XVFCMESISA N MeSHName Uridinemonophosphate Section2 Chembox Properties Formula C sub 9 sub ... lide Section3 Chembox Hazards MainHazards FlashPt Autoignition Uridinemonophosphate , also known ... . Biosynthesis Uridinemonophosphate is formed from Orotidine 5 monophosphate orotidylic acid in a decarboxylation ... of uridinemonophosphate, choline, and docosahexaenoic acid DHA were found to have significantly ..., July 3, 2008 ref UridineMonophosphate in Foods In brain research studies such as those mentioned in this article, uridinemonophosphate is used as a convenient delivery compound for uridine . Uridine is the active ingredient of the compound. A common misconception is that uridine and its compounds ... or prescription drugs. This is not so. Uridinemonophosphate is a major component of RNA . Any food ... fr Uridinemonophosphate gl Urid n monofosfato it Uridina monofosfato nl Uridinemonofosfaat ... of phosphoric acid with the nucleoside uridine . UMP consists of the phosphate Functional group group , the pentose sugar ribose , and the nucleobase uracil hence, it is a ribonucleoside monophosphate ... information, consult the article on uridine . References reflist See also Nucleoside Nucleotide DNA RNA Oligonucleotide Pyrimidine biosynthesis Ribonucleoside monophosphate Nucleobases, nucleosides ... more details
PBB geneid 7372 Uridinemonophosphate synthetase UMPS orotate phosphoribosyl transferase and orotidine 5 decarboxylase is the enzyme EC number 4.1.1.23 that catalyses the formation of uridinemonophosphate UMP , an energy carrying molecule in many important biosynthetic pathways. ref name entrez cite web title Entrez Gene UMPS uridinemonophosphate synthetase orotate phosphoribosyl transferase and orotidine 5 decarboxylase url http www.ncbi.nlm.nih.gov sites entrez?Db gene&Cmd ShowDetailView&TermToSearch 7372 accessdate ref In humans, the gene that codes for this enzyme is located on the long arm ... DP title Localization of the gene for uridinemonophosphate synthase to human chromosome region 3q13 ... sites catalyze the last two steps of the de novo uridinemonophosphate UMP biosynthetic pathway. After addition of ribose P to orotate by OPRTase to form orotidine 5 monophosphate OMP , OMP is decarboxylated to form uridinemonophosphate by ODCase. In microorganisms, these two domains are separate ..., uridinemonophosphate synthetase. ref name Jones 1980 Jones, M. E. 1980 Annu. Rev. Biochem. 49 ... Shanks RD, Robinson JL title Embryonic mortality attributed to inherited deficiency of uridinemonophosphate ... WP1601 highlight Uridinemonophosphate synthetase See also orotidine 5 phosphate decarboxylase ... and initial characterization of the single polypeptide that synthesizes uridine 5 monophosphate from orotate in Ehrlich ascites carcinoma. Purification by tandem affinity chromatography of uridine 5 monophosphate synthase journal Biochemistry volume 19 issue 20 pages 4699 706 year 1981 pmid 6893554 ... of uridinemonophosphate synthase UMPS gene to river buffalo chromosomes by FISH journal Chromosome ... web title Uracil metabolism UMP synthesis from orotic acid or uridine and conversion of uracil to beta ... doi cite journal author Qumsiyeh MB, Valentine MB, Suttle DP title Localization of the gene for uridinemonophosphate synthase to human chromosome region 3q13 by in situ hybridization journal Genomics ... more details
