Cat. No. | Product Name | Target | Signaling Pathways |
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T67919 |
NMT-IN-1
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Others | Others |
NMT-IN-1 是一种有效的 N-肉豆豆酰转移酶(NMT) 抑制剂,对 TbNMT 的 IC50为31μM , 对 hNMT 的 IC50为66μM。NMT-IN-1是治疗非洲锥虫病的潜在化合物。 | |||
T27135 |
DDD85646
DDD 85646,DDD-85646 |
Parasite | Microbiology/Virology |
DDD85646 是 T. brucei N-myristoyltransferase 的抑制剂,Ki 为 1.44 nM,IC50 为 2 nM,EC50 为 2 nM。 hNMT 的 IC50 为 4 nM。 | |||
T8760 |
NNMTi
5-Amino-1-methylquinolinium |
Others | Others |
NNMTi (5-Amino-1-methylquinolinium) 是烟酰胺 N -甲基转移酶的抑制剂 (IC50=1.2 μM),可选择性地结合 NNMT 底物结合位点残基。它能诱导体外成肌细胞分化,提高老年小鼠肌肉干细胞融合和再生能力。 | |||
T63493 | NNMT-IN-2 | ||
NNMT-IN-2 是一种很强的NNMT 抑制剂 (IC50: 3.7 nM)。 | |||
T38437 |
NMTCA
N-Nitroso-2-methylthiazolidine4-carboxylicacid,NMTPRO,N-nitrosomethylthioproline |
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NMTCA (NMTPRO) is a sulfur-containing N-nitrosamino acid utilized as an endogenous nitrosation indicator in gas chromatography-thermal energy analysis. | |||
T81661 |
NNMT-IN-4
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NNMT-IN-4(compound 38),一种选择性、非竞争性且具有膜通透性的烟酰胺N-甲基转移酶(NNMT)抑制剂,在体外生化及细胞实验中的IC50值为42 nM和38 nM。该抑制剂展现出良好的PK/PD关系和安全性,同时具备优秀的口服生物利用度和药物制剂性质,适合作为NNMT活性研究的体内化学探针。 | |||
T81432 |
PNMT-IN-1
|
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PNMT-IN-1(Inhibitor 4)是一种高特异性的PNMT抑制剂,具有1.2 nM的Ki值和81 nM的IC50值。它对DNMT1和DNMT3b也表现出活性,IC50值分别为61 μM和17 μM,并且对肾上腺素具有拮抗效果。PNMT-IN-1属于第二代抑制剂。 | |||
T64189 |
NNMT-IN-3
|
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NNMT-IN-3 (compound 14) 是一种有效的、选择性的烟酰胺 N-甲基转移酶 (NNMT) 抑制剂,在无细胞和基于细胞的实验中的 IC50 值分别为 1.1 nM 和 0.4 μM。NNMT-IN-3 能够用于肥胖、癌症、II 型糖尿病及骨骼肌减少症等疾病的研究。 | |||
T63859 |
DNMT3A-IN-1
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DNMT3A-IN-1 是选择性的、有效的 DNMT3A 抑制剂。 DNMT3A-IN-1 对 DNMT3A 表现出抑制活性,其 KI 的范围为 9.16-18.85 μM (AdoMet) 和 11.37-23.34 μM (poly dI-dC)。 | |||
T23477 |
tris(dibenzylideneacetone)dipalladium
Tris DBA,三(二亚苄基丙酮)二钯 |
Others | Others |
tris(dibenzylideneacetone)dipalladium (Tris DBA) 是一种 N-myristoyltransferase-1 (NMT-1) 抑制剂。 | |||
T63788 |
PCLX-001
|
Others | Others |
PCLX-001 is a small-molecule compound that acts as an orally active inhibitor of N-myristoyltransferase (NMT), specifically targeting NMT1 and NMT2 with IC50 values of 5 nM and 8 nM, respectively. This compound demonstrates anti-tumor effects and effectively inhibits the early signaling of B-cell receptor (BCR). Consequently, PCLX-001 is a valuable tool for researching B-cell malignancies [1] [2]. | |||
T27831 |
Lifibrate
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Lifibrate is an inhibitor of cholinephosphotransferase (CPT), phosphatidyl-N,N-dimethylethanolamine N-methyltransferase (PDE-NMT), and phosphatidyl-N-methylethanolamine N-methyltransferase (PME-NMT). | |||
T28701 |
SC-58272
SC58272 |
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SC-58272 is an inhibitor of N-myristoyltransferase (Nmt), a target for anti-fungal and anti-viral therapy. | |||
T27127 |
DCAT Maleate
DCAT |
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DCAT Maleate is an inhibitor of N-methyl transferases (NMT). DCAT Maleate methylate non-methylated pre-neurotoxins to prevent the formation of Parkinson's syndrome neurotoxins. | |||
T68562 |
FTR-1335
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FTR1335 is a CaNMT inhibitor (IC50 = 0.49 nM) with good fungal selectivity. CaNMT inhibitors are fungicidal and show antifungal activity against Candida (especially fluconazole-resistant strains). They function by inhibiting N-myristoyltransferase (NMT), which catalyzes the transfer of a C14 fatty acif from myristoyl-CoA to the N-terminal of glycine in many fungal proteins. Without this process, fungi can die. This process also occurs in humans, and as such selectivity is an important characteri... |