MK-5 with vented cover (polycarbonate 

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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].


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].


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.


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].


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].


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 vitro: . Despite the increased serum shift of these compounds, the representative 1e was highly potent


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


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].


B1207-5 each
EUR 222


B1250-5 each
EUR 261.6


B1255-5 each
EUR 261.6


B1315-5 each
EUR 614.4


B1344-5 each
EUR 314.4


B1641-5 each
EUR 333.6


B1942-5 each
EUR 183.6


B1980-5 each
EUR 548.4


B2118-5 each
EUR 222


B2289-5 each
EUR 235.2


B2317-5 each
EUR 235.2


B2431-5 each
EUR 496.8

MK-5 with vented cover (polycarbonate