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T28498rac-CCT-250863；化合物 T28498rac-CCT-250863
Rac-CCT-250863, a potent Nek2 inhibitor, exhibits selectivity for Nek2 over PLK1, MPS1, Cdk2 and Aurora A.
价 格：￥电议型 号：T28498产 地：中国大陆
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T26969CCT365623；化合物CCT365623CCT-365623|||CCT 365623；CCT-365623|||CCT 365623
CCT365623 is an orally bioavailable Lysyl Oxidase inhibitor with good anti-LOX potency, selectivity, pharmacokinetic properties, as well as anti-metastatic efficacy.
价 格：￥电议型 号：T26969产 地：中国大陆
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T26968CCT036477；化合物 T26968CCT 036477|||CCT-036477；CCT 036477|||CCT-036477
CCT036477 is a selective inhibitor of wingless-type MMTV integration site family dependent transcription. CCT036477reduces the transcriptional activity of the T-cell factor and lymphoid enhancer factor transcription factor family at the ?-catenin level.
价 格：￥电议型 号：T26968产 地：中国大陆
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T2611CCT 137690；化合物CCT137690CCT137690；CCT137690
CCT 137690 is a highly specific and oral-available aurora kinase inhibitor, for aurora A(IC50=15 nM ), B(IC50=25 nM) and C(IC50=19 nM).
价 格：￥电议型 号：T2611产 地：中国大陆
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T25215CCT077791；化合物CCT077791CCT 077791|||CCT-077791；CCT 077791|||CCT-077791
CCT077791 is a potent inhibitor of p300 and PCAF histone acetyltransferase activity for cancer research.
价 格：￥电议型 号：T25215产 地：中国大陆
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T23865CCT-271850；化合物 T23865MPS1-IN-77|||MPS1IN77|||CCT271850|||CCT 271850|||MPS1 IN 77；MPS1-IN-77|||MPS1IN
CCT-271850 is an inhibitor of the spindle checkpoint function of Monospindle 1.
价 格：￥电议型 号：T23865产 地：中国大陆
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T2268VER49009；化合物VER-49009CCT0129397|||VER 49009|||VER-49009；CCT0129397|||VER 49009|||VER-49009
VER49009 (CCT0129397) is an effective HSP90 inhibitor(IC50 =25 nM, Kd=78 nM).
价 格：￥电议型 号：T2268产 地：中国大陆
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T22633CCT251545 analogue, Compound 51；化合物 T22633CCT251545 analogue, Compound 51
CCT251545 analog is a potent and selective CDK8/19 inhibitor (IC50: 5.1 nM and 5.6 nM, respectively). Mediator complex-associated kinases CDK8 and CDK19 are involved in the regulation of multiple transcription pathways. CDK8 plays as an oncogene in gastric and colorectal cancers through the activation of WNT signaling.
价 格：￥电议型 号：T22633产 地：中国大陆
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T21872CCT018159；化合物CCT018159CCT018159
CCT018159 is a 3,4-diarylpyrazole resorcinol, an ATP-competitive HSP90ATPase inhibitor that inhibits human Hsp90β and yeast Hsp90 with IC50s of 3.2 and 6.6 μM, respectively.CCT018159 inhibits key endothelial and tumor cell functions associated with invasion and angiogenesis. CCT018159 caused cellular inhibition associated with G1 phase block and induced apoptosis.
价 格：￥电议型 号：T21872产 地：中国大陆
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T21685CCT 031374 hydrobromide；化合物CCT 031374 hydrobromideCCT 031374 hydrobromide
CCT 031374 hydrobromide is a TCF/β-catenin inhibitor with antitumor activities.
价 格：￥电议型 号：T21685产 地：中国大陆
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T1927CCT007093；化合物CCT007093CCT007093
CCT007093 is an effective PPM1D (WIP1) inhibitor (IC50: 8.4 μM).
价 格：￥电议型 号：T1927产 地：中国大陆
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T14908CCT367766；化合物CCT367766CCT367766
CCT367766 is a potent, PROTAC-based, third-generation, iso-functional pirin-targeted protein degradation probe (PDP) that depletes pirin expression at low concentrations.CCT367766 has an IC50 value of 490 nM for the CRBN-DDB1 complex.CCT367766 has a good affinity for recombinant pirin and CRBN. CCT367766 has a good affinity for recombinant pirin and CRBN, with Kd values of 55 nM and 120 nM, respectively. cct367766 is a potent orally active protein that reduces the expression of pirin at low conc
价 格：￥电议型 号：T14908产 地：中国大陆
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T14907CCT251545；化合物CCT251545CCT251545
CCT251545 is an potent and oral-bioavailable WNT signaling inhibitor(IC50 of 5 nM in 7dF3 cells).
价 格：￥电议型 号：T14907产 地：中国大陆
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T14906CCT251455；化合物 T14906CCT251455
CCT251455 is an inhibitor of mitotic kinase monopolar spindle 1 (MPS1; IC50: 3 nM).
价 格：￥电议型 号：T14906产 地：中国大陆
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T14905CCT251236；化合物 CCT251236CCT251236
CCT251236 is a cell-based phenotypic high-throughput screening (HTS) chemical probe developed to screen for inhibitors of the HSF1 stress pathway.CCT251236 exhibits antimyeloma activity and inhibits HSF1.
价 格：￥电议型 号：T14905产 地：中国大陆
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T14904CCT244747；化合物 T14904CCT244747
CCT244747 is a CHK1 inhibitor (IC50: 7.7 nM) and also abrogates G2 checkpoint (IC50: 29 nM).
价 格：￥电议型 号：T14904产 地：中国大陆
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T14903CCT129957；化合物CCT129957CCT129957
CCT129957 is a novel and potent phospholipase C-γ (PLC-γ) inhibitor with an IC50 of about 3 μM and a GC50 of 15 μM.CCT129957 exhibits anticancer activity and inhibits Ca2+ release in squamous cells.
价 格：￥电议型 号：T14903产 地：中国大陆
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T14902CCT020312；化合物CCT020312CCT020312
CCT020312 is a selective activator of EIF2AK3 and PERK. CCT020312 durably inhibits cell proliferation and elicits the phosphorylation of EIF2A.
价 格：￥电议型 号：T14902产 地：中国大陆
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T14901CCT-251921；化合物CCT-251921CCT-251921
CCT-251921 is a potent, selective, and orally bioavailable CDK8 inhibitor (IC50: 2.3 nM).
价 格：￥电议型 号：T14901产 地：中国大陆
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T10719CCT365623 hydrochloride；化合物 T10719CCT365623 hydrochloride
CCT365623 hydrochloride is an orally active inhibitor of lysyl oxidase (LOX) (IC50: 0.89 μM). It suppresses EGFR (pY1068) and AKT phosphorylation driven by EGF.
价 格：￥电议型 号：T10719产 地：中国大陆
