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Lapatinib Ditosylate analytical pure 0.999

Lapatinib ditosylate is a potent EGFR and ErbB2 inhibitor with IC50 of 10.8 and 9.2 nM, respectively.

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PF-04929113 Mesylate analytical pure 0.997

PF-04929113 mesylate is a potent and selective Hsp90 inhibitor with an IC50 of median 50 nM.

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Gefitinib-Based PROTAC 3 analytical pure 0.99

Gefitinib-based PROTAC 3 is a VHL-recruiting PROTAC that induces the degradation of EGFR and EGFR mutants with DC50 of 11.7 nM and 22.3 nM for HCC827 cell (Exon 19 del) and H3255 cell (L858R).

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Palbociclib Isethionate analytical pure 0.999

Palbociclib isethionate is a highly specific inhibitor of Cdk4 (IC50=11 nM) and Cdk6 (IC50=16 nM), having no activity against a panel of 36 additional protein kinases.

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LY2835219 Methanesulfonate analytical pure 0.999

Abemaciclib Methanesulfonate is a potent and selective inhibitor of CDK4 and CDK6 with IC50 of 2 nM and 10 nM respectively, used for the treatment of advanced or metastatic breast cancers.

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Caffeic Acid Phenethyl Ester analytical pure 0.993

Caffeic acid phenethyl ester, a natural product isolated and purified from the barks of Cinnamomum cassia Presl, is a potent and specific inhibitor of NF-κB activation, and also displays antioxidant, immunomodulatory and antiinflammatory activities.

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Glucagon Receptor Antagonists-4 analytical pure 0.981

Glucagon receptor antagonists-4 is an selective antagonist of glucagon receptor.

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Ammonium Pyrrolidine-1-Carbodithioate analytical pure 98%

Ammonium pyrrolidine-1-carbodithioate is a selective NF-κB inhibitor, inhibits translation of nitric oxide synthase mRNA to prevent induction.

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Calcium Chloride

Calcium Chloride is comprised of calcium and chlorine elements. It is highly soluble, colorless crystalline inorganic salt, having the formula CaCl2. Calcium Chloride deduced from limestone as a by-product of the Solvay process. It is widely used for de-icing, to increase water hardness in swimming pools, food sequestrant, and also used in reinforced concrete.

 

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IU1

IU1 is a reversible, small molecule inhibitor of deubiquitination by USP14 that demonstrates an IC50 value of 4-5 μM. IU1 selectively stimulates ubiquitin-dependent protein degradation in vitro at 34 μM and in MEF cells at 50 μM.

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