Synonyms(1): Phosphoric Acid Monohydrazinocarbonylmethyl Ester Synonyms from Alternative Forms(1):
Canonical SMILES: NNC(=O)COP(=O)(O)O
Standard InChI: InChI=1S/C2H7N2O5P/c3-4-2(5)1-9-10(6,7)8/h1,3H2,(H,4,5)(H2,6,7,8)
Standard InChI Key: OTQGCPIGFCJBDI-UHFFFAOYSA-N
Associated Targets(Human)
Triosephosphate isomerase 22 Activities
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Associated Targets(non-human)
Triosephosphate isomerase 6 Activities
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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
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Properties
Molecular Weight: 170.06
Molecular Weight (Monoisotopic): 170.0093
AlogP: -1.91
#Rotatable Bonds: 3
Polar Surface Area: 121.88
Molecular Species: ACID
HBA: 4
HBD: 4
#RO5 Violations: 0
HBA (Lipinski): 7
HBD (Lipinski): 5
#RO5 Violations (Lipinski): 0
CX Acidic pKa: 1.38
CX Basic pKa: 3.22
CX LogP: -3.43
CX LogD: -5.65
Aromatic Rings: 0
Heavy Atoms: 10
QED Weighted: 0.17
Np Likeness Score: -0.16
References
1.Fonvielle M, Weber P, Dabkowska K, Therisod M.. (2004) New highly selective inhibitors of class II fructose-1,6-bisphosphate aldolases., 14 (11):[PMID:15125960][10.1016/j.bmcl.2004.03.040]
2.Fonvielle M, Mariano S, Therisod M.. (2005) New inhibitors of rabbit muscle triose-phosphate isomerase., 15 (11):[PMID:15911278][10.1016/j.bmcl.2005.03.061]
3.Fonvielle M, Therisod H, Hemery M, Therisod M.. (2007) New competitive inhibitors of cytosolic (NADH-dependent) rabbit muscle glycerophosphate dehydrogenase., 17 (2):[PMID:17088060][10.1016/j.bmcl.2006.10.030]