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1beta,3beta,15alpha-trihydroxy-urs-9(11)-12-diene

Canonical Smiles	C[C@@H]1CC[C@]2([C@@H]([C@H]1C)C1=CC=C3[C@@]([C@@]1([C@H](C2)O)C)(C)CC[C@@H]1[C@]3(C)[C@H](O)C[C@@H](C1(C)C)O)C
InChI	InChI=1S/C30H48O3/c1-17-11-13-27(5)16-24(33)30(8)19(25(27)18(17)2)9-10-21-28(30,6)14-12-20-26(3,4)22(31)15-23(32)29(20,21)7/h9-10,17-18,20,22-25,31-33H,11-16H2,1-8H3/t17-,18+,20+,22+,23-,24+,25+,27-,28-,29+,30+/m1/s1
InChIKey	CTCOHAYTJYAGAT-OSIMVUHNSA-N
Formula	C₃₀H₄₈O₃
HBA	3
HBD	3
MW	456.71
Rotatable Bonds	0
TPSA	60.69
LogP	5.89
Number Rings	5
Number Aromatic Rings	0
Heavy Atom Count	33
Formal Charge	0
Fraction CSP3	0.87
Exact Mass	456.36
Number of Lipinski Rule Violations	1

#	Species	Family	Kingdom	NCBI Taxonomy ID
1	Salvia argentea	Lamiaceae	Plantae	49208

Showing of synonyms

Bechkri S, Alabdul Magid A, et al. (2019). Triterpenes from Salvia argentea var. aurasiaca and their antibacterial and cytotoxic activities.. Fitoterapia, 2019, 139, 104296. [View] [PubMed]

No compound-protein relationship available.

SMILES: C1CCCC2C1CCC(C2=3)C4C(=CC3)C5C(CC4)CCCC5

Level: 0

Mol. Weight: 456.71 g/mol

Anti-alzheimer

Anti-hyperlipidemic

Anti-hypertensive

Anti-inflammatory

Antimicrobial

Antioxidant

Antipyretic

Antitumor

Expectorant

Hepatoprotective

Sedative

Spasmolytic

Absorption

Protein Name	UniProt ID	Entry Name	Species	#Pharmacophore Points	Probability (0.7 ≤ Tversky Score ≤ 1.0)
Fatty acid-binding protein 10-A, liver basic	Q9I8L5	FA10A_DANRE	Danio rerio	2	0.7450
3-ketosteroid dehydrogenase	Q9RA02	Q9RA02_RHOER	Rhodococcus erythropolis	2	0.7435