1264
325
20
16
3
Cat. No. | Product Name | ||
---|---|---|---|
L2100 | 抗癌化合物库 | 7234 compounds | |
7234 种肿瘤相关的生物活性小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L2180 | 抗肿瘤库Plus | 1468 compounds | |
1468 种抗肿瘤相关、结构新颖的化合物; | |||
L2150 | 抗癌药物库 | 3080 compounds | |
3080 个具有抗癌活性小分子的独特集合,生物活性已经临床前实验证实,可用于高通量、高内涵筛选; | |||
L2110 | 抗癌上市药物库 | 1779 compounds | |
1779 个具有抗癌活性小分子的独特集合,所有化合物都经过了严格的临床前研究和临床试验,由FDA、EMA 或NMPA 批准上市,可用于高通量、高内涵筛选。 | |||
L2130 | 抗癌细胞代谢库 | 1268 compounds | |
1268 种癌细胞代谢相关的生物活性小分子化合物的特有集合,用于肿瘤相关的研究以及抗肿瘤药物的筛选,用于高通量、高内涵筛选; | |||
L2160 | 抗癌活性化合物库 | 3188 compounds | |
3188 种具有抗肿瘤活性的化合物的特有集合,用于高通量、高内涵筛选; | |||
L2120 | 抗癌临床化合物库 | 2545 compounds | |
2545 个具有抗癌活性小分子的独特集合,可用于高通量高内涵筛选。 | |||
L6900 | 稀有天然产物库 | 693 compounds | |
693 种稀有天然产物的集合,可以用于高通量和高内涵筛选; | |||
L1110 | 微管靶向化合物库 | 142 compounds | |
142 种靶向微管的分子集合,用于高通量筛选和高内涵筛选; | |||
L2151 | 化疗药物库 | 48 compounds | |
48 个肿瘤化疗药物,可以用于高通量和高内涵筛选; | |||
L6110 | 生物碱类天然产物库 | 500 compounds | |
500 种生物碱类天然产物的独特集合,可用于高通量筛选和高内涵筛选; | |||
NY1000 | 天然产物衍生物库 | 4000 compounds | |
22个天然产物骨架,3745个天然产物衍生物; | |||
L6100 | 天然多酚类化合物库 | 635 compounds | |
635 个天然多酚化合物的独特集合,可用于高通量、高内涵筛选; | |||
L6130 | 萜类天然产物库 | 622 compounds | |
622 种萜类天然产物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L6700 | 抗癌天然产物库 | 1772 compounds | |
1772 种已知活性天然产物的独特集合,是肿瘤药物开发、抗癌先导化合物筛选等领域的有力工具,可用于HTS 和HCS。 | |||
L1100 | 蛋白酶抑制剂库 | 343 compounds | |
343 种已知的小分子蛋白酶抑制剂的特有集合,可用于高通量筛选和高内涵筛选; | |||
L5100 | 含氟化合物库 | 574 compounds | |
574 个含氟化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L9240 | 农药化合物库 | 270 compounds | |
270种农药相关化合物的独特集合,可用于高通量筛选和高内涵筛选; | |||
L6020 | 天然产物单体化合物库 | 16627 compounds | |
16627 种精选天然产物集合,结构多样,遍布多种动植物与微生物; | |||
L6820 | 烟草单体化合物库 | 747 compounds | |
747种烟草单体化合物的独特集合,可用于高通量筛选和高内涵筛选 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T39868 |
Anticancer agent 11
|
Others | Others |
Anticancer agent 11 an effective broad-spectrum anticancer agent, exerts its therapeutic potential by suppressing angiogenesis and facilitating the formation of DNA cross-links. | |||
T60420 |
Anticancer agent 73
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Anticancer agent 73 是一种抗癌剂,它能有效地靶向反式激活反应(TAR)RNA 结合蛋白2(TRBP),并破坏TRBP-Dicer 的相互作用。Anticancer agent 73 通过调节 HCC 细胞中 miRNA 组和蛋白质组的表达谱,在体外和体内抑制 HCC 的生长和转移。 | |||
T60852 |
Anticancer agent 46
|
Others | Others |
Anticancer agent 46是一种有效的抗癌剂, 在细胞实验中显示出抗增殖活性,对 MGC803细胞的 IC50为0.986μM。 | |||
T61046 |
Anticancer agent 43
|
Apoptosis | Apoptosis |
Anticancer agent 43 是一种有效的抗癌剂,通过 caspase 3, PARP1,Bax 蛋白依赖性途径诱导癌细胞凋亡 (apoptosis)。Anticancer agent 43 能够诱导 DNA 损伤,可用于研究大鼠胶质母细胞瘤 。 | |||
T40479 |
Anticancer agent 13
|
Others | Others |
Anticancer agent 13 is an anticancer agent from dicarboxylic acids and amines. | |||
T39501 |
Anticancer agent 7
|
Others | Others |
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. | |||
T40330 |
Anticancer agent 15
|
Others | Others |
Anticancer agent 15, an anticancer agent, exerts its efficacy by elevating intracellular levels of reactive oxygen species (ROS) and inducing cell death in melanoma cancer cells through necroptosis. | |||
T10331 |
Anticancer agent 3
|
Others | Others |
Anticancer agent 3 (Compound 4) is a anti-cancer agent. | |||
T27998 |
MDK-4204
Anticancer AgentI,MDK 4204,Anticancer Agent I,MDK4204,Anticancer Agent-I |
Others | Others |
MDK-4204, an anticancer agent, shows significant anti-cancer activity with IC50 values of 8.8 µM and 9.5 µM in PC-3 and DU-145 cells, respectively. | |||
T62667 |
Anticancer agent 51
|
Others | Others |
Anticancer agent 51 (compound 3d) 是一种有效的抗癌剂 (Ki: 731.62 nM),具有抗癌活性。Anticancer agent 51 具有潜力进行前列腺癌的研究。 | |||
T64002 |
Anticancer agent 61
|
Others | Others |
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。 | |||
T72502 |
Anticancer agent 92
|
Others | Others |
Anticancer agent 92 是一种对非癌细胞无毒的抗癌剂。 | |||
T61412 |
Anticancer agent 47
|
Others | Others |
