Vincamine (41S,12S,13aS)-13a-乙基-12-羟基-2,3,41,5,6,12,13,13a-八氢-1H-吲哚并[3,2,1-de]吡啶并[3,2,1-ij][1,5]萘啶-12-羧酸甲酯

CAS 1617-90-9 MFCD00078054

化学结构图

1617-90-9
SMILES: CC[C@]12CCCN3CCc4c(n(c5ccccc45)[C@@](O)(C(=O)OC)C1)[C@@H]32

化学属性

Mol. FormulaC21 H26 N2 O3
Mol. Weight354.44
Melting Point232
TSCANo
Density1.36

别名和识别编码

Chemical NameVincamine
MDL NumberMFCD00078054
CAS Number1617-90-9
EC Number216-576-3
PubChem Substance ID87577853
Synonym (3aS,5S,11S)-3a-Ethyl-5-hydroxy-1,2,3,3a,4,5,10,11b-octahydro-11H-5a,11a-diaza-benzo[cd]fluoranthene-5-carboxylic acid methyl ester 14,15-Dihydro-14-hydroxyeburnamenine-14-carboxylic acid methyl ester Anasclerol Angiopac Arteriovinca Decincan Devincan Devinkan Eburnamenine-14-carboxylic acid, 14,15-dihydro-14-hydroxy-, methyl ester, Vincamine {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {SNA} 长春胺
Merck Number9983
Beilstein Registry Number25(3/4)1252
Chemical Name Translation(41S,12S,13aS)-13a-乙基-12-羟基-2,3,41,5,6,12,13,13a-八氢-1H-吲哚并[3,2,1-de]吡啶并[3,2,1-ij][1,5]萘啶-12-羧酸甲酯
Wiswesser Line NotationT D6 B5666 2AB S CN MN&&TTTJ Q2 SVO1 SQ
信息真实价格透明    资金保障    专业采购外包团队在线服务   
信息真实价格透明    资金保障    专业采购外包团队在线服务   
品牌质保精细包装    现货库存    一流品牌服务   

分类

  • {SNA} Alkaloid, Asymmetric Synthesis, Chemical Synthesis, Chiral Building Blocks, Complex Molecules, Nutrition Research, Phytochemicals by Chemical Classification
  • {SNA} Alkaloid, Asymmetric Synthesis, Cell Biology, Chemical Synthesis, Chiral Building Blocks, Complex Molecules, Nutrition Research, Phytochemicals by Chemical Classification

相关文献及参考

  • [2]. Li Wu, et al. Vincamine prevents lipopolysaccharide induced inflammation and oxidative stress via thioredoxin reductase activation in human corneal epithelial cells. Am J Transl Res. 2018 Jul 15;10(7):2195-2204. eCollection
  • Merck: 14,9983
  • Merck: 14,9983 Beilstein:25(3/4)1252
  • [1]. Te Du, et al. Vincamine as a GPR40 agonist improves glucose homeostasis in type 2 diabetic mice. J Endocrinol. 2019 Feb 1;240(2):195-214.
  • [1]. Te Du, et al. Vincamine as a GPR40 agonist improves glucose homeostasis in type 2 diabetic mice. J Endocrinol. 2019 Feb 1;240(2):195-214.
  • [2]. Li Wu, et al. Vincamine prevents lipopolysaccharide induced inflammation and oxidative stress via thioredoxin reductase activation in human corneal epithelial cells. Am J Transl Res. 2018 Jul 15;10(7):2195-2204. eCollection

安全信息

WGK Germany3
RTECSYY8575000
GHS Symbol
Hazard statements
  • H302 Harmful if swallowed 吞食有害
Signal word
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes Xn
Safety Statements
  • S36 Wear suitable protective clothing 穿戴适当的防护服;
Risk Statements
Precautionary statements
  • P264 Wash hands thoroughly after handling. 处理后要彻底洗净双手。
  • P501 Dispose of contents/container to..… 处理内容物/容器.....
  • P262 Do not get in eyes, on skin, or on clothing. 不要接触眼睛,皮肤或衣服。
  • P301+P312+P330
  • P270 Do not eat, drink or smoke when using this product. 使用本产品时不要吃东西,喝水或吸烟。
TYPE OF TEST            : LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE       : Oral
SPECIES OBSERVED

TYPE OF TEST            : LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE       : Intraperitoneal
SPECIES OBSERVED        : Rodent - mouse
DOSE/DURATION           : 195 mg/kg
TOXIC EFFECTS :
   Details of toxic effects not reported other than lethal dose value
REFERENCE :
   EPXXDW European Patent Application. (U.S. Patent and Trademark Office,
   Foreign Patents, Washington, DC 20231)  Volume(issue)/page/year: #0052238

TYPE OF TEST            : LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE       : Intravenous
SPECIES OBSERVED        : Rodent - rabbit
DOSE/DURATION           : 33 mg/kg
TOXIC EFFECTS :
   Details of toxic effects not reported other than lethal dose value
REFERENCE :
   AEPPAE Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und
   Pharmakologie.  (Berlin, Ger.) V.110-253, 1925-66.  For publisher
   information, see NSAPCC.  Volume(issue)/page/year: 236,296,1959

TYPE OF TEST            : LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE       : Intravenous
SPECIES OBSERVED        : Rodent - mouse
DOSE/DURATION           : 47740 ug/kg
TOXIC EFFECTS :
   Details of toxic effects not reported other than lethal dose value
REFERENCE :
   AGSOA6 Agressologie.  Revue Internationale de Physio-Biologie et de
   Pharmacologie Appliquees aux Effets de l'Agression.  (SPPIF, B.P.22, F-41353
   Vineuil, France)  V.1-    1960-  Volume(issue)/page/year: 19,211,1978

TYPE OF TEST            : LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE       : Intraperitoneal
SPECIES OBSERVED        : Rodent - rat
DOSE/DURATION           : 253 mg/kg
TOXIC EFFECTS :
   Details of toxic effects not reported other than lethal dose value
REFERENCE :
   ARZNAD Arzneimittel-Forschung. Drug Research.  (Editio Cantor Verlag,
   Postfach 1255, W

Storage condition -20°C

系列性分类


相关产品推荐