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Alpha ketoglutaric acid
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Encyclopedia results for Alpha ketoglutaric acid

Alpha ketoglutaric acid





Encyclopedia results for Alpha ketoglutaric acid

  1. Alpha-Ketoglutaric acid

    Refimprove date September 2011 DISPLAYTITLE alpha Ketoglutaric acid chembox Watchedfields changed verifiedrevid 443659412 Name Ketoglutaric acid Reference ref Merck Index , 13th Edition, 5320 . ref ImageFile Alpha ketoglutaric acid.png ImageSize 150px IUPACName 2 Oxopentanedioic acid OtherNames 2 Ketoglutaric acid br alpha Ketoglutaric acid br 2 Oxoglutaric acid br Oxoglutaric acid Section1 Chembox ... Ref drugbankcite correct drugbank DrugBank DB03806 SMILES O C O C O CCC O O MeSHName alpha ketoglutaric acid Section2 Chembox Properties Formula C sub 5 sub H sub 6 sub O sub 5 sub MolarMass 146.11 ... FlashPt Autoignition Ketoglutaric acid is one of two ketone derivatives of glutaric acid . The term ketoglutaric acid, when not further qualified, almost always refers to the alpha variant. Acetonedicarboxylic acid Ketoglutaric acid varies only by the position of the ketone functional group ... 1 Collagen . Dietary supplement Ketoglutaric acid is sold as a dietary supplement and to body ... biological compound. It is the keto acid produced by de amination of glutamate , and is an intermediate ... the oxygen level in its environment. In combination with molecular oxygen, alpha ketoglutarate ... on studies that show excess ammonia in the body can combine with alpha ketoglutarate, reducing ... 144 ALPHA KETOGLUTARATE.aspx?activeIngredientId 144&activeIngredientName ALPHA KETOGLUTARATE Alpha Ketoglutarate , WebMD ref However, the only studies that show alpha ketoglutarate can reduce ... deamination of glutamate by glutamate dehydrogenase . Alpha ketoglutarate can be used to produce Creatine alpha ketoglutarate Interactive pathway map TCACycle WP78 highlight Alpha Ketoglutaric acid References Reflist Citric acid cycle Amino acid metabolism intermediates DEFAULTSORT Ketoglutaric Acid, Alpha Category Dicarboxylic acids Category Keto acids Category Citric acid cycle compounds cs 2 oxoglutar t da Alfa ketoglutarat de Ketoglutars ure fr Acide alpha c toglutarique gl cido alfa ...   more details



  1. Ketoglutaric acid

    Ketoglutaric acid or oxoglutaric acid may refer to either of two chemical compounds alpha Ketoglutaric acid Ketoglutaric acid acetonedicarboxylic acid Ketoglutaric acid acetonedicarboxylic acid disambig ...   more details



  1. Alpha acid

    File R Humulone.svg thumb right Chemical structure of humulone , the most prevalent alpha acid in hops Alpha acids acids are a class of chemical compounds primarily of importance to the production of beer . They are found in the resin glands of the flowers of the hops hop plant and are the source of hop Taste Bitterness bitterness . Alpha acids may be isomerized to form iso alpha acids by the application of heat in solution . Iso alpha acids iso acids are typically produced in beer from the addition of hops to the boiling wort . The degree of isomerization and the amount of bitter flavor produced by the addition of hops is highly dependent on the length of time the hops are boiled. Longer boil times will result in isomerization of more of the available alpha acids. Common alpha acids include humulone , adhumulone , cohumulone , posthumulone , and prehumulone . The most common iso alpha acids are cis and trans isohumulone . Bittering The alpha acid rating on hops indicates the amount of alpha acid as a percentage of total weight of the hop. Hops with a higher alpha acid content will contribute more bitterness than a lower alpha acid hop when using the same amount of hops. High alpha acid varieties of hops are more efficient for producing highly bitter beers. Alpha acid percentages ... factors. For example, this list shows the typical range of Alpha Acids found in some common ... 5 Mt. Hood 3.5 8 Saaz 2 5 Styrian Goldings 4.5 7 Willamette 4 7 Anti bacterial properties Iso alpha ... alpha acids are very effective preventing serious contamination from Gram positive bacteria such as the lactic acid bacteria and Pediococcus , there are some strains that are quite resistant to the effects ... 3 ref The iso alpha acids have no effect on Gram negative bacteria, and therefore the brewer must ... stability. ref name Sakamoto References references External links Commons category inline alpha acids chemical structures of alpha acids Category Organic acids Category Brewing Category Bitter compounds ...   more details



  1. Alpha-Hydroxyglutaric acid

    DISPLAYTITLE alpha Hydroxyglutaric acid chembox verifiedrevid 443379483 Name Hydroxyglutaric acid ImageFile alpha hydroxyglutaric acid.png ImageSize 200px IUPACName 2 Hydroxypentanedioic acid OtherNames 2 Hydroxyglutaric acid Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 42 KEGG Ref keggcite correct kegg KEGG C02630 InChI 1 C5H8O5 c6 3 5 9 10 1 2 4 7 8 h3,6H,1 2H2, H,7,8 H,9,10 InChIKey HWXBTNAVRSUOJR UHFFFAOYAI SMILES1 O C O C O CCC O O StdInChI Ref stdinchicite correct chemspider StdInChI 1S C5H8O5 c6 3 5 9 10 1 2 4 7 8 h3,6H,1 2H2, H,7,8 H,9,10 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey HWXBTNAVRSUOJR UHFFFAOYSA N CASNo 2889 31 8 PubChem 43 ChEBI Ref ebicite correct EBI ChEBI 17084 SMILES C CC O O C C O O O MeSHName Alpha hydroxyglutarate Section2 Chembox Properties C 5 H 8 O 5 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Hydroxyglutaric acid 2 hydroxyglutaric acid is an alpha hydroxy acid . In humans the compound is formed by a hydroxyacid oxoacid transhydrogenase whereas in bacteria is formed by a 2 hydroxyglutarate synthase . The compound can be converted to alpha Ketoglutaric acid ketoglutaric acid through the action of a 2 hydroxyglutarate dehydrogenase which, in humans, are two enzymes called D2HGDH and L2HGDH . Deficiency in either of these two enzymes lead to a disease known as 2 Hydroxyglutaric aciduria 2 hydroxyglutaric aciduria . DEFAULTSORT Hydroxyglutaric acid, alpha Category Dicarboxylic acids Category Hydroxy acids organic compound stub de 2 Hydroxyglutars ure pt cido alfa hidroxi glut rico ...   more details



