2O or 2 O may refer to 2o Sector, see Secondary sector of the economy 2 O methylation 2O, IATA code for Island Air Service in Alaska see Essential Air Service See also 2OOO , a Sydney, Australia radio station O2 disambiguation H2O J20 disambiguation L20 disambiguation N2O disambiguation Letter NumberCombDisambig ... more details
chembox verifiedrevid 470483247 Name Suberic acid ImageFile Suberic acid.png ImageSize 200px ImageName Suberic acid ImageFile1 Suberic acid 3D balls.png ImageSize1 230px IUPACName octanedioic acid Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 10025 PubChem 10457 InChI 1 C8H14O4 c9 7 10 5 3 1 2 4 6 8 11 12 h1 6H2, H,9,10 H,11,12 InChIKey TYFQFVWCELRYAO UHFFFAOYAN ChEMBL Ref ebicite correct EBI ChEMBL 1162491 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C8H14O4 c9 7 10 5 3 1 2 4 6 8 11 12 h1 6H2, H,9,10 H,11,12 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey TYFQFVWCELRYAO UHFFFAOYSA N CASNo Ref cascite correct CAS CASNo 505 48 6 ChEBI Ref ebicite correct EBI ChEBI 9300 SMILES O C O CCCCCCC O O Section2 Chembox Properties Formula C sub 8 sub H sub 14 sub O sub 4 sub MolarMass 174.20 g mol Density 1.272 g cm sup 3 sup 25 C MeltingPt 141 144 C BoilingPt 230 C at 15 mmHg pKa 4.526, 5.498 ref name pka cite journal title Solubility and Activity Coefficients of Acidic and Basic Nonelectrolytes in Aqueous Salt Solutions. 2. Solubility and Activity Coefficients of Suberic, Azelaic, and Sebacic Acids in NaCl aq , CH3 4NCl aq , and C2H5 4NI aq at Different Ionic Strengths and at t 25 C author Bretti, C. Crea, F. Foti, C. Sammartano, S. journal J. Chem. Eng. Data year 2006 volume 51 issue 5 pages 1660 1667 doi 10.1021 je060132t ref Solubility 2.46 g L ref name pka Suberic acid , also octanedioic acid , is a dicarboxylic acid , with formula C sub 6 sub H sub 12 sub COOH sub 2 sub . References reflist Category Dicarboxylic acids organic compound stub cs Kyselina suberov de Korks ure es cido sub rico lv Kor sk be nl Kurkzuur pl Kwas korkowy pt cido sub rico sv Korksyra ... more details
Infobox Bone Name Intertubercular groove Latin sulcus intertubercularis humeri GraySubject 51 GrayPage 209 Image Gray207.png Caption Left humerus . Anterior view. Intertubercular groove visible at top. Image2 Caption2 System MeshName MeshNumber DorlandsPre s 28 DorlandsSuf 12768832 The Greater tubercle of the humerus greater and Lesser tubercle of the humerus lesser tubercles of the humerus are separated from each other by a deep groove, the intertubercular groove bicipital groove , sulcus intertubercular , which lodges the long tendon of the Biceps brachii and transmits a branch of the anterior humeral circumflex artery to the shoulder joint . It runs obliquely downward, and ends near the junction of the upper with the middle third of the bone. It is the lateral wall of the axilla . ref name titleDissector Answers Axilla and Arm cite web url http anatomy.med.umich.edu limbs axilla ans.html 2o title Dissector Answers Axilla and Arm accessdate 2007 12 23 format work archiveurl http web.archive.org web 20071210033208 http anatomy.med.umich.edu limbs axilla ans.html 2o Bot retrieved archive archivedate 2007 12 10 ref See also radial groove medial bicipital groove References reflist External links SUNYAnatomyLabs 03 st 02 04 Gray s Bones of upper extremity musculoskeletal stub gl Canle bicipital umeral hu Sulcus intertubercularis humeri th ... more details
Chembox ImageFile Sophoricoside.svg ImageSize 200px IUPACName 4 5,7 Dihydroxy 4 oxo 4 H chromen 3 yl phenyl small D small glucopyranoside OtherNames Genistein glucoside 4 small D small glucopyranosyloxy 5,7 dihydroxyisoflavone 4 5,7 dihydroxy 4 oxo 4H chromen 3 yl phenylbeta small D small glucopyranoside 4 5,7 Dihydroxy 4 oxo 4H chromen 3 yl phenylalpha small L small gulopyranoside Section1 Chembox Identifiers CASNo 152 95 4 PubChem 5321398 ChemSpiderID 4479150 SMILES O C 1c4c O cc O cc4O C C 1c3ccc O C H 2O C H C H O C H O C H 2O CO cc3 InChI 1 C21H20O10 c22 7 15 18 26 19 27 20 28 21 31 15 30 11 3 1 9 2 4 11 12 8 29 14 6 10 23 5 13 24 16 14 17 12 25 h1 6,8,15,18 24,26 28H,7H2 t15 ,18 ,19 ,20 ,21 m1 s1 InChIKey ISQRJFLLIDGZEP CMWLGVBABN StdInChI 1S C21H20O10 c22 7 15 18 26 19 27 20 28 21 31 15 30 11 3 1 9 2 4 11 12 8 29 14 6 10 23 5 13 24 16 14 17 12 25 h1 6,8,15,18 24,26 28H,7H2 t15 ,18 ,19 ,20 ,21 m1 s1 StdInChIKey ISQRJFLLIDGZEP CMWLGVBASA N Section2 Chembox Properties C 21 H 20 O 10 Appearance Pale yellow solid Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Sophoricoside is an isoflavone glycoside found Sophora japonica L., an herb used in traditional Chinese medicine . Category Isoflavone glucosides zh ... more details
