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T24362L 756423；化合物L 756423L756423|||MK-944a|||MK944a|||L-756,423|||L-756423|||MK 944a；L756423|||MK-944a|||
L 756423 (L756423) is a novel potent and selective and competitive HIV protease inhibitor with a Ki value of 0.049 nM for HIV-1 PR.L 756423 blocks the spread of HIV(IIIb)-infected MT25 lymphocytes at 0.50-0.1 nM and can be used for the study of Acquired Immunodeficiency Syndrome (AIDS).
价 格：￥电议型 号：T24362产 地：中国大陆
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T23555Z-VEID-FMK；化合物 T23555Z-VEID-FMK
When compared to other caspase inhibitors, Z-DRHD-FMK inhibited caspase 6 activity more effectively than the general caspase inhibitor of Z-Val-Ala-Asp (OMe)-fluoromethy ketone (Z-VAD-FMK) or the caspase 6 inhibitor Z-Val-Glu(Ome)-Ile-Asp(OMe)-fluoromethyl ketone.However, it was less effective in inhibiting TNFα-induced apoptosis than Z-VAD-FMK or Z-VEID-FMK, presumably.
价 格：￥电议型 号：T23555产 地：中国大陆
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T23358Sitagliptin phosphate磷酸西他列汀磷酸西他列汀|||Januvia|||MK-0431 phosphate|||Sitagliptin (phosphate)
Sitagliptin phosphate (MK-0431 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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T2316Omarigliptin；奥格列汀MK-3102；MK-3102|||奥格列汀
Omarigliptin (MK-3102) 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 Racemate；化合物T22988Niraparib Racemate|||2-(4-piperidin-3-ylphenyl)indazole-7-carboxamide；Nira
MK-4827 Racemate (Niraparib 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；2-氯-6-哌嗪吡嗪盐酸盐MK 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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T22986MK 1903；化合物MK 1903MK-1903|||MK 1903|||MK 1903|||MK1903；0
MK 1903 is a potent and selective complete agonist for the hydroxy-carboxylic acid receptor 2 (HCA2). HCA2 is also known as G protein-coupled receptor 109A(GPR109A). MK 1903 reduced Foschlin-induced cAMP production in uniform time-resolved fluorescence (htf) measurements using CHO cells expressing the human receptor (ECso-12.9 nM).
价 格：￥电议型 号：T22986产 地：中国大陆
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T2239LRaltegravir；雷特格韦MK-0518；雷特格韦|||MK-0518
Raltegravir (MK-0518) 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；MK 0518 potassium sa
Raltegravir potassium (MK 0518 potassium salt) 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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T21835Z-LEHD-fmk；多肽Z-LEHD-fmkZ-LEHD-fmk
Z-LEHD-FMK is a selective and potent caspase-9 inhibitor that protects against reperfusion injury and slows apoptosis.Z-LEHD-FMK exhibits antitumor and neuroprotective activity, increases the yield of in vitro-produced preimplantation embryos of Bubalus bubalis and alters the cellular stress response.
价 格：￥电议型 号：T21835产 地：中国大陆
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T2159CaMKP Inhibitor；化合物CaMKP InhibitorCaMKP Inhibitor
CaMKP Inhibitor can inhibit CaMKP.
价 格：￥电议型 号：T2159产 地：中国大陆
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T21466MK-212；化合物 T21466MK 212|||MK212；MK 212|||MK212
MK-212 is a 5HT2C-receptor agonist. Intraperitoneal injection of MK-212 in 0.5 and 1.0 mg/kg increased the blood level of corticosterone in mice and reduced their motor activity. In 0.1 and 0.2 mg/kg, the agonist reduced anxiety with no effect on motor activity.
价 格：￥电议型 号：T21466产 地：中国大陆
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T21456Grazoprevir hydrate；化合物 T21456Grazoprevir|||MK5172|||MK 5172|||MK-5172；Grazoprevir|||MK5172|||MK 517
Grazoprevir, a second generation hepatitis C virus protease inhibitor acting at the NS3/4a protease targets, has good activity against a range of hepatitis C virus genotype variants, including some that are resistant to most currently used antiviral medications.
价 格：￥电议型 号：T21456产 地：中国大陆
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T2134Dorzolamide hydrochloride盐酸多佐胺MK507 hydrochloride|||L671152 hydrochloride|||MK-507 (L-671152) HCl|||
Dorzolamide hydrochloride (MK507 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. Distributed throughout many cells and tissues, various carbonic anhydrases play important roles in mineral and metabolic homeostasis.
价 格：￥电议型 号：T2134产 地：中国大陆
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T21321MK-0731；化合物 T21321MK-0731
MK-0731, a synthetic small molecule with potential antineoplastic activity, selectively inhibits kinesin spindle protein (KSP), leading to the inhibition of mitotic spindle assembly, induction of cell cycle arrest during the mitotic phase and apoptosis in tumor cells that overexpress KSP.
价 格：￥电议型 号：T21321产 地：中国大陆
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T2126MK-5046；化合物MK5046MK-5046
MK-5046 is a novel BRS-3 agonist, binding to BRS-3 with high affinity (mouse Ki = 1.6 nM, human Ki = 25 nM).
价 格：￥电议型 号：T2126产 地：中国大陆
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T21039PL 100；化合物 T21039MK-8122|||PL-100|||PPL-100|||PPL 100|||MX-100；MK-8122|||PL-100|||PPL-100|||PPL 100|
PL 100 could inhibit HIV-1 protease.
价 格：￥电议型 号：T21039产 地：中国大陆
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T20950MK-8245 analog；化合物 T20950MK-8245-analog|||MK 8245 analog；MK-8245-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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T2077Adavosertib；化合物AdavosertibAZD1775|||MK-1775|||Adavosertib (MK-1775)；AZD1775|||MK-1775|||Adavosertib
Adavosertib (MK-1775) is a selective inhibitor of the cell cycle regulatory protein Wee1 (IC50=5.2 nM). Adavosertib has antitumor activity that blocks the cell cycle and inhibits tumor cell proliferation.
价 格：￥电议型 号：T2077产 地：中国大陆
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T20552Tirofiban HCl；化合物 T20552MK 383|||Aggrastat|||MK383|||MK-383|||Tirofiban hydrochloride；MK 383|||Aggra
Tirofiban HCl is an antagonist of platelet glycoprotein-IIb/IIIa receptor.
价 格：￥电议型 号：T20552产 地：中国大陆
