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Search Results for " anticancer agent 7 "

23

抑制剂 & 化合物

5

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T39501	Anticancer agent 7
	Anticancer agent 7 (Example 5) is an anti-cancer agent that exhibits potent anticancer activity against H1650 lung cancer cells, with an IC50 value of 5 μM.
T64348	Antiproliferative agent-16 Antiproliferative agent-16	Others	Others
	Antiproliferative agent-16 (Antiproliferative agent-16)是一种具有抗癌活性的吲哚酰肼-腙化合物。 Antiproliferative agent-16 对乳腺癌细胞表现出特异性 (对 MCF-7 细胞的 IC50 为 6.94 μM)。
T64002	Anticancer agent 61
	Anticancer agent 61 是一种口服具有活力的抗癌剂。Anticancer agent 61 能够抗 HepG2、Bel-7402 和 MCF-7 癌细胞的增殖，他们的 IC50 值分别为 1.12、1.97 和 1.08 μM。Anticancer agent 61 能够抑制肿瘤生长。
T63787	Anticancer agent 62
	Anticancer agent 62 是有效的抗癌剂。Anticancer agent 62 对 HepG2、Bel-7402 和 MCF-7 癌细胞表现出抗增殖作用，其 IC50值分别为 0.019、0.060 和 0.016 μM。Anticancer agent 62 能够抑制肿瘤生长。
T63917	Anticancer agent 67
	Anticancer agent 67 是环丙沙星类似物，是一种抗癌剂，在 MCF-7 细胞中能够诱导细胞凋亡 (apoptosis) 并增加亚 G1 细胞群。
T72479	Anticancer agent 66
	Anticancer agent 66 是一种抗癌剂。Anticancer agent 66 在 MCF-7 细胞中诱导细胞凋亡 (apoptosis) 并增加亚 G1 细胞群。Anticancer agent 66 是一种环丙沙星类似物。
T61823	Anticancer agent 63
	Anticancer agent 63 (compound 3h) exhibits significant cytotoxic activity against multiple cancer cell lines, including SW480, HeLa, A549, and MCF-7, with IC 50 values of 4.9, 11.5, 9.4, and 3.4 μM, respectively, after 24 hours of treatment. In particular, Anticancer agent 63 induces apoptosis in MCF-7 cells by down-regulating Bcl-2 expression and up-regulating IL-2 and Caspase-3 expression. Additionally, Anticancer agent 63 demonstrates antioxidative properties [1].
T61286	Glyoxalase I inhibitor 7
	Glyoxalase I inhibitor 7 (Compound 6) is a potent inhibitor of glyoxalase I (Glo-I) with an IC50 of 3.65 μM. It exhibits potential as an anticancer agent [1].
T61879	PARP1-IN-7
	PARP1-IN-7 是一种聚 ADP 核糖聚合酶-1（PARP1）的抑制剂，作为抗癌剂。
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。
T61582	Anticancer agent 57
	Anticancer agent 57 (compound 14) demonstrates potent inhibition of MDA-MB-231, MDA-MB-468, and MCF-7 cell lines, with IC 50 values ranging from 6.43 to 8.00 μM. Additionally, this agent induces cell cycle arrest and promotes apoptosis. In vivo studies using nude mice xenografted with MADMB-231 cells have shown that Anticancer agent 57 effectively inhibits tumor growth. Consequently, Anticancer agent 57 can serve as a valuable tool for researching triple negative breast cancer (TNBC) [1].
T61673	Anticancer agent 56
	Anticancer agent 56 (compound 4d) is a powerful anti-cancer compound with favorable drug-like properties. It shows significant anticancer activity against multiple cancer cell lines, with an IC50 value of less than 3 μM. Anticancer agent 56 exerts its effects by causing cell cycle arrest at the G2/M phase and activating the mitochondrial apoptosis pathway. Mechanistically, it induces the accumulation of reactive oxygen species (ROS), upregulates BAX, downregulates Bcl-2, and triggers the activat...
T72756	Gly-7-MAD-MDCPT
