3-(Quinolin-2-ylmethoxy)benzoic Acid

ID: ALA5169385

Chembl Id: CHEMBL5169385

PubChem CID: 14774173

Max Phase: Preclinical

Molecular Formula: C17H13NO3

Molecular Weight: 279.30

Names and Identifiers

Canonical SMILES:  O=C(O)c1cccc(OCc2ccc3ccccc3n2)c1

Standard InChI:  InChI=1S/C17H13NO3/c19-17(20)13-5-3-6-15(10-13)21-11-14-9-8-12-4-1-2-7-16(12)18-14/h1-10H,11H2,(H,19,20)

Standard InChI Key:  IJTITQLHFRUEQF-UHFFFAOYSA-N

Alternative Forms

1. Parent:

   

   ALA5169385

   3-(2-Quinolinylmethoxy)benzoic acid

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type:

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 279.30

Molecular Weight (Monoisotopic): 279.0895

AlogP: 3.51

#Rotatable Bonds: 4

Polar Surface Area: 59.42

Molecular Species: ACID

HBA: 3

HBD: 1

#RO5 Violations: ┄

HBA (Lipinski): 4

HBD (Lipinski): 1

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: 3.92

CX Basic pKa: 3.09

CX LogP: 2.99

CX LogD: 0.19

Aromatic Rings: 3

Heavy Atoms: 21

QED Weighted: 0.79

Np Likeness Score: -0.83

References

1. Fiorillo B, Sepe V, Conflitti P, Roselli R, Biagioli M, Marchianò S, De Luca P, Baronissi G, Rapacciuolo P, Cassiano C, Catalanotti B, Zampella A, Limongelli V, Fiorucci S..  (2021)  Structural Basis for Developing Multitarget Compounds Acting on Cysteinyl Leukotriene Receptor 1 and G-Protein-Coupled Bile Acid Receptor 1.,  64  (22.0): [PMID:34767347] [10.1021/acs.jmedchem.1c01078]

Source

Source(1):

• Scientific Literature