(S)-2-amino-N-((S)-1-((S)-1-(benzylamino)-3-guanidino-1-oxopropan-2-ylamino)-3-(biphenyl-4-yl)-1-oxopropan-2-yl)-5-guanidinopentanamide

ID: ALA2163899

Chembl Id: CHEMBL2163899

PubChem CID: 71449723

Max Phase: Preclinical

Molecular Formula: C32H42N10O3

Molecular Weight: 614.76

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  N=C(N)NCCC[C@H](N)C(=O)N[C@@H](Cc1ccc(-c2ccccc2)cc1)C(=O)N[C@@H](CNC(=N)N)C(=O)NCc1ccccc1

Standard InChI:  InChI=1S/C32H42N10O3/c33-25(12-7-17-38-31(34)35)28(43)41-26(18-21-13-15-24(16-14-21)23-10-5-2-6-11-23)30(45)42-27(20-40-32(36)37)29(44)39-19-22-8-3-1-4-9-22/h1-6,8-11,13-16,25-27H,7,12,17-20,33H2,(H,39,44)(H,41,43)(H,42,45)(H4,34,35,38)(H4,36,37,40)/t25-,26-,27-/m0/s1

Standard InChI Key:  RNUKRQOJXMLLFM-QKDODKLFSA-N

Alternative Forms

1. Parent:

   

   ALA2163899

   H-Arg-Bip-Ala(guanidino)-NHBn

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 614.76

Molecular Weight (Monoisotopic): 614.3441

AlogP: 0.26

#Rotatable Bonds: 16

Polar Surface Area: 237.12

Molecular Species: BASE

HBA: 6

HBD: 10

#RO5 Violations: 2

HBA (Lipinski): 13

HBD (Lipinski): 13

#RO5 Violations (Lipinski): 3

CX Acidic pKa: 12.21

CX Basic pKa: 11.83

CX LogP: -0.03

CX LogD: -4.92

Aromatic Rings: 3

Heavy Atoms: 45

QED Weighted: 0.06

Np Likeness Score: -0.06

References

1. Karstad R, Isaksen G, Wynendaele E, Guttormsen Y, De Spiegeleer B, Brandsdal BO, Svendsen JS, Svenson J..  (2012)  Targeting the S1 and S3 subsite of trypsin with unnatural cationic amino acids generates antimicrobial peptides with potential for oral administration.,  55  (14): [PMID:22720778] [10.1021/jm3002058]

Source

Source(1):

• Scientific Literature