MK-5 with vented cover (polycarbonate 

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MK-0974

A3612-5 5 mg
EUR 474
Description: MK-0974 (Telcagepant) is a highly potent, selective, and orally bioavailable antagonist of CGRP receptor with IC50 value of 0.77 nM [1].

MK-2894

A3613-5 5 mg
EUR 428.4
Description: MK-2894 is a highly potent and selective inhibitor of EP4 receptor with IC50 value of 2.5 nM [1].

MK-3207

A3615-5 5 mg
EUR 408
Description: MK-3207 is a new, highly selective CGRP receptor antagonist that is approximately 40- to 65-fold more potent than telcagepant for the human CGRP receptor. The IC50 is 0.12 nM and The Ki value is 0.024 nM. It is highly selective versus human AM1, AM2, CTR, and AMY3.

MK-4827

A3617-5 5 mg
EUR 250.8
Description: MK-4827 is a novel, selective and orally bioavailable PARP1/PARP2 inhibitor with IC50 of 3.8 nM and 2.1 nM, respevctively.MK-4827 has shown great activity against cancer cells with mutant BRCA-1 and BRCA-2; >330-fold selective against PARP3, V-PARP and Tank1 [1].

MK-5172

A3618-5 5 mg
EUR 184.8
Description: MK-5172 is a selective inhibitor of Hepatitis C Virus NS3/4a Protease [1].Hepatitis C (HCV) virus is a member of the Flaviviridae family of viruses in the Hepacivirus genus and encoded by a 9.6-kb positive strand RNA genome [2].

MK-6892

A3623-5 5 mg
EUR 602.4
Description: Description:IC50 Value: 4.0 nM (Ki for Human GPR109A) [1]MK-6892 is a highly potential GPR109A agonists.in vitro: . Despite the increased serum shift of these compounds, the representative 1e was highly potent

MK-8033

A3624-5 5 mg
EUR 559.2
Description: MK-8033 is a c-MET inhibitor in clinical trials. MK8033 is a selective small-molecule inhibitor, ATP competitive. Phase I investigation of the cMet inhibitor MK-8033 is ongoing.

MK 886

B6684-5 5 mg
EUR 164.4

MK-4101

B7803-5 5 mg
EUR 313.2
Description: IC50: 1.5 ?mol/L for in mouse Light II cells by Gli_luc assayMK-4101 is a Hedgehog (Hh) signaling pathway inhibitor.Abnormal activation of the Hedgehog (Hh) signaling pathway is reported in the pathogenesis of various cancers, such as medulloblastoma and basal cell carcinoma.

MK 571

B7023-5 5 mg
EUR 153.6
Description: MK 571 (L-660,711) is a novel potent and selective antagonist of leukotriene D4 receptor with Ki values of 0.22 nM and 2.1 nM in guinea pig and human lung membranes, respectively [1].

MK-0941

B1207-5 each
EUR 222

MK-1439

B1250-5 each
EUR 261.6

MK-4101

B1255-5 each
EUR 261.6

MK-8931

B1315-5 each
EUR 614.4

MK-5108

B1344-5 each
EUR 314.4

MK-1064

B1641-5 each
EUR 333.6

MK-8745

B1942-5 each
EUR 183.6

MK-0752

B1980-5 each
EUR 548.4

MK-5172

B2118-5 each
EUR 222

MK-7655

B2289-5 each
EUR 235.2

MK-0557

B2317-5 each
EUR 235.2

MK-3903

B2431-5 each
EUR 496.8

MK-5 with vented cover (polycarbonate