15
1
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T23371 |
SMER3
SMER 3 |
Others; Ligand for E3 Ligase | Others; PROTAC |
SMER3 是选择性的 Skp1-Cullin-F-box (SCF)Met30泛素连接酶抑制剂。SMER 3 通过抑制 SCFMet30来增强 Rapamycin 的生长抑制作用。 | |||
T22604 |
(-)-Bicuculline methiodide
|
Others | Others |
(-)-Bicuculline methiodide is a GABAA receptor antagonist. | |||
T12044 |
(-)-Bicuculline methochloride
l-Bicuculline methochloride |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
(-)-Bicuculline methochloride is a potent antagonist of GABAA receptor. | |||
T12043 |
(-)-Bicuculline methobromide
l-Bicuculline methobromide |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
(-)-Bicuculline methobromide is a potent antagonist of GABAA receptor . | |||
T72246 |
Bicuculline methobromide
(+)-Bicuculline methobromide,d-Bicuculline methobromide,(+)-Bicuculline methobromide ; d-Bicuculline methobromide |
||
Bicuculline methobromide 是选择性GABAA 受体拮抗剂,具IC50值为3 μM。该化合物可引起哺乳类动物阵挛性强直性惊厥,且能阻断Ca2+激活的钾通道,用于癫痫等精神疾病研究。 | |||
T74112 |
Bicuculline methochloride
|
||
Bicuculline ((+)-Bicuculline; d-Bicuculline) 甲基氯化物是一种惊厥生物碱,是选择性GABAA 受体 (GABAA receptor) 的拮抗剂,IC50为 3 μM。Bicuculline 甲基氯化物在哺乳动物中可以诱导阵挛性强直性惊厥,还可用于阻断 Ca2+激活的钾通道。Bicuculline 甲基氯化物可用于癫痫等相关精神疾病的研究。 | |||
T9140 |
NAcM-OPT HCl(2089293-61-6 free base)
|
NEDD8 | Metabolism |
NAcM-OPT HCl(2089293-61-6 free base) 是一种可口服的 cullin neddylation 1 (DCN1) 抑制剂,靶向 N-Acetyl-UBE2M(E2 结合酶,UBC12)与 DCN1 的相互作用,IC50 为 79 nM。 | |||
T77525 |
EN450
|
NF-κB | NF-κB |
EN450 是一种针对的 NF-κB 的半胱氨酸反应性共价分子胶降解剂,具有抗增殖活性和潜在的抗癌活性,通过依赖Cullin E3 连接酶和蛋白酶发挥作用,可用于研究白血病。 | |||
T5374 |
NAcM-OPT
|
E1/E2/E3 Enzyme; NEDD8 | Metabolism; Ubiquitination |
NAcM-OPT 是口服活性、有效的 cullin neddylation 1 抑制剂,可以抑制 DCN1-UBE2M 相互作用。 | |||
T0213 |
Thalidomide
Thalomid,沙利度胺,Sedoval |
Apoptosis; TNF; Autophagy; Ligand for E3 Ligase; Molecular Glues | Apoptosis; Autophagy; PROTAC |
Thalidomide (Thalomid) 能够抑制 cereblon,即 cullin-4 E3 泛素连接酶复合物 CUL4-RBX1-DDB1 的一部分,Kd 值约为 250 nM,具有免疫调节、抗炎、抗肿瘤作用。它可以作为分子胶来增强底物。 | |||
T23989 |
DI-404
|
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DI-404 is a high-Affinity Peptidomimetic the DCN1-UBC12 Protein-Protein Interaction inhibitor (Kd= 6.9 nM). DI-404 effectively and selectively inhibits the neddylation of cullin 3 over other cullin members. | |||
T71830 |
DT204
|
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DT204 is a SCFSkp2 inhibitor which blocks Skp2 binding to Cullin-1 and Commd1, thereby synergistically enhancing BTZ-induced apoptosis and stabilization. DT204 also increases p27 levels. | |||
T63930 |
DI-1859
|
||
DI-1859 是选择性的、有效的、共价的 DCN1 抑制剂。低纳摩尔浓度下,DI-1859 能够抑制细胞中 cullin 3 的 neddylation。DI-1859 能够促使小鼠肝脏中 NRF2 蛋白(一种 CRL3 底物)显著提高,并有效保护小鼠,防止乙酰氨基酚诱导的肝损伤。 | |||
T78194 |
Skp2 inhibitor 2
|
E1/E2/E3 Enzyme | Ubiquitination |
Skp2 inhibitor 2 (14f)为F-box蛋白S期激酶相关蛋白2(Skp2)的抑制剂,其IC50值为10.2 μM(针对Skp2-Cks1复合体)。该化合物是cullin-RING 连接酶的组成部分,负责招募并使底物泛素化,从而涉及蛋白质的水解和非水解相关过程。 | |||
T18598 |
PROTAC BRD2/BRD4 degrader-1
|
Others | Others |
PROTAC BRD2/BRD4 degrader-1 (compound 15) serves as a potent, selective degrader of BET proteins BRD4 and BRD2, achieving rapid, reversible, and unexpectedly selective elimination of BRD4 and BRD2 compared to BRD3. Its efficacy in suppressing solid tumors manifest with minimal cytotoxic effects. This compound comprises a BET inhibitor, a connecting linker, and thalidomide as the ligand for cereblon (CRBN)/cullin 4A[1]. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2850 |
Bicuculline
荷包牡丹碱,(+)-Bicuculline,d-Bicuculline |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Bicuculline ((+)-Bicuculline) 是从东北延胡索中提取的一种生物碱,能阻断 Ca2+激活钾 (SK) 通道。它是一种竞争性的神经递质 GABAA 受体拮抗剂,IC50为 2 μM。 |