Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T36880 |
NHC-diphosphate
|
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NHC-diphosphate is an active phosphorylated intracellular metabolite of β-d-N4-Hydroxycytidine (NHC) as a diphosphate form[1]. NHC is a pyrimidine ribonucleoside and behaves as a potent anti-virus agent. NHC effectively inhibits the replication of venezuelan equine encephalitis virus (VEEV), Chikungunya virus (CHIKV) and hepatitis C virus (HCV)[1]. Huh-7 cells are incubated with (10-50 μM; 4 h) NHC or a McGuigan phosphoramidate prodrug of NHC.Intracellular levels of the parental compounds and ... | |||
T36881 | NHC-diphosphate triammonium | ||
NHC-triphosphate triammonium is an active phosphorylated intracellular metabolite of β-d-N4-Hydroxycytidine (NHC) as a triphosphate form[1]. NHC-triphosphate triammonium is a weak alternative substrate for the viral polymerase and can be incorporated into HCV replicon RNA[1][2]. In an intracellular metabolism assay, HCV replicon cells are treated with 10 μM 3H-labeled NHC, and intracellular nucleotide levels are determined after 1, 2 and 8 hours incubations. NHC is rapidly convered into the mono... | |||
T19476 |
NHC-triphosphate
|
Others | Others |
NHC-triphosphate is a weak alternative substrate for the viral polymerase and changes the mobility of the product in polyacrylamide electrophoresis gels. | |||
T74070 | NHC-triphosphate tetrasodium | ||
NHC-triphosphate tetrasodium 是 NHC 的活性胞内磷酸盐代谢物 (intracellular metabolite),以三磷酸盐的形式存在。NHC-triphosphate tetrasodium 是病毒聚合酶 (viral polymerase) 的弱底物替代物,会被并入HCV 复制子 RNA 中。 | |||
T8498 |
EIDD-1931
Beta-d-N4-hydroxycytidine |
Virus Protease; HCV Protease; SARS-CoV; Topoisomerase | DNA Damage/DNA Repair; Microbiology/Virology; Proteases/Proteasome |
EIDD-1931 (Beta-d-N4-hydroxycytidine) 是一种核苷类抗病毒试剂 ,可抑制丙型肝炎病毒、基孔肯亚病毒和委内瑞拉马脑炎病毒的复制活性。 | |||
T18794 |
Tetrazine-Ph-NHCO-C3-NHS ester
|
Others; PROTAC Linker | Others; PROTAC |
Tetrazine-Ph-NHCO-C3-NHS ester是一种源于PEG的PROTACs合成连接剂。 | |||
T17763 |
DBCO-NHCO-PEG2-amine
|
Others | Others |
DBCO-NHCO-PEG2-amine is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17768 |
DBCO-NHCO-PEG3-acid
|
Others | Others |
DBCO-NHCO-PEG3-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T15061 |
DBCO-NHCO-PEG4-acid
|
Others | Others |
DBCO-Amide-PEG5-acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T18795 |
Tetrazine-Ph-NHCO-PEG3-alcohol
|
Others | Others |
Tetrazine-Ph-NHCO-PEG3-alcohol is a polyethylene glycol (PEG) derived linker specifically designed for use in the synthesis of proteolysis targeting chimeras (PROTACs)[1]. | |||
T39186 |
Boc-NHCH2CH2-PEG1-azide
Boc-NHCH2CH2-PEG1-azide |
||
Boc-NHCH2CH2-PEG1-azide is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17761 |
DBCO-NHCO-PEG13-acid
|
Others | Others |
DBCO-NHCO-PEG13-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17773 |
DBCO-NHCO-PEG7-acid
|
Others | Others |
DBCO-NHCO-PEG7-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17759 |
DBCO-NHCO-PEG12-biotin
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Others | Others |
DBCO-NHCO-PEG12-biotin is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T15064 |
DBCO-NHCO-PEG4-NHS ester
|
Others | Others |
DBCO-NHCO-PEG4-NHS ester ester is a MMP-2- and cathepsin B- (CatB) cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T18798 | Tetrazine-Ph-NHCO-PEG6-NH-Boc | Others | Others |
Tetrazine-Ph-NHCO-PEG6-NH-Boc is a PEG-based PROTAC linker utilized for PROTACs synthesis[1]. | |||
T17774 | DBCO-NHCO-S-S-NHS ester | Others | Others |
DBCO-NHCO-S-S-NHS ester is a cleavable linker employed for the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T17757 | DBCO-NHCO-C4-NHS ester | Others | Others |
