avenasterol

chemical compound

C₂₉H₄₈O

avenasterol is …
instance of (P31):
type of chemical entityQ113145171

sublass of (P279):
(24E/Z)-avenasterolQ83048205

External links are
P11160Cannabis Database ID000287
P233canonical SMILESOC1CCC2(C)C3C(=CCC2C1)C4CCC(C(C)CCC(=CC)C(C)C)C4(C)CC3
P231CAS Registry Number23290-26-8
P683ChEBI ID166888
P2057Human Metabolome Database IDHMDB0006851
P234InChIInChI=1S/C29H48O/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/h7,11,19-20,22-23,25-27,30H,8-10,12-18H2,1-6H3/b21-7-/t20-,22+,23+,25-,26+,27+,28+,29-/m1/s1
P235InChIKeyMCWVPSBQQXUCTB-OQTIOYDCSA-N
P2017isomeric SMILESC/C=C(/CC[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3C2=CC[C@@H]4[C@@]3(CC[C@@H](C4)O)C)C)\C(C)C
P665KEGG IDC15782
P2063LIPID MAPS IDLMST01040154
P11199Probes And Drugs IDPD131415
P662PubChem CID12795736
P11089UniChem compound ID31999732
P652UNIII0WYR6393O

P703found in taxonmaizeQ11575
Avena sativaQ12104
Vitis viniferaQ30046
Campanula mediumQ127555
Carthamus tinctoriusQ156625
Amelanchier canadensisQ159030
Amaranthus cruentusQ159191
Scarlet firethornQ159269
Cucurbita maximaQ161180
Amaranthus hypochondriacusQ159611
Nigella sativaQ160575
Euonymus japonicusQ161383
Amaranthus caudatusQ162791
Chinese peonyQ163076
common sunflowerQ171497
Bryonia dioicaQ163815
Delphinium staphisagriaQ163934
Nicotiana tabacumQ181095
Solanum sisymbriifoliumQ565399
Amaranthus hybridusQ1021182
Canavalia ensiformisQ1677262
Eryngium foetidumQ1146782
Lagenaria sicerariaQ1277255
Vernonia galamensisQ3556010
Vanilla tahitensisQ2388303
American ginsengQ2737217
sesameQ2763698
Kalanchoe marmorataQ1722001
Axinella cannabinaQ2218430
Mangifera indicaQ3919027
Vanilla planifoliaQ7224923
Cucurbita pepoQ7229863
Sesamum angustifoliumQ17715919
Sesamum alatumQ17715922
Baccharoides anthelminticaQ50840344
Solanum argentinumQ15533210
Trigonella callicerasQ15546460
Ethulia gracilisQ15596505
Staphisagria macrospermaQ80708332
Sesamum radiatumQ7456020
Medicago monspeliacaQ12230843
Ethulia conyzoidesQ15231086
P2067mass412.370516156
P3364stereoisomer of(3S,5R,9S,10S,13R,14S,17S)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-olQ105161499
(3S,5R,9R,10S,13R,14R,17R)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-olQ105161506
(3S,5S,9R,10S,13R,14R,17R)-17-((R,E)-5-Isopropylhept-5-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-olQ105161507

Reverse relations

stereoisomer of (P3364)
Q105161506(3S,5R,9R,10S,13R,14R,17R)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
Q105161499(3S,5R,9S,10S,13R,14S,17S)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
Q105161507(3S,5S,9R,10S,13R,14R,17R)-17-((R,E)-5-Isopropylhept-5-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

main subject (P921)
Q105161500(24R)- and (24S)-24-hydoxy-24-vinyllathosterols and other sterols from the aerial part of Bryonia dioica
Q1043839414-Demethylsterols and triterpene alcohols from two Vanilla bean species: Vanilla fragrans and V. tahitensis
Q104924622A 5-methylcoumarin glucoside from Ethulia conyzoides
Q104415015A comparative study of sterols in oil seeds of Solanum species
Q104951276Bioactive Compounds and Antiradical Potential of Campanula medium Lipids
Q104375030Canavalia ensiformis neutral lipids, a rich source of lupeol
Q104863133Carthami flos extract and its component, stigmasterol, inhibit tumour promotion in mouse skin two-stage carcinogenesis
Q102375115Characterization of fatty acids, triacylglycerols, phytosterols and tocopherols in peony seed oil from five different major areas in China
Q115965584Chemical composition of seeds of four Bulgarian grape varieties
Q104383953Chemical composition of tobacco seeds (Nicotiana tabacum L.)
Q104375050Chemotaxonomic value of sterols and steroidal sapogenins in the genusTrigonella
Q104383900Co-occurrence of C-24 epimeric 24-ethylsterols possessing and lacking a Δ25-bond inKalanchoe petitiana
Q104253053Composition and Biological Activity of the Fatty Seed Oil ofDelphinium Staphisagria— Note I
Q104383964Determination of sterol and triterpene alcohol acetates in natural products by reversed-phase liquid chromatography and gas chromatography—mass spectrometry
Q104838395Eight Novel Sterols from the Roots of Bryonia dioica JACQ.
Q104415220Investigations on the Δ23-, Δ24(28)- and Δ25-Sterols of zea mays
Q104383940Lipid composition of Evonimus japonicus L., Piracanttia coccinea L. and Amelanchier cannadensis L. seed oils
Q104415668Minor and trace sterols in marine invertebrates. Part 35. Isolation and structure elucidation of seventy-four sterols from the sponge Axinella cannabina
Q104383906Occurrence of Δ5-sterols in plants producing predominantly Δ7-sterols: Studies on the sterol compositions of six cucurbitaceae seeds
Q43878069Phytosterol content in American ginseng seed oil.
Q104375028Seed lipid components of Solanum argentinum
Q104383934Seed lipids ofSesamum indicum and related wild species in Sudan. The sterols
Q104383931Sterols and sterylglycosides of oats (Avena sativa). Distribution in the leaf tissue and medium-induced glycosylation of sterols during protoplast isolation
Q40151831Sterols in seeds and leaves of oats (Avena sativa L.).
Q105161501Sterols in vernonia anthelmintica seed
Q104247227Sterols of seed oils ofVernonia galamensis,Amaranthus cruentus,Amaranthus caudatus,Amaranthus hybridus andAmaranthus hypochondriacus grown in the humid tropics
Q104247802Sterols, methyl sterols, triterpene alcohols and fatty acids of the kernel fat of different malagasy mango(Mangifera indica) varieties
Q104913987Studies on the C-24 configurations of Δ7-sterols in theseeds of Cucurbita maxima
Q104383952The sterols of Nigella sativa seed oil
Q34502919Topical antiinflammatory activity of phytosterols isolated from Eryngium foetidum on chronic and acute inflammation models