SCS
CAS No. 3232-36-8
SCS( Salicylidene salicylhydrazide )
Catalog No. M27708 CAS No. 3232-36-8
SCS a potent selective inhibitor of α2β1γ1θ GABA(A) receptors with a maximum inhibition of 56+/-5% and an IC50 of 32 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 25MG | 43 | In Stock |
|
| 50MG | 61 | In Stock |
|
| 100MG | 89 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 216 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameSCS
-
NoteResearch use only, not for human use.
-
Brief DescriptionSCS a potent selective inhibitor of α2β1γ1θ GABA(A) receptors with a maximum inhibition of 56+/-5% and an IC50 of 32 nM.
-
DescriptionSCS a potent selective inhibitor of α2β1γ1θ GABA(A) receptors with a maximum inhibition of 56+/-5% and an IC50 of 32 nM.
-
In Vitro——
-
In VivoAnimal Model:BALB/c mice; tonic, phasic and Capsaicin (HY-10448) nociception modelDosage:10, 25, 50, and 75 mg/kg Administration:IP, single dose Result:Produced a significant protection on tonic, phasic and capsaicin nociception in a dose-dependent manner.Animal Model:BALB/c mice, Oxaliplatin (HY-17371)-induced neuropathic nociception model Dosage:50 and 75 mg/kg Administration:IP, single dose Result:Significantly attenuated the paw withdrawal threshold changes associated with Oxaliplatin. Significantly increased the percent antinociception during 30-120 min.
-
SynonymsSalicylidene salicylhydrazide
-
PathwayOthers
-
TargetOther Targets
-
RecptorHistamine Receptor|Autophagy|Apoptosis
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number3232-36-8
-
Formula Weight256.261
-
Molecular FormulaC14H12N2O3
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 50 mg/mL (195.11 mM)
-
SMILESOc1ccccc1C(=O)NN\C=C1\C=CC=CC1=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Cui J, et al. Alginic acid induces oxidative stress-mediated hormone secretion disorder, apoptosis and autophagy in mouse granulosa cells and ovaries. Toxicology. 2022;467:153099.
molnova catalog
related products
-
Sulfosuccinimidyl ol...
Sulfosuccinimidyl oleate sodium is a long-chain fatty acid that inhibits the transport of fatty acids to cells. Sulfosuccinimidyl oleate sodium is an effective, irreversible inhibitor of mitochondrial respiratory chain. Sulfosuccinimidyl oleate sodium binds to CD36 receptors on the surface of microglia.
-
Clanfenur
Clanfenur belongs to a new group of substituted benzoylphenylureas. The drug shows both in vitro and in vivo antitumour activity.
-
HTBA
HTBA is a low-cost enzymatic paper-based analytical device (enz-PAD) for determining urine creatinine.
Cart
sales@molnova.com