Cart
sales@molnova.com
Molsidomine
CAS No. 25717-80-0
Molsidomine( Corvaton | Morsydomine )
Catalog No. M13777 CAS No. 25717-80-0
Molsidomine is an orally active, long acting vasodilating drug, metabolized in the liver to the active metabolite linsidomine.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 200MG | 29 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameMolsidomine
-
NoteResearch use only, not for human use.
-
Brief DescriptionMolsidomine is an orally active, long acting vasodilating drug, metabolized in the liver to the active metabolite linsidomine.
-
DescriptionMolsidomine is an orally active, long acting vasodilating drug, metabolized in the liver to the active metabolite linsidomine, which is an unstable compound that releases nitric oxide (NO) upon decay as the actual vasodilating compound.
-
In Vitro——
-
In Vivo——
-
SynonymsCorvaton | Morsydomine
-
PathwayNF-κB
-
TargetNOD
-
RecptorNOD
-
Research AreaCardiovascular Disease
-
Indication——
Chemical Information
-
CAS Number25717-80-0
-
Formula Weight242.23
-
Molecular FormulaC9H14N4O4
-
Purity>98% (HPLC)
-
SolubilitySoluble in Water
-
SMILESO=C([N-]C1=C[N+](N2CCOCC2)=NO1)OCC
-
Chemical Name(ethoxycarbonyl)(3-morpholino-1,2,3-oxadiazol-3-ium-5-yl)amide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Rosenkranz B, et al. Clin Pharmacokinet. 1996 May;30(5):372-84.
molnova catalog
related products
-
JC-171
JC-171 is a selective NLRP3 inflammasome inhibitor that inhibits LPS/ATP-induced IL-1β release from macrophages with IC50 of 8.45 uM.
-
NLRP3 agonist 1
NLRP3 agonist 1 (compound 23) is a potent, orally active agent that activates Caspase-1 enzyme, resulting in the cleavage of proinflammatory cytokines pro-IL-1β and pro-IL-18 into their active forms .
-
NLRP3-IN-9
NLRP3-IN-9 is an inhibitor of NLRP3 ATPase and caspase-1. NLRP3-IN-9 acts by irreversibly trapping thiol nucleophiles, which prevents both ATP- and nigericin-triggered pyroptosis of human THP-1 cells in a time- and concentration-dependent manner.
