A277 1726 (Medchemexpress

A77 1726
1973-25 each
EUR 489.6

Human IgG antibody Laboratories manufactures the a277 1726 (medchemexpress reagents distributed by Genprice. The A277 1726 (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 . Other A277 products are available in stock. Specificity: A277 Category: 1726 Group: (Medchemexpress

True Blue
10mg Ask for price
Description: True Blue

True Blue
1g Ask for price
Description: True Blue

True Blue
1mg Ask for price
Description: True Blue

True Blue
50mg Ask for price
Description: True Blue

True Blue
5mg Ask for price
Description: True Blue

True Blue
5(mg
EUR 635

True Blue
5x5(mg
EUR 2705

(Medchemexpress information

A-443654
HY-10425 5mg
EUR 514.8

A-966492
HY-10614 50mg
EUR 1035.6

A-967079
HY-108463 25mg
EUR 391.2

A-484954
HY-110096 25mg
EUR 596.4

A-770041
HY-11011 5mg
EUR 501.6

A-803467
HY-11079 50mg
EUR 391.2

A-802715
HY-U00142 10mM/1mL
EUR 529.2

A-437203
HY-U00185 1mg
EUR 555.6

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-933548
HY-113639 Get quote Ask for price
Description: A-933548 is a potent and selective inhibitor of calpain, with a Ki of 18 nM. A-933548 can be used for the research of Alzheimer's disease[1].

A-940894
HY-113669 Get quote Ask for price
Description: A-940894 is a potent histamine H4 receptor antagonist, with Ki values of 7.6 nM (rat H4) and 71 nM (human H4). A-940894 exhibits with anti-inflammatory properties[1].

A-935142
HY-113673 1mg
EUR 617.98
Description: A-935142 is a human ether-a-go-go-related gene (hERG, Kv 11.1) channel activator. A-935142 enhances hERG current in a complex manner by facilitation of activation, reduction of inactivation, and slowing of deactivation, and abbreviates atrial and ventricular repolarization[1][2].

A-943931
HY-113936 Get quote Ask for price
Description: A-943931 is a potent and selective histamine H4 receptor (H4R) antagonist with pKi values of 4.6, 3.8 nM for human and rat H4R, respectively. A-943931 shows anti-inflammatory and antinociceptive efficacy[1][2].

A-127722
HY-114674 Get quote Ask for price
Description: A-127722 is A 2, 4-dialarylpyrrolidine-3-carboxylic acid ETA selective endothelin receptor (ET receptor) antagonist with IC50 value of 0.36 nM[1].

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-987306
HY-14364 Get quote Ask for price
Description: A-987306 is a potent and oral bioavailable histamine H4 antagonist, with Kis of 3.4 nM and 5.8 nM for rat H4, and human H4. A-987306 shows anti-inflammatory activity in mice peritonitis model[1].