	Gly-7-MAD-MDCPT 是一种抗癌剂。Gly-7-MAD-MDCPT 是一种喜树碱 (Camptothecin) 化合物，对多种癌细胞有细胞毒性，IC50为 10-1000 nM。
T79482	Anticancer agent 137	PI3K	PI3K/Akt/mTOR signaling
	Anticanceragent 137 (8q) 是一种高效的 PI3k 抑制剂，展现出广谱的抗肿瘤活性。它能够诱导 G2/M 阶段的细胞周期阻滞与细胞凋亡（apoptosis），并促进 PARP、caspase 3 和 caspase 7 的裂解。该化合物主要用于癌症相关的生物医学研究。
T78051	Necrocide 1	Others	Others
	Necrocide 1（化合物(S)-38）是一款有效的抗癌药物，具备显著的抗增殖效果，针对MCF-7和PC3细胞株的IC50值分别为0.48 nM及2 nM。
T83078	Anticancer agent 33
	Anticanceragent 33 (compound 3) 为Squamocin与Bullatacin衍生物，展现出有效的抗癌特性。本化合物对4T1乳腺癌细胞系（包括A549、HeLa、HepG2和MCF-7细胞）的生长抑制作用显著，其IC50范围为1.9-5.4 µM。
T74491	Antitumor agent-61
	Antitumor agent-61 (Compound 9b)，Irinotecan (Ir)的衍生物，展现出对多种肿瘤细胞（包括SK-OV-3、SK-OV-3/CDDP、U2OS、MCF-7、A549与MG-63）具有显著的抑制效果，其IC50值分别为0.92、1.39、1.75、2.20、3.05和3.23 μM。该化合物主要通过线粒体途径引发SK-OV-3细胞的凋亡。
T36869	5'-chloro-5'-Deoxyadenosine (hydrate)
	5'-chloro-5'-Deoxyadenosine (hydrate) is a nucleoside analog used as a substrate in polyketide biosynthesis. S-(5'-adenosyl)-L-methionine can be converted to 5'-chloro-5'-deoxyadenosine in a reaction catalyzed by a SAM-dependent chlorinase. Through a 7-step route, 5'-chloro-5'-deoxyadenosine can be converted to chloroethylmalonyl-CoA, which has been shown to be involved in the biosynthesis of the anticancer agent salinosporamide A in the marine bacterium S. tropica.
T83099	Antibacterial agent 162 trifluoromethanesulfonate
	Antibacterialagent 162 trifluoromethanesulfonate (化合物 7) 作为一种高效抗菌剂，对金黄色葡萄球菌（包括MRSA）展示了显著的抑制效果。同时，此化合物在抗癌领域也具有潜力，特别是对结肠癌和非小细胞肺癌细胞的抗增殖活性。因此，Antibacterialagent 162 trifluoromethanesulfonate 在抗癌和抗菌领域的研究中具有广泛的应用前景。
T79388	Anticancer agent 154	Reactive Oxygen Species	Immunology/Inflammation; Metabolism; NF-κB
	Anticanceragent 154 (Compound 8h) 增加活性氧水平、导致线粒体损伤，并诱导细胞凋亡和 DNA 损伤。此外，该化合物通过降低 GSH 和 GPX4 水平，增加脂质过氧化，进而诱导铁死亡。Anticanceragent 154 对多种癌细胞株（HT29、H1975、A549 及 MCF-7）显示抑制作用，IC50 值在 1.0-1.9 μM 范围。
T78608	Anticancer agent 164	Apoptosis	Apoptosis
	CML-IN-1（compound 7）是一种高效抗癌药物，针对人类慢性粒细胞白血病（CML）细胞系K562，能有效诱导凋亡（apoptosis）。该化合物主要通过显著抑制PI3K/Akt信号通路的蛋白磷酸化来发挥作用，同时CML-IN-1（compound 4）也能通过抑制结直肠癌的MEK/ERK信号通路来阻止细胞增殖。
T83680	Azurin (50-77) (P. aeruginosa) TFA Azurin p28,p28
	Azurin (50-77)是一种含铜细菌蛋白azurin的肽段，存在于P. aeruginosa中，具有细胞周期停滞、抑制癌细胞增殖和调节血管生成活性。作为VEGFR2的抑制剂（IC20约为10.7 µM），Azurin (50-77)（20 µM）能在MCF-7乳腺癌细胞中诱导G2/M期的细胞周期停滞。在50 µM的浓度下，减少MCF-7和ZR-75-1乳腺癌细胞的增殖。Azurin (50-77)以25 µM的浓度减少VEGF-A诱导的毛细管管腔形成（IC50 = 12 µM），降低人脐静脉内皮细胞（HUVECs）中与细胞膜相关的F-actin、焦点粘附激酶（FAK）和paxillin的水平，并增加胞外的血小板内皮细胞粘附分子-1（PECAM-1）的水平。在体内，Azurin (50-77)（每日10 mg/kg）在MCF-7小鼠异种移植模型中减少肿瘤体积。
T35683	2-deoxy-D-Glucose-13C6 2-deoxy-D-Glucose-13C6
	2-deoxy-D-Glucose-13C6is intended for use as an internal standard for the quantification of 2-deoxy-D-glucose by GC- or LC-MS. 2-deoxy-D-Glucose is a glucose antimetabolite and an inhibitor of glycolysis.1,2It inhibits hexokinase, the enzyme that converts glucose to glucose-6-phosphate, as well as phosphoglucose isomerase, the enzyme that converts glucose-6-phosphate to fructose-6-phosphate.32-deoxy-D-Glucose (16 mM) induces apoptosis in SK-BR-3 cells, as well as inhibits the growth of 143B oste...

