Antiproliferative agent-8

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Antiproliferative agent-8 

Antiproliferative against-9 (Compound 5a) 是一种抗癌剂。Antiproliferative against-9 具有抗增殖活性。Antiproliferative against-9 显着增加 P53 水平。

Antiproliferative agent-8

Antiproliferative agent-8 Chemical Structure

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生物活性

Antiproliferative against-9 (Compound 5a) is an anti-cancer agent. Antiproliferative against-9 has antiproliferative activity. Antiproliferative against-9 significantly increases the P53 levels[1].

分子量

405.83

Formula

C22H16ClN3O3

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Ramadan M, et al. Design and synthesis of new pyranoquinolinone heteroannulated to triazolopyrimidine of potential apoptotic antiproliferative activity. Bioorg Chem. 2020;105:104392.

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Antiproliferative against-7

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Antiproliferative against-7 

Antiproliferative against-7 (compound 8a) 是一种有效的抗肿瘤剂。Antiproliferative against-7 对癌细胞系 HCT116、MCF-7、H460 和非肿瘤非整倍体永生角质细胞 HaCaT 具有抗增殖活性,GI50 分别为 0.5 μM、2 μM、0.7 μM 和 3.5 μM。

Antiproliferative against-7

Antiproliferative against-7 Chemical Structure

CAS No. : 2389016-82-2

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生物活性

Antiproliferative against-7 (compound 8a) is a potent antitumor agent. Antiproliferative against-7 has antiproliferative activity against cancer cell lines HCT116, MCF-7, H460 and non-tumor aneuploid immortal keratinocyte HaCaT cells with GI50s of 0.5 μM, 2 μM, 0.7 μM and 3.5 μM, respectively[1].

IC50 & Target

GI50: 0.5 μM (HCT116), 2 μM (MCF-7), 0.7 μM (H460), 3.5 μM (HaCaT)[1]

分子量

404.83

Formula

C21H14ClFN6

CAS 号

2389016-82-2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Meščić Macan A, et al. Synthesis, antiproliferative activity and DNA/RNA-binding properties of mono- and bis-(1,2,3-triazolyl)-appended benzimidazo[1,2-a]quinoline derivatives. Eur J Med Chem. 2020;185:111845.

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Antiproliferative against-6

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Antiproliferative against-6 

Antiproliferative against-6 (compound 4o) 对胃癌细胞增殖有明显的不可逆抑制作用。Antiproliferative against-6 可引起细胞在 G2/M 期阻滞,诱导 ROS 积累,激活细胞自噬 (autophagy)。Antiproliferative against-6 可用于抗癌研究。

Antiproliferative against-6

Antiproliferative against-6 Chemical Structure

CAS No. : 2459892-41-0

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生物活性

Antiproliferative against-6 (compound 4o) can significantly and irreversibly inhibit proliferation of gastric cancer cells. Antiproliferative against-6 causes the G2/M phase arrest, and induces ROS accumulation and activation of autophagy. Antiproliferative against-6 can be used for researching anticancer[1].

IC50 & Target

ROS, Autophagy[1]

分子量

597.49

Formula

C28H21BrN8OS

CAS 号

2459892-41-0

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Wang S, et al. Discovery of new [1,2,4] Triazolo[1,5-a]Pyrimidine derivatives that Kill gastric cancer cells via the mitochondria pathway. Eur J Med Chem. 2020;203:112630.

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Antiproliferative against-5

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Antiproliferative against-5 

Antiproliferative against-5 (compound 2y) 对一些癌细胞有很好的抗增殖活性。Antiproliferative against-5 可降低 EC109 细胞线粒体膜电位,增加细胞凋亡率和 ROS 水平。Antiproliferative against-5 抑制裸鼠肿瘤生长,且具有低毒性。

Antiproliferative against-5

Antiproliferative against-5 Chemical Structure

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生物活性

Antiproliferative against-5 (compound 2y) has excellent anti-proliferative activity against certain cancer cell lines. Antiproliferative against-5 reduces the mitochondrial membrane potential, and increases the apoptosis rate and the level of ROS on EC109. Antiproliferative against-5 inhibits tumour growth in nude mice, with low toxicity[1].