as a deoxyuridine . Dietary sources of uridineUridine is one of the four basic components of ribonucleic ... containing RNA, uridine is released from RNA and is absorbed intact in the gut. Some food sources of uridine are Sugarcane extract ref http www.thebody.com content art30244.html Thebody.com ref Tomatoes 0.5 to 1.0 g uridine per kilogram dry weight ref http www.aseanfood.info Articles 11018411.pdf Aseanfood.info ref Brewer s yeast 3 uridine by dry weight ref name pmid11786646 cite journal author ... of beer on the plasma concentrations of uridine and purine bases journal Metab Clin Exp volume 51 .... Moderate consumption of yeast, about 5 grams per day, should provide adequate uridine for improved ... of uridine and EPA DHA omega 3 fatty acids has antidepressant activity equivalent to that of commonly ... like effects of uridine and omega 3 fatty acids are potentiated by combined treatment in rats journal ... j.biopsych.2004.11.038 url ref Uridine in the Glycolysis Pathway Uridine plays a role in the glycolysis ... molecule bonded to a UDP uridine di phosphate molecule. This process is catalyzed by the enzyme ... Ribosides bg ca Uridina cs Uridin de Uridin es Uridina fa fr Uridine gl Uridina it Uridina lt Uridinas nl Uridine ja oc Uridina pl Urydyna pt Uridina sr Uridin sv Uridin zh ... more details
enzyme Name uridine kinase EC number 2.7.1.48 CAS number 9026 39 5 IUBMB EC number 2 7 1 48 GO code 0004849 image width caption In enzymology , an uridine kinase EC number 2.7.1.48 is an enzyme that catalysis catalyzes the chemical reaction ATP uridine math rightleftharpoons math ADP UMP Thus, the two substrate biochemistry substrates of this enzyme are adenosine triphosphate ATP and uridine , whereas its two product chemistry products are adenosine diphosphate ADP and uridinemonophosphate UMP . This enzyme belongs to the family of transferase s, specifically those transferring phosphorus containing groups phosphotransferase s with an alcohol group as acceptor. The systematic name of this enzyme class is ATP uridine 5 phosphotransferase . Other names in common use include pyrimidine ribonucleoside kinase , uridine cytidine kinase , uridine kinase phosphorylating , and uridine phosphokinase . This enzyme participates in pyrimidine metabolism . Structural studies As of late 2007, 8 tertiary structure structures have been solved for this class of enzymes, with Protein Data Bank PDB accession codes PDB link 1UDW , PDB link 1UEI , PDB link 1UEJ , PDB link 1UFQ , PDB link 1UJ2 , PDB link 1XRJ , PDB link 2JEO , and PDB link 2UVQ . References reflist 1 cite journal author Orengo A date 1969 title Regulation of enzymic activity by metabolites. I. Uridine cytidine kinase of Novikoff ascites rat tumor journal J. Biol. Chem. volume 244 pages 2204&ndash 9 pmid 5782006 issue 8 cite journal author Skold O date 1960 title Uridine kinase from Erlich ascites tumor purification and properties journal J. Biol. Chem. volume 235 pages 3273&ndash 3279 enzyme stub Category EC 2.7.1 Category Enzymes of known structure ... more details
chembox Verifiedfields changed verifiedrevid 413157820 ImageFile DUMP chemical structure.png ImageSize IUPACName OtherNames dUMP Section1 Chembox Identifiers CASNo Ref cascite correct ?? CASNo 964 26 1 PubChem 688 SMILES ChEMBL Ref ebicite changed EBI ChEMBL 211312 MeSHName 2 deoxyuridine 5 monophosphate Section2 Chembox Properties Formula C sub 9 sub H sub 13 sub N sub 2 sub O sub 8 sub P MolarMass 308.182 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Deoxyuridine monophosphate is a deoxynucleotide . It is an intermediate in the metabolism of deoxyribonucleotide s. See also uridine monophosphate DCMP deaminase Nucleobases, nucleosides, and nucleotides biochem stub Category Nucleotides ca Monofosfat de desoxiuridina fa fr D soxyuridine monophosphate gl Desoxiuridina monofosfato nl Deoxyuridinemonofosfaat ja sr Dezoksiuridin monofosfat ... more details
