ID: ALA4128971

Max Phase: Preclinical

Molecular Formula: C24H30N6O4

Molecular Weight: 466.54

Molecule Type: Small molecule

Representations

Canonical SMILES:  CC(C)C[C@H](NC(=O)NCc1cn(Cc2cccc(OCc3ccccc3)c2)nn1)C(=O)NO

Standard InChI:  InChI=1S/C24H30N6O4/c1-17(2)11-22(23(31)28-33)26-24(32)25-13-20-15-30(29-27-20)14-19-9-6-10-21(12-19)34-16-18-7-4-3-5-8-18/h3-10,12,15,17,22,33H,11,13-14,16H2,1-2H3,(H,28,31)(H2,25,26,32)/t22-/m0/s1

Standard InChI Key:  HWJCWGXHJDEXFW-QFIPXVFZSA-N

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

Properties

Molecular Weight: 466.54

Molecular Weight (Monoisotopic): 466.2329

AlogP: 2.62

#Rotatable Bonds: 11

Polar Surface Area: 130.40

Molecular Species: NEUTRAL

HBA: 7

HBD: 4

#RO5 Violations: 0

HBA (Lipinski): 10

HBD (Lipinski): 4

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 8.72

CX Basic pKa: 0.04

CX LogP: 2.72

CX LogD: 2.70

Aromatic Rings: 3

Heavy Atoms: 34

QED Weighted: 0.25

Np Likeness Score: -1.45

References

1. Cao J, Ma C, Zang J, Gao S, Gao Q, Kong X, Yan Y, Liang X, Ding Q, Zhao C, Wang B, Xu W, Zhang Y..  (2018)  Novel leucine ureido derivatives as aminopeptidase N inhibitors using click chemistry.,  26  (12): [PMID:29859750] [10.1016/j.bmc.2018.04.041]

Source

Source(1):

• Scientific Literature