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Add to Cart The item has been addedK650163-25mgKAT6-IN-1 is a potent KAT6 inhibitor. KAT6-IN-1 can be used in research of cancer. -
Add to Cart The item has been addedK650163-50mgKAT6-IN-1 is a potent KAT6 inhibitor. KAT6-IN-1 can be used in research of cancer. -
Add to Cart The item has been addedK650163-5mgKAT6-IN-1 is a potent KAT6 inhibitor. KAT6-IN-1 can be used in research of cancer. -
Add to Cart The item has been addedK649087-10mgKB-0742 dihydrochloride is a potent, selective and orally active CDK9 inhibitor with an IC 50 of 6 nM for CDK9/cyclin T1 . KB-0742 dihydrochloride is selective for CDK9/cyclin T1 with >:50-fold selectivity over other CDK kinases. KB-0742 -
Add to Cart The item has been addedK649087-1mgKB-0742 dihydrochloride is a potent, selective and orally active CDK9 inhibitor with an IC 50 of 6 nM for CDK9/cyclin T1 . KB-0742 dihydrochloride is selective for CDK9/cyclin T1 with >:50-fold selectivity over other CDK kinases. KB-0742 -
Add to Cart The item has been addedK649087-25mgKB-0742 dihydrochloride is a potent, selective and orally active CDK9 inhibitor with an IC 50 of 6 nM for CDK9/cyclin T1 . KB-0742 dihydrochloride is selective for CDK9/cyclin T1 with >:50-fold selectivity over other CDK kinases. KB-0742 -
Add to Cart The item has been addedK649087-50mgKB-0742 dihydrochloride is a potent, selective and orally active CDK9 inhibitor with an IC 50 of 6 nM for CDK9/cyclin T1 . KB-0742 dihydrochloride is selective for CDK9/cyclin T1 with >:50-fold selectivity over other CDK kinases. KB-0742 -
Add to Cart The item has been addedK649087-5mgKB-0742 dihydrochloride is a potent, selective and orally active CDK9 inhibitor with an IC 50 of 6 nM for CDK9/cyclin T1 . KB-0742 dihydrochloride is selective for CDK9/cyclin T1 with >:50-fold selectivity over other CDK kinases. KB-0742 -
Add to Cart The item has been addedK650997-5mgKB-5492 anhydrous is a potent and selective inhibitor of sigma receptor , inhibits specific [ 3 H]1,3-di(2-tolyl)guanidine (DTG) binding to the sigma receptor with an IC 50 of 3.15 μM. KB-5492 anhydrous is an anti-ulcer agentIn VitroKB-5492 -
Add to Cart The item has been addedK648251-100mgKB-5492 free base is a potent and selective inhibitor of sigma receptor , inhibits specific [ 3 H]1,3-di(2-tolyl)guanidine (DTG) binding to the sigma receptor with an IC 50 of 3.15 μM. KB-5492 free base is an anti-ulcer agentIn VitroKB-5492 -
Add to Cart The item has been addedK648251-10mgKB-5492 free base is a potent and selective inhibitor of sigma receptor , inhibits specific [ 3 H]1,3-di(2-tolyl)guanidine (DTG) binding to the sigma receptor with an IC 50 of 3.15 μM. KB-5492 free base is an anti-ulcer agentIn VitroKB-5492 -
Add to Cart The item has been addedK648251-25mgKB-5492 free base is a potent and selective inhibitor of sigma receptor , inhibits specific [ 3 H]1,3-di(2-tolyl)guanidine (DTG) binding to the sigma receptor with an IC 50 of 3.15 μM. KB-5492 free base is an anti-ulcer agentIn VitroKB-5492
