6 Results for "

HEK-293A

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

6 Results for "HEK-293A" in MCE Product Catalog:

11
11 Cited Publications
Cat. No.: HY-13285
CAS No.: 355025-24-0
Purity:  98.88%
Synonyms: Debio 0719
Target:  

LPL Receptor YAP

Research Areas:  

Neurological Disease Cancer

Ki16425 (Debio 0719) is a subtype-selective, competitive antagonist of the EDG-family receptors, LPA1 and LPA3 with Kis of 0.34 μM and 0.93 μM, respectively. Ki16425 (Debio 0719) reduces the LPA-induced activation of p42/p44 MAPK . Ki16425 can also inhibit LPA-induced dephosphorylation of Yes-associated protein (YAP)/TAZ in HEK293A cells .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-153523
CAS No.: 374567-94-9
Purity:  99.90%
Synonyms: NNC0076-0079; 76-0079
Target:  

Lipase

Research Areas:  

Metabolic Disease

Hi 76-0079 (NNC0076-0079; 76-0079) is a lipase inhibitor that specifically targets hormone-sensitive lipase (HSL). Hi 76-0079 inhibits PNPB Hydrolysis in cell lysates of HEK293A cells overexpressing Lipe with an IC50 value of 0.1 μM. Hi 76-0079 synergizes with the ATGL inhibitor Atglistatin (HY-15859) to block lipolysis in vitro. Hi 76-0079 can be used for the study of lipid metabolism .
loading...
    loading...
Cat. No.: HY-13285R
CAS No.: 355025-24-0
Synonyms: Debio 0719 (Standard)
Ki16425 (Standard) is the analytical standard of Ki16425. This product is intended for research and analytical applications. Ki16425 (Debio 0719) is a subtype-selective, competitive antagonist of the EDG-family receptors, LPA1 and LPA3 with Kis of 0.34 μM and 0.93 μM, respectively. Ki16425 (Debio 0719) reduces the LPA-induced activation of p42/p44 MAPK . Ki16425 can also inhibit LPA-induced dephosphorylation of Yes-associated protein (YAP)/TAZ in HEK293A cells .
loading...
    loading...
Cat. No.: HY-183657
Target:  

Orphan GPCR

Research Areas:  

Neurological Disease

GPR3 inverse agonist-1 is a GPR3 inverse agonist with low micromolar potency in conformational analysis. GPR3 inverse agonist-1 inhibits GPR3-dependent Gs activity in HEK293A cells with an EC50 of 250 nM, and exhibits an EC50 of 2 μM in cAMP assays. GPR3 inverse agonist-1 induces concentration-dependent changes in BRET signals in GPR3 conformational biosensors (EC50 = 5 μM), reduces basal Gs activity downstream of GPR3, and competes for binding sites with the GPR3 agonist DPI (HY-100965). GPR3 inverse agonist-1 can be used in research related to Alzheimer's disease .
loading...
    loading...
Cat. No.: HY-183657A
Target:  

Orphan GPCR

Research Areas:  

Neurological Disease

GPR3 inverse agonist-1 TFA is a GPR3 inverse agonist with low micromolar potency in conformational analysis. GPR3 inverse agonist-1 TFA inhibits GPR3-dependent Gs activity in HEK293A cells with an EC50 of 250 nM, and exhibits an EC50 of 2 μM in cAMP assays. GPR3 inverse agonist-1 TFA induces concentration-dependent BRET signal changes in GPR3 conformational biosensors (EC50 = 5 μM), reduces basal Gs activity downstream of GPR3, competes for binding sites with the GPR3 agonist DPI (HY-100965). GPR3 inverse agonist-1 TFA can be used in research related to Alzheimer's disease .
loading...
    loading...
Cat. No.: HY-N21988
Adinanquercetiside is a flavonoid glycoside found in the leaves of Adinandra megaphylla Hu, and it shows no significant activity in α-glucosidase inhibition assays or cytotoxicity assays .
loading...
    loading...