Anticancer agent 47 (compound 4j) exhibits potent anticancer properties, demonstrating antiproliferative activities and inducing apoptosis as well as cell cycle arrest at G0/G1 phase. Moreover, Anticancer agent 47 has exhibited significant in vivo antitumor activities [1]. | |||
T62124 |
Anticancer agent 80
|
Others | Others |
Anticancer agent 80 (Compound 3c) 是一种抗癌剂。Anticancer agent 80 对 T47-D 表现出明显的暗毒性作用 (IC50: 10.14 μM)。 | |||
T63982 |
Anticancer agent 50
|
Others | Others |
Anticancer agent 50 (compound 6) 是 ABCB1 外排泵的有效调节剂,具有细胞毒活性和抗增殖活性。Anticancer agent 50 能够减少细胞周期蛋白 D1 的表达,并诱导 p53 表达。Anticancer agent 50 对 T 淋巴瘤表现出研究潜力。 | |||
T61379 |
Anticancer agent 30
|
Others | Others |
Anticancer agent 30 (compound 6f-Z) is a potent anticancer compound. It belongs to the class of 3-arylidene-2-oxindole derivatives and acts as a selective inhibitor of CDK2. Extensive research has demonstrated its significant anticancer activity, making it a promising candidate for cancer treatment [1]. | |||
T78929 |
Anticancer agent 126
|
Histone Methyltransferase | Chromatin/Epigenetic |
Anticanceragent 126 (compound 12) 作为WDR5抑制剂,能够破坏WDR5-MYC间的相互作用,并降低MYC靶基因的表达,表现出其抗癌活性。 | |||
T60776 |
Anticancer agent 68
|
Others | Others |
Anticancer agent 68 is (Compound 12) 是一种抗癌剂。Anticancer agent 68 将细胞阻滞在 G2/M 期并诱导程序性细胞死亡。Anticancer agent 68 通过激活 p53 和 PTEN 诱导上调肿瘤抑制。 | |||
T64179 |
Anticancer agent 65
|
Others | Others |
Anticancer agent 65 在肿瘤细胞系中显示出良好的效果,尤其是 A549 细胞 (IC50: 1.07 μM)。Anticancer agent 65 能够将 A549 细胞的细胞周期阻滞在 S 期,诱导细胞凋亡,增加 p53、p21 的表达水平,并促使 ROS 生成和 MMP 崩溃。 | |||
T83093 |
Anticancer agent 107
|
Others | Others |
Anticancer agent 107(Compd 11jc) 具有显著的抗肿瘤活性,是研究肺转移性黑色素瘤的潜在抗癌剂。 | |||
T79301 |
Anticancer agent 140
|
Parasite | Microbiology/Virology |
Anticanceragent 140(Compd 3)是一种化合物,具备潜在的抗癌和抗寄生虫活性。 | |||
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。 | |||
T79844 |
Anticancer agent 143
|
Phosphatase | Metabolism |
Anticanceragent 143(化合物 369),作为PTPN2/PTP1B双重抑制剂,表现出强效活性,其IC50值均低于2.5 nM。该化合物主要用于癌症研究领域。 | |||
T79202 |
Anticancer agent 118
|
Others | Others |
Anticanceragent 118是一种N-酰化环丙沙星衍生物,展现了针对革兰氏阳性(bacterial)菌株的高度活性,以及对前列腺癌PC3细胞的抗增殖能力,适用于抗肿瘤研究。 | |||
T78780 |
Anticancer agent 139
|
Others | Others |
Anticanceragent 139(Compound 6h)展现了针对多种癌细胞株的抗癌效能。该化合物能够与Tubulin的Lys352残基发生π-阳离子相互作用。在对SNB-19、OVCAR-8和NCI-H460细胞株的测试中,Anticanceragent 139展现出较高的生长抑制率(PGI),数值分别为86.61、85.26和75.99。同时,该化合物对于HOP-62、SNB-75、ACHN、NCI/ADR-RES、786-O、A549/ATCC、HCT-116以及MDA-MB-231细胞株亦表现出中等的生长抑制作用,其PGI值分别为67.55、65.46、59.09、59.02、57.88、56.88、56.53和56.4、51.88。 | |||
T83078 |
Anticancer agent 33
|
Others | Others |
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。 | |||
T83087 |
Anticancer agent 158
|
Others | Others |
Anticanceragent 158 (compound 7c) 作为一种有效的抗癌剂,其对HepG-2、MDA-MB-231、HCT-116细胞系的IC50值分别为7.93 μM、9.28 μM、13.28 μM。 | |||
T62601 |
Anticancer agent 48
|
Others | Others |
Anticancer agent 48 (compound 48) 是一种广谱抗癌剂,其表现出抗增殖活性。Anticancer agent 48 对微管蛋白聚合具有抑制作用。Anticancer agent 48 在体内显示抗肿瘤活性。Anticancer agent 48 具有潜力进行实体瘤和血液肿瘤的研究。主语 | |||
T61777 |
Anticancer agent 42
|
Others | Others |
Anticancer agent 42 (compound 10d) is an orally active, potent anticancer agent with demonstrated efficacy against MDA-MB-231 cells, exhibiting an IC50 of 0.07 μM. It exerts its anticancer activity through the activation of apoptotic pathways and p53 expression. Anticancer agent 42 is a valuable tool for investigating metastatic breast cancer [1]. | |||
T61750 |
Anticancer agent 72
|
Others | Others |
Anticancer agent 72 (compound 8c) effectively inhibits the K+ channel, displaying significant potential as an anticancer treatment. Additionally, it induces apoptosis, a programmed cell death process [1]. | |||
T63587 |
Anticancer agent 45
|
Others | Others |
Anticancer agent 46 是有效的、选择性的抗癌剂,能够诱导细胞凋亡 (apoptosis)。Anticancer agent 46 在癌细胞中表现出细胞毒效果,对人血的活化淋巴细胞显示出低毒性。 | |||
T63913 |
Anticancer agent 41
|
Others | Others |
Anticancer agent 41 是一种有效的抗癌剂,对 MDA-MB-231 细胞表现出良好的抗肿瘤效果 (IC50: 3.99 μM)。 | |||
T63917 |