  1. Alpha-amino-acid esterase

    orphan date January 2010 enzyme Name alpha amino acid esterase EC number 3.1.1.43 CAS number 74506 40 4 IUBMB EC number 3 1 1 43 GO code 0047658 image width caption In enzymology , an alpha amino acid esterase EC number 3.1.1.43 is an enzyme that catalysis catalyzes the chemical reaction an alpha amino acid ester H sub 2 sub O math rightleftharpoons math an alpha amino acid an alcohol Thus, the two substrate biochemistry substrates of this enzyme are alpha amino acid ester and water H sub 2 sub O , whereas its two product chemistry products are alpha amino acid and alcohol . This enzyme belongs to the family of hydrolase s, specifically those acting on carboxylic ester bonds. The systematic name of this enzyme class is alpha amino acid ester aminoacylhydrolase . This enzyme is also called alpha amino acid ester hydrolase . Structural studies As of late 2007, 5 tertiary structure structures have been solved for this class of enzymes, with Protein Data Bank PDB accession codes PDB link 1MPX , PDB link 1NX9 , PDB link 1RYY , PDB link 2B4K , and PDB link 2B9V . References reflist 1 cite journal author Kato K, Kawahara K, Takahashi T and Kakinuma A date 1980 title Purification of an alpha amino acid ester hydrolase from Xanthomonas citri journal Agric. Biol. Chem. volume 44 pages 1069&ndash 1074 cite journal author Kato K, Kawahara K, Takahashi T and Kakinuma A date 1980 title Substrate specificity of an alpha amino acid ester hydrolase from Xanthomonas citri journal Agric. Biol. Chem. volume 44 pages 1075&ndash 1081 cite journal author Takahashi T, Yamazaki Y, Kato K date 1974 title Substrate specificity of an alpha amino acid ester hydrolase produced by Acetobacter turbidans A.T.C.C. 9325 journal Biochem. J. volume 137 pages 497&ndash 503 pmid 4424889 issue 3 pmc 1166149 Category EC 3.1.1 Category Enzymes of known structure hydrolase stub ...   more details



  1. Alpha-Ketoisovaleric acid

    DISPLAYTITLE alpha Ketoisovaleric acid chembox verifiedrevid 443378375 Name Ketoisovaleric acid ImageFile alpha Ketovaline.svg ImageSize IUPACName 3 Methyl 2 oxobutanoic acid OtherNames 2 Ketoisovaleric acid Ketovaline Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 48 KEGG Ref keggcite correct kegg KEGG C00141 InChI 1 C5H8O3 c1 3 2 4 6 5 7 8 h3H,1 2H3, H,7,8 InChIKey QHKABHOOEWYVLI UHFFFAOYAY ChEMBL Ref ebicite correct EBI ChEMBL 146554 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C5H8O3 c1 3 2 4 6 5 7 8 h3H,1 2H3, H,7,8 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey QHKABHOOEWYVLI UHFFFAOYSA N CASNo Ref cascite correct CAS CASNo 759 05 7 DrugBank Ref drugbankcite correct drugbank DrugBank DB04074 PubChem 49 ChEBI Ref ebicite correct EBI ChEBI 16530 SMILES O C C O O C C C Section2 Chembox Properties C 5 H 8 O 3 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Ketoisovaleric acid is a metabolite of valine . See also alpha Ketovaleric acid Ketovaleric acid Amino acid metabolism intermediates DEFAULTSORT Ketoisovaleric acid, alpha Category Keto acids biochem stub fr Acide 3 m thyl 2 oxobutano que ja ...   more details



  1. Alpha-Ketoadipic acid

    DISPLAYTITLE alpha Ketoadipic acid Chembox verifiedrevid 438036721 Name Ketoadipic acid Reference ref http pubchem.ncbi.nlm.nih.gov summary summary.cgi?cid 71 2 oxoadipate Compound Summary , PubChem . ref ImageFileL1 Alpha ketoadipic acid.svg ImageFileL1 Ref chemboximage correct ?? ImageSizeL1 121 ImageNameL1 Skeletal formula of ketoadipic acid ImageFileR1 Alpha keotadipic acid 3D balls.png ImageFileR1 Ref chemboximage correct ?? ImageSizeR1 121 ImageNameR1 Ball and stick model of ketoadipic acid IUPACName 2 Oxohexanedioic acid SystematicName 2 Oxohexanedioic acid ref Cite web url http pubchem.ncbi.nlm.nih.gov summary summary.cgi?cid 71&loc ec rcs title Alpha ketoadipic acid work The PubChem Project publisher National Center for Biotechnology Information ref 2 Oxoadipate Section1 Chembox Identifiers CASNo 3184 35 8 CASNo Ref cascite correct ?? PubChem 71 PubChem Ref Pubchemcite correct PubChem ChemSpiderID 70 ChemSpiderID Ref chemspidercite correct chemspider KEGG C00322 KEGG Ref keggcite correct kegg MeSHName Alpha ketoadipic acid ChEBI Ref ebicite correct EBI ChEBI 15753 3DMet B00088 SMILES C CC O C O O CC O O SMILES1 O C C O O CCCC O O StdInChI 1S C6H8O5 c7 4 6 10 11 2 1 3 5 8 9 h1 3H2, H,8,9 H,10,11 StdInChI Ref stdinchicite correct chemspider InChI 1 C6H8O5 c7 4 6 10 11 2 1 3 5 8 9 h1 3H2, H,8,9 H,10,11 StdInChIKey FGSBNBBHOZHUBO UHFFFAOYSA N StdInChIKey Ref stdinchicite correct chemspider InChIKey FGSBNBBHOZHUBO UHFFFAOYAU Section2 Chembox Properties C 6 H 8 O 5 ExactMass 160.037173366 g mol sup 1 sup &alpha Ketoadipic acid or 2 oxoadipate is an intermediate in the metabolism of lysine . See also Homoisocitrate dehydrogenase References Reflist Biochem stub Organic compound stub Amino acid metabolism intermediates DEFAULTSORT Ketoadipic acid, alpha Category Dicarboxylic acids Category Keto acids fr Acide 2 oxoadipique ...   more details



