Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T15141 |
DM4
Ravtansine,美登素 DM4 |
Others; Microtubule Associated | Cytoskeletal Signaling; Others |
DM4 (Ravtansine)可用于制备抗体药物偶联物,是抗微管蛋白剂。 它抑制细胞分裂。 | |||
T38682 |
Lys-Nε-SPDB-DM4
Lys-Nε-SPDB-DM4 |
||
Lys-Nε-SPDB-DM4 is a drug-linker conjugate composed of a potent a tubulin inhibitor DM4 and a linker Lys-Nε-SPDB to make antibody drug conjugate (ADC). | |||
T17834 |
DM4-SPDP
|
Others | Others |
DM4-SPDP, a drug-linker conjugate, integrates the antitubulin agent DM4 with the linker SMCC, facilitating the creation of antibody drug conjugates[1]. Additionally, SPDP serves as a short-chain crosslinker enabling amine-to-sulfhydryl conjugation, leveraging NHS-ester and pyridyldithiol groups to establish cleavable (reducible) disulfide bonds with cysteine sulfhydryls[2][3]. | |||
T18701 |
SPDB-DM4
|
Others | Others |
SPDB-DM4 is a drug-linker conjugate designed for antibody-drug conjugate (ADC) applications, employing the maytansine-based payload DM4 (a tubulin inhibitor) connected through a SPDB linker. This compound demonstrates significant anti-tumor efficacy. | |||
T11059 |
DM4-SMe
|
Others | Others |
DM4-SMe is a cytotoxic part of antibody-drug conjugates (ADCs) and a metabolite of antibody-maytansin conjugates (AMCs) and tubulin inhibitors, which can also be stabilized by disulfide bonds or thioether The bond binds to the antibody. The IC50 of DM4-SM | |||
T13766 |
Maytansinoid DM4
|
Others | Others |
Maytansinoid DM4, a thiol-containing maytansine derivative, is a highly potent cytotoxic moiety utilized in ADC applications. | |||
T17833 |
DM4-SMCC
|
Others | Others |
DM4-SMCC, a non-cleavable drug-linker conjugate for antibody-drug conjugates (ADC), leverages the antitumor efficacy of DM4 (an antitubulin agent) through attachment with the SMCC linker, exhibiting antitumor activity[1]. | |||
T18702 |
DBA-DM4
|
Others | Others |
DBA-DM4 is a drug-linker conjugate for antibody-drug conjugate (ADC) synthesis, combining the tubulin inhibitor DM1 with the SPDP linker[1]. | |||
T18730 |
sulfo-SPDB-DM4
|
Others | Others |
Sulfo-SPDB-DM4 is a drug-linker conjugate designed for antibody-drug conjugates (ADCs) that employs the maytansine-based payload (DM4, an antitubulin agent) connected through the sulfo-SPDB linker. | |||
T18731 |
Sulfo-PDBA-DM4
|
Others | Others |
Sulfo-PDBA-DM4 is a drug-linker conjugate for antibody-drug conjugate (ADC) applications, combining the potent tubulin inhibitor DM4 with the gluthatione-cleavable linker Sulfo-PDBA. This configuration harnesses DM4's cytotoxic potential through Sulfo-PDBA's targeted delivery mechanism. | |||
T77907 |
Tusamitamab ravtansine
HuMAb2-3-SPDB-DM4,SAR-408701 |
||
Tusamitamab ravtansine (SAR-408701) 是一款针对CEACAM5的人源化单克隆抗体与DM4细胞毒性药物经活性分子连接而成的抗体-药物偶联物(ADC),专门靶向CEACAM5表达的肿瘤细胞。 | |||
T77872 |
S-Me-DM4
|
||
S-Me-DM4是DM4在胞内酶作用下发生S-甲基化反应形成的代谢产物。DM4本身是一种具有强细胞毒性的含硫醇类微管解聚剂,并可作为ADC Cytotoxin分子应用。 | |||
T4214 |
KDM4D-IN-1
|
Histone Demethylase | Chromatin/Epigenetic |
KDM4D-IN-1 是一种 KDM4D 抑制剂,IC50为 0.41±0.03 μM。 | |||
T60654 |
KDM4C-IN-1
|
Histone Demethylase | Chromatin/Epigenetic |
KDM4C-IN-1 是一种具有选择性和高效性的KDM4C 抑制剂(IC50:8 nM),具有潜在的抗癌活性。KDM4C-IN-1 抑制 HepG2 和 A549 细胞的生长,可用于研究白血病。 | |||
T27721 |
KDM4C-IN-35
KDM4C IN 35,KDM4CIN35 |
||
KDM4C-IN-35 is a novel and selective KDM4C inhibitor. | |||
T11749 |
KDM4-IN-2
|
Glucokinase | Metabolism |
KDM4-IN-2 is a potent and selective KDM4/KDM5 dual inhibitor with Kis of 4 and 7 nM for KDM4A and KDM5B, respectively. | |||
T60354 |
KDM4-IN-4
|
||
KDM4-IN-4 (compound 47) 是一种有效的组蛋白赖氨酸特异性脱甲基酶 4 (KDM4)抑制剂,与 KDM4A-Tudor 结构域约有 80 μM 的亲和力。KDM4-IN-4 可以抑制细胞内 H3K4Me3 与 Tudor 结构域的结合,EC50为 105 μM。KDM4-IN-4 可用于抗癌研究。 | |||
T27722 | KDM4-IN-I | ||
KDM4-IN-I is a novel inhibitor of KDM4. | |||
T25142 |
BDM44768
BDM 44768,BDM-44768 |
||
BDM44768 is an insulin-degrading enzyme (IDE) inhibitor that acts by inducing glucose intolerance. | |||
T60593 |
KDM4-IN-3
|
||
KDM4-IN-3 是赖氨酸脱甲基酶4(KDM4)的抑制剂。KDM4-IN-3 具有细胞渗透性,可在低微摩尔浓度下杀死前列腺癌细胞。 | |||
T4346 |
SPDB
|
Others | Others |
SPDB 是一种可降解的 ADC 连接剂,可用于合成抗体偶联药物。它是一个与 DM4 偶联物相连的小片段,利用二硫键与抗体偶联。 | |||
T40162 |
Acid-C3-SSPy
Acid-C3-SSPy |
||
Acid-C3-SSPy is a cleavable DBA-DM4 linker used in the synthesis of DBA-DM4 , a drug-linker conjugate for ADC. | |||
T76940 |
Cantuzumab ravtansine
|
||
Cantuzumab ravtansine (IMGN242; huC242-DM4) 是一种 ADC,由一种人源化单克隆抗体 huC242,通过二硫键与 DM4 (DM4) 共价连接。Cantuzumab ravtansine 对一系列 CanAg 阳性人肿瘤异种移植物具有广泛的抗肿瘤功效。 | |||
T77825 |
Mirvetuximab soravtansine
IMGN853 |
||
Mirvetuximab soravtansine (IMGN853)是一种抗体药物偶联物(ADC),包含与人源化单克隆抗体M9346A共价连接的细胞毒素maytansoid DM4。该药物特异性地结合于叶酸受体1 (FOLR1),显示出抑制细胞生长和增强DNA损伤的抗增殖效果。 |