Anticancer agent 67
|
Others | Others |
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。 | |||
T63671 |
Anticancer agent 60
|
Others | Others |
Anticancer agent 60 对人 HepG2 细胞具有抗增殖效果,其 IC50 值为 4.13 μM。在人 HepG2 异种移植小鼠模型中,Anticancer agent 60 表现出抗肿瘤活性。 | |||
T63159 |
Anticancer agent 28
|
Others | Others |
Anticancer agent 28 在体内 H22 同种异体移植小鼠中具有良好的抗肿瘤作用。Anticancer agent 28 对 K562 细胞的作用是 Oridonin 的50倍,其 IC50 值为 0.09 μM。 | |||
T79204 |
Anticancer agent 122
|
Others | Others |
Anticanceragent 122,作为一种hLDHA抑制剂,表现出显著的抗癌活性,主要应用于抗肿瘤研究。 | |||
T63354 |
Anticancer agent 17
|
Others | Others |
Anticancer agent 17 对 HeLa 细胞 (IC50: 0.19 μM) 和 A2780 细胞 (IC50: 0.09 μM) 具有有效抗癌作用。 | |||
T61673 |
Anticancer agent 56
|
Others | Others |
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... | |||
T83080 |
Anticancer agent 171
|
Others | Others |
Anticanceragent 171(Compound 6a)是一款肟类似物,对HCT116细胞表现出显著的抗癌活性,IC50值为3.43 μM,主要用于癌症研究领域。 | |||
T78957 |
Anticancer agent 105
|
Apoptosis | Apoptosis |
Anticanceragent 105 是基于噻吩嘧啶支架的抗癌化合物,显示出高度的安全性与抗肿瘤活性。该化合物对黑色素瘤细胞表现出选择性毒性,并能诱导细胞凋亡(apoptosis)。在肺转移性黑色素瘤小鼠模型中,Anticanceragent 105 能够显著地抑制转移性结节的形成。 | |||
T83084 |
Anticancer agent 162
|
Others | Others |
Anticanceragent 162 (compound 1d)作为一种抗癌药物,显示出亲脂性和针对性细胞毒性,能够特异性诱导Hela细胞系的癌细胞死亡。 | |||
T83075 |
Anticancer agent 94
|
Others | Others |
Anticanceragent 94, 一种4-羟基香豆素衍生物,能抑制肺癌细胞的侵袭和迁移,其机制为调节(EMT)效应子表达。 | |||
T83076 |
Anticancer agent 93
|
Others | Others |
Anticanceragent 93, 一种4-羟基香豆素衍生物,能够抑制肺癌细胞的侵袭与迁移,其机制为调节上皮间质转化(EMT)效应子的表达。 | |||
T83090 |
Anticancer agent 131
|
Others | Others |
HCT-116-IN-1, 一种与γ-内酰胺融合的吡啶酮衍生物,展现了针对HCT116细胞的强抗癌活性,其细胞毒性测定显示IC50值为5.59 μM。 | |||
T79359 |
Anticancer agent 147
|
Ferroptosis | Apoptosis |
Anticanceragent 147(化合物6j),作为槐定碱的衍生物,功能为铁死亡(Ferroptosis)诱导剂。该化合物能促进Fe2+、活性氧(ROS)及丙二醛(MDA)在细胞内的积累,并通过增加内质网(ER)应激和上调转录因子ATF3的表达发挥作用。在体外及体内实验中,Anticanceragent 147展现了出色的抗肝癌活性。 | |||
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。 | |||
T62427 |
Anticancer agent 32
|
Others | Others |
Anticancer agent 32 (compound 2g) 是一种抗癌剂。Anticancer agent 32 能够影响细胞周期并诱导细胞凋亡,表现出抗癌效果。Anticancer agent 32 能够用于研究癌症。 | |||
T62602 |
Anticancer agent 49
|
Others | Others |
Anticancer agent 49 (compound 69) 是一种广谱抗癌剂,其表现出抗增殖活性。Anticancer agent 49 对微管蛋白聚合具有抑制作用。Anticancer agent 49 在体内显示抗肿瘤活性。Anticancer agent 49 具有潜力进行实体瘤和血液肿瘤的研究。 | |||
T61230 |
Anticancer agent 74
|
Others | Others |
Anticancer agent 74 exhibits moderate anticancer activity with lower selectivity and cytotoxicity compared to doxorubicin towards normal cells [1]. | |||
T63599 |
Anticancer agent 54
|
Others | Others |
Anticancer agent 54 是有效的抗癌剂,其抗癌活性取决于 DNA 嵌入和 ROS 生成。 Anticancer agent 54 能够将细胞周期阻滞在 G0/G1 期,并诱导细胞凋亡 (apoptosis),具有抗增殖效果。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
T83073 |
Anticancer agent 96
|
||
Anticanceragent 96 (Compound 4) 对人癌细胞表现出显著的细胞毒性。 | |||
T83086 |
Anticancer agent 160
|
Others | Others |
Anticanceragent 160 (Compound 6),源自Parthenium hysterophorus的天然化合物,对HCT-116细胞表现出细胞毒作用,其半数抑制浓度(IC50)为5.0 μM。 | |||
T83088 |
Anticancer agent 156
|
||
Anticanceragent 156(compound 11)是一种基于Miliusanes的强效抗癌剂,有效抑制人源癌细胞生长,并对胃癌细胞展现出显著细胞毒性。 | |||
TN1873 |
Lirinidine
|
Others; Antioxidant | Others; oxidation-reduction |
Lirinidine 是一种分离自L. tulipifera叶片生物碱,具有抗氧化 (antioxidant) 和抗癌作用。它在体外表现出中等的铁还原能力和较小的自由基清除能力,可用于研究化妆品。 | |||
T9144 |
Telekin
|
Others | Others |
Telekin 是一种从中草药 Carpesium divaricatum 中分离出来的 eudesmane 型倍半萜内酯化合物,据报道可强烈抑制癌细胞的增殖。 | |||
T21065 |
Artemisitene
|
Others | Others |
Artemisitene 是青蒿素的氧化形式,是一种抗疟药。青蒿素前体是青蒿素生物合成的重要基础物质,包括青蒿素 B、青蒿素、青蒿酸等。 | |||
T10668 |
Camalexin
|
Reactive Oxygen Species; ROS; Antibacterial; Antifungal | Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Camalexin 是从Camelina sativa 和Arabidopsis 中分离出来的一种植物抗毒素,可诱导活性氧的产生,具有抗菌、抗真菌、抗增殖和抗癌活性。 | |||
TN6771 |
Malabaricone B
|
Others | Others |
Malabaricone B 是一种源自香料的酚类物质,它通过不依赖 p53 的途径诱导肺癌细胞中的线粒体损伤。 | |||
TN6739 |
Angoline
6-Methoxyldihydrochelerythrine |
