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T73990Lipid M；化合物 Lipid MLipid M
Lipid M (pKa: 6.75) is a potential carrier for mRNA vaccines, offering enhanced immune responses and increased tolerability [1].
价 格：￥电议型 号：T73990产 地：中国大陆
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T73918Lauroyl coenzyme A lithium；化合物 Lauroyl coenzyme A lithiumLauroyl coenzyme A lithium
Lauroyl coenzyme A lithium salt is a kind of coenzyme A. Coenzyme A acts as an acyl carrier, namely acetyl-CoA. Lauryl-CoA (C12-CoA) is a long-chain (C-12) saturated fatty acyl-CoA that functions as an intermediate in lipid metabolism, involved in lipid biosynthesis and fatty acid transport. Lauroyl-CoA is a substrate for the FAM34A protein and the product of firefly luciferase.
价 格：￥电议型 号：T73918产 地：中国大陆
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T7366NGI-1；化合物NGI-1ML414；ML414
NGI-1 (ML414) is a a cell-permeable inhibitor of oligosaccharyltransferase (OST).can effectively reduce virus infectivity without affecting cell viability.
价 格：￥电议型 号：T7366产 地：中国大陆
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T73647Boc-MLF TFA；化合物 Boc-MLF TFABoc-MLF TFA
Boc-MLF (TFA), a peptide antagonist specific to the formyl peptide receptor (FPR), also inhibits signaling through formyl peptide receptor like 1 (FPRL1) at elevated concentrations [1].
价 格：￥电议型 号：T73647产 地：中国大陆
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T73525ML202；化合物 ML202ML202
ML202 is a highly specific allosteric activator of human pyruvate kinase M2 (hPK-M2), enhancing the cooperativity of phosphoenolpyruvate (PEP) binding, with negligible effect on adenosine diphosphate (ADP) binding.
价 格：￥电议型 号：T73525产 地：中国大陆
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T73279MLKL-IN-5；化合物 MLKL-IN-5MLKL-IN-5
MLKL-IN-5 is a potent MLKL inhibitor that mediates necroptosis [1] .
价 格：￥电议型 号：T73279产 地：中国大陆
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T72913(R)-MLN-4760；化合物 (R)-MLN-4760(R)-MLN-4760
(R)-MLN-4760, the R-enantiomer of MLN-4760, functions as an ACE2 inhibitor and exhibits a half maximal inhibitory concentration (IC50) of 8.4 μM, identifying it as the less active isomer.
价 格：￥电议型 号：T72913产 地：中国大陆
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T72861(6R)-ML753286；化合物 (6R)-ML753286(6R)-ML753286
´(6R)-ML753286, an isomer of ML753286, is an orally active, selective Breast Cancer Resistance Protein (BCRP) inhibitor, demonstrating an IC50 of 0.6 μM. It exhibits high permeability and low to medium clearance in rodent and human liver S9 fractions, with cross-species plasma stability [1].´
价 格：￥电议型 号：T72861产 地：中国大陆
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T72360Menin-MLL inhibitor 26；化合物 Menin-MLL inhibitor 26Menin-MLL inhibitor 26
Menin-MLL inhibitor 26 is a Menin-MLL inhibitor. Menin-MLL inhibitor 26 also is an active reference. Menin-MLL inhibitor 26 can inhibits cell growth. Menin-MLL inhibitor 26 can be used for the research of leukemia [1] .
价 格：￥电议型 号：T72360产 地：中国大陆
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T7214TEPP-46；化合物ML265ML265；ML265
TEPP-46 (ML265) is a potent PKM2 activator (AC50 : 92 nM) showing little or no effect on PKM1, PKL and PKR,induces tetramerization and reduces tumor formation and size in a mouse xenograft model. .
价 格：￥电议型 号：T7214产 地：中国大陆
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T72135(1s,4s)-Menin-MLL inhibitor-23；化合物 (1s,4s)-Menin-MLL inhibitor-23(1s,4s)-Menin-MLL inhibitor-23
(1s,4s)-Menin-MLL Inhibitor-23, an enantiomer of Menin-MLL Inhibitor-23 (Example 99A), functions as an inhibitor of the menin-MLL interaction [1].
价 格：￥电议型 号：T72135产 地：中国大陆
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T71992ML-077；化合物 ML-077Lipoxal-d10|||ML077|||Oxaliplatin d10|||ML-077|||ML 077|||Lipoxal d10；Lipoxal-d10||
ML-077, also known as VU0255011, is a highly selective, potent, saline soluble, best in class" KCC2 antagonist for high fidelity in vitro studies on KCC2 function with IC(50)=537 nM. ML-077 is cell permeable and exhibits submicromolar potency
价 格：￥电议型 号：T71992产 地：中国大陆
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T71583Amlodipine hydrochloride, (R)-；化合物 Amlodipine hydrochloride, (R)-Amlodipine hydrochloride, (R)-
Amlodipine hydrochloride, (R)-, is a medication used to lower blood pressure and prevent chest pain. It belongs to a group of medications known as dihydropyridine-type calcium channel blockers. By widening of blood vessels it lowers blood pressure. In angina, amlodipine increases blood flow to the heart muscle to relieve pain due to angina.
价 格：￥电议型 号：T71583产 地：中国大陆
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T71504MLS-2384；化合物 MLS-2384MLS-2384
MLS-2384 is a dual JAK/Src kinase inhibitor, suppressing growth of diverse cancer cells.
价 格：￥电议型 号：T71504产 地：中国大陆
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T71380MLN-0415；化合物 MLN-0415MLN-0415
MLN-0415 is an IKK2 inhibitor which decreases NF-κB activation and down-regulates the expression of a number of inflammatory proteins.
价 格：￥电议型 号：T71380产 地：中国大陆
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T71352MLS000099089；化合物 MLS000099089MLS000099089
MLS000099089 is a selective and potent inhibitor of recombinant human 12/15-LOX and cellular murine 12/15-LOX.
价 格：￥电议型 号：T71352产 地：中国大陆
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T7091N-Formyl-Met-Leu-Phe；酪胺盐酸盐fMLP|||N-Formyl-MLF；fMLP|||N-Formyl-MLF
N-Formyl-Met-Leu-Phe (N-Formyl-MLF) (fMLF) is a synthetic peptide that acts as an agonist at formyl peptide receptors (FPR; Ki = 0.8 pM).
价 格：￥电议型 号：T7091产 地：中国大陆
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T70890ML309；化合物 ML309ML309
ML309 is a potent inhibitor of R132H mutant IDH1 capable of reducing 2-hydroxyglutarate production in U87 MG glioblastoma cells. ML309 is capable of potent and selective inhibition of mutant IDH1 and effectively lowers cell-based production of 2-HG in a U87MG mutant glioblastoma cell line.
价 格：￥电议型 号：T70890产 地：中国大陆
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T70822Gemlapodect；化合物 GemlapodectRO554965；RO554965
Gemlapodect (RO554965), a phosphodiesterase 10A (PDE10A) inhibitor, is utilized in schizophrenia research.
价 格：￥电议型 号：T70822产 地：中国大陆
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T70786ML252；化合物 ML 252ML252
ML252 is a selective potassium channel inhibitor, specifically targeting the KCNQ2 channel (Kv7.2) with an IC50 value of 69 nM. Additionally, ML252 demonstrates inhibitory activity against Cytochrome P450 isoforms, including IC50 values of 6.1 nM (CYP1A2), 18.9 nM (CYP2C9), 3.9 nM (CYP3A4), and 19.9 nM (CYP2D6).
价 格：￥电议型 号：T70786产 地：中国大陆
