifera
inferredcites →https://doi.org/10.1016/j.phytochem.2013.12.005openalex-snapshot
Triterpenoid saponins from Polycarpaea corymbosa Lamk. var. eriantha Hochst
inferredcites →https://doi.org/10.1016/j.phytochem.2013.12.017openalex-snapshot
Terpenoids from the roots of Drypetes hoaensis and their cytotoxic activities
inferredcites →https://doi.org/10.1016/j.phytochem.2014.01.002openalex-snapshot
Novel chemical constituents with anti-inflammatory activity from the leaves of Sesbania aculeata
inferredcites →https://doi.org/10.1016/j.phytochem.2014.01.019openalex-snapshot
Caspicaosides E–K, triterpenoid saponins and cytotoxic acylated saponins from fruits of Gleditsia caspica Desf.
inferredcites →https://doi.org/10.1016/j.phytochem.2014.02.005openalex-snapshot
Cycloartane triterpenes from the leaves of Neoboutonia macrocalyx L.
inferredcites →https://doi.org/10.1016/j.phytochem.2014.02.018openalex-snapshot
Triterpenoid saponins from the roots of two Gypsophila species
inferredcites →https://doi.org/10.1016/j.phytochem.2014.03.002openalex-snapshot
Hepatoprotective triterpenes from traditional Tibetan medicine Potentilla anserina
inferredcites →https://doi.org/10.1016/j.phytochem.2014.03.009openalex-snapshot
Triterpenoids from Salvia argentea var. aurasiaca (Pomel) Batt. & Trab. and their chemotaxonomic significance
inferredcites →https://doi.org/10.1016/j.phytochem.2014.04.002openalex-snapshot
Oleanane triterpenes as protein tyrosine phosphatase 1B (PTP1B) inhibitors from Camellia japonica
inferredcites →https://doi.org/10.1016/j.phytochem.2014.05.012openalex-snapshot
Chemical constituents of Abies delavayi
inferredcites →https://doi.org/10.1016/j.phytochem.2014.07.003openalex-snapshot
Chemical constituents of Abies nukiangensis
inferredcites →https://doi.org/10.1016/j.phytochem.2014.07.012openalex-snapshot
Saponins in the genus Panax L. (Araliaceae): A systematic review of their chemical diversity
inferredcites →https://doi.org/10.1016/j.phytochem.2014.08.009openalex-snapshot
Limonoids from the fruits of Melia toosendan and their NF-κB modulating activities
inferredcites →https://doi.org/10.1016/j.phytochem.2014.08.011openalex-snapshot
Constituents of Vigna angularis and their in vitro anti-inflammatory activity
inferredcites →https://doi.org/10.1016/j.phytochem.2014.08.029openalex-snapshot
Terpenoids, flavonoids and caffeic acid derivatives from Salvia viridis L. cvar. Blue Jeans
inferredcites →https://doi.org/10.1016/j.phytochem.2014.09.017openalex-snapshot
Triterpene glycosides and other polar constituents of shea (Vitellaria paradoxa) kernels and their bioactivities
inferredcites →https://doi.org/10.1016/j.phytochem.2014.09.022openalex-snapshot
Terpenoids with alpha-glucosidase inhibitory activity from the submerged culture of Inonotus obliquus
inferredcites →https://doi.org/10.1016/j.phytol.2013.09.004openalex-snapshot
A new nortriterpenoid from the fruiting bodies of Ganoderma tropicum
inferredcites →https://doi.org/10.1016/j.phytol.2013.09.015openalex-snapshot
Further cycloartane and friedelane triterpenoids from the leaves of Caloncoba glauca
inferredcites →https://doi.org/10.1016/j.phytol.2014.01.006openalex-snapshot
New triterpene saponins from the seed cake of Camellia Oleifera and their cytotoxic activity
inferredcites →https://doi.org/10.1016/j.phytol.2014.02.011openalex-snapshot
Chemical constituents from Sarcopyramis nepalensis Wall
inferredcites →https://doi.org/10.1016/j.phytol.2014.03.001openalex-snapshot
Aristatosides A-C, hederagenin-type triterpene saponins from Cephalaria aristata
inferredcites →https://doi.org/10.1016/j.phytol.2014.03.009openalex-snapshot
New 19α-hydroxyursane-type triterpenes from the leaves of Meyna spinosa (=Vangueria spinosa), Rubiaceae
inferredcites →https://doi.org/10.1016/j.phytol.2014.03.014openalex-snapshot
A new triterpenoid and eremophilanolide from Ligularia przewalskii
inferredcites →https://doi.org/10.1016/j.phytol.2014.04.011openalex-snapshot
Two tirucallane derivatives from Paramignya scandens and their cytotoxic activity
inferredcites →https://doi.org/10.1016/j.phytol.2014.06.017openalex-snapshot
Two new apotirucallane-type isomeric triterpenoids from the root bark of Dictamnus dasycarpus with their anti-proliferative activity
inferredcites →https://doi.org/10.1016/j.phytol.2014.07.006openalex-snapshot
Two novel saponins from Cephalaria davisiana (Dipsacaceae)
inferredcites →https://doi.org/10.1016/j.phytol.2014.08.009openalex-snapshot
One new flavonoid xyloside and one new natural triterpene rhamnoside from the leaves of Syzygium grande
inferredcites →https://doi.org/10.1016/j.phytol.2014.08.019openalex-snapshot
A protostane and two lanostanes from the bark of Garcinia ferrea
inferredcites →https://doi.org/10.1016/j.phytol.2014.09.011openalex-snapshot
Terpenoids and other constituents from Euphorbia bupleuroides
inferredcites →https://doi.org/10.1016/j.phytol.2014.09.015openalex-snapshot
Antibacterial and cytotoxic triterpenoids from the ethanol extract of Dysoxylum densiflorum (Blume) Miq
inferredcites →https://doi.org/10.1016/j.phytol.2014.10.007openalex-snapshot
Bafouoside C, a new triterpenoid saponin from the roots of Cussonia bancoensis Aubrev. & Pellegr.