enzyme Name uridine nucleosidase EC number 3.2.2.3 CAS number 9025 47 2 IUBMB EC number 3 2 2 3 GO code 0045437 image width caption In enzymology , an uridine nucleosidase EC number 3.2.2.3 is an enzyme that catalysis catalyzes the chemical reaction uridine H sub 2 sub O math rightleftharpoons math D ribose uracil Thus, the two substrate biochemistry substrates of this enzyme are uridine and water H sub 2 sub O , whereas its two product chemistry products are D ribose and uracil . This enzyme belongs to the family of hydrolase s, specifically those glycosylases that hydrolyse N glycosyl compounds. The systematic name of this enzyme class is uridine ribohydrolase . This enzyme is also called uridine hydrolase . This enzyme participates in pyrimidine metabolism . Structural studies As of late 2007, 23 tertiary structure structures have been solved for this class of enzymes, with Protein Data Bank PDB accession codes PDB link 1EMH , PDB link 1EMJ , PDB link 1EUG , PDB link 1FLZ , PDB link 1OKB , PDB link 1SSP , PDB link 1UDG , PDB link 1UDH , PDB link 1UDI , PDB link 1UGH , PDB link 1UUG , PDB link 1YUO , PDB link 2BOO , PDB link 2C53 , PDB link 2C56 , PDB link 2EUG , PDB link 2J8X , PDB link 2SSP , PDB link 2UUG , PDB link 3EUG , PDB link 4EUG , PDB link 4SKN , and PDB link 5EUG . References reflist 1 cite journal author Carter CE date 1951 title Partial purification of a non phosphorylytic uridine nucleosidase from yeast journal J. Am. Chem. Soc. volume 73 pages 1508&ndash 1510 doi 10.1021 ja01148a028 issue 4 hydrolase stub Category EC 3.2.2 Category Enzymes of known structure ... more details
Unreferenced stub auto yes date December 2009 Chembox Verifiedfields changed verifiedrevid 470620324 ImageFile Uridindiphosphat protoniert.svg ImageSize IUPACName Uridine 5 trihydrogen diphosphate OtherNames Section1 Chembox Identifiers CASNo 58 98 0 CASNo Ref cascite correct CAS PubChem 1158 ChEMBL Ref ebicite changed EBI ChEMBL 130266 IUPHAR ligand 1749 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 19952429 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C9H12N2O6.2H3O4P c12 3 4 6 14 7 15 8 17 4 11 2 1 5 13 10 9 11 16 2 1 5 2,3 4 h1 2,4,6 8,12,14 15H,3H2, H,10,13,16 2 H3,1,2,3,4 t4 ,6 ,7 ,8 m1.. s1 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey PMPFLUWUGZHTOK WFIJOQBCSA N SMILES MeSHName Uridine diphosphate Section2 Chembox Properties Formula C sub 9 sub H sub 14 sub N sub 2 sub O sub 12 sub P sub 2 sub MolarMass 404.161 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Uridine diphosphate , abbreviated UDP , is a nucleoside diphosphate . It is an ester of pyrophosphoric acid with the nucleoside uridine . UDP consists of the pyrophosphate Functional group group , the pentose sugar ribose , and the nucleobase uracil . See also Nucleoside Nucleotide DNA RNA Oligonucleotide UGGT Nucleobases, nucleosides, and nucleotides DEFAULTSORT Uridine Diphosphate Category Nucleotides Category Pyrimidinediones Biochem stub ca Difosfat d uridina da Uridindifosfat de Uridindiphosphat es Uridina difosfato fa fr Uridine diphosphate gl Urid n difosfato it Uridina difosfato nl Uridinedifosfaat ja pl Urydyno 5 difosforan sr Uridin difosfat fi Uridiinidifosfaatti zh ... more details
group group , the pentose sugar ribose , and the nucleobase cytosine hence, a ribonucleoside monophosphate ... by amination of uridine triphosphate , the main source of CMP is from RNA being decomposed, e.g. ... DNA RNA Oligonucleotide Ribonucleoside monophosphate References reflist 2 Nucleobases, nucleosides, and nucleotides DEFAULTSORT Cytidine Monophosphate Category Nucleotides Category Pyrimidones Biochem ... fr Cytidine monophosphate gl Citid n monofosfato it Citosina monofosfato nl Cytidinemonofosfaat ... more details
