Cart
sales@molnova.com
BMS-195270
CAS No. 202822-23-9
BMS-195270( —— )
Catalog No. M34523 CAS No. 202822-23-9
BMS-195270 is a tissue-specific inhibitor of bladder muscle tone and spontaneous contraction in rats. It can inhibit Carbachol-induced tone and inhibit calcium flux in isolated rat bladder tissue strips in an isolated bladder model.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 90 | In Stock |
|
| 5MG | 136 | In Stock |
|
| 10MG | 217 | In Stock |
|
| 25MG | 426 | In Stock |
|
| 50MG | 685 | In Stock |
|
| 100MG | 888 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameBMS-195270
-
NoteResearch use only, not for human use.
-
Brief DescriptionBMS-195270 is a tissue-specific inhibitor of bladder muscle tone and spontaneous contraction in rats. It can inhibit Carbachol-induced tone and inhibit calcium flux in isolated rat bladder tissue strips in an isolated bladder model.
-
DescriptionBMS-195270 is a small molecule that inhibits Carbachol (HY-B1208)-evoked tonicity of isolated rat bladder strips. BMS-195270 inhibits calcium flux.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayGPCR/G Protein
-
TargetCalcium Channel
-
RecptorCalcium Channel
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number202822-23-9
-
Formula Weight355.7
-
Molecular FormulaC15H9ClF3N3O2
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 125 mg/mL (351.42 mM; Ultrasonic )
-
SMILESO=C1NC(=NN1C2=CC(Cl)=CC=C2O)C=3C=CC=CC3C(F)(F)F
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Fitzgerald K, et al. Chemical genetics reveals an RGS/G-protein role in the action of a compound. PLoS Genet. 2006 Apr;2(4):e57.?
molnova catalog
related products
-
Levamlodipine
Levamlodipine also known as S-amlodipine is a pharmacologically active enantiomer of amlodipine an antihypertensive and anti-anginal medication.
-
Bay K-8644
Bay K-8644 is a potent L-type calcium channels (LTCCs) activator with EC50 of 17.3 nM.
-
Ethyl cinnamate
Ethyl cinnamate has antifungal, and vasorelaxant effects. Ethyl cinnamate can lead to the damage of cell membrane system and metabolic disorder through inducing lipid peroxidation via initiating ROS overproduction.
