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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC0918 | Bcl6-protac-15 |
Novel B-Cell Lymphoma 6 (BCL6) PROTAC
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| DCC0917 | Bcl-2 Inhibitor S1 |
Novel pan-Bcl-2 family inhibitor, upregulating the BH3-only protein Noxa, which inhibits Mcl-1, inducing autophagy through (ER) stress and disruption of the interaction of Beclin 1 with Bcl-2
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| DCC0916 | Bcl-2 Inhibitor Pdf |
Novel efficient Bcl-2 inhibitor, exhibiting high specificity and stabilizing effect toward G-quadruplexes
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| DCC0915 | Bcl2 Degrader C5 |
Novel potent and selective degrader of Bcl-2
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| DCC0914 | Bc-k01 |
Novel inhibitor of the KRS-67LR interaction
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| DCC0913 | Bche Inhibitor 1 |
Novel butyrylcholinesterase inhibitor (BChEi) for the treatment of canine cognitive dysfunction
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| DCC0912 | bce-001 |
Memory Enhancer and Free Radical Scavenger
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| DCC0911 | Bc1464 |
Novel FBXO7/PINK1 interaction antagonist, abrogating FBXO7 and PINK1 association, leading to increased cellular PINK1 concentrations and activities, and limiting mitochondrial damage
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| DCC0910 | Bc12-4 |
Novel potent inhibitor of IL-2 secretion, demonstrating potent immunomodulatory activity
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| DCC0909 | Bbh-chal |
Novel potent apoptotic inducer of human leukaemia cells by activation of the extrinsic pathway and the generation of reactive oxygen species
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| DCC0908 | Bbb_26580140 |
Novel inhibitor of SARS-CoV-2 main protease (MPro)
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| DCC0906 | bb-78484 |
Potent inhibitor of LpxC
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| DCC0905 | Bb-0322703 |
Novel potent TRPM8 antagonist (IC 50 1.25 ± 0.26 μM)
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| DCC0904 | Bb-0300674 |
Novel inhibitor of prion replication
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| DCC0903 | Bazinaprine |
Selective inhibitor of type A monoamine oxidase with dopaminergic properties
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| DCC0902 | Bay-acc002 |
Novel potent and selective acetyl-CoA carboxylase (ACC) inhibitor, blocking WNT3A lipidation, secretion, and signaling
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| DCC0901 | Bay-acc001 |
Novel potent and selective acetyl-CoA carboxylase (ACC) inhibitor
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| DCC0900 | Bay-9897 |
Negaitve control for BAY-390
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| DCC0899 | Bay-846 |
Novel allosteric MEK inhibitor with long half-lives, high bioavailabilities, low brain penetration potential and high efficacy in a K-Ras-mutated A549 xenograft model
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| DCC0898 | Bay-677 |
Negative control for BAY-678, a potent and selective human neutrophil elastase (HNE) inhibitor
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| DCC0897 | Bay-4900 |
Negative control for BAY-549
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| DCC0896 | Bay-438 |
Novel allosteric MEK inhibitor with long half-lives, high bioavailabilities, low brain penetration potential and high efficacy in a K-Ras-mutated A549 xenograft model
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| DCC0895 | Bay-369 |
Control compound for BAY-598, a novel potent inhibitor of SMYD2
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| DCC0894 | Bay-364 |
Negative control for BAY299
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| DCC0893 | Bay1830839 |
Novel potent interleukin-1 receptor-associated kinase 4 (IRAK4) inhibitor (IC 50 of 3 nM)
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| DCC0892 | Bay-173 |
Negative control for BAY-3153
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| DCC0891 | Bay1143269 |
Novel MNK1 inhibitor, targeting oncogenic protein expression and showing potent anti-tumor activity
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| DCC0890 | Bay-0361 |
Negative control for BAY-091
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| DCC0889 | Bay 27-9955 |
Novel glucagon receptor antagonist
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| DCC0888 | Bax Inhibitor P5 |
Novel cell-permeable synthetic peptide inhibitor of Bax, blocking apoptosis
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