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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC5075 | Tdcipp |
Hepatotoxicity inducer, significantly up-regulating the expression of genes involved in endoplasmic reticulum stress and Toll-like receptor (TLR) pathway
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| DCC5074 | Td-5471 Hydrochloride |
Novel long-acting β 2 -adrenoceptor agonist
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| DCC5073 | Td-428 |
Novel potent BET protein degrader, inhibiting cell proliferation due to suppressed C-MYC transcription
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| DCC5072 | Td-1211 |
Novel selective opioid receptor antagonist at all three receptor types
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| DCC5071 | Td-106 |
Novel IKZF1/3 degrader, inhibiting the proliferation of multiple myeloma cells in vitro as well as in vivo
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| DCC5070 | Td-004 |
Novel degrader of the anaplastic lymphoma kinase (ALK) fusion protein, effectively inducing ALK degradation and inhibiting the growth of ALK fusion positive cell lines, SU-DHL-1 and H3122, significantly reducing the tumor growth in H3122 xenograft model
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| DCC5069 | T-cupm |
Sorafenib analogue, retaining cytotoxicity similar to sorafenib in various human cancer cell lines and strongly inhibiting growth in the NCI-60 cell line panel
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| DCC5068 | Tc-t 6000 |
Potent equilibrative nucleoside transporter 4 (ENT4) inhibitor
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| DCC5067 | Tcs-401 |
Insulin receptor sensitizing agent; Selective inhibitor of protein-tyrosine phosphatase 1B (PTP1B)
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| DCC5066 | Tcs-3035 |
Novel GPR35 agonist
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| DCC5064 | Tcs2312 |
Novel potent and selective CHK1 kinase inhibitor
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| DCC5063 | Tc-s 7005 |
Potent and selective polo-like kinase 2 (PLK2) inhibitor
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| DCC5062 | Tc-ot-39 |
Nonpeptide partial agonist of oxytocin (OT) and vasopressin V2 receptors
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| DCC5061 | Tcn-237 Dihydrochloride |
Highly potent NR2B-selective NMDA receptor antagonist
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| DCC5060 | Tcmdc-135051 Tfa Salt |
Novel Inhibitor of the malaria parasite protein kinase CLK3, inhibiting the development of liver-stage parasites, killing asexual blood-stage parasites at the trophozoite and schizont stages of the erythrocytic cycle, blocking the development of sexual ga
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| DCC5059 | tcmdc-125802 |
Antimalarial; Novel inhibitor of HepG2
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| DCC5058 | Tc-i 2014 |
Potent TRPM8 antagonist, exhibiting antiallodynic properties in pain models
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| DCC5056 | Tch-013 |
Non-competitive modulator of the proteasome inducing apoptosis a panel of myeloma and leukemia cell lines
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| DCC5055 | Tc-g1004 |
Potent and selective antagonist of adenosine A2A receptors
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| DCC5053 | Tc-e 5006 |
Novel orally bioavailableγ-secretase modulator, reducing Aβ42 levels
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| DCC5052 | tc-c-14g |
Potent CB1 receptor inverse agonist
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| DCC5051 | Tc-aqp1-1 |
Aquaporin 1 (AQP1) channel blocker
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| DCC5050 | Tc-ac28 |
Novel potent and selective ligand of Brd2(2)
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| DCC5049 | Tc299423 |
Novel agonist for nicotinic acetylcholine receptors (nAChRs), modestly selectively targeting α6β2 subtype
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| DCC5048 | Tbz-19 |
Novel anti-angiogenesis and vascular disrupting agent, exhibiting moderate inhibitory cell proliferation activity
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| DCC5047 | Tbz-07 |
Novel anti-angiogenesis and vascular disrupting agent, exhibiting moderate inhibitory cell proliferation activity
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| DCC5046 | Tbk1 Inhibitor-1 |
Novel TBK1/IKKε inhibitor
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| DCC5045 | Tbe-31 |
Highly potent activator of Nrf2; Potent phase 2 cytoprotective pathway inducer and liver carcinogenesis blocker
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| DCC5044 | Tbdps-chc |
Novel potent MCT1 inhibitor, exhibiting good single agent anticancer efficacy properties
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| DCC5043 | Tbbl-0000316 |
Novel antibiotic against Mycobacterium tuberculosis (Mtb), potently killing replicating, virulent Mtb H37Rv in a clavulanate-dependent manner
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