  1. Alpha-Ketoisocaproic acid

    DISPLAYTITLE alpha Ketoisocaproic acid Chembox verifiedrevid 411952246 Name &alpha Ketoisocaproic acid ImageFile Alpha ketoisocaproic acid.png ImageFile Ref chemboximage correct ?? ImageSize 244 ImageName Skeletal formula of alpha ketoisocaproic acid IUPACName 4 Methyl 2 oxopentanoic acid SystematicName 4 Methyl 2 oxopentanoic acid ref http pubchem.ncbi.nlm.nih.gov summary summary.cgi?cid 70 ref OtherNames 4 Methyl 2 oxovaleric acid Section1 Chembox Identifiers CASNo 816 66 0 CASNo Ref cascite correct CAS PubChem 70 PubChem Ref Pubchemcite correct PubChem ChemSpiderID 69 ChemSpiderID Ref chemspidercite correct chemspider EINECS 212 435 5 UNNumber 3265 DrugBank DB03229 KEGG C00233 KEGG Ref keggcite correct kegg MeSHName Alpha ketoisocaproic acid ChEBI 48430 ChEMBL 445647 ChEMBL Ref ebicite correct EBI Beilstein 1701823 3DMet B00066 SMILES CC C CC O C O O SMILES1 O C C O O CC C C StdInChI 1S C6H10O3 c1 4 2 3 5 7 6 8 9 h4H,3H2,1 2H3, H,8,9 StdInChI Ref stdinchicite correct chemspider InChI 1 C6H10O3 c1 4 2 3 5 7 6 8 9 h4H,3H2,1 2H3, H,8,9 StdInChIKey BKAJNAXTPSGJCU UHFFFAOYSA N StdInChIKey Ref stdinchicite correct chemspider InChIKey BKAJNAXTPSGJCU UHFFFAOYAG Section2 Chembox Properties C 6 H 10 O 3 ExactMass 130.062994186 g mol sup 1 sup Density 1.055 g cm sup 3 sup at 20 C MeltingPtCL 8 MeltingPtCH 10 BoilingPtC 85 Boiling notes at 13 mmHg LogP 0.133 pKa 2.651 pKb 11.346 Section3 Chembox Hazards EUClass Hazchem C RPhrases R34 SPhrases S26 , S36 37 39 , S45 &alpha Ketoisocaproic acid is an intermediate in the metabolism of leucine . References Reflist Organic compound stub Amino acid metabolism intermediates DEFAULTSORT Ketoisocaproic acid, alpha Category Keto acids fr Acide 4 m thyl 2 oxoval rique hu Alfa ketoizokapronsav ja ...   more details



  1. Alpha-Ketobutyric acid

    DISPLAYTITLE alpha Ketobutyric acid chembox verifiedrevid 443659318 Name Ketobutyric acid ImageFile Alpha ketobutyric acid.svg ImageSize ImageFile1 Alpha Ketobutyric acid.png ImageSize IUPACName 2 oxobutanoic acid OtherNames Section1 Chembox Identifiers KEGG Ref keggcite correct kegg KEGG C00109 InChI 1 C4H6O3 c1 2 3 5 4 6 7 h2H2,1H3, H,6,7 InChIKey TYEYBOSBBBHJIV UHFFFAOYAT ChEMBL Ref ebicite correct EBI ChEMBL 171246 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C4H6O3 c1 2 3 5 4 6 7 h2H2,1H3, H,6,7 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey TYEYBOSBBBHJIV UHFFFAOYSA N CASNo Ref cascite correct CAS CASNo 600 18 0 PubChem 58 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 57 ChEBI Ref ebicite correct EBI ChEBI 30831 DrugBank Ref drugbankcite correct drugbank DrugBank DB04553 SMILES O C C O O CC MeSHName Alpha ketobutyric acid Section2 Chembox ... of sotolon from alpha ketobutyric acid. ref Optimal Conditions for the Formation of Sotolon from .alpha. Ketobutyric Acid in the French Vin Jaune . Pham Thu Thuy, Guichard Elisabeth, Schlich Pascal ... acid is a product of the lysis of cystathionine . It is also one of the degradation products of threonine , produced by the catabolism of the amino acid by threonine dehydratase . It is also produced by the degradation of homocysteine and the metabolism of methionine . Ketobutyric acid is transported into the mitochondrial matrix, where it is converted to propionyl CoA by Branched Chain Alpha Keto Acid Dehydrogenase Complex . Further mitochondrial reactions produce succinyl CoA . This is first ... produces succinyl CoA which enters the citric acid cycle . ref http pathman.smpdb.ca pathways SMP00452 ... 10.1007 BF02275793 ref See also Butyric acid References reflist Amino acid metabolism intermediates DEFAULTSORT Ketobutyric acid, alpha Category Keto acids biochem stub de 2 Oxobutans ure fa fr Acide alpha c tobutyrique ja zh ...   more details



