N-[(S)-1-(4-Chloro-3-methoxy-1-oxo-isochroman-7-ylcarbamoyl)-2-phenyl-ethyl]-nicotinamide

ID: ALA153562

PubChem CID: 44367844

Max Phase: Preclinical

Molecular Formula: C25H22ClN3O5

Molecular Weight: 479.92

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  COC1OC(=O)c2cc(NC(=O)[C@H](Cc3ccccc3)NC(=O)c3cccnc3)ccc2C1Cl

Standard InChI:  InChI=1S/C25H22ClN3O5/c1-33-25-21(26)18-10-9-17(13-19(18)24(32)34-25)28-23(31)20(12-15-6-3-2-4-7-15)29-22(30)16-8-5-11-27-14-16/h2-11,13-14,20-21,25H,12H2,1H3,(H,28,31)(H,29,30)/t20-,21?,25?/m0/s1

Standard InChI Key:  OYNAQLRQGXRVDC-LQAIBEDLSA-N

Molfile:  

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M  END

Associated Targets(Human)

ELANE Tclin Leukocyte elastase (8173 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

CELA2A Elastase 2A (403 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Alpha-chymotrypsin (819 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: 479.92Molecular Weight (Monoisotopic): 479.1248AlogP: 3.48#Rotatable Bonds: 7
Polar Surface Area: 106.62Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 12.87CX Basic pKa: 3.62CX LogP: 3.53CX LogD: 3.53
Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.40Np Likeness Score: -0.28

References

1. Kerrigan JE, Oleksyszyn J, Kam CM, Selzler J, Powers JC..  (1995)  Mechanism-based isocoumarin inhibitors for human leukocyte elastase. Effect of the 7-amino substituent and 3-alkoxy group in 3-alkoxy-7-amino-4-chloroisocoumarins on inhibitory potency.,  38  (3): [PMID:7853347] [10.1021/jm00003a017]

Source