ID: ALA3425722

Max Phase: Preclinical

Molecular Formula: C8H6N2O2S

Molecular Weight: 194.22

Molecule Type: Small molecule

Representations

Canonical SMILES:  O=c1[nH]c(-c2cccs2)ncc1O

Standard InChI:  InChI=1S/C8H6N2O2S/c11-5-4-9-7(10-8(5)12)6-2-1-3-13-6/h1-4,11H,(H,9,10,12)

Standard InChI Key:  CNUHCLHSRVNQAG-UHFFFAOYSA-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: 194.22

Molecular Weight (Monoisotopic): 194.0150

AlogP: 1.20

#Rotatable Bonds: 1

Polar Surface Area: 65.98

Molecular Species: NEUTRAL

HBA: 4

HBD: 2

#RO5 Violations: 0

HBA (Lipinski): 4

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 6.96

CX Basic pKa:

CX LogP: 1.01

CX LogD: 0.48

Aromatic Rings: 2

Heavy Atoms: 13

QED Weighted: 0.72

Np Likeness Score: -1.25

References

1. Harrison ST, Poslusney MS, Mulhearn JJ, Zhao Z, Kett NR, Schubert JW, Melamed JY, Allison TJ, Patel SB, Sanders JM, Sharma S, Smith RF, Hall DL, Robinson RG, Sachs NA, Hutson PH, Wolkenberg SE, Barrow JC..  (2015)  Synthesis and Evaluation of Heterocyclic Catechol Mimics as Inhibitors of Catechol-O-methyltransferase (COMT).,  6  (3): [PMID:25815153] [10.1021/ml500502d]

Source

Source(1):

• Scientific Literature