ID: ALA3142353

Max Phase: Preclinical

Molecular Formula: C28H55N3O5

Molecular Weight: 513.76

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCCCCCC(O)[C@H](CCC)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)C(C)C

Standard InChI:  InChI=1S/C28H55N3O5/c1-10-12-13-14-15-16-18-22(32)21(17-11-2)29-25(33)23(19(3)4)30-26(34)24(20(5)6)31-27(35)36-28(7,8)9/h19-24,32H,10-18H2,1-9H3,(H,29,33)(H,30,34)(H,31,35)/t21-,22?,23-,24-/m0/s1

Standard InChI Key:  YVIIRSKNNANXSZ-CNTOOOFYSA-N

Associated Targets(Human)

Pepsin A 59 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: 513.76Molecular Weight (Monoisotopic): 513.4142AlogP: 5.07#Rotatable Bonds: 17
Polar Surface Area: 116.76Molecular Species: NEUTRALHBA: 5HBD: 4
#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): 4#RO5 Violations (Lipinski): 2
CX Acidic pKa: 12.70CX Basic pKa: CX LogP: 5.87CX LogD: 5.87
Aromatic Rings: 0Heavy Atoms: 36QED Weighted: 0.20Np Likeness Score: 0.27

References

1. Kratzel M, Hiessböck R, Bernkop-Schnürch A..  (1998)  Auxiliary agents for the peroral administration of peptide and protein drugs: synthesis and evaluation of novel pepstatin analogues.,  41  (13): [PMID:9632367] [10.1021/jm980015w]

Source