On the public citation graph

Steroids and Flavonoids from Physalis alkekengi var. franchetii and Their Inhibitory Effects on Nitric Oxide Production

https://doi.org/10.1021/np700713r
0 signed · 133 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/cbdv.200590086openalex-snapshot
Antileishmanial Physalins fromPhysalis minima
inferredcites →https://doi.org/10.1002/hlca.200790098openalex-snapshot
Two Novel Neophysalins from Physalis alkekengi L. var. franchetii
inferredcites →https://doi.org/10.1002/ptr.939openalex-snapshot
Antimycobacterial physalins from Physalis angulata L. (Solanaceae)
inferredcites →https://doi.org/10.1016/0031-9422(92)80462-nopenalex-snapshot
Physalins N and O from Physalis alkekengi
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/10.1016/0040-4020(78)88336-7openalex-snapshot
Carbon-13 NMR studies of flavonoids—III
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/s0014-2999(02)02829-7openalex-snapshot
Inhibition of macrophage activation and lipopolysaccaride-induced death by seco-steroids purified from Physalis angulata L.
inferredcites →https://doi.org/10.1016/s0031-9422(00)82495-4openalex-snapshot
A New physalin from Physalis alkekengi: structure of physalin L
inferredcites →https://doi.org/10.1016/s0031-9422(00)94659-4openalex-snapshot
Physalins E and H, new physalins from Physalis angulata and P. lancifolia
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(01)00066-8openalex-snapshot
Two flavonoids and other compounds from the aerial parts of Centaurea bracteata from Italy
inferredcites →https://doi.org/10.1016/s0304-4238(97)00124-6openalex-snapshot
Flavonoid and carotenoid pigments in flower tissue of Sandersonia aurantiaca (Hook.)
inferredcites →https://doi.org/10.1016/s0308-8146(96)00287-7openalex-snapshot
Identification and quantification of major polyphenols in apple pomace
inferredcites →https://doi.org/10.1021/jf980614bopenalex-snapshot
Antioxidative Phenolic Compounds from Sage (Salvia officinalis)
inferredcites →https://doi.org/10.1021/np50125a004openalex-snapshot
Structural Revision of Physalin H Isolated from Physalis angulata
inferredcites →https://doi.org/10.1038/sj.bjp.0706321openalex-snapshot
Mechanisms of the anti‐inflammatory effects of the natural secosteroids physalins in a model of intestinal ischaemia and reperfusion injury
inferredcites →https://doi.org/10.1039/j29700000812openalex-snapshot
Crystal and molecular structure of 5α-acetoxy-6β-bromohexahydrophysalin A
inferredcites →https://doi.org/10.1055/s-2006-957473openalex-snapshot
The Griess Assay: Suitable for a Bio-Guided Fractionation of Anti-Inflammatory Plant Extracts?
inferredcites →https://doi.org/10.1107/s0108270191004031openalex-snapshot
Structure of 4,7-didehydroneophysalin B, acid-induced rearrangement product of physalin A
inferredcites →https://doi.org/10.1211/jpp.58.2.0011openalex-snapshot
In-vitro and in-vivo antitumour activity of physalins B and D from Physalis angulata
inferredcites →https://doi.org/10.1246/bcsj.66.299openalex-snapshot
Factors Influencing the Antioxidant Activities of Phenols by an Ab Initio Study
inferredcites →https://doi.org/10.1246/bcsj.67.222openalex-snapshot
Crystal Structures of 5α,6α-Epoxy and 2,3-Dihydro Derivatives of Physalin B, a 13,14-Seco-16,24-cyclosteroid, and Their 1H NMR Spectral Analysis

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/10.1016/j.phytochem.2022.113301zenodo-depositor-declared