Infobox Anatomy Name Anterior axillary fold Latin GraySubject 289 GrayPage 1328 Image Gray1231.png Caption Front of right upper extremity. Anterior axillary fold not labeled, but visible at right. Image2 Gray411.png Caption2 Deep muscles of the chest and front of the arm, with the boundaries of the axilla. System MeshName MeshNumber DorlandsPre f 11 DorlandsSuf 12371050 The lower border of Pectoralis major forms the rounded anterior axillary fold . Some sources also include the pectoralis minor . ref NormanAnatomy lesson3axilla ref It can elongate after weight loss. ref cite pmid 17602378 ref See also underarm References reflist External links eMedicineDictionary anterior axillary fold http anatomy.med.umich.edu limbs axilla ans.html 2o Description at umich.edu muscle stub Superficial anatomy Category Muscular system ... more details
chembox UNII Ref fdacite correct FDA UNII VI1001O2DI verifiedrevid 437203063 ImageFile norclostebol.png ImageSize 200px IUPACName 8R,9S,10R,13S,14S,17S 4 chloro 17 hydroxy 13 methyl 2,6,7,8,9,10,11,12,14,15,16,17 dodecahydro 1H cyclopenta a phenanthren 3 one OtherNames 4 Chloro 17 hydroxyestr 4 en 3 one Section1 Chembox Identifiers CASNo 13583 21 6 PubChem 166576 SMILES C C 12CC C H 3 C H C H 1CC C H 2O CCC4 C C O CC C H 34 Cl Section2 Chembox Properties Formula C sub 18 sub H sub 25 sub ClO sub 2 sub MolarMass 308.84 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Norclostebol is an anabolic steroid . steroid stub Anabolic steroids Category Steroids Category Organochlorides ... more details
chembox verifiedrevid 448145852 Name Sebacic acid ImageFile Sebacic acid.png ImageSize 220px ImageName Sebacic acid ImageFile1 Sebacic acid 3D balls.png ImageSize1 240px IUPACName decanedioic acid OtherNames 1,8 octanedicarboxylic acid Section1 Chembox Identifiers CASNo Ref cascite correct CAS CASNo 111 20 6 SMILES OC O CCCCCCCCC O O Section2 Chembox Properties Formula C sub 10 sub H sub 18 sub O sub 4 sub MolarMass 202.25 g mol Density 1.209 g cm sup 3 sup 25 C MeltingPt 131 134.5 C BoilingPt 294.4 C at 100 mmHg pKa 4.720, 5.450 ref name pka cite journal title Solubility and Activity Coefficients of Acidic and Basic Nonelectrolytes in Aqueous Salt Solutions. 2. Solubility and Activity Coefficients of Suberic, Azelaic, and Sebacic Acids in NaCl aq , CH3 4NCl aq , and C2H5 4NI aq at Different Ionic Strengths and at t 25 C author Bretti, C. Crea, F. Foti, C. Sammartano, S. journal J. Chem. Eng. Data year 2006 volume 51 issue 5 pages 1660 1667 doi 10.1021 je060132t ref Solubility 0.25 g L ref name pka Sebacic acid is a dicarboxylic acid with structure carboxyl group HOOC CH sub 2 sub sub 8 sub COOH , and is naturally occurring. In its pure state it is a white flake or powdered crystal. The product is described as non hazardous, though in its powdered form it can be prone to flash ignition a typical risk in handling fine organic powders . Sebaceus is Latin for tallow candle, sebum tallow is Latin for tallow, and refers to its use in the manufacture of candles. Sebacic acid is a derivative of castor oil , with the vast majority of world production occurring in China which annually exports over 20,000 metric tonnes, representing over 90 of global trade of the product Fact date February 2007 . In the industrial setting, sebacic acid and its homologues such as azelaic acid can be used in plasticizers, lubricants, hydraulic fluids, cosmetics, candles, etc. Sebacic acid is also used as an intermediate for aromatics, antiseptics, and painting materials. References Reflist Exte ... more details
