Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C35H52O4 |
Molecular Weight | 536.785 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 4 / 4 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C(=O)[C@]12C(=O)[C@](CC=C(C)C)(C[C@H](CC=C(C)C)[C@@]1(C)CCC=C(C)C)C(=O)C(CC=C(C)C)=C2O
InChI
InChIKey=IWBJJCOKGLUQIZ-HQKKAZOISA-N
InChI=1S/C35H52O4/c1-22(2)13-12-19-33(11)27(16-14-23(3)4)21-34(20-18-25(7)8)30(37)28(17-15-24(5)6)31(38)35(33,32(34)39)29(36)26(9)10/h13-15,18,26-27,38H,12,16-17,19-21H2,1-11H3/t27-,33+,34+,35-/m0/s1
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
St. John's wort extracts and some of their constituents potently inhibit ultimate carcinogen formation from benzo[a]pyrene-7,8-dihydrodiol by human CYP1A1. | 2003 Nov 15 |
|
Induction of human CYP2C9 by rifampicin, hyperforin, and phenobarbital is mediated by the pregnane X receptor. | 2004 Feb |
|
MDR- and CYP3A4-mediated drug-herbal interactions. | 2006 Mar 27 |
|
Hyperforin--a key constituent of St. John's wort specifically activates TRPC6 channels. | 2007 Dec |
|
Synthesis of novel vitamin K2 analogues with modification at the ω-terminal position and their biological evaluation as potent steroid and xenobiotic receptor (SXR) agonists. | 2011 Jun 23 |
|
Improved assays for xenosensor activation based on reverse transfection. | 2015 Oct |
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
DSLD |
1122 (Number of products:1)
Created by
admin on Fri Dec 15 19:44:01 GMT 2023 , Edited by admin on Fri Dec 15 19:44:01 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
5834
Created by
admin on Fri Dec 15 19:44:01 GMT 2023 , Edited by admin on Fri Dec 15 19:44:01 GMT 2023
|
PRIMARY | |||
|
11079-53-1
Created by
admin on Fri Dec 15 19:44:01 GMT 2023 , Edited by admin on Fri Dec 15 19:44:01 GMT 2023
|
PRIMARY | |||
|
m6171
Created by
admin on Fri Dec 15 19:44:01 GMT 2023 , Edited by admin on Fri Dec 15 19:44:01 GMT 2023
|
PRIMARY | Merck Index | ||
|
C001654
Created by
admin on Fri Dec 15 19:44:01 GMT 2023 , Edited by admin on Fri Dec 15 19:44:01 GMT 2023
|
PRIMARY | |||
|
7646
Created by
admin on Fri Dec 15 19:44:01 GMT 2023 , Edited by admin on Fri Dec 15 19:44:01 GMT 2023
|
PRIMARY | |||
|
DB01892
Created by
admin on Fri Dec 15 19:44:01 GMT 2023 , Edited by admin on Fri Dec 15 19:44:01 GMT 2023
|
PRIMARY | |||
|
DTXSID90891409
Created by
admin on Fri Dec 15 19:44:01 GMT 2023 , Edited by admin on Fri Dec 15 19:44:01 GMT 2023
|
PRIMARY | |||
|
SUB183753
Created by
admin on Fri Dec 15 19:44:01 GMT 2023 , Edited by admin on Fri Dec 15 19:44:01 GMT 2023
|
PRIMARY | |||
|
100000169967
Created by
admin on Fri Dec 15 19:44:01 GMT 2023 , Edited by admin on Fri Dec 15 19:44:01 GMT 2023
|
PRIMARY | |||
|
RM741E34FP
Created by
admin on Fri Dec 15 19:44:01 GMT 2023 , Edited by admin on Fri Dec 15 19:44:01 GMT 2023
|
PRIMARY | |||
|
HYPERFORIN
Created by
admin on Fri Dec 15 19:44:01 GMT 2023 , Edited by admin on Fri Dec 15 19:44:01 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD