25-Chloro-27-norcholest-4-en-3-one

ID: ALA2048332

Chembl Id: CHEMBL2048332

PubChem CID: 70694627

Max Phase: Preclinical

Molecular Formula: C26H41ClO

Molecular Weight: 405.07

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(Cl)CCC[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/C26H41ClO/c1-17(6-5-7-18(2)27)22-10-11-23-21-9-8-19-16-20(28)12-14-25(19,3)24(21)13-15-26(22,23)4/h16-18,21-24H,5-15H2,1-4H3/t17-,18?,21+,22-,23+,24+,25+,26-/m1/s1

Standard InChI Key:  YPBFNQUIPOQWQC-VRPZDKJBSA-N

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: 405.07Molecular Weight (Monoisotopic): 404.2846AlogP: 7.57#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: 7.28CX LogD: 7.28
Aromatic Rings: Heavy Atoms: 28QED Weighted: 0.43Np Likeness Score: 2.15

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