DBCO-NHCO-C4-NHS ester is an alkyl chain-derived PROTAC linker applicable for PROTACs synthesis[1]. | |||
T17758 |
DBCO-NHCO-PEG12-amine
|
Others | Others |
DBCO-NHCO-PEG12-amine is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17770 |
DBCO-NHCO-PEG6-amine
|
Others | Others |
DBCO-NHCO-PEG6-amine is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T18796 |
Tetrazine-Ph-NHCO-PEG4-alkyne
|
Others | Others |
Tetrazine-Ph-NHCO-PEG4-alkyne is a PEG4-based linker for PROTACs synthesis[1]. | |||
T40049 |
MC-AAA-NHCH2OCH2COO-7-aminomethyl-10-methyl-11-fluoro camptothecin
MC-AAA-NHCH2OCH2COO-7-aminomethyl-10-methyl-11-fluoro camptothecin |
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MC-AAA-NHCH2OCH2COO-7-aminomethyl-10-methyl-11-fluoro camptothecin (compound 21a), is a camptothecin payload which can be utilized in the synthesis of a camptothecin antibody-drug conjugate (ADC) by conjugation to a monoclonal antibody (mAb). | |||
T15062 | DBCO-NHCO-PEG4-amine | Others | Others |
DBCO-NHCO-PEG4-amine is a cleavable ADC linker used to conjugate MMAE and antibody (e.g., DBCO-VCpAB MMAE and DBCO-TRX MMAE with EC50s of 280 nM and 22 nM in SKBR3 cells, respectively)[1]. | |||
T17771 |
DBCO-NHCO-PEG6-Biotin
|
Others | Others |
DBCO-NHCO-PEG6-Biotin is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17760 |
DBCO-NHCO-PEG12-maleimide
|
Others | Others |
DBCO-NHCO-PEG12-maleimide is a PEG-based PROTAC linker utilized in the synthesis of PROTACs[1]. | |||
T17767 |
DBCO-NHCO-PEG2-NHS ester
|
Others | Others |
DBCO-NHCO-PEG2-NHS ester, a PEG-based PROTAC linker, enables the synthesis of PROTACs[1]. | |||
T17766 |
DBCO-NHCO-PEG2-maleimide
|
Others | Others |
DBCO-NHCO-PEG2-maleimide is a polyethylene glycol (PEG) derived PROTAC linker utilized during PROTAC synthesis[1]. | |||
T15065 | DBCO-NHCO-PEG5-NHS ester | Others | Others |
DBCO-NHCO-PEG5-NHS ester is a polyethylene glycol (PEG)-based linker utilized in the synthesis of PROTACs[1]. | |||
T17772 | DBCO-NHCO-PEG6-maleimide | Others | Others |
DBCO-NHCO-PEG6-maleimide is a polyethylene glycol (PEG)-based linker compound employed in the synthesis of proteolysis-targeting chimeras (PROTACs)[1]. | |||
T17764 |
DBCO-NHCO-PEG2-Biotin
|
Others | Others |
DBCO-NHCO-PEG2-Biotin is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17765 |
DBCO-NHCO-PEG2-CH2COOH
|
Others | Others |
DBCO-NHCO-PEG2-CH2COOH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17769 |
DBCO-NHCO-PEG3-Fmoc
|
Others | Others |
DBCO-NHCO-PEG3-Fmoc is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T18797 |
Tetrazine-Ph-NHCO-PEG4-NH-Boc
|
Others | Others |
Tetrazine-Ph-NHCO-PEG4-NH-Boc is a PEGylated PROTAC linker suitable for PROTAC synthesis[1]. | |||
T17762 |
DBCO-NHCO-PEG13-NHS ester
|
Others | Others |
DBCO-NHCO-PEG13-NHS ester is a pegylated PROteolysis-TArgeting Chimera (PROTAC) linker, serving as a valuable tool for PROTAC synthesis[1]. | |||
T15063 |
DBCO-NHCO-PEG4-NH-Boc
|
Others | Others |
DBCO-NHCO-PEG4-NH-Boc is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T40048 |
MC-AAA-NHCH2OCH2COOH
MC-AAA-NHCH2OCH2COOH |
||
MC-AAA-NHCH2OCH2COOH (compound 20) is a cleavable antibody-drug conjugate (ADC) linker. Its primary application lies in the synthesis of ADCs. | |||
T82934 | AuM1Phe | Topoisomerase | DNA Damage/DNA Repair |
AuM1Phe是一种N-杂环卡宾(NHC)金属络合物,其作用机制包括抑制人类拓扑异构酶I活性和阻碍肌动蛋白聚合。在MDA-MB-231乳腺癌细胞上,AuM1Phe展现了抑制细胞生长的效果,具有1.2 μM的IC50值。 | |||
T74225 | ROS-ERS inducer 1 | ||
ROS-ERS inducer 1 是一种基于4,5-二芳基咪唑的Pt(II)-N-杂环卡宾 (Pt(II)-NHC) 复合物,属于 II 型免疫原性细胞死亡(ICD)诱导剂。它能促使内质网应激(ERS)并伴随活性氧(ROS)的生成,进而在HCC细胞中触发损伤相关分子模式(DAMP)的释放。相比Cisplatin,ROS-ERS inducer 1 表现出更高的抗癌效能。 |