inferredcites →https://doi.org/10.1016/j.phytol.2014.10.010openalex-snapshot
New oleanane saponins from Schefflera kwangsiensis
inferredcites →https://doi.org/10.1016/j.tet.2013.12.023openalex-snapshot
Nortriterpenoids from Schisandra chinensis and their absolute configurational assignments by electronic circular dichroism study
inferredcites →https://doi.org/10.1016/j.tet.2014.04.007openalex-snapshot
Ivorenoids A–F: limonoids from Khaya ivorensis
inferredcites →https://doi.org/10.1016/j.tet.2014.04.062openalex-snapshot
Xylomexicanins E-H, new limonoids from Xylocarpus granatum
inferredcites →https://doi.org/10.1016/j.tet.2014.07.006openalex-snapshot
Diverse prieurianin-type limonoid derivatives from the fruits of Aphanamixis grandifolia and their absolute configuration determination
inferredcites →https://doi.org/10.1016/j.tet.2014.07.027openalex-snapshot
Bioactive rearranged limonoids from the Chinese mangrove Xylocarpus granatum Koenig
inferredcites →https://doi.org/10.1016/j.tet.2014.09.013openalex-snapshot
Three lanostane triterpenoids with antitrypanosomal activity from the fruiting body of Hexagonia tenuis
inferredcites →https://doi.org/10.1016/j.tet.2014.10.070openalex-snapshot
Dysotriflorins A–M, triterpenoids from Dysoxylum densiflorum
inferredcites →https://doi.org/10.1016/j.tetlet.2013.12.010openalex-snapshot
Exploration of possible biosynthetic origin of 1/8/9-orthoester moiety in phragmalins
inferredcites →https://doi.org/10.1016/j.tetlet.2014.02.057openalex-snapshot
An unusual 9,11-seco limonoid from Toona ciliata
inferredcites →https://doi.org/10.1016/j.tiv.2014.04.011openalex-snapshot
Chemopreventive and therapeutic effects of nimbolide in cancer: The underlying mechanisms
inferredcites →https://doi.org/10.1021/bk-2014-1185.ch003openalex-snapshot
Separation and Identification of Cucurbitane-Type Triterpenoids from Bitter Melon
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New Triterpenoid Saponins from Ilex cornuta and Their Protective Effects against H2O2-Induced Myocardial Cell Injury
inferredcites →https://doi.org/10.1021/jf503047aopenalex-snapshot
Biological Functionality of Soyasaponins and Soyasapogenols
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Colossolactones, New Triterpenoid Metabolites from a Vietnamese Mushroom Ganoderma colossum
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Hepatoprotective Effects of Triterpenoids from Ganoderma cochlear
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Chemical Constituents from Inonotus obliquus and Their Biological Activities
inferredcites →https://doi.org/10.1021/np400678hopenalex-snapshot
Limonoids from Aphanamixis polystachya and Their Antifeedant Activity
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Cytotoxic Dammarane-Type Triterpenoids from the Stem Bark of Dysoxylum binecteriferum
inferredcites →https://doi.org/10.1021/np400701kopenalex-snapshot
NF-κB Inhibitors from Eurycoma longifolia
inferredcites →https://doi.org/10.1021/np400797sopenalex-snapshot
A,D-seco-Limonoids from the Stems of Clausena emarginata
inferredcites →https://doi.org/10.1021/np400838aopenalex-snapshot
Leonurusoleanolides E–J, Minor Spirocyclic Triterpenoids from Leonurus japonicus Fruits
inferredcites →https://doi.org/10.1021/np4008415openalex-snapshot
Unusual Fernane and Gammacerane Glycosides from the Aerial Parts of Spergula fallax
inferredcites →https://doi.org/10.1021/np400846kopenalex-snapshot
Triterpene Lactones from Cultures of Ganoderma sp. KM01
inferredcites →https://doi.org/10.1021/np400851kopenalex-snapshot
Lupane Triterpenoids from the Stems of Euonymus carnosus
inferredcites →https://doi.org/10.1021/np400863dopenalex-snapshot
Bioactive Limonoids from the Leaves of Azaridachta indica (Neem)
inferredcites →https://doi.org/10.1021/np400937fopenalex-snapshot
Iridal-Type Triterpenoids with Neuroprotective Activities from Iris tectorum
inferredcites →https://doi.org/10.1021/np400971ropenalex-snapshot
Biologically Active Dichapetalins from Dichapetalum gelonioides
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Limonoids from the Leaves and Twigs of Walsura yunnanensis
