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

ID: ALA511184

Chembl Id: CHEMBL511184

PubChem CID: 44581584

Max Phase: Preclinical

Molecular Formula: C16H23NO3S2

Molecular Weight: 341.50

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCc1ccc(CSC[C@H](NC(=O)[C@H](C)CS)C(=O)O)cc1

Standard InChI:  InChI=1S/C16H23NO3S2/c1-3-12-4-6-13(7-5-12)9-22-10-14(16(19)20)17-15(18)11(2)8-21/h4-7,11,14,21H,3,8-10H2,1-2H3,(H,17,18)(H,19,20)/t11-,14+/m1/s1

Standard InChI Key:  DQQAGWYNBSJKIU-RISCZKNCSA-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: 341.50Molecular Weight (Monoisotopic): 341.1119AlogP: 2.62#Rotatable Bonds: 9
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: 3.47CX LogD: 0.29
Aromatic Rings: 1Heavy Atoms: 22QED Weighted: 0.60Np Likeness Score: -0.29

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