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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC0939 | Benmoxin |
Irreversible and nonselective Monoamine_oxidase_inhibitor>monoamine oxidase inhibitor (MAOI)
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| DCC0938 | Benfluron Hydrochloride |
Novel inhibitor of HIV-1 Rev function, also acting as a cytostatic agent with substantial antiretroviral activity
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| DCC0937 | Benc-511 |
Novel potent PI3K inhibitor, suppressing metastasis of non-small cell lung cancer cells by modulating β-catenin/ZEB1 regulatory loop, blocking AKT phosphorylation
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| DCC0936 | Benazepril |
Inhibitor of angiotensin-converting enzyme (ACE); Prodrug of benazeprilat
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| DCC0935 | Benanserin Hydrochloride |
Inhibitor of monoamine oxidase; Anti-serotonin agent
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| DCC0934 | Bemppox |
Novel potent and specific inhibitor of dog gastric lipase (DGL)
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| DCC0933 | Behenyl Palmitate |
Fatty Ester for Lipid Research
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| DCC0932 | beclomethasone 17-monopropionate |
Active metabolite of beclomethasone dipropionate
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| DCC0931 | Bdoia383 |
Novel CBP/p300 Bromodomains inhibitor, binding BRD4 almost identical to SGC-CBP30
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| DCC0930 | Bdm41906 |
Novel specific bona fide EthR-inhibitor, boosting ETH 4 times in an intravenously infected TB mice model
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| DCC0929 | Bdm31827 |
Novel EthR inhibitor and ethionamide booster
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| DCC0928 | Bdm31369 |
Novel activator of ethionamide
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| DCC0927 | Bdm31343 |
Novel EthR inhibitor, boosting antituberculous activity of ethionamide
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| DCC0926 | Bdm14471 |
Potent and selective hydroxamate PfAM1 inhibitor
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| DCC0925 | Bdf-9148 |
Sodium channel enhancer
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| DCC0924 | bddpm |
Novel small molecule PTP1B inhibitor
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| DCC0923 | bd-1008 |
Potent and selective
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| DCC0922 | Bcr-abl-in-y9 |
Novel Bcr-Abl inhibitor, potently inhibited Bcr-AblWT and Bcr-AblT315I kinases with IC 50 of 0.043 μM and 0.17 μM, respectively
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| DCC0921 | bcr-abl Inhibitor 9b |
Novel highly potent inhibitor of breakpoint cluster region-abelson kinase (Bcr-Abl) including the T315I mutant
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| DCC0920 | Bcn-peg6-oh |
Clearing cycloalkyne for click reaction with Azido-Warfarin WN3 or other Azido-containing drugs
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| DCC0919 | Bcn-e-bcn |
Novel Cell-Permeable Probe for the Identification of Protein Sulfenic Acids
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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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