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经验公式(希尔记法):
C22H31N3O5 · C4H4O4
化学文摘社编号:
分子量:
533.57
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352125
MDL number:
InChI key
XSTJTOKYCAJVMJ-GVTSEVKNSA-N
SMILES string
O=C(O)/C=C\C(O)=O.O=C(N1CCN(CC(N2CCCC2)=O)CC1)/C=C/C3=CC(OC)=C(OC)C(OC)=C3
InChI
1S/C22H31N3O5.C4H4O4/c1-28-18-14-17(15-19(29-2)22(18)30-3)6-7-20(26)25-12-10-23(11-13-25)16-21(27)24-8-4-5-9-24;5-3(6)1-2-4(7)8/h6-7,14-15H,4-5,8-13,16H2,1-3H3;1-2H,(H,5,6)(H,7,8)/b7-6+;2-1-
assay
≥98% (HPLC)
form
powder
storage condition
desiccated
color
white to beige
solubility
H2O: 20 mg/mL, clear
storage temp.
2-8°C
Quality Level
General description
Cinepazide maleate can be synthesized from ethyl chlorocarbonate activation and (E) 3,4,5-trimethoxycinnamylic acid.
Biochem/physiol Actions
Cinepazide maleate is a vasodilator used clinically in China used for the treatment of cardiovascular and cerebrovascular diseases, and peripheral vascular diseases.
Cinepazide maleate is a vasodilator used clinically in China used in China for the treatment of cardiovascular and cerebrovascular diseases, and peripheral vascular diseases. Cinepazide maleate is thought to act as a potentiator of adenosine A2 receptors and has also been characterized as a calcium channel blocker. It was withdrawn for agranulocytosis in several countries.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
An Improved Synthesis of Cinepazide Maleate.
LIU, Hua-xiang, et al.
Fine Chemicals / ????, 10, 012-012 (2009)
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