ID: ALA3951037

Max Phase: Preclinical

Molecular Formula: C20H21N3OS

Molecular Weight: 351.48

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(Nc2nc(C3CC3)nc3sc4c(c23)CCCC4)cc1

Standard InChI:  InChI=1S/C20H21N3OS/c1-24-14-10-8-13(9-11-14)21-19-17-15-4-2-3-5-16(15)25-20(17)23-18(22-19)12-6-7-12/h8-12H,2-7H2,1H3,(H,21,22,23)

Standard InChI Key:  WRYIIIQLTILTLD-UHFFFAOYSA-N

Associated Targets(non-human)

Mycobacterium tuberculosis 203094 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Probable L-lysine-epsilon aminotransferase 60 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mus musculus 284745 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: 351.48Molecular Weight (Monoisotopic): 351.1405AlogP: 5.20#Rotatable Bonds: 4
Polar Surface Area: 47.04Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 3.55CX LogP: 5.76CX LogD: 5.76
Aromatic Rings: 3Heavy Atoms: 25QED Weighted: 0.70Np Likeness Score: -1.81

References

1. Samala G, Brindha Devi P, Saxena S, Gunda S, Yogeeswari P, Sriram D..  (2016)  Anti-tubercular activities of 5,6,7,8-tetrahydrobenzo[4,5]thieno[2,3-d]pyrimidin-4-amine analogues endowed with high activity toward non-replicative Mycobacterium tuberculosis.,  24  (21): [PMID:27667550] [10.1016/j.bmc.2016.09.012]

Source