ID: ALA3958071

Max Phase: Preclinical

Molecular Formula: C24H23N3S

Molecular Weight: 385.54

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(Nc2nc(-c3ccccc3)nc3sc4c(c23)CCCC4)c(C)c1

Standard InChI:  InChI=1S/C24H23N3S/c1-15-12-13-19(16(2)14-15)25-23-21-18-10-6-7-11-20(18)28-24(21)27-22(26-23)17-8-4-3-5-9-17/h3-5,8-9,12-14H,6-7,10-11H2,1-2H3,(H,25,26,27)

Standard InChI Key:  MPLLJIWCGPWBOA-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: 6.60#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: 3.25CX LogP: 8.08CX LogD: 8.08
Aromatic Rings: 4Heavy Atoms: 28QED Weighted: 0.43Np Likeness Score: -2.17

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