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T7292FITMFITM,mGluR,Metabotropic glutamate receptors,inhibit,Inhibitor
FITM is a potent negative allosteric modulator of mGlu1 receptor(Ki : 2.5 nM).
价 格：￥电议型 号：T7292产 地：中国大陆
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T8830Foslinanib SodiumFoslinanib Sodium
Foslinanib Sodium is an anticancer compound.It inhibits vasculogenic mimicry network formation in C8161 and SK-MEL-28 melanoma cells when used at concentrations ranging from less than or equal to 5 to 10 nM
价 格：￥电议型 号：T8830产 地：中国大陆
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T6424Bromfenac SodiumInhibitor,inhibit,Bromfenac,Cyclooxygenase,HLEC-B3,Bromfenac Sodium,COX,ocular infla
Bromfenac Sodium is a nonsteroidal anti-inflammatory drug (NSAID), which has anti-inflammatory activity and may block prostaglandin synthesis by inhibiting cyclooxygenase 1 and 2.
价 格：￥电议型 号：T6424产 地：中国大陆
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T4065Fluorescein SodiumFluorescein Sodium,Fluorescein,inhibit,fluorescent probes,Inhibitor,tumor,Uranine,
Fluorescein Sodium is a phthalic indicator dye. It is used therapeutically as a diagnostic aid in corneal injuries and corneal trauma.
价 格：￥电议型 号：T4065产 地：中国大陆
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T8924MFCD28987368MFCD28987368,ADC Linkers,inhibit,MFCD-28987368,Antibody-drug conjugates linkers,Inhibito
MFCD28987368 is a chemical compound
价 格：￥电议型 号：T8924产 地：中国大陆
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T10802CHMFL-EGFR-202CHMFLEGFR202,CHMFL EGFR 202
CHMFL-EGFR-202 is a potent, irreversible inhibitor of EGFR mutant kinase (IC50s: 5.3 nM and 8.3 nM for drug-resistant mutant EGFR T790M and WT EGFR kinases).
价 格：￥电议型 号：T10802产 地：中国大陆
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T9118KEA1-97Apoptosis,KEA1 97,Proliferation,Apoptotic,Caspase,inhibit,KEA-1-97,DCTalkyne,KEA1-97,231MFP,I
Kea1-97 is a selective disruptor of interaction between thioredoxin and caspase-3 (IC50 = 10 μ M). Kea1-97 destroys the interaction between thioredoxin and caspase 3 and activates caspases without affecting the activity of thioredoxin.
价 格：￥电议型 号：T9118产 地：中国大陆
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T9622MF-766EP4,arthritis,inflammation disease,AIA,inhibit,anti-tumor,MF766,MF 766,MF-766,Prostaglandin Re
MF-766 is a highly potent, selective and orally active EP4 antagonist with a Ki of 0.23 nM. It behaves as a full antagonist with an IC50 of 1.4 nM (shifted to 1.8 nM in the presence of 10% HS) in the functional assay. It can be used for cancer and inflammation diseases research[1][2].
价 格：￥电议型 号：T9622产 地：中国大陆
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TQ0221Rufloxacin hydrochlorideRufloxacin,MF-934,Rufloxacin hydrochloride,MF934,MF 934,Inhibitor,inhibit,Ba
Rufloxacin hydrochloride is a fluoroquinolone antibacterial and inhibits topoisomerase. Rufloxacin hydrochloride inhibits B-cell differentiation in human mononuclear cells.
价 格：￥电议型 号：TQ0221产 地：中国大陆
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T64381BMF-219
BMF-219 is a specific irreversible inhibitor of Menin-MLL interactions. BMF-219 can be used in the study of alloimmune diseases, autoimmune diseases, cancer and other diseases dependent on menin-MLL.
价 格：￥电议型 号：T64381产 地：中国大陆
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T10800CHMFL-ABL-121CHMFLABL121,CHMFL ABL 121
CHMFL-ABL-121 is a highly potent inhibitor of type II ABL kinase (IC50s: 2 nM and 0.2 nM against purified inactive ABL wt and T315I kinase protein).
价 格：￥电议型 号：T10800产 地：中国大陆
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T7651Rose Bengal sodiumfluorescein,Inhibitor,dye,crimson-coloured,ophthalmic,antiviral,inhibit,Rose Benga
Rose Bengal is a potent inhibitor of VGlut and vesicular monoamine transporter (VMAT) (Ki of 19 and 64 nM for VGlut andVMAT, respectively）
价 格：￥电议型 号：T7651产 地：中国大陆
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T10799CHMFL-ABL-039CHMFLABL039,CHMFL ABL 039
CHMFL-ABL-039 is a type II native ABL kinase and drug-resistant V299L mutant BCR-ABL inhibitor (IC50s: 7.9 nM and 27.9 nM) used in the research of chronic myeloid leukemia.
价 格：￥电议型 号：T10799产 地：中国大陆
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T8909MFCD01917484MFCD01917484,MFCD-01917484
MFCD01917484 is a chemical compound.
价 格：￥电议型 号：T8909产 地：中国大陆
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T2403Bromfenac sodium hydrateinhibit,COX,Bromfenac sodium hydrate,ocular inflammation,HLEC-B3,Cyclooxygen
Bromfenac Sodium Sesquihydrate is the sodium salt form of bromfenac, a nonsteroidal anti-inflammatory drug (NSAID) with analgesic and anti-inflammatory activities. Upon ophthalmic administration, bromfenac binds to and inhibits the activity of cyclooxygenase II (COX II), an enzyme which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins (PG). By inhibiting PG formation, bromfenac is able to inhibit PG-induced inflammation, thereby preventing vasodilation, leukocytosi
价 格：￥电议型 号：T2403产 地：中国大陆
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T10803CHMFL-KIT-033CHMFL KIT 033,CHMFLKIT033
CHMFL-KIT-033 is an effective and selective c-KIT inhibitor with an IC50 value of 45 nM for c-KIT T670I mutant in gastrointestinal stromal tumors.
价 格：￥电议型 号：T10803产 地：中国大陆
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T8914MFCD01827729MFCD01827729,MFCD-01827729
MFCD01827729 is a chemical compound.
价 格：￥电议型 号：T8914产 地：中国大陆
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T8567amflutizoleamflutizole
Amflutizole used for the treatment of gout, and is a Xanthine oxidase inhibitor
价 格：￥电议型 号：T8567产 地：中国大陆
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T13683Epsilon-momfluorothrin
Epsilon-momfluorothrin is a type I synthetic pyrethroid insecticide, activates constitutive androstane receptor (CAR), and induces hepatocellular tumors in rats.
价 格：￥电议型 号：T13683产 地：中国大陆
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T10804CHMFL-PI3KD-317CHMFL-PI-3KD-317,CHMFLPI3KD317,CHMFL PI3KD 317
CHMFL-PI3KD-317 is a highly potent, selective and orally active PI3Kδ inhibitor, with an IC50 of 6 nM, and exhibits over 10-1500 fold selectivity over other class I, II and III PIKK family isoforms, such as PI3Kα (IC50, 62.6 nM), PI3Kβ (IC50, 284 nM), PI3Kγ (IC50, 202.7 nM), PIK3C2A (IC50, >10000 nM), PIK3C2B (IC50, 882.3 nM), VPS34 (IC50, 1801.7 nM), PI4KIIIA (IC50, 574.1 nM) and PI4KIIIB (IC50, 300.2 nM). CHMFL-PI3KD-317 inhibits PI3Kδ-mediated Akt T308 phosphorylation in Raji cells, with an E
价 格：￥电议型 号：T10804产 地：中国大陆
