31
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Cat. No. | Product Name | Target | Signaling Pathways |
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T36126 |
TMP-153
|
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Acyl-CoA:cholesterol acyltransferase (ACAT) catalyses the esterification of excess cellular cholesterol with fatty acids and is important for intestinal cholesterol absorption, hepatic lipoprotein secretion, and cholesterol accumulation in vascular tissues. ACAT inhibitors improve plasma lipid profile and ameliorate proteinuria in nephrotic animals. TMP-153 is a quinolyl derivative that inhibits ACAT with IC50 values of 5-10 nM in various animals. At 0.5-1.5 mg/kg, TMP-153 dose-dependently reduc... | |||
T13172L1 |
TMP-778
|
ROR | Metabolism |
TMP-778是一种RORγt 的选择性逆向激动剂。 | |||
T13174 |
TMPyP4 tosylate
TMP 1363 |
DNA/RNA Synthesis; Telomerase | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
TMPyP4 tosylate (TMP 1363) 是四链体 (G-quadruplex) 的特异性配体,抑制四链体和 IGF-1 之间的相互作用。它也是端粒酶抑制剂,在骨肉瘤细胞系中显示抗肿瘤作用。 | |||
T3983 |
TMP195
TFMO 2,TMP 195 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
TMP195 (TFMO 2) 是一种选择性 IIa 类组蛋白脱乙酰酶 (HDAC) 抑制剂。对 HDAC4、HDAC5、HDAC7,HDAC9的 Ki 值分别为59、60、26,5 nM。 | |||
T1857 |
TMP269
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
TMP269 是一种有效的特异性 IIa 类 HDAC 抑制剂,分别抑制 HDAC 4/HDAC 5/HDAC 7/HDAC 9,IC50值分别为 157 nM,97 nM,43 nM 和 23 nM。 | |||
T31017 |
Coumarin-TMP-Halo
Coumarin TMP Halo,CTH |
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Coumarin-TMP-Halo is a specific fluorescent protein labeling agent. | |||
T34893 |
TMP-NVOC-Halo
TNH |
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TMP-NVOC-Halo is a caged protein labeling agent. | |||
T80972 |
TNH
TMP-NVOC linker-Halo |
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TNH为一种二聚体,能够渗透活细胞并招募蛋白质至细胞结构。 | |||
T78534 |
NVOC cage-TMP-Halo
|
Others | Others |
NVOC cage-TMP-Halo是一种具有细胞渗透能力和光激活特性的蛋白质二聚化诱导剂。该化合物可对活细胞内蛋白质定位进行快速且可逆的控制,适用于研究动态细胞过程。 | |||
T24899 |
Trimosulfa
Trimethoprim-sulfamethoxazole,Sulfamethoxazole-trimethoprim,TMP-SMX,Trimforte,Trimethoprimsulfa |
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Trimosulfa is a fixed antibiotic combination that widely used for mild-to-moderate bacterial infections and as prophylaxis against opportunistic infections. | |||
T13172L | TMP778 | Others | Others |
TMP778 is an effective and selective RORγt inverse agonist (IC50: 7 nM in FRET assay). | |||
T17108 |
TMP920
|
ROR | Metabolism |
TMP920 inhibits RORγt binding to the SRC1 peptide (IC50: 0.03 μM). TMP920 is a highly potent and selective RORγt antagonist. | |||
T13172 | TMP780 | ROR | Metabolism |
TMP780 is an inverse RORγt agonist (IC50: 13 nM). RORγt is a tractable drug target for the treatment of cutaneous inflammatory disorders. | |||
T83821 |
Thymidine-5'-O-(α,β-methylene)diphosphate sodium
α,β-Methylenethymidine diphosphate,Thymidine-5'-O-methylenediphosphate,TMP-CP,α,β-MTDP |
