2-ethoxy-6-(phenylsulfonyl)pyridin-4-ol

ID: ALA460399

Chembl Id: CHEMBL460399

PubChem CID: 44588115

Max Phase: Preclinical

Molecular Formula: C13H13NO4S

Molecular Weight: 279.32

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  CCOc1cc(O)cc(S(=O)(=O)c2ccccc2)n1

Standard InChI:  InChI=1S/C13H13NO4S/c1-2-18-12-8-10(15)9-13(14-12)19(16,17)11-6-4-3-5-7-11/h3-9H,2H2,1H3,(H,14,15)

Standard InChI Key:  FVANNPYYNYCRDF-UHFFFAOYSA-N

Alternative Forms

1. Parent:

   

   ALA460399

   2-(benzenesulfonyl)-6-ethoxy-1H-pyridin-4-one

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: 279.32

Molecular Weight (Monoisotopic): 279.0565

AlogP: 2.02

#Rotatable Bonds: 4

Polar Surface Area: 76.49

Molecular Species: NEUTRAL

HBA: 5

HBD: 1

#RO5 Violations: ┄

HBA (Lipinski): 5

HBD (Lipinski): 1

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: 9.04

CX Basic pKa: ┄

CX LogP: 2.79

CX LogD: 2.79

Aromatic Rings: 2

Heavy Atoms: 19

QED Weighted: 0.93

Np Likeness Score: -1.00

References

1. Hussain I, Yawer MA, Lalk M, Lindequist U, Villinger A, Fischer C, Langer P..  (2008)  Hetero-Diels-Alder reaction of 1,3-bis(trimethylsilyloxy)-1,3-butadienes with arylsulfonylcyanides. Synthesis and antimicrobial activity of 4-hydroxy-2-(arylsulfonyl)pyridines.,  16  (23): [PMID:18990580] [10.1016/j.bmc.2008.10.033]

Source

Source(1):

• Scientific Literature