153
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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T20907 |
DBC
3,4,5,6-Dibenzocarbazole |
Others | Others |
DBC, a ubiquitous environmental pollutant, induces significant DNA strand break levels and micronuclei in HepG2 cells. | |||
T20214 |
Bucladesine
Bucladesina,DT 5621,DBC-AMP,Actosin |
Others | Others |
Bucladesine is a cyclic nucleotide derivative which mimics the action of endogenous cAMP and is capable of permeating the cell membrane. Bucladesine is a phosphodiesterase inhibitor. The compound is used in a wide variety of research applications because | |||
T15067 |
DBCO-NHS ester
|
Others | Others |
DBCO-NHS ester 是一种 ADC 连接剂,可裂解的 3 单元 PEG,还可以用于合成抗体药物共轭物 (ADC)。 | |||
T15069 |
DBCO-PEG4-Biotin
ADIBO-NH-PEG2-Biotin |
Others | Others |
DBCO-PEG4-Biotin (ADIBO-NH-PEG2-Biotin) 是一种 azadibenzocyclooctyne-biotin 衍生物,含有生物素基团和 4 个 PEG。DBCO-PEG4-Biotin 是一种用途广泛的生物素酰化试剂,能通过无铜催化烷基叠氮化反应 (SPAAC) 将生物素的一部分引入叠氮标记的生物分子中。 | |||
T15073 |
DBCO-PEG4-NHS ester
|
PROTAC Linker | PROTAC |
DBCO-PEG4-NHS ester 是一种属于 PEG 类的 PROTAC linker,可用于 PROTAC 分子的合成。 | |||
T77948 |
Tri-GalNAc-DBCO
|
PROTACs | PROTAC |
Tri-GalNAc-DBCO是一种PIP-GalNAc 偶联物,通过无铜菌株促进的叠氮化物-炔烃环加成与非特异性标记抗体上的叠氮化物偶联,可结合ASGPR以驱动蛋白质下调和靶向蛋白质降解的化合物。 | |||
T15076 |
DBCO-S-S-PEG3-biotin
生物素-PEG3-二硫-DBCO |
Others; PROTAC Linker | Others; PROTAC |
DBCO-S-S-PEG3-biotin 是一种属于 PEG 类的 PROTAC linker,可用于 PROTAC 分子的合成。 | |||
T17791 |
DBCO-PEG3-NHS ester
|
Others | Others |
DBCO-PEG3-NHS ester是一种可降解的 ADC linker,可用于合成抗体偶联活性分子 。 | |||
T15058 |
DBCO-amine
|
||
DBCO-amine 是一种可切割的 ADC 接头,用于合成抗体-药物偶联物。 | |||
T17753 |
DBCO-mPEG (MW 5kDa)
|
Others | Others |
DBCO-mPEG (MW 5kDa) 是一种基于 PEG 的 PROTAC 连接物,可用于合成 PROTAC。 | |||
T9282 |
DBCO-C3-Acid
DBCO-ACID |
Others | Others |
DBCO-(CH2)3-Acid 是一种用于抗体-药物偶联物的 Click Chemistry 中间体,可用以合成 ADC linker。 | |||
T17859 |
DSPE-PEG4-DBCO
|
PROTACs | PROTAC |
DSPE-PEG4-DBCO 是一种属于 PEG 类的 PROTAC linker。DSPE-PEG4-DBCO 可细胞成像和生物医学研究中用作生物材料。 | |||
T18137 |
m-PEG12-DBCO
|
Others | Others |
m-PEG12-DBCO 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. | |||
T17748 | DBCO-CONH-S-S-NHS ester | Others | Others |
DBCO-CONH-S-S-NHS ester is a disulfide-linked ADC linker employed for the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T17804 |
DBCO-PEG5-DBCO
|
Others | Others |
DBCO-PEG5-DBCO 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. | |||
T17839 |
DNP-PEG4-DBCO
|
Others | Others |
DNP-PEG4-DBCO 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. | |||
T17780 |
DBCO-PEG1
|
Others | Others |
DBCO-PEG1 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. | |||
T17805 |
DBCO-PEG6-amine
|
Others | Others |
DBCO-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. | |||
T17775 |
DBCO-NHS ester 3
|
Others | Others |
DBCO-NHS ester 3 (Compound 12) is a cleavable linker utilized in the synthesis of antibody-drug conjugate (ADC). It is a derivative of Dibenzylcyclooctyne (DBCO) resulting from the activation of N-hydroxysuccinimide by the carboxylic acid moiety of both methyl-oxanorbornadiene (MeOND) and dibenzoazacyclooctyne (DIBAC)[1][2]. | |||
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]. | |||
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]. | |||
T15075 |
DBCO-PEG5-NHS ester
|
Others | Others |
DBCO-PEG4-NHS ester is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T16956 |
Sulfo DBCO-amine
|
Others | Others |
Sulfo DBCO-amine is an alkyl chain-derived PROTAC linker utilized for synthesizing PROTACs[1]. | |||
T17796 |
DBCO-PEG4-Desthiobiotin
|
Others | Others |
DBCO-PEG4-Desthiobiotin is a polyethylene glycol (PEG) derivative utilized as a linker for the synthesis of proteolysis-targeting chimeras (PROTACs)[1]. | |||
T17801 |
DBCO-PEG4-VA-PBD
|
Others | Others |
DBCO-PEG4-VA-PBD is a cleavable 4 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[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]. | |||
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. | |||
