1-ethoxy-1-oxopropan-2-yl 2-((S)-1-((S)-2-((S)-1-acetylpyrrolidine-2-carboxamido)propanoyl)pyrrolidine-2-carbonyl)-1-methylhydrazinecarboxylate

ID: ALA3272700

PubChem CID: 90677666

Max Phase: Preclinical

Molecular Formula: C22H35N5O8

Molecular Weight: 497.55

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCOC(=O)C(C)OC(=O)N(C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](C)NC(=O)[C@@H]1CCCN1C(C)=O

Standard InChI:  InChI=1S/C22H35N5O8/c1-6-34-21(32)14(3)35-22(33)25(5)24-19(30)17-10-8-12-27(17)20(31)13(2)23-18(29)16-9-7-11-26(16)15(4)28/h13-14,16-17H,6-12H2,1-5H3,(H,23,29)(H,24,30)/t13-,14?,16-,17-/m0/s1

Standard InChI Key:  WPRULIVJKFUPFR-PEDUJENPSA-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 Pancreatic elastase (395 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: 497.55Molecular Weight (Monoisotopic): 497.2486AlogP: -0.46#Rotatable Bonds: 7
Polar Surface Area: 154.66Molecular Species: NEUTRALHBA: 8HBD: 2
#RO5 Violations: HBA (Lipinski): 13HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 10.05CX Basic pKa: CX LogP: -1.29CX LogD: -1.29
Aromatic Rings: Heavy Atoms: 35QED Weighted: 0.35Np Likeness Score: -0.72

References

1. Dorn CP, Zimmerman M, Yang SS, Yurewicz EC, Ashe BM, Frankshun R, Jones H..  (1977)  Proteinase inhibitors. I. Inhibitors of elastase.,  20  (11): [PMID:915907] [10.1021/jm00221a020]

Source