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T62891α-Glucosidase-IN-19；化合物 α-Glucosidase-IN-19α-Glucosidase-IN-19
Alpha-Glucosidase-IN-19 (Compound 6B) is an orally active alpha-glucosidase inhibitor (IC50: 3.63 μM) with antidiabetic effects.
价 格：￥电议型 号：T62891产 地：中国大陆
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T62890OXPHOS-IN-1；化合物 OXPHOS-IN-1OXPHOS-IN-1
OXPHOS-IN-1 (compound 2) is an inhibitor of oxidative phosphorylation (OXPHOS) and inhibits the growth of MIA PaCa-2 cells (IC50: 2.34 μM) and BxPC-3 cells (IC50: 13.82 μM).
价 格：￥电议型 号：T62890产 地：中国大陆
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T6289Dovitinib；多韦替尼TKI258|||CHIR-258；TKI258|||多韦替尼|||CHIR-258|||度维替尼
Dovitinib (CHIR-258) (TKI258, CHIR258) is a multitargeted RTK inhibitor, mostly for class III (FLT3/c-Kit, IC50: 1/2 nM), also effective to class IV (FGFR1/3) and class V (VEGFR1-4) RTKs (IC50: 8-13 nM), less potent to EGFR, InsR, EphA2, c-Met, IGF-1R, Tie2, and HER2.
价 格：￥电议型 号：T6289产 地：中国大陆
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T62889Fenoverine；化合物 FenoverineFenoverine
Fenoverine is an antispasmodic drug that inhibits calcium channel currents and can cause rhabdomyolysis.
价 格：￥电议型 号：T62889产 地：中国大陆
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T62888Influenza A virus-IN-7；化合物 Influenza A virus-IN-7Influenza A virus-IN-7
Influenza A virus-IN-7 (compound 16r) is a potent, orally active inhibitor of influenza A virus (IC50: 3.43 μM, CC50>100 μM). Influenza A virus-IN-7 is an anti-IAV agent with low cytotoxicity and inhibits viral RNA transcription and replication.
价 格：￥电议型 号：T62888产 地：中国大陆
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T62887Topoisomerase II inhibitor 4；化合物 Topoisomerase II inhibitor 4Topoisomerase II inhibitor 4
Topoisomerase II inhibitor 4 (compound E17) is a potent inhibitor of topoisomerase II. Topoisomerase II inhibitor 4 has antitumour effects, blocking the cell cycle in the G2/M phase, inhibiting the proliferation of cancer cells and exhibiting cytotoxicity. It inhibits the proliferation of cancer cells and exhibits cytotoxicity.
价 格：￥电议型 号：T62887产 地：中国大陆
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T62886S1PR1 agonist 2；化合物 S1PR1 agonist 2S1PR1 agonist 2
S1PR1 agonist 2 is a potent agonist of S1PR1. S1PR1 agonist 2 has potential for studies of autoimmune diseases.
价 格：￥电议型 号：T62886产 地：中国大陆
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T62885GABAA receptor modulator-2；化合物 GABAA?receptor?modulator-2GABAA receptor modulator-2
GABAA receptor modulator-2 (Compound 20) is a selective, orally active α5-GABAAR negative conformation modulator (Ki: 4.1 nM). gABAA receptor modulator-2 exhibits high metabolic stability and a good central nervous system safety profile.
价 格：￥电议型 号：T62885产 地：中国大陆
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T62884eIF4A3-IN-6；化合物 eIF4A3-IN-6eIF4A3-IN-6
eIF4A3-IN-6 is a potent inhibitor of eukaryotic initiation factor 4A (eIF4A) (e.g. eIF4AI and eIF4AII). eIF4A3-IN-6 has the potential to be investigated in eIF4A-dependent diseases, including cancer.
价 格：￥电议型 号：T62884产 地：中国大陆
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T62883BRD4 Inhibitor-23；化合物 BRD4 Inhibitor-23BRD4 Inhibitor-23
BRD4 Inhibitor-23 is a potent, orally active BRD4 inhibitor that acts on BRD4 BD-1 (IC50: 6.21 nM) and BRD4 BD-2 (IC50: 1.44 nM).
