(Q104251263)

inferred from SMILES

mass

426.38616622 dalton

1 reference

(3S,4S,5R,10S,13R,14R,17R)-4,10,13,14-tetramethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-1,2,3,4,5,6,7,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol

inferred from SMILES

stereoisomer of

1 reference

inferred from InChI

chemical formula

C₃₀H₅₀O

0 references

canonical SMILES

OC1CCC2(C3=C(CCC2C1C)C4(C)CCC(C(C)CCC(=C)C(C)C)C4(C)CC3)C

0 references

isomeric SMILES

C=C(CC[C@@H](C)[C@H]1CC[C@@]2(C)C3=C(CC[C@]12C)[C@@]1(C)CC[C@H](O)[C@@H](C)[C@@H]1CC3)C(C)C

0 references

found in taxon

sesame

2 references

Final Report on the Safety Assessment of Sesame Oil

Seed lipids ofSesamum indicum and related wild species in Sudan. The sterols

Baccharoides anthelmintica

1 reference

4α-methylvernosterol and other sterols from Vernonia anthelmintica seeds

Mangifera indica

1 reference

Sterols, methyl sterols, triterpene alcohols and fatty acids of the kernel fat of different malagasy mango(Mangifera indica) varieties

Euphorbia guyoniana

3 references

Diterpenoids and triterpenoids from Euphorbia guyoniana

Diterpenoids and triterpenoids from Euphorbia guyoniana

Diterpenoids and triterpenoids from Euphorbia guyoniana

Euphorbia officinarum

3 references

Bioactive triterpene derivatives from latex of two Euphorbia species.

Bioactive triterpene derivatives from latex of two Euphorbia species.

Bioactive triterpene derivatives from latex of two Euphorbia species.

Euphorbia peplus

2 references

Nonpolar components of the latex of Euphorbia peplus

Triterpenoids and steroids of Euphorbia pilulifera

Leptosphaeria maculans

2 references

Sterol composition of mycelia of the plant pathogenic ascomycete Leptosphaeria maculans

Sterol composition of mycelia of the plant pathogenic ascomycete Leptosphaeria maculans

Nicotiana benthamiana

1 reference

Virus-induced silencing of sterol biosynthetic genes: identification of a Nicotiana tabacum L. obtusifoliol-14alpha-demethylase (CYP51) by genetic manipulation of the sterol biosynthetic pathway in Nicotiana benthamiana L.

Sideritis discolor

3 references

A chemotaxonomic study of nine Canarian Sideritis species

A chemotaxonomic study of nine Canarian Sideritis species

A chemotaxonomic study of nine Canarian Sideritis species

Euphorbia bupleuroides

1 reference

Terpenoids and other constituents from Euphorbia bupleuroides

Bryonia dioica

1 reference

Eight Novel Sterols from the Roots of Bryonia dioica JACQ.

Cheiropleuria bicuspis

1 reference

Fern constituents: Triterpenoids isolated from the leaves of Cheiropleuria bicuspis.

Volkameria inermis

2 references

24,24-Dimethyl-25-dehydrolophenol, a 4α-methylsterol from Clerodendrum inerme

24,24-Dimethyl-25-dehydrolophenol, a 4α-methylsterol from Clerodendrum inerme

Euphorbia chamaesyce

4 references

Obtusifoliol and related steroids from the whole herb of Euphorbia chamaesyce

Bioactive steroids from the whole herb of Euphorbia chamaesyce

Bioactive steroids from the whole herb of Euphorbia chamaesyce

Obtusifoliol and related steroids from the whole herb of Euphorbia chamaesyce

Euphorbia piscatoria

2 references

Tetra- and Pentacyclic Triterpenes from the Aerial Parts of Euphorbia piscatoria

Tetra- and Pentacyclic Triterpenes from the Aerial Parts of Euphorbia piscatoria

Euphorbia retusa

2 references

Diterpenoids and triterpenoids from Euphorbia guyoniana

Diterpenoids and triterpenoids from Euphorbia retusa

Gleichenia japonica

1 reference

Triterpene Alcohols and Sterols from the Fern Gleichenia japonica SPR.

