CEACAM19 (human) monoclonal antibody (HY-8H10) |
MBS566382-01mg |
MyBiosource |
0.1mg |
EUR 705 |
Human IgG antibody Laboratories manufactures the medchemexpress hy-19720a reagents distributed by Genprice. The Medchemexpress Hy-19720A 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 Medchemexpress products are available in stock. Specificity: Medchemexpress Category: Hy-19720A
Human True Insulin ELISA Kit |
MyBiosource |
10x96-Strip-Wells |
EUR 6725 |
Human True Insulin ELISA Kit |
MyBiosource |
48-Strip-Wells |
EUR 550 |
Human True Insulin ELISA Kit |
MyBiosource |
5x96-Strip-Wells |
EUR 3420 |
Human True Insulin ELISA Kit |
MyBiosource |
96-Strip-Wells |
EUR 765 |
Human True Insulin GENLISA ELISA |
Krishgen |
1 x 96 wells |
EUR 286 |
Human True insulin ELISA kit |
BlueGene |
96T |
EUR 700 |
Description: ELISA |
Chemicals information
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]. |
A-967079 |
HY-108463 |
MedChemExpress |
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 |
MedChemExpress |
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 |
MedChemExpress |
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 |
MedChemExpress |
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 |
MedChemExpress |
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 |
MedChemExpress |
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 |
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-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-123189 |
HY-116623 |
MedChemExpress |
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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 |
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]. |