Anti-inflammatory withanolides from the aerial parts of Physalis minima
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/ange.201500112openalex-snapshot
Biology‐Oriented Synthesis of a Withanolide‐Inspired Compound Collection Reveals Novel Modulators of Hedgehog Signaling
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/anie.201500112openalex-snapshot
Biology‐Oriented Synthesis of a Withanolide‐Inspired Compound Collection Reveals Novel Modulators of Hedgehog Signaling
inferred← citeshttps://doi.org/10.1002/bmc.3970openalex-snapshot
LC–MS/MS method for simultaneous determination of flavonoids and physalins in rat plasma: Application to pharmacokinetic study after oral administration of Physalis alkekengi var. franchetii (Chinese lantern) extract
inferred← citeshttps://doi.org/10.1002/bmc.4121openalex-snapshot
Identification of absorbed constituents and in vivo metabolites in rats after oral administration of Physalis alkekengi var. franchetii by ultra‐high‐pressure liquid chromatography quadrupole time‐of‐flight mass spectrometry
inferred← citeshttps://doi.org/10.1002/cbdv.201400371openalex-snapshot
Triterpenoids and Flavonoids from the Leaves of Astragalus membranaceus and Their Inhibitory Effects on Nitric Oxide Production
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/cm.70131openalex-snapshot
Apoptosis Induction, Disruption of Cytoskeleton Remodeling and EMT Inhibition as Major Mechanism(s) Underlying the Pleiotropic Action of Withania somnifera in Breast Cancer
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/rcm.7456openalex-snapshot
Metabolic profiling of luteolin‐7‐ O ‐glucoside in rat urine, plasma, bile and feces after oral administration using ultra‐high‐performance liquid chromatography/quadrupole time‐of‐flight mass spectrometry
inferred← citeshttps://doi.org/10.1007/978-3-319-41334-1_14openalex-snapshot
Natural Withanolides in the Treatment of Chronic Diseases
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/s00425-020-03434-xopenalex-snapshot
Transcriptomic variation of the flower–fruit transition in Physalis and Solanum
inferred← citeshttps://doi.org/10.1007/s10298-017-1183-3openalex-snapshot
Alkékenge : Physalis alkekengi L. (Solanaceae)
inferred← citeshttps://doi.org/10.1007/s10340-024-01826-6openalex-snapshot
Physalis floridana suppresses the expression of trehalase gene HvTREs in Henosepilachna vigintioctopunctata (Coleoptera: Coccinellidae) for defense against herbivorous insects
inferred← citeshttps://doi.org/10.1007/s10600-015-1517-zopenalex-snapshot
Chemical Constituents of Physalis alkekengi var. franchetii
inferred← citeshttps://doi.org/10.1007/s11010-016-2686-1openalex-snapshot
Physalin A induces G2/M phase cell cycle arrest in human non-small cell lung cancer cells: involvement of the p38 MAPK/ROS pathway
inferred← citeshttps://doi.org/10.1007/s11694-019-00213-5openalex-snapshot
Microwave-assisted extraction of total saponins from Physalis alkekengi L. var. franchetii (Mast.) Makino and their in vitro anti-inflammatory activity
inferred← citeshttps://doi.org/10.1007/s12192-018-0887-0openalex-snapshot
HO-1 dependent antioxidant effects of ethyl acetate fraction from Physalis alkekengi fruit ameliorates scopolamine-induced cognitive impairments
inferred← citeshttps://doi.org/10.1007/s12272-015-0620-9openalex-snapshot
A new 9,11-secosterol with a 1,4-quinone from a Korean marine sponge Ircinia sp.
