233951
Methylenediphosphonic acid
98%
Synonym(s):
MDP, Medronic acid
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About This Item
Linear Formula:
CH2[P(O)(OH)2]2
CAS Number:
Molecular Weight:
176.00
Beilstein/REAXYS Number:
1708494
MDL number:
UNSPSC Code:
12352100
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assay
98%
impurities
<0.5% methyl alcohol
1% ethyl alcohol
mp
197-199 °C (lit.)
SMILES string
OP(O)(=O)CP(O)(O)=O
InChI
1S/CH6O6P2/c2-8(3,4)1-9(5,6)7/h1H2,(H2,2,3,4)(H2,5,6,7)
InChI key
MBKDYNNUVRNNRF-UHFFFAOYSA-N
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Marie R Webster et al.
Journal of medicinal chemistry, 54(19), 6647-6656 (2011-08-26)
Bisphoshonates are used clinically to treat disorders of calcium metabolism, hypercalcemia and osteoporosis, and malignant bone disease. Although these agents are commonly used in cancer patients and have potential direct anticancer effects, their use for the treatment of extraskeletal disease
Jean-Yves Winum et al.
Bioorganic & medicinal chemistry letters, 15(6), 1683-1686 (2005-03-05)
The interaction of five human carbonic anhydrase (hCA, EC 4.2.1.1) isozymes, that is, hCA I, II, IV, V, and IX with a small library of phosphonic acids/organic phosphates, including methylphosphonic acid, MPA; phenylphosphonic acid, PPA; N-(phosphonoacetyl)-L-aspartic acid, PALA, methylene diphosphonic
Scott A Lujan et al.
Proceedings of the National Academy of Sciences of the United States of America, 104(30), 12282-12287 (2007-07-17)
Conjugative transfer of plasmid DNA via close cell-cell junctions is the main route by which antibiotic resistance genes spread between bacterial strains. Relaxases are essential for conjugative transfer and act by cleaving DNA strands and forming covalent phosphotyrosine linkages. Based
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