N-[3-(2-amino-5-methoxyphenyl)-3-oxopropyl]cyclopentanocarboxamide

ID: ALA381464

Chembl Id: CHEMBL381464

PubChem CID: 11543842

Max Phase: Preclinical

Molecular Formula: C16H22N2O3

Molecular Weight: 290.36

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  COc1ccc(N)c(C(=O)CCNC(=O)C2CCCC2)c1

Standard InChI:  InChI=1S/C16H22N2O3/c1-21-12-6-7-14(17)13(10-12)15(19)8-9-18-16(20)11-4-2-3-5-11/h6-7,10-11H,2-5,8-9,17H2,1H3,(H,18,20)

Standard InChI Key:  NMSXKXYWYUARSV-UHFFFAOYSA-N

Alternative Forms

1. Parent:

   

   ALA381464

   N-[3-(2-amino-5-methoxyphenyl)-3-oxopropyl]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: 290.36

Molecular Weight (Monoisotopic): 290.1630

AlogP: 2.16

#Rotatable Bonds: 6

Polar Surface Area: 81.42

Molecular Species: NEUTRAL

HBA: 4

HBD: 2

#RO5 Violations: 0

HBA (Lipinski): 5

HBD (Lipinski): 3

#RO5 Violations (Lipinski): 0

CX Acidic pKa:

CX Basic pKa: 3.17

CX LogP: 1.99

CX LogD: 1.99

Aromatic Rings: 1

Heavy Atoms: 21

QED Weighted: 0.62

Np Likeness Score: -0.87

References

1. Entrena A, Camacho ME, Carrión MD, López-Cara LC, Velasco G, León J, Escames G, Acuña-Castroviejo D, Tapias V, Gallo MA, Vivó A, Espinosa A..  (2005)  Kynurenamines as neural nitric oxide synthase inhibitors.,  48  (26): [PMID:16366599] [10.1021/jm050740o]

2. Chayah M, Camacho ME, Carrion MD, Gallo MA, Romero M, Duarte J.  (2016)  N,N-Disubstituted thiourea and urea derivatives: design, synthesis, docking studies and biological evaluation against nitric oxide synthase,  7  (4): [10.1039/C5MD00477B]

Source

Source(1):

• Scientific Literature