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C-17 Lactam-Bearing Limonoids from the Twigs and Leaves of Amoora tsangii
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Dammarane-Type Triterpenoids from Gentianella azurea
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Anti-inflammatory Diterpenoids from the Root Bark of Acanthopanax gracilistylus
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Dammarane Triterpenes as Potential SIRT1 Activators from the Leaves of Panax ginseng
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Cycloartane Triterpenoids and Their Glycosides from the Rhizomes of Cimicifuga foetida
inferredcites →https://doi.org/10.1021/np500253mopenalex-snapshot
Uralsaponins M–Y, Antiviral Triterpenoid Saponins from the Roots of Glycyrrhiza uralensis
inferredcites →https://doi.org/10.1021/np5002829openalex-snapshot
Limonoids from the Seeds of Swietenia macrophylla with Inhibitory Activity against Dengue Virus 2
inferredcites →https://doi.org/10.1021/np5002863openalex-snapshot
Ganoboninketals A–C, Antiplasmodial 3,4- seco -27-Norlanostane Triterpenes from Ganoderma boninense Pat.
inferredcites →https://doi.org/10.1021/np5003687openalex-snapshot
Weakly Anti-inflammatory Limonoids from the Seeds of Xylocarpus rumphii
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Lithocarpic Acids A–N, 3,4- seco -Cycloartane Derivatives from the Cupules of Lithocarpus polystachyus
inferredcites →https://doi.org/10.1021/np500509qopenalex-snapshot
Anti-inflammatory Ursane- and Oleanane-Type Triterpenoids from Vitex negundo var. cannabifolia
inferredcites →https://doi.org/10.1021/np500575qopenalex-snapshot
Synthesis of Cyclocaric Acid A and Comparison to Material from Cyclocarya paliurus
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Structural Characterization and Antioxidative Activity of Lancifonins: Unique Nortriterpenoids from Schisandra lancifolia
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Nitrogen-Containing Dimeric nor -Multiflorane Triterpene from a Turraea sp.
inferredcites →https://doi.org/10.1021/ol5027552openalex-snapshot
Trichiconins A–C, Limonoids with New Carbon Skeletons from Trichilia connaroides
inferredcites →https://doi.org/10.1039/c3ra46412aopenalex-snapshot
Anti-inflammatory terpenoids from Boswellia ovalifoliolata
inferredcites →https://doi.org/10.1039/c4ob00807copenalex-snapshot
Dammarane-type triterpenoids as 11β-HSD1 inhibitors from Homonoia riparia
inferredcites →https://doi.org/10.1039/c4ra00708eopenalex-snapshot
New rearranged limonoids from Walsura cochinchinensis
inferredcites →https://doi.org/10.1039/c4ra02784aopenalex-snapshot
Multifunctional pentacyclic triterpenoids as adjuvants in cancer chemotherapy: a review
inferredcites →https://doi.org/10.1055/s-0033-1360363openalex-snapshot
Fatsioside A, a Rare Baccharane-Type Glycoside Inhibiting the Growth of Glioma Cells from the Fruits of Fatsia japonica
inferredcites →https://doi.org/10.1055/s-0033-1360390openalex-snapshot
Libiguins A and B: Novel Phragmalin Limonoids Isolated from Neobeguea mahafalensis Causing Profound Enhancement of Sexual Activity
inferredcites →https://doi.org/10.1055/s-0034-1368428openalex-snapshot
Cytotoxic Triterpenoid Glycosides from the Roots of Camellia oleifera
inferredcites →https://doi.org/10.1055/s-0034-1368455openalex-snapshot
Triterpene Saponins from the Stems of Entada phaseoloides
inferredcites →https://doi.org/10.1055/s-0034-1368612openalex-snapshot
Two New 2,3-Seco-Hopane Triterpene Derivatives from Megacodon stylophorus and Their Antiproliferative and Antimicrobial Activities
inferredcites →https://doi.org/10.1055/s-0034-1382464openalex-snapshot
Rhododendroside A, an unprecedentedly cyclized antiseptic megastigmane glycoside from Rhododendron brachycarpum
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Novel pentacyclic triterpenes exhibiting strong neuroprotective activity in SH-SY5Y cells in salsolinol- and glutamate-induced neurodegeneration models
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Substituted dienes prepared from betulinic acid – Synthesis, cytotoxicity, mechanism of action, and pharmacological parameters
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