  1. Alpha-Cyano-4-hydroxycinnamic acid

    DISPLAYTITLE alpha Cyano 4 hydroxycinnamic acid chembox Watchedfields changed verifiedrevid 446778754 Name Cyano 4 hydroxycinnamic acid ImageFile Cyanohydroxycinnamic acid.png ImageSize 200px IUPACName E 2 cyano 3 4 hydroxyphenyl prop 2 enoate OtherNames alpha cyano 4 hydroxycinnamic acid br alpha cyano 4 hydroxycinnamate br 2 cyano 4 hydroxycinnamate Section1 Chembox Identifiers CASNo Ref cascite correct ?? CASNo 28166 41 8 PubChem 6931228 SMILES C1 CC CC C1C C C N C O OH O Section2 Chembox Properties C 10 H 7 O 3 N 1 Appearance Yellow powder Density MeltingPt 245 250  C BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Cyano 4 hydroxycinnamic acid , also written as alpha cyano 4 hydroxycinnamic acid and abbreviated CHCA , is a cinnamic acid derivative and is a member of the phenylpropanoid family. It is used as a matrix for peptide s and nucleotides in Matrix assisted laser desorption ionization MALDI mass spectrometry analyses. ref cite journal title Cyano 4 hydroxycinnamic acid as a matrix for matrix assisted laser desorption mass spectrometry journal Org. Mass Spectrom. volume 27 issue 2 pages 156 8 year 1992 doi 10.1002 oms.1210270217 author Beavis, R. C. last2 Chaudhary first2 T. last3 Chait first3 B. T. ref See also Sinapinic acid References Reflist DEFAULTSORT Cyano 4 hydroxycinnamic acid, alpha Category Carboxylic acids Category Aromatic compounds Category Phenylpropanoids Category Nitriles fa ja 4 ru 4 ...   more details



  1. Alpha-Aminobutyric acid

    DISPLAYTITLE alpha Aminobutyric acid Chembox verifiedrevid 443377761 Name Aminobutyric acid ImageFile alpha aminobutyric acid.png ImageSize 180px IUPACName 2 Aminobutanoic acid OtherNames 2 Aminobutyric acid Aminobutanoic acid Ethylglycine Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 6405 UNII Ref fdacite correct FDA UNII 8306QPJ19P InChI 1 C4H9NO2 c1 2 3 5 4 6 7 h3H,2,5H2,1H3, H,6,7 InChIKey QWCKQJZIFLGMSD UHFFFAOYAG ChEMBL Ref ebicite correct EBI ChEMBL 55242 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C4H9NO2 c1 2 3 5 4 6 7 h3H,2,5H2,1H3, H,6,7 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey QWCKQJZIFLGMSD UHFFFAOYSA N CASNo Ref cascite correct CAS CASNo 2835 81 6 PubChem 6657 ChEBI Ref ebicite correct EBI ChEBI 35621 SMILES O C O C N CC Section2 Chembox Properties Formula C sub 4 sub H sub 9 sub NO sub 2 sub MolarMass 103.12 g mol Appearance Density MeltingPt BoilingPt pKa 2.55 carboxyl , 9.60 amino ref Dawson, R.M.C., et al., Data for Biochemical Research , Oxford, Clarendon Press, 1959. ref Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Aminobutyric acid AABA is an isomer of the amino acid aminobutyric acid with chemical formula C sub 4 sub H sub 9 sub NO sub 2 sub . It has two other isomers, gamma aminobutyric acid GABA and beta aminobutyric acid . It is a key intermediate in the biosynthesis of ophthalmic acid or ophthalmate, which was first isolated from calf lens. References Reflist DEFAULTSORT Aminobutyric Acid, Alpha Category Amino acids Amine stub de Aminobutters ure fa it Acido alfa amminobutirrico ja pl Kwas aminomas owy pt cido alfa aminobut rico ru ...   more details



  1. Alpha-Ketovaleric acid

    DISPLAYTITLE alpha Ketovaleric acid Chembox Verifiedfields changed verifiedrevid 477319291 Name Ketovaleric acid ImageFile Alpha ketovaleric acid.svg ImageSize 200px IUPACName 2 Oxopentanoic acid OtherNames Ketovalerate Oxovaleric acid 2 Ketopentanoic acid 2 Oxo n valeric acid Section1 Chembox Identifiers CASNo 1821 02 9 CASNo Ref cascite changed ?? ChEMBL Ref ebicite correct EBI ChEMBL 1162544 PubChem 74563 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 67142 ChEBI Ref ebicite correct EBI ChEBI 33033 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C5H8O3 c1 2 3 4 6 5 7 8 h2 3H2,1H3, H,7,8 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey KDVFRMMRZOCFLS UHFFFAOYSA N SMILES O C C O O CCC InChI InChI 1S C5H8O3 c1 2 3 4 6 5 7 8 h2 3H2,1H3, H,7,8 Section2 Chembox Properties C 5 H 8 O 3 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Ketovaleric acid is a keto acid that is found in human blood. ref cite journal last1 Fu first1 X last2 Kimura first2 M last3 Iga first3 M last4 Yamaguchi first4 S title Gas chromatographic mass spectrometric screening for organic acidemias using dried urine filter paper determination of alpha ketoacids journal Journal of Chromatography B volume 758 issue 1 pages 87 94 year 2001 pmid 11482739 ref ref cite journal last1 Lee first1 SH last2 Kim first2 SO last3 Chung first3 BC title Gas chromatographic mass spectrometric determination of urinary oxoacids using O 2,3,4,5,6 pentafluorobenzyl oxime trimethylsilyl ester derivatization and cation exchange chromatography .... ref http www.nugowiki.org index.php 2 Oxovaleric acid European Nutrigenomics Organisation Metabolite Database ref See also Alpha Ketoisovaleric acid Ketoisovaleric acid 3 Oxopentanoic acid ketovaleric acid Levulinic acid ketovaleric acid References reflist DEFAULTSORT Ketovaleric acid, alpha ... performance liquid chromatographic determination of alpha keto acids in human serum and urine using ...   more details



