Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C30H50O2 |
| Molecular Weight | 442.7168 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 10 / 10 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@H]1CC[C@]2(CO)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2[C@H]1C
InChI
InChIKey=XUARCIYIVXVTAE-ZAPOICBTSA-N
InChI=1S/C30H50O2/c1-19-10-15-30(18-31)17-16-28(6)21(25(30)20(19)2)8-9-23-27(5)13-12-24(32)26(3,4)22(27)11-14-29(23,28)7/h8,19-20,22-25,31-32H,9-18H2,1-7H3/t19-,20+,22+,23-,24+,25+,27+,28-,29-,30-/m1/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| CYP716A subfamily members are multifunctional oxidases in triterpenoid biosynthesis. | 2011-12 |
|
| Antitubercular activity of triterpenoids from Asteraceae flowers. | 2005-01 |
|
| Antimycobacterial plant terpenoids. | 2001-11 |
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| Inhibitory effects of triterpenoids and sterols on human immunodeficiency virus-1 reverse transcriptase. | 2001-05 |
|
| Inhibitory effect of triterpenes from Crataegus pinatifida on HIV-I protease. | 1999-05 |
|
| Triterpenes as potential dimerization inhibitors of HIV-1 protease. | 1996-10-14 |
Patents
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545-46-0
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SUBSTANCE RECORD
