ID: ALA1706590

Max Phase: Preclinical

Molecular Formula: C16H17N3O2

Molecular Weight: 283.33

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  NC(Cc1c[nH]c2ccccc12)C(=O)NCc1ccco1

Standard InChI:  InChI=1S/C16H17N3O2/c17-14(16(20)19-10-12-4-3-7-21-12)8-11-9-18-15-6-2-1-5-13(11)15/h1-7,9,14,18H,8,10,17H2,(H,19,20)

Standard InChI Key:  FQLXKOCHDBPFLL-UHFFFAOYSA-N

Associated Targets(Human)

Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 93046 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Plasmodium falciparum 966862 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Isocitrate lyase 1 45 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: YesOral: 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: 283.33Molecular Weight (Monoisotopic): 283.1321AlogP: 1.95#Rotatable Bonds: 5
Polar Surface Area: 84.05Molecular Species: NEUTRALHBA: 3HBD: 3
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.09CX Basic pKa: 7.96CX LogP: 1.38CX LogD: 0.71
Aromatic Rings: 3Heavy Atoms: 21QED Weighted: 0.67Np Likeness Score: -0.69

References

1. PubChem BioAssay data set, 
2. Bhusal RP, Patel K, Kwai BXC, Swartjes A, Bashiri G, Reynisson J, Sperry J, Leung IKH..  (2017)  Development of NMR and thermal shift assays for the evaluation of Mycobacterium tuberculosis isocitrate lyase inhibitors.,  (11): [PMID:30108733] [10.1039/C7MD00456G]