inferred← citeshttps://doi.org/10.1007/s13659-013-0021-zopenalex-snapshot
Three new physalins from Physalis alkekengi var. franchetii
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14816-4openalex-snapshot
Eight-Membered Rings With One Oxygen Atom
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.01219-0openalex-snapshot
Eight-membered Rings with One Oxygen Atom
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.106106openalex-snapshot
A review on natural products with cage-like structure
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.108082openalex-snapshot
Physalins and neophysalins from the calyx of Physalis alkekengi: Structures and anti-inflammatory efficacy
inferred← citeshttps://doi.org/10.1016/j.bse.2013.12.030openalex-snapshot
Chemical constituents from the calyces of Physalis alkekengi var. franchetii
inferred← citeshttps://doi.org/10.1016/j.carres.2012.02.003openalex-snapshot
New sucrose esters from the fruits of Physalis solanaceus
inferred← citeshttps://doi.org/10.1016/j.carres.2017.07.010openalex-snapshot
Physakengoses K-Q, seven new sucrose esters from Physalis alkekengi var. franchetii
inferred← citeshttps://doi.org/10.1016/j.chroma.2014.08.004openalex-snapshot
The rapid discovery and identification of physalins in the calyx of Physalis alkekengi L.var.franchetii (Mast.) Makino using ultra-high performance liquid chromatography–quadrupole time of flight tandem mass spectrometry together with a novel three-step data mining strategy
inferred← citeshttps://doi.org/10.1016/j.fct.2014.06.007openalex-snapshot
Nitric oxide induces apoptosis and autophagy; autophagy down-regulates NO synthesis in physalin A-treated A375-S2 human melanoma cells
inferred← citeshttps://doi.org/10.1016/j.fitote.2016.05.010openalex-snapshot
Six new physalins from Physalis alkekengi var. franchetii and their cytotoxicity and antibacterial activity
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104728openalex-snapshot
New cytotoxic withanolides from Physalis minima
inferred← citeshttps://doi.org/10.1016/j.gene.2009.10.004openalex-snapshot
One-step identification of conserved miRNAs, their targets, potential transcription factors and effector genes of complete secondary metabolism pathways after 454 pyrosequencing of calyx cDNAs from the Labiate Salvia sclarea L
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e20030openalex-snapshot
Research progress on the chemical components and pharmacological effects of Physalis alkekengi L. var. franchetii (Mast.) Makino
inferred← citeshttps://doi.org/10.1016/j.jchromb.2010.12.032openalex-snapshot
Plasma pharmacokinetics and tissue distribution study of physalin D in rats by ultra-pressure liquid chromatography with tandem mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.jchromb.2017.01.037openalex-snapshot
Metabolic profiles of physalin A in rats using ultra-high performance liquid chromatography coupled with quadrupole time-of-flight tandem mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.jep.2013.04.051openalex-snapshot
Physalin A induces apoptosis via p53-Noxa-mediated ROS generation, and autophagy plays a protective role against apoptosis through p38-NF-κB survival pathway in A375-S2 cells
inferred← citeshttps://doi.org/10.1016/j.jep.2016.01.023openalex-snapshot
The ethyl acetate fraction from Physalis alkekengi inhibits LPS-induced pro-inflammatory mediators in BV2 cells and inflammatory pain in mice
inferred← citeshttps://doi.org/10.1016/j.jep.2017.08.022openalex-snapshot
Physalis alkekengi L. var. franchetii (Mast.) Makino: An ethnomedical, phytochemical and pharmacological review
inferred← citeshttps://doi.org/10.1016/j.jep.2020.112956openalex-snapshot
Anti-colitic effects of Physalin B on dextran sodium sulfate-induced BALB/c mice by suppressing multiple inflammatory signaling pathways
inferred← citeshttps://doi.org/10.1016/j.jep.2020.113490openalex-snapshot
Anti-inflammatory action of physalin A by blocking the activation of NF-κB signaling pathway
inferred← citeshttps://doi.org/10.1016/j.jep.2024.117736openalex-snapshot
Genus Physalis L.: A review of resources and cultivation, chemical composition, pharmacological effects and applications
inferred← citeshttps://doi.org/10.1016/j.jep.2024.118446openalex-snapshot
In vitro and in vivo studies of the therapeutic potential of Tinospora crispa extracts in osteoarthritis: Targeting oxidation, inflammation, and chondroprotection
inferred← citeshttps://doi.org/10.1016/j.jff.2017.10.043openalex-snapshot
Withanolides isolated from Nicandra physaloides protect liver cells against oxidative stress-induced damage
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.jpba.2024.116388openalex-snapshot
Metabolic profiling of different parts of Physalis alkekengi L. var. franchetii (Mast.) Makino based on UPLC-Q-Orbitrap-HRMS coupled with bioactivity assays
inferred← citeshttps://doi.org/10.1016/j.nutos.2022.06.005openalex-snapshot
Efficacy of physalis peruviana on restoring histopathological alternations against lead induced toxicity in albino rats
inferred← citeshttps://doi.org/10.1016/j.phymed.2022.154328openalex-snapshot
Physalis alkekengi L. var. franchetii (Mast.) Makino: A review of the pharmacognosy, chemical constituents, pharmacological effects, quality control, and applications
inferred← citeshttps://doi.org/10.1016/j.phytol.2026.104210openalex-snapshot
Plantagiolides O and P, withanolides from rhizomes of Tacca chantrieri and their anti-nematode activity
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.2014.01.004openalex-snapshot
Withanolides from Physalis minima and their inhibitory effects on nitric oxide production
inferred← citeshttps://doi.org/10.1016/j.steroids.2016.09.002openalex-snapshot
Withanolides from the stems and leaves of Physalis pubescens and their cytotoxic activity
inferred← citeshttps://doi.org/10.1016/j.steroids.2018.08.009openalex-snapshot
Two new bioactive steroids from a mangrove-derived fungus Aspergillus sp.
