ID: ALA4173973

Max Phase: Preclinical

Molecular Formula: C24H28N4O3S

Molecular Weight: 452.58

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCOC(=O)c1cnc2ccc(OCc3ccc(N[C@@H]4CCNC4)nc3)cc2c1SCC

Standard InChI:  InChI=1S/C24H28N4O3S/c1-3-30-24(29)20-14-26-21-7-6-18(11-19(21)23(20)32-4-2)31-15-16-5-8-22(27-12-16)28-17-9-10-25-13-17/h5-8,11-12,14,17,25H,3-4,9-10,13,15H2,1-2H3,(H,27,28)/t17-/m1/s1

Standard InChI Key:  MQRALJYJKNFYFY-QGZVFWFLSA-N

Associated Targets(Human)

Peptide N-myristoyltransferase 1 643 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Peptide N-myristoyltransferase 2 44 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Glycylpeptide N-tetradecanoyltransferase 128 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: 452.58Molecular Weight (Monoisotopic): 452.1882AlogP: 4.27#Rotatable Bonds: 9
Polar Surface Area: 85.37Molecular Species: BASEHBA: 8HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 10.38CX LogP: 3.37CX LogD: 0.58
Aromatic Rings: 3Heavy Atoms: 32QED Weighted: 0.37Np Likeness Score: -1.16

References

1. Goncalves V, Brannigan JA, Laporte A, Bell AS, Roberts SM, Wilkinson AJ, Leatherbarrow RJ, Tate EW..  (2017)  Structure-guided optimization of quinoline inhibitors of Plasmodium N-myristoyltransferase.,  (1): [PMID:28626547] [10.1039/C6MD00531D]

Source