On the public citation graph

Leishmanicidal, Antiplasmodial, and Cytotoxic Activity of Novel Diterpenoid 1,2-Quinones from Perovskia abrotanoides : New Source of Tanshinones

https://doi.org/10.1021/np010032f
0 signed · 181 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1016/0031-9422(89)80294-8openalex-snapshot
Abietane type diterpenoids from Salvia miltiorrhiza
inferredcites →https://doi.org/10.1016/s0006-291x(86)80136-xopenalex-snapshot
The mdrl gene, responsible for multidrug-resistance, codes for P-glycoprotein
inferredcites →https://doi.org/10.1016/s0021-9673(01)88770-7openalex-snapshot
High-performance liquid chromatography of abietane-type compounds
inferredcites →https://doi.org/10.1016/s0031-9422(00)81178-4openalex-snapshot
20-Nor-abietane and rearranged abietane diterpenoids from the root of Salvia argentea
inferredcites →https://doi.org/10.1016/s0031-9422(99)00343-xopenalex-snapshot
Diterpenoids from Salvia glutinosa, S. austriaca, S. tomentosa and S. verticillata roots
inferredcites →https://doi.org/10.1016/s0032-9592(99)00146-6openalex-snapshot
Effects of yeast elicitor on the growth and secondary metabolism of a high-tanshinone-producing line of the Ti transformed Salvia miltiorrhiza cells in suspension culture
inferredcites →https://doi.org/10.1016/s0040-4020(01)92414-7openalex-snapshot
Synthesis of tanshinones
inferredcites →https://doi.org/10.1016/s0040-4039(00)73991-8openalex-snapshot
Isolation and structure determination of peradione (1) a novel triterpene with a rearranged perovskane skeleton from Perovskia abrotanoides
inferredcites →https://doi.org/10.1016/s0040-4039(00)80559-6openalex-snapshot
Salviolone, a cytotoxic bisnorditerpene with a benzotropolone chromophore from a chinese drug dan-shen ()
inferredcites →https://doi.org/10.1016/s0040-4039(00)99187-1openalex-snapshot
Absolute configurations of marine diterpenes possessing a xenicane skeleton. An application of an advanced mosher's method
inferredcites →https://doi.org/10.1016/s0168-1656(97)00144-2openalex-snapshot
Tanshinone production in Ti-transformed Salvia miltiorrhiza cell suspension cultures
inferredcites →https://doi.org/10.1016/s0378-8741(99)00059-8openalex-snapshot
Tanshinone IIA isolated from Salvia miltiorrhiza BUNGE induced apoptosis in HL60 human premyelocytic leukemia cell line
inferredcites →https://doi.org/10.1021/ja00011a006openalex-snapshot
High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
inferredcites →https://doi.org/10.1021/jm00109a022openalex-snapshot
Compounds from Danshen. Part 4. Structure-activity relationship of miltirone, an active central benzodiazepine receptor ligand isolated from Salvia miltiorrhiza Bunge (Danshen)
inferredcites →https://doi.org/10.1021/jm00109a023openalex-snapshot
Synthesis of the 2-amino-4-phosphonobutanoic acid analogs (E)- and (Z)-2-amino-2,3-methano-4-phosphonobutanoic acid and their evaluation as inhibitors of hippocampal excitatory neurotransmission
inferredcites →https://doi.org/10.1021/jo00042a006openalex-snapshot
Perovskone: a triterpene with a novel carbon skeleton from Perovskia abrotanoides
inferredcites →https://doi.org/10.1021/jo00131a006openalex-snapshot
Aromatic Annulation Strategy for the Synthesis of Angularly-Fused Diterpenoid Quinones. Total Synthesis of (+)-Neocryptotanshinone, (-)-Cryptotanshinone, Tanshinone IIA, and (.+-.)-Royleanone
inferredcites →https://doi.org/10.1021/jo00304a009openalex-snapshot
Asymmetric syntheses of Salvia miltiorrhiza abietanoid o-quinones: methyl tanshinonate, tanshinone IIB, tanshindiol B and 3-hydroxytanshinone
inferredcites →https://doi.org/10.1021/jo00304a010openalex-snapshot
Synthesis of miltirone by an ultrasound-promoted cycloaddition
inferredcites →https://doi.org/10.1021/np50085a015openalex-snapshot
Constituents of High Altitude Himalayan Herbs, Part V. A New Diterpenoid Quinone from Salvia hians
inferredcites →https://doi.org/10.1055/s-0028-1097363openalex-snapshot
Gas–Chromatographic Analysis of the Volatile Oil of Perovskia abrotanoides Karel.
