ID: ALA551672

Max Phase: Preclinical

Molecular Formula: C20H18ClN5O3S

Molecular Weight: 443.92

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cc(S(=O)(=O)N(Cc2ccco2)Cc2ccccc2Cl)ccc1-n1cnnn1

Standard InChI:  InChI=1S/C20H18ClN5O3S/c1-15-11-18(8-9-20(15)26-14-22-23-24-26)30(27,28)25(13-17-6-4-10-29-17)12-16-5-2-3-7-19(16)21/h2-11,14H,12-13H2,1H3

Standard InChI Key:  YDLHDYNJJFAMSV-UHFFFAOYSA-N

Associated Targets(Human)

Carboxypeptidase B 100 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Carboxypeptidase B 26 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Carboxypeptidase A1 174 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: 443.92Molecular Weight (Monoisotopic): 443.0819AlogP: 3.61#Rotatable Bonds: 7
Polar Surface Area: 94.12Molecular Species: NEUTRALHBA: 7HBD: 0
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.69CX LogD: 3.69
Aromatic Rings: 4Heavy Atoms: 30QED Weighted: 0.43Np Likeness Score: -2.78

References

1. Fernández D, Avilés FX, Vendrell J..  (2009)  A new type of five-membered heterocyclic inhibitors of basic metallocarboxypeptidases.,  44  (8): [PMID:19386397] [10.1016/j.ejmech.2009.03.034]

Source