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T19784DBTNSC-701994；NSC 701994；NSC701994；4,7-Bis(thiophen-2-yl)benzo[c][1,2,5]thiadiazole
DBT is a far-red/near-infrared fluorescent probe for specific in vitro and in vivo imaging of tumor-associated proteins.
价 格：￥电议型 号：T19784产 地：中国大陆
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T1944LDN-214117LDN214117；LDN 214117
LDN-214117 is a potent and selective ALK2 inhibitor.
价 格：￥电议型 号：T1944产 地：中国大陆
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T1900LDN-212854LDN212854；BMP Inhibitor III
LDN-212854, a novel BMP inhibitor, exhibits greater selectivity for BMP versus the TGF-β type I receptors; possesses differences towards ALK2(IC50=1.3 nM) versus ALK1/3 compared to other inhibitors.
价 格：￥电议型 号：T1900产 地：中国大陆
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T18529PDEC-NB4-Nitrophenyl 2-(Pyridin-2-Yldisulfanyl)Ethyl Carbonate
PDEC-NB is a disulfide cleavable linker used for the antibody-drug conjugate?(ADC).
价 格：￥电议型 号：T18529产 地：中国大陆
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T1839Mps1-IN-2
Mps1-IN-2 is a potent, selective and ATP-competitive dual Mps1/Plk1 inhibitor.
价 格：￥电议型 号：T1839产 地：中国大陆
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T16834S26131N-[2-[7-[3-[8-(2-acetamidoethyl)naphthalen-2-yl]oxypropoxy]naphthalen-1-yl]ethyl]acetamide
S26131 behaves as an antagonist on MT1 and MT2 receptors with Ki of 0.5 and 112 nM respectively.
价 格：￥电议型 号：T16834产 地：中国大陆
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T16277NCT-502N-(4,6-dimethylpyridin-2-yl)-4-[5-(trifluoromethyl)pyridin-2-yl]piperazine-1-carbothioamide
NCT-502 is a human phosphoglycerate dehydrogenase inhibitor, cytotoxic to PHGDH-dependent cancer cells. It decreases glucose-derived serine production and it has an IC50 of 3.7 μM against PHGDH.
价 格：￥电议型 号：T16277产 地：中国大陆
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T16028IMB-XH1Mcl1-IN-2；7-[(2-吡啶基氨基)-2-噻吩基甲基]-8-喹啉醇
Mcl1-IN-2 is a myeloid cell factor 1 (Mcl-1) inhibitor.
价 格：￥电议型 号：T16028产 地：中国大陆
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T15728LDN-212320OSU-0212320；LDN/OSU-0212320；LDN-0212320
LDN-212320 is a glutamate transporter EAAT2 activator. It also enhances EAAT2 levels by > 6 fold at concentrations < 5 μM after 24 h.
价 格：￥电议型 号：T15728产 地：中国大陆
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T15271DenifanstatTVB-2640；TVB2640；FASN-IN-2
FASN-IN-2 is a Fatty Acid Synthase (FASN) inhibitor(IC50 of 0.052 μM and an EC50 of 0.072 μM),with potential antineoplastic activity.
价 格：￥电议型 号：T15271产 地：中国大陆
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T15268FAAH-IN-2O-Desmorpholinopropyl Gefitinib；4-(3-氯-4-氟苯氨基)-7-甲氧基喹唑啉-6-醇
FAAH-IN-2 is a potent inhibitor of FAAH(fatty acid amide hydrolase).
价 格：￥电议型 号：T15268产 地：中国大陆
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T14341ATN-224Bis(choline)tetrathiomolybdate；四硫钼酸二胆碱
ATN-224 inhibits SOD1 activity in endothelial cells, an effect that is dose dependent with an IC50 of 17.5±3.7 nM. ATN-224 is an oral Cu2+/Zn2+-superoxide dismutase 1 (SOD1) inhibitor.
价 格：￥电议型 号：T14341产 地：中国大陆
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T13194CSF1R-IN-2
CSF1R-IN-2 is an oral-active SRC, MET and c-FMS inhibitor (IC50s: 0.12 nM, 0.14 nM and 0.76 nM for SRC, MET and c-FMS respectively).
价 格：￥电议型 号：T13194产 地：中国大陆
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T13115Telomerase-IN-2Telomerase inhibitor 2；端粒酶抑制剂2
Telomerase-IN-2 shows potent inhibitory activity against telomerase by decreasing the expression of dyskerin (IC50: 0.89??M).
价 格：￥电议型 号：T13115产 地：中国大陆
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T12919SIRT-IN-2
SIRT-IN-2 is a potent SIRT1/2/3 inhibitor(IC50s of 4, 1, 7 μM, respectively).
价 格：￥电议型 号：T12919产 地：中国大陆
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T12894SGN-2FF
SGN-2FF is an oral fucosyltransferase inhibitor with antitumor activity.
价 格：￥电议型 号：T12894产 地：中国大陆
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T12747ROCK2-IN-2
ROCK2-IN-2 is a selective inhibitor of ROCK2 (IC50 of <1 μM).
价 格：￥电议型 号：T12747产 地：中国大陆