chembox verifiedrevid 443555075 ImageFile Cytidindiphosphat protoniert.svg ImageSize IUPACName OtherNames Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 5902 InChI 1 C9H15N3O11P2 c10 5 1 2 12 9 15 11 5 8 7 14 6 13 4 22 8 3 21 25 19,20 23 24 16,17 18 h1 2,4,6 8,13 14H,3H2, H,19,20 H2,10,11,15 H2,16,17,18 t4 ,6 ,7 ,8 m1 s1 InChIKey ZWIADYZPOWUWEW XVFCMESIBF ChEMBL Ref ebicite correct EBI ChEMBL 425252 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C9H15N3O11P2 c10 5 1 2 12 9 15 11 5 8 7 14 6 13 4 22 8 3 21 25 19,20 23 24 16,17 18 h1 2,4,6 8,13 14H,3H2, H,19,20 H2,10,11,15 H2,16,17,18 t4 ,6 ,7 ,8 m1 s1 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey ZWIADYZPOWUWEW XVFCMESISA N CASNo 63 38 7 CASNo Ref cascite correct CAS CASOther br 34393 59 4 disodium salt NOT CAS verified PubChem 290 ChEBI Ref ebicite correct EBI ChEBI 17239 SMILES O P O O OP O O OC C H 2O C H N 1C O N C N C C 1 C H O C H 2O Section2 Chembox Properties Formula C sub 9 sub H sub 15 sub N sub 3 sub O sub 11 sub P sub 2 sub MolarMass 403.176422 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Cytidine diphosphate , abbreviated CDP , is a nucleoside diphosphate . It is an ester of pyrophosphoric acid with the nucleoside cytidine . CDP consists of the pyrophosphate Functional group group , the pentose sugar ribose , and the nucleobase cytosine . See also Nucleoside Nucleotide DNA RNA Oligonucleotide External links Nucleobases, nucleosides, and nucleotides Category Nucleotides Category Pyrimidones biochem stub ca Difosfat de citidina da Cytidindifosfat de Cytidindiphosphat fr Cytidine diphosphate gl Citid n difosfato it Citosindifosfato nl Cytidinedifosfaat ja sr Citidin difosfat zh ... more details
Chembox Verifiedfields changed verifiedrevid 477225363 ImageFile 5 Methyluridin.svg ImageSize 150px IUPACName 1 2 R ,3 R ,4 S ,5 R 3,4 dihydroxy 5 hydroxymethyl oxolan 2 yl 5 methylpyrimidine 2,4 dione OtherNames Ribothymidine, Ribosylthymine Thymine riboside, m5u Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 1363755 InChI 1 C10H14N2O6 c1 4 2 12 10 17 11 8 4 16 9 7 15 6 14 5 3 13 18 9 h2,5 7,9,13 15H,3H2,1H3, H,11,16,17 t5 ,6 ,7 ,9 m0 s1 InChIKey DWRXFEITVBNRMK AZRUVXNYBS StdInChI Ref stdinchicite correct chemspider StdInChI 1S C10H14N2O6 c1 4 2 12 10 17 11 8 4 16 9 7 15 6 14 5 3 13 18 9 h2,5 7,9,13 15H,3H2,1H3, H,11,16,17 t5 ,6 ,7 ,9 m0 s1 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey DWRXFEITVBNRMK AZRUVXNYSA N CASNo Ref cascite changed ?? CASNo 1463 10 1 PubChem 445408 SMILES O C 1NC O N C C 1C C H 2O C H C H O C H 2O CO Section2 Chembox Properties Formula C sub 10 sub H sub 14 sub N sub 2 sub O sub 6 sub MolarMass 258.23 g mol Appearance Density MeltingPtC 185 BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition The chemical compound 5 methyluridine , also called ribothymidine , is a pyrimidine nucleoside . It is the ribonucleoside counterpart to the deoxyribonucleoside thymidine , which lacks a hydroxyl group at the 2 position. 5 Methyluridine contains a thymine base joined to a ribose pentose sugar . It exists in solid form as small white crystals or white crystalline Powder substance powder , has a molecular weight of 258.23 unified atomic mass unit u , and has a melting point of 185 C. The stability of 5 methyluridine under standard temperature and pressure STP is very high. References Unreferenced date December 2009 Nucleobases, nucleosides, and nucleotides Nucleic acids DEFAULTSORT Methyluridine, 5 Category Nucleosides Category Pyrimidinediones Category Ribosides bg 5 cs 5 Methyluridin de Ribothymidin fr Ribothymidine ja 5 ... more details