IL Receptor; STAT | Immunology/Inflammation; JAK/STAT signaling; Stem Cells |
Angoline (6-Methoxyldihydrochelerythrine) 是选择性 IL6/STAT3信号通路的抑制剂,IC50为 11.56 μM。它抑制 STAT3 磷酸化及其靶基因表达,并抑制癌细胞增殖。 | |||
TN1079 |
Deoxyelephantopin
|
NF-κB | NF-κB |
Deoxyelephantopin 是来自Elephantopus scaber 的,具有生物活性的天然倍半萜烯内酯,能够抑制NF-κB,MAPK,PI3K/Akt 和β-catenin 信号传导。它可广泛用于癌症方面的研究。 | |||
TN7060 |
Methyl oleanonate
|
PPAR | DNA Damage/DNA Repair; Metabolism |
Methyl oleanonate 是从柃木中分离得到的一种三萜类天然产物,是齐墩果酸衍生物,是一种PPARγ激动剂,具有抗癌作用。 | |||
TN1712 |
Gossypin
|
NF-κB; S6 Kinase | MAPK; NF-κB; PI3K/Akt/mTOR signaling |
Gossypin 是一种从Hibiscus vitifolius 中分离得到的黄酮,能够抑制NF-κB 和 NF-κB 的调节基因表达。在小鼠原代骨髓细胞和 RAW264.7 细胞中,它也可抑制 RANKL 诱导的破骨细胞形成。它具有抗氧化、抗炎、抗癌、抗衰老、抗糖尿病和保护肝脏的活性。 | |||
T11685 |
Isolongifolene
异长叶烯,(-)-Isolongifolene |
Apoptosis; Others | Apoptosis; Others |
Isolongifolene ((-)-Isolongifolene) 是一种从调料九里香中分离的三环倍半萜烯,具有抗氧化,抗炎,抗癌和神经保护的特性。它通过调节 PI3K/AKT/GSK-3β 信号通路来减轻鱼藤酮诱导的氧化应激,线粒体功能障碍和细胞凋亡。 | |||
T7544 |
Fucoidan
岩藻多糖 |
Others | Others |
Fucoidan 是一种 α-淀粉酶和 α-葡萄糖苷酶的有效抑制剂,是一种生物特性多糖。 它具有抗凝血,抗肿瘤,抗氧化和抗脂肪特性。 | |||
T7052 |
Gnetol
|
Tyrosinase; COX; HDAC; AChR | Chromatin/Epigenetic; DNA Damage/DNA Repair; Immunology/Inflammation; Neuroscience; Proteases/Proteasome |
Gnetol 是从买麻藤的根中分离出来的一种酚类。它是酪氨酸酶抑制剂,对鼠酪氨酸酶的 IC50为 4.5 μM,可抑制黑色素的生物合成。它有效抑制 COX-1和 HDAC,具有抗氧化、抗增殖、抗癌和保肝活性,还具有浓度依赖性的 α-淀粉酶、α-葡萄糖苷酶和脂肪形成活性。 | |||
T5613 |
Squalane
角鲨烷,Dodecahydrosqualene,Perhydrosqualene |
Others | Others |
Squalane 是某些鱼油 (尤其是鲨鱼肝油) 和某些植物油中存在的脂质。它具有抗癌,抗氧化作用,可用作皮肤保湿和润肤剂。 | |||
T2853 |
Curcumol
莪术醇,(-)-Curcumol,姜黄醇 |
Apoptosis; JAK | Angiogenesis; Apoptosis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
Curcumol ((-)-Curcumol) 是一种倍半萜,具有抗癌,抗微生物,抗真菌,抗病毒和抗炎活性。它通过靶向关键信号通路,在许多癌细胞中有效地诱导凋亡。 | |||
T1134 |
Clofoctol
叔辛酚氯,氯福克酚 |
Antibacterial; Antibiotic | Microbiology/Virology |
Clofoctol 是一种抗生素,,可研究革兰氏阳性菌感染。它仅对革兰氏阳性菌起作用, 可渗透入人类肺组织。 | |||
T3332 |
Isosteviol
异甜菊醇,(-)-Isosteviol |
IL Receptor; Potassium Channel; TNF; NF-κB; Reactive Oxygen Species; COX; Topoisomerase | Apoptosis; DNA Damage/DNA Repair; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience; NF-κB |
Isosteviol ((-)-Isosteviol) 是一种常见的天然甜味剂,属于四环二萜糖苷,是甜菊糖苷通过酸催化水解产生的。它抑制 DNA 聚合酶和 DNA 拓扑异构酶,具有抗菌、抗癌和抗结核作用。 | |||
T2731 |
Usnic Acid
Usniacin,松萝酸,地衣酸 |
Antibacterial; Autophagy | Autophagy; Microbiology/Virology |
Usnic Acid (Usniacin) 是地衣次生代谢产物,具有独特的二苯并呋喃骨架。它是一种抗菌剂、抗肿瘤剂和酶抑制剂。 | |||
T9715 |
Aplidine
|
SARS-CoV; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Aplidine 是有效的eEF1A2(KD=80 nM) 靶向的抗癌药物。Aplidine 具有抗病毒活性,抑制SARS-CoV-2的 IC90为 0.88 nM。Aplidine 在多发性骨髓瘤,晚期癌症及 COVID-19 领域有研究的价值。 | |||
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。 | |||
TN1990 |
Norathyriol
芒果苷元 |
Akt; DNA/RNA Synthesis; AMPK; PPAR | Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; Metabolism; PI3K/Akt/mTOR signaling |
Norathyriol 是来自芒果的芒果苷代谢物,具有抗氧化、抗癌、抗菌和抗炎活性。它以非竞争性方式抑制 α-葡萄糖苷酶,IC50为 3.12 μM。它还抑制PPARα、PPARβ和PPARγ,IC50分别为 92.8、102.4 和 153.5 µM。 | |||
TN7059 |
Deoxylimonin
NSC 314317,脱氧柠檬苦素,desoxylimonin |
Others | Others |
Deoxylimonin (NSC 314317) 是一种分离自葡萄柚籽中的三萜化合物。它是一种母体衍生物,其抗癌、缓解疼痛和抗炎活性比母体化合物强。 | |||
T3921 |
Punicalagin
安石榴甙,安石榴苷 |
SARS-CoV; HBV | Microbiology/Virology |
Punicalagin 是一种在石榴中发现的主要鞣花单宁,是可逆且非竞争性的 3CLpro 抑制剂。Punicalagin 具有抗氧化、抗炎和抗肿瘤活性。 | |||
T6995 |
Ochromycinone
STA 21,STA21,STA-21 |
Antibacterial; STAT | JAK/STAT signaling; Microbiology/Virology; Stem Cells |
Ochromycinone (STA 21) 是一种天然抗生素,也是一种 STAT3抑制剂。它可抑制 STAT3DNA 结合活性,STAT3二聚化。它具有抗癌和抗菌活性。 | |||
T7730 |
Aminopterin
APGA,氨基蝶呤,4-Aminofolic acid |
Antifolate | Cell Cycle/Checkpoint |
Aminopterin (4-Aminofolic acid) 是叶酸的 4-氨基衍生物,是叶酸拮抗剂,具有抗癌和免疫抑制活性,用于研究儿童白血病。它催化叶酸还原为四氢叶酸,竞争性抑制二氢叶酸还原酶,Ki 值为 3.7 pM。 | |||
T5S0055 |
Chelidonine
Helidonine,Khelidonin,白屈菜碱,Stylophorin |
Apoptosis; Others; Influenza Virus | Apoptosis; Microbiology/Virology; Others |
Chelidonine (Stylophorin) 是白屈菜中的一种异喹啉生物碱,有抗肿瘤和抗病毒作用。它可导致细胞周期 G2/M 停滞,诱导 caspase 依赖和非依赖性的细胞凋亡。 | |||
T2800 |
L-Theanine
L-茶氨酸,左旋茶氨酸 |