enzyme Name uridine phosphorylase EC number 2.4.2.3 CAS number 9030 22 2 IUBMB EC number 2 4 2 3 GO code 0004850 image width caption In enzymology , an uridine phosphorylase EC number 2.4.2.3 is an enzyme that catalysis catalyzes the chemical reaction uridine phosphate math rightleftharpoons math uracil alpha D ribose 1 phosphate Thus, the two substrate biochemistry substrates of this enzyme are uridine and phosphate , whereas its two product chemistry products are uracil and alpha D ribose 1 phosphate . This enzyme belongs to the family of glycosyltransferase s, specifically the pentosyltransferases. The systematic name of this enzyme class is uridine phosphate alpha D ribosyltransferase . Other names in common use include pyrimidine phosphorylase , UrdPase , UPH , and UPase . This enzyme participates in pyrimidine metabolism . Structural studies As of late 2007, 27 tertiary structure structures have been solved for this class of enzymes, with Protein Data Bank PDB accession codes PDB link 1K3F , PDB link 1LX7 , PDB link 1RXC , PDB link 1RXS , PDB link 1RXU , PDB link 1RXY , PDB link 1RYZ , PDB link 1SJ9 , PDB link 1SQ6 , PDB link 1T0U , PDB link 1TGV , PDB link 1TGY , PDB link 1U1C , PDB link 1U1D , PDB link 1U1E , PDB link 1U1F , PDB link 1U1G , PDB link 1Y1Q , PDB link 1Y1R , PDB link 1Y1S , PDB link 1Y1T , PDB link 1ZL2 , PDB link 2HN9 , PDB link 2HRD , PDB link 2HSW , PDB link 2HWU , and PDB link 2I8A . References reflist 1 cite journal author CANELLAKIS ES date 1957 title Pyrimidine metabolism. II. Enzymatic pathways of uracil anabolism journal J. Biol. Chem. volume 227 pages 329&ndash 38 pmid 13449076 issue 1 cite journal author PAEGE LM, SCHLENK F date 1952 title Bacterial uracil riboside phosphorylase journal Arch. Biochem. Biophys. volume 40 pages 42&ndash 9 pmid 12997187 doi 10.1016 0003 9861 52 90071 4 issue 1 cite journal author Pontis H, Degerstedt G and Reichard P date 1961 title Uridine and deoxyuridine phosphorylases from Ehrlich ascites tumor journal ... more details
Unreferenced date October 2006 Chembox verifiedrevid 447289738 ImageFile Desoxyguanosinmonophosphat protoniert.svg ImageSize IUPACName OtherNames Section1 Chembox Identifiers CASNo Ref cascite correct CAS CASNo 902 04 5 PubChem 161075 SMILES C1C C OC1N2C NC3 C2NC NC3 O N COP O O O O.N Section2 Chembox Properties Formula C sub 10 sub H sub 14 sub N sub 5 sub O sub 7 sub P MolarMass 347.2243 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Deoxyguanosine monophosphate , also known as deoxyguanylate , or dGMP , is a derivative of the common nucleic acid guanosine triphosphate GTP , in which the OH hydroxyl group on the 2 carbon on the nucleotide s pentose has been reduced to just a hydrogen atom hence the deoxy part of the name . It is used as a monomer in DNA . See also Nucleic acid DNA metabolism Cofactor biochemistry Cofactor Guanosine Nucleobases, nucleosides, and nucleotides DEFAULTSORT Deoxyguanosine Monophosphate Category Nucleotides ca Monofosfat de desoxiguanosina fa fr D soxyguanosine monophosphate gl Desoxiguanosina monofosfato nl Deoxyguanosinemonofosfaat sr Dezoksiguanozin monofosfat zh ... more details
chembox verifiedrevid 460776176 ImageFile DCMP chemical structure.png ImageSize IUPACName OtherNames Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 13343 InChI 1 C9H14N3O7P c10 7 1 2 12 9 14 11 7 8 3 5 13 6 19 8 4 18 20 15,16 17 h1 2,5 6,8,13H,3 4H2, H2,10,11,14 H2,15,16,17 t5 ,6 ,8 m0 s1 InChIKey NCMVOABPESMRCP SHYZEUOFBL StdInChI Ref stdinchicite correct chemspider StdInChI 1S C9H14N3O7P c10 7 1 2 12 9 14 11 7 8 3 5 13 6 19 8 4 18 20 15,16 17 h1 2,5 6,8,13H,3 4H2, H2,10,11,14 H2,15,16,17 t5 ,6 ,8 m0 s1 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey NCMVOABPESMRCP SHYZEUOFSA N CASNo Ref cascite correct CAS CASNo 1032 65 1 ChEMBL Ref ebicite correct EBI ChEMBL 374699 PubChem 624 ChEBI Ref ebicite correct EBI ChEBI 15918 SMILES c1cn c O nc1N C H 2C C H C H O2 COP O O O O MeSHName