Unreferenced date December 2009 DISPLAYTITLE ortho Nitrophenyl galactoside Chembox Name ortho Nitrophenyl galactoside ImageFile ONPG structure.png ImageSize 200px IUPACName 2R,3R,4S,5R 2 Hydroxymethyl 6 2 nitrophenoxy oxane 3,4,5 triol OtherNames 2 Nitrophenylgalactoside Abbreviations ONPG Section1 Chembox Identifiers CASNo 19710 96 4 PubChem 123646 SMILES O N O C1 CC CC C1O C H 2O C H CO C H O C H O C H 2O MeSHName 2 nitrophenylgalactoside Section2 Chembox Properties Formula C sub 12 sub H sub 15 sub NO sub 8 sub MolarMass 301.249 Appearance Density MeltingPt BoilingPt Section3 Chembox Hazards Solubility MainHazards FlashPt Autoignition Lowercase ortho Nitrophenyl galactoside ortho Nitrophenyl galactoside ONPG is a Colorimeter chemistry colorimetric and spectrophotometry spectrophotometric substrate biochemistry substrate for detection of beta galactosidase activity. This compound is normally colorless. However if galactosidase is present, it Hydrolysis hydrolyzes the ONPG molecule into galactose and ortho nitrophenol . The latter compound has a yellow color that can be used to check for enzyme activity by means of a Colorimeter chemistry colorimetric assay at 420 nm wavelength . galactosidase is required for lactose utilization, so the intensity of the color produced can be used as a measure of the enzymatic rate. Though ONPG mimics lactose and is hydrolyzed by galactosidase, it is unable to act as an inducer for the lac operon. Without another lactose analog that can act as an inducer, such as IPTG , galactosidase will not be transcribed and ONPG will not be hydrolyzed. Glycosides DEFAULTSORT Ortho Nitrophenyl Galactoside Category Galactosides Nitrophenyl galactoside, ortho Category Nitrobenzenes Biochem stub de O Nitrophenyl D galactopyranosid fr Ortho nitroph nyl galactoside ... more details
chembox verifiedrevid 443371557 ImageFile Adenylosuccinate.svg ImageSize IUPACName OtherNames Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 389122 InChI 1 C14H18N5O11P c20 7 21 1 5 14 24 25 18 11 8 12 16 3 15 11 19 4 17 8 13 10 23 9 22 6 30 13 2 29 31 26,27 28 h3 6,9 10,13,22 23H,1 2H2, H,20,21 H,24,25 H,15,16,18 H2,26,27,28 t5?,6 ,9 ,10 ,13 m1 s1 InChIKey OFBHPPMPBOJXRT DPXQIYNJBG StdInChI Ref stdinchicite correct chemspider StdInChI 1S C14H18N5O11P c20 7 21 1 5 14 24 25 18 11 8 12 16 3 15 11 19 4 17 8 13 10 23 9 22 6 30 13 2 29 31 26,27 28 h3 6,9 10,13,22 23H,1 2H2, H,20,21 H,24,25 H,15,16,18 H2,26,27,28 t5?,6 ,9 ,10 ,13 m1 s1 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey OFBHPPMPBOJXRT DPXQIYNJSA N CASNo Ref cascite correct ?? CASNo 19240 42 7 PubChem 195 ChEBI Ref ebicite correct EBI ChEBI 15919 SMILES O C O CC C O O Nc3ncnc1c3ncn1 C H 2O C H C H O C H 2O COP O O O MeSHName Adenylosuccinate Section2 Chembox Properties Formula C sub 14 sub H sub 18 sub N sub 5 sub O sub 11 sub P MolarMass 463.294 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Adenylosuccinate is an intermediate in the interconversion of purine nucleotide s inosine monophosphate IMP and adenosine monophosphate AMP . The enzyme adenylosuccinate synthase carries out the reaction by the addition of aspartate to IMP and requires the input of energy from a phosphoanhydride bond in the form of guanosine triphosphate GTP . ref Figures 20.4 and 20.7 in Textbook of Biochemistry , with clinical correlations, Sixth Edition, Thomas M. Devlin, Ed., Wiley Liss, Inc., New York, NY, 2006 ref GTP is used instead of adenosine triphosphate ATP , so the reaction is not dependent on its products. See also Adenylosuccinate lyase deficiency Purine nucleotide cycle References reflist Nucleotide metabolism intermediates Category Nucleotides biochem stub fr Acide ad nylosuccinique ... more details
chembox ImageFile Coniferin structure.svg ImageSize 300px IUPACName small 2 R ,3 S ,4 S ,5 R ,6 S 2 Hydroxymethyl 6 4 E 3 hydroxyprop 1 enyl 2 methoxyphenoxy oxane 3,4,5 triol small OtherNames small D small Glucopyranoside 4 3 hydroxy 1 propenyl 2 methoxyphenyl br Coniferyl alcohol small D small glucoside Section1 Chembox Identifiers ChemSpiderID 4444067 InChI 1 C16H22O8 c1 22 11 7 9 3 2 6 17 4 5 10 11 23 16 15 21 14 20 13 19 12 8 18 24 16 h2 5,7,12 21H,6,8H2,1H3 b3 2 t12 ,13 ,14 ,15 ,16 m1 s1 InChIKey SFLMUHDGSQZDOW FAOXUISGBA CASNo 531 29 3 PubChem 5280372 SMILES O c1c OC cc C C CO cc1 C H 2O C H C H O C H O C H 2O CO Section2 Chembox Properties Formula C sub 16 sub H sub 22 sub O sub 8 sub MolarMass 342.35 g mol ExactMass 342.13147 u Appearance Density MeltingPtC 186 BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Coniferin is a glucoside of coniferyl alcohol . This white crystalline solid is a metabolite in conifer s, serving as an intermediate in cell wall lignification , as well as having other biological roles. Vanillin was first synthesized from coniferin by chemists Ferdinand Tiemann and Wilhelm Haarmann . References Unreferenced date February 2008 Reflist Monolignol Category Monolignol glucosides Natural phenol stub cs Koniferin de Coniferin sv Koniferin ... more details
