ID: ALA217191

Max Phase: Preclinical

Molecular Formula: C13H11N3O3S

Molecular Weight: 289.32

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(/C=C/Sc1nc(O)cc(-c2ccccc2)n1)NO

Standard InChI:  InChI=1S/C13H11N3O3S/c17-11(16-19)6-7-20-13-14-10(8-12(18)15-13)9-4-2-1-3-5-9/h1-8,19H,(H,16,17)(H,14,15,18)/b7-6+

Standard InChI Key:  TWLUULROUSJAIP-VOTSOKGWSA-N

Associated Targets(non-human)

Histone deacetylase HD2 351 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Histone deacetylase HD1B 86 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: 289.32Molecular Weight (Monoisotopic): 289.0521AlogP: 1.96#Rotatable Bonds: 4
Polar Surface Area: 95.34Molecular Species: NEUTRALHBA: 6HBD: 3
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.46CX Basic pKa: 1.87CX LogP: 2.41CX LogD: 2.41
Aromatic Rings: 2Heavy Atoms: 20QED Weighted: 0.26Np Likeness Score: -0.75

References

1. Mai A, Massa S, Rotili D, Simeoni S, Ragno R, Botta G, Nebbioso A, Miceli M, Altucci L, Brosch G..  (2006)  Synthesis and biological properties of novel, uracil-containing histone deacetylase inhibitors.,  49  (20): [PMID:17004718] [10.1021/jm0605536]

Source