Hippophae rhamnoides

3 references

Chemical investigation ofHippophaë rhamnoides. II. Main components of the neutral reaction of the saponification products of an extract of the leaves of the sea buckthorn

Phytosterols in Sea Buckthorn ( Hippophaë rhamnoides L.) Berries: Identification and Effects of Different Origins and Harvesting Times

Hippophae rhamnoides L.: chromatographic methods to determine chemical composition, use in traditional medicine and pharmacological effects

Nigella sativa

1 reference

The sterols of Nigella sativa seed oil

Olea europaea

1 reference

Triterpene alcohols and sterols of Spanish olive oil

Panax ginseng

1 reference

Composition of unsaponifiable lipid from seed oils ofPanax ginseng andP. quiquefolium

Phaseolus vulgaris

1 reference

25-Methylgramisterol and other 4α-methylsterols from Phaseolus vulgaris seeds

Sesamum alatum

1 reference

Seed lipids ofSesamum indicum and related wild species in Sudan. The sterols

Sesamum angustifolium

1 reference

Seed lipids ofSesamum indicum and related wild species in Sudan. The sterols

Sesamum radiatum

1 reference

Seed lipids ofSesamum indicum and related wild species in Sudan. The sterols

Symphoricarpos albus

1 reference

The occurrence of lanosterol and 24-methylenelanost-8-en-3β-ol in leaves of symphoricarpus albus

Tabernaemontana cymosa

1 reference

Alkaloids and other compounds from seeds of Tabernaemontana cymosa

Vigna angularis

1 reference

Triterpenic lipids in Azuki bean seeds.

Vitis vinifera

1 reference

The main triterpene compounds of vine leaves and rachises

maize

1 reference

Comparative study of the inhibition of sterol biosynthesis in Rubus fruticosus suspension cultures and zea mays seedlings by N-(1,5,9-trimethyldecyl)-4α,10-dimethyl-8-aza-trans-decal-3β-ol and derivatives

Botrytis cinerea

1 reference

Effect on ergosterol biosynthesis of a fungicide, SSF-109, in Botrytis cinerea

Graesiella emersonii

1 reference

Triparanol inhibition of sterol biosynthesis in Chlorella emersonii

Euphorbia nicaeensis

1 reference

Über Inhaltsstoffe von Euphorbiaceae, 8. Mitt. [1]. Triterpenester und Triterpenalkohole aus Euphorbia biglandulosa Desf. / Constituents of Euphorbiaceae, 8. Comm. [1]. Triterpen Esters and Triterpen Alcohols from Euphorbia biglandulosa Desf.

Euphorbia rigida

1 reference

Über Inhaltsstoffe von Euphorbiaceae, 8. Mitt. [1]. Triterpenester und Triterpenalkohole aus Euphorbia biglandulosa Desf. / Constituents of Euphorbiaceae, 8. Comm. [1]. Triterpen Esters and Triterpen Alcohols from Euphorbia biglandulosa Desf.

Gynostemma pentaphyllum

1 reference

4α,14α-Dimethyl-5α-ergosta-7,9(11),24(28)-trien-3β-ol from Phaseolus vulgaris and Gynostemma pentaphyllum

Hoya australis

1 reference

Investigations on Hoya Species. I

Psilotum nudum

1 reference

Sterols and fatty acids of a whisk fernPsilotum nudum

Euphorbia broteri

1 reference

Triterpenes from Euphorbia broteri

potato

2 references

Biosynthesis and metabolism of sesquiterpenoid phytoalexins and triterpenoids in potato cell suspension cultures

Effect of ageing on sterol metabolism in potato tuber slices

Oryza sativa

1 reference

Sterols in Rice Bran

Diplopterygium glaucum

1 reference

Triterpene Alcohols and Sterols from the Fern Gleichenia japonica SPR.

Goniophlebium formosanum

1 reference

24S-Chirality of 24-alkylsterols possessing a Δ25-double bond from Polypodium formosanum

Euphorbia sulcata

2 references

Diterpenoids and triterpenoids from Euphorbia guyoniana

Diterpenoids and triterpenoids from Euphorbia retusa

Euphorbia oxyphylla

1 reference

Triterpenes from Euphorbia broteri

Identifiers

InChI

InChI=1S/C30H50O/c1-19(2)20(3)9-10-21(4)23-13-17-30(8)26-12-11-24-22(5)27(31)15-16-28(24,6)25(26)14-18-29(23,30)7/h19,21-24,27,31H,3,9-18H2,1-2,4-8H3/t21-,22+,23-,24+,27+,28+,29-,30+/m1/s1

0 references

0 references

CAS Registry Number

16910-32-0

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

1 reference

17 September 2022

inferred from InChIKey

ChEBI ID

17791

mapping relation type

exact match

1 reference

International Chemical Identifier

InChI

InChI=1S/C30H50O/c1-19(2)20(3)9-10-21(4)23-13-17-30(8)26-12-11-24-22(5)27(31)15-16-28(24,6)25(26)14-18-29(23,30)7/h19,21-24,27,31H,3,9-18H2,1-2,4-8H3/t21-,22+,23-,24+,27+,28+,29-,30+/m1/s1

1 reference

1 reference

Human Metabolome Database ID

HMDB0001242

2 references

inferred from InChIKey

UNII

3RH57E39ER

1 reference

LIPID MAPS ID

LMST01030101

1 reference