stigmastanol (Q3973521)

From Wikidata

Jump to navigation Jump to search

chemical compound

sitostanol
fucostanol
(3S,5S,8R,9S,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

Language	Label	Description	Also known as
English	stigmastanol	chemical compound	sitostanol fucostanol (3S,5S,8R,9S,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

Statements

type of chemical entity

0 references

Stigmastan-3beta-ol

1 reference

based on heuristic

inferred from SMILES

chemical structure

Stigmastanol.svg
512 × 311; 24 KB

0 references

416.401816284 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

Stigmastan-3-ol, (3beta)-

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

24-Ethylcoprostanol

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

(3R,5S,8R,9S,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

(3R,5S,8R,9S,10S,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

(3S,5S,8R,9R,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

1 reference

based on heuristic

inferred from InChI

(3R,5R,8R,9S,10S,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

1 reference

based on heuristic

inferred from InChI

(24S)-5beta-stigmastan-3beta-ol

1 reference

based on heuristic

inferred from InChI

1 reference

based on heuristic

inferred from InChI

(3S,5S,8S,9S,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₉H₅₂O

2 references

imported from Wikimedia project

Italian Wikipedia

canonical SMILES

CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C

0 references

isomeric SMILES

CC[C@H](CC[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC[C@@H]4[C@@]3(CC[C@@H](C4)O)C)C)C(C)C

0 references

Campanula medium

1 reference

Bioactive Compounds and Antiradical Potential of Campanula medium Lipids

Salpa thompsoni

2 references

Fatty acids and sterols of the tunicate, Salpa thompsoni, from the Antarctic Ocean: chemical composition and hemolytic activity

Fatty acids and sterols of the tunicate, Salpa thompsoni, from the Antarctic Ocean: chemical composition and hemolytic activity

Abies sachalinensis

1 reference

Occurrence of epijuvabione-type sesquiterpenoids in Abies sachalinensis

1 reference

Biarylheptanoids and other constituents from wood of Alnus japonica

Arabidopsis thaliana

1 reference

Sterols and phytyl esters of Arabidopsis thaliana under normal and chilling temperatures

Armillaria mellea

1 reference

Metabolites of the honey mushroom, Armillariamellea

Phallusia nigra

1 reference

Minor sterols of marine invertebrates 37. Isolation of novel coprostanols and 4 alpha-methyl sterols from the tunicate Ascidia nigra

Axinella cannabina

1 reference

Minor and trace sterols in marine invertebrates. Part 35. Isolation and structure elucidation of seventy-four sterols from the sponge Axinella cannabina

Calycanthus floridus

1 reference

92. The sterols of Calycanthus floridus

Clerodendrum chinense

1 reference

Sterols of some Clerodendrum species (Verbenaceae): occurrence of the 24 alpha- and 24 beta-epimers of 24-ethylsterols lacking a delta 25-bond

Conium maculatum

1 reference

Steroids from Poison Hemlock (Conium maculatum L.): A GC-MS analysis

Cymodocea nodosa

1 reference

Configuration at C-24 of sterols from the marine phanerogames Posidonia oceanica and Cymodocea nodosa

Dracaena cinnabari

1 reference

Sterols and triterpenoids from Dracaena cinnabari

Dysidea fragilis

1 reference

New cytotoxic steroids from the marine sponge Dysidea fragilis coming from the lagoon of Venice

Amphilectus digitatus

1 reference

Steroid compounds of marine sponges. I. Sterols ofEsperiopsis digitata

Neoesperiopsis digitata

1 reference

Steroid compounds of marine sponges. I. Sterols ofEsperiopsis digitata

Amphilectus fucorum

1 reference

Novel sterols from the sponge esperiopsis edwardii

1 reference

Steroid alcohols from the ascidianHalocynthia aurantium

Hedysarum setigerum

1 reference

Secondary Metabolites from Hedysarum setigerum

Chelonanthus albus

1 reference

Chemical constituents from the stems of Michelia alba

Heterotheca inuloides

1 reference

Sesquiterpene, Triterpene und Sterine aus Blüten von Heterotheca inuloides (“Mexikanische Arnikablüten”)

Isodon japonicus

1 reference

Biosynthesis of oleanene- and ursene-type triterpenes from [4-13C]mevalonolactone and sodium [1,2-13C2]acetate in tissue cultures of Isodon japonicus Hara

Kalanchoe petitiana

1 reference

Co-occurrence of C-24 epimeric 24-ethylsterols possessing and lacking a Δ25-bond inKalanchoe petitiana

Muricea californica

1 reference

Occurrence and seasonal variation of 19-norcholest-4-en-3-one and 3 beta-monohydroxy sterols in the Californian gorgonian, Muricea californica

1 reference

Bioactive constituents of Chinese natural medicines. VII. Inhibitors of degranulation in RBL-2H3 cells and absolute stereostructures of three new diarylheptanoid glycosides from the bark of Myrica rubra

1 reference

Bioactive constituents of Chinese natural medicines. VII. Inhibitors of degranulation in RBL-2H3 cells and absolute stereostructures of three new diarylheptanoid glycosides from the bark of Myrica rubra

Petrosia ficiformis

1 reference

Minor and trace sterols in marine invertebrates XVII. (24R)-24,26-Dimethylcholesta-5,26-dien-3 beta-OL, a new sterol from the sponge Petrosia ficiformis

Axinella aruensis

1 reference

Minor and trace sterols in marine invertebrates. 61. Isolation and structure elucidation of new A-nor sterols from the marine sponge Phakellia aruensis