inferredcites →https://doi.org/10.1055/s-0028-1099377openalex-snapshot
DAS VORKOMMEN VON PHENANTHRENCHINONEN IN ARTEN DER GATTUNG SALVIA
inferredcites →https://doi.org/10.1055/s-0028-1099487openalex-snapshot
DITERPENCHINONE AUS LABIATENWURZELN1
inferredcites →https://doi.org/10.1055/s-2006-960219openalex-snapshot
Abietane-Type Diterpene Quinones fromSalvia nipponica
inferredcites →https://doi.org/10.1080/10412905.1997.9700753openalex-snapshot
Essential Oil ofLomatopodium staurophyllum(Rech. f.) Rech. f.
inferredcites →https://doi.org/10.1128/aac.16.6.710openalex-snapshot
Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique
inferredcites →https://doi.org/10.1128/aac.37.12.2550openalex-snapshot
Licochalcone A, a novel antiparasitic agent with potent activity against human pathogenic protozoan species of Leishmania
inferredcites →https://doi.org/10.1142/s0192415x90000046openalex-snapshot
Protective Effect of Danshen During Myocaredial Ischemia and Reperfusion: An Isolated Rat Heart Study
inferredcites →https://doi.org/10.1146/annurev.bi.62.070193.002125openalex-snapshot
BIOCHEMISTRY OF MULTIDRUG RESISTANCE MEDIATED BY THE MULTIDRUG TRANSPORTER
inferredcites →https://doi.org/10.1248/cpb.45.1306openalex-snapshot
Aldose Reductase Inhibitory Constituents of the Root of Salvia miltiorhiza BUNGE.
inferredcites →https://doi.org/10.1248/cpb.46.107openalex-snapshot
Constituents of Roots of Salvia deserta SCHANG. (Xinjiang-Danshen).

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112926zenodo-depositor-declared
Two seco-norabietane diterpenoids with unprecedented skeletons from the roots of Salvia abrotanoides (Kar.) Sytsma
inferred← citeshttps://doi.org/10.1002/9781118801512.ch15openalex-snapshot
Reconstitution of Medicinally Important Plant Natural Products in Microorganisms
inferred← citeshttps://doi.org/10.1002/9783527694082.ch3openalex-snapshot
Contribution of Natural Products to Drug Discovery in Tropical Diseases
inferred← citeshttps://doi.org/10.1002/ardp.70341openalex-snapshot
Novel Diterpenoids From Salvia rosmarinus Reveal a Compound With Antiproliferative and Antioxidant Activities
inferred← citeshttps://doi.org/10.1002/bdrc.21050openalex-snapshot
Pregnancy outcomes, embryonic and fetal development in maternal exposure to chinese medicines
inferred← citeshttps://doi.org/10.1002/bkcs.10122openalex-snapshot
Abietane Diterpenoids from Perovskia atriplicifolia and Their Anti‐ HBV Activities
inferred← citeshttps://doi.org/10.1002/cbdv.201700071openalex-snapshot
Four New Diterpene Glucosides from Perovskia atriplicifolia
inferred← citeshttps://doi.org/10.1002/cbdv.201700565openalex-snapshot
Variations in Essential Oil Composition and Antioxidant Activity in Perovskia abrotanoides Kar . Collected from Different Regions in Iran
inferred← citeshttps://doi.org/10.1002/cbdv.71589openalex-snapshot
Abietane‐Type Diterpenoids From Salvia kiangsiensis : Isolation, Semisynthesis, and Cytotoxicity of Their Oxime Ester Derivatives
inferred← citeshttps://doi.org/10.1002/ffj.1508openalex-snapshot
Chemical composition of the essential oil ofPerovskia abrotanoides Karel. growing wild in Iran
inferred← citeshttps://doi.org/10.1002/hlca.201500514openalex-snapshot
A Novel C22Terpenoid from the CulturedPerovskia atriplicifolia
inferred← citeshttps://doi.org/10.1002/pfm2.70007openalex-snapshot
Orthoquinone, Cyclic, and Acyclic α‐Diketone Natural Products: From Food Applications to Pharmacotherapy
inferred← citeshttps://doi.org/10.1002/ptr.2305openalex-snapshot
Antileishmanial, antiplasmodial and cytotoxic activities of 12,16‐dideoxy aegyptinone B from Zhumeria majdae Rech.f. & Wendelbo
inferred← citeshttps://doi.org/10.1002/ptr.5749openalex-snapshot
Diterpenes as lead molecules against neglected tropical diseases
inferred← citeshttps://doi.org/10.1007/978-3-030-81218-8_3openalex-snapshot
Phoma on Medicinal and Aromatic Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-43806-1_10openalex-snapshot
Teratogenicity and Developmental Toxicity of Herbal Products
inferred← citeshttps://doi.org/10.1007/978-3-642-22144-6_120openalex-snapshot
Terpenes: Chemistry, Biological Role, and Therapeutic Applications
inferred← citeshttps://doi.org/10.1007/s00005-007-0039-1openalex-snapshot
Terpenes: substances useful in human healthcare
inferred← citeshttps://doi.org/10.1007/s00210-026-05664-4openalex-snapshot
