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13

抑制剂 & 化合物

3

天然产物

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Cat. No. Product Name Target Signaling Pathways
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

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

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

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...

化合物

UCB-9260
Cat.No: T13951
Synonym:
Target: TNF
Ibulocydine
Cat.No: T70988
Synonym:
Target:
Gamma-Methylleucine
Cat.No: T31907
Synonym: L-Neopentylglycine,gamma-Methyl-L-leucine,3-叔丁基-L-丙氨酸,2-Amino-3-tert-butylpropionic acid
Target: Others
1,3,3,5,5-pentamethylcyclohexan-1-amine hydrochloride
Cat.No: T50096
Synonym:
Target: Others
HBED-CC-tris(tert-butyl ester)
Cat.No: T82236
Synonym:
Target: Others
IMM-01
Cat.No: T25529
Synonym:
Target: GTPase
7-Methoxy-1-naphthaleneacetic acid
Cat.No: T9897
Synonym:
Target: Others
Nb-enantride
Cat.No: T33603
Synonym:
Target:
Alnuctamab
Cat.No: T83141
Synonym: EM901,CC-93269
Target:
UCB-6876
Cat.No: T68954
Synonym:
Target:
UCB-6786
Cat.No: T71807
Synonym:
Target:
SGC 6870
Cat.No: T36976
Synonym:
Target:
L-Pyrohomoglutamic Acid
Cat.No: T36110
Synonym:
Target:
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.

天然产物

Asymmetric dimethylarginine
Cat.No: T7682
Synonym:
Target: Endogenous Metabolite, NO Synthase, NOD
Dimethylamine hydrochloride
Cat.No: T5309
Synonym: N,N-Dimethylamine,二甲胺盐酸盐
Target: Others
7-Isopentenyloxy-gamma-fagarine
Cat.No: TN3237
Synonym:
Target: Others
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