  1. Alpha-Phenylcinnamic acid

    DISPLAYTITLE alpha Phenylcinnamic acid Chembox Watchedfields changed verifiedrevid 404024540 Name Phenycinnamic acid ImageFile Alpha Phenylcinnamic acid.png ImageSize 150 ImageAlt Skeletal formula ImageFile1 Alpha Phenylcinnamic acid 3D balls.png ImageAlt1 Ball and stick model IUPACName 2 E 2,3 Diphenylprop 2 enoic acid OtherNames Phenylcinnamic acid, Phenylmethylene benzeneacetic acid, Phenyl trans cinnamic acid Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 610577 InChI 1 C15H12O2 c16 15 17 14 13 9 5 2 6 10 13 11 12 7 3 1 4 8 12 h1 11H, H,16,17 b14 11 InChIKey BIDDLDNGQCUOJQ SDNWHVSQBV SMILES1 O C O C C c1ccccc1 c2ccccc2 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C15H12O2 c16 15 17 14 13 9 5 2 6 10 13 11 12 7 3 1 4 8 12 h1 11H, H,16,17 b14 11 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey BIDDLDNGQCUOJQ SDNWHVSQSA N CASNo Ref cascite correct ?? CASNo 91 48 5 SMILES OC O C C C1 CC CC C1 C2 CC CC C2 Section2 Chembox Properties C 15 H 12 O 2 Appearance White to light yellow powder MeltingPt 172 174  C BoilingPt 224 225  C Solubility Slightly soluble Section3 Chembox Hazards MainHazards Irritant ref http msds.chem.ox.ac.uk PH alpha phenyl cinnamic acid.html ref Phenylcinnamic acid is a phenylpropanoid , or, more specifically, a derivative of cinnamic acid . It has the chemical formula formula ... reflist DEFAULTSORT Phenylcinnamic Acid, Alpha Category Aromatic acids ... search cas 91485.html ref . Uses Phenylcinnamic acid is frequently used as a compound ... phenylcinnamic acid. Some of the more popular methods of formation include the condensation ... of benzylmandelic acid , or by the reaction of sodium phenylacetate with benzaldehyde in acetic anhydride ... and Computational Tools for Mechanistic Study A Modified Perkin Condensation leading to Alpha Phenylcinnamic Acid Isomers author Istv n P link , B la T r k, Gyula Tasi, Tam s K rtv lyesi publisher ...   more details



  1. 15,16-Dihydroxy-alpha-eleostearic acid

    DISPLAYTITLE 15,16 Dihydroxy alpha eleostearic acid Chembox verifiedrevid 406475594 Name 15,16 Dihydroxy eleostearic acid ImageFile 15,16 Dihydroxy alpha eleostearic acid.svg ImageSize 200px ImageAlt IUPACName 9 Z ,11 E ,13 E 15,16 Dihydroxyoctadeca 9,11,13 trienoic acid OtherNames Section1 Chembox Identifiers CASNo 1083078 83 4 CASNo Ref cascite correct CAS PubChem SMILES OC CCCCCCC C C C C C C C O C O CC O Section2 Chembox Properties C 18 H 30 O 4 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition 15,16 Dihydroxy eleostearic acid , or 15,16 Dihydroxy 9Z,11E,13E 9,11,13 octadecatrienoic acid , is an organic compound with formula chem C 18 H 30 O 4 , or H sub 3 sub C CH sub 2 sub CH OH sub 2 sub CH CH sub 3 sub CH sub 2 sub sub 7 sub C O OH. It can be seen as derived from alpha eleostearic acid eleostearic acid by the replacement of two hydrogen atoms by two hydroxyl OH groups. The compound is found in the pulp and seeds of bitter melon s the fruits of Momordica charantia . It has been found to induce apoptosis in HL60 leukemia cells in vitro at a concentration of 160 micromolar M , although it is less potent in this regard than the unsubstituted eleostearic acid also found in the seed oil . While eleostearic acid has been found to prevent carcinogenesis in rat s, this derivative does not seem to have that effect. ref name kob2008 Masuko Kobori, Mayumi Ohnishi Kameyama, Yukari Akimoto, Chizuko Yukizaki and Mitsuru Yoshida 2008 Eleostearic Acid and Its Dihydroxy Derivative Are MajorApoptosis Inducing Components of Bitter Gourd . Journal of Agricultural and Food Chemistry, volume 56, issue 22, pages 10515 10520. doi 10.1021 jf8020877 ref The compound can be extracted from the fruit with ethanol , and is soluble in ethyl acetate but not in water or acetone . See also alpha eleostearic acid Eleostearic acid References reflist DEFAULTSORT Dihydroxy alpha eleostearic acid, 15,16 Category Fatty acids ...   more details



  1. Alpha-Aminoadipic acid

    DISPLAYTITLE alpha Aminoadipic acid chembox verifiedrevid 443377661 Name Aminoadipic acid ImageFile Alpha aminoadipic acid.svg ImageSize IUPACName 2 aminohexanedioic acid OtherNames Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 456 SMILES1 O C O CCCC N C O O InChI 1 C6H11NO4 c7 4 6 10 11 2 1 3 5 8 9 h4H,1 3,7H2, H,8,9 H,10,11 InChIKey OYIFNHCXNCRBQI UHFFFAOYAC ChEMBL Ref ebicite correct EBI ChEMBL 433238 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C6H11NO4 c7 4 6 10 11 2 1 3 5 8 9 h4H,1 3,7H2, H,8,9 H,10,11 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey OYIFNHCXNCRBQI UHFFFAOYSA N CASNo 542 32 5 PubChem 469 ChEBI Ref ebicite correct EBI ChEBI 37024 SMILES C CC C O O N CC O O MeSHName 2 Aminoadipic Acid Section2 Chembox Properties Formula C sub 6 sub H sub 11 sub NO sub 4 sub MolarMass 161.156 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Aminoadipic acid is an intermediate in the metabolism of lysine and saccharopine . See also Adipic acid Amino acid metabolism intermediates DEFAULTSORT Aminoadipic Acid, Alpha biochem stub Category Dicarboxylic acids Category Amino acids fr Acide 2 aminoadipique ja pt cido alfa aminoad pico ...   more details



