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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC11800 | G1T38 dihydrochloride |
A novel, potent and selective inhibitor of CDK4/6 with biochemical IC50 of 1 nM and 2 nM for CDK4/cyclin D1 and CDK6/cyclin D3, respectively.
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| DC11799 | G1T38 |
A novel, potent and selective inhibitor of CDK4/6 with biochemical IC50 of 1 nM and 2 nM for CDK4/cyclin D1 and CDK6/cyclin D3, respectively.
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| DC11909 | Ralaniten acetate |
A novel small-molecule inhibitor of androgen receptor (AR) N-terminal domain inhibitor for the treatment of advanced prostate cancer.
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| DC11908 | Ralaniten |
A novel small-molecule inhibitor of androgen receptor (AR) N-terminal domain inhibitor for the treatment of advanced prostate cancer.
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| DC11631 | INCB040093 |
A novel potent, selective, orally available PI3Kδ inhibitor with IC50 of 31 nM.
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| DC11929 | ME-344 |
A novel mitochondrial and mTOR inhibitor with potent anti-cancer activity, inhibits leukemia cell lines with IC50 of 70-260 nM.
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| DC11861 | TAK-441 |
A highly potent, orally active hedgehog signaling (Hh) inhibitor with IC50 of 4.4 nM in Gli-luc reporter assays.
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| DC11932 | GPX-150 |
A doxorubicin analog that demonstrates anti-cancer activity without cardiotoxicity, does not inhibit topoisomerase IIβ activity at 100 uM.
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| DC8944 | 5-Fluorouracil |
5-Fluorouracil is a potent antitumor agent that affects pyrimidine synthesis by inhibiting thymidylate synthetase thus depleting intracellular dTTP pools.
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| DCC-002 | Vinblastine |
>98%,Standard References
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| DCS-091 | Cephalomannine |
>98%,Standard References
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| DCL-047 | Sulforaphane |
>98%,Standard References
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| DCF-001 | Tetrandrine |
>98%,Standard References
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| DCC-073 | Gossypol-acetic acid |
>98%,Standard References
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