N-Hydroxysuccinyl-L-phenylalanylglycyl[(2,4,6-Trimethylbenzoyl)oxy)methyl ketone

ID: ALA53410

PubChem CID: 44297707

Max Phase: Preclinical

Molecular Formula: C31H34N2O6

Molecular Weight: 530.62

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  Cc1cc(C)c(C(=O)OCC(=O)[C@@H](C)NC(=O)[C@H](Cc2ccccc2)NC(=O)OCc2ccccc2)c(C)c1

Standard InChI:  InChI=1S/C31H34N2O6/c1-20-15-21(2)28(22(3)16-20)30(36)38-19-27(34)23(4)32-29(35)26(17-24-11-7-5-8-12-24)33-31(37)39-18-25-13-9-6-10-14-25/h5-16,23,26H,17-19H2,1-4H3,(H,32,35)(H,33,37)/t23-,26+/m1/s1

Standard InChI Key:  OFCOJPYLXMKAGH-BVAGGSTKSA-N

Molfile:  

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M  END

Associated Targets(non-human)

CTSB Cathepsin B (273 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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: 530.62Molecular Weight (Monoisotopic): 530.2417AlogP: 4.38#Rotatable Bonds: 11
Polar Surface Area: 110.80Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.49CX Basic pKa: CX LogP: 6.25CX LogD: 6.25
Aromatic Rings: 3Heavy Atoms: 39QED Weighted: 0.36Np Likeness Score: -0.30

References

1. Wagner BM, Smith RA, Coles PJ, Copp LJ, Ernest MJ, Krantz A..  (1994)  In vivo inhibition of cathepsin B by peptidyl (acyloxy)methyl ketones.,  37  (12): [PMID:8021922] [10.1021/jm00038a012]

Source