Mk-7145 Medchemexpress

MK-7145
HY-18277 Get quote Ask for price
Description: MK-7145 is a ROMK inhibitor, with an IC50 of 0.045 μM.

Human IgG antibody Laboratories manufactures the mk-7145 medchemexpress reagents distributed by Genprice. The Mk-7145 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 Mk-7145 products are available in stock. Specificity: Mk-7145 Category: Medchemexpress

MK-7145
50mg Ask for price
Description: MK-7145

MK-7145
5mg Ask for price
Description: MK-7145

True Blue
5.0mg
EUR 595

True Blue
5(mg
EUR 635

True Blue
5x5(mg
EUR 2705

True Blue
10mg Ask for price
Description: True Blue

True Blue
1g Ask for price
Description: True Blue

Chemicals information

MK-8745
HY-13819 10mM/1mL
EUR 200.22
Description: MK-8745 is an aurora A kinase inhibitor with an IC50 of 0.6 nM.

MK-0159
HY-150508 10 mg
EUR 833.35
Description: MK-0159 is an orally active, potent and selective CD38 inhibitor, with IC50 values of 22, 3, and 70 nM for human, mouse and rat CD38, respectively. MK-0159 also shows good microsomal stability for human and rodent liver microsomes. MK-0159 increases NAD+ (nicotinamide adenine dinucleotide) and reduces ADPR (adenosine diphosphate ribose) in whole blood and heart[1].

MK-0429
HY-15102 100mg
EUR 2435.1
Description: MK-0429 (L-000845704) is an orally active, potent, selective and nonpeptide pan-integrin antagonist with IC50 values of 1.6 nM, 2.8 nM, 0.1 nM, 0.7 nM, 0.5 nM and 12.2 nM for αvβ1, αvβ3, αvβ5, αvβ6, αvβ8 and α5β1, respectively[1][2][3].

MK-0249
HY-U00076 5mg
EUR 2745.6

MK-8189
HY-153093 10 mg
EUR 2110.42
Description: MK-8189 is a potent, orally active and selective PDE10A inhibitor with a Ki value of 29 pM. MK-8189 can be used in research of schizophrenia[1].

MK-0557
HY-15411 10mM/1mL
EUR 857.16
Description: MK-0557 is a highly selective, orally available neuropeptide Y5 receptor antagonist with a Ki of 1.6 nM.

MK-4101
HY-100036 100mg
EUR 411.26
Description: MK-4101 is a Smoothened (SMO) antagonist (IC50 of 1.1 µM for 293 cells ) and also a potent inhibitor of the hedgehog pathway (IC50 of 1.5 µM for mouse cells; IC50 of 1 µM for KYSE180 oesophageal cancer cells). MK-4101 has robust antitumor activity that inhibits tumor cell proliferation and induces extensive apoptosis[1].

MK-3328
HY-100275 1mg
EUR 617.98
Description: MK-3328 is a β-Amyloid PET ligand, which exhibits high binding potency with an IC50 of 10.5 nM[1][2].

MK-447
HY-100297 10mg
EUR 2047.2
Description: MK-447 is a free radical scavenger, also a nonsteroidal antiinflammatory agent, and enhances the formation of the endoperoxide, PGH2, and other prostaglandins.

MK-6913
HY-100327 10mg
EUR 7346.4
Description: MK-6913 (Tetrahydrofluoroene 52) is a potent and selective estrogen receptor β agonist.

MK-8617
HY-101023 50mg
EUR 443.73
Description: MK-8617 is an orally active pan-inhibitor of hypoxia-inducible factor prolyl hydroxylase 1-3 (HIF PHD1-3) with an IC50 of 1 nM for PHD2.

MK-6240
HY-101186 50mg
EUR 3847.2

MK-212
HY-101324 Get quote Ask for price
Description: MK-212 (CPP) is a centrally acting 5-HT1C/5-HT2 agonist. MK-212 can stimulate phosphoinositide hydrolysis in cerebral cortex[1].

MK-0343
HY-101869 10 mg
EUR 865.81
Description: MK0343 (MRK-409) is an orally bioavailable GABAA receptor subtype-selective partial agonist. MK0343 is a non-sedating anxiolytic[1].

MK-0608
HY-10244 10 mg
EUR 1190.49
Description: MK-0608 is a potent and orally bioavailable inhibitor of HCV replication in vitro with an EC50 of 0.3 μM (EC90=1.3 μM) in the subgenomic-replicon assay[1].

MK-0674
HY-10290 Get quote Ask for price
Description: MK-0674 is a potent, orally bioavailable and selective cathepsin K inhibitor, with an IC50 of 0.4 nM, shows 1156, 1465, 11857 and 243 fold selectivity over Cat B, Cat F, Cat L and Cat S[1].

MK-3207
HY-10301 5mg
EUR 207.8
Description: MK-3207 is an orally active, highly selective and species-specific CGRP receptor antagonist (for human CGRP receptor: IC50=0.12 nM; Ki=0.024 nM). MK-3207 can be used for migraine studies[1].