Antibody product name |
ProductCode |
TRI Biotech |
Pack Size |
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Human IgG antibody Laboratories manufactures the 852a medchemexpress reagents distributed by Genprice. The 852A Medchemexpress reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact MedChemExpress Inc.. Other 852A products are available in stock. Specificity: 852A Category: Medchemexpress
Chemicals information
A-381393 |
HY-116941 |
MedChemExpress |
25mg |
EUR 703.47 |
Description: A-381393 is a potent, selective, brain penetrate dopamine D4 receptor antagonist, with Kis of 1.5, 1.9 and 1.6 nM for human dopamine D4.4, D4.2, and D4.7 receptor, respectively, >2700-fold selectivity over D1, D2, D3 and D5 dopamine receptors. A-381393 shows moderate affinity for 5-HT2A (Ki, 370 nM)[1]. |
A-315675 |
HY-117151 |
MedChemExpress |
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Description: A-315675 is a potent highly potent inhibitor of A and B strain influenza virus neuraminidases inhibitor[1]. |
A-192621 |
HY-120295 |
MedChemExpress |
10 mg |
EUR 1688.34 |
Description: A-192621 is a potent, nonpeptide, orally active and selective endothelin B (ETB) receptor antagonist with an IC50 of 4.5 nM and a Ki of 8.8 nM. The selectivity of A-192621 is 636-fold higher than ETA (IC50 of 4280 nM and Ki of 5600 nM). A-192621 promotes apoptosis in PASMCs. A-192621 alos causes elevation of arterial blood pressure and an elevation in the plasma ET-1 level[1][2][3]. |
A-412997 |
HY-129103 |
MedChemExpress |
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Description: A-412997 is a selective Dopamine D4 agonist with Ki values of 12 and 7.9 nM for the rat and human receptors. A-412997 improves short term memory and cognitive properties in rodent models[1]. |
A-674563 |
HY-13254 |
MedChemExpress |
100mg |
EUR 703.47 |
Description: A-674563 is an orally active and selective Akt1 inhibitor with a Ki of 11 nM. |
A-908292 |
HY-147004 |
MedChemExpress |
10 mg |
EUR 1623.4 |
Description: A-908292 is a potent and selective acetyl-CoA carboxylase 2 (ACC2) inhibitor, with an IC50 of 23 nM for human ACC2. A-908292 can be used for the research of fatty acid metabolism[1][2]. A-908292 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. |
A-317491 |
HY-15568 |
MedChemExpress |
10mM/1mL |
EUR 432.91 |
Description: A-317491 is a potent, selective and non-nucleotide antagonist of P2X3 and P2X2/3 receptors, with Kis of 22, 22, 9, and 92 nM for hP2X3, rP2X3, hP2X2/3, and rP2X2/3, respectively. A-317491 is highly selective (IC50>10 μM) over other P2 receptors and other neurotransmitter receptors, ion channels, and enzymes. A-317491 reduces inflammatory and neuropathic pain by blocking P2X3 and P2X2/3 receptor-mediated calcium flux[1][2]. |
A-385358 |
HY-16014 |
MedChemExpress |
10mg |
EUR 2002.2 |
Description: A-385358 is a selective inhibitor of Bcl-XL with Kis of 0.80 and 67 nM for Bcl-XL and Bcl-2, respectively. |
A-769662 |
HY-50662 |
MedChemExpress |
100mg |
EUR 357.15 |
Description: A-769662 is a potent, reversible AMPK activator with EC50 of 0.8 μM. |
A-740003 |
HY-50697 |
MedChemExpress |
10mM/1mL |
EUR 99.57 |
Description: A-740003 is a potent, selective and competitive P2X7 receptor antagonist with IC50 values are 18 and 40 nM for rat and human P2X7 receptors, respectively. |
A939572 |
HY-50709 |
MedChemExpress |
2mg |
EUR 623.39 |
Description: A939572 is a potent, and orally bioavailable stearoyl-CoA desaturase1 (SCD1) inhibitor with IC50 values of <4 nM and 37 nM for mSCD1 and hSCD1, respectively. |
A-841720 |
HY-103550 |
MedChemExpress |
1 mg |
EUR 80.09 |
Description: A-841720 is a potent, non-competitive and selective mGlu1 receptor antagonist with an IC50 of 10 nM for human mGlu1 receptor. A-841720 displays 34-fold selectivity over mGlu5 (IC50 of 342 nM), and no significant activity at a range of other neurotransmitter receptors, ion channels, and transporters. A-841720 has the potential for chronic pain research[1][2]. |
A-443654 |
HY-10425 |
MedChemExpress |
5mg |
EUR 1190.49 |
Description: A-443654 is a pan-Akt inhibitor and has equal potency against Akt1, Akt2, or Akt3 within cells (Ki=160 pM)[1]. |
A-966492 |
HY-10614 |
MedChemExpress |
50mg |
EUR 766.25 |
Description: A-966492 is a novel and potent inhibitor of PARP1 and PARP2 with Ki of 1 nM and 1.5 nM, respectively. |
A-286982 |
HY-107587 |
MedChemExpress |
1 mg |
EUR 487.02 |
Description: A-286982 is a potent and allosteric LFA-1/ICAM-1 interaction inhibitor with IC50s of 44 nM and 35 nM in an LFA-1/ICAM-1 binding and LFA-1-mediated cellular adhesion assay, respectively[1][2]. |
A-784168 |
HY-108460 |
MedChemExpress |
10 mg |
EUR 270.57 |
Description: A-784168 is a potent and orally active inhibitor of vanilloid receptor type 1 (TRPV1). Vanilloid receptor type 1 (TRPV1) is a ligand-gated nonselective cation channel that is considered to be an important integrator of various pain stimuli such as endogenous lipids, capsaicin, heat, and low pH. A-784168 has good CNS penetration[1]. |