Deoxycytidine monophosphate Section2 Chembox Properties Formula C sub 9 sub H sub 14 sub N sub 3 sub O sub 7 sub P MolarMass 307.197 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Deoxycytidine monophosphate , also known as deoxycytidylate , or dCMP , is a deoxynucleotide , and one of the four monomer s that make up DNA . In a DNA double helix, it will base pair with deoxyguanosine monophosphate . Nucleobases, nucleosides, and nucleotides Category Nucleotides biochem stub ca Monofosfat de desoxicitidina fa fr D soxycytidine monophosphate gl Desoxicitidina monofosfato nl Deoxycytidinemonofosfaat sr Dezoksicitidin monofosfat zh ... more details
Unreferenced date October 2006 Chembox verifiedrevid 447288275 ImageFile DAMP chemical structure.png ImageSize IUPACName OtherNames Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 12079 InChI 1 C10H14N5O6P c11 9 8 10 13 3 12 9 15 4 14 8 7 1 5 16 6 21 7 2 20 22 17,18 19 h3 7,16H,1 2H2, H2,11,12,13 H2,17,18,19 t5 ,6 ,7 m0 s1 InChIKey KHWCHTKSEGGWEX RRKCRQDMBS StdInChI Ref stdinchicite correct chemspider StdInChI 1S C10H14N5O6P c11 9 8 10 13 3 12 9 15 4 14 8 7 1 5 16 6 21 7 2 20 22 17,18 19 h3 7,16H,1 2H2, H2,11,12,13 H2,17,18,19 t5 ,6 ,7 m0 s1 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey KHWCHTKSEGGWEX RRKCRQDMSA N CASNo Ref cascite correct CAS CASNo 653 63 4 PubChem 621 ChEBI Ref ebicite correct EBI ChEBI 17713 SMILES c1nc c2c n1 n cn2 C H 3C C H C H O3 COP O O O O N MeSHName Deoxyadenosine monophosphate Section2 Chembox Properties Formula C sub 10 sub H sub 14 sub N sub 5 sub O sub 6 sub P MolarMass 331.222 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Context article date October 2009 Deoxyadenosine monophosphate , also known as deoxyadenylate , or dAMP , is a derivative of the common nucleic acid AMP, or adenosine monophosphate , in which the OH hydroxyl group on the 2 carbon on the nucleotide s pentose has been reduced to just a hydrogen atom hence the deoxy part of the name . Deoxyadenosine monophosphate is abbreviated dAMP. It is a monomer used in DNA . See also Nucleic acid DNA metabolism Cofactor biochemistry Cofactor Guanosine Cyclic AMP cAMP Adenosine Triphosphate ATP Nucleobases, nucleosides, and nucleotides DEFAULTSORT Deoxyadenosine Monophosphate Category Nucleotides Biochemistry stub ca Monofosfat de desoxiadenosina fa fr D soxyad nosine monophosphate gl Desoxiadenosina monofosfato nl Deoxyadenosinemonofosfaat ja sr Dezoksiadenozin monofosfat zh ... more details
FlashPt Autoignition Adenosine monophosphate AMP , also known as 5 adenylic acid , is a nucleotide ... down by living systems, nucleoside monophosphates, including adenosine monophosphate, are formed. AMP ... AMP can be converted into inosine monophosphate IMP by the enzyme myoadenylate deaminase , freeing an ammonia group. In a catabolic pathway, adenosine monophosphate can be converted to uric ... adenosine monophosphate cyclic AMP or cAMP . Within certain cells the enzyme adenylate cyclase ... fr Ad nosine monophosphate gl Adenosina monofosfato ko hr Adenozin monofosfat ... ur Adenosine monophosphate zh ... more details
s, thymidine monophosphate does not contain the deoxy prefix in its name. ref cite ... es Timidilato fa fr Thymidine monophosphate gl Desoxitimidina monofosfato nl ... more details
