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产品数：86101
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T6347Ki16198lung,Ki 16198,inhibit,Inhibitor,LPL Receptor,BxPC-3,liver metastasis,Ki16198,Ki-16198,Lysopho
Ki16198 is the methyl ester of Ki16425, which is a LPA antagonist and inhibits LPA1- and LPA3-induced inositol phosphate production with Ki of 0.34 μM and 0.93 μM, respectively, shows weaker inhibition for LPA2, no activity at LPA4, LPA5, LPA6.
价 格：￥电议型 号：T6347产 地：中国大陆
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T9608KL201KL201,CRY1,Inhibitor,Per2-dLuc,FBXL3,inhibit,clock,KL 201,circadian,cryptochrome,KL-201
KL201 a circadian clock modulator, is a isoform-selective cryptochrome 1 (CRY1) stabilizer. KL201 lengthens the period of circadian rhythms in cells and tissues[1].
价 格：￥电议型 号：T9608产 地：中国大陆
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T9231Mbx2329pandemic influenza virus A,inhibit,inhibitory activities,Influenza Virus,influenza virus entr
MBX2329 is a specific inhibitor of HA-mediated viral entry that inhibits H1N1 virus strain high pathogenic avian influenza H5N1 virus strain.
价 格：￥电议型 号：T9231产 地：中国大陆
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T9976OBX02-011
OBX02-011 is an effective and reversible inhibitor of EGFR tyrosine kinase with IC50s of 0.134 and 2.09 nM for triple mutants Del19/T790M/C797S and L858R/T790M/C797S.
价 格：￥电议型 号：T9976产 地：中国大陆
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T9595LP-261NCI-H522,tubulin polymerization,tumor,SW-620,BXPC-3,H522,anti-mitotic,inhibit,LP261,MCF-7,Inhi
LP-261 is a novel tubulin targeting anticancer agent that binds at the colchicine site on tubulin, inducing G2/M arrest.
价 格：￥电议型 号：T9595产 地：中国大陆
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T8956BC-?1258LRR,F-box,inhibit,repeat,BC-?1258,BC ?1258,FBXL2,Apoptosis,tumor,Inhibitor,BC?1258
BC-1258 is a unique small molecule F-box/LRR-repeat protein 2 (FBXL2) activator.
价 格：￥电议型 号：T8956产 地：中国大陆
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T8311ObefazimodObefazimod,HIV,Inhibitor,Human immunodeficiency virus,inhibit,ABX 464
ABX-464 is a potent anti-HIV agent. ABX464 inhibits HIV-1 replication in stimulated peripheral blood mononuclear cells (PBMCs) (IC50 : 0.1 μM - 0.5 μM)
价 格：￥电议型 号：T8311产 地：中国大陆
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TQ0166TesevatinibXL647,Tesevatinib,EXEL 7647,KD019,HER1,Ephrin Receptor,Inhibitor,VEGFR,KD 019,Vascular en
Tesevatinib is an orally available, multi-target tyrosine kinase inhibitor (IC50s: 0.3, 16, 1.5, 8.7, and 1.4 nM for EGFR, ErbB2, KDR, Flt4, and EphB4).
价 格：￥电议型 号：TQ0166产 地：中国大陆
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T5353ABX-1431
ABX-1431 is a selective and orally available CNS-penetrant monoacylglycerol lipase (MAGL/MGLL) inhibitor (IC50: 14 nM).
价 格：￥电议型 号：T5353产 地：中国大陆
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T4628SeladelparMBX 8025
MBX-8025 has been used in trials studying the treatment of Hyperlipidemia.
价 格：￥电议型 号：T4628产 地：中国大陆
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T4046BX517BX 517；BX-517；PDK1 inhibitor 2
BX-517 is a potent and selective inhibitor of PDK1.
价 格：￥电议型 号：T4046产 地：中国大陆
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T2663GTS-21 dihydrochlorideGTS 21 dihydrochloride；DMBX-anabaseine；DMXB-A
GTS 21 dihydrochloride is a nAChRs agonist. nAChRs are neuron receptor proteins that activated by the binding of the neurotransmitter ACh.
价 格：￥电议型 号：T2663产 地：中国大陆
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T2375BX471ZK-811752；BX 471；BX-471
BX471 is a potent, selective non-peptide CCR1 antagonist.
价 格：￥电议型 号：T2375产 地：中国大陆
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T2365PilaralisibXL-147；SAR245408
Pilaralisib is an orally available small molecule that selectively inhibits the activity of phosphoinositide-3 kinase (PI3K). Pilaralisib has been used in trials studying the treatment of Cancer, Lymphoma, Solid Tumors, Glioblastoma, and Breast Cancer, am
价 格：￥电议型 号：T2365产 地：中国大陆
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T21527HBX 41108HBX-41108；7-氯-9-氧代-9H-茚并[1,2-B]吡嗪-2,3-二甲腈
HBx 41108 is a non-competitive, reversible inhibitor of USP7 with an IC50 of 424nM. HBx 41108 inhibited deubiquitination of p53 mediated by USP7 in a dose-dependent manner with an IC50 of 0.8μM.
价 格：￥电议型 号：T21527产 地：中国大陆
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T1837BX-912BX912
BX-912 is a specific inhibitor of 3-Phosphoinositide-dependent Kinase-1 (PDK1, IC50: 12 nM). The selectivity of BX-912 is more 10 fold than C-Kit, EGFR, PKA, PKC etc.
价 格：￥电议型 号：T1837产 地：中国大陆
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T1830BX795
BX795 is an effective and selective PDK1 inhibitor (IC50: 6 nM), and its selectivity is 140- and 1600-fold for PDK1 over PKA and PKC in cell-free assays, respectively. Meanwhile, the selectivity for PDK1 is 100-fold than GSK3β.
价 格：￥电议型 号：T1830产 地：中国大陆
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T1793MBX-2982MBX2982
MBX-2982 is a selective, orally-available GPR119 agonist, used for the treatment of diabetes.
价 格：￥电议型 号：T1793产 地：中国大陆
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T16022ArhalofenateJNJ 39659100；MBX 102；芳卤芬酯；4-氯-ALPHA-[3-(三氟甲基)苯氧基]苯乙酸 2-(乙酰基氨基)乙酯
Arhalofenate is a selective partial agonist of peroxisome proliferator-activated receptor PPARγ. It is used for the treatment of type 2 diabetes.
价 格：￥电议型 号：T16022产 地：中国大陆
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T15464HBX 19818
HBX 19818 is a specific ubiquitin-specific protease 7 (USP7) inhibitor (IC50: 28.1 μM).
价 格：￥电议型 号：T15464产 地：中国大陆
