6 Results for "

compound 9j

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "compound 9j" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-147648
CAS No.: 2455508-19-5
Purity:  99.26%
Target:  

Glyoxalase (GLO)

Research Areas:  

Cancer

Glyoxalase I inhibitor 6 (Compound 9j) is a glyoxalase I (Glo-I) inhibitor with an IC50 of 1.13 μM. Glyoxalase I inhibitor 6 can be used as anticancer agent with low toxicity .
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Cat. No.: HY-149968
CAS No.: 2911585-60-7
Research Areas:  

Cancer

LSD1-IN-25 (Compound 9j) is a potent, selective and orally active LSD1 inhibitor with an IC50 of 46 nM (Ki = 30.3 nM). LSD1-IN-25 induces cancer cell apoptosis .
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Cat. No.: HY-150558
CAS No.: 727730-24-7
Target:  

Cytochrome P450

Research Areas:  

Cancer

CYP1B1-IN-2 (compound 9j) is a potent and selective CYP1B1 (cytochrome P450 1B1) inhibitor, with an IC50 of 0.52 nM .
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Cat. No.: HY-155821
CAS No.: 2924156-51-2
Anti-inflammatory agent 55 (compound 9j) is a derivative of Coixol and has anti-inflammatory activity. Anti-inflammatory agent 54 inhibits the NF-κB pathway and downregulates the expression of iNOS, TNF-α, IL-6 and IL-1β. Anti-inflammatory agent 54 inhibits LPS-induced nitric oxide (NO) production in RAW264.7 macrophages (IC50: 0.8 μM) and exerts in vivo anti-inflammatory activity in a mouse auricular edema model .
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Cat. No.: HY-164111
CAS No.: 1128096-58-1
Target:  

JAK

Research Areas:  

Neurological Disease

JNK-IN-17 (Compound 9J) is a selective and potent JNK inhibitor with IC50 values of 0.039, 0.079 μM for JNK1 and JNK3. JNK-IN-17 can inhibit c-Jun phosphorylation with an IC50 of 0.082 μM in Streptozotocin (HY-13753)-infuced INS-1 pancreatic islet β cells. JNK-IN-17 shows inhibition rate ≤ 33% on the four main P450 subtypes (2C9, 2D6, 3A4, 1A2) in human liver microsomes, indicating a relatively low risk of drug interactions. JNK-IN-17 can be used for researches of neurological and metabolic disease, such as Parkinson's disease .
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Cat. No.: HY-180212A
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

SYK-1106 dihydrochloride is a selective δ opioid receptor (DOR) agonist with an EC50 of 0.089 nM. SYK-1106 dihydrochloride shows high selectivity over MOR and KOR. SYK-1106 dihydrochloride exhibits antidepressant-like effects in the mouse forced-swimming tests. SYK-1106 dihydrochloride can be used for the research of depression .
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