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YK-4-279
Description of:YK-4-279
YK-4-279(cas:1037184-44-3)is a ETV1 inhibitor, which inhibitor protein-protein interactions between ES-FLI1 and RHA.YK-...
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COH29
Description of:COH29(cas:1190932-38-7)
COH29 is a potent ribonucleotide reductase (RNR) inhibitor with anticancer activity with an IC50 of 8 &m...
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TMP195
Description of:TMP195(cas:1314891-22-9)
TMP195 is a potent and selective class IIa HDAC inhibitor with IC50s of 59 nM, 60 nM, 26 nM and 15 nM f...
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TMP269
Chemical Information
M.Wt
514.52
Storage
Please store the product under ...
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Nexturastat A
Chemical Information
M.Wt
341.4
Storage
Please store the product under t...
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Valrubicin
With a mechanism of action that appears to differ from doxorubicin, valrubicin is converted intracytoplasmically into N-trifluoroacetyladriamycin, whi...
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Ixabepilone (BMS -247550)
Ixabepilone (BMS-247550) is an orally bioavailable semisynthetic analogue of epothilone B with antineoplastic activity. Ixabepilone binds to tubulin a...
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Pirarubicin
Pirarubicin is an anthracycline agent. Pirarubicin intercalates into DNA and interacts with topoisomerase II, thereby inhibiting DNA replication and r...
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EPZ 5676
EPZ-5676 is an S-adenosyl methionine (SAM) competitive inhibitor of DOT11L with Ki of 80 pM. -EPZ-5676 is a small molecule inhibitor of histone methyl...
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Amrubicin
Amrubicin intercalates into DNA and inhibits the activity of topoisomerase II, resulting in inhibition of DNA replication, and RNA and protein synthes...
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M 344
M344 is a potent HDAC inhibitor with IC50 of 100 nM. M344 induces terminal cell differentiation and causes an increase in hyperacetylated histone H4. ...
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Tacedinaline (CI 994, PD 123654)
CI994 (Tacedinaline) is an anti-cancer drug which inhibits HDAC1 with IC50 of 0.57 μM. Tacedinaline inhibits histone deacetylation, which may resul...
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Daunorubicin (Daunomycin)
Daunorubicin HCl (Daunomycin) inhibits both DNA and RNA synthesis and inhibits DNA synthesis with Ki of 0.02 μM. Daunorubicin is a DNA intercalatin...
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Apoptosis
DHFR
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