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T24477MK6-83MK6 83；MK683
MK6-83 is the transient receptor potential channel ML3 agonist.
价 格：￥电议型 号：T24477产 地：中国大陆
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T24410LIMK-IN-22jLIMK inhibitor-22j；LIMK IN 22j；LIMK inhibitor 22j；LIMKIN22j
LIMK-IN-22j is an effective and selective inhibitor of LIMK.
价 格：￥电议型 号：T24410产 地：中国大陆
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T23358Sitagliptin phosphateJanuvia；Sitagliptin (phosphate)；MK-0431 phosphate；磷酸西他列汀
Sitagliptin phosphate is a dipeptidyl peptidase-4 (DPP4) inhibitor.
价 格：￥电议型 号：T23358产 地：中国大陆
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T2316OmarigliptinMK-3102；奥格列汀
Omarigliptin has been used in trials studying the treatment of Type 2 Diabetes Mellitus and Chronic Renal Insufficiency.
价 格：￥电议型 号：T2316产 地：中国大陆
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T22988MK-4827 RacemateNiraparib Racemate；2-(4-piperidin-3-ylphenyl)indazole-7-carboxamide
MK-4827 Racemate is a selective PARP1 and PARP2 inhibitor with IC50s of 3.8 nM and 2.1 nM, respectively, over 330-fold selectivity for PARP3, V-PARP and Tank1.
价 格：￥电议型 号：T22988产 地：中国大陆
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T22987MK 212 hydrochloride
MK 212 hydrochloride is a 5-HT2C receptor agonist
价 格：￥电议型 号：T22987产 地：中国大陆
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T2239LRaltegravirMK-0518；雷特格韦
Raltegravir is a pyrrolidinone derivative and HIV INTEGRASE INHIBITOR that is used in combination with other ANTI-HIV AGENTS for the treatment of HIV INFECTION.
价 格：￥电议型 号：T2239L产 地：中国大陆
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T2239Raltegravir potassium雷特格韦钾盐；MK 0518 potassium salt；Raltegravir potassium salt
Raltegravir potassium salt(MK0518 potassium salt) is a potent integrase (IN) inhibitor, used to treat HIV infection.
价 格：￥电议型 号：T2239产 地：中国大陆
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T2134Dorzolamide hydrochloride盐酸多佐胺；Dorzolamide HCl；MK507 hydrochloride；L671152 hydrochloride；MK-507 (L-6
Dorzolamide Hydrochloride is the hydrochloride salt form of dorzolamide, an inhibitor of carbonic anhydrase, a zinc-containing enzyme that catalyzes the rapid conversion of carbon dioxide and water into carbonic acid, protons and bicarbonate ions. Distrib
价 格：￥电议型 号：T2134产 地：中国大陆
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T20950MK-8245 analogMK 8245 analog；MK8245 analog；MK-8245-analog
MK-8245 analog is an analog of MK-8245 which is a liver-targeted Inhibitor of Stearoyl-CoA Desaturase (SCD). It is useful for the Treatment of Dyslipidemia and Diabetes.
价 格：￥电议型 号：T20950产 地：中国大陆
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T2077AdavosertibMK-1775；AZD1775；Adavosertib (MK-1775)
MK-1775 is a small molecule inhibitor of the checkpoint kinase WEE1 (IC50: 5.2 nM). It hinders the G2 DNA damage checkpoint.
价 格：￥电议型 号：T2077产 地：中国大陆
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T20095IbutamorenL163191；MK677；MK-677；L-163191；MK 677；L 163191
Ibutamoren is a drug which acts as a potent, orally active growth hormone secretagogue, mimicking the GH stimulating action of the endogenous hormone ghrelin. It also alters the metabolism of body fat and so may have an application in the treatment of obe
价 格：￥电议型 号：T20095产 地：中国大陆
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T1952MK-2206 dihydrochlorideMK-2206 2HCl
MK-2206 is a highly specific inhibitor of Akt1/2/3 (IC50: 8/12/65 nM in cell-free assays) and no effect on the activities of 250 other protein kinases.
价 格：￥电议型 号：T1952产 地：中国大陆
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T1928AnacetrapibMK-0859；安塞曲匹
Anacetrapib (MK0859) is an effective, specific, reversible rhCETP and mutant CETP(C13S) inhibitor (IC50: 7.9 nM and 11.8 nM). Anacetrapib reduces the transfer of cholesteryl ester from HDL to LDL and/or VLDL thereby, producing an increase in serum HDL-cho
价 格：￥电议型 号：T1928产 地：中国大陆
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T1913MK-3697MK3697
MK-3697, an isonicotinamide small molecule, acts as a potent and selective Orexin 2 receptor antagonist (Ki: 0.95 nM).
价 格：￥电议型 号：T1913产 地：中国大陆
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T1872Fenretinide芬维A胺；4-HPR；4-hydroxy(phenyl)retinamide；MK-4016
Fenretinide is an orally-active synthetic retinoid derivative with potential antineoplastic and chemopreventive activities.
价 格：￥电议型 号：T1872产 地：中国大陆
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T1799Caspofungin AcetateMK 0991；Cancidas；L 743872；L 743873；醋酸卡泊芬净
Cancidas is the acetate salt of an antimycotic echinocandin lipopeptide, semisynthetically derived from a fermentation product of the fungus Glarea lozoyensis. This agent is active against Aspergillus and Candida species.
价 格：￥电议型 号：T1799产 地：中国大陆
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T1790Fosaprepitant dimeglumineMK-0517；Fosaprepitant dimeglumine salt；L785298；福沙匹坦二甲葡胺；福沙吡坦二甲葡胺
Fosaprepitant Dimeglumine is the dimeglumine salt form of fosaprepitant, the water-soluble, N-phosphorylated prodrug of aprepitant, with antiemetic activity. Upon intravenous administration and rapid conversion to aprepitant, this agent binds selectively
价 格：￥电议型 号：T1790产 地：中国大陆
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T1743AprepitantMK-869；Aprepitant`；MK-0869；L-754030；阿瑞匹坦
Aprepitant is a Substance P/Neurokinin-1 Receptor Antagonist. The mechanism of action of aprepitant is as a Neurokinin 1 Antagonist, and Cytochrome P450 3A4 Inhibitor, and Cytochrome P450 2C9 Inducer, and Cytochrome P450 3A4 Inducer.
价 格：￥电议型 号：T1743产 地：中国大陆
