Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T9370 |
dCBP-1
|
Epigenetic Reader Domain; Ligand for E3 Ligase | Chromatin/Epigenetic; PROTAC |
dCBP-1 是基于Cereblon 配体的p300/CBP 的选择性双功能降解剂。dCBP-1可以有效的杀死多发性骨髓瘤细胞,并降低驱动 MYC 表达的致癌增强子活性。 | |||
T8667 |
MC-Gly-Gly-Phe-Gly
DSN28369 |
Others | Others |
MC-Gly-Gly-Phe-Gly (DSN28369) 是一种可降解的 ADC linker,是一种异双功能接头,可用于制备抗体药物偶联物。 | |||
T9116 |
SMCC
N-Succinimidyl 4-(N-maleimidomethyl)cycl,4-(N-马来酰亚胺基甲基)环己烷-1-羧酸琥珀酰亚胺酯 |
Others | Others |
SMCC (N-Succinimidyl 4-(N-maleimidomethyl)cycl) 是一种异双功能蛋白质交联剂。它接合抗原耦合脾脏细胞来诱导抗原特异性免疫反应。 | |||
T14061 |
EMCS
6-Maleimidohexanoic acid N-hydroxysuccinimide ester |
Others | Others |
EMCS (6-Maleimidohexanoic acid N-hydroxysuccinimide ester) 是一种异双官能团交联剂,是一种制备半抗原结合物和酶免疫偶联物的化合物,是抗体药物偶联物中一种有效的保护基团。 | |||
T5440 |
Dbet57
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
dBET57 是基于 PROTAC 技术的 BRD4 异双功能降解剂,对 BRD4BD1 有显著降解作用,DC50/5h 为 500 nM。 | |||
T17389 |
AMAS
|
Others | Others |
AMAS 是一种不可裂解的异双功能交联剂,具有 NHS 酯和马来酰亚胺基团,可实现含胺和巯基分子的共价结合。 | |||
T5434 |
ARV-825
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
ARV-825 是一种双功能 PROTAC,蛋白水解靶向嵌合体,将 BRD4 募集到 E3 泛素连接酶大脑中,导致 BRD4 在所有测试的 BL 细胞系中快速、有效和延长降解。对 BRD4 的 BD1 和 BD2 结构域具有高亲和力,Kd 值分别为 90 和 28 nM。 | |||
T18725 |
Sulfo-LC-SPDP
|
Others | Others |
Sulfo-LC-SPDP is a heterobifunctional crosslinker characterized by its thiol-cleavable and membrane impermeable properties. | |||
T21269 |
Sulfo-EMCS
|
||
Sulfo-EMCS is a heterobifunctional sulfhydryl- and amine-reactive crosslinker. | |||
T24841 |
Sulfo-MBS Crosslinker
Sulfo-MBS Cross linker,Sulfo-MBS Cross-linker |
||
Sulfo-MBS Crosslinker is a non-cleavable, water-soluble, heterobifunctional protein crosslinking reagent. It is commonly used to crosslink haptens to carrier proteins and enzymes to antibodies. | |||
T19568 |
Sulfo-SMPB sodium
|
Others | Others |
Sulfo-SMPB sodium is a non-cleavable heterobifunctional chemical cross-linking reagent that combines N-hydroxysuccinimide ester and maleimide groups. This compound enables the covalent conjugation of molecules possessing amine and sulfhydryl functionalities. | |||
T19941 |
MBS Crosslinker
MBS protein crosslinker |
||
MBS crosslinker is a non-cleavable, water-insoluble, heterobifunctional protein crosslinking reagent. The MBS protein crosslinker extended spacer arm analog is SMPB crosslinker SATA Protein Modifier can be used to add sulfhydryl groups to proteins or pept | |||
T11292 |
FKBP12 PROTAC dTAG-7
dTAG-7 |
Epigenetic Reader Domain | Chromatin/Epigenetic |
FKBP12 PROTAC dTAG-7 (dTAG-7) is a heterobifunctional compound that selectively degrades the BET bromodomain transcriptional co-activator BRD4 by connecting BET bromodomains to the E3 ubiquitin ligase CRBN. Additionally, it serves as a degrader of FKBP12F36V when FKBP12F36V is expressed in-frame with a targeted protein. | |||
T15395 |
GMBS
|
Others | Others |
GMBS is a heterobifunctional cross-linker. | |||
T24842 |
Sulfo-SIA Crosslinker
Sulfo-SIA Cross-linker,Sulfo-SIA Cross linker |
||
Sulfo-SIA Crosslinker is a non-cleavable, heterobifunctional protein crosslinker. Sulfo-SIA Crosslinker is useful in making antibody-drug conjugates. | |||
T19942 |
SBA Crosslinker
SBA Cross-linker,SBA Cross linker |
||
SBA crosslinker is a sulfhydryl and amino reactive heterobifunctional protein crosslinking reagent. SBA protein crosslinker is non-cleavable and is among the shortest amine and sulfhydryl reactive crosslinking reagents known with a spacer arm length of on | |||
T18734 | Sulfo-SPP | Others | Others |
Sulfo-SPP is a heterobifunctional, thiol-cleavable and membrane impermeable crosslinker. | |||
