Cart
sales@molnova.com
Kv2-IN-A1
CAS No. 689297-68-5
Kv2-IN-A1( RY785 )
Catalog No. M24703 CAS No. 689297-68-5
Kv2-IN-A1 is an inhibitor of Kv2.1 and Kv2.2.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 138 | In Stock |
|
| 5MG | 122 | In Stock |
|
| 10MG | 202 | In Stock |
|
| 25MG | 341 | In Stock |
|
| 50MG | 498 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameKv2-IN-A1
-
NoteResearch use only, not for human use.
-
Brief DescriptionKv2-IN-A1 is an inhibitor of Kv2.1 and Kv2.2.
-
DescriptionKv2-IN-A1 is an inhibitor of Kv2.1 and Kv2.2.
-
In Vitro——
-
In Vivo——
-
SynonymsRY785
-
PathwayCell Cycle/DNA Damage
-
TargetPotassium Channel
-
RecptorKv2.1|Kv2.2
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number689297-68-5
-
Formula Weight396.89
-
Molecular FormulaC20H17ClN4OS
-
Purity>98% (HPLC)
-
SolubilityDMSO:10 mM
-
SMILESCC(CC(=O)NC1=CC2=C(C=C1)N=C(N2)C3=CSC=N3)C4=CC(=CC=C4)Cl
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Herrington J , Solly K , Ratliff K S , et al. Identification of novel and selective Kv2 channel inhibitors.[J]. Molecular Pharmacology, 2011, 80(6):959-964.
molnova catalog
related products
-
BeKm 1
Potent and selective KV11.1 (hERG) channel blocker. Selective for KV11.1 over a panel of 14 other potassium channels. Dose-dependently prolongs QTc interval in isolated rabbit heart.
-
XE 991 dihydrochlori...
A potent, selective and orally active blocker of voltage-gated potassium channels Kv7 (KCNQ) that blocks KCNQ1, KCNQ2 and KCNQ2+KCNQ3 with Kd of 0.78, 0.7 and 0.6 uM, respectively.
-
TKIM
TKIM is a TWIK-related potassium channel 1 (TREK-1) inhibitor, binding to the pocket of the intermediate (IM) state of TREK-1.TKIM binds to the pocket of the IM state of TREK-1, which differs from the binding of common inhibitors, which bind to channels in the inactive state.?