  1. Alpha-Eleostearic acid

    DISPLAYTITLE alpha Eleostearic acid chembox verifiedrevid 445131831 Name Eleostearic acid ImageFile Alpha eleostearic acid.svg ImageSize 200px ImageName Eleostearic acid IUPACName 9 Z ,11 E ,13 E Octadeca 9,11,13 trienoic acid Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ... also 15,16 Dihydroxy alpha eleostearic acid 15,16 Dihydroxy eleostearic acid References reflist DEFAULTSORT Eleostearic Acid, alpha Category Fatty acids cs Kyselina alfa eleostearov lv Eleostear nsk be ... 97 issue 1 pages 1 9 ref Eleostearic acid or 9 Z ,11 E ,13 E octadeca 9,11,13 trienoic acid , is an organic compound , a conjugated fatty acids conjugated linolenic acid and one of the isomer s of octadecatrienoic acid . It is often called simply eleostearic acid although there is also a beta eleostearic acid eleostearic acid the all trans or 9 E ,11 E ,13 E isomer The acid makes up approximately ... fatty acid degree of unsaturation gives tung oil its properties as a drying oil . Biochemical properties Image bittermelonfruit.jpg thumb left Eleostearic acid makes up about 60 of the fatty acids from bitter gourd oil. In their pioneering work on essential fatty acid s, Burr, Burr and Miller compared the nutritional properties of eleostearic acid ELA to that of its isomer alpha linolenic acid ALA . ALA relieved essential fatty acid deficiency ELA did not. ref name Burr In rats, eleostearic acid is converted to a conjugated linoleic acid . ref name Tsuzuki cite journal url http jn.nutrition.org ... issue 8 pages 2153 9. title Conjugated linolenic acid is slowly absorbed in rat intestine, but quickly converted to conjugated linoleic acid author Tsuzuki T, Kawakami Y, Abe R, et al. accessdate 2007 ... Kameyama, Yukari Akimoto, Chizuko Yukizaki and Mitsuru Yoshida 2008 Eleostearic Acid and Its Dihydroxy ... 0.01 bitter gourd seed oil 0.006 as eleostearic acid were found to prevent azoxymethane induced ..., T. Tanaka 2004 , Dietary seed oil rich in conjugated linolenic acid from bitter melon inhibits ...   more details



  1. Alpha hydroxy acid

    title An evaluation of the effect of an alpha hydroxy acid blend skin cream in the cosmetic improvement ... U.S. Food and Drug Administration Alpha Hydroxy Acids in Cosmetics DEFAULTSORT Alpha Hydroxy Acid ... , and hydroxy acids Hydroxy acids , or alpha hydroxy acids AHAs , are a class of chemical compounds that consist of a carboxylic acid substituted with a hydroxyl hydroxyl group on the adjacent ... and simple are glycolic acid , lactic acid , citric acid , mandelic acid . Cosmetic applications ... food products including glycolic acid from sugar cane , lactic acid from sour milk , malic acid from apples , citric acid from citrus fruits and tartaric acid from grape wine . For any topical compound ... compound s ability to penetrate the top layer of the skin. Glycolic acid having the smallest molecular ... appear to have deeper dermal effects. Glycolic acid, lactic acid and citric acid, on topical application ... ref Ditre CM, Griffin TD, Murphy GF, Vasn Scott EJ Improvement of photodamaged skin with alpha hydroxy acid AHA A clinical, histological, and ultra structural study. Dermatology 2000 Congress. Vienna, Austria. May 18 21, 1993 175. ref Alpha hydroxy acids at different concentrations In low concentrations, 5 10 , as is found in many over the counter products, glycolic acid reduces cell adhesion in the top ... for smoother texture following regular use of topical glycolic acid GA . This relatively low ... Glycolic acid versus trichloroacetic acid in melasma ref name Glycolic acid peeling in the treatment ... or other pigmentary problems. Newer formulations combine glycolic acid with an amino acid such as arginine ... acid efficacy. ref Glycolic Acid Peels By Ronald L. Moy, Debra Luftman, Lenore S. Kakita ref The use of an anti irritant like allantoin is also helpful. Because of its safety, glycolic acid at the concentrations ... sensitive skin . ref What Is Glycolic Acid All About? By Peter T. Pacik, M.D., F.A.C.S. href http www.skincare ... for more efficacious glycolic acid concentrations 50 70 as well as prime the skin for deeper chemical ...   more details



  1. Alpha-Linolenic acid

    Use dmy dates date April 2012 Distinguish linoleic acid About alpha linolenic acid Linolenic acid disambiguation Linolenic acid lowercase chembox verifiedrevid 477319349 Name Linolenic acid ImageFile ALAnumbering.png ImageSize 250px ImageFile1 Linolenic acid 3D vdW.png ImageSize1 250px OtherNames ALA Linolenic acid cis , cis , cis 9,12,15 Octadecatrienoic acid 9 Z ,12 Z ,15 Z 9,12,15 Octadecatrienoic acid 9 Z ,12 Z ,15 Z octadeca 9,12,15 trienoic acid ref cite journal last1 Loreau first1 O last2 ... carbon from the methyl end of the fatty acid chain, known as the n end. Thus, linolenic acid is a polyunsaturated fatty acid polyunsaturated omega 3 fatty acid n 3 omega 3 fatty acid. It is an isomer of gamma linolenic acid , a polyunsaturated omega 6 fatty acid n 6 omega 6 fatty acid. History Alpha linolenic acid was first isolated by Rollett ref cite journal author Rollett, A. journal ... preparation of Z,Z 1,4 dienic units with a new C6 homologating agent synthesis of alpha linolenic acid ... PC title Conversion of alpha linolenic acid to longer chain polyunsaturated fatty acids in human adults ... IA last2 Katan first2 MB last3 Zock first3 PL title Dietary alpha linolenic acid is associated ... shown a relationship between alpha linolenic acid ALA , which is abundant in linseed oil, and an increased ... Boffetta first3 P last4 Ronco first4 A last5 Mendilaharsu first5 M title Alpha linolenic acid and risk ... last2 Chen first2 YH last3 Bent first3 S title The relation of alpha linolenic acid to the risk of prostate ... 10.3945 ajcn.111.011817 pmc 3095504 ref Stability and Hydrogenation Alpha linolenic acid is relatively ... acid, 9Z,12Z,15E 1 13 C octadeca 9,12,15 trienoic acid and their 1 13 C all cis isomers journal ... Section2 Chembox Properties C 18 H 30 O 2 Density MeltingPt BoilingPt Linolenic acid is an organic ... of organic chemistry structure , it is named all cis 9,12,15 octadecatrienoic acid. ref name ... literature, it is given the name 18 3 n 3 . Linolenic acid is a carboxylic acid with an 18 ...   more details



