(2S,4aR,4bR,6R,8S,8aR,10aR)-1,1,4a,8,8a-pentamethyl-7-oxo-8-(3-oxopentyl)tetradecahydrophenanthrene-2,6-diyl diacetate

ID: ALA4066034

PubChem CID: 137633932

Max Phase: Preclinical

Molecular Formula: C28H44O6

Molecular Weight: 476.65

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CCC(=O)CC[C@]1(C)C(=O)[C@H](OC(C)=O)C[C@@H]2[C@@]3(C)CC[C@H](OC(C)=O)C(C)(C)[C@@H]3CC[C@]21C

Standard InChI:  InChI=1S/C28H44O6/c1-9-19(31)10-14-28(8)24(32)20(33-17(2)29)16-22-26(6)13-12-23(34-18(3)30)25(4,5)21(26)11-15-27(22,28)7/h20-23H,9-16H2,1-8H3/t20-,21+,22-,23+,26+,27-,28-/m1/s1

Standard InChI Key:  MWSYQQIVSNHTSV-WXXOXURNSA-N

Molfile:  

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M  END

Alternative Forms

  1. Parent:

    ALA4066034

    ---

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: 476.65Molecular Weight (Monoisotopic): 476.3138AlogP: 5.45#Rotatable Bonds: 6
Polar Surface Area: 86.74Molecular Species: NEUTRALHBA: 6HBD:
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): #RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 5.15CX LogD: 5.15
Aromatic Rings: Heavy Atoms: 34QED Weighted: 0.47Np Likeness Score: 2.30

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