chembox Verifiedfields changed verifiedrevid 477224023 ImageFile Aminoimidazole ribotide.svg ImageSize IUPACName 5 5 amino imidazole imidazol 1 yl 3,4 dihydroxy oxolane oxolan 2 yl methyl dihydrogen phosphate OtherNames AIR, br 5 5 amino 1 imidazolyl 3,4 dihydroxy 2 tetrahydrofuranyl methyl dihydrogen phosphate Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 141854 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C8H14N3O7P c9 5 1 10 3 11 5 8 7 13 6 12 4 18 8 2 17 19 14,15 16 h1,3 4,6 8,12 13H,2,9H2, H2,14,15,16 t4 ,6 ,7 ,8 m1 s1 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey PDACUKOKVHBVHJ XVFCMESISA N CASNo Ref cascite changed ?? CASNo 25635 88 5 ChEBI Ref ebicite changed EBI ChEBI 28843 KEGG Ref keggcite changed kegg KEGG C03373 PubChem 153 SMILES O P O O OC C H 2O C H n1cncc1N C H O C H 2O MeSHName aminoimidazole ribotide Section2 Chembox Properties Formula C sub 8 sub H sub 14 sub N sub 3 sub O sub 7 sub P MolarMass 295.186 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition 5 Phosphoribosyl 5 aminoimidazole or aminoimidazole ribotide is an intermediate in the formation of purine s. Thus, it is an intermediate in the adenine pathway , and is synthesized from 5 phosphoribosylformylglycinamidine by AIR synthetase . See also Phosphoribosylaminoimidazole carboxylase 5 carboxyamino imidazole ribonucleotide synthase 5 carboxyamino imidazole ribonucleotide mutase Nucleotide metabolism intermediates DEFAULTSORT Aminoimidazole ribotide, 5 Category Nucleotides biochemistry stub ... more details
chembox verifiedrevid 399329235 ImageFile 5 phosphoribosyl 4 carboxy 5 aminoimidazole.svg ImageSize IUPACName 5 Amino 1 2 R ,3 R ,4 S ,5 R 3,4 dihydroxy 5 phosphonooxymethyl oxolan 2 yl imidazole 4 carboxylic acid OtherNames Carboxyaminoimidazole ribotide, br Carboxyaminoimidazole ribonucleotide, br CAIR, br 5 amino 1 5 O phosphono small D small ribofuranosyl 1 H imidazole 4 carboxylic acid Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 144983 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 InChIKey XFVULMDJZXYMSG ZIYNGMLEBD SMILES1 O P O O OC C H 2O C H n1cnc C O O c1N C H O C H 2O StdInChI Ref stdinchicite correct chemspider StdInChI 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 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey XFVULMDJZXYMSG ZIYNGMLESA N CASNo 6001 14 5 PubChem 165388 ChEBI 28413 SMILES C1 NC C N1 C H 2 C H C H C H O2 COP O O O O O N C O O Section2 Chembox Properties Formula C sub 9 sub H sub 14 sub N sub 3 sub O sub 9 sub P MolarMass 339.196 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition 5 Phosphoribosyl 4 carboxy 5 aminoimidazole or CAIR is an Reaction intermediate intermediate in the formation of purine s. It is formed by phosphoribosylaminoimidazole carboxylase . Nucleotide metabolism intermediates DEFAULTSORT Phosphoribosyl 4 carboxy 5 aminoimidazole, 5 organic compound stub Category Nucleotides ... more details
orphan date December 2008 chembox verifiedrevid 399302161 ImageFile 2alpha Mannobiose.svg ImageSize IUPACName 2 R ,3 S ,4 S ,5 S ,6 R 2 hydroxymethyl 6 3 S ,4 S ,5 S ,6 R 2,4,5 trihydroxy 6 hydroxymethyl oxan 3 yl oxyoxane 3,4,5 triol OtherNames Reference ref http pubchem.ncbi.nlm.nih.gov summary summary.cgi?cid 11099946 2alpha Mannobiose Compound Summary , PubChem ref Section1 Chembox Identifiers ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 9275088 InChI 1 C12H22O11 c13 1 3 6 16 8 18 10 11 20 21 3 23 12 9 19 7 17 5 15 4 2 14 22 12 h3 20H,1 2H2 t3 ,4 ,5 ,6 ,7 ,8 ,9 ,10 ,11?,12 m1 s1 InChIKey HIWPGCMGAMJNRG VXSGSMIHBW SMILES1 C C1C C C C O1 O OC2C C C C O2 CO O O O O O O StdInChI Ref