ID: ALA213408

Max Phase: Preclinical

Molecular Formula: C18H21N3O6

Molecular Weight: 375.38

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1ccccc1C(=O)NNC(=O)C1(C(=O)N[C@H]2CC(=O)OC2O)CCC1

Standard InChI:  InChI=1S/C18H21N3O6/c1-10-5-2-3-6-11(10)14(23)20-21-17(26)18(7-4-8-18)16(25)19-12-9-13(22)27-15(12)24/h2-3,5-6,12,15,24H,4,7-9H2,1H3,(H,19,25)(H,20,23)(H,21,26)/t12-,15?/m0/s1

Standard InChI Key:  ZSOPKWJQJKUHFH-SFVWDYPZSA-N

Associated Targets(Human)

Caspase-8 1006 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Caspase-1 6235 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

THP-1 11052 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Caspase-3 3632 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: 375.38Molecular Weight (Monoisotopic): 375.1430AlogP: -0.32#Rotatable Bonds: 4
Polar Surface Area: 133.83Molecular Species: NEUTRALHBA: 6HBD: 4
#RO5 Violations: 0HBA (Lipinski): 9HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.97CX Basic pKa: CX LogP: 0.52CX LogD: 0.52
Aromatic Rings: 1Heavy Atoms: 27QED Weighted: 0.32Np Likeness Score: -0.44

References

1. Soper DL, Sheville J, O'Neil SV, Wang Y, Laufersweiler MC, Oppong KA, Wos JA, Ellis CD, Fancher AN, Lu W, Suchanek MK, Wang RL, De B, Demuth TP..  (2006)  Synthesis and evaluation of novel 1-(2-acylhydrazinocarbonyl)-cycloalkyl carboxamides as interleukin-1beta converting enzyme (ICE) inhibitors.,  16  (16): [PMID:16782334] [10.1016/j.bmcl.2006.05.076]

Source