ID: ALA3898575

Max Phase: Preclinical

Molecular Formula: C24H23N3S

Molecular Weight: 385.54

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  c1ccc(CCNc2nc(-c3ccccc3)nc3sc4c(c23)CCCC4)cc1

Standard InChI:  InChI=1S/C24H23N3S/c1-3-9-17(10-4-1)15-16-25-23-21-19-13-7-8-14-20(19)28-24(21)27-22(26-23)18-11-5-2-6-12-18/h1-6,9-12H,7-8,13-16H2,(H,25,26,27)

Standard InChI Key:  KYFVQYRIHFWANA-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: 385.54Molecular Weight (Monoisotopic): 385.1613AlogP: 5.89#Rotatable Bonds: 5
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: 4.03CX LogP: 7.34CX LogD: 7.34
Aromatic Rings: 4Heavy Atoms: 28QED Weighted: 0.47Np Likeness Score: -1.73

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