inferred← citeshttps://doi.org/10.1016/s1875-5364(10)60008-8openalex-snapshot
Natural Products Chemistry Research 2008's Progress in China
inferred← citeshttps://doi.org/10.1016/s1875-5364(19)30054-8openalex-snapshot
Withaminimas A—F, six withanolides with potential anti-inflammatory activity from Physalis minima
inferred← citeshttps://doi.org/10.1016/s1875-5364(25)60881-8openalex-snapshot
Withanolide derivatives from Physalis angulata var. villosa and their cytotoxic activities
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c01359openalex-snapshot
Secondary Metabolites of the Lichen Lethariella cladonioides and Their Neuroprotective Potential
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00911openalex-snapshot
17β-Hydroxy-18-acetoxywithanolides from Aeroponically Grown Physalis crassifolia and Their Potent and Selective Cytotoxicity for Prostate Cancer Cells
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00094openalex-snapshot
Antiproliferative and Anti-inflammatory Withanolides from Physalis angulata
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02679openalex-snapshot
Asperflotone, an 8(14→15)-abeo-Ergostane from the Sponge-Derived Fungus 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.6b03557openalex-snapshot
Phomopsterones A and B, Two Functionalized Ergostane-Type Steroids from the Endophytic Fungus Phomopsis sp. TJ507A
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03530openalex-snapshot
Aspersecosteroids A and B, Two 11(9 → 10)-abeo-5,10-Secosteroids with a Dioxatetraheterocyclic Ring System from Aspergillus flocculosus 16D-1
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/np100392mopenalex-snapshot
Diarylheptanoids from the Rhizomes of Curcuma kwangsiensis
inferred← citeshttps://doi.org/10.1021/np1007922openalex-snapshot
Anti-inflammatory Triterpenes from the Leaves of Rosa laevigata
inferred← citeshttps://doi.org/10.1021/np400017kopenalex-snapshot
Physalin A Induces Apoptotic Cell Death and Protective Autophagy in HT1080 Human Fibrosarcoma Cells
inferred← citeshttps://doi.org/10.1021/np400296sopenalex-snapshot
Withanolide Artifacts Formed in Methanol
inferred← citeshttps://doi.org/10.1021/np900538ropenalex-snapshot
Quassidines A−D, Bis-β-carboline Alkaloids from the Stems of Picrasma quassioides
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/c0np00045kopenalex-snapshot
Natural withanolides: an overview
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/c6ra07031kopenalex-snapshot
New withanolides with TRAIL-sensitizing effect from Physalis pubescens L.
inferred← citeshttps://doi.org/10.1039/c6ra16424bopenalex-snapshot
Anti-inflammatory labdane-type diterpenoids 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/c7ob02551copenalex-snapshot
Withapubesides A–D: natural inducible nitric oxide synthase (iNOS) inhibitors from Physalis pubescens
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/10.1063/5.0172801openalex-snapshot
Comparison of some chemical indices of the fruit calyces of Physalis peruviana L. and Physalis alkekengi L. from different genotypes
inferred← citeshttps://doi.org/10.1080/00498254.2016.1271961openalex-snapshot
Two sulfonate metabolites of physalin A in rats
inferred← citeshttps://doi.org/10.1080/14786419.2016.1269102openalex-snapshot
A new phenol glycoside from Physalis angulata
inferred← citeshttps://doi.org/10.1080/14786419.2017.1294176openalex-snapshot
A new eremophilane glycoside from the fruits of Physalis pubescens and its cytotoxic activity
inferred← citeshttps://doi.org/10.1111/j.1745-4514.2010.00400.xopenalex-snapshot
PURIFICATION, CHARACTERIZATION AND IN VITRO ANTIOXIDANT ACTIVITIES OF POLYSACCHARIDE FRACTIONS ISOLATED FROM THE FRUITS OF PHYSALIS ALKEKENGI L.