chembox verifiedrevid 395738406 ImageFile Orotidine monophosphate.svg ImageSize IUPACName 3 2R,3R,4S,5R 3,4 dihydroxy 5 & 8203 phosphonooxymethyl oxolan 2 yl & 8203 2,6 dioxo pyrimidine 4 carboxylic acid OtherNames Orotidylic acid, br OMP Section1 Chembox Identifiers CASNo 2149 82 8 PubChem 968 SMILES C1 C N C O NC1 O C2C C C O2 COP O O O O O C O O MeSHName Orotidine 5 monophosphate Section2 Chembox Properties Formula C sub 10 sub H sub 13 sub N sub 2 sub O sub 11 sub P MolarMass 368.191 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Orotidine 5 monophosphate OMP , also known as orotidylic acid, is a pyrimidine nucleotide which is the last intermediate in the biosynthesis of uridine monophosphate . OMP is formed from orotic acid orotate and phosphoribosyl pyrophosphate by the enzyme Orotate phosphoribosyltransferase In humans, the enzyme UMP synthase converts OMP into uridine 5 monophosphate . If UMP synthase is defective, orotic aciduria can result. Nucleotide metabolism intermediates Category Nucleotides Category Pyrimidinediones biochem stub fa ja 5 sr Orotidin 5 monofosfat ... more details
enzyme Name tRNA uridine aminocarboxypropyltransferase EC number 2.5.1.25 CAS number IUBMB EC number 2 5 1 25 GO code 0016432 image width caption lowercase In enzymology , a tRNA uridine aminocarboxypropyltransferase EC number 2.5.1.25 is an enzyme that catalysis catalyzes the chemical reaction S adenosyl L methionine tRNA uridine math rightleftharpoons math 5 methylthioadenosine tRNA 3 3 amino 3 carboxypropyl uridine Thus, the two substrate biochemistry substrates of this enzyme are S adenosyl L methionine and tRNA uridine , whereas its two product chemistry products are 5 methylthioadenosine and tRNA 3 3 amino 3 carboxypropyl uridine . This enzyme belongs to the family of transferase s, specifically those transferring aryl or alkyl groups other than methyl groups. The systematic name of this enzyme class is S adenosyl L methionine tRNA uridine 3 3 amino 3 carboxypropyl transferase . References reflist 1 cite journal author Nishimura S, Taya Y, Kuchino Y, Oashi Z date 1974 title Enzymatic synthesis of 3 3 amino 3 carboxypropyl uridine in Escherichia coli phenylalanine transfer RNA transfer of the 3 amino acid 3 carboxypropyl group from S adenosylmethionine journal Biochem. Biophys. Res. Commun. volume 57 pages 702&ndash 8 pmid 4597321 issue 3 doi 10.1016 0006 291X 74 90603 2 transferase stub Category EC 2.5.1 Category Enzymes of unknown structure ... more details
chembox Verifiedfields changed verifiedrevid 476997454 ImageFile UDP Galactose.svg ImageSize IUPACName OtherNames Section1 Chembox Identifiers InChI 1 C9H12N2O6.C6H14O12P2 c12 3 4 6 14 7 15 8 17 4 11 2 1 5 13 10 9 11 16 7 1 3 9 5 10 6 18 20 14,15 16 4 2 8 17 19 11,12 13 h1 2,4,6 8,12,14 15H,3H2, H,10,13,16 2 7,9 10H,1H2, H2,11,12,13 H2,14,15,16 p 4 t4 ,6 ,7 ,8 3 ,4 ,5 ,6 m11 s1 InChIKey UYLAOKYVSPTOGT HUYLZDLQBS StdInChI Ref stdinchicite correct chemspider StdInChI 1S C9H12N2O6.C6H14O12P2 c12 3 4 6 14 7 15 8 17 4 11 2 1 5 13 10 9 11 16 7 1 3 9 5 10 6 18 20 14,15 16 4 2 8 17 19 11,12 13 h1 2,4,6 8,12,14 15H,3H2, H,10,13,16 2 7,9 10H,1H2, H2,11,12,13 H2,14,15,16 p 4 t4 ,6 ,7 ,8 3 ,4 ,5 ,6 m11 s1 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey UYLAOKYVSPTOGT UESRDHDISA J CASNo Ref cascite changed ?? CASNo 2956 16 3 PubChem 1166 ChEMBL Ref ebicite changed EBI ChEMBL 1743884 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 19951534 SMILES OC C H O C H O C H OP O O O C H C O OP O O O.O C 1NC O N C C 1 C H 2O C H CO C H O C H 2O MeSHName Uridine diphosphate galactose Section2 Chembox Properties Formula C sub 15 sub H sub 24 sub N sub 2 sub O sub 17 sub P sub 2 sub MolarMass 566.302 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Uridine diphosphate galactose Uridine diphosphate UDP galactose is an intermediate in the production of polysaccharide s. It is important in nucleotide sugars metabolism , and is the substrate for the transferase B4GALT5 . See also UDP galactose epimerase uridine diphosphate galactose Category Coenzymes Category Nucleotides biochem stub Fructose and galactose metabolic intermediates fa ja ... more details
