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T62425sEH inhibitor-3；化合物 sEH inhibitor-3sEH inhibitor-3
sEH inhibitor-3 (compound 35) is a potent, orally active inhibitor of soluble epoxide hydrolase (sEH) that acts on human sEH (Ki: 0.75 nM).
价 格：￥电议型 号：T62425产 地：中国大陆
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T62353HIV-1 inhibitor-33；化合物 HIV-1 inhibitor-33HIV-1 inhibitor-33
HIV-1 inhibitor-33 (compound 5n) is a potent and selective HIV-1 inhibitor that acts on HIV-1 (EC50: 8.6 nM), MT-4 cells (CC50: 18 μM). HIV-1 inhibitor-33 can be used in the study of AIDS.
价 格：￥电议型 号：T62353产 地：中国大陆
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T62070HIV-1 inhibitor-31；化合物 HIV-1 inhibitor-31HIV-1 inhibitor-31
HIV-1 inhibitor-31 (compound 4) is a potent inhibitor of HIV-1. HIV-1 inhibitor-31 can be used in the study of AIDS.
价 格：￥电议型 号：T62070产 地：中国大陆
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T6192Alogliptin；阿格列汀SYR-322；SYR-322|||阿格列汀|||阿洛利停
Alogliptin (SYR-322)(SYR-322) is a potent, selective inhibitor of DPP-4 with IC50 of <10 nM, exhibits greater than 10, 000-fold selectivity over DPP-8 and DPP-9.
价 格：￥电议型 号：T6192产 地：中国大陆
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T61801HIV-1 inhibitor-35；化合物 HIV-1 inhibitor-35HIV-1 inhibitor-35
HIV-1 inhibitor-35 (compound 74) is a highly potent inhibitor of the HIV-1 virus, exhibiting EC50 values of 80 nM and 70 nM for LTR and CMV, respectively, in HEK293 cells. Additionally, HIV-1 inhibitor-35 demonstrates inhibitory activity against HepG2 liver cancer cells, with a CC50 value of 40 nM. Moreover, HIV-1 inhibitor-35 shows promise as a potential HIV-1 latency reversing agent [1].
价 格：￥电议型 号：T61801产 地：中国大陆
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T61670HIV-1 inhibitor-38；化合物 HIV-1 inhibitor-38HIV-1 inhibitor-38
HIV-1 inhibitor-38 (Compound 91) is a powerful agent that inhibits the activity of HIV-1. It exhibits great potential as a novel latency reversing agent, making it a promising candidate for further development [1].
价 格：￥电议型 号：T61670产 地：中国大陆
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T61516PI3K/mTOR Inhibitor-3；化合物 PI3K/mTOR Inhibitor-3PI3K/mTOR Inhibitor-3
PI3K/mTOR Inhibitor-3 (compound 12) is an imidazoline compound with potent dual inhibitory effects on PI3K and mTOR. This compound exhibits notable anti-cancer activity [1].
价 格：￥电议型 号：T61516产 地：中国大陆
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T61311HIV-1 inhibitor-30；化合物 HIV-1 inhibitor-30HIV-1 inhibitor-30
HIV-1 inhibitor-30 (compound 10i) is a potent inhibitor of HIV-1, specifically targeting the RT DNA polymerase enzyme. It exhibits strong antiretroviral activity, with an EC 50 value of 40 nM and an IC 50 value of 80 nM. Furthermore, HIV-1 inhibitor-30 demonstrates significant effectiveness against seven NNRTI-resistant strains of HIV-1 (RT-K103N; RT-Y181C; RT-K103N, Y181C; RT-L100I, K103N; RT-Y188L; RT-K103N, G190A; RT-K103N, V108I), with IC 50 values ranging from 0.04 to 1.42 μM. This compound
价 格：￥电议型 号：T61311产 地：中国大陆
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T61310HIV-1 inhibitor-37；化合物 HIV-1 inhibitor-37HIV-1 inhibitor-37
HIV-1 inhibitor-37 (Compound 83) is a highly powerful HIV-1 inhibitor. It exhibits significant potential for use as an innovative latent HIV-1 reactivating agent [1].
价 格：￥电议型 号：T61310产 地：中国大陆
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T61134HIV-1 inhibitor-36；化合物 HIV-1 inhibitor-36HIV-1 inhibitor-36
HIV-1 inhibitor-36 (Compound 2) is a potent HIV-1 inhibitor with significant potential as a novel latency reversing agent [1].
