Minodronic acid

Minodronic acid
Names
	IUPAC name (1-Hydroxy-2-imidazo[1,2-a]pyridin-3-yl-1-phosphonoethyl)phosphonic acid
	Other names Minodronate; YM 529
Identifiers
CAS Number	180064-38-4 ; 155648-60-5 (hydrate) ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL319144 ;
ChemSpider	115805 ;
IUPHAR/BPS	3164;
PubChem CID	130956;
UNII	40SGR63TGL ;
CompTox Dashboard (EPA)	DTXSID4048779 ;
	InChI InChI=1S/C9H12N2O7P2/c12-9(19(13,14)15,20(16,17)18)5-7-6-10-8-3-1-2-4-11(7)8/h1-4,6,12H,5H2,(H2,13,14,15)(H2,16,17,18) Key: VMMKGHQPQIEGSQ-UHFFFAOYSA-N ;
	SMILES O=P(O)(O)C(O)(P(=O)(O)O)Cc1cnc2ccccn12;
Properties
Chemical formula	C9H12N2O7P2
Molar mass	322.150 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

Minodronic acid is a third-generation bisphosphonate drug. It is approved for use in Japan for the treatment of osteoporosis.[1] Its mechanism of action involves inhibition of farnesyl pyrophosphate synthase activity.[2]

References

Shridhar Hegde and Michelle Schmidt (2009). "To Market, To Market - 2009. 16. Minodronic acid". Annual Reports in Medicinal Chemistry. 45: 509–510. doi:10.1016/s0065-7743(10)45028-9.
Sorbera, L.A.; Castañer, J.; Leeson, P.A. (2002). "Minodronic Acid". Drugs of the Future. 27 (10): 935–941. doi:10.1358/dof.2002.027.10.701186.

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[1] Shridhar Hegde and Michelle Schmidt (2009). "To Market, To Market - 2009. 16. Minodronic acid". Annual Reports in Medicinal Chemistry. 45: 509–510. doi:10.1016/s0065-7743(10)45028-9.

[2] Sorbera, L.A.; Castañer, J.; Leeson, P.A. (2002). "Minodronic Acid". Drugs of the Future. 27 (10): 935–941. doi:10.1358/dof.2002.027.10.701186.