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T15806LY2562175；化合物LY2562175LY2562175
LY2562175 is an effective and selective FXR agonist (EC50: 193 nM).
价 格：￥电议型 号：T15806产 地：中国大陆
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T15805LLY2510924 acetate(1088715-84-7 free base)；化合物LY2510924 acetateLY2510924 acetate(1088715-84-7 free ba
Ly2510924 acetate is an potent and selective CXCR4 antagonist. It prevents the binding of SDF-1 to CXCR4 with an IC50 of 0.079 nM.
价 格：￥电议型 号：T15805L产 地：中国大陆
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T15805LY2510924；化合物 T15805LY2510924
LY2510924 is an effective and selective CXCR4 antagonist. It blocks SDF-1 binding to CXCR4 (IC50: 0.079 nM).
价 格：￥电议型 号：T15805产 地：中国大陆
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T15804LY2452473；化合物 T15804LY2452473
LY2452473 is an orally bioavailable and selective androgen receptor modulator.
价 格：￥电议型 号：T15804产 地：中国大陆
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T15803LY223982化合物 T15803SKF107324|||CGS23131
LY223982 is an effective and specific inhibitor of the leukotriene B4 receptor (IC50: 13.2 nM). It also can against [3H]LTB4 binding to LTB4 receptor.
价 格：￥电议型 号：T15803产 地：中国大陆
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T15801LY210073；化合物 T15801LY210073
LY210073 is an antagonist of the Leukotriene B4 (LTB4) receptor (IC50: 6.2 nM).
价 格：￥电议型 号：T15801产 地：中国大陆
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T15800LY117018；化合物 T15800LY117018
LY117018 shows antiproliferative effects on breast cancer cell lines. LY117018 is a Raloxifene analog and is a selective estrogen receptor modulator.
价 格：￥电议型 号：T15800产 地：中国大陆
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T1580Desvenlafaxine；去甲文拉法辛WY 45233 Succinate|||O-Desmethylvenlafaxine；去甲文拉法辛|||WY 45233 Succinate|||O-Des
Desvenlafaxine (O-Desmethylvenlafaxine) is a cyclohexanol and phenol derivative and metabolite of venlafaxine that functions as a serotonin and noradrenaline reuptake inhibitor (SNRI) and is used as an antidepressive agent.
价 格：￥电议型 号：T1580产 地：中国大陆
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T15772Lodoxamide tromethamine；洛度沙胺氨丁三醇U-42585E；U-42585E
Lodoxamide tromethamine is a mast cell stabilizer with anti-allergic properties and can be used in studies about the treatment of asthma and allergic conjunctivitis.
价 格：￥电议型 号：T15772产 地：中国大陆
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T15758Linopirdine；利诺吡啶DuP 996；利诺吡啶|||DuP 996
Linopirdine (DuP 996) is a TRPV1 agonist. Linopirdine is an orally active and selective M-type K+ current (IM; Kv7; KCNQ Channels) inhibitor (IC50: 2.4 μM). Linopirdine is a cognitive enhancer. It acts by stimulating release of acetylcholine and other neurotransmitters.Linopirdine is a putative cognition-enhancing drug that increases acetylcholine release in rat brain tissue.
价 格：￥电议型 号：T15758产 地：中国大陆
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T15670KT5823；化合物KT5823KT5823
KT5823 is a selective and potent cGMP-dependent protein kinase (PKG) inhibitor with inhibitory effects on PKA and PKC.KT5823 increases thyroid-stimulating hormone-induced (Na+/I- symporter) NIS expression and iodide ion uptake by modulating sodium iodide symporter protein expression and activity in thyroid cells. KT5823 induces apoptosis.
价 格：￥电议型 号：T15670产 地：中国大陆
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T15589Iodo-PEG4-N3；化合物 T15589Iodo-PEG4-N3
Iodo-PEG4-N3 is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T15589产 地：中国大陆
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T15588Iobenguane sulfate；硫酸碘苄胍 EP标准品MIBG sulfate；硫酸碘苄胍 EP标准品|||MIBG sulfate
Iobenguane sulfate (MIBG sulfate) is a high-affinity substrate for cholera toxin that interferes with cellular mono(ADP-ribosylation). Radioiodinated Iobenguane sulfate is clinically used as a tumor-targeted radiopharmaceutical in the diagnosis and treatment of adrenergic tumors.
价 格：￥电议型 号：T15588产 地：中国大陆
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T15587Inz-5；化合物 T15587Inz-5
Inz-5 is a fungal-selective inhibitor of mitochondrial cytochrome bc1. Inz-5 impairs fungal virulence. It also prevents the evolution of drug resistance.
价 格：￥电议型 号：T15587产 地：中国大陆
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T15586Intoplicine；茚托利辛Intoplicine
Intoplicine is an inhibitor of DNA topoisomerase I and II.
价 格：￥电议型 号：T15586产 地：中国大陆
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T15585IRBP(668-687) (TFA)；化合物 T15585Interphotoreceptor retinoid-binding protein(668-687) TFA；Interphotorec
Interphotoreceptor retinoid-binding protein TFA is the amino acid residue 668 to 687 of human interphotoreceptor retinoid-binding protein (IRBP). It also induces uveitis.
价 格：￥电议型 号：T15585产 地：中国大陆
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T15584Integrin Antagonists 27；化合物 T15584Integrin Antagonists 27
Integrin Antagonists 27 is a small molecule integrin αvβ3 antagonist. It has a binding affinity of 18 nM and as a novel anticancer agent.
价 格：￥电议型 号：T15584产 地：中国大陆
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T15583GSK 3008348 hydrochloride；化合物 T15583GSK 3008348 hydrochloride
GSK 3008348 hydrochloride is an integrin αvβ6 antagonist. The affinity (pIC50) for the human - a 6 protein in the Fluorescence Polarisation Assay for GSK 3008348 is 8.1, whereas its affinity in the cell Adhesion Assays was for ανβ6 (pIC50: 8.4); ανβ3 (pIC50: 6); ανβ5 (pIC50: 6.9); ανβ8 (pIC50: 7.7).
价 格：￥电议型 号：T15583产 地：中国大陆
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T15582inS3-54A18；化合物inS3-54A18inS3-54A18
inS3-54A18 is an effective inhibitor of STAT3. inS3-54A18 has anticancer effects.
价 格：￥电议型 号：T15582产 地：中国大陆
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T15580Inolitazone dihydrochloride化合物 T15580RS5444 dihydrochloride|||CS-7017 dihydrochloride|||Efatutazone
Inolitazone dihydrochloride is an effective, high-affinity PPARγ agonist; its biological activity is dependent on PPARγ (IC50:0.8 nM) to inhibit cell growth. Inolitazone dihydrochloride enhances the role of cell cycle kinase inhibitor p21 WAF1/CIP1.
价 格：￥电议型 号：T15580产 地：中国大陆
