ID: ALA2407812

Max Phase: Preclinical

Molecular Formula: C9H10N2O3

Molecular Weight: 194.19

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1nc2c(c(C)c1O)COC(=O)N2

Standard InChI:  InChI=1S/C9H10N2O3/c1-4-6-3-14-9(13)11-8(6)10-5(2)7(4)12/h12H,3H2,1-2H3,(H,10,11,13)

Standard InChI Key:  UYNZLQZOVOYPQD-UHFFFAOYSA-N

Associated Targets(Human)

MB Tbio Myoglobin (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Liver microsomes (16955 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

PTGS1 Cyclooxygenase-1 (5266 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Liver microsomes (8692 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 194.19Molecular Weight (Monoisotopic): 194.0691AlogP: 1.47#Rotatable Bonds: 0
Polar Surface Area: 71.45Molecular Species: NEUTRALHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.36CX Basic pKa: 5.19CX LogP: 1.30CX LogD: 1.29
Aromatic Rings: 1Heavy Atoms: 14QED Weighted: 0.66Np Likeness Score: 0.51

References

1. Shchepin RV, Liu W, Yin H, Zagol-Ikapitte I, Amin T, Jeong BS, Roberts LJ, Oates JA, Porter NA, Boutaud O..  (2013)  Rational Design of Novel Pyridinol-Fused Ring Acetaminophen Analogues.,  (8): [PMID:24482730] [10.1021/ml4000904]

Source