| Weight | 218.101 g/mol |
|---|---|
| Formula | C7H7O6P |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
fosfosal (6064-83-1)
o-carboxyphenylphosphate · o-carboxyphenyl phosphate · Disdolen
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- Kinetic studies of the transphosphorylation reactions catalyzed by alkaline phosphatase from E. coli: Hydrolysis of p-nitrophenyl phosphate and o-carboxyphenyl phosphate in presence of tris (International Journal of Biochemistry, 1982)
- Phosphoryl transfer from o-carboxyphenyl phosphate to tri(hydroxymethyl)-aminomethane catalysed by alkaline phosphatase from E. coli (International Journal of Biochemistry, 1980)
- Reactivity of the alkaline phosphatases of bovine milk and intestinal mucosa with the substrates phenyl phosphate and o-carboxyphenyl phosphate. (Archives of Biochemistry and Biophysics, 1960)
- The effect of fosfosal and acetylsalicylic acid on leukocyte migration and PGE2 concentration in experimentally induced acute inflammation (European Journal of Pharmacology, 1988)
- Pharmacological study of 2-phosphonoxybenzoic acid (fosfosal), a new analgesic drug. (Drug Research, 1980)
- Acute, subacute and chronic toxicity of fosfosal. (Drug Research, 1980)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - o-carboxyphenylphosphate
- o-carboxyphenyl phosphate
- Disdolen
- o-cpp cpd
- 2-phosphonoxybenzoic acid
- Protalgia
- o-carboxyphenylphosphoric acid
- 2-carboxyphenylphosphoric acid
- Aydolid
-
SMILESC1=CC=C(C(=C1)C(=O)O)OP(=O)(O)O
-
InChIKeyFFKUDWZICMJVPA-UHFFFAOYSA-N
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fosfosal
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