ID: ALA3142364

Max Phase: Preclinical

Molecular Formula: C26H51N3O5

Molecular Weight: 485.71

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCCCC(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/C26H51N3O5/c1-10-12-13-14-16-20(30)19(15-11-2)27-23(31)21(17(3)4)28-24(32)22(18(5)6)29-25(33)34-26(7,8)9/h17-22,30H,10-16H2,1-9H3,(H,27,31)(H,28,32)(H,29,33)/t19-,20?,21-,22-/m0/s1

Standard InChI Key:  IZHJRKJUNADDBG-UZVDJONISA-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: 485.71Molecular Weight (Monoisotopic): 485.3829AlogP: 4.29#Rotatable Bonds: 15
Polar Surface Area: 116.76Molecular Species: NEUTRALHBA: 5HBD: 4
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.70CX Basic pKa: CX LogP: 4.98CX LogD: 4.98
Aromatic Rings: 0Heavy Atoms: 34QED Weighted: 0.26Np Likeness Score: 0.28

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