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Antileishmanial Physalins fromPhysalis minima
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ptr.2650010106openalex-snapshot
Antileishmanial activity of harmaline and other tryptamine derivatives
inferredcites →https://doi.org/10.1002/ptr.2650040402openalex-snapshot
Natural products and the development of selective antiprotozoal drugs
inferredcites →https://doi.org/10.1002/ptr.939openalex-snapshot
Antimycobacterial physalins from Physalis angulata L. (Solanaceae)
inferredcites →https://doi.org/10.1016/0031-9422(93)80040-yopenalex-snapshot
Physalin and neophysalins from Physalis alkekengi var. francheti and their differentiation inducing activity
inferredcites →https://doi.org/10.1016/0035-9203(87)90013-7openalex-snapshot
Antiprotozoal activity of diospyrin towards Leishmania donovani promastigotes in vitro
inferredcites →https://doi.org/10.1016/0040-4020(95)00807-kopenalex-snapshot
New physalins possessing an additional carbon-carbon bond from Physalis alkekengi var. francheti
inferredcites →https://doi.org/10.1016/0378-8741(95)01288-oopenalex-snapshot
Antigonorrhoeal activity of plants used in Guatemala for the treatment of sexually transmitted diseases
inferredcites →https://doi.org/10.1016/s0031-9422(00)82292-xopenalex-snapshot
Withaminimin, a withanolide from Physalis minima
inferredcites →https://doi.org/10.1016/s0031-9422(00)94660-0openalex-snapshot
The structure of Physalins F and J from Physalis angulata and P. Lancifolia
inferredcites →https://doi.org/10.1016/s0031-9422(99)00416-1openalex-snapshot
Three withanolides from Withania coagulans
inferredcites →https://doi.org/10.1016/s0040-4039(01)97745-7openalex-snapshot
Bitter principles of structure of physalin a
inferredcites →https://doi.org/10.1016/s0378-8741(03)00280-0openalex-snapshot
Investigations of anti-inflammatory and antinociceptive activities of Piper cubeba, Physalis angulata and Rosa hybrida
inferredcites →https://doi.org/10.1016/s0944-7113(00)80052-5openalex-snapshot
In vitro antimycobacterial activities of Physalis angulata L
inferredcites →https://doi.org/10.1021/np50125a004openalex-snapshot
Structural Revision of Physalin H Isolated from Physalis angulata
inferredcites →https://doi.org/10.1039/b100455gopenalex-snapshot
Plant natural products with leishmanicidal activity.
inferredcites →https://doi.org/10.1039/j29700000812openalex-snapshot
Crystal and molecular structure of 5α-acetoxy-6β-bromohexahydrophysalin A
inferredcites →https://doi.org/10.1039/j39710002032openalex-snapshot
Constitutents of Withania somnifera Dun. Part XII. The withanolides of an indian chemotype
inferredcites →https://doi.org/10.1080/1057563021000040835openalex-snapshot
Microbial Transformation of Dehydroepiandrosterone
inferredcites →https://doi.org/10.1142/s0192415x92000242openalex-snapshot
Immunomodulatory Activity of Various Fractions Derived from Physalis angulata L Extract
inferredcites →https://doi.org/10.1246/bcsj.68.219openalex-snapshot
Physalins Possessing an Endoperoxy Structure from Physalis alkekengi var. francheti. Structural Revision of Physalin K
inferredcites →https://doi.org/10.1248/bpb.27.193openalex-snapshot
Trypanocidal Constituents in Plants: 4. Withanolides from the Aerial Parts of Physalis angulata
inferredcites →https://doi.org/10.1248/cpb.36.4316openalex-snapshot
The structural elucidation of fritillaria alkaloids from Fritillaria ebeiensis var. purpurea. I. The structures of ebeienine, ebeiedine and ebeiedinone.
