Classified by application
All Products
Signaling Pathways
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Neuro Signaling Pathway
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Protease/Metabolic Enzyme
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Research Areas
- Metabolic Disease
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Nature products
Antibodies
Peptides
Catalysts
Impurities
Intermediate
- Amino acid
- Ammonia Series
- Pyridazine Series
- Quinazoline
- Nucleoside Series
- Azaindazole
- Pyrazole Series
- Quinoline Series
- Pyrimidine Series
- Boric acid
- Pyrrole Series
- Thiophene Series
- Saccharide
- Azaindole
- Indole Series
- Piperidine Series
- Indazole Series
- Heterocyclic Series
- Pyridine Series
- Benzene Series
Raw Materials
CDK
Chemical Structure | Cat. No. | Product Name | CAS No. |
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BCP24646 | Fascaplysin New | 114719-57-2 |
Fascaplysin is an inhibitor of cyclin D kinase 4/ cyclin D1 (IC50 = 0.35 μM). Fascaplysin induces caspase mediated crosstalk between apoptosis and autophagy through the inhibition of PI3K/AKT/mTOR signaling cascade in human leukemia HL-60 cells.
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BCP33291 | (-)-BAY-1251152 New | 1610358-59-2 |
(-)-BAY-1251152 is an enanthiomer of BAY-1251152 with rotation (-).
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BCP36919 | KB-0742 hydrochloride New | 2416874-75-2 |
KB-0742 dihydrochloride is a potent, selective and orally inhibitor of CDK9.
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BCP48019 | LY3143921 New | 1627696-52-9 |
LY3143921 is a potent and selective CDC7 kinase inhibitor.
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BCP48020 | LY3143921 hydrate New | 1627696-53-0 |
LY3143921 hydrate is an orally administered ATP-competitive CDC7 inhibitor.
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BCP48567 | SRX3177 New | 2241237-51-2 |
SRX3177 is a novel potent triple action inhibitor, targeting BRD, PI3K, and CDK.
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BCP48519 | GSK-3/CDK5/CDK2-IN-1 New | 395074-72-3 |
GSK-3/CDK5/CDK2-IN-1, an imidazole derivative, is an inhibitor of cdk5, cdk2, and GSK-3 extracted from patent WO2002010141A1, example 9a.
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BCP47151 | HQ461 New | 1226443-41-9 |
HQ461 is a molecular glue that promotes CDK12-DDB1 interaction to trigger cyclin K degradation.
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BCP46934 | Cdk2/9 Inhibitor New | 507487-89-0 |
Cdk2/9 Inhibitor is a small molecule/inhibitor primarily used for phosphorylation and dephosphorylation applications.
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BCP46783 | Aminopurvalanol A New | 220792-57-4 |
Aminopurvalanol A selectively inhibits TgCK1alpha. Aminopurvalanol A also acts as a cell-permeable cyclin-dependent kinase inhibitor, inhibiting cdk1/cyclin B, cdk2/cyclin A, cdk2/cyclin E, and cdk5/p35.
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