  1. Alpha-Parinaric acid

    DISPLAYTITLE alpha Parinaric acid chembox verifiedrevid 443380378 ImageFile alpha Parinaric acid.png ImageSize 300px Name &alpha Parinaric acid IUPACName 9 Z ,11 E ,13 E ,15 Z octadeca 9,11,13,15 tetraenoic acid OtherNames cis parinaric acid br parinaric acid Section1 Chembox Identifiers ChemSpiderID ... W, Zucolotto M. 1996 . Identification of alpha parinaric acid in the seed oil of Sebastiana brasiliensis ... ref References reflist 2 DEFAULTSORT Parinaric acid, alpha Category Fatty acids fa ... Parinaric acid is a conjugated fatty acid conjugated polyunsaturated fatty acid . Discovered by Tsujimoto and Koyanagi in 1933, ref Tsujimoto M, Koyanagi H. 1933 . New unsaturated acid in the kernel ... double bond structure of parinaric acid distinguishes it structurally and chemically from the usual methylene interrupted arrangement of polyunsaturated fatty acid s that have double bonds and single ... by the alternating double bonds, parinaric acid is commonly used as a molecular probe in the study of biological membranes biomembranes . Natural sources Parinaric acid occurs naturally in the seeds ... seeds contain about 46 parinaric acid, 34 eleostearic acid as major components, with lesser amounts of saturated fatty acid s, oleic acid and linoleic acid . ref Hilditch TP et al. 1964 . The Chemical Constitution of Natural Fats, Fourth Edition. pg. 253. ref Parinaric acid is also found ... of Impatiens balsamina are 4.7 palmitic acid , 5.8 stearic acid , 2.8 arachidic acid , 18.3 oleic acid, 9.2 linoleic acid, 30.1 linolenic acid and 29.1 parinaric acid. ref name isbn0 8342 1342 7 cite book author Gunstone F.D. title Fatty Acid and Lipid Chemistry publisher Springer Verlag location ... Synthesis Biosynthesis The biochemical mechanism by which parinaric acid is formed in the plant ... a conjugase . This enzyme is related to the family of fatty acid desaturase enzymes responsible ... double bonds production of fatty acid components of high value drying oils in transgenic soybean embryos ...   more details



  1. Acid alpha-glucosidase

    PBB geneid 2548 Lysosomal alpha glucosidase is an enzyme that in humans is encoded by the GAA gene . ref name entrez cite web title Entrez Gene GAA glucosidase, alpha acid Pompe disease, glycogen storage disease type II url http www.ncbi.nlm.nih.gov sites entrez?Db gene&Cmd ShowDetailView&TermToSearch 2548 accessdate ref Errors in this gene cause glycogen storage disease type II Pompe disease . The PBB Summary template is automatically maintained by Protein Box Bot. See Template PBB Controls to Stop updates. PBB Summary section title summary text This gene encodes acid alpha glucosidase , which is essential for the degradation of glycogen to glucose in lysosome s. Different forms of acid alpha glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease type II glycogen storage disease II , also known as Pompe disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. ref name entrez References reflist External links http www.ncbi.nlm.nih.gov bookshelf br.fcgi?book gene&part gsd2 GeneReview NIH UW entry on Glycogen Storage Disease ... S, et al. title Sequence of the cDNA and 5 flanking region for human acid alpha glucosidase, detection ... R title Identification of the base pair substitution responsible for a human acid alpha glucosidase ... MM, et al. title Glycogenosis type II acid maltase deficiency . journal Muscle Nerve volume 3 issue ... L, vander Heyden N, Dedera D title Inhibition of HIV and SIV infectivity by blockade of alpha glucosidase ... author Hermans MM, Kroos MA, van Beeumen J, et al. title Human lysosomal alpha glucosidase. Characterization ... of a point mutation in the human lysosomal alpha glucosidase gene causing infantile glycogenosis ... with previous cDNA and amino acid sequences journal DNA Cell Biol. volume 9 issue 2 pages 85 ... lysosomal alpha glucosidase gene journal Biochem. J. volume 272 issue 2 pages 493 7 year ...   more details



