SAR7334
CAS No. 1333210-07-3
SAR7334( TRCP6-IN-1 )
Catalog No. M23484 CAS No. 1333210-07-3
SAR7334 is a potent and specific inhibitor of TRPC6(IC50 of 7.9 nM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 147 | In Stock |
|
| 10MG | 237 | In Stock |
|
| 25MG | 383 | In Stock |
|
| 50MG | 537 | In Stock |
|
| 100MG | 672 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameSAR7334
-
NoteResearch use only, not for human use.
-
Brief DescriptionSAR7334 is a potent and specific inhibitor of TRPC6(IC50 of 7.9 nM).
-
DescriptionSAR7334 is a potent and specific inhibitor of TRPC6(IC50 of 7.9 nM).
-
In VitroSAR7334 inhibits TRPC6, TRPC3 and TRPC7-mediated Ca2+ influx into cells with IC50s of 9.5, 282 and 226?nM, whereas TRPC4 and TRPC5-mediated Ca2+ entry is not affected. SAR7334 (1?μM) results in a major block of the Ang II-evoked calcium influx in the podocytes. SAR7334 (1 μM) has negligible effect on SOCE. SAR7334 dose-dependently reduces TRPC6 currents with an IC50 of 7.9?nM. SAR7334 (100?nM) substantially reduces TRPC6 currents.
-
In VivoSAR7334 (10?mg/kg, p.o.) suppresses TRPC6-dependent acute HPV in isolated perfused lungs from mice. SAR7334 demonstrates that it is suitable for chronic oral administration. In an initial short-term study, SAR7334 does not change mean arterial pressure in spontaneously hypertensive rats (SHR).
-
SynonymsTRCP6-IN-1
-
PathwayMembrane Transporter/Ion Channel
-
TargetTRP/TRPV Channel
-
RecptorTRPC6
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1333210-07-3
-
Formula Weight367.87
-
Molecular FormulaC21H22ClN3O
-
Purity>98% (HPLC)
-
SolubilityDMSO:350 mg/mL (951.42 mM)
-
SMILESN[C@H](CCC1)CN1[C@H](Cc1c2cccc1)[C@@H]2Oc(ccc(C#N)c1)c1Cl
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Ilatovskaya DV, et al. The Role of Angiotensin II in Glomerular Volume Dynamics and Podocyte Calcium Handling. Sci Rep. 2017 Mar 22;7(1):299.
molnova catalog
related products
-
TC-I2000
TC-I2000 is an TRPM8 channel blocker. Inhibits?icilin-induced TRPM8 channel activation in rTRPM8-expressing CHO cells with IC50?of 53 nM.
-
A 425619
A 425619 is a potent TRPV1 antagonistsystemic administration of the TRPV1 antagonist, A-425619, reversed the decrease in digging behavior induced by CFA injection, further confirming the role of TRPV1, expressed by knee neurons, in acute inflammatory joint pain.
-
Mesendogen
Mesendogen is an inhibitor of transient receptor potential cation channel, subfamily M, member 6 (TRPM6) and 7 (TRPM7) and acts by inhibiting TRPM6/TRPM7 magnesium channel activity.
Cart
sales@molnova.com