Unraveling potent therapeutic potentials of tanshinones, lipophilic abietane diterpenes: a holistic literature review
inferred← citeshttps://doi.org/10.1007/s00436-002-0768-3openalex-snapshot
Natural products as antiparasitic drugs
inferred← citeshttps://doi.org/10.1007/s00436-020-06787-0openalex-snapshot
Recent researches in effective antileishmanial herbal compounds: narrative review
inferred← citeshttps://doi.org/10.1007/s11094-025-03441-wopenalex-snapshot
Isolation of Cryptotanshinone from Perovskia angustifolia and its Anti-Inflammatory Activity
inferred← citeshttps://doi.org/10.1007/s11373-005-0973-zopenalex-snapshot
Tanshinone IIA isolated from Salvia miltiorrhiza elicits the cell death of human endothelial cells
inferred← citeshttps://doi.org/10.1007/s11373-005-4564-9openalex-snapshot
Biomedical Vignette
inferred← citeshttps://doi.org/10.1007/s13659-013-0034-7openalex-snapshot
Total synthesis of 1-oxomiltirone via Suzuki coupling
inferred← citeshttps://doi.org/10.1016/b978-0-12-822800-5.00011-1openalex-snapshot
Natural products as a novel source for antileishmanial drug development
inferred← citeshttps://doi.org/10.1016/j.bcab.2019.101113openalex-snapshot
In vitro propagation and phytochemical assessment of Perovskia abrotanoides Karel. (Lamiaceae) – A medicinally important source of phenolic compounds
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104261openalex-snapshot
Antiproliferative abietane quinone diterpenoids from the roots of Salvia deserta
inferred← citeshttps://doi.org/10.1016/j.bmc.2003.10.010openalex-snapshot
Erythrocyte membrane modifying agents and the inhibition of Plasmodium falciparum growth
inferred← citeshttps://doi.org/10.1016/j.bmc.2006.03.047openalex-snapshot
Cytotoxicity of abietane diterpenoids from Perovskia abrotanoides and of their semisynthetic analogues
inferred← citeshttps://doi.org/10.1016/j.bmc.2009.02.050openalex-snapshot
Antimalarials from nature
inferred← citeshttps://doi.org/10.1016/j.bmc.2011.06.067openalex-snapshot
In vitro cytotoxic activity of abietane diterpenes from Peltodon longipes as well as Salvia miltiorrhiza and Salvia sahendica
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.08.096openalex-snapshot
Chemotherapy of leishmaniasis. Part IX: Synthesis and bioevaluation of aryl substituted ketene dithioacetals as antileishmanial agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.09.024openalex-snapshot
Chemotherapy of leishmaniasis. Part XI: Synthesis and bioevaluation of novel isoxazole containing heteroretinoid and its amide derivatives
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.10.110openalex-snapshot
Chemotherapy of leishmaniasis part X: Synthesis and bioevaluation of novel terpenyl heterocycles
inferred← citeshttps://doi.org/10.1016/j.bmcl.2013.04.025openalex-snapshot
Synthesis and biological evaluation of a novel series of aryl S,N-ketene acetals as antileishmanial agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2013.10.040openalex-snapshot
Cytotoxic compounds from invasive giant salvinia (Salvinia molesta) against human tumor cells
inferred← citeshttps://doi.org/10.1016/j.canlet.2011.10.006openalex-snapshot
Cryptotanshinone suppresses androgen receptor-mediated growth in androgen dependent and castration resistant prostate cancer cells
inferred← citeshttps://doi.org/10.1016/j.ejmech.2004.03.007openalex-snapshot
Synthesis and antileishmanial profile of some novel terpenyl pyrimidines
inferred← citeshttps://doi.org/10.1016/j.ejmech.2005.02.007openalex-snapshot
Chemotherapy of leishmaniasis part II: synthesis and bioevaluation of substituted arylketene dithioacetals as antileishmanial agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2006.02.004openalex-snapshot
Chemotherapy of leishmaniasis part III: synthesis and bioevaluation of novel aryl substituted terpenyl pyrimidines as antileishmanial agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2006.09.016openalex-snapshot
Chemotherapy of leishmaniasis Part VI: Synthesis and bioevaluation of some novel terpenyl S,N- and N,N-acetals
inferred← citeshttps://doi.org/10.1016/j.ejmech.2007.12.014openalex-snapshot
Chemotherapy of leishmaniasis part-VIII: Synthesis and bioevaluation of novel chalcones
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.113084openalex-snapshot
Antimalarial application of quinones: A recent update
