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Physanolide A, a Novel Skeleton Steroid, and Other Cytotoxic Principles from Physalis angulata
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0006-291x(89)92226-2openalex-snapshot
A new compound, withangulatin A, promotes type II DNA topoisomerase-mediated DNA damage
inferredcites →https://doi.org/10.1016/s0031-9422(03)00183-3openalex-snapshot
Chemical and cytotoxic constituents from Peperomia sui
inferredcites →https://doi.org/10.1016/s0367-326x(01)00281-7openalex-snapshot
A novel cytotoxic flavonoid glycoside from Physalis angulata
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/np50098a021openalex-snapshot
Insect Inhibitory Steroidal Saccharide Esters from Physalis peruviana
inferredcites →https://doi.org/10.1021/np50105a003openalex-snapshot
Insect Inhibitory Steroidal Saccharide Esters from Physalis peruviana
inferredcites →https://doi.org/10.1021/np50125a004openalex-snapshot
Structural Revision of Physalin H Isolated from Physalis angulata
inferredcites →https://doi.org/10.1039/np9910800415openalex-snapshot
Withanolides and related ergostane-type steroids
inferredcites →https://doi.org/10.1080/10286020108041391openalex-snapshot
The Structure of Physalin T fromPhysalis alkekengivar.francheti
inferredcites →https://doi.org/10.1248/cpb.39.1591openalex-snapshot
Studies on the constituents of the solanaceous plants. Part XXI. Physagulin C, a New Withanolide from Physalis angulata L.
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.2020.112651zenodo-depositor-declared
Structurally diverse steroids with nitric oxide inhibitory activities from Aglaia lawii leaves
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/ange.200900634openalex-snapshot
Synthesis of the DFGH ring system of Type B Physalins: Highly Oxygenated, Cage‐Shaped Molecules
inferred← citeshttps://doi.org/10.1002/anie.200900634openalex-snapshot
Synthesis of the DFGH ring system of Type B Physalins: Highly Oxygenated, Cage‐Shaped Molecules
inferred← citeshttps://doi.org/10.1002/bmc.3678openalex-snapshot
In vivo pharmacokinetics of and tissue distribution study of physalin B after intravenous administration in rats by liquid chromatography with tandem mass spectrometry
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/chin.200646214openalex-snapshot
Physanolide A, a Novel Skeleton Steroid, and Other Cytotoxic Principles from Physalis angulata.
inferred← citeshttps://doi.org/10.1002/ejoc.200700172openalex-snapshot
Versatile Methodology to Synthesize Oxygen‐Bridged Nine‐ and Ten‐Membered Cycloalkanes by the Hypoiodite Reaction
inferred← citeshttps://doi.org/10.1002/hlca.200890248openalex-snapshot
Withanolides from Physalis alkekengi var. francheti
inferred← citeshttps://doi.org/10.1002/ijch.201600110openalex-snapshot
Synthesis of the Right‐Side Structure of Type B Physalins
inferred← citeshttps://doi.org/10.1002/jssc.201700038openalex-snapshot
Identification and quantitative analysis of physalin D and its metabolites in rat urine and feces by liquid chromatography with triple quadrupole time‐of‐flight mass spectrometry
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/10.1016/j.ejmech.2012.12.017openalex-snapshot
A new cytotoxic quinolone alkaloid and a pentacyclic steroidal glycoside from the stem bark of Crataeva nurvala: Study of anti-proliferative and apoptosis inducing property
inferred← citeshttps://doi.org/10.1016/j.fitote.2024.106124openalex-snapshot
Anti-tumor withanolides as signal transducers and activators of transcription 3 (STAT3)-inhibition from Withania obtusifolia
inferred← citeshttps://doi.org/10.1016/j.jinsphys.2007.12.004openalex-snapshot
Immune depression in Rhodnius prolixus by seco-steroids, physalins
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2010.09.025openalex-snapshot
Synthetic evolutions in the nucleophilic addition to alkynes
inferred← citeshttps://doi.org/10.1016/j.jpba.2011.09.012openalex-snapshot
An ultra-pressure liquid chromatography–tandem mass spectrometry method for the simultaneous determination of three physalins in rat plasma and its application to pharmacokinetic study of Physalis alkekengi var. franchetii (Chinese lantern) in rats
inferred← citeshttps://doi.org/10.1016/j.jpba.2012.08.020openalex-snapshot
Characterization of physalins and fingerprint analysis for the quality evaluation of Physalis alkekengi L. var. franchetii by ultra-performance liquid chromatography combined with diode array detection and electrospray ionization tandem mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.jsbmb.2013.05.011openalex-snapshot
Current status on development of steroids as anticancer agents
inferred← citeshttps://doi.org/10.1016/j.procbio.2010.09.022openalex-snapshot
Immunosuppression effect of Withangulatin A from Physalis angulata via heme oxygenase 1-dependent pathways
inferred← citeshttps://doi.org/10.1016/j.steroids.2010.01.014openalex-snapshot
Virginols A–C, three new withanolides from Physalis virginiana
inferred← citeshttps://doi.org/10.1016/j.steroids.2014.04.015openalex-snapshot
Induction of quinone reductase (QR) by withanolides isolated from Physalis angulata L. var. villosa Bonati (Solanaceae)
inferred← citeshttps://doi.org/10.1016/j.steroids.2015.08.015openalex-snapshot
Cytotoxic 20,24-epoxywithanolides from Physalis angulata
inferred← citeshttps://doi.org/10.1016/j.tet.2009.09.066openalex-snapshot