stdinchicite correct chemspider StdInChI 1S C12H22O11 c13 1 3 6 16 8 18 10 11 20 21 3 23 12 9 19 7 17 5 15 4 2 14 22 12 h3 20H,1 2H2 t3 ,4 ,5 ,6 ,7 ,8 ,9 ,10 ,11?,12 m1 s1 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey HIWPGCMGAMJNRG VXSGSMIHSA N CASNo 15548 39 7 PubChem 11099946 SMILES OC C H 1 C H O C H O C H O C H O C H C O O C H CO C H 2O C H 2O O1 Section2 Chembox Properties Formula C sub 12 sub H sub 22 sub O sub 11 sub MolarMass 342.30 g mol Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition 2 Mannobiose is a disaccharide . References reflist DEFAULTSORT Mannobiose, 2 Category Disaccharides organic compound stub biochem stub ... more details
chembox Verifiedfields changed verifiedrevid 457811880 Name Apiin Reference ImageFile Apiin.svg ImageSize 270px ImageName Apigenin IUPACName 7 2S,3R,4S,5S,6R 3 2S,3R,4R 3,4 dihydroxy 4 hydroxymethyl oxolan 2 yl oxy 4,5 dihydroxy 6 hydroxymethyl oxan 2 yl oxy 5 hydroxy 2 4 hydroxyphenyl chromen 4 one OtherNames Apioside Section1 Chembox Identifiers CASNo Ref cascite changed ?? CASNo 26544 34 3 ChEBI Ref ebicite correct EBI ChEBI 15932 PubChem 5280746 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 4444321 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey NTDLXWMIWOECHG YRCFQSNFSA N SMILES O C 4c5c O cc O C H 2O C H CO C H O C H O C H 2O C H 1OC C O CO C H 1O cc5O C c3ccc O cc3 C 4 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C26H28O14 c27 8 18 20 32 21 33 22 40 25 23 34 26 35,9 28 10 36 25 24 39 18 37 13 5 14 30 19 15 31 7 16 38 17 19 6 13 11 1 3 12 29 4 2 11 h1 7,18,20 25,27 30,32 35H,8 10H2 t18 ,20 ,21 ,22 ,23 ,24 ,25 ,26 m1 s1 Section2 Chembox Properties Formula C sub 26 sub H sub 28 sub O sub 14 sub MolarMass 564.49 g mol ExactMass 564.15 MeltingPt C Apiin is a chemical compound isolated from parsley ref http content.karger.com ProdukteDB produkte.asp?Aktion ShowPDF&ProduktNr 223977&Ausgabe 231622&ArtikelNr 90736&filename 90736.pdf Bioavailability of Apigenin from Apiin Rich Parsley in Humans br Hellen Meyera, Adrian Bolarinwaa, Guenther Wolframb, Jakob Linseisena, c ref and celery . The aglycone of apiin is apigenin . References Reflist External links flavone Category Flavone glycosides Natural phenol stub fr Apiine ... more details
chembox Verifiedfields changed verifiedrevid 477855186 Name Rhoifolin ImageFile Rhoifolin.svg ImageSize 250px ImageName Rhoifolin structure IUPACName 7 4,5 dihydroxy 6 hydroxymethyl 3 3,4,5 trihydroxy 6 methyloxan 2 yl oxyoxan 2 yl oxy 5 hydroxy 2 4 hydroxyphenyl chromen 4 one OtherNames Apigenin 7 O neohesperidoside Section1 Chembox Identifiers CASNo Ref cascite changed ?? CASNo 17306 46 6 PubChem 5282150 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 4445347 ChEMBL Ref ebicite correct EBI ChEMBL 395990 ChEBI Ref ebicite correct EBI ChEBI 31227 SMILES O C 4c5c O cc O C H 2O C H CO C H O C H O C H 2O C H 1O C H C H O C H O C H 1O C cc5O C c3ccc O cc3 C 4 StdInChI Ref stdinchicite correct chemspider StdInChI 1S C27H30O14 c1 10 20 32 22 34 24 36 26 37 10 41 25 23 35 21 33 18 9 28 40 27 25 38 13 6 14 30 19 15 31 8 16 39 17 19 7 13 11 2 4 12 29 5 3 11 h2 8,10,18,20 30,32 36H,9H2,1H3 t10 ,18 ,20 ,21 ,22 ,23 ,24 ,25 ,26 ,27 m0 s1 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey RPMNUQRUHXIGHK PYXJVEIZSA N Section2 Chembox Properties Formula C sub 27 sub H sub 30 sub O sub 14 sub MolarMass 578.52 g mol ExactMass 578.163556 u Density MeltingPt BoilingPt Rhoifolin is a chemical compound. It is a flavone , a type of flavonoid isolated from Boehmeria nivea , China grass or ramie leaf , from Citrus limon , Canton lemon leaf , from Citrus x aurantium , the bigarade or bitter orange plant , from Citrus x paradisi , the grapefruit leaf , from Ononis campestris , the cammock shoot and from Sabal serratula , the serenoa or sabal fruit plant ref http www.liberherbarum.com Minor UK IN2516.htm Rhoifolin on Liber Herbarum Minor ref . Glycosides References Reflist External links flavone Category Flavone glycosides Natural phenol stub fr Rhoifoline ... more details