Apoptosis; Others | Apoptosis; Others |
L-Theanine 是一种存在于绿茶叶片中的非蛋白氨基酸物质,能阻断大脑中谷氨酸与谷氨酸受体结合,具有神经保护和抗氧化活性。 它通过口服能抑制皮层神经元兴奋从而产生抗应激作用。 | |||
T3912 |
Saikosaponin B1
柴胡皂苷B1,柴胡皂苷 B1 |
Others | Others |
Saikosaponin B1 是柴胡的生物活性成分,具有抗癌作用。它能够靶向SMO 抑制 Hedgehog 通路,显著抑制髓母细胞瘤模型中的肿瘤生长。 | |||
T6169 |
Indirubin
Indigopurpurin,Indigo red,NSC 105327,Couroupitine B,靛玉红 |
Apoptosis; Raf; GSK-3; CDK | Apoptosis; Cell Cycle/Checkpoint; MAPK; PI3K/Akt/mTOR signaling; Stem Cells |
Indirubin (Couroupitine B) 是一种具有抗炎症和抗癌活性的天然产物。 | |||
T0610 |
Piceatannol
白皮杉醇,trans-Piceatannol,Astringenin |
Apoptosis; Serine/threonin kinase; PKA; Syk; PKC; Autophagy | Angiogenesis; Apoptosis; Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; Metabolism; Tyrosine Kinase/Adaptors |
Piceatannol (Astringenin) 是一种Syk 抑制剂,可降低由 TNF 诱导的 iNOS 表达,可研究急性肺损伤。它是存在于各种水果和蔬菜中天然存在的多酚二苯乙烯,可诱导细胞自噬和凋亡,具有抗癌和抗炎特性。 | |||
TN1195 |
17-Hydroxy sprengerinin C
17-羟基麦冬皂苷C |
BCL; Others; Caspase | Apoptosis; Others; Proteases/Proteasome |
17-Hydroxy sprengerinin C 是从黄精的根茎中分离得到的一种糖苷化合物,具有更强的抗癌活性。17-Hydroxy sprengerinin C 降低 Blc-2 和 pro-caspase3 的表达并增加 Bax 的产生。 | |||
T6431 |
Levoleucovorin Calcium
左亚叶酸钙,Calcium Levofolinate,CL307782 |
Others; Antifolate | Cell Cycle/Checkpoint; Others |
Levoleucovorin Calcium (CL307782) 是一种亚叶酸的钙盐,在癌症化疗中用作辅助剂。 | |||
T2230 |
Paeoniflorin
芍药苷,Peoniflorin |
HSP; COX | Cytoskeletal Signaling; Immunology/Inflammation; Metabolism; Neuroscience |
Paeoniflorin (Peoniflorin) 是从芍药根中提取的一种蒎烷单萜糖苷,具有抗癌作用、抗氧化应激、抗血小板聚集、血管扩张、降低血液粘度和抗炎活性等多种生物活性。它是一种热休克蛋白诱导剂,通过自噬途径保护 PC12 细胞免受 MPP+和酸性损伤。 | |||
T4S0094 |
Hydroxygenkwanin
羟基芫花素,Luteolin 7-methylether,7-O-Methylluteolin |
Antioxidant | oxidation-reduction |
Hydroxygenkwanin (Luteolin 7-methylether) 是一种丁香达芙妮的主要成分,是一种天然的类黄酮化合物。它具有抗氧化,抗神经胶质瘤能力和抗癌作用。 | |||
T1011 |
Itraconazole
伊曲康唑,R51211 |
P450; Hedgehog/Smoothened; Antibiotic; Autophagy; Antifungal | Autophagy; GPCR/G Protein; Metabolism; Microbiology/Virology; Stem Cells |
Itraconazole (R51211) 属于三唑类天然产物,是一种抗真菌剂,具有口服活性。Itraconazole 是一种 Hedgehog 信号通路拮抗剂,一种 oxysterol-binding protein (OSBP) 抑制剂,也是一种细胞色素 P-450 依赖性酶的抑制剂。 | |||
T1611 |
Isotretinoin
13-cis-Retinoic acid,异维A酸 |
Retinoid Receptor; Endogenous Metabolite; Autophagy | Autophagy; Metabolism |
Isotretinoin (13-cis-Retinoic acid) 是一种天然存在的维甲酸,具有潜在的抗肿瘤活性。 它结合并激活核视黄酸受体 (RAR), 活化的 RARs 作为促进细胞分化和凋亡的转录因子。它是一种类维生素A 和维生素A 衍生物,用于治疗严重的痤疮和某些形式的皮肤、头颈癌。 | |||
T2763 |
Panaxadiol
人参二醇,20(R)-Panaxadiol |
Others; HIF/HIF Prolyl-Hydroxylase | Chromatin/Epigenetic; Metabolism; Others |
Panaxadiol (20(R)-Panaxadiol) 是从人参根中获得,具有神经保护和抗肿瘤作用,能够抑制程序性细胞死亡配体-1(PD-L1)的表达和肿瘤增殖。 | |||
T7786 |
Tryptanthrin
|
DNA gyrase | DNA Damage/DNA Repair |
Tryptanthrin 是一种口服具有活性的细胞内Leukotriene (LT) biosynthesis 抑制剂。 它能够降低大鼠胸膜炎模型中的 LTB4 水平,并抑制人全血中Leukotriene 的形成 (IC50= 10 µM)。 | |||
T2S0961 |
Chalcone
benzylideneacetophenone,phenyl styryl ketone,Cinnamophenone,benzalacetophenone,β-phenylacrylophenone,查耳酮 |
EGFR; Antibacterial | Angiogenesis; JAK/STAT signaling; Microbiology/Virology; Tyrosine Kinase/Adaptors |
Chalcone (Cinnamophenone) 是从甘草中分离得到的一种芳香酮,可合成查耳酮衍生物。它具有多种生物和药理的活性,如抗炎、抗菌、抗癌、抗氧化、抗寄生虫等活性。 | |||
T4S21320 |
ISOGINKGETIN
异银杏素,4',4'''-Dimethylamentoflavone,异银杏双黄酮 |
MMP; Others | Others; Proteases/Proteasome |
ISOGINKGETIN (4',4'''-Dimethylamentoflavone) 是一种MMP9抑制剂,也是一种Pre-mRNA Splicing 抑制剂。 | |||
T5668 |
Triacetylresveratrol
乙酰化白藜芦醇,三乙酰基白藜芦醇,Acetyl-trans-resveratrol |
BCL; NF-κB; STAT | Apoptosis; JAK/STAT signaling; NF-κB; Stem Cells |
Triacetylresveratrol (Acetyl-trans-resveratrol) 是 Resveratrol 的乙酰化类似物,可降低 STAT3和 NF-κB 磷酸化,具有抗癌作用。 | |||
T2902 |
Costunolide
Costus lactone,NSC 106404,Costunolid,(+)-Costunolide,木香烃内酯 |
Apoptosis; Endogenous Metabolite; Telomerase | Apoptosis; DNA Damage/DNA Repair; Metabolism |
Costunolide (Costus lactone) 是一种天然的倍半萜内酯,具有抗氧化、抗炎、抗过敏、骨重塑、神经保护、促进毛发生长、抗癌和抗糖尿病的特性,可诱导乳腺癌细胞周期阻滞和凋亡。 | |||
T0687 |
Simvastatin
辛伐他汀,MK-0733,MK 733 |