5,10:13,14-Disecosteroids: novel modified steroids containing 10- and 9-membered rings
inferred← citeshttps://doi.org/10.1016/j.tet.2017.03.029openalex-snapshot
Ionic hydrogenation-directed stereoselective construction of C-20(H) stereogenic center in steroid side chains: Scope and limitations
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.11.081openalex-snapshot
Withaphysanolide A, a novel C-27 norwithanolide skeleton, and other cytotoxic compounds from Physalis divericata
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151555openalex-snapshot
Phosteoid A, a highly oxygenated norsteroid from the deep-sea-derived fungus Phomopsis tersa FS441
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00380openalex-snapshot
Cytotoxic Physalins from Aeroponically Grown Physalis acutifolia
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02049openalex-snapshot
Asperfloketals A and B, the First Two Ergostanes with Rearranged A and D Rings: From the Sponge-Associated Aspergillus flocculosus 16D-1
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03255openalex-snapshot
Synthesis of DFGH-Ring Derivatives of Physalins via One-Pot Construction of GH-Ring and Evaluation of Their NF-κB-Inhibitory Activity
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02821openalex-snapshot
Tricholumin A, a Highly Transformed Ergosterol Derivative from the Alga-Endophytic Fungus Trichoderma asperellum
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00539openalex-snapshot
Urceoloids A and B, Two C19 Steroids with a Rearranged Spirocyclic Carbon Skeleton from Urceola quintaretii
inferred← citeshttps://doi.org/10.1021/cr4004083openalex-snapshot
A Concise Account of Various Approaches for Stereoselective Construction of the C-20(H) Stereogenic Center in Steroid Side Chain
inferred← citeshttps://doi.org/10.1021/je100227kopenalex-snapshot
Solubility of Physalin D in Ethanol, Methanol, Propanone, Trichloromethane, Ethyl Ethanoate, and Water at Temperatures from (283.2 to 313.2) K
inferred← citeshttps://doi.org/10.1021/np400296sopenalex-snapshot
Withanolide Artifacts Formed in Methanol
inferred← citeshttps://doi.org/10.1021/ol203498aopenalex-snapshot
Physangulidines A, B, and C: Three New Antiproliferative Withanolides from Physalis angulata L.
inferred← citeshttps://doi.org/10.1021/ol902215nopenalex-snapshot
Highly Efficient and Tunable Synthesis of Dioxabicyclo[4.2.1] Ketals and Tetrahydropyrans via Gold-Catalyzed Cycloisomerization of 2-Alkynyl-1,5-diols
inferred← citeshttps://doi.org/10.1039/b611850jopenalex-snapshot
Editorial: Natural products chemistry in China
inferred← citeshttps://doi.org/10.1080/00032719.2017.1331238openalex-snapshot
Rapid Determination of Phenolics, Flavonoids, and Antioxidant Properties ofPhysalis ixocarpaBrot. ex Hornem. andPhysalis angulataL. by Infrared Spectroscopy and Partial Least Squares
inferred← citeshttps://doi.org/10.1080/14786419.2018.1550766openalex-snapshot
A new 22,26-seco physalin steroid from Physalis angulata
inferred← citeshttps://doi.org/10.1097/cad.0000000000000701openalex-snapshot
Physalin B induces G2/M cell cycle arrest and apoptosis in A549 human non-small-cell lung cancer cells by altering mitochondrial function
inferred← citeshttps://doi.org/10.1155/2018/7943140openalex-snapshot
Physalin B Suppresses Inflammatory Response to Lipopolysaccharide in RAW264.7 Cells by Inhibiting NF-κB Signaling
inferred← citeshttps://doi.org/10.1155/2022/1589877openalex-snapshot
Traditional and Phytochemical Bases of Herbs, Shrubs, Climbers, and Trees from Ethiopia for Their Anticancer Response
inferred← citeshttps://doi.org/10.1177/1934578x0800300420openalex-snapshot
Toxic Chemical Compounds of the Solanaceae
inferred← citeshttps://doi.org/10.1177/1934578x1701201016openalex-snapshot
A Novel Cytotoxic Physalin from Physalis angulata
inferred← citeshttps://doi.org/10.1248/cpb.56.234openalex-snapshot
Withangulatin I, a New Cytotoxic Withanolide from Physalis angulata
inferred← citeshttps://doi.org/10.1371/journal.pone.0040727openalex-snapshot
Physalin F Induces Cell Apoptosis in Human Renal Carcinoma Cells by Targeting NF-kappaB and Generating Reactive Oxygen Species
inferred← citeshttps://doi.org/10.1590/s0102-695x2011005000106openalex-snapshot
Plants from Solanaceae family with possible anxiolytic effect reported on 19th century's Brazilian medical journal
inferred← citeshttps://doi.org/10.26656/fr.2017.3(6).169openalex-snapshot
Extract of ceplukan (Physalis angulata L.) inhibited proliferation and induced apoptosis in myeloma cell line
inferred← citeshttps://doi.org/10.26722/rpmi.2023.v8n1.709openalex-snapshot
Revisión de reportes etnomédicos antitumorales de las plantas del Jardín Botánico del Instituto de Medicina Tradicional de EsSalud en Iquitos, Perú
inferred← citeshttps://doi.org/10.32604/biocell.2008.32.195openalex-snapshot
Genotoxic effect of Physalis angulata L. (Solanaceae) extract on human lymphocytes treated in vitro
inferred← citeshttps://doi.org/10.3390/md19060324openalex-snapshot
Antitumor Profile of Carbon-Bridged Steroids (CBS) and Triterpenoids
inferred← citeshttps://doi.org/10.3390/molecules28155669openalex-snapshot
Fascinating Furanosteroids and Their Pharmacological Profile
inferred← citeshttps://doi.org/10.3390/ph16020160openalex-snapshot
Withaferin A: A Pleiotropic Anticancer Agent from the Indian Medicinal Plant Withania somnifera (L.) Dunal
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