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10

抑制剂 & 化合物

2

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Cat. No. Product Name Target Signaling Pathways
T0370 Pheniramine maleate

Daneral,Inhiston,Trimetose,马来酸非尼拉敏

5-HT Receptor; Histamine Receptor GPCR/G Protein; Immunology/Inflammation; Neuroscience
Pheniramine maleate (Trimetose) 是一种具有抗组胺和血管扩张特性的烷基胺衍生物,可与组胺 H1 受体结合,从而抑制磷脂酶 A2 和内皮源性松弛因子一氧化氮的产生。
T6018 Zosuquidar trihydrochloride

唑喹达三盐酸盐,Zosuquidar (LY335979) 3HCl,RS 33295-198 trihydrochloride,RS 33295-198 (D06387) 3HCl,Zosuquidar 3HCl,LY-335979 trihydrochloride

P-gp Membrane transporter/Ion channel; Neuroscience
Zosuquidar trihydrochloride (LY-335979 trihydrochloride) 是一种P-糖蛋白抑制剂,Ki 值为 59 nM。
T5858 Sertindole

Lu 23-174,舍吲哚

Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; Autophagy Autophagy; GPCR/G Protein; Neuroscience
Sertindole (Lu 23-174) 是一种非典型抗精神病药,可与多巴胺 D2 受体和血清素受体亚型 5-HT1D、5-HT2A 和 5-HT2C 结合,Kd 值分别为 2.7、20、0.14 和 6 nM。
T83008 Antitumor agent-119

Antitumor agent-119(化合物13K)为2-苯并恶唑基腙衍生物,显示抗癌活性。该化合物对Butkitt、CCRF-CEM、HeLa和HT-29细胞系展现出细胞生长抑制作用,其IC50值分别为30 nM、140 nM、100 nM和40 nM。
T60359 cis-4-Br-2,5-F2-PCPA

cis-4-Br-2,5-F2-PCPA (S1024) 抑制 LSD1 和 LSD2,Ki 值分别为 94 nM 和 8.4 μM。癌症干细胞中 LSD1异常表达,cis-4-Br-2,5-F2-PCPA 能够通过增加 CCRF-CEM 细胞中二甲基化组蛋白 H3 的 K4 (H3K4) 水平,抑制 LSD1活性和癌细胞增殖。
T63522 Anticancer agent 64

Anticancer agent 64 (化合物 5m) 对 CCRF-CEM 细胞具有细胞毒性,其IC50为2.4 μM。Anticancer agent 64 通过诱导细胞凋亡表现出良好的抗癌活性。Anticancer agent 64 诱导caspase 3和 7 的激活和PARP 的裂解。Anticancer agent 64 具有明显的线粒体去极化作用。
T61017 Topoisomerase II inhibitor 6

Topoisomerase II inhibitor 6 (Compound 5) 是色胺酮的衍生物。它是一种有效的拓扑异构酶的选择性抑制剂。Topoisomerase II inhibitor 6 在 G2 期阻断 CCRF-CEM 的细胞周期并诱导 DNA 双链断裂。Topoisomerase II inhibitor 6 对不同的肿瘤细胞系具有抗增殖活性,在癌症疾病研究中具有潜力。
T62405 KDM1/CDK1-IN-1

KDM1/CDK1-IN-1 (compound 4) 是一种有效的 KDM1 (IC50: 0.096 μM) 和 CDK1 (IC50: 0.078 μM) 抑制剂。KDM1/CDK1-IN-1 能够将 HOP-92 细胞的细胞周期阻滞在 G2/M 期,并诱导其凋亡 (apoptosis)。KDM1/CDK1-IN-1 对 CCRF-CEM 细胞 (IC50: 16.34 μM)、HOP-92 细胞 (IC50: 3.45 μM) 和 Hep-G2 细胞 (IC50: 7.79 μM) 具有较强的细胞毒性。
T35810 C24 dihydro Ceramide (d18:0/24:0)

