180
99
9
1
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T23552 |
YZ9
|
Glucokinase | Metabolism |
Y29 是 PFKFB3抑制剂,IC50为 0.183 µM。Y29是 Fru-6-P 的竞争性抑制剂,Ki 为 0.094 µM。Y29 抑制 HeLa 细胞生长,GI50为 2.7 µM。 | |||
T8513 |
Spastazoline
|
Others | Others |
Spastazoline 是spastin(一种微管切断AAA 蛋白) 的选择性抑制剂,对人 spastin 的IC50值为 99 nM。它不能影响重组人 VPS4 的 ATPase 活性。 | |||
T21992 |
Vacuolin-1
|
PI3K; Autophagy | Autophagy; PI3K/Akt/mTOR signaling |
Vacuolin-1 是一种细胞渗透性抑制剂,可抑制 Ca2+ 依赖性溶酶体与细胞膜的融合。它通过抑制溶酶体内容物的释放起作用。它是一种有效的选择性 PIKfyve 抑制剂,通过损害溶酶体成熟来抑制晚期自噬。 | |||
T0855 |
(R)-Naproxen
|
COX | Immunology/Inflammation; Neuroscience |
(R)-Naproxen 是一种抗炎剂,具有解热和镇痛作用。酸及其钠盐都用于治疗急性痛风或痛经、肌肉骨骼疾病、类风湿性关节炎和其他风湿病。 | |||
T11563 |
Histone Acetyltransferase Inhibitor II
|
Epigenetic Reader Domain; Histone Acetyltransferase | Chromatin/Epigenetic |
Histone Acetyltransferase Inhibitor II 是一种选择性的细胞渗透性 p300 组蛋白乙酰转移酶抑制剂,IC50值为 5 µM。它在哺乳动物细胞中具有抗乙酰化酶活性,可用于癌症研究。 | |||
T9119 |
SU0268
|
Others | Others |
SU0268 是有效的 8-8-氧鸟嘌呤 DNA 糖基化酶1的选择性抑制剂,具有调控铜绿假单胞杆菌感染免疫反应的能力。 | |||
T23372 |
SMIFH2
|
Others | Others |
SMIFH2 是formin 特异性抑制剂。它利用 Formins 阻碍肌动蛋白聚合,影响肌动蛋白细胞骨架。 | |||
T6421 |
BRD73954
|
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
BRD73954 是一种有效且特异性的 HDAC 抑制剂,对 HDAC6 和 HDAC8 的 IC50 分别为 36 nM 和 120 nM。 | |||
T11553 |
Heptamidine dimethanesulfonate
SBi4211 dimethanesulfonate |
Others | Others |
Heptamidine dimethanesulfonate (SBi4211 dimethanesulfonate) 是一种与喷他脒有关的、强效的钙结合蛋白 S100B 的抑制剂 (Kd=6.9 μM),选择性地杀死表达 S100B 的黑素瘤细胞。它是有效的强直性肌营养不良 (DM) 研究工具。 | |||
T34603 |
L-Selenocystine
L-Selenocystine,L-硒代胱胺基乙酸 |
Others | Others |
L-Selenocystine (L-Selenocystine) 可用作生物活性硒醇化合物的组成部分。 | |||
T50005 |
Sertaconazole
|
Antifungal | Microbiology/Virology |
Sertaconazole 是一种广谱抗真菌药。 | |||
T12006 |
Metarrestin
ML246 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Metarrestin (ML246) 是一种口服有效的选择性核仁周区室 (PNC) 抑制剂,可有效抑制转移。Metarrestin 破坏核仁结构并抑制 RNA 聚合酶 (Pol) I 转录,部分是通过与翻译延伸因子 eEF1A2 的相互作用。 | |||
T12579 |
RAMB4
PTP1B-IN-9 |
Proteasome | Proteases/Proteasome; Ubiquitination |
RAMB4 (PTP1B-IN-9) 是一种泛素-蛋白酶体系统(UPS)应激源,是通过抑制 20S 蛋白酶体催化活性物质上游泛素介导的蛋白质降解而产生。它能够在不影响 20S 蛋白酶体催化活性的情况下触发泛素蛋白酶体系统 (UPS) 应激反应。 | |||
T5399 |
GeA-69
|
PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair |
GeA-69 是一种选择性变构 PARP14 大结构域 2 (MD2) 抑制剂,Kd 值为 2.1 µM。 | |||
T3076 |
GLPG0634 analog
GLPG0634 analogue |
Tyrosine Kinases; JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors |
GLPG0634 analog (GLPG0634 analogue) 是一种 JAK 广谱性抑制剂,对 JAK1/JAK2/JAK3 的 IC50值为 50 到 200 nM 之间。 | |||
T9024 |
OUL35
NSC39047 |
Others; PARP | Chromatin/Epigenetic; DNA Damage/DNA Repair; Others |
OUL35 (NSC-39047) 是一种选择性 PARP-10 抑制剂和小分子 ARTD10 抑制剂,其 IC50值为 329 nM。 | |||