价 格：￥电议型 号：T62883产 地：中国大陆
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T62882Ezurpimtrostat hydrochloride；Ezurpimtrostat 盐酸盐GNS561 hydrochloride；GNS561 hydrochloride
Ezurpimtrostat hydrochloride (GNS561 hydrochloride) is an orally available palmitoyl protein thioesterase-1 inhibitor with antifibrotic, antiviral, and anticancer effects that blocks cancer cell proliferation by interacting with palmitoyl protein thioesterase to inhibit late autophagy and dose-dependently increase lysosomal accumulation.
价 格：￥电议型 号：T62882产 地：中国大陆
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T62881(R)-BAY-899；化合物 (R)-BAY-899(R)-BAY-899
(R)-BAY-899 is an R-isomer of BAY-899. BAY-899 is a selective, orally active luteinizing hormone receptor (LH-R) antagonist that acts on hLH (human LH) (IC50: 185 nM) and rLH (rat LH) (IC50: 46 nM).
价 格：￥电议型 号：T62881产 地：中国大陆
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T62880Antibacterial agent 99；化合物 Antibacterial agent 99Antibacterial agent 99
Antibacterial agent 99 (compound 7b) is an effective antibacterial agent. antibacterial agent 99 has significant antibacterial and antifungal effects and no haemolytic activity.
价 格：￥电议型 号：T62880产 地：中国大陆
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T6287LTariquidar dimesylate；化合物 T6287LD 06008|||XR9576|||D06008|||XR 9576|||Tariquidar dimesilate|||XR-957
Tariquidar is a P-glycoprotein inhibitor undergoing research as an adjuvant against multidrug resistance in cancer. Tariquidar non-competitively binds to the p-glycoprotein transporter, thereby inhibiting transmembrane transport of anticancer drugs.
价 格：￥电议型 号：T6287L产 地：中国大陆
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T62879OncoFAP；化合物 OncoFAPOncoFAP
OncoFAP is an ultra-high affinity fibroblast activating protein (FAP) ligand with potential tumour targeting.
价 格：￥电议型 号：T62879产 地：中国大陆
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T62878Zalunfiban dihydrochloride；化合物 Zalunfiban dihydrochlorideZalunfiban dihydrochloride
Zalunfiban (RUC-4) dihydrochloride is a selective and potent platelet αIIbβ3 antagonist with an IC50 value of 45 nM. Zalunfiban dihydrochloride can be used to study myocardial infarction.
价 格：￥电议型 号：T62878产 地：中国大陆
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T62877RET-IN-7；化合物 RET-IN-7RET-IN-7
RET-IN-7 exhibits strong inhibitory effects against RET kinase in vitro and shows significant efficacy in treating RET-driven tumor xenografts in mice through multiple-day dosing.
价 格：￥电议型 号：T62877产 地：中国大陆
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T62876MONIRO-1；化合物 MONIRO-1MONIRO-1
MONIRO-1 is a T- and N-type calcium channel blocker that acts on hCav2.2 (IC50: 34 μM), hCav3.1 (IC50: 3.3 μM), hCav3.2 (IC50: 1.7 μM) and hCav3.3 (IC50: 7.2 μM).
价 格：￥电议型 号：T62876产 地：中国大陆
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T62875NF-κB-IN-3；化合物 NF-κB-IN-3NF-κB-IN-3
NF-κB-IN-3 (Compound 2) is an NF-κB inhibitor (IC50: 0.70 μM) and can be used as an anti-tumour agent.
价 格：￥电议型 号：T62875产 地：中国大陆
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T62874(Z)-Fluoxastrobin；化合物 (Z)-Fluoxastrobin(Z)-Fluoxastrobin
(Z)-Fluoxastrobin is a fungicide that exhibits effective control of important seed and soil-borne pathogens.
价 格：￥电议型 号：T62874产 地：中国大陆
