Oxodipine
CAS No. 90729-41-2
Oxodipine( —— )
Catalog No. M36210 CAS No. 90729-41-2
Oxodipine, a dihydropyridine-type calcium antagonist, inhibited KCl-induced aortic contraction in rabbits and reduced cardiac force in less potent rat ventricular test-paper contractions.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 116 | Get Quote |
|
| 5MG | 168 | Get Quote |
|
| 10MG | 247 | Get Quote |
|
| 25MG | 466 | Get Quote |
|
| 50MG | 635 | Get Quote |
|
| 100MG | 884 | Get Quote |
|
| 500MG | 1773 | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameOxodipine
-
NoteResearch use only, not for human use.
-
Brief DescriptionOxodipine, a dihydropyridine-type calcium antagonist, inhibited KCl-induced aortic contraction in rabbits and reduced cardiac force in less potent rat ventricular test-paper contractions.
-
DescriptionOxodipine, a dihydropyridine-type calcium antagonist, inhibited KCl-induced aortic contraction in rabbits and reduced cardiac force in less potent rat ventricular test-paper contractions. In rat cultured neonatal ventricular myocytes, Oxodipine reduced L-type Ca currents (I) with an IC of 0.24 μM, and against T-type Ca currents (I) with an IC of 0.41 μM. Oxodipine causes constipation in mice and gingival hyperplasia in dogs.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayGPCR/G Protein
-
TargetCalcium Channel
-
RecptorCalcium Channel
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number90729-41-2
-
Formula Weight359.37
-
Molecular FormulaC19H21NO6
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESC(OCC)(=O)C=1C(C(C(OC)=O)=C(C)NC1C)C2=C3C(=CC=C2)OCO3
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog
related products
-
AMG1
A novel specific CRAC channel inhibitor that blocks function of effector.
-
Felodipine
Felodipine is a long-acting 1,4-dihydropyridine calcium channel blocker.
-
ORM-10103
ORM-10103 is a novel potent and selective inhibitor of the Na+/Ca2+ exchanger (NCX).
Cart
sales@molnova.com