17beta-[(N-Heptyl)methylamino]-4-aza-5alpha-androstan-3-one

ID: ALA1079514

Chembl Id: CHEMBL1079514

PubChem CID: 46882312

Max Phase: Preclinical

Molecular Formula: C26H46N2O

Molecular Weight: 402.67

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCCCCCN(C)C1CC[C@H]2[C@@H]3CC[C@H]4NC(=O)CC[C@]4(C)[C@H]3CC[C@]12C

Standard InChI:  InChI=1S/C26H46N2O/c1-5-6-7-8-9-18-28(4)23-13-11-20-19-10-12-22-25(2,17-15-24(29)27-22)21(19)14-16-26(20,23)3/h19-23H,5-18H2,1-4H3,(H,27,29)/t19-,20-,21-,22+,23?,25+,26-/m0/s1

Standard InChI Key:  KUWNYQSGXDSFCP-OMVPJQILSA-N

Associated Targets(Human)

HSD17B7 Tchem 3-keto-steroid reductase (330 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: 402.67Molecular Weight (Monoisotopic): 402.3610AlogP: 5.78#Rotatable Bonds: 7
Polar Surface Area: 32.34Molecular Species: BASEHBA: 2HBD: 1
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 10.79CX LogP: 5.52CX LogD: 2.37
Aromatic Rings: Heavy Atoms: 29QED Weighted: 0.55Np Likeness Score: 0.99

References

1. Bellavance E, Luu-The V, Poirier D..  (2009)  Potent and selective steroidal inhibitors of 17beta-hydroxysteroid dehydrogenase type 7, an enzyme that catalyzes the reduction of the key hormones estrone and dihydrotestosterone.,  52  (23): [PMID:19772289] [10.1021/jm900921c]

Source