Boc-Phe-His-Leu-CF3-Ile-Amp

ID: ALA154795

Chembl Id: CHEMBL154795

PubChem CID: 44371838

Max Phase: Preclinical

Molecular Formula: C40H54F2N8O7

Molecular Weight: 796.92

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  CC[C@H](C)[C@H](NC(=O)C(F)(F)C(=O)C(CC(C)C)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)NCc1ccccn1

Standard InChI:  InChI=1S/C40H54F2N8O7/c1-8-25(4)32(36(54)45-22-27-16-12-13-17-44-27)50-37(55)40(41,42)33(51)29(18-24(2)3)47-35(53)31(20-28-21-43-23-46-28)48-34(52)30(19-26-14-10-9-11-15-26)49-38(56)57-39(5,6)7/h9-17,21,23-25,29-32H,8,18-20,22H2,1-7H3,(H,43,46)(H,45,54)(H,47,53)(H,48,52)(H,49,56)(H,50,55)/t25-,29?,30-,31-,32-/m0/s1

Standard InChI Key:  YJEITIRWMUEULI-WNTFFZHHSA-N

Alternative Forms

1. Parent:

   

   ALA154795

   Boc-Phe-His-Leu-CF3-Ile-Amp

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: 796.92

Molecular Weight (Monoisotopic): 796.4084

AlogP: 3.55

#Rotatable Bonds: 20

Polar Surface Area: 213.37

Molecular Species: NEUTRAL

HBA: 9

HBD: 6

#RO5 Violations: 2

HBA (Lipinski): 15

HBD (Lipinski): 6

#RO5 Violations (Lipinski): 3

CX Acidic pKa: 8.87

CX Basic pKa: 6.53

CX LogP: 4.11

CX LogD: 4.05

Aromatic Rings: 3

Heavy Atoms: 57

QED Weighted: 0.09

Np Likeness Score: -0.57

References

1. Maibaum J, Rich DH..  (1988)  Inhibition of porcine pepsin by two substrate analogues containing statine. The effect of histidine at the P2 subsite on the inhibition of aspartic proteinases.,  31  (3): [PMID:3126296] [10.1021/jm00398a022]

Source

Source(1):

• Scientific Literature