(2R)-2,5-diamino-N-(1-oxo-4-phenyl-1-(quinolin-3-ylamino)butan-2-yl)pentanamide

ID: ALA1940620

Chembl Id: CHEMBL1940620

PubChem CID: 57403443

Max Phase: Preclinical

Molecular Formula: C24H29N5O2

Molecular Weight: 419.53

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  NCCC[C@@H](N)C(=O)NC(CCc1ccccc1)C(=O)Nc1cnc2ccccc2c1

Standard InChI:  InChI=1S/C24H29N5O2/c25-14-6-10-20(26)23(30)29-22(13-12-17-7-2-1-3-8-17)24(31)28-19-15-18-9-4-5-11-21(18)27-16-19/h1-5,7-9,11,15-16,20,22H,6,10,12-14,25-26H2,(H,28,31)(H,29,30)/t20-,22?/m1/s1

Standard InChI Key:  KUXYCYLURMIFID-PSDZMVHGSA-N

Associated Targets(non-human)

Streptomyces coelicolor (161 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

Calculated Properties

Molecular Weight: 419.53Molecular Weight (Monoisotopic): 419.2321AlogP: 2.36#Rotatable Bonds: 10
Polar Surface Area: 123.13Molecular Species: BASEHBA: 5HBD: 4
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): 6#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.47CX Basic pKa: 9.91CX LogP: 2.00CX LogD: -1.19
Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.40Np Likeness Score: -0.46

References

1. Okandeji BO, Greenwald DM, Wroten J, Sello JK..  (2011)  Synthesis and evaluation of inhibitors of bacterial drug efflux pumps of the major facilitator superfamily.,  19  (24): [PMID:22055717] [10.1016/j.bmc.2011.10.011]

Source