Posidonia oceanica

1 reference

Configuration at C-24 of sterols from the marine phanerogames Posidonia oceanica and Cymodocea nodosa

Isodon lophanthoides

1 reference

Abietane quinones from rabdosia lophanthoides

1 reference

An investigation of the chemical composition of the seeds of Salsola collina

Salsola collina

1 reference

An investigation of the chemical composition of the seeds of Salsola collina

Saussurea controversa

1 reference

The chemical composition of the extractive substances ofSaussurea controversa

Syzygium siamense

1 reference

New cytotoxic steroids from the fruits of Syzygium siamense

Thomandersia laurifolia

1 reference

Thomandersine and isothomandersine, 2-indolinone alkaloids from Thomandersia laurifolia

Drimia sanguinea

1 reference

Bufadienolides and other constituents of Urginea sanguinea

1 reference

Flavones and lignans in flowers, fruits and seedlings ofVirola venosa

1 reference

Investigations on the Δ23-, Δ24(28)- and Δ25-Sterols of zea mays

1 reference

Dominance of Δ5-sterols in eight species of the cactaceae

Costus tonkinensis

1 reference

24-Methylpollinastanone, related triterpenoids and sterols from Costus tonkinensis

Festuca hieronymi

1 reference

Festuca argentina and Festuca hieronymi : Chemical relationships between non-polar constituents

Setaria italica

2 references

Regional Variations of Sitostanol Content in the Seeds of Setaria italics Beauv.

Identification of Trace Sterols in the Seeds of Foxtail Millet (Setaria italica Beauv.).

1 reference

Features of 4-Desmethylsterols in Tomato Shoots.

American ginseng

1 reference

Phytosterol content in American ginseng seed oil.

Lessingianthus mollissimus

1 reference

Sesquiterpene Lactones and Other Constituents of Vernonia mollissima and Vernonia squamulosa

Vernonia mollissima

1 reference

Sesquiterpene Lactones and Other Constituents of Vernonia mollissima and Vernonia squamulosa

Alsophila podophylla

1 reference

Fern Constituents: Dryocrassy Formate, Sitostanyl Formate and 12α-Hydroxyfern-9(11)-ene from Cyathea podophylla.

Alsophila spinulosa

1 reference

Fern Constituents: Triterpenoids Isolated from Leaflets of Cyathea spinulosa.

Cymbopogon martinii

1 reference

Fatty acids and sterols from Cymbopogon martinii var. motia roots

Cymbopogon martinii

1 reference

Fatty acids and sterols from Cymbopogon martinii var. motia roots

Aloe rubroviolacea

1 reference

Constituents of Aloe rubroviolacea

Cannabis sativa

1 reference

Identification of Teasterone and Phytosterols in the Lipid Fraction from Seeds of Cannabis sativa L.

1 reference

Dominance of Δ5-sterols in eight species of the cactaceae

Cyathea kalbreyeri

1 reference

Fern Constituents: Dryocrassy Formate, Sitostanyl Formate and 12α-Hydroxyfern-9(11)-ene from Cyathea podophylla.

Strychnos spinosa

1 reference

Antitrypanosomal activity of triterpenoids and sterols from the leaves of Strychnos spinosa and related compounds

Acacia longifolia

1 reference

Identification of delta7 phytosterols and phytosteryl glucosides in the wood and bark of several Acacia species

Acacia dealbata

1 reference

Identification of delta7 phytosterols and phytosteryl glucosides in the wood and bark of several Acacia species

Acacia melanoxylon

1 reference

Identification of delta7 phytosterols and phytosteryl glucosides in the wood and bark of several Acacia species

Acacia retinodes

1 reference

Identification of delta7 phytosterols and phytosteryl glucosides in the wood and bark of several Acacia species

subject has role

anticholesteremic agents

1 reference

Medical Subject Headings

MeSH descriptor ID

15 March 2018

Commons category

Stigmastanol

0 references

Identifiers

InChI=1S/C29H52O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h19-27,30H,7-18H2,1-6H3/t20-,21-,22+,23+,24+,25-,26+,27+,28+,29-/m1/s1

1 reference

LGJMUZUPVCAVPU-HRJGVYIJSA-N

1 reference

ChEBI release 2020-09-01

CAS Registry Number

2 references

imported from Wikimedia project

Italian Wikipedia

LGJMUZUPVCAVPU-HRJGVYIJSA-N

CAS Common Chemistry

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=83-45-4

0 references

0 references

Reaxys registry number

2564508

0 references

mapping relation type

0 references

1 reference

imported from Wikimedia project

English Wikipedia

UniChem compound ID

1 reference

splash10-002s-0029000000-27f3a2a4c1a3fb969075

0 references

splash10-01p2-0029000000-3b26f2c6dbb919b7d0ac

0 references

splash10-066u-4942100000-604c3357e69c5eff6d37

0 references

0 references

201-479-0

0 references

ECHA Substance Infocard ID

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

(3β,5α)-stigmastan-3-ol (English)

CAS no.: 83-45-4 (English)

AICS Chemical ID (BEING DELETED)

0 references

MeSH descriptor ID

1 reference

Medical Subject Headings

MeSH descriptor ID

14 March 2018

0 references

0 references

Probes And Drugs ID

0 references

0 references

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

15 January 2022

LGJMUZUPVCAVPU-HRJGVYIJSA-N

1 reference

Freebase Data Dumps

publication date

28 October 2013

Microsoft Academic ID

0 references

Sitelinks

Wikipedia(7 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(1 entry)

commonswiki Category:Stigmastanol

Retrieved from "https://www.wikidata.org/w/index.php?title=Q3973521&oldid=2130058504"