Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C21H31ClN6O3 |
Molecular Weight | 450.962 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
N[C@H](CC1=CC=CC=C1)C(=O)N2CCC[C@H]2C(=O)N[C@@H](CCCNC(N)=N)C(=O)CCl
InChI
InChIKey=KWPACVJPAFGBEQ-IKGGRYGDSA-N
InChI=1S/C21H31ClN6O3/c22-13-18(29)16(8-4-10-26-21(24)25)27-19(30)17-9-5-11-28(17)20(31)15(23)12-14-6-2-1-3-7-14/h1-3,6-7,15-17H,4-5,8-13,23H2,(H,27,30)(H4,24,25,26)/t15-,16+,17+/m1/s1
Molecular Formula | C21H31ClN6O3 |
Molecular Weight | 450.962 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
PPACK is a synthetic peptide that irreversibly inhibits thrombin-mediated platelet activation by binding to the active site of thrombin with a Ki = 0.24 nM. PPACK competes with alpha-thrombin at the high-affinity site and is an antagonist of alpha-thrombin induced activation. PPACK is used as a tool for assessment of Platelet function.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3362867
Vascular graft-bearing baboons (Papio anubis) were administered PPACK (100 nmol/kg per min) by continuous intravenous infusion. The treatment abolished platelet deposition, vascular graft occlusion, thrombus associated release of platelet-specific proteins and fibrino-peptides, platelet hemostatic plug formation, platelet aggregation and thrombin-induced blood clotting. The effects of PPACK disappeared within 15 min after the infusion was discontinued.
Route of Administration:
Intravenous
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1832095
Platelet-rich plasma was incubated with 10 uM PPACK and the drug completely inhibited thrombin-induced platelet aggregation. The effect of PPACK on platelet deposition at the site of balloon injury was measured with 10 uM of the drug. Platelet deposition at the site of balloon injury was reduced by 47%.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:35:55 GMT 2023
by
admin
on
Fri Dec 15 16:35:55 GMT 2023
|
Record UNII |
N62UL02WW4
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
N62UL02WW4
Created by
admin on Fri Dec 15 16:35:55 GMT 2023 , Edited by admin on Fri Dec 15 16:35:55 GMT 2023
|
PRIMARY | |||
|
m9086
Created by
admin on Fri Dec 15 16:35:55 GMT 2023 , Edited by admin on Fri Dec 15 16:35:55 GMT 2023
|
PRIMARY | Merck Index | ||
|
71142-71-7
Created by
admin on Fri Dec 15 16:35:55 GMT 2023 , Edited by admin on Fri Dec 15 16:35:55 GMT 2023
|
PRIMARY | |||
|
5311176
Created by
admin on Fri Dec 15 16:35:55 GMT 2023 , Edited by admin on Fri Dec 15 16:35:55 GMT 2023
|
PRIMARY | |||
|
DTXSID20991446
Created by
admin on Fri Dec 15 16:35:55 GMT 2023 , Edited by admin on Fri Dec 15 16:35:55 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
SALT/SOLVATE -> PARENT | |||
|
SALT/SOLVATE -> PARENT |