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环(甘氨酰-L-组氨酰) | 15266-88-3

环(甘氨酰-L-组氨酰)结构式图片|15266-88-3结构式图片
环(甘氨酰-L-组氨酰)
Cyclo(-Gly-L-His)
15266-88-3
C8H10N4O2
194.1906
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:环(甘氨酰-L-组氨酰)结构式
7408484
名称和标识符
MDL MFCD00237614
InChIKey FYFJTCMGWLBLPG-LURJTMIESA-N
Inchi InChI=1S/C8H10N4O2/c13-7-3-10-8(14)6(12-7)1-5-2-9-4-11-5/h2,4,6H,1,3H2,(H,9,11)(H,10,14)(H,12,13)/t6-/m0/s1
SMILES O=C1N[C@H](C(NC1)=O)CC2=CN=CN2
别名信息
- 中文别名 -
  • 环(甘氨酰-L-组氨酰)
- 英文别名 -
  • 2,5-Piperazinedione,3-(1H-imidazol-5-ylmethyl)-, (3S)-
  • CYCLO(-GLY-HIS)
  • Cyclo(-Gly-L-His)
  • (S)-3-(1H-Imidazol-4-ylmethyl)-2,5-piperazinedione
  • cyclo-(glycyl-L-histidyl)
  • CYCLO(GLY-L-HIS)
  • cyclo-Gly-His
  • Cyclo(glycyl-L-histidyl)
  • SCHEMBL10515887
  • HY-P5033
  • CS-0675750
  • Cyclo(Gly-His)
  • (3S)-3-(1H-imidazol-5-ylmethyl)piperazine-2,5-dione
  • 15266-88-3
  • MFCD00237614
  • (S)-3-((1H-Imidazol-5-yl)methyl)piperazine-2,5-dione
  • AKOS006275241
  • (3S)-3-[(1H-imidazol-5-yl)methyl]piperazine-2,5-dione
  • Cyclo(-Gly-His)
  • cyclo(glycyl-l-histidyl)
物化性质
实验特性
LogP -0.77560
PSA 86.88000
沸点 758.7±50.0 °C at 760 mmHg
熔点 Not available
蒸气压 0.0±2.6 mmHg at 25°C
闪点 412.6±30.1 °C
密度 1.4±0.1 g/cm3
计算特性
精确分子量 194.08000
氢键供体数量 3
氢键受体数量 6
可旋转化学键数量 2
同位素质量 194.08
重原子数量 14
复杂度 256
同位素原子数量 0
确定原子立构中心数量 1
不确定原子立构中心数量 0
确定化学键立构中心数量 0
不确定化学键立构中心数量 0
共价键单元数量 1
疏水参数计算参考值(XlogP) -1.1
拓扑分子极性表面积 86.9A^2
海关数据
海关编码 2933990090
海关数据

中国海关编码:

2933990090

概述:

2933990090. 其他仅含氮杂原子的杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

申报要素:

品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期

Summary:

2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

相关文献
  • 1. Co-ordinating properties of cyclopeptides. Thermodynamic and spectroscopic study on the formation of copper(II) complexes with cyclo(Gly-His)4 and cyclo(Gly-His-Gly)2 and their superoxide dismutase-like activity
    Raffaele P. Bonomo,Giuseppe Impellizzeri,Giuseppe Pappalardo,Roberto Purrello,Enrico Rizzarelli,Giovanni Tabbì J. Chem. Soc. Dalton Trans. 1998 3851
  • 2. Co-ordination properties of cyclopeptides. Formation and stability of zinc(II) and copper(II) complexes of histidine-containing cyclopeptides, or imidazole
    Giuseppe Arena,Giuseppe Impellizzeri,Giuseppe Maccarrone,Giuseppe Pappalardo,Enrico Rizzarelli J. Chem. Soc. Dalton Trans. 1994 1227
  • 3. Co-ordination properties of cyclopeptides. Formation and stability of zinc(II) and copper(II) complexes of histidine-containing cyclopeptides, or imidazole
    Giuseppe Arena,Giuseppe Impellizzeri,Giuseppe Maccarrone,Giuseppe Pappalardo,Enrico Rizzarelli J. Chem. Soc. Dalton Trans. 1994 1227
  • 4. Organic chemistry
    L. Crombie,V. Gold,B. Capon,C. W. Rees,E. F. Caldin,D. J. Millen,R. F. M. White,C. J. Timmons,E. S. Waight,R. H. Thomson,R. McCrindle,K. H. Overton,R. M. Acheson,K. W. Bentley,J. S. Whitehurst,D. J. Manners,R. C. Sheppard Annu. Rep. Prog. Chem. 1963 60 245
  • 5. Organic chemistry
    L. Crombie,V. Gold,B. Capon,C. W. Rees,E. F. Caldin,D. J. Millen,R. F. M. White,C. J. Timmons,E. S. Waight,R. H. Thomson,R. McCrindle,K. H. Overton,R. M. Acheson,K. W. Bentley,J. S. Whitehurst,D. J. Manners,R. C. Sheppard Annu. Rep. Prog. Chem. 1963 60 245
  • 6. Contents pages
    J. Chem. Soc. Dalton Trans. 1994 P049
专业数据库参考
PubChemId 7408484
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