ID: ALA2430785

Max Phase: Preclinical

Molecular Formula: C19H26O

Molecular Weight: 270.42

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C[C@@]12CCC[C@H]1[C@@H]1C(=O)C=C3C=CCC[C@]3(C)[C@H]1CC2

Standard InChI:  InChI=1S/C19H26O/c1-18-9-5-7-14(18)17-15(8-11-18)19(2)10-4-3-6-13(19)12-16(17)20/h3,6,12,14-15,17H,4-5,7-11H2,1-2H3/t14-,15-,17-,18-,19-/m0/s1

Standard InChI Key:  KTFHYOMAVCUFEY-FQQAFBJJSA-N

Associated Targets(Human)

MCF7 126967 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MKN-28 466 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HeLa 62764 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

KB 17409 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

Properties

Molecular Weight: 270.42Molecular Weight (Monoisotopic): 270.1984AlogP: 4.68#Rotatable Bonds: 0
Polar Surface Area: 17.07Molecular Species: NEUTRALHBA: 1HBD: 0
#RO5 Violations: 0HBA (Lipinski): 1HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.49CX LogD: 4.49
Aromatic Rings: 0Heavy Atoms: 20QED Weighted: 0.62Np Likeness Score: 2.81

References

1. Yao J, Ye W, Liu J, Liu J, Wang C.  (2013)  Synthesis and cytotoxicity of (3)-3-acetyloxy-5(6)-androsten-7-one oxime and 3,5(6)-androstadien-7-one oxime,  [10.1007/s00044-013-0788-9]

Source