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5′-Phosphoribosyl-4-carboxy-5-aminoimidazole

5′-Phosphoribosyl-4-carboxy-5-aminoimidazole (or CAIR) is an intermediate in the formation of purines.

5′-Phosphoribosyl-4-carboxy-5-aminoimidazole
Names
IUPAC name
5-Amino-1-(5-O-phosphono-β-D-ribofuranosyl)-1H-imidazole-4-carboxylic acid
Systematic IUPAC name
5-Amino-1-{(2R,3R,4S,5R)-3,4-dihydroxy-5-[(phosphonooxy)methyl]oxolan-2-yl}-1H-imidazole-4-carboxylic acid
Other names
Carboxyaminoimidazole ribotide,
Carboxyaminoimidazole ribonucleotide,
CAIR,
Identifiers
  • 6001-14-5 Y
3D model (JSmol)
  • Interactive image
  • Interactive image
ChEBI
  • CHEBI:28413 Y
ChemSpider
  • 144983 Y
  • 165388
UNII
  • 5MA501Z5DO Y
  • DTXSID50208716
  • InChI=1S/C9H14N3O9P/c10-7-4(9(15)16)11-2-12(7)8-6(14)5(13)3(21-8)1-20-22(17,18)19/h2-3,5-6,8,13-14H,1,10H2,(H,15,16)(H2,17,18,19)/t3-,5-,6-,8-/m1/s1 Y
    Key: XFVULMDJZXYMSG-ZIYNGMLESA-N Y
  • InChI=1/C9H14N3O9P/c10-7-4(9(15)16)11-2-12(7)8-6(14)5(13)3(21-8)1-20-22(17,18)19/h2-3,5-6,8,13-14H,1,10H2,(H,15,16)(H2,17,18,19)/t3-,5-,6-,8-/m1/s1
    Key: XFVULMDJZXYMSG-ZIYNGMLEBD
  • C1=NC(=C(N1[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)O)O)O)N)C(=O)O
  • O=P(O)(O)OC[C@H]2O[C@@H](n1cnc(C(=O)O)c1N)[C@H](O)[C@@H]2O
Properties
C9H14N3O9P
Molar mass 339.196 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)

It is formed by phosphoribosylaminoimidazole carboxylase.


phosphoribosyl, carboxy, aminoimidazole, cair, intermediate, formation, purines, names, iupac, name, amino, phosphono, ribofuranosyl, imidazole, carboxylic, acid, systematic, iupac, name, amino, dihydroxy, phosphonooxy, methyl, oxolan, imidazole, carboxylic, a. 5 Phosphoribosyl 4 carboxy 5 aminoimidazole or CAIR is an intermediate in the formation of purines 5 Phosphoribosyl 4 carboxy 5 aminoimidazole Names IUPAC name 5 Amino 1 5 O phosphono b D ribofuranosyl 1H imidazole 4 carboxylic acid Systematic IUPAC name 5 Amino 1 2R 3R 4S 5R 3 4 dihydroxy 5 phosphonooxy methyl oxolan 2 yl 1H imidazole 4 carboxylic acid Other names Carboxyaminoimidazole ribotide Carboxyaminoimidazole ribonucleotide CAIR Identifiers CAS Number 6001 14 5 Y 3D model JSmol Interactive imageInteractive image ChEBI CHEBI 28413 Y ChemSpider 144983 Y PubChem CID 165388 UNII 5MA501Z5DO Y CompTox Dashboard EPA DTXSID50208716 InChI InChI 1S C9H14N3O9P c10 7 4 9 15 16 11 2 12 7 8 6 14 5 13 3 21 8 1 20 22 17 18 19 h2 3 5 6 8 13 14H 1 10H2 H 15 16 H2 17 18 19 t3 5 6 8 m1 s1 YKey XFVULMDJZXYMSG ZIYNGMLESA N YInChI 1 C9H14N3O9P c10 7 4 9 15 16 11 2 12 7 8 6 14 5 13 3 21 8 1 20 22 17 18 19 h2 3 5 6 8 13 14H 1 10H2 H 15 16 H2 17 18 19 t3 5 6 8 m1 s1Key XFVULMDJZXYMSG ZIYNGMLEBD SMILES C1 NC C N1 C H 2 C H C H C H O2 COP O O O O O N C O OO P O O OC C H 2O C H n1cnc C O O c1N C H O C H 2O Properties Chemical formula C9H14N3O9P Molar mass 339 196 g mol Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa N verify what is Y N Infobox references It is formed by phosphoribosylaminoimidazole carboxylase This article about an organic compound is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title 5 Phosphoribosyl 4 carboxy 5 aminoimidazole amp oldid 1151997843, wikipedia, wiki, book, books, library,

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