inferred← citeshttps://doi.org/10.1016/j.fct.2007.08.009openalex-snapshot
Genotoxic effects of tanshinones from Hyptis martiusii in V79 cell line
inferred← citeshttps://doi.org/10.1016/j.fitote.2012.05.005openalex-snapshot
Norditerpenoids from Salvia castanea Diels f. pubescens
inferred← citeshttps://doi.org/10.1016/j.fitote.2014.09.022openalex-snapshot
Salviprzols A and B, C21- and C22-terpenoids from the roots of Salvia przewalskii Maxim
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.08.024openalex-snapshot
Two novel terpenoids from the cultured Perovskia atriplicifolia
inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104826openalex-snapshot
Diterpenes from an Uzbek medicinal plant Perovskia scrophulariifolia: Their structures and anti-neuroinflammatory activity
inferred← citeshttps://doi.org/10.1016/j.indcrop.2015.01.015openalex-snapshot
Effects of some elicitors on tanshinone production in adventitious root cultures of Perovskia abrotanoides Karel
inferred← citeshttps://doi.org/10.1016/j.indcrop.2019.111592openalex-snapshot
Variation in the primary and secondary metabolites derived from the isoprenoid pathway in the Perovskia species in response to different wavelengths generated by light emitting diodes (LEDs)
inferred← citeshttps://doi.org/10.1016/j.indcrop.2022.115429openalex-snapshot
Essential oil composition, physiological and morphological variation in Salvia abrotanoides and S. yangii under drought stress and chitosan treatments
inferred← citeshttps://doi.org/10.1016/j.jchromb.2004.08.007openalex-snapshot
Separation methods of quinonoid constituents of plants used in Oriental traditional medicines
inferred← citeshttps://doi.org/10.1016/j.jep.2008.01.020openalex-snapshot
Study of embryotoxicity of Perovskia abrotanoides, an adulterant in folk-medicine, during organogenesis in mice
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2020.121360openalex-snapshot
Synthesis of novel 2,5-substituted p-aminophenols and 2,5-substituted p-quinones in a one-pot reaction between α-alkoxyvinyl(ethoxy)carbene complexes, amines and alkynes
inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.129447openalex-snapshot
Antileishmanial and pharmacophore modeling of abietane-type diterpenoids extracted from the roots of Salvia hydrangea
inferred← citeshttps://doi.org/10.1016/j.phrs.2010.02.007openalex-snapshot
Discovery of cyclooxygenase inhibitors from medicinal plants used to treat inflammation
inferred← citeshttps://doi.org/10.1016/j.phytochem.2009.05.004openalex-snapshot
Accelerated dereplication of crude extracts using HPLC–PDA–MS–SPE–NMR: Quinolinone alkaloids of Haplophyllum acutifolium
inferred← citeshttps://doi.org/10.1016/j.phytochem.2012.02.015openalex-snapshot
Abietane diterpenes induce cytotoxic effects in human pancreatic cancer cell line MIA PaCa-2 through different modes of action
inferred← citeshttps://doi.org/10.1016/j.phytochem.2016.10.012openalex-snapshot
Selective in vitro and in silico butyrylcholinesterase inhibitory activity of diterpenes and rosmarinic acid isolated from Perovskia atriplicifolia Benth. and Salvia glutinosa L.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113433openalex-snapshot
Reassessing the molecular structures of some previously isolated abietane diterpenoids with a naphthalene moiety and the structure-activity relationship (SAR) of quinone diterpenoids
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114523openalex-snapshot
Anti-inflammatory abietane-type diterpenoids from the roots of Salvia przewalskii
inferred← citeshttps://doi.org/10.1016/j.reprotox.2019.06.001openalex-snapshot
Evaluation of in vitro embryotoxicity tests for Chinese herbal medicines
inferred← citeshttps://doi.org/10.1016/j.resmic.2016.08.002openalex-snapshot
A tanshinone I derivative enhances the activities of antibiotics against Staphylococcus aureus in vitro and in vivo
inferred← citeshttps://doi.org/10.1016/j.sajb.2013.10.014openalex-snapshot
Antileishmanial activity of 12-methoxycarnosic acid from Salvia repens Burch. ex Benth. (Lamiaceae)
inferred← citeshttps://doi.org/10.1016/j.tet.2004.09.116openalex-snapshot
Synthesis of tri- and tetracyclic diterpenes. Cyclisations promoted by SmI2
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.05.056openalex-snapshot
Perovskatone A: a novel C23 terpenoid from Perovskia atriplicifolia
