
Analgin
CAS No. 5907-38-0
Analgin( Dipyrone | NSC-73205 | NSC 73205 | NSC73205 | Anador | Novalgin )
Catalog No. M15189 CAS No. 5907-38-0
A drug that has analgesic, anti-inflammatory, and antipyretic properties.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
200MG | 89 | In Stock |
![]() ![]() |
500MG | Get Quote | In Stock |
![]() ![]() |
1G | Get Quote | In Stock |
![]() ![]() |
Biological Information
-
Product NameAnalgin
-
NoteResearch use only, not for human use.
-
Brief DescriptionA drug that has analgesic, anti-inflammatory, and antipyretic properties.
-
DescriptionA drug that has analgesic, anti-inflammatory, and antipyretic properties. It is the sodium sulfonate of aminopyrine. Because of the risk of serious adverse effects its use is justified only in serious situations where no alternative is available or suitable.
-
In VitroCell Proliferation Assay Cell Line:PaTu 8988 t, Panc-1 Concentration:1, 10, 100, 250, 500 μM Incubation Time:48 h Result:Inhibited proliferation in the PaTu 8988 t cell line with 1–500 μM and with concentrations of 1 μM, 10 μM, 100 μM, and 250 μM in the Panc-1 cell line.
-
In VivoAnimal Model:Neuropathic pain rat model Dosage:500 mg/kg Administration:intraperitoneally preemptively at 16 and 1 h before Chronic constriction injury (CCI) and then twice a day for 7 days.Result:Decreased the expression of pronociceptive interleukins (IL-1beta, IL-6, and IL-18) and chemokines (CCL2, CCL4, and CCL7).Animal Model:Pain model in rats Dosage:250 or 500 mg/kg Administration:p.o.Result:Decreased the COX-2 gene expression at 500 mg/kg and increased the MPO gene expression.Reduced MDA levels in the carrageenan paw test and increased tGSH levels.
-
SynonymsDipyrone | NSC-73205 | NSC 73205 | NSC73205 | Anador | Novalgin
-
PathwayChromatin/Epigenetic
-
TargetCOX
-
RecptorCOX-1
-
Research AreaInflammation/Immunology
-
Indication——
Chemical Information
-
CAS Number5907-38-0
-
Formula Weight333.34
-
Molecular FormulaC13H16N3NaO4S
-
Purity>98% (HPLC)
-
Solubility10 mM in DMSO
-
SMILESO=S(CN(C1=C(C)N(C)N(C2=CC=CC=C2)C1=O)C)([O-])=O.[H]O[H].[Na+]
-
Chemical Namesodium ((1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)(methyl)amino)methanesulfonate hydrate
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
molnova catalog



related products
-
Parecoxib sodium
A potent and selective COX-2 inhibitor; a water-soluble prodrug of valdecoxib.
-
Desmethyl Celecoxib
Demethyl celecoxib is a selective inhibitor of COX-2 with anti-inflammatory activity (IC50 of 32 nM).?
-
Bromfenac sodium
Bromfenac Sodium is the sodium salt form of bromfenac, a nonsteroidal anti-inflammatory drug (NSAID) with analgesic and anti-inflammatory activities.