ID: ALA3941246

Max Phase: Preclinical

Molecular Formula: C19H18FN3S

Molecular Weight: 339.44

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Fc1ccc(Nc2nc(C3CC3)nc3sc4c(c23)CCCC4)cc1

Standard InChI:  InChI=1S/C19H18FN3S/c20-12-7-9-13(10-8-12)21-18-16-14-3-1-2-4-15(14)24-19(16)23-17(22-18)11-5-6-11/h7-11H,1-6H2,(H,21,22,23)

Standard InChI Key:  QYNNGIVTIKPXDF-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: 339.44Molecular Weight (Monoisotopic): 339.1205AlogP: 5.33#Rotatable Bonds: 3
Polar Surface Area: 37.81Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 3.55CX LogP: 6.10CX LogD: 6.10
Aromatic Rings: 3Heavy Atoms: 24QED Weighted: 0.70Np Likeness Score: -2.20

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