inferred← citeshttps://doi.org/10.1016/s0079-6468(05)43006-4openalex-snapshot
Recent Advances in the Search for Newer Antimalarial Agents
inferred← citeshttps://doi.org/10.1016/s0959-6380(02)80009-5openalex-snapshot
Chapter 5.3 Five-membered ring systems: Furans and benzofurans
inferred← citeshttps://doi.org/10.1016/s1572-5995(05)80036-5openalex-snapshot
Biological Activity of Quinones
inferred← citeshttps://doi.org/10.1017/s1742758408079861openalex-snapshot
Chemical composition and insecticidal activity of essential oil from Perovskia abrotanoides (Lamiaceae) against Sitophilus oryzae (Coleoptera: Curculionidae) and Tribolium castaneum (Coleoptera: Tenebrionidae)
inferred← citeshttps://doi.org/10.1021/acs.analchem.9b02377openalex-snapshot
Simplify: A Mass Spectrometry Metabolomics Approach to Identify Additives and Synergists from Complex Mixtures
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00832openalex-snapshot
Terpenoid Constituents of Perovskia artemisioides Aerial Parts with Inhibitory Effects on Bacterial Biofilm Growth
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c01256openalex-snapshot
Nor-abietane Diterpenoids fromPerovskia abrotanoidesRoots with Anti-inflammatory Potential
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c01004openalex-snapshot
Anti-inflammatory Activity of Tanshinone-Related Diterpenes from Perovskia artemisioides Roots
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02855openalex-snapshot
C28 Terpenoids from Lamiaceous Plant Perovskia scrophulariifolia: Their Structures and Anti-neuroinflammatory Activity
inferred← citeshttps://doi.org/10.1021/cr400552xopenalex-snapshot
Fruitful Decade for Antileishmanial Compounds from 2002 to Late 2011
inferred← citeshttps://doi.org/10.1021/jf058045copenalex-snapshot
Diterpenes from Salvia broussonetii Transformed Roots and Their Insecticidal Activity
inferred← citeshttps://doi.org/10.1021/mp700151bopenalex-snapshot
Terpenoids: Opportunities for Biosynthesis of Natural Product Drugs Using Engineered Microorganisms
inferred← citeshttps://doi.org/10.1021/np0106384openalex-snapshot
In Vitro Cytotoxic Activity of Phenanthroindolizidine Alkaloids from Cynanchum v incetoxicum and Tylophora t anakae against Drug-Sensitive and Multidrug-Resistant Cancer Cells
inferred← citeshttps://doi.org/10.1021/np0201826openalex-snapshot
New Dammarane and Malabaricane Triterpenes from Caloncoba echinata
inferred← citeshttps://doi.org/10.1021/np020244sopenalex-snapshot
Leishmanicidal and Antiplasmodial Activity of Constituents of Smirnowia iranica
inferred← citeshttps://doi.org/10.1021/np034033eopenalex-snapshot
Labdanes and Isopimaranes fromPlatycladus orientalisand Their Effects on Erythrocyte Membrane and onPlasmodiumfalciparumGrowth in the Erythrocyte Host Cells
inferred← citeshttps://doi.org/10.1021/np800119kopenalex-snapshot
Vascular Effects of Different Lipophilic Components of “Danshen”, a Traditional Chinese Medicine, in the Isolated Porcine Coronary Artery
inferred← citeshttps://doi.org/10.1021/np900047popenalex-snapshot
Semisynthesis and Biological Evaluation of Abietane-Type Diterpenes. Revision of the Structure of Rosmaquinone
inferred← citeshttps://doi.org/10.1021/ol034716lopenalex-snapshot
A New Class of Spermidine-Derived Alkaloids
inferred← citeshttps://doi.org/10.1038/s41467-019-12269-4openalex-snapshot
Organocatalytic atroposelective construction of axially chiral arylquinones
inferred← citeshttps://doi.org/10.1038/s41598-024-53510-5openalex-snapshot
Comparative transcriptomics of two Salvia subg. Perovskia species contribute towards molecular background of abietane-type diterpenoid biosynthesis
inferred← citeshttps://doi.org/10.1039/c3ra45146aopenalex-snapshot
Biotransformation of diterpenes
inferred← citeshttps://doi.org/10.1039/d3gc04154aopenalex-snapshot
Enantioselective cross-dehydrogenative coupling enabled by organocatalysis
inferred← citeshttps://doi.org/10.1055/a-0608-4946openalex-snapshot
Antiprotozoal Diterpenes from Perovskia abrotanoides
inferred← citeshttps://doi.org/10.1055/s-0030-1270933openalex-snapshot
Antiplasmodial and Antitrypanosomal Activity of Tanshinone-Type Diterpenoids fromSalvia miltiorrhiza
inferred← citeshttps://doi.org/10.1080/0972060x.2017.1358672openalex-snapshot
Effect of Abiotic Environmental Factors on Growth and Essential Oil Characteristics ofPerovskia abrotanoidesKarel.
