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T15748LG100754；化合物LG100754UVI 2112；UVI 2112
LG100754 (UVI 2112) is an insulin sensitizer that functions through RXR. LG100754 is an RXR dimer modulator. LG100754 acts as an RXR: RXR homodimer antagonist, but functions as an agonist towards RXR: PPARα and RXR: PPARγ heterodimers.
价 格：￥电议型 号：T15748产 地：中国大陆
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T15747Lexithromycin；来红霉素Erythromycin A 9-methoxime|||Wy 48314；Erythromycin A 9-methoxime|||Wy 48314|||来红霉素
Lexithromycin is an erythromycin A derivative. It has antibacterial activity.
价 格：￥电议型 号：T15747产 地：中国大陆
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T15746Lexibulin dihydrochloride；化合物 T15746CYT-997 dihydrochloride；CYT-997 dihydrochloride
Lexibulin 2Hcl is an effective tubulin polymerization inhibitor (IC50: 10-100 nM in cancer cell lines). It also has potent cytotoxic and vascular disrupting activity in vitro and in vivo.
价 格：￥电议型 号：T15746产 地：中国大陆
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T15745Lexacalcitol；来沙骨化醇KH1060；来沙骨化醇|||KH1060
Lexacalcitol is over 100 times more active than 1alpha,25-dihydroxyvitamin D3 [1alpha,25-(OH)2D3], as judged by in vitro antiproliferative and cell differentiating assays.
价 格：￥电议型 号：T15745产 地：中国大陆
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T15743Levomepromazine；化合物 T15743Methotrimeprazine；Methotrimeprazine
Methotrimeprazine is an orally available neuroleptic agent. It is commonly used to relieve nausea and vomiting in palliative care settings. Levomepromazine has antagonist actions at multiple neurotransmitter receptor sites, including cholinergic, dopaminergic, serotonin, and histamine receptors.
价 格：￥电议型 号：T15743产 地：中国大陆
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T1574Etoricoxib；依托考昔Arcoxia|||MK-663|||Tauxib|||L-791456|||Nucoxia|||Desvenlafaxine；Arcoxia|||MK-663|||Ta
Etoricoxib (MK-663) is a synthetic, nonsteroidal anti-inflammatory drug (NSAID) with antipyretic, analgesic, and potential antineoplastic properties. Etoricoxib specifically binds to and inhibits the enzyme cyclooxygenase-2 (COX-2), resulting in inhibition of the conversion of arachidonic acid into prostaglandins. Inhibition of COX-2 may induce apoptosis and inhibit tumor cell proliferation and angiogenesis.
价 格：￥电议型 号：T1574产 地：中国大陆
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T15736Leriglitazone；化合物 T15736Hydroxypioglitazone；Hydroxypioglitazone
Leriglitazone, a metabolite of pioglitazone, binds to the PPARγ C-terminal ligand-binding domain (Ki: 1.2 μM) and induces transcriptional efficacy of the PPARγ (EC50: 680 nM). Leriglitazone PioOH is a PPARγ agonist, stabilizes the PPARγ activation function-2 (AF-2) co-activator binding surface.
价 格：￥电议型 号：T15736产 地：中国大陆
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T15735Leptomycin B；来普霉素BCI 940|||LMB；CI 940|||LMB|||来普霉素B
Leptomycin B (LMB) is a potent inhibitor of the nuclear export of proteins and is a potent antifungal antibiotic blocking the eukaryotic cell cycle. Leptomycin B inactivates CRM1/exportin 1 by covalent modification at a cysteine residue.
价 格：￥电议型 号：T15735产 地：中国大陆
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T15733Lemildipine；化合物 T15733NB-818|||NPK-1886；NB-818|||NPK-1886
Lemildipine is a new blocker of dihydropyridine calcium entry.
价 格：￥电议型 号：T15733产 地：中国大陆
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T15732Ribociclib succinate；瑞博西尼琥珀酸盐LEE011 succinate；LEE011 琥珀酸盐|||瑞博西尼琥珀酸盐|||LEE011 succinate
Ribociclib succinate (LEE011 succinate) is a highly specific CDK4/6 inhibitor (IC50: 10 nM and 39 nM, respectively). It also is over 1,000-fold less potent against the cyclin B/CDK1 complex.
价 格：￥电议型 号：T15732产 地：中国大陆
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T15731Ribociclib succinate hydrate化合物 T15731LEE011 succinate hydrate
Ribociclib succinate hydrate is a highly specific CDK4/6 inhibitor (IC50s: 10 nM and 39 nM, respectively). It also is over 1,000-fold less potent against the cyclin B/CDK1 complex.
价 格：￥电议型 号：T15731产 地：中国大陆
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T15730Ribociclib hydrochloride瑞博西尼盐酸盐LEE011 hydrochloride|||瑞博西尼盐酸盐
Ribociclib hydrochloride is a highly specific CDK4/6 inhibitor (IC50: 10 nM and 39 nM, respectively). It is over 1,000-fold less potent against the cyclin B/CDK1 complex.
价 格：￥电议型 号：T15730产 地：中国大陆
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T15729LDN-91946；化合物LDN-91946LDN-91946
LDN-91946 is an effective and selective inhibitor of ubiquitin C-terminal hydrolase-L1 (UCH-L1) (Ki = 2.8 μM).
价 格：￥电议型 号：T15729产 地：中国大陆
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T15728LDN-212320；化合物LDN-212320LDN-0212320|||LDN/OSU-0212320|||OSU-0212320；LDN-0212320|||LDN/OSU-0212320|||
LDN-212320 (OSU-0212320) is a glutamate transporter EAAT2 activator. It also enhances EAAT2 levels by > 6 fold at concentrations < 5 μM after 24 h.
价 格：￥电议型 号：T15728产 地：中国大陆
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T15727Sonidegib diphosphate；化合物Erismodegib diphosphateNVP-LDE 225 diphosphate|||Erismodegib diphosphate|||
Sonidegib diphosphate (LDE225 diphosphate) is an effective and selective Smo antagonist (IC50: 1.3 nM and 2.5 nM for mouse and human Smo in a binding assay, respectively).
价 格：￥电议型 号：T15727产 地：中国大陆
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T15725Lck inhibitor 2化合物 T15725Lck inhibitor 2
Lck inhibitor 2 is a bis-anilinopyrimidine inhibitor of tyrosine kinases including LCK, BTK, LYN, SYK, and TXK (IC50s: 13nM, 9nM, 3nM, 26nM, and 2nM for Lck, Btk, Lyn, Btk, and Txk respectively).
价 格：￥电议型 号：T15725产 地：中国大陆
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T15724LC-PEG8-SPDP；化合物 T15724LC-PEG8-SPDP
LC-PEG8-SPDP is a cleavable ADC linker used for the antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15724产 地：中国大陆
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T15723LBW242；化合物 T15723LBW242
LBW242 is a 3-mer and Smac mimetic and is an effective and orally active proapoptotic IAP inhibitor. LBW242 has activity against multiple myeloma and potentiates TRAIL- and anticancer drug-mediated cell death of ovarian cancer cells. LBW242 displays effects on mutant FLT3-expressing cells.
价 格：￥电议型 号：T15723产 地：中国大陆
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T15722Lavoltidine；化合物 T15722Loxtidine|||AH-234844；Loxtidine|||AH-234844
Lavoltidine is an orally active and irreversible histamine H2-receptor antagonist. Lavoltidine strongly suppresses gastric acid secretion and also induces hypergastrinemia.
价 格：￥电议型 号：T15722产 地：中国大陆
