Ranelic acid

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Ranelic acid
Structural formula of ranelic acid
Ball-and-stick model of the ranelic acid molecule
Names
IUPAC name
5-(Bis(carboxymethyl)amino)-3-(carboxymethyl)-4-cyano-2-thiophenecarboxylic acid
Systematic IUPAC name
5-[Bis(carboxymethyl)amino]-3-(carboxymethyl)-4-cyanothiophene-2-carboxylic acid[1]
Identifiers
135459-90-4 YesY
5459-90-4 N
ChemSpider 2314551 YesY
Jmol 3D model Interactive image
Interactive image
KEGG D08467 YesY
PubChem 3052774
UNII K9CCS0RIBT YesY
  • InChI=1S/C12H10N2O8S/c13-2-6-5(1-7(15)16)10(12(21)22)23-11(6)14(3-8(17)18)4-9(19)20/h1,3-4H2,(H,15,16)(H,17,18)(H,19,20)(H,21,22) YesY
    Key: DJSXNILVACEBLP-UHFFFAOYSA-N YesY
  • OC(=O)CN(CC(O)=O)C1=C(C#N)C(CC(O)=O)=C(S1)C(O)=O
  • C(C1=C(SC(=C1C#N)N(CC(=O)O)CC(=O)O)C(=O)O)C(=O)O
Properties
C12H10N2O8S
Molar mass 342.28 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Ranelic acid is an organic acid capable of chelating metal cations.[2]

It forms the ranelate ion, C12H6N2O8S4−. Strontium ranelate, the strontium salt of ranelic acid, is a drug used to treat osteoporosis and increase bone mineral density (BMD).

References

  1. CID 3052774 from PubChem
  2. Bivalent metal salts of 2-N,N-di(carboxymethyl)amino,3-cyano,4-carboxymethyl,5-carboxy-thiophene-acid, process for their preparation and pharmaceutical compositions containing them. EP 415850 

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