inferred← citeshttps://doi.org/10.1080/10826068.2016.1168745openalex-snapshot
The production and antiprotozoal activity of abietane diterpenes in Salvia austriaca hairy roots grown in shake flasks and bioreactor
inferred← citeshttps://doi.org/10.1080/13880200490514078openalex-snapshot
The Essential Oil Composition ofPerovskia abrotanoidesfrom Iran
inferred← citeshttps://doi.org/10.1080/14786419.2015.1101694openalex-snapshot
Chemical composition and antimicrobial activities of Perovskia artemisioides Boiss. essential oil
inferred← citeshttps://doi.org/10.1080/14786419.2019.1684280openalex-snapshot
Perovskanol, a new sesquiterpenoid with an unprecedented skeleton from Perovskia Abrotanoides
inferred← citeshttps://doi.org/10.1080/14786419.2022.2057492openalex-snapshot
Exploring SARS-CoV-2 Delta variant spike protein receptor-binding domain (RBD) as a target for tanshinones and antimalarials
inferred← citeshttps://doi.org/10.1080/14786419.2024.2372829openalex-snapshot
Two undescribed constituents from Salvia castanea Diels and evaluation of their cytotoxic activity
inferred← citeshttps://doi.org/10.1080/15569543.2019.1691013openalex-snapshot
The genus Perovskia Kar.: ethnobotany, chemotaxonomy and phytochemistry: a review
inferred← citeshttps://doi.org/10.1080/16878507.2021.1957397openalex-snapshot
Assessment of pollution at the former uranium waste dumpsite near kaji-Say Village/Kyrgyzstan: a genetic and physiological investigation
inferred← citeshttps://doi.org/10.1093/chromsci/42.4.211openalex-snapshot
Evaluation of Pressurized Liquid Extraction and Pressurized Hot Water Extraction for Tanshinone I and IIA in Salvia miltiorrhiza Using LC and LC-ESI-MS
inferred← citeshttps://doi.org/10.1097/00001432-200212000-00007openalex-snapshot
Advances in the treatment of leishmaniasis
inferred← citeshttps://doi.org/10.1111/cbdd.13197openalex-snapshot
Coptisine, a natural alkaloid from Coptidis Rhizoma, inhibits plasmodium falciparum dihydroorotate dehydrogenase
inferred← citeshttps://doi.org/10.1155/2014/540516openalex-snapshot
Tanshinone IIA Induces Apoptosis in Human Oral Cancer KB Cells through a Mitochondria-Dependent Pathway
inferred← citeshttps://doi.org/10.1155/2024/5526562openalex-snapshot
The Use of Perovskia abrotanoides Extract in Ameliorating Heat Stress‐Induced Oxidative Damage and Improving Growth Efficiency in Carp Juveniles (Cyprinus carpio)
inferred← citeshttps://doi.org/10.1177/1934578x0600101218openalex-snapshot
Non-nitrogenous Plant-derived Constituents with Antiplasmodial Activity
inferred← citeshttps://doi.org/10.1177/1934578x1300801133openalex-snapshot
Chemical Analysis and Calcium Channel Blocking Activity of the Essential Oil of Perovskia abrotanoides
inferred← citeshttps://doi.org/10.1177/1934578x1501000703openalex-snapshot
Isolation and Fast Selective Determination of Nor-abietanoid Diterpenoids from Perovskia atriplicifolia Roots Using LC-ESI-MS/MS with Multiple Reaction Monitoring
inferred← citeshttps://doi.org/10.1186/0717-6287-47-12openalex-snapshot
Compositional studies and Biological activities of Perovskia abrotanoides Kar. oils
inferred← citeshttps://doi.org/10.1248/bpb.26.845openalex-snapshot
Isolation and Quantitative Analysis of Cryptotanshinone, an Active Quinoid Diterpene Formed in Callus of Salvia miltiorrhiza BUNGE
inferred← citeshttps://doi.org/10.1248/cpb.53.1524openalex-snapshot
Quinone Derivatives by Chemical Transformations of 16-Hydroxycarnosol from Salvia Species
inferred← citeshttps://doi.org/10.1248/cpb.54.1602openalex-snapshot
Semisynthesis of Isetexane Diterpenoid Analogues and Their Cytotoxic Activity
inferred← citeshttps://doi.org/10.1515/znc-2006-3-404openalex-snapshot
Cytotoxic Abietane Diterpenes from Hyptis martiusii Benth.