T9350 |
IMP-1088
|
Others; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Others |
IMP-1088 是一种人N-肉豆蔻酰基转移酶NMT1和NMT2双重抑制剂,对 HsNMT1 和 HsNMT2 的IC50小于1 nM,对 HsNMT1 的Kd 小于210 pM。它有保护宿主细胞免受病毒感染的细胞毒作用,通过阻断鼻病毒的 N-肉豆蔻酰化蛋白来阻断鼻病毒的复制。 | |||
T9098 |
DMG-PEG 2000
DMG-PEG2000 |
Others | Others |
DMG-PEG 2000 (DMG-PEG2000) 可用于脂质纳米颗粒制备,用于口服质粒 DNA 的体内传递途径,提高纳米颗粒的黏液渗透性和传递效率。它也可用于 siRNA 转染的脂质体的制备,能够提高转染效率。 | |||
T0711 |
Niclosamide
BAY2353,Niclocide,氯硝柳胺 |
Antibiotic; STAT; Parasite | JAK/STAT signaling; Microbiology/Virology; Stem Cells |
Niclosamide (Niclocide) 是一种口服生物可利用的氯化水杨酰苯胺。它通过抑制 DNA 复制,具有驱虫和潜在的抗肿瘤活性。 | |||
T3103 |
L67
DNA Ligase Inhibitor |
DNA; DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
L67 (DNA Ligase Inhibitor) 是一种竞争性人类 DNA 连接酶抑制剂,抑制 DNA 连接酶 I 和 III,IC50为10μM。 | |||
T2617 |
SNS-314 Mesylate
SNS-314 |
Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic |
SNS-314 Mesylate (SNS-314) 是一种有效且特异性的极光激酶抑制剂,对极光激酶 A、B、C 的 IC50值分别为 9,31 和 3 nM。 | |||
T9079 |
Apostatin-1
Apt-1 |
Others | Others |
Apostatin-1 (Apt-1) 是一种新型 TRADD 抑制剂。 Apostatin-1 可以与 TRADD 的 N 末端 TRAF2 结合域上的口袋结合。 | |||
T7020 |
Z-VAD-FMK
Z-VAD(OH)-FMK,Caspase Inhibitor VI,Z-VAD |
Caspase | Apoptosis; Proteases/Proteasome |
Z-VAD-FMK (Caspase Inhibitor VI) 是一种 caspase 的广谱抑制剂。Z-VAD-FMK 可以与活化的 caspase 结合,从而抑制细胞凋亡。Z-VAD-FMK即使在高达 440μM 的浓度下也不会抑制 UCHL1 的活性。 | |||
T4327 |
Prexasertib dihydrochloride
LY2606368 (dihydrochloride),Prexasertib HCl,LY2606368 |
Apoptosis; Chk; S6 Kinase | Apoptosis; Cell Cycle/Checkpoint; MAPK; PI3K/Akt/mTOR signaling |
Prexasertib dihydrochloride (LY2606368) 是一种选择性的,ATP 竞争性的细胞周期检测点激酶 1 抑制剂,Ki 为 0.9 nM,IC50为 <1 nM。它抑制 CHK2(IC50=8 nM) 和 RSK1 (IC50=9 nM)。它引起双链 DNA 断裂和复制突变,导致细胞凋亡,有抗肿瘤活性。 | |||
T0455 |
Clozapine
氯氮平,HF 1854,LX 100-129 |
Dopamine Receptor; Adrenergic Receptor; AChR | GPCR/G Protein; Neuroscience |
Clozapine (HF 1854) 是一种三环二苯二氮卓类药物,属于非典型抗精神病药物。它结合几种类型的中枢神经系统受体,并显示出独特的药理学特征。 它是一种血清素拮抗剂,与 5-HT 2A/2C 受体亚型具有强结合力。它还对几种多巴胺能受体表现出很强的亲和力,但对多巴胺 D2 受体仅表现出较弱的拮抗作用,这种受体通常被认为可调节精神抑制活性。 | |||
T6665 |
Sertaconazole nitrate
FI-7045,Ginedermofix,FI7056,Ertaczo,硝酸舍他康唑 |
Antibiotic; Antifungal | Microbiology/Virology |
Sertaconazole nitrate (FI-7045) 是一种局部广谱抗真菌药,可用于治疗浅表皮肤和粘膜感染。 | |||
T15396 |
GN44028
N-(2,3-Dihydro-1,4-benzodioxin-6-yl)-1,4-dihydroindeno[1,2-c]pyrazol-3-amine |
HIF | Angiogenesis; Chromatin/Epigenetic |
GN44028 (N-(2,3-Dihydro-1,4-benzodioxin-6-yl)-1,4-dihydroindeno[1,2-c]pyrazol-3-amine) 是缺氧诱导因子(HIF)-1的有效抑制剂,其 IC50=14 nM。它可以抑制低氧诱导的 HIF-1α 的转录特性,但不抑制 HIF-1α mRNA 的表达,HIF-1α 蛋白的累积或HIF-1α/HIF-1β 的异缘二聚化。 | |||
T4310 |
Prexasertib
5-[[5-[2-(3-氨基丙氧基)-6-甲氧基苯基]-1H-吡唑-3-基]氨基]-2-吡嗪甲腈,LY2606368 |
