lithium(1+) ion {[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-2-{[({[(3R)-3-[(2-{[2-(dodecanoylsulfanyl)ethyl]carbamoyl}ethyl)carbamoyl]-3-hydroxy-2,2-dimethylpropyl phosphonato]oxy}(hydroxy)phosphoryl)oxy]methyl}-4-hydroxyoxolan-3-yl]oxy}phosphonic acid

• ChemBase编号: 155208
• 分子式: C33H57LiN7O17P3S
• 平均质量: 955.769663
• 单一同位素质量: 955.29045384
• SMILES: [Li+].CCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@@H](C(C)(C)COP(=O)([O-])OP(=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)n1cnc2c1ncnc2N)O)OP(=O)(O)O)O
• Canonical SMILES: CCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@@H](C(COP(=O)(OP(=O)(OC[C@H]1O[C@H]([C@@H]([C@@H]1OP(=O)(O)O)O)n1cnc2c1ncnc2N)O)[O-])(C)C)O.[Li+]
• InChI: InChI=1S/C33H58N7O17P3S.Li/c1-4-5-6-7-8-9-10-11-12-13-24(42)61-17-16-35-23(41)14-15-36-31(45)28(44)33(2,3)19-54-60(51,52)57-59(49,50)53-18-22-27(56-58(46,47)48)26(43)32(55-22)40-21-39-25-29(34)37-20-38-30(25)40;/h20-22,26-28,32,43-44H,4-19H2,1-3H3,(H,35,41)(H,36,45)(H,49,50)(H,51,52)(H2,34,37,38)(H2,46,47,48);/q;+1/p-1/t22-,26-,27-,28+,32-;/m1./s1
• InChIKey: FWNUZMNRIPYTPZ-CDSRRKEDSA-M

名称和登记号

名称

• IUPAC标准名: lithium(1+) ion {[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-2-{[({[(3R)-3-[(2-{[2-(dodecanoylsulfanyl)ethyl]carbamoyl}ethyl)carbamoyl]-3-hydroxy-2,2-dimethylpropyl phosphonato]oxy}(hydroxy)phosphoryl)oxy]methyl}-4-hydroxyoxolan-3-yl]oxy}phosphonic acid
• IUPAC传统名: lithium(1+) ion [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-2-[({[(3R)-3-[(2-{[2-(dodecanoylsulfanyl)ethyl]carbamoyl}ethyl)carbamoyl]-3-hydroxy-2,2-dimethylpropyl phosphonato]oxy(hydroxy)phosphoryl}oxy)methyl]-4-hydroxyoxolan-3-yl]oxyphosphonic acid
• 别名: C12-CoA; Dodecanoyl-Coenzyme A lithium salt; Lauroyl coenzyme A lithium salt

登记号

• CAS号: 190063-12-8
• MDL号: MFCD01310860
• PubChem SID: 162249346; 24896322
• PubChem CID: 23702138

理论计算性质

• Acid pKa: 0.8207477
• 质子受体: 17
• 质子供体: 8
• LogD (pH = 5.5): -5.825725
• LogD (pH = 7.4): -7.4420323
• Log P: -1.2230906
• 摩尔折射率: 217.1222 cm^3
• 极化性: 86.69031 Å^3
• 极化表面积: 366.46 Å^2
• 可自由旋转的化学键: 30
• 里宾斯基五规则: false

分子性质

安全信息

• 德国WGK号: 3
• 个人保护装置: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• 保存温度: -20°C

产品相关信息

• 纯度: ≥90% (HPLC)
• 线性分子式: C33H58N7O17P3S

详细说明

Sigma Aldrich - L2659

Biochem/physiol Actions
Coenzyme A functions as an acyl group carrier, acetyl-CoA. Dodecanoyl-Coenzyme A (C12-CoA), a long-chain (C-12) saturated fatty acyl-CoA, is used as an intermediate in lipid metabolism and is involved in lipid biosynthesis and fatty acid transport.. Lauroyl CoA is a substrate for FAM34A proteins and a product of firefly luciferase.
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. L2659.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.