inferred← citeshttps://doi.org/10.1517/14728222.6.4.407openalex-snapshot
Promising therapeutic targets for antileishmanial drugs
inferred← citeshttps://doi.org/10.1517/17425240903548232openalex-snapshot
Drug delivery strategies for therapy of visceral leishmaniasis
inferred← citeshttps://doi.org/10.21203/rs.3.rs-10063911/v1openalex-snapshot
Fungal–Fungal Interactions Drive Metabolic Reprogramming in Root-Associated Endophytes of Salvia abrotanoides
inferred← citeshttps://doi.org/10.2174/092986712800229023openalex-snapshot
The Potential of Secondary Metabolites from Plants as Drugs or Leads Against Protozoan Neglected Diseases - Part I
inferred← citeshttps://doi.org/10.2174/09298673113206660291openalex-snapshot
Combating Malaria with Plant Molecules: A Brief Update
inferred← citeshttps://doi.org/10.2174/1389201020666190618121218openalex-snapshot
Green and Simple Synthesis of Silver Nanoparticles by Aqueous Extract of Perovskia abrotanoides: Characterization, Optimization and Antimicrobial Activity
inferred← citeshttps://doi.org/10.2174/1574884709999140606161413openalex-snapshot
Plants Used in Traditional Medicine: Extracts and Secondary Metabolites Exhibiting Antileishmanial Activity
inferred← citeshttps://doi.org/10.2174/1874842202007010026openalex-snapshot
Evaluation of Safety, Antileishmanial, and Chemistry of Ethanolic Leaves Extracts of Seven Medicinal Plants: An In-vitro Study
inferred← citeshttps://doi.org/10.2174/2210315509666190425125312openalex-snapshot
Protective Ability of Perovskia abrotanoides Karel Root Extract on the Aggregation of Protein In Vitro
inferred← citeshttps://doi.org/10.22038/ijbms.2017.9568openalex-snapshot
Cytotoxic and apoptotic effects of root extract and tanshinones isolated from Perovskiaabrotanoides Kar.
inferred← citeshttps://doi.org/10.22038/ijbms.2023.67730.14828openalex-snapshot
Beneficial effects of endophytic fungi inoculation on tanshinones and phenolic compounds of Salvia abrotanoides.
inferred← citeshttps://doi.org/10.29252/koomesh.23.2.291openalex-snapshot
Anticancer effects of Perovskia abrotanoides hydroalcoholic extracts on MKN45 gastric cancer cells
inferred← citeshttps://doi.org/10.30699/jambs.27.122.17openalex-snapshot
A Study on the Effects of Perovskia abrotanoides Karel on Experimental Skin Burn in Male Rat: in-vivo and in-vitro Findings
inferred← citeshttps://doi.org/10.31083/ph.2009.9543openalex-snapshot
Antimicrobial and cytotoxic abietane diterpenoids from the roots of Meriandera benghalensis (Roxb.) Benth
inferred← citeshttps://doi.org/10.3184/174751913x13618945224197openalex-snapshot
Synthesis of Diterpenoid Rosmic Acid Derivatives
inferred← citeshttps://doi.org/10.3389/fmicb.2019.03013openalex-snapshot
Endophytic Fungi of Native Salvia abrotanoides Plants Reveal High Taxonomic Diversity and Unique Profiles of Secondary Metabolites
inferred← citeshttps://doi.org/10.3390/agriculture10110543openalex-snapshot
Bioactive Products from Endophytic Fungi of Sages (Salvia spp.)