IC50 & Target

IC50: 0.13 ± 0.01 μM in EC109, 0.27 ± 0.02 μM in TE-1, 0.20 ± 0.01 μM in MGC-803, 0.35 ± 0.03 μM in MCF-7[1]

体外研究
(In Vitro)

Antiproliferative against-5 has inhibitory activity against cancer cell lines EC109, TE-1, MGC-803 and MCF-7 with IC50s of 0.13 ± 0.01 μM, 0.27 ± 0.02 μM, 0.20 ± 0.01 μM and 0.35 ± 0.03 μM[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

547.04

Formula

C29H35ClO8

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Huo JF, et al. Synthesis and in vitro and in vivo biological evaluation of novel derivatives of flexicaulin A as antiproliferative agents. Eur J Med Chem. 2020;208:112789.

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Antiproliferative against-8

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Antiproliferative against-8 

Antiproliferative against-8 (compound 8f) 是一种有效的抗增殖剂。Antiproliferative against-8 对癌细胞 MCF-7、MDA-MB-231、HCT-116 和 FR-2 具有抗增殖活性,IC50 分别为 3.5 μM、15.54 μM、30.43 μM 和 34.8 μM。Antiproliferative against-8 可促进 ROS 产生,诱导细胞凋亡 (apoptosis)。

Antiproliferative against-8

Antiproliferative against-8 Chemical Structure

CAS No. : 2497687-47-3

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生物活性

Antiproliferative against-8 (compound 8f) is a potent anti-proliferative agent. Antiproliferative against-8 has antiproliferative activity against cancer cell lines MCF-7, MDA-MB-231, HCT-116 and FR-2 with IC50s of 3.5 μM, 15.54 μM, 30.43 μM and 34.8 μM, respectively. Antiproliferative against-8 can increase ROS production and induce apoptosis[1].

IC50 & Target

IC50: 3.5 μM (MCF-7), 15.54 μM (MDA-MB-231), 30.43 μM (HCT-116), 34.8 μM (FR-2)[1]

分子量

440.58

Formula

C28H32N4O

CAS 号

2497687-47-3

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Dheer D,et al.Design, synthesis and comparative analysis of triphenyl-1,2,3-triazoles as anti-proliferative agents. Eur J Med Chem. 2020 Dec 1;207:112813.

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Antiproliferative against-4

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Antiproliferative against-4 

Antiproliferative against-4 (comp 4) 显示对 MCF-7 癌细胞具有良好的活性 (IC50 = 0.19 nM)。

Antiproliferative against-4

Antiproliferative against-4 Chemical Structure

规格 是否有货
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生物活性

Antiproliferative against-4 (comp 4) shows the highest potency for MCF-7 cells (IC50 = 0.19 nM)[1].

体内研究
(In Vivo)

Antiproliferative against-4 (comp 4) is non-toxic in vivo (Danio rerio) at concentrations up to 125 μM[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

284.29

Formula

C11H12N2O5S

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Miloš Svirčev, et al. Design, synthesis, and biological evaluation of thiazole bioisosteres of goniofufurone through in vitro antiproliferative activity and in vivo toxicity. Bioorg Chem. 2022 Apr;121:105691.

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Antiproliferative against-4

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Antiproliferative against-4 

Antiproliferative against-4 (comp 4) 显示对 MCF-7 癌细胞具有良好的活性 (IC50 = 0.19 nM)。

Antiproliferative against-4

Antiproliferative against-4 Chemical Structure

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

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生物活性

Antiproliferative against-4 (comp 4) shows the highest potency for MCF-7 cells (IC50 = 0.19 nM)[1].

体内研究
(In Vivo)

Antiproliferative against-4 (comp 4) is non-toxic in vivo (Danio rerio) at concentrations up to 125 μM[1].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

284.29

Formula

C11H12N2O5S

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Miloš Svirčev, et al. Design, synthesis, and biological evaluation of thiazole bioisosteres of goniofufurone through in vitro antiproliferative activity and in vivo toxicity. Bioorg Chem. 2022 Apr;121:105691.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Antiproliferative against-4

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Antiproliferative against-4 

Antiproliferative against-4 (comp 4) 显示对 MCF-7 癌细胞具有良好的活性 (IC50 = 0.19 nM)。

Antiproliferative against-4

Antiproliferative against-4 Chemical Structure

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

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生物活性

Antiproliferative against-4 (comp 4) shows the highest potency for MCF-7 cells (IC50 = 0.19 nM)[1].

体内研究
(In Vivo)

Antiproliferative against-4 (comp 4) is non-toxic in vivo (Danio rerio) at concentrations up to 125 μM[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

284.29

Formula

C11H12N2O5S

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Miloš Svirčev, et al. Design, synthesis, and biological evaluation of thiazole bioisosteres of goniofufurone through in vitro antiproliferative activity and in vivo toxicity. Bioorg Chem. 2022 Apr;121:105691.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务