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TMP-CP(Thymidine-5’-O-(α,β-methylene)diphosphate)是TDP的一种水解稳定衍生物,同时也是一种thymidine kinase抑制剂(Ki = 23 µM)。它已被用作α,β-methylene-2’-deoxythymidine 5’-triphosphate合成的前体,该合成物是DNA polymerase的一种不可切割底物。 | |||
T40732 |
TMPD dihydrochloride
|
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TMPD dihydrochloride 是酶促转化氧化还原的活性底物和用于还原血红素过氧化物酶的电子供体。 | |||
T13173 |
TMPA
|
Others; AMPK | Chromatin/Epigenetic; Others; PI3K/Akt/mTOR signaling |
TMPA 是一种核受体 Nur77 和 LKB1 相互作用的拮抗剂。 | |||
T60080 |
TMPH
2,2,6,6-Tetramethylpiperidin-4-yl heptanoate |
AChR | Neuroscience |
TMPH 是一种 nAChR 抑制剂,可抑制缺乏 α5、α6 或 β3 亚基的 nAChR。 TMPH 可用于关于 nAChR 功能障碍或神经系统疾病的研究。 | |||
T61780 |
MtTMPK-IN-4
|
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MtTMPK-IN-4 (compound 2), a para-piperidine, is a highly potent inhibitor of thymidylate kinase (MtTMPK) in Mycobacterium tuberculosis, exhibiting an IC50 value of 6.1 μM. Additionally, it possesses remarkable inhibitory activity against tyrosinase. Furthermore, MtTMPK-IN-4 exhibits potent antibacterial properties [1] [2]. | |||
T63657 | MtTMPK-IN-9 | ||
MtTMPK-IN-9 是中等效力的分支杆菌胸苷酸激酶 (MtbTMPK)抑制剂 (IC50: 48 μM)。MtTMPK-IN-9 对抗分枝杆菌具有亚微摩尔活性,但没有显著的细胞毒性。MtTMPK-IN-9 能够用于研究结核病。 | |||
T63491 | MtTMPK-IN-8 | ||
MtTMPK-IN-8 是具有中等效力的分支杆菌胸苷酸激酶 (MtbTMPK)抑制剂,没有显著的细胞毒性,对抗分枝杆菌表现出亚微摩尔活性 (MICs = 0.78~9.4 μM),能够用于研究结核病。 | |||
T78238 |
4′-DTMP
4-Demethyltrimethoprim |
DHFR; Antifungal | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
4′-DTMP (4-Demethyltrimethoprim) 是一种有效的 DHFR 抑制剂,具有抗菌活性,诱导与酶的额外局部相互作用,对大肠杆菌具有抑制作用。 | |||
T27314 |
Fe-TMPyP
|
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Fe-TMPyP binds to the prion protein PrP and inhibits misfolding. Fe-TMPyP is also a peroxynitrite decomposition catalyst. | |||
T61781 |
MtTMPK-IN-6
|
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MtTMPK-IN-6 (compound 1) is a highly effective inhibitor (IC 50 = 29 μM) of M. tuberculosis thymidylate kinase (Mtb TMPK). It is a valuable compound for tuberculosis research [1]. | |||
T62305 |
MtTMPK-IN-2
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MtTMPK-IN-2 (compound 15)为一高效MtbTMPK抑制剂,IC50值达1.1 μM。该化合物对MtbH37Rv表现出抑制活性(MIC = 12.5 μM),同时对人成纤维细胞MRC-5显示出一定细胞毒性(EC50= 6.1 μM)。MtTMPK-IN-2适用于结核病研究。 | |||
T61796 | MtTMPK-IN-1 | ||
MtTMPK-IN-1 (compound 3) is a highly effective inhibitor of Mycobacterium tuberculosis thymidylate kinase (Mt TMPK), exhibiting an IC50 value of 2.5 μM. It displays moderate to weak activity against Mtb H37Rv while demonstrating low cytotoxicity in human fibroblast cells MRC-5. MtTMPK-IN-1 is a valuable tool for tuberculosis research [1]. | |||
T63639 | MtTMPK-IN-7 | ||
MtTMPK-IN-7 是中等效力的分支杆菌胸苷酸激酶 (MtbTMPK) 抑制剂 (IC50: 47 μM)。MtTMPK-IN-7 对抗分枝杆菌表现出亚微摩尔活性,其 MICs 值为 2.3~4.7 μM。MtTMPK-IN-7 能够用于研究结核病。 | |||
T61573 | MtTMPK-IN-5 | ||
