(3S,5R,8R,9R,10R,12R,13S,14R,17S)-4,4,8,10,14-Pentamethylhexadecahydro-1H-cyclopenta[a]phenanthrene-3,12,17-triol

ID: ALA4084915

PubChem CID: 137647769

Max Phase: Preclinical

Molecular Formula: C22H38O3

Molecular Weight: 350.54

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CC1(C)[C@@H](O)CC[C@]2(C)[C@H]3C[C@@H](O)[C@@H]4[C@@H](O)CC[C@@]4(C)[C@]3(C)CC[C@@H]12

Standard InChI:  InChI=1S/C22H38O3/c1-19(2)15-7-11-21(4)16(20(15,3)9-8-17(19)25)12-14(24)18-13(23)6-10-22(18,21)5/h13-18,23-25H,6-12H2,1-5H3/t13-,14+,15-,16+,17-,18-,20-,21+,22+/m0/s1

Standard InChI Key:  GHEDPBNXBNIAIZ-XVDOCLBUSA-N

Molfile:  

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M  END

Alternative Forms

  1. Parent:

    ALA4084915

    ---

Associated Targets(Human)

HSD11B1 Tclin 11-beta-hydroxysteroid dehydrogenase 1 (5910 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hsd11b1 11-beta-hydroxysteroid dehydrogenase 1 (1542 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 350.54Molecular Weight (Monoisotopic): 350.2821AlogP: 3.75#Rotatable Bonds:
Polar Surface Area: 60.69Molecular Species: NEUTRALHBA: 3HBD: 3
#RO5 Violations: HBA (Lipinski): 3HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: 2.82CX LogD: 2.82
Aromatic Rings: Heavy Atoms: 25QED Weighted: 0.62Np Likeness Score: 2.89

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