Apoptosis; Mitophagy; Ferroptosis; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Simvastatin (MK 733) 是一种 HMG-CoA 还原酶抑制剂 (Ki=0.2 nM),具有口服活性。Simvastatin 具有降血脂活性,可以抑制肝脏产生胆固醇,还可以用于预防心血管疾病。 | |||
T4036 |
Solasodine
Solancarpidine,Purapuridine,澳洲茄铵,Solasodin |
Apoptosis; Others; E1/E2/E3 Enzyme; Antifungal | Apoptosis; Microbiology/Virology; Others; Ubiquitination |
Solasodine (Purapuridine) 是存在于茄科植物中的一种类固醇生物碱。它具有神经保护、降压、抗真菌、抗癌、抗动脉粥样硬化、抗雄激素和抗炎活性。 | |||
TN6864 |
Prosaikogenin F
前柴胡皂苷F |
Others | Others |
Prosaikogenin F ((2R,3R,4S,5R,6R)-2-{[(1S,2R,4S,5R,8R,9S,10R,13S,14R,17S,18R)-2-hydroxy-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,1?.0?,1?.0?,1?.0?,13]tetracos-15-en-10-yl]oxy}-6-methyloxane-3,4,5-triol) 是一种单糖苷,具有溶血和抗癌特性。 | |||
T3604 |
Sodium dichloroacetate
Sodium Dichloroacetate,DCA,bichloroacetic acid,二氯乙酸钠,Sodium dichloroacetate (DCA),二氯醋酸酯 |
Apoptosis; Dehydrogenase; Reactive Oxygen Species; PDK | Apoptosis; Immunology/Inflammation; Metabolism; NF-κB; PI3K/Akt/mTOR signaling |
Sodium dichloroacetate (DCA) 是一种肿瘤细胞线粒体中的代谢调节剂,一种丙酮酸脱氢酶激酶 (PDK) 抑制剂。Sodium dichloroacetate 具有抗肿瘤活性,可以降低肿瘤微环境中的乳酸,增加活性氧的产生并促进肿瘤细胞凋亡。 | |||
T2755 |
Rhoifolin
野漆树苷,Apigenin-7-O-rhamnoglucoside,Apigenin 7-O-neohesperidoside,Rhoifoloside |
Others; p38 MAPK; NF-κB; transporter; IGF-1R; Autophagy | Autophagy; MAPK; Metabolism; NF-κB; Others; Tyrosine Kinase/Adaptors |
Rhoifolin (Apigenin 7-O-neohesperidoside) 是从琯溪蜜柚叶子分离的一种黄酮糖苷。它通过 RANKL 诱导的NF-κB 和MAPK 途径改善钛颗粒刺激的骨溶解并减少破骨细胞生成。它通过增强脂联素分泌,胰岛素受体-β的酪氨酸磷酸化和GLUT4易位有助于治疗糖尿病并发症。 | |||
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Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-05033 |
5T4/TPBG Protein, Human, Recombinant (aa 60-345, His)
5T4AG,trophoblast glycoprotein,WAIF1,M6P1,5T4 |
Human | HEK293 Cells |
Trophoblast glycoprotein (TPBG), also known as 5T4, is the therapeutic target of several anticancer agents currently in clinical development, largely due to its high expression in tumors and low expression in normal adult tissues. 5T4/TPBG Protein, Human, Recombinant (aa 60-345, His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 33.1 kDa and the accession number is Q13641. | |||
TMPY-04644 |
PDGFB Protein, Human, Recombinant (His)
platelet-derived growth factor beta polypeptide,SSV,c-sis,SI... |
Human | P. pastoris (Yeast) |
Platelet-derived growth factor-B (PDGFB) is necessary for normal cardiovascular development. The administration of PDGFB alone normalized tumor vasculature by increasing periendothelial coverage and vascular functionality. Interestingly, this effect exerted by PDGFB was also observed in the presence of DAPT. So PDGFB is able to improve tumor vascularity and allows the anticancer action of DAPT in the tumor. PDGFB Protein, Human, Recombinant (His) is expressed in yeast with His tag. The predicted... | |||
TMPY-06191 |
5T4/TPBG Protein, Mouse, Recombinant (His)
trophoblast glycoprotein,WAIF1,5T4,AW495680 |
Mouse | HEK293 Cells |
Trophoblast glycoprotein (TPBG), also known as 5T4, is the therapeutic target of several anticancer agents currently in clinical development, largely due to its high expression in tumors and low expression in normal adult tissues. 5T4/TPBG Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 37.2 kDa and the accession number is Q9Z0L0. | |||
TMPY-06214 |
5T4/TPBG Protein, Mouse, Recombinant (hFc)
trophoblast glycoprotein,AW495680,5T4,WAIF1 |
Mouse | HEK293 Cells |
Trophoblast glycoprotein (TPBG), also known as 5T4, is the therapeutic target of several anticancer agents currently in clinical development, largely due to its high expression in tumors and low expression in normal adult tissues. 5T4/TPBG Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 62.5 kDa and the accession number is Q9Z0L0. | |||
TMPK-01310 |
Syndecan-1 Protein, Rabbit, Recombinant (His)
SDC1,SYND1,SDC,CD138,Syndecan 1 |
Rabbit | HEK293 Cells |
