ID: ALA4285480

Max Phase: Preclinical

Molecular Formula: C26H30N4O6

Molecular Weight: 494.55

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(C)C(NC(=O)OCc1ccccc1)C(=O)NCC(=O)NC(Cc1c[nH]c2ccccc12)C(=O)O

Standard InChI:  InChI=1S/C26H30N4O6/c1-16(2)23(30-26(35)36-15-17-8-4-3-5-9-17)24(32)28-14-22(31)29-21(25(33)34)12-18-13-27-20-11-7-6-10-19(18)20/h3-11,13,16,21,23,27H,12,14-15H2,1-2H3,(H,28,32)(H,29,31)(H,30,35)(H,33,34)

Standard InChI Key:  QLXOMMQGDJICAR-UHFFFAOYSA-N

Associated Targets(non-human)

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: 494.55Molecular Weight (Monoisotopic): 494.2165AlogP: 2.35#Rotatable Bonds: 11
Polar Surface Area: 149.62Molecular Species: ACIDHBA: 5HBD: 5
#RO5 Violations: 0HBA (Lipinski): 10HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: 3.81CX Basic pKa: CX LogP: 2.58CX LogD: -0.67
Aromatic Rings: 3Heavy Atoms: 36QED Weighted: 0.28Np Likeness Score: -0.43

References

1. 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]

Source