ID: ALA40804

Max Phase: Preclinical

Molecular Formula: C4H8N2O2

Molecular Weight: 116.12

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  NC[C@H]1CC(=O)NO1

Standard InChI:  InChI=1S/C4H8N2O2/c5-2-3-1-4(7)6-8-3/h3H,1-2,5H2,(H,6,7)/t3-/m1/s1

Standard InChI Key:  ZHCZZTNIHDWRNS-GSVOUGTGSA-N

Associated Targets(non-human)

Felis catus (3858 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Gabrg1 GABA receptor gamma-1 subunit (26 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Gabrp GABA-A receptor; anion channel (5731 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc6a11 GABA transporter (97 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: 116.12Molecular Weight (Monoisotopic): 116.0586AlogP: -1.23#Rotatable Bonds: 1
Polar Surface Area: 64.35Molecular Species: BASEHBA: 3HBD: 2
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.69CX Basic pKa: 9.32CX LogP: -2.28CX LogD: -2.68
Aromatic Rings: 0Heavy Atoms: 8QED Weighted: 0.45Np Likeness Score: 1.19

References

1. Krogsgaard-Larsen P, Nielsen L, Falch E, Curtis DR..  (1985)  GABA agonists. Resolution, absolute stereochemistry, and enantioselectivity of (S)-(+)- and (R)-(-)-dihydromuscimol.,  28  (11): [PMID:2999396] [10.1021/jm00149a012]

Source