CD138 (syndecan-1, Sdc-1) is a member of the syndecan family that comprises heparan sulfate proteoglycans. CD138 is significant for cell-cell and cell-matrix interactions.CD138 plays a crucial role in carcinogenesis and is an attractive target for anticancer treatment with heparanase inhibitors and anti-CD138 antibodies for immunotherapy. | |||
TMPY-06317 |
5T4/TPBG Protein, Human, Recombinant (aa 1-355, His)
trophoblast glycoprotein,WAIF1,5T4AG,M6P1,5T4 |
Human | HEK293 Cells |
Trophoblast glycoprotein (TPBG), also known as 5T4, is the therapeutic target of several anticancer agents currently in clinical development, largely due to its high expression in tumors and low expression in normal adult tissues. 5T4/TPBG Protein, Human, Recombinant (aa 1-355, His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 36.15 kDa and the accession number is NP_006661.1. | |||
TMPK-00721 |
CX3CL1/Fractalkine Protein, Mouse, Recombinant (His & Avi), Biotinylated
Neurotactin,CXC3C,ABCD-3,Fkn,Fractalkine,NTT,Cx3cl1,SCYD1,Cx... |
Mouse | HEK293 Cells |
Fractalkine/CX3C chemokine ligand 1 (CX3CL1) is a chemokine involved in the anticancer function of lymphocytes-mainly NK cells, T cells and dendritic cells. Its increased levels in tumors improve the prognosis for cancer patients, although it is also associated with a poorer prognosis in some types of cancers, such as pancreatic ductal adenocarcinoma. | |||
TMPY-05077 |
PDGFB Protein, Rhesus, Recombinant (His)
platelet-derived growth factor β polypeptide,platelet-derive... |
Rhesus | P. pastoris (Yeast) |
Platelet-derived growth factor-B (PDGFB) is necessary for normal cardiovascular development. The administration of PDGFB alone normalized tumor vasculature by increasing periendothelial coverage and vascular functionality. Interestingly, this effect exerted by PDGFB was also observed in the presence of DAPT. So PDGFB is able to improve tumor vascularity and allows the anticancer action of DAPT in the tumor. PDGFB Protein, Rhesus, Recombinant (His) is expressed in yeast with His tag. The predicte... | |||
TMPK-00060 |
IL-17B Protein, Mouse, Recombinant (His)
IL20,interleukin 17B,interleukin 20,IL-17B,MGC138901,ZCYTO7,... |
Mouse | E. coli |
IL-17A, the prototypic member of the IL-17 family, several experimental findings strongly support the role of the IL-17B/IL-17 receptor B (IL-17RB) pathway in tumorigenesis and resistance to anticancer therapies. IL-17B/IL-17RB expression patterns and biological activities in cancer and highlight issues that remain to be addressed to better characterize IL-17B and its receptor as potential targets for enhancing the effectiveness of the existing cancer therapies. | |||
TMPY-04877 |
PDGFB Protein, Mouse, Recombinant (His)
platelet-derived growth factor β polypeptide,血小板源生长因子,Sis,pl... |
Mouse | P. pastoris (Yeast) |
Platelet-derived growth factor-B (PDGFB) is necessary for normal cardiovascular development. The administration of PDGFB alone normalized tumor vasculature by increasing periendothelial coverage and vascular functionality. Interestingly, this effect exerted by PDGFB was also observed in the presence of DAPT. So PDGFB is able to improve tumor vascularity and allows the anticancer action of DAPT in the tumor. PDGFB Protein, Mouse, Recombinant (His) is expressed in yeast with His tag. The predicted... | |||
TMPY-02395 |
PDGFB Protein, Cynomolgus, Recombinant (mFc)
血小板源生长因子,platelet-derived growth factor beta polypeptide,pla... |
Cynomolgus | HEK293 Cells |
Platelet-derived growth factor-B (PDGFB) is necessary for normal cardiovascular development. The administration of PDGFB alone normalized tumor vasculature by increasing periendothelial coverage and vascular functionality. Interestingly, this effect exerted by PDGFB was also observed in the presence of DAPT. So PDGFB is able to improve tumor vascularity and allows the anticancer action of DAPT in the tumor. PDGFB Protein, Cynomolgus, Recombinant (mFc) is expressed in HEK293 mammalian cells with ... | |||
TMPK-00710 |
Claudin-4 Protein-VLP, Human, Recombinant
