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T1744BIX02188；化合物BIX02188BIX02188
BIX02188 is a selective and potent MEK5 inhibitor that inhibits MEK5-induced apoptosis in cells expressing the oncogenic mutant FLT3-ITD.
价 格：￥电议型 号：T1744产 地：中国大陆
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T17188U-101017；化合物 T17188PNU 101017；PNU 101017
U-101017 is a partial benzodiazepine receptor and GABAA receptor agonist.
价 格：￥电议型 号：T17188产 地：中国大陆
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T17001Tazanolast；他扎司特Tazalest|||TO 188|||Tazanol；他扎司特|||Tazalest|||TO 188|||Tazanol
Tazanolast is a selective mast-cell-stabilizing drug.
价 格：￥电议型 号：T17001产 地：中国大陆
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T16188N-(Azido-PEG3)-N-Boc-PEG3-acid；化合物 T16188N-(Azido-PEG3)-N-Boc-PEG3-acid
N-(Azido-PEG3)-N-Boc-PEG3-acid is a polyethylene glycol (PEG)-based linker specifically designed for the construction of proteolysis-targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T16188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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T15345FR-188582；化合物 T15345FR-188582
FR-188582 is a highly selective cyclooxygenase (COX)-2 inhibitor (IC50: 17 nM).
价 格：￥电议型 号：T15345产 地：中国大陆
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T15188E-?6123；化合物 T15188E-?6123
E-6123 is an antagonist of platelet-activating factor (PAF) receptor.
价 格：￥电议型 号：T15188产 地：中国大陆
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T1447Fenclonine芬克洛宁Fenchlonine|||PCPA|||CP-10188|||芬克洛宁|||4-Chloro-DL-phenylalanine|||DL-4-Chlorophenylal
Fenclonine (CP-10188) is a selective and irreversible inhibitor of tryptophan hydroxylase, a rate-limiting enzyme in the biosynthesis of serotonin (5-HYDROXYTRYPTAMINE). Fenclonine(CP-10188) acts pharmacologically to deplete endogenous levels of serotonin.
价 格：￥电议型 号：T1447产 地：中国大陆
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T14188ALLO-2；化合物ALLO-2ALLO-2
ALLO-2 is a Inhibitor of Drug-Resistant Smo Mutant.It inhibits Smo agonist Hh-Ag1.5-induced luciferase expression in TM3-Gli-Luc cells with IC50 of 6 nM.
价 格：￥电议型 号：T14188产 地：中国大陆
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T13188TP-004；化合物 T13188TP-004
TP-004 is a potent and reversible methionine aminopeptidase 2 (MetAP2) inhibitor (IC50: 6 nM).
价 格：￥电议型 号：T13188产 地：中国大陆
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T131188Compound N066-0070；化合物 N066-0070Compound N066-0070
Compound N066-0070 is a useful organic compound for research related to life sciences and the catalog number is T131188.
价 格：￥电议型 号：T131188产 地：中国大陆
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T126188Ajugamarin G1；化合物 Ajugamarin G1Ajugamarin G1
Ajugamarin G1 is a useful organic compound for research related to life sciences and the catalog number is T126188.
价 格：￥电议型 号：T126188产 地：中国大陆
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T1241883-Methoxy-5-pentyl-2-prenylphenol；化合物 3-Methoxy-5-pentyl-2-prenylphenol3-Methoxy-5-pentyl-2-prenylph
3-Methoxy-5-pentyl-2-prenylphenol is a useful organic compound for research related to life sciences. The catalog number is T124188 and the CAS number is 80489-92-5.
价 格：￥电议型 号：T124188产 地：中国大陆
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T12201Nebracetam hydrochloride；化合物Nebracetam hydrochlorideWEB 1881 FU hydrochloride；WEB 1881 FU hydrochlor
Nebracetam hydrochloride (WEB 1881 FU hydrochloride) is an agonist nootropic M1-muscarinic. Nebracetam hydrochloride induces a rise of intracellular Ca2+ concentration. Nebracetam hydrochloride exhibits an EC50 of 1.59 mM for elevating [Ca2+]i.
价 格：￥电议型 号：T12201产 地：中国大陆
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T12188NB-360；化合物NB-360NB-360
NB-360 is a potent and brain-penetrable inhibitor of BACE1 and BACE2 with IC50s of 5, 5, and 6 nM for mouse and human BACE1 and BACE2. NB-360 exhibits excellent selectivity over the related aspartyl proteases pepsin, cathepsin E, and cathepsin D.
价 格：￥电议型 号：T12188产 地：中国大陆
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T11889LTV-1；化合物 T11889LTV-1
LTV-1 has the potential for autoimmunity treatment. LTV-1 is a potent lymphoid tyrosine phosphatase (LYP) inhibitor in T cells with an IC50 of 508 nM.
价 格：￥电议型 号：T11889产 地：中国大陆
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T11888LtaS-IN-1；化合物LtaS-IN-1LtaS-IN-1
LtaS-IN-1 is an effective inhibitor of Lipoteichoic acid synthesis in multidrug-resistant (MDR) E. faecium and by altering the cell wall morphology. LtaS-IN-1 is against Enterococcus spp 28 strains with varying MIC values ranging from 0.5 μg/mL to 64 μg/mL. LtaS-IN-1 inhibits strain E1630 and E1590 with MIC values of 0.5 μg/mL.
价 格：￥电议型 号：T11888产 地：中国大陆
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T11887LT052；化合物 T11887LT052
LT052, a highly active and selective BET BD1 inhibitor with an IC50 of 87.7 nM, demonstrates nanomolar BRD4 BD1 potency and significant selectivity, being 138-fold more selective for BRD4 BD1 over BRD4 BD2 (IC50 =12.130 μM). Its anti-inflammatory properties make it a potential candidate for acute gout arthritis research [1].
价 格：￥电议型 号：T11887产 地：中国大陆
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T11885LSP-249；化合物LSP-249LSP-249
LSP-249 is a plasma kallikrein inhibitor under the study for angioedema, with an EC50 less than 100 nM in cell.
价 格：￥电议型 号：T11885产 地：中国大陆
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T11884LSN 3213128；化合物 T11884LSN 3213128
LSN 3213128, anti-tumor activity. is a selective, nonclassical, orally bioavailable antifolate with potent and specific inhibitory activity for aminoimidazole-4-carboxamide ribonucleotide formyltransferase (AICARFT), with IC50 of 16 nM for AICARFT enzyme inhibiton and 19 nM in cells.
价 格：￥电议型 号：T11884产 地：中国大陆