Cer(d18:0/24:0)

C24 dihydro Ceramide is a sphingolipid that has been found in the stratum corneum of human skin.[1] It is found in higher concentrations in female sebum compared to male sebum.[2] C24 dihydro Ceramide levels positively correlate with cytotoxicity in CCRF-CEM, MOLT-4, COG-LL-317h, and COG-LL-332h T cell acute lymphoblastic leukemia (ALL) cell lines.[4] Levels of C24 dihydro ceramide are increased by 149.49-fold in dihydroceramide desaturase 1 (DEGS1) knockdown UM-SCC-22A human head and neck squam...
T36695 TAS-103

TAS-103 is a dual inhibitor of DNA topoisomerase I/II, used for cancer research. TAS-103 is a dual inhibitor of DNA topoisomerase I/II. TAS-103 (0.1-10 μM) is active on CCRF-CEM cells, with an IC50 value of 5 nM. TAS-103 (0.1 μM) significantly increases levels of topo IIα FITC immunofluorescence in individual CCRF-CEM cells[1]. TAS-103 (0.01-1 μM) is highly cytotoxic to Lewis lung carcinoma (LLC) cells, and Liposomal TAS-103 is almost as active as free TAS-103[2]. TAS-103 inhibits the viability ...

化合物

Pheniramine maleate
Cat.No: T0370
Synonym: Daneral,Inhiston,Trimetose,马来酸非尼拉敏
Target: 5-HT Receptor, Histamine Receptor
Zosuquidar trihydrochloride
Cat.No: T6018
Synonym: 唑喹达三盐酸盐,Zosuquidar (LY335979) 3HCl,RS 33295-198 trihydrochloride,RS 33295-198 (D06387) 3HCl,Zosuquidar 3HCl,LY-335979 trihydrochloride
Target: P-gp
Sertindole
Cat.No: T5858
Synonym: Lu 23-174,舍吲哚
Target: Dopamine Receptor, 5-HT Receptor, Adrenergic Receptor, Autophagy
Antitumor agent-119
Cat.No: T83008
Synonym:
Target:
cis-4-Br-2,5-F2-PCPA
Cat.No: T60359
Synonym:
Target:
Anticancer agent 64
Cat.No: T63522
Synonym:
Target:
Topoisomerase II inhibitor 6
Cat.No: T61017
Synonym:
Target:
KDM1/CDK1-IN-1
Cat.No: T62405
Synonym:
Target:
C24 dihydro Ceramide (d18:0/24:0)
Cat.No: T35810
Synonym: Cer(d18:0/24:0)
Target:
TAS-103
Cat.No: T36695
Synonym:
Target:
Cat. No. Product Name Target Signaling Pathways
T3815 Isoscopoletin

异莨菪亭,7-Methoxyesculetin,6-Hydroxy-7-methoxycoumarin

Others; HBV Microbiology/Virology; Others
Isoscopoletin (7-Methoxyesculetin) 是艾叶中的一种活性成分。它具有显著的细胞增殖抑制作用,对人类 CCRF-CEM 白血病细胞和耐药亚系 CEM/ADR5000 作用的 IC50值分别为 4.0 μM 和 1.6 μM。它具有抑制 HBV 复制的活性。
TN3438 Arborinine

HCV Protease; Antifection Microbiology/Virology; Proteases/Proteasome
Arborinine shows mild in vitro antibacterial activity, it possesses moderate levels of anti-hepatitis C virus(HCV) activities with the IC50 values being 6.4 ± 0.7 ug/ml. Arborinine shows antifeedant activity against Spodoptera frugiperda. Arborinin shows

天然产物

Isoscopoletin
Cat.No: T3815
Synonym: 异莨菪亭,7-Methoxyesculetin,6-Hydroxy-7-methoxycoumarin
Target: Others, HBV
Arborinine
Cat.No: TN3438
Synonym:
Target: HCV Protease, Antifection
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