inferredcites →https://doi.org/10.1248/cpb.51.530openalex-snapshot
Minor Withanolides from Physalis philadelphica: Structures, Quinone Reductase Induction Activities, and Liquid Chromatography (LC)-MS-MS Investigation as Artifacts
inferredcites →https://doi.org/10.1248/cpb.52.1358openalex-snapshot
Cholinesterase Inhibiting Withanolides from Withania somnifera
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.2021.112925zenodo-depositor-declared
Naturally occurring physalins from the genus Physalis: A review
inferred← citeshttps://doi.org/10.1002/cbdv.201400435openalex-snapshot
Chemical Constituents and Biological Activities of Plants from the Genus Physalis
inferred← citeshttps://doi.org/10.1002/cbdv.201500282openalex-snapshot
13,14‐seco‐Withanolides from Physalis minima with Potential Anti‐inflammatory Activity
inferred← citeshttps://doi.org/10.1002/hlca.200890248openalex-snapshot
Withanolides from Physalis alkekengi var. francheti
inferred← citeshttps://doi.org/10.1002/hlca.201000126openalex-snapshot
Withanolides from Aureliana fasciculata var. fasciculata
inferred← citeshttps://doi.org/10.1007/978-3-642-22144-6_150openalex-snapshot
Withanolides: Chemistry and Antitumor Activity
inferred← citeshttps://doi.org/10.1007/978-3-7091-0748-5_3openalex-snapshot
Withanolides and Related Steroids
inferred← citeshttps://doi.org/10.1007/s00210-026-05354-1openalex-snapshot
Physalis minima L.: A comprehensive review on phytochemistry, pharmacology, and food applications
inferred← citeshttps://doi.org/10.1007/s10600-015-1517-zopenalex-snapshot
Chemical Constituents of Physalis alkekengi var. franchetii
inferred← citeshttps://doi.org/10.1007/s11101-015-9420-6openalex-snapshot
Phytochemistry and biosynthesis of δ-lactone withanolides
inferred← citeshttps://doi.org/10.1007/s11130-020-00821-3openalex-snapshot
A review of nutritional properties and health benefits of Physalis species
inferred← citeshttps://doi.org/10.1016/j.aspen.2026.102533openalex-snapshot
Insecticidal activity against mosquito larvae, leishmanicidal activity, and cytotoxicity against human cells of a synthesized thiourea compound and a column chromatography fraction (AF5) from the n-hexane soluble fraction of Artemisia scoparia
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107630openalex-snapshot
13,14-Seco Withaphysalins from Physalis Minima and Their Inhibitory Effects on Nlrp3 Inflammasome Activation
inferred← citeshttps://doi.org/10.1016/j.biopha.2022.114012openalex-snapshot
Withaferin A-silyl ether analogs as potential anti-kinetoplastid agents targeting the programmed cell death
inferred← citeshttps://doi.org/10.1016/j.fitote.2012.10.015openalex-snapshot
Editorial for Special Issue of Fitoterapia
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104728openalex-snapshot
New cytotoxic withanolides from Physalis minima
inferred← citeshttps://doi.org/10.1016/j.foohum.2024.100395openalex-snapshot
Global insights into Physalis research: A bibliometric journey from origin to recent advances
inferred← citeshttps://doi.org/10.1016/j.hermed.2023.100763openalex-snapshot
An insight into indigenous ethnobotanical and pharmacological potential of Solanaceae family in Pakistan: a review
inferred← citeshttps://doi.org/10.1016/j.inoche.2025.114546openalex-snapshot
Synthesis of Physalis minima L. based AuNPs: Insights in their antimicrobial, antioxidant and anticancer activity
inferred← citeshttps://doi.org/10.1016/j.jep.2021.114588openalex-snapshot
Medicinal plants used against hepatic disorders in Bangladesh: A comprehensive review
inferred← citeshttps://doi.org/10.1016/j.phytol.2017.06.014openalex-snapshot
New coumestan and coumaronochromone derivatives from Dalbergia boehmii Taub. (Fabaceae)
inferred← citeshttps://doi.org/10.1016/j.redox.2017.02.017openalex-snapshot
Importance of ROS-mediated autophagy in determining apoptotic cell death induced by physapubescin B
inferred← citeshttps://doi.org/10.1016/s1875-5364(21)60090-0openalex-snapshot
Physalin B reduces Aβ secretion through down-regulation of BACE1 expression by activating FoxO1 and inhibiting STAT3 phosphorylation
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c12654openalex-snapshot
Withanolides from Physalis angulata as Potent Antimelanoma Agents: Activation of the p53 Pathway In Vitro and In Vivo
inferred← citeshttps://doi.org/10.1021/cr400552xopenalex-snapshot
Fruitful Decade for Antileishmanial Compounds from 2002 to Late 2011
