Cart
sales@molnova.com
Anti-inflammatory agent 42
CAS No. 877468-30-9
Anti-inflammatory agent 42( —— )
Catalog No. M36629 CAS No. 877468-30-9
Anti-inflammatory agent 42 has anti-inflammatory activity and inhibits the expression of TNF-α and IL-6 in LPS-stimulated macrophages.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 29 | In Stock |
|
| 10MG | 46 | In Stock |
|
| 25MG | 72 | In Stock |
|
| 50MG | 105 | In Stock |
|
| 100MG | 158 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameAnti-inflammatory agent 42
-
NoteResearch use only, not for human use.
-
Brief DescriptionAnti-inflammatory agent 42 has anti-inflammatory activity and inhibits the expression of TNF-α and IL-6 in LPS-stimulated macrophages.
-
DescriptionAnti-inflammatory agent 42 (Compound 10j) is an anti-inflammatory agent. Anti-inflammatory agent 42 shows excellent inhibition on the expression of TNF-α and IL-6 in LPS (HY-D1056)-stimulated macrophages.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayApoptosis
-
TargetIL Receptor
-
RecptorIL Receptor | TNF
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number877468-30-9
-
Formula Weight328.39
-
Molecular FormulaC20H12N2OS
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C1N2C(S\C1=C/C1=C3C=CC=CC3=CC=C1)=NC1=C2C=CC=C1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Hu J, et al. Synthesis and biological evaluation of novel thiazolidinone derivatives as potential anti-inflammatory agents. Eur J Med Chem. 2013 Jun;64:292-301.?
molnova catalog
related products
-
Caulophyllogenin
Caulophyllogenin is a partial PPARγ agonist (EC50?=?12.6?μM) derived from the stem bark of Kalopanax pictus (Araliaceae).
-
CP 424174
CP 424174 is an inhibitor of IL-1β post-translational processing with IC50 of 210 nM. Inhibits the formation of mature IL-1β. Indirectly inhibits NLRP3. Active in vivo and orally bioavailable.
-
3-O-Methylquercetin
3-O-Methylquercetin is a selective and competitive PDE3/PDE4 inhibitor, and inhibits PDE3 than PDE4 with a low Km value.