  1. Retinoic acid receptor alpha

    PBB geneid 5914 Retinoic acid receptor alpha RAR , also known as NR1B1 nuclear receptor subfamily 1 ... url issn ref Interactions Retinoic acid receptor alpha has been shown to Protein protein interaction ... ML title SMRT corepressor interacts with PLZF and with the PML retinoic acid receptor alpha RARalpha ... alpha, a promiscuous partner of retinoic acid and thyroid hormone receptors journal EMBO J. volume ... and transcriptional properties of two classes of retinoic acid receptor alpha fusion proteins in acute ... acid receptor alpha gene to a novel transcribed locus. journal Nature volume 347 issue 6293 ... M, Chambon P title Characterization of a functional promoter for the human retinoic acid receptor alpha ... Retinoic Acid Receptor Alpha Category Intracellular receptors Category Transcription factors ... for the morphogen retinoic acid journal Nature volume 330 issue 6149 pages 624 9 year 1987 pmid 2825036 ... by 2 families of nuclear receptors, retinoic acid receptor retinoic acid receptor RAR and retinoid ... Entrez Gene retinoic acid receptor url http www.ncbi.nlm.nih.gov sites entrez?Db gene&Cmd ShowDetailView&TermToSearch ... acid receptor and its inhibition of retinoic acid induced apoptosis in cancer cells journal J ... acid receptors, modulating their activity in the presence of cellular retinoic acid binding protein ... Identification of nuclear receptor corepressor as a peroxisome proliferator activated receptor alpha ... F, Ivins S, Zhu J, S derstr m M, Waxman S, Zelent A title Reduced retinoic acid sensitivities ... leukemia fusion protein, with retinoic acid receptor and STAT3 signaling pathways journal Blood ... interacting protein 140 on coregulator binding to retinoic acid receptor complexes, histone ... month November pmid 10610177 doi 10.1038 15463 url issn ref Retinoid X receptor alpha RXRA . ref ... title Retinoic acid receptors inhibit AP1 activation by regulating extracellular signal regulated kinase ... MH, Formstecher P, Lefebvre P title PLZF is a negative regulator of retinoic acid receptor transcriptional ...   more details



  1. L-amino-acid alpha-ligase

    enzyme Name L amino acid alpha ligase EC number 6.3.2.28 CAS number IUBMB EC number 6 3 2 28 GO code image width caption Orphan date February 2009 In enzymology , an L amino acid alpha ligase EC number 6.3.2.28 is an enzyme that catalysis catalyzes the chemical reaction ATP an L amino acid an L amino acid math rightleftharpoons math ADP phosphate L aminoacyl L amino acid Thus, the two substrate biochemistry substrates of this enzyme are adenosine triphosphate ATP and L amino acid , whereas its 3 product chemistry products are adenosine diphosphate ADP , phosphate , and L aminoacyl L amino acid . This enzyme belongs to the family of ligase s, specifically those forming carbon nitrogen bonds as acid D amino acid ligases peptide synthases . The systematic name of this enzyme class is L amino acid L amino acid ligase ADP forming . Other names in common use include L amino acid alpha ligase , bacilysin synthetase , YwfE , and L amino acid ligase . References reflist 1 cite journal author Tabata K, Ikeda H, Hashimoto S date 2005 title ywfE in Bacillus subtilis codes for a novel enzyme, L amino acid ligase journal J. Bacteriol. volume 187 pages 5195&ndash 202 pmid 16030213 doi 10.1128 JB.187.15.5195 5202.2005 issue 15 pmc 1196041 ligase stub Category EC 6.3.2 Category Enzymes of unknown structure ...   more details



  1. Branched-chain alpha-keto acid dehydrogenase complex

    The branched chain keto acid dehydrogenase complex is a combination of enzyme s responsible for the degradation of the branched chain amino acids . Examples of these include valine , isoleucine , and leucine . Cofactors This complex requires the following 5 cofactors Thiamine diphosphate FAD Nicotinamide adenine dinucleotide NAD sup sup Lipoic acid Lipoate Coenzyme A Similar enzymes This complex is also analogous to the alpha ketoglutarate dehydrogenase complex in the citric acid cycle and the pyruvate dehydrogenase complex creating acetyl CoA prior to the citric acid cycle. Pathology A deficiency in any of the enzymes of this complex as well as an enzyme inhibitor inhibition of the complex as a whole is responsible for maple syrup urine disease . This enzyme is an autoantigen recognized in primary biliary cirrhosis , a form of acute liver failure. These antibodies appear to recognize oxidized protein that has resulted from inflammatory immune responses. Some of these inflammatory responses are explained by gluten sensitivity . ref name pmid17657817 cite journal author Leung PS, Rossaro L, Davis PA, et al. title Antimitochondrial antibodies in acute liver failure Implications for primary biliary cirrhosis journal Hepatology volume 46 issue 5 pages 1436 year 2007 pmid 17657817 doi 10.1002 hep.21828 ref . Other mitochondrial autoantigens include pyruvate dehydrogenase and branched chain oxoglutarate dehydrogenase , which are antigens recognized by anti mitochondrial antibodies . References Reflist External links http www.ncbi.nlm.nih.gov bookshelf br.fcgi?book gene&part msud GeneReviews NCBI NIH UW entry on Maple Syrup Urine Disease MeshName Branched Chain Ketoacid Dehydrogenase EC number 1.2.4.4 Autoantigens Aldehyde Oxo oxidoreductases Amino acid metabolism enzymes Multienzyme complexes DEFAULTSORT Branched Chain Alpha Keto Acid Dehydrogenase Complex Category Autoantigens ...   more details



  1. Creatine-alpha ketoglutarate

    Creatine alpha ketoglutarate is a salt chemistry salt formed from alpha Ketoglutaric acid alpha ketoglutaric acid AKG and creatine . It is sold as a fitness supplement however, its effects are experimentally unproven. ref cite journal last1 Incledon first1 T last2 Kreider first2 RB title Creatine alpha ketoglutarate is experimentally unproven journal The Journal of sports medicine and physical fitness volume 40 issue 4 pages 373 6 year 2000 pmid 11297009 ref References reflist Category Bodybuilding supplements biochemistry stub ...   more details



  1. Alpha Alpha

    Expand German topic culture date July 2011 Alpha Alpha Infobox television show name Alpha Alpha image caption format camera runtime creator starring country Germany network Theme first aired last aired num seasons num episodes list episodes Alpha Alpha was a 1972 German science fiction fantasy television series which aired on ZDF . It starred Karl Michael Vogler , Lilith Ungerer , Arthur Brauss and Horst Sachtleben . See also List of German television series External links imdb title id title Alpha Alpha Category German science fiction television series Category 1972 television series debuts Category 1972 television series endings Category ZDF television series Category German fantasy Germany tv prog stub de Alpha Alpha ...   more details




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