Claudin4,CLDN4,Claudin-4,CPETR1,CPE-R,WBSCR8,CPE R |
Human | HEK293 Cells |
Claudin-4 (CLDN4) is a key component of tight junctions (TJs) in epithelial cells. CLDN4 is overexpressed in many epithelial malignancies and correlates with cancer progression. Changes in CLDN4 expression have been associated with epigenetic factors (such as hypomethylation of promoter DNA), inflammation associated with infection and cytokines, and growth factor signaling. CLDN4 helps to maintain the tumor microenvironment by forming TJs and acts as a barrier to the entry of anticancer drugs in... | |||
TMPY-05076 |
PDGFB Protein, Canine, Recombinant (His)
platelet-derived growth factor beta polypeptide,platelet-der... |
Canine | P. pastoris (Yeast) |
Platelet-derived growth factor-B (PDGFB) is necessary for normal cardiovascular development. The administration of PDGFB alone normalized tumor vasculature by increasing periendothelial coverage and vascular functionality. Interestingly, this effect exerted by PDGFB was also observed in the presence of DAPT. So PDGFB is able to improve tumor vascularity and allows the anticancer action of DAPT in the tumor. PDGFB Protein, Canine, Recombinant (His) is expressed in yeast with His tag. The predicte... | |||
TMPJ-00247 |
METAP1 Protein, Human, Recombinant
METAP1,Methionine aminopeptidase 1,MAP 1,MetAP 1,Peptidase M... |
Human | E. coli |
Methionine Aminopeptidase 1 is a member of the M24 family of metalloproteases. METAP1 plays an important role in G(2)/M phase regulation of the cell cycle and may serve as a promising target for the discovery and development of new anticancer agents. METAP1 and METAP2 have different substrate specificity due to the differences in both size and shape of the active sites. The proteolytic removal of N-terminal methionine from nascent peptides is catalyzed by a family of enzymes known as methionine... | |||
TMPY-01865 |
BLMH Protein, Mouse, Recombinant (His)
Bh,bleomycin hydrolase,Bmh,AI035728 |
Mouse | E. coli |
The papain superfamily member bleomycin hydrolase (BLMH) is a cytoplasmic cysteine peptidase that is highly conserved through evolution. The only known activity of the enzyme is metabolic inactivation of the glycopeptide bleomycin (BLM), an essential component of combination chemotherapy regimens for cancer. The papain superfamily member bleomycin hydrolase (BLMH) is a neutral cysteine protease with structural similarity to a 20S proteasome. Bleomycin (BLM), a clinically used glycopeptide antica... | |||
TMPY-02072 |
HSF1 Protein, Human, Recombinant (His)
HSTF1,heat shock transcription factor 1 |
Human | E. coli |
Heat shock factor protein 1, also known as heat shock transcription factor 1, HSF1, and HSTF1, is a cytoplasm and nucleus protein that belongs to the HSF family. HSF1 is the major transcription factor of HSPs (heat shock proteins) in response to various stresses. Wild type HSF1 (heat shock transcriptional factor 1) is normally inactive. HSF1 / HSTF1 is a DNA-binding protein that specifically binds heat shock promoter elements (HSE) and activates transcription. In higher eukaryotes, HSF is unable... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TMID-0058 |
Glycocholic acid-d4
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Glycocholic acid-d4 是 Glycocholic acid 的氘代化合物。Glycocholic acid 的 CAS 号为 475-31-0。Glycocholic acid 是一种胆汁酸,具有抗肿瘤活性,能够靶向作用于耐药泵和非耐药泵通路。 | |||
TMIJ-0050 |
Butyricacid-d7
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Butyricacid-d7 是 Butyricacid 的氘代化合物。Butyricacid 的 CAS 号为 107-92-6。Butyric acid 是一种从许多乳制品中分离出来的脂肪酸,具有抗癌活性。 它抑制组蛋白去乙酰化酶 (HDAC) 并诱导胶质瘤细胞凋亡和 G1 期细胞周期停滞。此外,它在低剂量时刺激上皮细胞增殖,在高剂量时抑制增殖。 | |||
TMIJ-0099 |
Minodronic acid-d4
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Minodronic acid-d4 是 Minodronic acid 的氘代化合物。Minodronic acid 的 CAS 号为 180064-38-4。Minodronic acid(YM-529) 是一种 P2X2/3 受体拮抗剂, 具有抗癌活性,可直接或间接的抑制癌细胞增殖,诱导细胞凋亡。Minodronic-acid 对各种类型的癌细胞的转移具有抑制作用。Minodronic-acid 可用于研究骨质疏松。 |