价 格：￥电议型 号：T61134产 地：中国大陆
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T61085TGP-377/421；化合物TGP-377/421Targapre-miR-377/421；Targapre-miR-377/421
TGP-377/421 (Targapre-miR-377/421) is a potent miR-377 and miR-421 dual inhibitor that inhibits miR-377 and miR-421 by binding to their functional sites.
价 格：￥电议型 号：T61085产 地：中国大陆
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T61035CBR-3465；化合物 CBR-3465CBR-3465
CBR-3465 is an inhibitor of mycobacterium tuberculosis (Mtb) type II NADH dehydrogenase. The MIC of CBR-3465 against Mtb is 0.16 μM [1].
价 格：￥电议型 号：T61035产 地：中国大陆
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T60909SSAO inhibitor-3；化合物 SSAO inhibitor-3SSAO inhibitor-3
SSAO inhibitor-3 (Compound 2) can be used in the study of atherosclerosis, diabetes and its complications, obesity, stroke, chronic kidney disease, retinopathy, chronic obstructive pulmonary disease (COPD), autoimmune diseases, multiple sclerosis, etc. SSAO inhibitor-3 is an inhibitor of semicarbazide-sensitive amine oxidase (SSAO) with IC 50 s of 0.1-10 μM and <10 nM for human AOC1 and SSAO, respectively [1].
价 格：￥电议型 号：T60909产 地：中国大陆
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T60646PCSK9 modulator-3；化合物 PCSK9 modulator-3PCSK9 modulator-3
PCSK9 modulator-3 (Compound 13) is a potent PCSK9 modulator with an EC 50 value of 2.46 nM that has the potential in the hyperlipidemia research. PCSK9 is a recently proved target for lowering low-density lipoprotein cholesterol (LDL-C) [1].
价 格：￥电议型 号：T60646产 地：中国大陆
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T60454NDM-1 inhibitor-3；化合物NDM-1 inhibitor-3NDM-1 inhibitor-3
NDM-1 inhibitor-3 is a New Delhi Metallo-β-lactamase-1 (NDM-1) inhibitor (Ki : 4 μM) widely found in nature and is associated with antibiotic resistance.
价 格：￥电议型 号：T60454产 地：中国大陆
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T5524Aurora kinase inhibitor-3；化合物Aurora Kinase Inhibitor IIIAurora Kinase Inhibitor III；Aurora Kinase In
Aurora kinase inhibitor-3 (Aurora Kinase Inhibitor III) is a potent inhibitor of Aurora A kinase (IC50 = 42 nM).1 It is selective for Aurora A over BMX, BTK, IGF-1R, c-Src, TRKB, SYK, and EGFR.
价 格：￥电议型 号：T5524产 地：中国大陆
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T4998L2Cefpodoxime sodium；化合物 T4998L2R3746|||R 3763|||R 3746|||R-3746|||R-3763；R3746|||R 3763|||R 3746|||R-
Cefpodoxime sodium is a third generation cephalosporin antibiotic agent. It targets gram-positive and gram-negative bacteria, especially those responsible for otitis media and pharyngitis.
价 格：￥电议型 号：T4998L2产 地：中国大陆
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T39920PROTAC IRAK4 degrader-3；PROTAC IRAK4 degrader-3PROTAC IRAK4 degrader-3；PROTAC IRAK4 degrader-3
PROTAC IRAK4 degrader-3 is a PROTAC-induced IRAK4 degrader based on von Hippel-Lindau.
价 格：￥电议型 号：T39920产 地：中国大陆
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T39837PROTAC ERRα Degrader-3；PROTAC ERRα Degrader-3PROTAC ERRα Degrader-3
PROTAC ERRα Degrader-3 is a highly effective and selective von Hippel-Lindau-based ligand that efficiently degrades the ERRα protein. At a concentration of 30 nM, this compound exhibits a remarkable degradation capability, reducing the ERRα protein levels by >80%. Importantly, PROTAC ERRα Degrader-3 shows no activity against the ERRβ and ERRγ proteins.
价 格：￥电议型 号：T39837产 地：中国大陆
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T3972SR-3029；化合物SR3029SR3029；SR3029
SR-3029 is a potent and highly specific CK1δ/CK1ε inhibitor.
价 格：￥电议型 号：T3972产 地：中国大陆
