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T1839Mps1-IN-2；化合物Mps1-IN-2Mps1-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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T17831Dioxoisoindolin-O-PEG-OMe (MW 2000)；化合物 T17831(1,3-dioxoisoindolin-2-yl)-O-PEG-OMe (MW 2000)；(1,3-di
Dioxoisoindolin-O-PEG-OMe (MW 2000) is a polyethylene glycol (PEG) based PROTAC linker, which finds application in the synthesis of PROTACs[1].
价 格：￥电议型 号：T17831产 地：中国大陆
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T17830Dioxoisoindolin-O-PEG-OH (MW 2000)；化合物 T17830(1,3-dioxoisoindolin-2-yl)-O-PEG-OH (MW 2000)；(1,3-diox
Dioxoisoindolin-O-PEG-OH (MW 2000) is a polyethylene glycol (PEG)-based linker utilized for the synthesis of PROTACs (proteolysis targeting chimeras)[1].
价 格：￥电议型 号：T17830产 地：中国大陆
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T173354-Methyl-4-(pyridin-2-yldisulfanyl)pentanoic acid；化合物 T173354-Methyl-4-(pyridin-2-yldisulfanyl)penta
4-Methyl-4-(pyridin-2-yldisulfanyl)pentanoic acid is a cleavable linker compound employed in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T17335产 地：中国大陆
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T16950Sudoxicam；舒多昔康4-Hydroxy-2-methyl-N-2-thiazolyl-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide；舒多昔康||
Sudoxicam (4-Hydroxy-2-methyl-N-2-thiazolyl-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide) is a reversible antagonist of COX with anti-inflammatory, anti-edema, and antipyretic properties.
价 格：￥电议型 号：T16950产 地：中国大陆
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T16947SU16f；化合物SU16f3-substituted indolin-2-one 16f|||SU-16F|||SU 16F；3-substituted indolin-2-one 16f|||SU
SU16f (3-substituted indolin-2-one 16f) is a potent and selective PDGFRβ inhibitor (IC50s: 10 nM, 140 nM, 2.29 μM for PDGFRβ, PDGFR1, PDGFR2, respectively). Neutralization of PDGFRβ receptor by SU16f blocks the promoting role of GC-MSCs conditioned medium in gastric cancer cell proliferation and migration.
价 格：￥电议型 号：T16947产 地：中国大陆
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T16940STAT5-IN-2；化合物STAT5-IN-2STAT5-IN-2
STAT5-IN-2 is an inhibitor of STAT5 with antileukemic effects (EC50s: 9 μM and 5 μM in K562 and KU812 cells, respectively).
价 格：￥电议型 号：T16940产 地：中国大陆
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T16834S26131；化合物S26131N-[2-[7-[3-[8-(2-acetamidoethyl)naphthalen-2-yl]oxypropoxy]naphthalen-1-yl]ethyl]ace
S26131 (N-[2-[7-[3-[8-(2-acetamidoethyl)naphthalen-2-yl]oxypropoxy]naphthalen-1-yl]ethyl]acetamide) 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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T16577PRMT5-IN-2；化合物 T16577PRMT5-IN-2
PRMT5-IN-2 is an inhibitor of protein arginine methyltransferase 5.
价 格：￥电议型 号：T16577产 地：中国大陆
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T16574Pregnenolone monosulfate sodium salt；化合物 T165743β-Hydroxy-5-pregnen-20-one monosulfate sodium salt；3
Pregnenolone monosulfate sodium salt is a powerful neurosteroid, the main precursor of various steroid hormones including steroid ketones. Pregnenolone monosulfate sodium salt can protect the brain from cannabis intoxication. Pregnenolone monosulfate sodium salt acts as a signaling-specific inhibitor of the cannabinoid CB1 receptor. Pregnenolone monosulfate sodium salt also inhibits the effects of tetrahydrocannabinol (THC) that are mediated by the CB1 receptors.
价 格：￥电议型 号：T16574产 地：中国大陆
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T16277NCT-502；化合物NCT-502N-(4,6-dimethylpyridin-2-yl)-4-[5-(trifluoromethyl)pyridin-2-yl]piperazine-1-carbo
NCT-502 (N-(4,6-dimethylpyridin-2-yl)-4-[5-(trifluoromethyl)pyridin-2-yl]piperazine-1-carbothioamide) 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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T16038Men 10376；化合物 T16038Neurokinin-2 receptor antagonist；Neurokinin-2 receptor antagonist
Men 10376 is a selective antagonist of tachykinin NK-2 receptor. It has a Ki of 4.4 μM for rat small intestine NK-2 receptor.
价 格：￥电议型 号：T16038产 地：中国大陆
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T16028IMB-XH1；7-[(2-吡啶基氨基)-2-噻吩基甲基]-8-喹啉醇Mcl1-IN-2；Mcl1-IN-2|||7-[(2-吡啶基氨基)-2-噻吩基甲基]-8-喹啉醇
IMB-XH1 (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-212320；化合物LDN-212320LDN-0212320|||LDN/OSU-0212320|||OSU-0212320；LDN-0212320|||LDN/OSU-0212320|||
LDN-212320 (OSU-0212320) 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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T15696NEP-IN-2；化合物 T15696NEP-IN-2
NEP-IN-2 is an inhibitor of neutral endopeptidase. It also is used in the research of proliferation in atherosclerosis, restenosis.
价 格：￥电议型 号：T15696产 地：中国大陆
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T15579INDY；化合物INDY1-(3-ethyl-5-hydroxy-1,3-benzothiazol-2-ylidene)propan-2-one；1-(3-ethyl-5-hydroxy-1,3-be
INDY is an ATP-competitive inhibitor of Dyrk1A and Dyrk1B with IC50s of 0.24 μM and 0.23 μM and a Ki of 0.18 μM for Dyrk1A ATP pocket, respectively.
价 格：￥电议型 号：T15579产 地：中国大陆
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T15559TBK1/IKKε-IN-2；化合物TBK1/IKKε-IN-2TBK1/IKKε-IN-2
TBK1/IKKε-IN-2 is a dual inhibitor of TBK1 and IKKε.
价 格：￥电议型 号：T15559产 地：中国大陆
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T15271Denifanstat；化合物FASN-IN-2FASN-IN-2|||TVB2640|||TVB-2640；FASN-IN-2|||TVB2640|||TVB-2640
Denifanstat (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-2；4-(3-氯-4-氟苯氨基)-7-甲氧基喹唑啉-6-醇O-Desmorpholinopropyl Gefitinib；O-Desmorpholinopropyl Gefitinib
FAAH-IN-2 (O-Desmorpholinopropyl Gefitinib) 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-224；四硫钼酸二胆碱Bis(choline)tetrathiomolybdate；四硫钼酸二胆碱|||Bis(choline)tetrathiomolybdate
ATN-224 (Bis(choline)tetrathiomolybdate) 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
