27-Norcholest-4-en-3-one

ID: ALA2048326

Chembl Id: CHEMBL2048326

Cas Number: 905300-93-8

PubChem CID: 70686269

Max Phase: Preclinical

Molecular Formula: C26H42O

Molecular Weight: 370.62

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C

Standard InChI:  InChI=1S/C26H42O/c1-5-6-7-8-18(2)22-11-12-23-21-10-9-19-17-20(27)13-15-25(19,3)24(21)14-16-26(22,23)4/h17-18,21-24H,5-16H2,1-4H3/t18-,21+,22-,23+,24+,25+,26-/m1/s1

Standard InChI Key:  MCFWQAHODJJXRF-GHSKVMHMSA-N

Alternative Forms

  1. Parent:

Associated Targets(non-human)

cyp125 Putative cytochrome P450 125 (56 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: 370.62Molecular Weight (Monoisotopic): 370.3236AlogP: 7.35#Rotatable Bonds: 5
Polar Surface Area: 17.07Molecular Species: NEUTRALHBA: 1HBD:
#RO5 Violations: 1HBA (Lipinski): 1HBD (Lipinski): #RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 7.39CX LogD: 7.39
Aromatic Rings: Heavy Atoms: 27QED Weighted: 0.46Np Likeness Score: 2.29

References

1. Johnston JB, Singh AA, Clary AA, Chen CK, Hayes PY, Chow S, De Voss JJ, Ortiz de Montellano PR..  (2012)  Substrate analog studies of the ω-regiospecificity of Mycobacterium tuberculosis cholesterol metabolizing cytochrome P450 enzymes CYP124A1, CYP125A1 and CYP142A1.,  20  (13): [PMID:22647881] [10.1016/j.bmc.2012.05.003]

Source