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T41345AFMK；化合物AFMKFormyl-N-acetyl-5-methoxykynurenamine|||Acetyl-N-formyl-5-methoxykynurenamine；Formyl-N-a
AFMK (Formyl-N-acetyl-5-methoxykynurenamine) is an active metabolite of Melatonin with antioxidant and free radical scavenging activity. AFMK is a modulator of apoptosis and improves the anti-tumor effect of Gemcitabine in PANC-1 cells.
价 格：￥电议型 号：T41345产 地：中国大陆
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T41269PMK ethyl glycidate；化合物 PMK ethyl glycidatePMK ethyl glycidate
PMK ethyl glycidate has a wide range of applications in life science related research.
价 格：￥电议型 号：T41269产 地：中国大陆
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T4106MK-8617；化合物MK8617MK8617；MK8617
MK-8617 is an orally available HIF PHD1 3 pan-inhibitor, inhibiting PHD1/2/3 (IC50: 1.0/1.0/14 nM).
价 格：￥电议型 号：T4106产 地：中国大陆
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T40930(S)-Sitagliptin phosphate；(S)-Sitagliptin phosphate(S)-Sitagliptin phosphate|||(S)-MK-0431 phosphate
(S)-Sitagliptin phosphate, the less active S-enantiomer of Sitagliptin phosphate, is a high-potency inhibitor of DPP4. It exhibits an IC50 of 19 nM in Caco-2 cell extracts.
价 格：￥电议型 号：T40930产 地：中国大陆
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T40602Z-LEHD-FMK TFA；Z-LEHD-FMK TFAZ-LEHD-FMK TFA
Z-LEHD-FMK TFA is a specific and irreversible inhibitor of caspase-9, offering protection against detrimental reperfusion injury and moderating apoptosis. Additionally, Z-LEHD-FMK TFA demonstrates its neuroprotective potential in a rat model of spinal cord trauma.
价 格：￥电议型 号：T40602产 地：中国大陆
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T40396FgGpmk1-IN-1FgGpmk1-IN-1FgGpmk1-IN-1
FgGpmk1-IN-1 is a new inhibitor of the fusarium graminearum mitogen-activated protein kinase (FgGpmk1), displaying a potency with an EC50 value of 3.46 μg/mL.
价 格：￥电议型 号：T40396产 地：中国大陆
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T4017Relebactam；瑞来巴坦MK-7655；瑞来巴坦|||MK-7655
Relebactam (MK-7655) is a diazabicyclooctane inhibitor with activity against a wide spectrum of β-lactamases.
价 格：￥电议型 号：T4017产 地：中国大陆
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T3984GLP-1(7-36), amide；胰高血糖素样肽-1MKC 253|||Human GLP-1-(7-36)-amide|||Glucagon-like Peptide 1 (7-36) amid
GLP-1(7-36), amide (MKC 253) is a peptide hormone released from intestinal L-cells upon nutrient consumption. It binds the GLP-1 receptor in the pancreas and displays various antidiabetic effects by potentiating glucose-induced secretion of insulin from pancreatic β-cells, increasing insulin expression.
价 格：￥电议型 号：T3984产 地：中国大陆
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T3960T56-LIMKi；化合物T56-LIMKiT5601640；T5601640
T56-LIMKi (T5601640) is a selective inhibitor of LIMK2.
价 格：￥电议型 号：T3960产 地：中国大陆
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T39545MK-6884；MK-6884MK-6884
MK-6884, a positive allosteric modulator (PAM) of M4 muscarinic receptors, exhibits a high affinity (Ki = 0.19 nM). It is a valuable compound for the investigation of neurodegenerative diseases. Additionally, MK-6884 can be efficiently radiolabeled with carbon-11, enabling its use as a PET imaging agent.
价 格：￥电议型 号：T39545产 地：中国大陆
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T39526Decanoyl-RVKR-CMK TFA；Decanoyl-RVKR-CMK TFADecRVKRcmk TFA|||Decanoyl-RVKR-CMK TFA；DecRVKRcmk TFA|||D
Decanoyl-RVKR-CMK (DecRVKRcmk) TFA effectively hinders the processing of over-expressed gp160 and suppresses HIV-1 replication.
价 格：￥电议型 号：T39526产 地：中国大陆
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T39521LEESGGGLVQPGGSMK；LEESGGGLVQPGGSMKLEESGGGLVQPGGSMK
LEESGGGLVQPGGSMK, a proteolysis peptide, is a constituent of Infliximab, a chimeric monoclonal IgG1 antibody that selectively binds to TNF-α. It can be employed for quantitative assessment of Infliximab.
价 格：￥电议型 号：T39521产 地：中国大陆
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T39489Ulevostinag；UlevostinagUlevostinag|||MK-1454；Ulevostinag|||MK-1454
Ulevostinag (MK-1454) is a STING agonist.
价 格：￥电议型 号：T39489产 地：中国大陆
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T39344Z-VDVA-(DL-Asp)-FMK；Z-VDVA-(DL-Asp)-FMKZ-VDVA-(DL-Asp)-FMK
Z-VDVA-(DL-Asp)-FMK is a derivative compound of Z-VDVAD-FMK specifically designed as an inhibitor targeting caspase-2.
价 格：￥电议型 号：T39344产 地：中国大陆
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T39086MK-4688；MK-4688MK-4688
MK-4688 is an efficient inhibitor of the HDM2-p53 protein-protein interaction.
价 格：￥电议型 号：T39086产 地：中国大陆
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T38908MK-8262；MK-8262MK-8262
MK-8262, an orally active and potent cholesteryl ester transfer protein (CETP) inhibitor (IC 50 = 53 nM, log D = 5.3), is a bistrifluoromethyl analogue that shows promise in research related to high-density lipoprotein (HDL) and low-density lipoprotein (LDL) with potential implications for coronary heart disease (CHD).
价 格：￥电议型 号：T38908产 地：中国大陆
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T38844MK-8245 Trifluoroacetate；MK-8245 TrifluoroacetateMK-8245 Trifluoroacetate
MK-8245 trifluoroacetate is a phenoxy piperidine isoxazole derivative functioning as a potent, liver-targeting stearoyl-CoA desaturase (SCD) inhibitor, demonstrating significant anti-diabetic and anti-dyslipidemic effects. It showcases high specificity and efficacy against SCD1 across various species, with IC50 values of 1 nM for human SCD1 and 3 nM for both rat and mouse SCD1. MK-8245´s mechanism includes a tetrazole acetic acid moiety that facilitates liver-targeting through OATPs recogn
价 格：￥电议型 号：T38844产 地：中国大陆
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T38594MK-5204；MK-5204MK-5204
MK-5204 is an orally active β-1,3-glucan synthesis inhibitor.
价 格：￥电议型 号：T38594产 地：中国大陆
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T38469(Rac)-Z-Phe-Phe-FMK；化合物(Rac)-Z-Phe-Phe-FMKCathepsin L-IN-2；Cathepsin L-IN-2
(Rac)-Z-Phe-Phe-FMK (Cathepsin L-IN-2) is a cathepsin L inhibitor that inhibits the tendency of β-amyloid to induce apoptotic changes .
价 格：￥电议型 号：T38469产 地：中国大陆
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T3722MK-1064；化合物MK1064Urokinase inhibitor 1|||MK 1064；Urokinase inhibitor 1|||MK 1064
MK-1064 (Urokinase inhibitor 1) is a selective orexin 2 receptor antagonist (2-SORA).
价 格：￥电议型 号：T3722产 地：中国大陆