Chembox ImageFile Robinobiose.svg ImageSize 200px IUPACName 6 O 6 deoxy small L small mannopyranosyl small D small galactopyranose OtherNames Robinobiose Section1 Chembox Identifiers CASNo 552 74 9 CASNo Ref cascite correct PubChem 441428 ChemSpiderID 390161 SMILES O C C H 1O C H O C H O C H O C H 1O C H 2O C H C H O C H O C H 2O C InChI 1 C12H22O10 c1 3 5 13 7 15 10 18 12 21 3 20 2 4 6 14 8 16 9 17 11 19 22 4 h3 19H,2H2,1H3 t3 ,4 ,5 ,6 ,7 ,8 ,9 ,10 ,11 ,12 m0 s1 InChIKey OVVGHDNPYGTYIT PEPLWKDOBI StdInChI 1S C12H22O10 c1 3 5 13 7 15 10 18 12 21 3 20 2 4 6 14 8 16 9 17 11 19 22 4 h3 19H,2H2,1H3 t3 ,4 ,5 ,6 ,7 ,8 ,9 ,10 ,11 ,12 m0 s1 StdInChIKey OVVGHDNPYGTYIT PEPLWKDOSA N Section2 Chembox Properties C 12 H 22 O 10 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Robinose is a disaccharide composed of 6 O rhamnose rhamno pyranosyl galactose galacto pyranoside. The sugar can be found in Acalypha hispida . ref cite journal doi 10.1016 S0031 9422 03 00494 1 title Anthocyanins acylated with gallic acid from chenille plant, Acalypha hispida year 2003 last1 Reiersen first1 Bergitte last2 Kiremire first2 Bernard T last3 Byamukama first3 Robert last4 Andersen first4 yvind M journal Phytochemistry volume 64 issue 4 pages 867 71 pmid 14559283 ref Robinin is a kaempferol 3 O robinoside 7 O rhamnoside. References reflist Category Disaccharides Category Deoxy sugars biochemistry stub fr Robinose ja ... more details
chembox verifiedrevid 423646115 Name Gastrodin ImageFile Gastrodin.svg ImageSize 250px ImageName Chemical structure of gastrodin ImageAlt Chemical structure of gastrodin IUPACName 2 R ,3 S ,4 S ,5 R ,6 S 2 hydroxymethyl 6 4 hydroxymethyl phenoxy oxane 3, 4,5 triol OtherNames br Gastrodine Section1 Chembox Identifiers CASNo 62499 27 8 CASNo Ref cascite correct ?? CASOther PubChem 115067 ChemSpiderID 102977 SMILES O c1ccc cc1 CO C H 2O C H C H O C H O C H 2O CO InChI 1 C13H18O7 c14 5 7 1 3 8 4 2 7 19 13 12 18 11 17 10 16 9 6 15 20 13 h1 4,9 18H,5 6H2 t9 ,10 ,11 ,12 ,13 m1 s1 InChIKey PUQSUZTXKPLAPR UJPOAAIJBX StdInChI 1S C13H18O7 c14 5 7 1 3 8 4 2 7 19 13 12 18 11 17 10 16 9 6 15 20 13 h1 4,9 18H,5 6H2 t9 ,10 ,11 ,12 ,13 m1 s1 StdInChIKey PUQSUZTXKPLAPR UJPOAAIJSA N MeSHName Section2 Chembox Properties Formula C sub 13 sub H sub 18 sub O sub 7 sub MolarMass 286.27 g mol ExactMass 286.105253 u Appearance Density MeltingPt C BoilingPt C Solubility Gastrodin is a natural phenol. It is the glucoside of 4 hydroxybenzyl alcohol gastrodigenin . It can be isolated from Gastrodia elata . It can be produced by biotransformation of 4 hydroxybenzaldehyde by Datura tatula cell cultures. ref Production of Gastrodin Through Biotransformation of p hydroxybenzaldehyde Using Cell Suspension Cultures of Datura tatula L. Jia Shun Gong, Wei Peng Ma, Jun Xue Pu, Shu Guan Xu, Shuang Qing Zheng and Chun Jie Xiao, Chinese Journal of Biotechnology, Volume 22, Issue 5, September 2006, Pages 800 805, doi 10.1016 S1872 2075 06 60056 3 ref References Reflist commons Category Natural phenol glucosides Natural phenol stub ... more details
Chembox ImageFile syringin.svg ImageSize 200px IUPACName 4 1 E 3 Hydroxyprop 1 en 1 yl 2,6 dimethoxyphenyl small D small glucopyranoside OtherNames Eleutheroside B Ilexanthin A Ligustrin Lilacin Magnolenin Methoxyconiferine Sinapyl alcohol 4 O glucoside Siringin Syringoside Section1 Chembox Identifiers CASNo 118 34 3 CASNo Ref cascite correct CAS PubChem 5316860 ChemSpiderID 4475831 SMILES O c1c OC cc C C CO cc1OC C H 2O C H C H O C H O C H 2O CO InChI 1 C17H24O9 c1 23 10 6 9 4 3 5 18 7 11 24 2 16 10 26 17 15 22 14 21 13 20 12 8 19 25 17 h3 4,6 7,12 15,17 22H,5,8H2,1 2H3 b4 3 t12 ,13 ,14 ,15 ,17 m1 s1 InChIKey QJVXKWHHAMZTBY GCPOEHJPBY StdInChI 1S C17H24O9 c1 23 10 6 9 4 3 5 18 7 11 24 2 16 10 26 17 15 22 14 21 13 20 12 8 19 25 17 h3 4,6 7,12 15,17 22H,5,8H2,1 2H3 b4 3 t12 ,13 ,14 ,15 ,17 m1 s1 StdInChIKey QJVXKWHHAMZTBY GCPOEHJPSA N Section2 Chembox Properties C 17 H 24 O 9 Appearance White crystalline solid Density MeltingPtC 192 Melting notes ref name Merck Merck Index , 11th Edition, 8997 ref BoilingPt Solubility Slightly soluble ref name Merck Section3 Chembox Hazards MainHazards FlashPt Autoignition Syringin is a natural chemical compound first isolated from the bark of lilac Syringa vulgaris by Meillet in 1841. ref name Merck It has since been found to be distributed widely throughout many types of plants. Chemically, it is the glucoside of sinapyl alcohol . References reflist Category Phenylpropanoid glucosides Natural phenol stub ... more details