inferred← citeshttps://doi.org/10.1021/np400296sopenalex-snapshot
Withanolide Artifacts Formed in Methanol
inferred← citeshttps://doi.org/10.1021/np700713ropenalex-snapshot
Steroids and Flavonoids from Physalis alkekengi var. franchetii and Their Inhibitory Effects on Nitric Oxide Production
inferred← citeshttps://doi.org/10.1038/s41598-017-03849-9openalex-snapshot
Physalins V-IX, 16,24-cyclo-13,14-seco withanolides from Physalis angulata and their antiproliferative and anti-inflammatory activities
inferred← citeshttps://doi.org/10.1039/c6ob02656gopenalex-snapshot
A novel withanolide with an unprecedented carbon skeleton from Physalis angulata
inferred← citeshttps://doi.org/10.1039/c7ob02205kopenalex-snapshot
Unprecedented 22,26-seco physalins from Physalis angulata and their anti-inflammatory potential
inferred← citeshttps://doi.org/10.1039/c8ob00194dopenalex-snapshot
Synthesis of the 10-oxabicyclo[5.2.1]decane framework present in bioactive natural products
inferred← citeshttps://doi.org/10.1039/d0ra04106hopenalex-snapshot
New withanolides from Physalis minima and their cytotoxicity against A375 human melanoma cells
inferred← citeshttps://doi.org/10.1080/14786419.2013.766053openalex-snapshot
Professor Atta-ur-Rahman: towering scientific achievements
inferred← citeshttps://doi.org/10.1080/14786419.2024.2354858openalex-snapshot
Two new withanolides from Physalis minima L
inferred← citeshttps://doi.org/10.1111/jphp.13209openalex-snapshot
Withanolides from the genus Physalis: a review on their phytochemical and pharmacological aspects
inferred← citeshttps://doi.org/10.1128/aac.00583-22openalex-snapshot
Antileishmanial Activities of ( Z )-2-(Nitroimidazolylmethylene)-3( 2H )-Benzofuranones: Synthesis, In Vitro Assessment, and Bioactivation by NTR 1 and 2
inferred← citeshttps://doi.org/10.1177/1934578x0800300420openalex-snapshot
Toxic Chemical Compounds of the Solanaceae
inferred← citeshttps://doi.org/10.12980/jclm.3.201514j92openalex-snapshot
Quantification of methyl esters of fatty acids in the oil of Physalis minima by GC-MS
inferred← citeshttps://doi.org/10.13140/rg.2.2.33877.09441openalex-snapshot
EFFECT OF DIFFERENT WEED MANAGEMENT PRACTICES ON SOIL BACTERIAL POPULATION UNDER DIFFERENT CROPS
inferred← citeshttps://doi.org/10.1351/pac200880081783openalex-snapshot
Discovery of leishmanicidal agents from medicinal plants
inferred← citeshttps://doi.org/10.1371/journal.pone.0274543openalex-snapshot
Anti-leishmanial physalins—Phytochemical investigation, in vitro evaluation against clinical and MIL-resistant L. tropica strains and in silico studies
inferred← citeshttps://doi.org/10.14233/ajchem.2021.23067openalex-snapshot
Bioactive Phytochemical Compounds of Physalis minima L. and its Anticholinesterase and Antioxidant Activities
inferred← citeshttps://doi.org/10.1590/s0102-695x2010005000036openalex-snapshot
Effects of seco-steroids purified from Physalis angulata L., Solanaceae, on the viability of Leishmania sp
inferred← citeshttps://doi.org/10.2174/1574884709999140606161413openalex-snapshot
Plants Used in Traditional Medicine: Extracts and Secondary Metabolites Exhibiting Antileishmanial Activity
inferred← citeshttps://doi.org/10.3109/13880200903062606openalex-snapshot
Antimicrobial activity of the extracts and physalin D fromPhysalis alkekengiand evaluation of antioxidant potential of physalin D
inferred← citeshttps://doi.org/10.3389/fphar.2022.864714openalex-snapshot
Therapeutic Applications of Physalins: Powerful Natural Weapons
inferred← citeshttps://doi.org/10.3389/fphar.2023.1119419openalex-snapshot
Prof. Dr. M. Iqbal Choudhary-A lifetime career dedicated to remarkable services in “natural products sciences”
inferred← citeshttps://doi.org/10.3390/molecules23123160openalex-snapshot
Leishmanicidal Activity of Withanolides from Aureliana fasciculata var. fasciculata
inferred← citeshttps://doi.org/10.3390/plants12091813openalex-snapshot
Potential Plant-Based New Antiplasmodial Agent Used in Papua Island, Indonesia
inferred← citeshttps://doi.org/10.5155/eurjchem.8.4.422-429.1651openalex-snapshot
Synthesis, single crystal X-ray diffraction, Hirshfeld surface and biological activity of quinolone derivatives
inferred← citeshttps://doi.org/10.6000/1927-5129.2016.12.37openalex-snapshot
In-Vitro Antileishmanial Activity of Raphanus sativus L. var. caudatus
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