inferred← citeshttps://doi.org/10.1155/2016/4359394openalex-snapshot
Antibacterial and Anti‐Inflammatory Activities ofPhysalis Alkekengivar.franchetiiand Its Main Constituents
inferred← citeshttps://doi.org/10.1159/000486641openalex-snapshot
Ethnopharmacological Study of Medicinal Plants Used for Treating Dysuria: A Collection from Traditional Markets in Shiraz
inferred← citeshttps://doi.org/10.11606/d.41.2012.tde-01052013-111617openalex-snapshot
Efeito induzido pelo vírus Y da batata (Potato virus Y) no metabolismo secundário do camapu (Physalis angulata L.)
inferred← citeshttps://doi.org/10.1186/s12906-019-2511-yopenalex-snapshot
Physalin A regulates the Nrf2 pathway through ERK and p38 for induction of detoxifying enzymes
inferred← citeshttps://doi.org/10.1248/bpb.34.1584openalex-snapshot
Physalins A and B Inhibit Androgen-Independent Prostate Cancer Cell Growth through Activation of Cell Apoptosis and Downregulation of Androgen Receptor Expression
inferred← citeshttps://doi.org/10.1248/cpb.59.359openalex-snapshot
Anti-inflammatory Alkaloids from the Stems of Picrasma quassioides BENNET
inferred← citeshttps://doi.org/10.15171/ps.2016.14openalex-snapshot
Inhibitory Effects of Urginea maritima (L.) Baker, Zhumeria majdae Rech. F. and Wendelbo and Physalis divaricata D. Don Ethanolic Extracts on Mushroom Tyrosinase
inferred← citeshttps://doi.org/10.1556/018.68.2017.3.7openalex-snapshot
Isolation and quantitative analysis of physalin D in the fruit and calyx of Physalis alkekengi L.
inferred← citeshttps://doi.org/10.2174/1871527314666150821112051openalex-snapshot
The beneficial effect of Cape gooseberry juice on carbon tetrachloride-induced neuronal damage
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/10.29252/jmp.4.72.s12.1openalex-snapshot
Overview on the Agronomic, Phytochemical and Therapeutic traits of Bladder Cherry (Physalis alkekengi L.)
inferred← citeshttps://doi.org/10.29356/jmcs.v59i1.16openalex-snapshot
Optimization of Extraction Conditions for Flavonoids of Physalis alkekengi var. franchetii Stems by Response Surface Methodology and Inhibition of Acetylcholinesterase Activity
inferred← citeshttps://doi.org/10.30721/fsab2020.v3.i1.80openalex-snapshot
Phytochemical composition and biological activity of Physalis spp.: A mini-review
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/10.3390/antiox12122101openalex-snapshot
Metabolite Profiling, through LC-ESI/LTQOrbitrap/MS Analysis, of Antioxidant Extracts from Physalis alkekengi L.
inferred← citeshttps://doi.org/10.3390/ijms21165642openalex-snapshot
Anti-Obesity Effects of Polyphenol Intake: Current Status and Future Possibilities
inferred← citeshttps://doi.org/10.3390/molecules24081608openalex-snapshot
Cytotoxic Withanolides from the Whole Herb of Physalis angulata L.
inferred← citeshttps://doi.org/10.3390/molecules25163747openalex-snapshot
Physalis alkekengi L. Extract Reduces the Oxidative Stress, Inflammation and Apoptosis in Endothelial Vascular Cells Exposed to Hyperglycemia
inferred← citeshttps://doi.org/10.3390/molecules27030695openalex-snapshot
Natural Products from Physalis alkekengi L. var. franchetii (Mast.) Makino: A Review on Their Structural Analysis, Quality Control, Pharmacology, and Pharmacokinetics
inferred← citeshttps://doi.org/10.3390/molecules27217272openalex-snapshot
A Rapid and Sensitive LC−MS/MS Method for the Quantitation of Physalin A with Special Consideration to Chemical Stability in Rat Plasma: Application to a Pharmacokinetic Study
inferred← citeshttps://doi.org/10.3390/molecules30143017openalex-snapshot
Three New Physalins from Physalis Alkekengi L. var. franchetii (Mast.) Makino
inferred← citeshttps://doi.org/10.5772/intechopen.1002226openalex-snapshot
Berries: A New Paradigm for Nutraceuticals
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.