Chembox Verifiedfields changed verifiedrevid 477346139 ImageFile 7 Methylguanosine.svg ImageSize 180px IUPACName 7 Methylguanosine OtherNames N7 Methylguanosine 2 Amino 1,6 dihydro 7 methyl 6 oxo 9 small D small ribofuranosylpurinium Section1 Chembox Identifiers Abbreviations m7G m sup 7 sup G CASNo 20244 86 4 CASNo Ref cascite changed ?? ChEBI Ref ebicite correct EBI ChEBI 20794 PubChem 445404 ChemSpiderID Ref chemspidercite correct chemspider ChemSpiderID 393054 SMILES O C3 N C N Nc1c3n c n 1 C H 2O C H C H O C H 2O CO C InChI 1 C11H15N5O5 c1 15 3 16 8 5 15 9 20 14 11 12 13 8 10 7 19 6 18 4 2 17 21 10 h3 4,6 7,10,17 19H,2H2,1H3, H2 ,12,13,14,20 p 1 t4 ,6 ,7 ,10 m1 s1 InChIKey OGHAROSJZRTIOK UJMNIJGGBX StdInChI Ref stdinchicite correct chemspider StdInChI 1S C11H15N5O5 c1 15 3 16 8 5 15 9 20 14 11 12 13 8 10 7 19 6 18 4 2 17 21 10 h3 4,6 7,10,17 19H,2H2,1H3, H2 ,12,13,14,20 p 1 t4 ,6 ,7 ,10 m1 s1 StdInChIKey Ref stdinchicite correct chemspider StdInChIKey OGHAROSJZRTIOK KQYNXXCUSA O Section2 Chembox Properties C 11 H 16 N 5 O 5 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition 7 Methylguanosine is a modified purine nucleobase . It is a methylation methylated version of guanosine and when found in human urine, it may be a biomarker of some types of cancer. ref cite journal pmid 1739950 year 1992 last1 Reynaud first1 C last2 Bruno first2 C last3 Boullanger first3 P last4 Grange first4 J last5 Barbesti first5 S last6 Niveleau first6 A title Monitoring of urinary excretion of modified nucleosides in cancer patients using a set of six monoclonal antibodies volume 61 issue 3 pages 255 62 journal Cancer letters ref References reflist External links http www.hmdb.ca metabolites HMDB01107 Metabocard for 7 Methylguanosine HMDB01107 , Human Metabolome Database, University of Alberta DEFAULTSORT Methylguanosine, 7 Category Nucleosides Category Purines organic compound stub ... more details
context date February 2008 Caravantius, an Illyrians Illyrian , was half brother ref The Illyrians by J. J. Wilkes, 1992, ISBN 0 631 19807 5, From Index, Caravantius, half brother of Gentius ref to Gentius ref The Illyrians by J. J. Wilkes, 1992, ISBN 0 631 19807 5, page 173, ... After detaching 1000 infantry and 50 horsemen under his half brother Caravantius to deal with the Cavi, otherwise unknown, Gentius advanced south for five miles and proceeded to attack 2O Livy 43. ... ref . He fought ref The Illyrians by J. J. Wilkes, 1992, ISBN 0 631 19807 5, page 174, ... Illyrian navy sent to attack supply routes, and the story resumes with Gentius trapped in Scodra and hoping for relief from Caravantius. ... ref with his brother against the Cavi . References reflist Sources The Illyrians by J. J. Wilkes, 1992 ISBN 0 631 19807 5 External links commons Illyria & Illyrians Category Illyrian people euro royal stub ca Caravanti it Caravanzio la Caravantius ... more details
chembox UNII Ref fdacite correct FDA UNII 7IVE3SDZ38 verifiedrevid 437160221 ImageFile Epimestrol.png ImageSize 200px IUPACName 8 R ,9 S ,13 S ,14 S ,16 R ,17 S 3 methoxy 13 methyl 6,7,8,9,11,12,14,15,16,17 decahydrocyclopenta a phenanthrene 16,17 diol IUPACName hidden yes OtherNames Stimovul 3 Methoxyestriol 3 Methoxy 17 epiestriol Section1 Chembox Identifiers CASNo 7004 98 0 PubChem 244809 KEGG Ref keggcite correct kegg KEGG D04021 SMILES C C 12CC C H 3 C H C H 1C C H C H 2O O CCC4 C3C CC C4 OC Section2 Chembox Properties Formula C sub 19 sub H sub 26 sub O sub 3 sub MolarMass 302.40794 Appearance Density MeltingPt BoilingPt Solubility Section3 Chembox Hazards MainHazards FlashPt Autoignition Epimestrol is an ovulation stimulant. steroid stub Category Steroids ... more details
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