N-((R)-1-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-3-methyl-1-oxobutan-2-yl)cyclopentanecarboxamide

ID: ALA2398747

Chembl Id: CHEMBL2398747

PubChem CID: 57889423

Max Phase: Preclinical

Molecular Formula: C24H35ClN2O3

Molecular Weight: 435.01

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  CC(C)[C@@H](NC(=O)C1CCCC1)C(=O)N1CC[C@](O)(c2ccc(Cl)cc2)C(C)(C)C1

Standard InChI:  InChI=1S/C24H35ClN2O3/c1-16(2)20(26-21(28)17-7-5-6-8-17)22(29)27-14-13-24(30,23(3,4)15-27)18-9-11-19(25)12-10-18/h9-12,16-17,20,30H,5-8,13-15H2,1-4H3,(H,26,28)/t20-,24+/m1/s1

Standard InChI Key:  UTGYFIZUYRNNRM-YKSBVNFPSA-N

Alternative Forms

1. Parent:

   

   ALA2398747

   N-((R)-1-((S)-4-(4-Chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-3-methyl-1-oxobutan-2-yl)cyclopentanecarboxamide

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: 435.01

Molecular Weight (Monoisotopic): 434.2336

AlogP: 4.12

#Rotatable Bonds: 5

Polar Surface Area: 69.64

Molecular Species: NEUTRAL

HBA: 3

HBD: 2

#RO5 Violations: 0

HBA (Lipinski): 5

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 12.74

CX Basic pKa:

CX LogP: 3.98

CX LogD: 3.98

Aromatic Rings: 1

Heavy Atoms: 30

QED Weighted: 0.73

Np Likeness Score: -0.39

References

1. Gardner DS, Santella JB, Duncia JV, Carter PH, Dhar TG, Wu H, Guo W, Cavallaro C, Van Kirk K, Yarde M, Briceno SW, Grafstrom RR, Liu R, Patel SR, Tebben AJ, Camac D, Khan J, Watson A, Yang G, Rose A, Foster WR, Cvijic ME, Davies P, Hynes J..  (2013)  The discovery of BMS-457, a potent and selective CCR1 antagonist.,  23  (13): [PMID:23707259] [10.1016/j.bmcl.2013.04.079]

2.  (2014)  Piperidinyl derivative as a modulator of chemokine receptor activity, 

Source

Source(2):

• Scientific Literature
• BindingDB Database