inferred← citeshttps://doi.org/10.3390/agriculture12020187openalex-snapshot
Using Next-Generation Sequencing Technology to Explore Genetic Pathways in Endophytic Fungi in the Syntheses of Plant Bioactive Metabolites
inferred← citeshttps://doi.org/10.3390/agronomy14040835openalex-snapshot
Salvia Species: Biotechnological Strategies Applied to In Vitro Cultures for the Controlled Production of Bioactive Diterpenoids
inferred← citeshttps://doi.org/10.3390/biology10060458openalex-snapshot
Seasonal Variations of Rosmarinic Acid and Its Glucoside and Expression of Genes Related to Their Biosynthesis in Two Medicinal and Aromatic Species of Salvia subg. Perovskia
inferred← citeshttps://doi.org/10.3390/biology11121757openalex-snapshot
Mycorrhizal Colonization Modulates the Essential Oil Profile and Enzymatic and Non-Enzymatic Antioxidants to Mitigate the Adverse Effects of Water Deficit in Salvia subg. Perovskia
inferred← citeshttps://doi.org/10.3390/cells10010112openalex-snapshot
Metabolomics and DNA-Based Authentication of Two Traditional Asian Medicinal and Aromatic Species of Salvia subg. Perovskia
inferred← citeshttps://doi.org/10.3390/genes14040871openalex-snapshot
The Influence of Methyl Jasmonate on Expression Patterns of Rosmarinic Acid Biosynthesis Genes, and Phenolic Compounds in Different Species of Salvia subg. Perovskia Kar L.
inferred← citeshttps://doi.org/10.3390/ijms15058360openalex-snapshot
In Vitro Antiprotozoal Activity of Abietane Diterpenoids Isolated from Plectranthus barbatus Andr.
inferred← citeshttps://doi.org/10.3390/ijms21124475openalex-snapshot
Norditerpenoids with Selective Anti-Cholinesterase Activity from the Roots of Perovskia atriplicifolia Benth.
inferred← citeshttps://doi.org/10.3390/ijms252312566openalex-snapshot
Chemical Composition, Physiological and Morphological Variations in Salvia subg. Perovskia Populations in Response to Different Salinity Levels
inferred← citeshttps://doi.org/10.3390/metabo12060534openalex-snapshot
Production and Functionalities of Specialized Metabolites from Different Organic Sources
inferred← citeshttps://doi.org/10.3390/molecules28114504openalex-snapshot
Identification of Chemical Constituents in Blumea balsamifera Using UPLC–Q–Orbitrap HRMS and Evaluation of Their Antioxidant Activities
inferred← citeshttps://doi.org/10.3390/plants7040105openalex-snapshot
Biological Activities of Extracts from Aerial Parts of Salvia pachyphylla Epling Ex Munz
inferred← citeshttps://doi.org/10.4103/0250-474x.56016openalex-snapshot
The antimicrobial activity of essential oil fromPerovskia abrotanoideskarel and its main components
inferred← citeshttps://doi.org/10.4103/1735-5362.371587openalex-snapshot
Bioassay-guided isolation in Salvia abrotanoides Karel. stem based on its anti-fungal and anti-trichomonas activity
inferred← citeshttps://doi.org/10.4103/abr.abr_243_23openalex-snapshot
The Therapeutic Effect of Shirvan Herbal Ointment on Human Cutaneous Leishmaniasis Compared with Glucantime
inferred← citeshttps://doi.org/10.4103/jrpp.jrpp_13_24openalex-snapshot
The Effectiveness of Perovskia abrotanoides Extract Topical Formulation on the Cutaneous Leishmaniasis: A Randomized Controlled Clinical Trial
inferred← citeshttps://doi.org/10.52547/koomesh.23.2.291openalex-snapshot
Anticancer effects of Perovskia abrotanoides hydroalcoholic extracts on MKN45 gastric cancer cells
inferred← citeshttps://doi.org/10.5897/jmpr2013.5095openalex-snapshot
Induction of callogenesis and rhizogenesis in Perovskia abrotanoides Karel., a little known medicinal plant
inferred← citeshttps://doi.org/10.61186/mlj.17.3.45openalex-snapshot
Perovskia abrotanoides Kar. as a Promising Source of Antimicrobial Compounds against Foodborne Pathogens
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.