3-((3S,3aS,4R,5aR,6R,9aR,9bR)-3,4-dihydroxy-7-(2-hydroxypropan-2-yl)-6,9a,9b-trimethyldodecahydro-1H-cyclopenta[a]naphthalen-6-yl)propanoic acid

Names and Identifiers

Canonical SMILES: CC(C)(O)[C@@H]1CC[C@]2(C)[C@H](C[C@@H](O)[C@@H]3[C@@H](O)CC[C@]32C)[C@@]1(C)CCC(=O)O

Standard InChI: InChI=1S/C22H38O5/c1-19(2,27)15-7-11-21(4)16(20(15,3)9-8-17(25)26)12-14(24)18-13(23)6-10-22(18,21)5/h13-16,18,23-24,27H,6-12H2,1-5H3,(H,25,26)/t13-,14+,15-,16+,18-,20-,21+,22+/m0/s1

Standard InChI Key: UMJSXJCFPRFKCG-WFNFYUGMSA-N

Molfile:

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M  END

Alternative Forms

Parent:

ALA4100206
---

Associated Targets(Human)

HSD11B1 Tclin 11-beta-hydroxysteroid dehydrogenase 1 (5910 Activities)

Discover Target: HSD11B1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Hsd11b1 11-beta-hydroxysteroid dehydrogenase 1 (1542 Activities)

Discover Target: Hsd11b1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Molecule Features

Natural Product: No	Oral: No	Chemical Probe: No	Parenteral: No
Molecule Type: Small molecule	Topical: No	First In Class: No	Black Box: No
Chirality: No	Availability: No	Prodrug: No

Drug Indications

MESH ID	MESH Heading	EFO IDs	EFO Terms	Max Phase for Indication	References

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Calculated Properties

Molecular Weight: 382.54	Molecular Weight (Monoisotopic): 382.2719	AlogP: 3.20	#Rotatable Bonds: 4
Polar Surface Area: 97.99	Molecular Species: ACID	HBA: 4	HBD: 4
#RO5 Violations: ┄	HBA (Lipinski): 5	HBD (Lipinski): 4	#RO5 Violations (Lipinski): ┄
CX Acidic pKa: 4.72	CX Basic pKa: ┄	CX LogP: 1.95	CX LogD: -0.68
Aromatic Rings: ┄	Heavy Atoms: 27	QED Weighted: 0.60	Np Likeness Score: 2.77

References

1. Shao LD, Bao Y, Shen Y, Su J, Leng Y, Zhao QS.. (2017) Synthesis of selective 11β-HSD1 inhibitors based on dammarane scaffold., 135 [PMID:28458137] [10.1016/j.ejmech.2017.04.059]

Source

Source(1):

Scientific Literature