Details
Stereochemistry | ACHIRAL |
Molecular Formula | C22H31N3O5 |
Molecular Weight | 417.4986 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(=CC(OC)=C1OC)\C=C\C(=O)N2CCN(CC(=O)N3CCCC3)CC2
InChI
InChIKey=RCUDFXMNPQNBDU-VOTSOKGWSA-N
InChI=1S/C22H31N3O5/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/h6-7,14-15H,4-5,8-13,16H2,1-3H3/b7-6+
DescriptionCurator's Comment: description was created based on several sources, including
http://www.cphi-online.com/cinepazide-maleate-prod079010.html
http://www.technology-x.net/CN54/201210324341.html
Curator's Comment: description was created based on several sources, including
http://www.cphi-online.com/cinepazide-maleate-prod079010.html
http://www.technology-x.net/CN54/201210324341.html
Cinepazide or cinepazide maleate (Kelinao or Anjieli in China) is a vasodilator used in China for the treatment of cardiovascular and cerebrovascular diseases, and peripheral vascular diseases. As a calcium channel blocker, cinepazide can stop calcium from entering vascular smooth muscle cells and relax smooth muscles of cerebral vessels, coronary arteries and peripheral vessels so as to relieve vasospasm, reduce vascular resistance, improve flexibility of red blood cells, increase blood circulation in cerebral vessels and improve microcirculation and brain metabolism. Cinepazide could also increase the number of cAMP by inhibiting cAMP phosphodiesterase and reduce oxygen consumption. In April 2002, cinepazide of Beijing Hwellso Pharmaceutical Co., Ltd was approved to enter the market with two dosage forms of oral formulation and injection under the trade name of Kelinao. Currently, Kelinao is the only domestic brand for the treatment of cardiovascular diseases. And in 2009, cinepazide was included in the national medicare drug list. Cinepazide maleate, after wide application, has gained the recognition of Chinese doctors and patients for the treatment of cerebral arteriosclerosis, transient ischemic attack, cerebral thrombosis, cerebral embolism, cerebral hemorrhage sequel and post-traumatic brain syndrome. Besides, due to its efficacy in cardiovascular diseases and peripheral vascular diseases, cinepazide maleate has become a leading product in cerebrovascular drug market.
Originator
Sources: http://pg.jrj.com.cn/acc/Res%5CHK_RES%5CSTOCK%5C2011%5C9%5C28%5C5025ec90-2ed1-473d-bc50-4bc5affe1d83.pdf
Curator's Comment: 1969
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2363032 Sources: https://www.ncbi.nlm.nih.gov/pubmed/27990002 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/6322212
cinepazide in concentrations ranging from 10(-6) to 10(-5) M selectively potentiates the relaxing response mediated through purinergic P1-receptors.
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
WHO-ATC |
C04AX27
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
||
|
WHO-VATC |
QC04AX27
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
||
|
NCI_THESAURUS |
C29707
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
23887-46-9
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
PRIMARY | |||
|
100000081063
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
PRIMARY | |||
|
SUB06293MIG
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
PRIMARY | |||
|
DB12123
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
PRIMARY | |||
|
m1071
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
PRIMARY | Merck Index | ||
|
245-928-9
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
PRIMARY | |||
|
C91001
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
PRIMARY | |||
|
CHEMBL1874750
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
PRIMARY | |||
|
CINEPAZIDE
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
PRIMARY | |||
|
C026896
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
PRIMARY | |||
|
3206
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
PRIMARY | |||
|
DTXSID5048261
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
PRIMARY | |||
|
651
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
PRIMARY | |||
|
5282459
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
PRIMARY | |||
|
67Y4P5C84X
Created by
admin on Fri Dec 15 16:07:17 GMT 2023 , Edited by admin on Fri Dec 15 16:07:17 GMT 2023
|
PRIMARY |
ACTIVE MOIETY
SALT/SOLVATE (PARENT)