DISPLAYTITLE Uridine diphosphate N acetylglucosamine Chembox verifiedrevid 399168372 Name Uridine diphosphate N acetylglucosamine ImageFile UDP N acetylglucosamine.png ImageSize 200px IUPACName 2 R ,3 R ,4 R ,5 S ,6 R 3 acetamido 4,5 dihydroxy 6 hydroxymethyl oxan 2 yl nowiki nowiki 2 R ,3 S ,4 R ,5 R 5 2,4 dioxopyrimidin 1 yl 3,4 dihydroxyoxolan 2 yl methoxy hydroxyphosphoryl hydrogen phosphate OtherNames UDP N acetylglucosamine UDP GlcNAc Section1 Chembox Identifiers CASNo 7277 98 7 PubChem 445675 SMILES CC O N C H 1 C H C H C H O C H 1OP O O OP O O OC C H 2 C H C H C H O2 N3C CC O NC3 O O O CO O O Section2 Chembox Properties C 17 H 27 N 3 O 17 P 2 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Uridine diphosphate N acetylglucosamine or UDP GlcNAc is a nucleotide sugar and a coenzyme in metabolism . It is used by glycosyltransferase s to transfer N Acetylglucosamine N acetylglucosamine residues to substrates. small D small Glucosamine is made naturally in the form of glucosamine 6 phosphate, and is the biochemical precursor of all amino sugar nitrogen containing sugars . ref cite journal doi 10.1074 jbc.R100053200 last1 Roseman first1 S title Reflections on glycobiology url http www.jbc.org cgi content full 276 45 41527 journal The Journal of Biological Chemistry volume 276 issue 45 pages 41527 42 year 2001 pmid 11553646 ref To be specific, glucosamine 6 phosphate is synthesized from fructose 6 phosphate and glutamine ref cite journal author1 Sudhamoy Ghosh last2 Blumenthal first2 HJ last3 Davidson first3 E last4 Roseman first4 S title Glucosamine Metabolism url http www.jbc.org cgi reprint 235 5 1265 journal Journal of Biological Chemistry volume 235 issue 5 pages 1265 date 1960 05 01 pmid 13827775 ref as the first step of the hexosamine biosynthesis pathway. ref http www.chem.qmul.ac.uk iubmb enzyme reaction polysacc UDPGlcN.html International Union of Biochemistry and Molecular Biology ref The end product ... more details
chembox verifiedrevid 402840353 ImageFile UDP glucuronic acid.png ImageSize 200px IUPACName OtherNames Section1 Chembox Identifiers InChI 1 C9H12N2O6.C6H12O13P2 c12 3 4 6 14 7 15 8 17 4 11 2 1 5 13 10 9 11 16 7 1 2 18 20 12,13 14 5 19 21 15,16 17 3 8 4 9 6 10 11 h1 2,4,6 8,12,14 15H,3H2, H,10,13,16 1 5,8 9H, H,10,11 H2,12,13,14 H2,15,16,17 p 4 t4 ,6 ,7 ,8 2 ,3 ,4 ,5 m10 s1 InChIKey GIFKDHYZEJQSDD DNQFPBLIBB StdInChI Ref stdinchicite correct chemspider StdInChI 1S C9H12N2O6.C6H12O13P2 c12 3 4 6 14 7 15 8 17 4 11 2 1 5 13 10 9 11 16 7 1 2 18 20 12,13 14 5 19 21 15,16 17 3 8 4 9 6 10 11 h1 2,4,6 8,12,14 15H,3H2, H,10,13,16 1 5,8 9H, H,10,11 H2,12,13,14 H2,15,16,17 p 4 t4 ,6 ,7 ,8 2 ,3 ,4 ,5 m10 s1 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey GIFKDHYZEJQSDD BZYIUNRFSA J CASNo 2616 64 0 PubChem 17473 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 19951236 IUPHAR ligand 1784 SMILES OC O C H O C H O C H OP O O O C H C O OP O O O.O C 1NC O N C C 1 C H 2O C H CO C H O C H 2O MeSHName UDP glucuronic acid Section2 Chembox Properties Formula C sub 15 sub H sub 22 sub N sub 2 sub O sub 18 sub P sub 2 sub MolarMass 580.285 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition UDP glucuronic acid is a sugar used in the creation of polysaccharide s and is an intermediate in the biosynthesis of ascorbic acid except in primate s and guinea pig s . It is made from UDP glucose by UDP glucose 6 dehydrogenase EC 1.1.1.22 using NAD as a cofactor. It is the source of the glucuronosyl group in glucuronosyltransferase reactions. See also glucuronic acid Uridine diphosphate UDP Nucleotide sugars Category Organophosphates Category Glycosides Category Coenzymes Category Nucleotides biochem stub fa ja pl Kwas urydyno 5 difosfo D glukuronowy fi UDP glukuronihappo ... more details
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