MtTMPK-IN-5 (compound 17) is a highly effective inhibitor of M. tuberculosis thymidylate kinase (Mtb TMPK), demonstrating remarkable enzyme inhibitory activity with an IC50 value of 34 μM. Additionally, MtTMPK-IN-5 exhibits notable activity against M. tuberculosis, as evidenced by a minimum inhibitory concentration (MIC) of 12.5 μM. Given its potent properties, MtTMPK-IN-5 serves as a valuable tool for tuberculosis research [1]. | |||
T35966 |
Mn(III)TMPyP
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Mn(III)TMPyP is a manganese-porphyrin which acts as a superoxide dismutase (SOD) mimetic and peroxynitrite decomposition catalyst. SOD mimetics described to date are unstable and are capable of catalyzing undesired side-reactions in addition to the dismutation of the superoxide radical (O2-). Mn(III)TMPyP is an SOD mimetic with increased stability to pH and hydrogen peroxide. The rate constant for superoxide dismutation and peroxynitrite decomposition are 3.9 x 107 M-1s-1 and ~2 x 106 M-1s-1, re... | |||
T28986 |
TMPPAA
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TMPPAA is an allosteric agonist of 5-HT3 receptor. | |||
T23462 |
TMPH hydrochloride
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Others | Others |
neuronal nicotinic ACh receptors (nAChRs) antagonist | |||
T62897 |
MtTMPK-IN-3
|
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MtTMPK-IN-3(compound 25)是一种针对结核分枝杆菌胸苷酸激酶(MtbTMPK)的有效抑制剂,具有0.12 μM的IC50值。该化合物对MtbH37Rv展示出了抑制效果(MIC=12.5 μM),同时对人成纤维细胞MRC-5显示出一定的细胞毒性(EC50=12.5 μM)。MtTMPK-IN-3适用于结核病研究领域。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T4730 |
Thymidine-5'-monophosphate disodium salt
胸苷酸二钠,Thymidine 5'-monophosphate disodium salt,TMP DISODIUM SALT |
Others; Endogenous Metabolite | Metabolism; Others |
Thymidine-5'-monophosphate disodium salt (TMP DISODIUM SALT) 是内源性代谢产物的一种。 | |||
T4558 |
Trioxsalen
三甲沙林,Trimethylpsoralen,Trioxysalen,Trisoralen |
DNA Alkylator/Crosslinker; DHFR | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism |
Trioxsalen (Trioxysalen) 是一种呋喃香豆素和补骨脂素衍生物,与 UV-A 一起用于光疗治疗白癜风和手部湿疹。它是一种光化学 DNA 交联剂,可用于激光激活定位的基因组链间交联可视化。 | |||
T7892 |
ATMP
|
Others | Others |
ATMP 是一种具有螯合特性的膦酸。它是一种阻垢剂。 | |||
T0572 |
Methyl 3,4,5-trimethoxybenzoate
Methyl gallate trimethyl ether,Methyl EudesMate,3,4,5-Trimethoxybenzoic acid methyl ester,Methyl tri-O-methylgallate,甲氧苄啶杂质H,Trimethylgallic acid methyl ester |
Others | Others |
Methyl 3,4,5-trimethoxybenzoate (Methyl EudesMate) 是由 Gallic acid 为原料合成得到,常用于生产磺胺增效剂中间体、甲氧苄氨嘧啶 (TMP)以及许多其它药物。 | |||
T83320 |
4'-Demethylpodophyllotoxone
|
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4'-Demethylpodophyllotoxone为链格孢(Alternaria alternata)S-f6的生物转化中间产物,经4-(2,3,5,6-tetramethylpyrazine-1) (4-TMP)修饰后形成的新化合物,可有效抑制人胃癌细胞系(BGC-823)的生长。 | |||
T75540 |
Ipomoeassin F
|
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Ipomoeassin F 是一种高效且具有选择性的内质网(ER)蛋白转位抑制剂,它通过作用于ER膜上的Sec61复合物(Sec61α)的成孔亚基来实现其功能。此化合物能特异性抑制SARS-CoV-2蛋白在ER膜上的转位,同时阻碍分泌蛋白和I型跨膜蛋白(TMP)的ER转运,但对III型TMP的转运不产生影响。 |