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T12200Firsocostat S enantiomer；化合物 T12200ND-630 S enantiomer|||NDI-010976 S enantiomer|||GS-0976 S enantio
Firsocostat S enantiomer is the less active S enantiomer of Firsocostat.
价 格：￥电议型 号：T12200产 地：中国大陆
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T12170Naminterol；那明特罗Naminterol
Naminterol is a phenethanolamine derivative is an agonist of β2 adrenoceptor with bronchodilatory properties, and used for treatment of asthma.
价 格：￥电议型 号：T12170产 地：中国大陆
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T12157ETA antagonist 1；化合物 T12157ETA antagonist 1
ETA antagonist 1 is an antagonist of ETA selective (IC50 of 0.08 μM).
价 格：￥电议型 号：T12157产 地：中国大陆
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T12155Y1 receptor antagonist 1；Y1 receptor 拮抗剂 1H 409-22 isomer；H 409-22 isomer
Y1 receptor antagonist 1 (H 409-22 isomer) is the active isomer of H-409/22, a neuropeptide Y (NPY) Y1 receptor antagonist that dose-dependently antagonizes the vascular response to exogenous and endogenous NPY in pigs. lagodeoxycholic acid (H 409-22 isomer) is the active isomer of H-409/22, an antagonist of neuropeptide Y (NPY) Y1 receptor.
价 格：￥电议型 号：T12155产 地：中国大陆
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T12129Mutant IDH1-IN-4；化合物 T12129Mutant IDH1-IN-4
Mutant IDH1-IN-4 is an mutant Isocitrate dehydrogenase 1 (IDH 1) inhibitor.
价 格：￥电议型 号：T12129产 地：中国大陆
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T12128Mutant IDH1-IN-2；化合物Mutant IDH1-IN-2Mutant IDH1-IN-2
Mutant IDH1-IN-2 is a inhibitor of mutant Isocitrate dehydrogenase (IDH) proteins, with IC50 of 16.6 nM in Fluorescence biochemical assay, IC50 of ＜22 nM in LS-MS biochemical assay.
价 格：￥电议型 号：T12128产 地：中国大陆
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T12096Morinidazole (R enantiomer)；R-吗啉硝唑R-Morinidazole；R-Morinidazole|||R-吗啉硝唑
Morinidazole (R enantiomer) is the R-enantiomer of Morinidazole.
价 格：￥电议型 号：T12096产 地：中国大陆
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T12092Monacolin J；辛伐他汀内酯二醇Antibiotic MB 530A|||Lovastatin diol lactone；Antibiotic MB 530A|||Lovastatin dio
Monacolin J (Antibiotic MB 530A) is a cholesterol biosynthesis inhibitor.
价 格：￥电议型 号：T12092产 地：中国大陆
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T12067MK-7246 S enantiomer；化合物 T12067MK-7246 S enantiomer
MK-7246 S enantiomer is a potent and selective CRTH2 antagonist.
价 格：￥电议型 号：T12067产 地：中国大陆
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T12064Niraparib (R-enantiomer)；化合物Niraparib R-enantiomerMK 4827 (R-enantiomer)|||Niraparib R-enantiomer；MK
Niraparib R-enantiomer (MK 4827 R-enantiomer) is an inhibitor of PARP1(IC50 of 2.4 nM).
价 格：￥电议型 号：T12064产 地：中国大陆
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T11997MELK-IN-1；尼达尼布杂质LNintedanib Impurity L|||MELK inhibitor 17；Nintedanib Impurity L|||MELK inhibitor 17
MELK-IN-1 (MELK inhibitor 17) is a potent inhibitor of maternal embryonic leucine zipper kinase (MELK),(IC50:3nm;Ki:0.39 nM).
价 格：￥电议型 号：T11997产 地：中国大陆
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T11991Mefentrifluconazole氯氟醚菌唑CYPs|||aromatase|||Inhibitor
Mefentrifluconazole is a potent, selective and orally active fungal CYP51 (Kd= 0.5 nM) inhibitor, but shows less inhibitory activity on human aromatase (IC50=0.92 μM). Mefentrifluconazole is a novel azole derivative and used as an agrochemical broad-spectrum antifungal agent.
价 格：￥电议型 号：T11991产 地：中国大陆
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T11967Mcl-1 antagonist 1；化合物 T11967Mcl-1 antagonist 1
Mcl-1 antagonist 1 is a Mcl-1 protein antagonist.
价 格：￥电议型 号：T11967产 地：中国大陆
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T11966MCHR1 antagonist 2；化合物MCHR1 antagonist 2MCHR1 antagonist 2
MCHR1 antagonist 2 is an antagonist of melanin-concentratin hormone receptor 1(MCH1-R, IC50 = 65 nM) and also inhibits hERG.
价 格：￥电议型 号：T11966产 地：中国大陆
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T11964MCH-1 antagonist 1；化合物 T11964MCH-1 antagonist 1
MCH-1 antagonist 1 also inhibits CYP3A4 (IC50: 10μM).MCH-1 antagonist 1 is a potent melanin concentrating hormone (MCH-1) antagonist (Ki: 2.6 nM).
价 格：￥电议型 号：T11964产 地：中国大陆
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T11951Mavoglurant racemate；化合物 T11951AFQ-056 racemate；AFQ-056 racemate
Mavoglurant is a novel, non-competitive mGlu5 receptor antagonist. Mavoglurant (racemate) is the racemate of mavoglurant.
价 格：￥电议型 号：T11951产 地：中国大陆
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T11935Macitentan (n-butyl analogue)；马西替坦正丁基类似物Macitentan (n-butyl analogue)
Macitentan n-butyl analogue, a derivative of Macitentan, functions as an orally active dual antagonist targeting both endothelin ETA and ETB receptors. This compound shows promise for treating idiopathic pulmonary fibrosis (IPF) and pulmonary arterial hypertension (PAH), leveraging its non-peptide structure for potential therapeutic applications.
价 格：￥电议型 号：T11935产 地：中国大陆
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T11934Macitentan-d4；马西替坦d4Macitentan D4|||ACT-064992 D4；Macitentan D4|||ACT-064992 D4
Macitentan-d4 (ACT-064992 D4) is a deuterated substitute for Macitentan and can be used as a dual antagonist of the non-peptides ETA and ETB (endothelin receptor).Macitentan-d4 is less toxic than Macitentan, has a longer half-life, and can be used to study endothelin receptor-mediated diseases.
价 格：￥电议型 号：T11934产 地：中国大陆
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T11902LY 344864 S-enantiomer；化合物 T11902LY 344864 S-enantiomer
LY 344864 S-enantiomer, the S-enantiomer of LY344864, serves as a 5-HT1F receptor agonist.
价 格：￥电议型 号：T11902产 地：中国大陆
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T11891Lumefantrine-d18；苯芴醇 D18Benflumetol D18|||Lumefantrine D18；Benflumetol D18|||苯芴醇 D18|||Lumefantrine
Lumefantrine D18 is an antimalarial drug, and is the deuterium labeled Lumefantrine.
价 格：￥电议型 号：T11891产 地：中国大陆
