About: Cytotoxic acetylenes from Panax quinquefolium

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scientific article published on 01 February 1991

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 1991 (uk) im Februar 1991 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en febreru de 1991 (ast) artikull shkencor i botuar më 01 shkurt 1991 (sq) scientific article published on 01 February 1991 (en)
publication date	wds:Q70198027-53EBEA06-7CAA-49AC-AAF9-45CE30080E24
publication date	1991-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q70198027-27494864-D7FB-48C3-95FD-9348BA352AB5
language of work or name	English
cites work	wds:Q70198027-C85DB30F-1B71-4AC1-B917-EB5F0D45294C
cites work	Studies on the panaxytriol of Panax ginseng C. A. Meyer. Isolation, determination and antitumor activity
access restriction status	wds:Q70198027-6A50B7CB-13BB-4825-836B-849FB4F374AE
access restriction status	open access
author name string	wds:Q70198027-109798A4-79E7-4C5B-8880-350DA1D73D45 wds:Q70198027-BA8DB373-5A4C-4AF2-8E3D-066360E93A27 wds:Q70198027-E47E29F1-4905-447F-BDD6-2D5BAE7A75C3 wds:Q70198027-EC6E5DD6-D3B8-4B2C-8940-7F659DF08320
author name string	M Satoh Y Fujimoto N Takeuchi M Kirisawa
rdfs:label	Cytotoxic acetylenes from Panax quinquefolium (en) Cytotoxic acetylenes from Panax quinquefolium (nl) Cytotoxic acetylenes from Panax quinquefolium (sq)
skos:prefLabel	Cytotoxic acetylenes from Panax quinquefolium (en) Cytotoxic acetylenes from Panax quinquefolium (nl) Cytotoxic acetylenes from Panax quinquefolium (sq)
name	Cytotoxic acetylenes from Panax quinquefolium (en) Cytotoxic acetylenes from Panax quinquefolium (nl) Cytotoxic acetylenes from Panax quinquefolium (sq)
title	wds:Q70198027-095E21B2-5E95-4360-B190-47CACD11F39E
title	Cytotoxic acetylenes from Panax quinquefolium (en)
page(s)	wds:Q70198027-524304B9-C806-4446-B8A9-9BA248FECA8C
page(s)	521-523
instance of	wds:Q70198027-90F10421-919F-4714-88DF-97C007B4DF63
instance of	scholarly article
main subject	wds:Q70198027-150DE31B-7F06-4954-AB14-DB0460498A41 wds:Q70198027-CD0EB70A-AB39-4D15-AA4E-8A653FF85F53 wds:Q70198027-F3A0F4B4-F681-4631-AF97-7B46ECC85166
main subject	American ginseng heptadec-1-ene-4,6-diyne-3,9,10-triol panaxydol
PubMed ID	wds:Q70198027-29BEB2C9-7CE5-41B0-AD66-100E550C7789
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/2054881
PubMed ID	2054881
published in	wds:Q70198027-78CF06E0-BB4C-494B-BFCF-9A5D4D0C141E
full work available at URL	wds:Q70198027-FCD836E6-BE24-4448-9632-F56C79AD37D3
published in	Chemical & Pharmaceutical Bulletin
full work available at URL	https://www.jstage.jst.go.jp/article/cpb1958/39/2/39_2_521/_pdf
issue	wds:Q70198027-2E313780-ABBE-4304-B56C-748416E0E3C1
volume	wds:Q70198027-CC63F106-A85A-4544-8777-664E967EC9DB
issue	2
volume	39
DOI	wds:Q70198027-7CE63654-4444-4904-A6BA-79C28F487FCE
DOI	http://dx.doi.org/10.1248/CPB.39.521
DOI	10.1248/CPB.39.521
online access status	wds:Q70198027-54954C87-BD76-4B51-9B2E-F3CCC5935EEA
online access status	open access
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q70198027
is cites work of	Bioactive saponins and glycosides. XIX. Notoginseng (3): immunological adjuvant activity of notoginsenosides and related saponins: structures of notoginsenosides-L, -M, and -N from the roots of Panax notoginseng (Burk.) F. H. Chen Inducible nitric oxide synthase inhibitors from Saposhnikovia divaricata and Panax quinquefolium Bioactive saponins and glycosides. XI. Structures of new dammarane-type triterpene oligoglycosides, quinquenosides I, II, III, IV, and V, from American ginseng, the roots of Panax quinquefolium L Polyacetylenes from sardinian Oenanthe fistulosa: a molecular clue to risus sardonicus Serotonergic activity-guided phytochemical investigation of the roots of Angelica sinensis Immunosuppressive diacetylenes, ceramides and cerebrosides from Hydrocotyle leucocephala Synthesis of naturally occurring polyynes Phytochemistry of wild populations of Panax quinquefolius L. (North American ginseng). Bioactive polyacetylenes in food plants of the Apiaceae family: occurrence, bioactivity and analysis Simultaneous determination of ginsenosides and polyacetylenes in American ginseng root (Panax quinquefolium L.) by high-performance liquid chromatography. Anticancer activity of natural and synthetic acetylenic lipids Quantification of two polyacetylenes in Radix Ginseng and roots of related Panax species using a gas chromatography-mass spectrometric method Protective effect of panaxydol and panaxynol on sodium nitroprusside-induced apoptosis in cortical neurons Screening of polyacetylenic alcohols in crude drugs using the ELISA for panaxytriol Synthesis and cytotoxic activity of a series of diacetylenic compounds related to falcarindiol Biomass and content of ginsenosides and polyacetylenes in American ginseng roots can be increased without affecting the profile of bioactive compounds Oploxynes A and B, polyacetylenes from the stems of Oplopanax elatus pS2 expression induced by American ginseng in MCF-7 breast cancer cells Anti-TB polyynes from the roots of Angelica sinensis Chemical analysis of Panax quinquefolius (North American ginseng): A review Determination of polyacetylenes and ginsenosides in Panax species using high performance liquid chromatography Polyacetylenes from the roots of cultivated-wild ginseng and their cytotoxicity in vitro Epoxy acetylenic lipids: their analogues and derivatives Acetylenic anticancer agents Effect of panaxydol on hypoxia-induced cell death and expression and secretion of neurotrophic factors (NTFs) in hypoxic primary cultured Schwann cells Differential effects of falcarinol and related aliphatic C(17)-polyacetylenes on intestinal cell proliferation Polyacetylenes in hairy roots of a panax hybrid Biphasic effect of falcarinol on caco-2 cell proliferation, DNA damage, and apoptosis. Dietary polyacetylenes, falcarinol and falcarindiol, isolated from carrots prevents the formation of neoplastic lesions in the colon of azoxymethane-induced rats. Bioactive acetylenic metabolites Synthese von Polyin-Naturstoffen Synthesis of panax acetylenes: chiral syntheses of acetylpanaxydol, PQ-3 and panaxydiol Polyacetylenes from Panax quinquefolium New dammarane-type saponin from roots of Panax notoginseng Antitrypanosomal properties of Panax ginseng C. A. Meyer: new possibilities for a remarkable traditional drug Regression of squamous cell carcinoma of the lung by Chinese herbal medicine: a case with an 8-year follow-up. Studies on panax acetylenes: absolute structure of a new panax acetylene, and inhibitory effects of related acetylenes on the growth of L-1210 cells. A polyacetylene gentiobioside from hairy roots of Lobelia inflata Panaxydol inhibits the proliferation and induces the differentiation of human hepatocarcinoma cell line HepG2.

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