852A Medchemexpress

Antibody product name

ProductCode Pack Size Ask for price

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

L-NAME hydrochloride

1g
EUR 159.23

L-NAME hydrochloride

1
EUR 15.9

L-NAME hydrochloride

1 g
EUR 55.2

L-NAME hydrochloride

25
EUR 174

L-NAME hydrochloride

25 g
EUR 246

L-NAME hydrochloride

5
EUR 55.4

L-NAME hydrochloride

5 g
EUR 103.2

Chemicals information

A-286982

HY-107587 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 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].

A-967079

HY-108463 25mg
EUR 432.91
Description: A-967079 is a selective TRPA1 receptor antagonist with IC50s of 67 nM and 289 nM at human and rat TRPA1 receptors, respectively, and has good penetration into the CNS.

A-484954

HY-110096 25mg
EUR 746.76
Description: A-484954 is a highly selective eukaryotic elongationfactor-2 kinase(eEF2K) inhibitor, with an IC50 of 280 nM.

A-770041

HY-11011 5mg
EUR 313.86
Description: A-770041 is a selective and orally active Src-family Lck inhibitor. A-770041 inhibits Lck with an IC50 value of 147 nM with the presence of 1 mM ATP. A-770041 shows 300-fold selective to Lck over Fyn, the other Src family kinase involved in T-cell signaling. A-770041 can be used for the research of acute rejection[1][2].

A-971432

HY-110291 5 mg
EUR 270.57
Description: A-971432 is a potent, selective and orally active sphingosine-1-phosphate (S1P) receptor 5 agonist with IC50s of .362, >10, 0.006 µM for S1P1, S1P3, S1P5 respectively. A-971432 protects blood–brain barrier (BBB) homeostasis. A-971432 reverses age-related cognitive decline. A-971432 has the potential for the research of alzheimer’s disease or multiple sclerosis [1][2].

A-425619

HY-110292 1 mg
EUR 340.91
Description: A-425619, a potent and selective TRPV1 receptor antagonist, is effective in alleviating acute and chronic inflammatory pain and postoperative pain[1].

A-803467

HY-11079 50mg
EUR 248.92
Description: A-803467 is a potent and selective tetrodotoxin-resistant Nav1.8 sodium channel blocker (IC50=8 nM). A-803467 has shown significant anti-nociception in neuropathic and inflammatory pain models. A-803467 enhances the chemosensitivity of conventional anticancer agents through interaction with the ATP-binding cassette subfamily G member 2 (ABCG2) transporter[1][2].

A-317491

HY-15568 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 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-836339

HY-12761 50mg
EUR 1060.62

A-412997

HY-129103 Get quote Ask for price
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 100mg
EUR 703.47
Description: A-674563 is an orally active and selective Akt1 inhibitor with a Ki of 11 nM.

A-123189

HY-116623 Get quote Ask for price
Description: A-123189 is a selective and potent α1D antagonist with Kis of 0.312 and 0.17 for human α1D and rat α1D, respectively. A-123189 displays selectivities between 10- to 20-fold for the α1D receptor over the human α1A and rat α1A receptors[1].

A-381393

HY-116941 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 Get quote Ask for price
Description: A-315675 is a potent highly potent inhibitor of A and B strain influenza virus neuraminidases inhibitor[1].

A-192621

HY-120295 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].