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Cat. No. | Product Name | Target | Signaling Pathways |
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T13951 |
UCB-9260
|
TNF | Apoptosis |
UCB-9260 是口服活性小分子,通过稳定三聚体的不对称形式抑制肿瘤坏死因子信号传导。它对肿瘤坏死因子的选择性高于其他超家族成员,并与肿瘤坏死因子结合,其Kd 值为 13 nM。 | |||
T70988 |
Ibulocydine
|
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Ibulocydine is a potent CDK inhibitor. Ibulocydine has high activity against Cdk7/cyclin H/Mat1 and Cdk9/cyclin T. Ibulocydine inhibited the growth of HCC cells more effectively than other Cdk inhibitors, including olomoucine and roscovitine, whereas ibulocydine as well as the other Cdk inhibitors and BMK-Y101 minimally influenced the growth of normal hepatocyte cells. Ibulocydine induced apoptosis in HCC cells, most likely by inhibiting Cdk7 and Cdk9. In vitro treatment of HCC cells with ibuloc... | |||
T31907 |
Gamma-Methylleucine
L-Neopentylglycine,gamma-Methyl-L-leucine,3-叔丁基-L-丙氨酸,2-Amino-3-tert-butylpropionic acid |
Others | Others |
Gamma-Methylleucine (2-Amino-3-tert-butylpropionic acid) 是铜催化的不对称迈克尔反应的辅助剂。 | |||
T50096 |
1,3,3,5,5-pentamethylcyclohexan-1-amine hydrochloride
|
Others | Others |
1,3,3,5,5-pentamethylcyclohexan-1-amine hydrochloride,又称PAC,是一种环胺,通常用作不对称合成中的手性助剂,包括Diels-Alder 反应、羟醛反应和Michael 加成。 | |||
T82236 |
HBED-CC-tris(tert-butyl ester)
|
Others | Others |
HBED-CC-tris(tert-butyl ester)是HBED-CC的一种单价变体,可用于合成基于非对称 HBED-CC 的放射性化合物,可用于肿瘤成像。 | |||
T25529 |
IMM-01
|
GTPase | GPCR/G Protein |
IMM-01 是一类新型的哺乳动物透明 (mDia) 相关形式的小分子激动剂,其作用于 Rho GTPase 下游以组装肌动蛋白丝,并与微丝组织在迁移和不对称分裂过程中建立和维持细胞极性. GTP 结合的 Rho 通过破坏 DID 和 DAD 自动调节结构域之间的相互作用来激活 mDia 家族成员,从而释放 FH2 结构域以调节肌动蛋白和微管动力学。 | |||
T9897 |
7-Methoxy-1-naphthaleneacetic acid
|
Others | Others |
7-Methoxy-1-naphthaleneacetic acid 是植物生长素作用的抑制剂。 7-Methoxy-1-naphthaleneacetic acid 抑制与拟南芥和玉米中生长素不对称分布相关的极性生长素转运和热带反应。 7-Methoxy-1-naphthaleneacetic acid 抑制由酵母中表达的 AUX1、PIN 和 ABCB 蛋白介导的生长素转运。 | |||
T33603 |
Nb-enantride
|
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Nb-enantride is a novel chiral trialkylborohydride for the asymmetric reduction of ketones. | |||
T83141 |
Alnuctamab
EM901,CC-93269 |
||
Alnuctamab (EM901)为一种不对称双臂人源化IgG T细胞接合器,主要应用于免疫学研究。 | |||
T68954 |
UCB-6876
|
||
UCB-6876 is a novel inhibitor of TNF signalling by stabilising an asymmetric form of the trimer, displaying a concentration-dependent response curve and selectivity over the TNFR1 extracellular domain and control proteins. | |||
T71807 |
UCB-6786
|
||
UCB-6786 is a novel inhibitor of TNF signalling by stabilising an asymmetric form of the trimer, displaying a concentration-dependent response curve and selectivity over the TNFR1 extracellular domain and control proteins. | |||
T36976 | SGC 6870 | ||
Potent and selective protein arginine methyltransferase 6 (PRMT6) inhibitor (IC50 = 77 nM). Exhibits selectivity over all other PRMTs and 23 methyltransferases. In HEK293T cells overexpressing PRMT6, inhibits asymmetric dimethylation of H3R2 (IC50 = 0.8 μM) Negative control SGC 6870N (Cat. No. 7184) also available. | |||
T36110 |
L-Pyrohomoglutamic Acid
|
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L-Pyrohomoglutamic acid is an amino acid building block.1,2It has been used in the synthesis of ligands for FK506-binding proteins (FKBPs) and histone deacetylase (HDAC) inhibitors. 1.Pomplun, S., Wang, Y., Kirschner, A., et al.Rational design and asymmetric synthesis of potent and neurotrophic ligands for FK506-binding proteins (FKBPs)Angew. Chem. Int. Ed.54(1)345-348(2015) 2.Taddei, M., Cini, E., Giannotti, L., et al.Lactam based 7-amino suberoylamide hydroxamic acids as potent HDAC inhibitors... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7682 |
Asymmetric dimethylarginine
|
Endogenous Metabolite; NO Synthase; NOD | Immunology/Inflammation; Metabolism; NF-κB |
Asymmetric dimethylarginine 是内源性一氧化氮合成酶抑制剂,可以作为内皮功能障碍的标志。 | |||
T5309 |
Dimethylamine hydrochloride
N,N-Dimethylamine,二甲胺盐酸盐 |
Others | Others |
Dimethylamine hydrochloride (N,N-Dimethylamine) 大量存在于人类尿液中。 | |||
TN3237 |
7-Isopentenyloxy-gamma-fagarine
|
Others | Others |
7-Isopentenyloxy-gamma-fagarine has highly cytotoxicity against the MCF-7and Jurkat cell line. It has been used as a precursor for the chemical asymmetric synthesis of the enantiopure alkaloids: evoxine, anhydroevoxine and evodine. |