Cart
sales@molnova.com
Protease-Activated Receptor-4 diTFA
CAS No. ——
Protease-Activated Receptor-4 diTFA( —— )
Catalog No. M21052 CAS No. ——
Protease-Activated Receptor-4 diTFA2454 is the proteinase-activated receptor-4 (PAR4)agonist.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 61 | Get Quote |
|
| 5MG | 85 | Get Quote |
|
| 10MG | 154 | Get Quote |
|
| 25MG | 315 | Get Quote |
|
| 50MG | 472 | Get Quote |
|
| 100MG | Get Quote | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameProtease-Activated Receptor-4 diTFA
-
NoteResearch use only, not for human use.
-
Brief DescriptionProtease-Activated Receptor-4 diTFA2454 is the proteinase-activated receptor-4 (PAR4)agonist.
-
DescriptionProtease-Activated Receptor-4 diTFA2454 is the proteinase-activated receptor-4 (PAR4)agonist.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayGPCR/G Protein
-
TargetPAR
-
RecptorPAR-4
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number——
-
Formula Weight894.81
-
Molecular FormulaC37H48F6N8O11
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESOC(=O)C(F)(F)F.OC(=O)C(F)(F)F.NCCCC[C@H](NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@H](CC1=CC=C(O)C=C1)NC(=O)CN)C(=O)N[C@@H](CC1=CC=CC=C1)C(N)=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Huang S C . Proteinase-activated receptor-1 (PAR1) and PAR2 mediate relaxation of guinea pig internal anal sphincter[J]. Gastroenterology 2014 189(5):46-50.
molnova catalog
related products
-
FSLLRY-NH2
Selective PAR2 peptide antagonist. Reverses taxol-induced mechanical allodynia, heat hyperalgesia and PKC activation in ICR mice. Blocks ERK activation and collagen production in isolated cardiac fibroblasts. Also reduces symptoms in a mouse model of dermatophyte-associated itch.
-
TFLLR-NH2
TFLLR-NH2 is a protease-activated receptor (PARs) agonist which is more selective to PAR-1 than SFLLRN-NH2.
-
Vorapaxar
A potent, selective and orally active thrombin receptor PAR-1 antagonist with Ki of 8.1 nM.
