(R)-2-((S)-3-mercapto-2-methylpropanamido)-3-(4-propylbenzylthio)propanoic acid

ID: ALA461021

Chembl Id: CHEMBL461021

PubChem CID: 44581585

Max Phase: Preclinical

Molecular Formula: C17H25NO3S2

Molecular Weight: 355.53

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCc1ccc(CSC[C@H](NC(=O)[C@H](C)CS)C(=O)O)cc1

Standard InChI:  InChI=1S/C17H25NO3S2/c1-3-4-13-5-7-14(8-6-13)10-23-11-15(17(20)21)18-16(19)12(2)9-22/h5-8,12,15,22H,3-4,9-11H2,1-2H3,(H,18,19)(H,20,21)/t12-,15+/m1/s1

Standard InChI Key:  ZSKJDRPLOVJZSR-DOMZBBRYSA-N

Associated Targets(Human)

ACE Tclin Angiotensin-converting enzyme (1423 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

LTA4H Leukotriene A-4 hydrolase (98 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: 355.53Molecular Weight (Monoisotopic): 355.1276AlogP: 3.01#Rotatable Bonds: 10
Polar Surface Area: 66.40Molecular Species: ACIDHBA: 4HBD: 3
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 3.96CX Basic pKa: CX LogP: 3.91CX LogD: 0.73
Aromatic Rings: 1Heavy Atoms: 23QED Weighted: 0.56Np Likeness Score: -0.14

References

1. Enomoto H, Morikawa Y, Miyake Y, Tsuji F, Mizuchi M, Suhara H, Fujimura K, Horiuchi M, Ban M..  (2009)  Synthesis and biological evaluation of N-mercaptoacylcysteine derivatives as leukotriene A4 hydrolase inhibitors.,  19  (2): [PMID:19042128] [10.1016/j.bmcl.2008.11.042]

Source