2-({[4-(Adamantan-1-yl)phenyl]carbonyl}amino)-5-chlorobenzoic acid

ID: ALA4207363

Chembl Id: CHEMBL4207363

PubChem CID: 66680617

Max Phase: Preclinical

Molecular Formula: C24H24ClNO3

Molecular Weight: 409.91

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C(Nc1ccc(Cl)cc1C(=O)O)c1ccc(C23CC4CC(CC(C4)C2)C3)cc1

Standard InChI:  InChI=1S/C24H24ClNO3/c25-19-5-6-21(20(10-19)23(28)29)26-22(27)17-1-3-18(4-2-17)24-11-14-7-15(12-24)9-16(8-14)13-24/h1-6,10,14-16H,7-9,11-13H2,(H,26,27)(H,28,29)

Standard InChI Key:  UYFRJXOBXCZLSO-UHFFFAOYSA-N

Alternative Forms

Associated Targets(Human)

SERPINE1 Tchem Plasminogen activator inhibitor-1 (498 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Rattus norvegicus (775804 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: 409.91Molecular Weight (Monoisotopic): 409.1445AlogP: 5.76#Rotatable Bonds: 4
Polar Surface Area: 66.40Molecular Species: ACIDHBA: 2HBD: 2
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 3.36CX Basic pKa: CX LogP: 6.33CX LogD: 2.91
Aromatic Rings: 2Heavy Atoms: 29QED Weighted: 0.67Np Likeness Score: -0.84

References

1. Yamaoka N, Murano K, Kodama H, Maeda A, Dan T, Nakabayashi T, Miyata T, Meguro K..  (2018)  Identification of novel plasminogen activator inhibitor-1 inhibitors with improved oral bioavailability: Structure optimization of N-acylanthranilic acid derivatives.,  28  (4): [PMID:29366646] [10.1016/j.bmcl.2017.11.016]

Source