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T6589MK-2048化合物MK2048MK2048
MK-2048 is a potent inhibitor of integrase (IN) and INR263K with IC50 of 2.6 nM and 1.5 nM, respectively.
价 格：￥电议型 号：T6589产 地：中国大陆
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T6486Enalapril Maleate马来酸依那普利MK-421 Maleate|||Renitec Maleate|||Glioten Maleate|||MK-421 (maleate)|||Vaso
Enalapril Maleate (MK-421 Maleate), an angiotensin-converting enzyme (ACE) inhibitor, is utilized in the treatment of hypertension, chronic heart failure , and diabetic nephropathy.
价 格：￥电议型 号：T6486产 地：中国大陆
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T6352(-)-Dizocilpine maleate；(-)-MK 801马来酸C13737|||(-)-MK 801 (Maleate)|||(-)-MK 801 Maleate；C13737|||(-)
(-)-Dizocilpine maleate ((-)-MK 801 (Maleate)) is a potent, selective and non-competitive NMDA receptor antagonist with Kd of 37.2 nM in rat brain membranes.
价 格：￥电议型 号：T6352产 地：中国大陆
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T6340LEnalaprilat；化合物 T6340LMK422|||MK 422|||MK 421 diacid|||Enalapril acid|||MK-422；MK422|||MK 422|||MK 4
Enalaprilat, the active metabolite of Enalapril, is a effective intravenously administered angiotensin-converting enzyme inhibitor. It is an effective agent for the treatment of essential hypertension and has beneficial hemodynamic effects in heart failure.
价 格：￥电议型 号：T6340L产 地：中国大陆
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T6340Enalaprilat Dihydrate；依那普利拉二水合物MK-422|||MK-422 Dihydrate；依那普利拉二水合物|||MK-422|||MK-422 Dihydrate
Enalaprilat Dihydrate (MK-422 Dihydrate) （IC50=1.94 nM） is a potent angiotensin-converting enzyme (ACE) inhibitor.
价 格：￥电议型 号：T6340产 地：中国大陆
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T62760ROMK-IN-32；化合物 ROMK-IN-32ROMK-IN-32
ROMK-IN-32 is an inhibitor of the extra-renal medullary potassium channel (ROMK) (IC50: 35 nM) and also inhibits hERG (IC50: 22 μM).
价 格：￥电议型 号：T62760产 地：中国大陆
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T62609MK-2206；化合物 MK-2206MK-2206
MK-2206 is an orally active, highly selective, metabotropic Akt inhibitor that acts on Akt1 (IC50: 8 nM), Akt2 (IC50: 12 nM) and Akt3 (IC50: 65 nM). Many breast cancer cell lines, PIK3CA mutants and PTEN-losing cell lines are sensitive to MK-2206, which has anti-cancer effects.
价 格：￥电议型 号：T62609产 地：中国大陆
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T6259Dizocilpine；地佐环平MK-801；地佐环平|||MK-801
MK-801 (Dizocilpine (MK-801)) is a potent N-methyl-D-aspartate (NMDA) receptor antagonist with Ki of 30.5 nM.
价 格：￥电议型 号：T6259产 地：中国大陆
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T62544MK-8153；化合物 MK-8153MK-8153
MK-8153 is a selective, potent, orally active inhibitor of extrarenal medullary potassium channels (ROMK), acting on ROMK EP (IC50: 5 μM) and hERG EP (IC50: 34 μM).MK-8153 can be used as a diuretic.
价 格：￥电议型 号：T62544产 地：中国大陆
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T62110MK2-IN-4；化合物 MK2-IN-4MK2-IN-4
MK2-IN-4 is a MAPKAPK2 (MK2) inhibitor (IC50: 45 nM). MK2-IN-4 can be used in cancer, inflammation and immunology studies.
价 格：￥电议型 号：T62110产 地：中国大陆
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T61933MK-0159；化合物 MK-0159MK-0159
MK-0159 is an orally available, highly potent CD38 inhibitor with myocardial injury protection for the study of cardiac ischemia and reperfusion injury.
价 格：￥电议型 号：T61933产 地：中国大陆
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T61878N-Demethyl MK-6884；化合物 N-Demethyl MK-6884N-Demethyl MK-6884
N-Demethyl MK-6884 (compound 34) is an influential allosteric modulator of the M4 mAChR, which finds applicability in Alzheimer´s disease research as well as the study of other diseases influenced by the M4 mAChR [1].
价 格：￥电议型 号：T61878产 地：中国大陆
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T61859MK-28；化合物 MK-28MK-28
MK-28 is a selective PERK agonist that reduces toxicity and prolongs survival in a Huntington´s disease model.MK-28 has a significant killing effect on MK28 gastric cancer cells.
价 格：￥电议型 号：T61859产 地：中国大陆
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T6182Tirofiban；替罗非班L700462|||Aggrastat|||MK383；L700462|||Aggrastat|||替罗非班|||MK383
Tirofiban (L700462) (MK-383) is a selective palate GPIIb/IIIa antagonist which inhibits platelet aggregation with IC50 of 9 nM.
价 格：￥电议型 号：T6182产 地：中国大陆
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T60951Molnupiravir；莫努匹韦EIDD-2801|||Lagevrio|||MK-4482；EIDD-2801|||Lagevrio|||MK-4482
Molnupiravir (MK-4482) (EIDD-2801) is a prodrug of the ribonucleoside analog EIDD-1931 which is orally bioavailable. Molnupiravir can be used in COVID-19, seasonal and pandemic influenza research that has broad spectrum antiviral activity against multiple coronaviruses and influenza virus, for example, SARS-CoV-2, MERS-CoV, SARS-CoV [1][2].
价 格：￥电议型 号：T60951产 地：中国大陆
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T6094MK-2461；化合物MK2461MK2461；MK2461
MK-2461 is a novel inhibitor that targets multiple proteins and competitively binds to ATP sites, specifically inhibiting the activated c-Met protein with an average inhibitory concentration (IC50) of 2.5 nM.
价 格：￥电议型 号：T6094产 地：中国大陆
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T60857MKK7-COV-9；MKK共价抑制剂9MKK7-COV-9
MKK7-COV-9 is a selective and potent covalent inhibitor of MKK7 with inhibitory effects on MKK7-induced protein-protein interactions.MKK7-COV-9 interrupts the activation of primary B-cells in response to LPS.MKK7-COV-9 shows low cytotoxicity at high concentrations.
价 格：￥电议型 号：T60857产 地：中国大陆
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T60688MKI-1；化合物MKI-1MASTL Kinase Inhibitor-1；MASTL Kinase Inhibitor-1
MKI-1 (MASTL Kinase Inhibitor-1) is an inhibitor of MASTL (microtubule-associated serine/threonine kinase-like, IC50= 9.9 μM). MKI-1 exerts radiosensitizer and antitumor activities through PP2A activation in breast cancer.
价 格：￥电议型 号：T60688产 地：中国大陆
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T6068MK-5108；化合物MK-5108VX-689|||MK5108；VX-689|||MK5108
MK-5108 (VX-689) is a highly potent and specific Aurora-A kinase inhibitor with an IC50 value of 0.064 nM.
价 格：￥电议型 号：T6068产 地：中国大陆
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T6061LMK-235；化合物LMK235LMK235；LMK235
LMK-235 is a potent HDAC inhibitor, and is used in cancer research.
价 格：￥电议型 号：T6061产 地：中国大陆
