Vindoline 文多灵

CAS 2182-14-1 MFCD01744432

化学结构图

2182-14-1
SMILES: CCC12C=CCN3CCC4(c5ccc(OC)cc5N(C)C4C(O)(C(=O)OC)C1OC(C)=O)C32

化学属性

Mol. FormulaC25 H32 N2 O6
Mol. Weight456.53
Density1.33
Melting Point162-1640C
Boiling Point
Flash Point-

别名和识别编码

Chemical NameVindoline
CAS Number2182-14-1
Synonym (-)-Vindoline (2?,3?,4?,5?,12?,19?)-4-(Acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-aspidospermidine-3-carboxylic Acid Methyl Ester (2beta,3beta,4beta,5alpha,12beta,19alpha)-4-(Acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-aspidospermidine-3-carboxylic acid methyl ester Methyl (2β,3β,4β,5α,12R,19α)-4-(Acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methylaspidospermidine-3-carboxylate NSC 91994 Vindolin Vindoline {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} { {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {} {
MDL Number-
EC Number218-558-0
Chemical Name Translation文多灵
Wiswesser Line NotationT C6 B5665 2AB S BX IN QN NU JH&&TTTJ FO1 I1 KVO1 KQLOV1 M2
PubChem Substance ID260535
InChIInChI=1S/C25H32N2O6/c1-6-23-10-7-12-27-13-11-24(19(23)27)17-9-8-16(31-4)14-18(17)26(3)20(24)25(30,22(29)32-5)21(23)33-15(2)28/h7-10,14,19-21,30H,6,11-13H2,1-5H3/t19-,20+,21+,23+,24+,25-/m0/s1
LabNetwork Molecule IDLN01326585
Canonical SMILES-
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分类

  • {SNA} Metabolic Pathways, Terpenoid Metabolism, Terpenoids, 代谢组学, 细胞生物学
  • {SNA} Cell Biology, Metabolic Pathways, Metabolomics, Terpenoid Metabolism, Terpenoids
  • {SNA} Terpenoids, 代谢组学, 代谢通路, 细胞生物学, 萜类代谢
  • Chiral Reagents
  • Pharmaceuticals
  • Intermediates & Fine Chemicals,

产品应用

  • A novel antitumor agent.

相关文献及参考

  • Altstadt, T., et al.: J. Med. Chem., 44, 4577 (2001),
  • Baloglu, E., et al.: Bioorg. Med. Chem., 11, 1557 (2003),
  • Distefano, M., et al.: Int. J. Cancer, 72, 844 (1997),
  • Merck: 14,9988
  • [1]. Prakash V, et al. Mechanism of interaction of vinca alkaloids with tubulin: catharanthine and vindoline. Biochemistry. 1991 Jan 22;30(3):873-80.

安全信息

Storage condition -20 -20°C -20℃ 2-8°C 2-8°C, protect from light 储存温度 2-8°C
GHS Symbol
WGK Germany3
Precautionary statements
  • P201 Obtain special instructions before use. 使用前获取专门指示。
  • P202 Do not handle until all safety precautions have been read and understood. 已阅读并理解所有的安全预防措施之前,切勿操作。
  • P203
  • P262 Do not get in eyes, on skin, or on clothing. 不要接触眼睛,皮肤或衣服。
  • P280 Wear protective gloves/protective clothing/eye protection/face protection. 戴防护手套/防护服/眼睛的保护物/面部保护物。
  • P281 Use personal protective equipment as required. 使用所需的个人防护装备。
  • P308+P313
  • P318
  • P405 Store locked up. 上锁保管。
  • P501 Dispose of contents/container to..… 处理内容物/容器.....
Hazard statements
  • H341 Suspected of causing genetic defects 怀疑导致遗传性缺陷
RTECSCJ0120000
Signal word Warning
Safety Statements
  • S24/25 Avoid contact with skin and eyes 避免皮肤和眼睛接触;
  • S36/37 Wear suitable protective clothing and gloves 穿戴适当的防护服和手套;
Hazard Codes Xn
Risk Statements
  • R68 Possible risk of irreversible effects 可能有不可挽回的作用的危险
TYPE OF TEST            : LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE       : Intraperitoneal
SPECIES OBSERVED        : Rodent - mouse
DOSE/DURATION           : 400 mg/kg
TOXIC EFFECTS :
   Behavioral - somnolence (general depressed activity)
   Behavioral - excitement
REFERENCE :
   33GVAL "Catharanthus Alkaloids," Taylor, W.I., and N.R. Farnsworth, eds.,
   New York, Marcel Dekker, 1975  Volume(issue)/page/year: -,73,1975

系列性分类


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