化合物

Anticancer agent 7

Cat.No: T39501

Antiproliferative agent-16

Cat.No: T64348

Synonym: Antiproliferative agent-16

Target: Others

Anticancer agent 61

Cat.No: T64002

Anticancer agent 62

Cat.No: T63787

Anticancer agent 67

Cat.No: T63917

Anticancer agent 66

Cat.No: T72479

Anticancer agent 63

Cat.No: T61823

Glyoxalase I inhibitor 7

Cat.No: T61286

Cat.No: T61879

Anticancer agent 64

Cat.No: T63522

Anticancer agent 57

Cat.No: T61582

Anticancer agent 56

Cat.No: T61673

Gly-7-MAD-MDCPT

Cat.No: T72756

Anticancer agent 137

Cat.No: T79482

Target: PI3K

Cat.No: T78051

Target: Others

Anticancer agent 33

Cat.No: T83078

Antitumor agent-61

Cat.No: T74491

5'-chloro-5'-Deoxyadenosine (hydrate)

Cat.No: T36869

Antibacterial agent 162 trifluoromethanesulfonate

Cat.No: T83099

Anticancer agent 154

Cat.No: T79388

Target: Reactive Oxygen Species

Anticancer agent 164

Cat.No: T78608

Target: Apoptosis

Azurin (50-77) (P. aeruginosa) TFA

Cat.No: T83680

Synonym: Azurin p28,p28

2-deoxy-D-Glucose-13C6

Cat.No: T35683

Synonym: 2-deoxy-D-Glucose-13C6

Cat. No.	Product Name	Target	Signaling Pathways
TN1727	Helichrysetin 4,2',4'-三羟基-6'-甲氧基查耳酮,蜡菊亭	Apoptosis; HIV Protease	Apoptosis; Microbiology/Virology; Proteases/Proteasome
	Helichrysetin 是从豆蔻果实中分离出的一种天然产物，是一种 DNA 结合抑制剂，可抑制原位导管癌DCIS 的形成。它抑制细胞生长，可诱导 A549 细胞凋亡。
T2S1865	Octyl gallate Gallic acid octyl ester,n-Octylgallate,Octyl 3,4,5-trihydroxybenzoate,Progallin O,Stabilizer GA-8,没食子酸辛酯	Antioxidant; Influenza Virus; Reactive Oxygen Species; Antibacterial; Antifungal; HSV	Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB; oxidation-reduction
	Octyl gallate (Octyl 3,4,5-trihydroxybenzoate) 具有抗菌、抗氧化作用，有选择性和敏感性的荧光特性，广泛用作食品添加剂。它对 HSV-1，水泡性口炎病毒和脊髓灰质炎病毒有显著的抗病毒作用。
T81690	Neocucurbitacin A	STAT	JAK/STAT signaling; Stem Cells
	Neocucurbitacin A (compound 7)是一种从沉香果皮提取的STAT3抑制剂，常用于抗癌研究。
T83089	Anticancer agent 149
	Anticanceragent 149 (compound 3) 是一种从薯蓣 (DM) 根茎中分离出的抗癌剂，其对MCF-7 细胞呈现选择性细胞毒活性，特有IC50值为31.41 μM。
T73403	Aviculin
	Aviculin 是一种木聚糖苷，是一种有效的抗癌剂 (anticanceragent)。Aviculin 可降低 MCF-7 细胞代谢活性到 50% 以下，IC50为 75.47 μM。Aviculin 通过内在凋亡途径诱导乳腺癌细胞凋亡 (apoptosis)。Aviculin 增加了 caspase-9、caspase-7和 PARP 的表达。Aviculin 使 Bax/Bcl-2 的比值升高。

天然产物

Cat.No: TN1727

Synonym: 4,2',4'-三羟基-6'-甲氧基查耳酮,蜡菊亭

Target: Apoptosis, HIV Protease

Cat.No: T2S1865

Synonym: Gallic acid octyl ester,n-Octylgallate,Octyl 3,4,5-trihydroxybenzoate,Progallin O,Stabilizer GA-8,没食子酸辛酯

Target: Antioxidant, Influenza Virus, Reactive Oxygen Species, Antibacterial, Antifungal, HSV

Neocucurbitacin A

Cat.No: T81690

Target: STAT

Anticancer agent 149

Cat.No: T83089

Cat.No: T73403

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