MULTIFLORENOL

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C30H50O
Molecular Weight	426.7174
Optical Activity	UNSPECIFIED
Defined Stereocenters	8 / 8
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CC1(C)CC[C@]2(C)CC[C@]3(C)C4=CC[C@H]5C(C)(C)[C@@H](O)CC[C@]5(C)[C@H]4CC[C@@]3(C)[C@@H]2C1

InChI

InChIKey=ZDFUASMRJUVZJP-GIIHIBIBSA-N

InChI=1S/C30H50O/c1-25(2)15-16-27(5)17-18-29(7)21-9-10-22-26(3,4)24(31)12-13-28(22,6)20(21)11-14-30(29,8)23(27)19-25/h9,20,22-24,31H,10-19H2,1-8H3/t20-,22-,23+,24-,27+,28+,29+,30-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C30H50O
Molecular Weight	426.7174
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	8 / 8
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

Title	Date	PubMed
Cloning and characterization of oxidosqualene cyclases from Kalanchoe daigremontiana: enzymes catalyzing up to 10 rearrangement steps yielding friedelin and other triterpenoids.	2010-09-24	20610397

Substance Class	Chemical Created by `admin` on `Mon Mar 31 20:21:27 GMT 2025` Edited by `admin` on `Mon Mar 31 20:21:27 GMT 2025`
Record UNII	S2TU3PU8DO
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

MULTIFLORENOL

Common Name

English

(3S-(3.ALPHA.,4A.BETA.,6B.ALPHA.,8A.ALPHA.,12A.ALPHA.,12B.BETA.,14A.BETA.,14B.ALPHA.))-1,2,3,4,4A,5,6B,7,8,8A,9,10,11,12,12A,12B,13,14,14A,14B-EICOSAHYDRO-4,4,6B,8A,11,11,12B,14B-OCTAMETHYL-3-PICENOL

Preferred Name

English

26-NOROLEAN-7-EN-3-OL, 13-METHYL-, (3.BETA.,13.ALPHA.,14.BETA.)-

Common Name

English

D:C-FRIEDOOLEAN-7-EN-3.BETA.-OL

Common Name

English

D:C-FRIEDOOLEAN-7-EN-3-OL, (3.BETA.)-

Common Name

English

Code System Code Type Description

CAS

2270-62-4

Created by admin on Mon Mar 31 20:21:27 GMT 2025 , Edited by admin on Mon Mar 31 20:21:27 GMT 2025

PRIMARY

PUBCHEM

12312990

Created by admin on Mon Mar 31 20:21:27 GMT 2025 , Edited by admin on Mon Mar 31 20:21:27 GMT 2025

PRIMARY

EPA CompTox

DTXSID50177231

Created by admin on Mon Mar 31 20:21:27 GMT 2025 , Edited by admin on Mon Mar 31 20:21:27 GMT 2025

PRIMARY

FDA UNII

S2TU3PU8DO

Created by admin on Mon Mar 31 20:21:27 GMT 2025 , Edited by admin on Mon Mar 31 20:21:27 GMT 2025

PRIMARY