T74412 | dTAGV-1-NEG TFA | ||
dTAGV-1-NEG TFA 是一种非对映异构体,是 dTAGV-1 的异双功能阴性对照。dTAGV-1-NEG TFA 是一种 FKBP12F36V 选择性降解剂。 | |||
T15883 |
m-PEG4-phosphonic acid ethyl ester
|
Others | Others |
m-PEG4-phosphonic acid ethyl ester is a PEGylation-based linker for the design and synthesis of PROTACs, which are heterobifunctional molecules facilitating targeted protein degradation[1]. | |||
T39352 | Piperidine-GNE-049-N-Boc | ||
Piperidine-GNE-049-N-Boc is a ligand that specifically binds to the target protein dCBP, enabling it to be degraded by a selective and potent heterobifunctional degrader, p300/CBP. | |||
T40144 |
CBP/p300 ligand 2
|
||
CBP/p300 ligand 2 is a selective ligand that binds to the target protein for PROTAC of dCBP-1, a potent and selective heterobifunctional degrader of p300/CBP. | |||
T40036 |
Thalidomide-NH-PEG4-COOH
Thalidomide-NH-PEG4-COOH |
||
Thalidomide-NH-PEG4-COOH is a conjugate comprising an E3 ligase ligand-linker, utilized in the synthesis of dCBP-1. dCBP-1 itself functions as a powerful and selective heterobifunctional degrader targeting p300/CBP. | |||
T14809 | Bromo-PEG5-phosphonic acid diethyl ester | Others | Others |
Bromo-PEG5-phosphonic acid diethyl ester is a polyethylene glycol (PEG)-based linker for PROTAC synthesis[1]. It is utilized in the construction of PROteolysis TArgeting Chimeras (PROTACs), which are heterobifunctional molecules designed to induce protein degradation. | |||
T19943 |
SMPB Crosslinker
SMPB Cross linker,SMPB Cross-linker |
||
SMPB crosslinker is a heterobifunctional protein crosslinking reagent that is reactive toward sulfhydryl and amino groups. The SMPB protein crosslinker is an extended chain length analog of MBS crosslinker. SMPB crosslinker's spacer arm is non-cleavable. | |||
T18189 |
m-PEG3-Sulfone-PEG4-propargyl
|
Others | Others |
m-PEG3-Sulfone-PEG4-propargyl is a polyethylene glycol (PEG)-based prodrug-induced degradation (PROTAC) linker. It is utilized in the efficient synthesis of PROTACs, a class of heterobifunctional molecules designed to selectively target and degrade specific protein targets[1]. | |||
T74556 |
dTAG-47
|
||
dTAG-47,异双功能 dTAG 分子,靶向突变型 FKBP12 (FKBP12F36V)。FKBP12F36V 可用作降解标签 (dTAG) 并与靶蛋白融合。dTAG-47可用于基底样乳腺癌(BBC)的研究。 | |||
T11291 |
FKBP12 PROTAC dTAG-13
dTAG-13 |
Epigenetic Reader Domain | Chromatin/Epigenetic |
FKBP12 PROTAC dTAG-13 (dTAG-13) is a degrader of FKBP12F36V with expression of FKBP12F36V in-frame with a protein of interest. FKBP12 PROTAC dTAG-13 (dTAG-13) also is a selective degrader of BET bromodomain transcriptional co-activator BRD4 by bridging BET bromodomains to an E3 ubiquitin ligase CRBN. FKBP12 PROTAC dTAG-13 (dTAG-13) is a PROTAC-based heterobifunctional degrader. | |||
T69506 | dBRD4-BD1 | ||
dBRD4-BD1 is a selective BRD4 bromodomain inhibitor. dBRD4-BD1 can selectively degrade BRD4 (DC50 = 280 nM). Notably, dBRD4-BD1 upregulates BRD2/3, a result not observed with degraders using pan-BET ligands. Designing BRD4 selectivity up front enables analysis of BRD4 biology without wider BET-inhibition and simplifies designing BRD4-selective heterobifunctional molecules, such as degraders with new E3 recruiting ligands or for additional probes beyond degraders. | |||
T82192 |
HLDA-221
|
||
HLDA-221是一种异双功能小分子,其为调节诱导邻近靶向嵌合体(RIPTAC)。该分子通过在癌组织中选择性表达的靶蛋白与泛表达蛋白间形成稳定的三元复合物,特异性诱导表达该靶蛋白细胞的cell death。 | |||
T77915 |
CCT367766 formic
|
PROTACs | PROTAC |
CCT367766 formic 是一款有效的口服第三代异功能蛋白降解探针(PROTAC),基于Cereblon配体,能在低浓度降低pirin蛋白表达。该化合物对CRBN-DDB1复合物具中等亲和力,IC50值为490 nM;同时,对重组pirin和CRBN的亲和力良好,Kd值分别为55 nM和120 nM。CCT367766 formic作为化学工具,对研究某些未开发蛋白质具有重要价值。 |