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. | |||
T17815 |
DBCO-Val-Cit-PABC-OH
|
Others | Others |
DBCO-Val-Cit-PABC-OH is a cleavable linker employed in the synthesis of antibody-drug conjugates (ADCs) [1]. | |||
T18341 |
Methyltetrazine-PEG12-DBCO
|
Others | Others |
Methyltetrazine-PEG12-DBCO is a polyethylene glycol (PEG)-based linker compound utilized 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. | |||
T17782 |
DBCO-PEG12-acid
|
Others | Others |
DBCO-PEG12-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. | |||
T84734 |
DBCO-PEG4-GGFG-Dxd
|
Others | Others |
DBCO-PEG4-GGFG-Dxd作为一种点击化学试剂,是抗体-活性分子偶联物的关键组成部分,它结合了DNA拓扑异构酶I抑制剂Dxd与可裂解的ADC linker DBCO-PEG4-GGFG。此化合物利用DBCO基团与含Azide基团的分子之间通过菌株促进的炔-叠氮环加成反应(SPAAC)实现快速且特异的连接。 | |||
T39297 |
Bis-sulfone-PEG4-DBCO
Bis-sulfone-PEG4-DBCO |
Others | Others |
Bis-sulfone-PEG4-DBCO 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. | |||
T15059 | DBCO-C6-acid | Others | Others |
DBCO-C6-acid is a non-cleavable linker utilized for the synthesis of antibody-drug conjugates (ADCs) and carmaphycin analogues[1]. | |||
T17742 |
DBCO-Biotin
Azadibenzocyclooctyne-Biotin conjugate |
||
DBCO-Biotin (Azadibenzocyclooctyne-Biotin conjugate) 是一种基于烷基链的 PROTAC linker。 | |||
T17797 |
DBCO-PEG4-NH-Boc
|
Others | Others |
DBCO-PEG4-NH-Boc 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. | |||
T18200 |
m-PEG4-NH-DBCO
|
Others | Others |
m-PEG4-NH-DBCO 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. | |||
T17794 |
DBCO-PEG4-alcohol
|
Others | Others |
DBCO-PEG4-alcohol 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]. | |||
T18948 |
Cy5-DBCO
DBCO-Sulfo-Cy5 |
Others | Others |
Cy5-DBCO (DBCO-Sulfo-Cy5) is a near-infrared (NIR) red fluorescent dye (λabs: 646 nm, λem: 670 nm). Cy5-DBCO is not suitable for staining intracellular components of the permeabilized cells because it may exhibit a high background. | |||
T18410 |
N-DBCO-N-bis(PEG2-C2-NHS ester)
|
Others | Others |
N-DBCO-N-bis(PEG2-C2-NHS ester) is a Polyethylene Glycol (PEG) derived linker that finds utility in the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1]. | |||
T17789 |
DBCO-(PEG2-VC-PAB-MMAE)2
|
Others | Others |
DBCO-(PEG2-VC-PAB-MMAE)2 consists of Monomethyl auristatin E (MMAE), a toxin payload in antibody-drug conjugate [1], conjugated to the cleavable linker DBCO-(PEG2-VC-PAB)2. MMAE, a potent tubulin inhibitor, serves as the cytotoxic component in this formulation. | |||
T17812 |
DBCO-SS-amine
|
Others | Others |
DBCO-SS-amine is a cleavable linker vital in ADC synthesis. DBCO-SS-amine joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing ADC effectiveness. | |||
T15060 |
DBCO-Maleimide
|
Others | Others |
DBCO-Maleimide is a cleavable linker utilized in the synthesis of antibody-drug conjugates (ADCs). [1] | |||
T18411 |
N-(DBCO-PEG4)-N-Biotin-PEG4-NHS
|
Others | Others |
N-(DBCO-PEG4)-N-Biotin-PEG4-NHS is a PEG-based PROTAC linker suitable for synthesizing PROTACs[1]. | |||
T18970 |
DBCO-PEG12-TCO
|
Others | Others |
DBCO-PEG12-TCO contains a DBCO and a TCO moiety. | |||
T15074 |
DBCO-PEG4-TAMRA
|
Others | Others |
DBCO-PEG4-TAMRA, contains a DBCO group, is a PEG-based TARMA dye. The TAMRA dye is a dye widely used in oligonucleotide labeling. | |||
T17832 |
DM1-PEG4-DBCO
|
Others | Others |
DM1-(PEG)4-DBCO is a drug-linker conjugate that combines the potent microtubulin inhibitor mertansine (DM1) with the DBCO-PEG4-Ahx linker for the development of antibody-drug conjugates (ADCs). This conjugation aims to mitigate the systemic toxicity associated with maytansine while improving tumor-specific delivery, leveraging DM1’s capabilities as an antibody-conjugatable maytansinoid. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2787 |
Picroside I
6'-Cinnamoylcatalpol,胡黄连苦苷I |
MMP; STAT | JAK/STAT signaling; Proteases/Proteasome; Stem Cells |
Picroside I (6'-Cinnamoylcatalpol) 是胡黄连的一种天然产物,是有肝脏保护作用的代谢成分,可用于哮喘研究,有减轻炎症作用,还下调 pSTAT6 和 GATA3 表达。 |