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Obtusifoliol

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Obtusifoliol
Identifiers

CAS Number	16910-32-0
3D model (JSmol)	Interactive image
ChEBI	CHEBI:17791
ChEMBL	ChEMBL1978954
ChemSpider	167937
KEGG	C01943
PubChem CID	5047
UNII	3RH57E39ER
CompTox Dashboard(EPA)	DTXSID60168650
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 Key: MMNYKQIDRZNIKT-YLANKJTKSA-N 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 Key: MMNYKQIDRZNIKT-YLANKJTKSA-N
SMILES C[C@@H]1[C@H](CC[C@]2(C1CCC3=C2CC[C@]4([C@]3(CC[C@@H]4[C@H](C)CCC(=C)C(C)C)C)C)C)O
Properties
Chemical formula	C₃₀H₅₀O
Molar mass	426.729 g·mol⁻¹
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). Infobox references

Chemical compound

Obtusifoliol is ametabolic intermediate ofsterols made by certainfungi. It can be converted todelta8,14-sterol by the enzymeERG11 (CYP51F1).^[1]

toHMG-CoA	Acetyl-CoA Acetoacetyl-CoA HMB HMB-CoA HMG-CoA
Ketone bodies	Acetone Acetoacetic acid β-Hydroxybutyric acid
toDMAPP	Mevalonic acid Phosphomevalonic acid 5-Diphosphomevalonic acid Isopentenyl pyrophosphate Dimethylallyl pyrophosphate
Geranyl-	Geranyl pyrophosphate Geranylgeranyl pyrophosphate
Carotenoid	Prephytoene diphosphate Phytoene

Nonhuman

ToSitosterol	Cycloartenol Cycloeucalenol Obtusifoliol 4α-methylfecosterol Isofucosterol 24-Methylenelophenol Sitosterol MorePhytosterols seehere instead.
ToErgocalciferol	Fecosterol Episterol Ergostatrienol Ergostatetraenol Ergosterol Ergocalciferol

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