Apoptosis; Chk | Apoptosis; Cell Cycle/Checkpoint |
Prexasertib (LY2606368) 是一种具有潜在抗肿瘤活性的检查点激酶 1 抑制剂。它可引起双链 DNA 断裂和复制突变,导致细胞凋亡。 | |||
T13639 |
Deferasirox (Fe3+ chelate)
|
Apoptosis | Apoptosis |
Deferasirox (Fe3+ chelate) 是一种可口服的铁螯合剂,具有潜在的抗癌活性,抑制 MCL-1 的抗凋亡活性,可用于研究铁超负荷。 | |||
T81479 |
Phytochelatin 3
PC 3 |
||
Phytochelatin 3 (PC 3)是一种具有金属螯合能力的小型肽,主要用途为螯合重金属离子。 | |||
T30873 |
Chelator 1a
Chelator1a,Chelator-1a |
Antifungal | Microbiology/Virology |
Chelator 1a 具有抗真菌活性,抑制曲霉菌和念珠菌,可用于研究真菌感染和癌症。 | |||
T81475 |
Phytochelatin 5
PC 5 |
||
Phytochelatin 5为植物合成的金属结合化合物,具有可能降低如镉等膳食有毒金属的生物利用度。 | |||
T81472 |
Phytochelatin 6 TFA
PC 6 TFA |
||
Phytochelatin 6 TFA为植物合成的金属结合化合物,具有降低如镉等膳食有毒金属的生物可利用性的潜能。 | |||
T81477 |
Phytochelatin 4
PC 4 |
||
Phytochelatin 4 (PC 4)为植物体内富含Cys的小分子短肽,其结构特征为含有γ-Glu-Cys基序。 | |||
T81474 |
Phytochelatin 5 TFA
PC 5 TFA |
||
Phytochelatin 5 TFA为植物合成的金属结合化合物,有潜在降低食物中有毒金属(例如镉)生物可利用性的作用。 | |||
T81480 |
Phytochelatin 2 (PC2) (TFA)
|
||
Phytochelatin 2 (PC2) TFA是一种具有植物螯合素性质的重要肽类,能有效地与重金属离子形成稳定的螯合物,起到防护作用,避免金属离子的毒性影响,并促进体内金属离子的平衡稳定。 | |||
T81478 |
Phytochelatin 3 TFA
PC 3 TFA |
||
Phytochelatin 3 (PC 3) TFA,一小分子螯合肽,专用于重金属离子螯合。 | |||
T41109 |
Phytochelatin 2 (PC2)
|
||
Phytochelatin 2, a short plant peptide, serves as an essential metal-binding compound. Phytochelatins are a diverse group of plant compounds that play a crucial role in chelating metals, safeguarding against metal toxicity, and maintaining metal homeostasis. | |||
T81476 |
Phytochelatin 4 TFA
PC 4 TFA |
||
Phytochelatin 4 (PC 4) TFA,一种在植物中发现的短肽,富含 Cys,且具有 γ-Glu-Cys 基序。 | |||
T81473 |
Phytochelatin 6
PC 6 |
||
Phytochelatin 6是一种植物所产生的金属结合化合物,其可能降低(如镉)等膳食有毒金属的生物利用度。 | |||
T124710 |
Trachelanthamidine
|
Others | Others |
Trachelanthamidine 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T124710。 | |||
T8517 |
Belinostat
PX105684,PXD101,贝利司他,PXD-101 |
HDAC; Autophagy | Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair |
Belinostat (PXD101) 是一种异羟肟酸型组蛋白脱乙酰酶抑制剂,具有抗肿瘤活性,在 HeLa 细胞提取物中的IC50为 27 nM。 | |||
T11657 |
INH154
|
Others | Others |
INH154 是一种高效的 Nek2 和 Hec1 结合抑制剂,能够抑制 Hela 细胞(IC50:200 nM)、 MB468 细胞(IC50:120 nM)。 | |||
T7181 |
IDO-IN-1
4-氨基-N-(3-溴-4-氟苯基)-N'-羟基-1,2,5-恶二唑-3-甲脒 |
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
IDO-IN-1 是吲哚胺-2,3-双加氧酶抑制剂,IC50=59 nM。 | |||
T77771 |
Compound 10w
|
Others | Others |
Compound 10w,一种取代吡唑并[1,5-a]嘧啶酰胺化合物,是一种ZSTK474 类似物,对 HeLa细胞显示出抗癌活性。 | |||
T25214 |
CCR-11
CCR11,CCR 11 |
Antibiotic | Microbiology/Virology |
CCR-11 是一种具有抗菌活性的绕丹宁衍生物。 CCR-11 可以抑制 B. subtilis细胞和 HeLa 细胞增殖。 CCR-11 通过抑制 FtsZ 的组装和 GTPase 活性来抑制细菌增殖和细菌胞质分裂。 CCR-11 具有潜在的抗肿瘤活性,可用于研究乳腺癌和小儿骨髓增生异常。 | |||
T5342 |
IWP-O1
|
Wnt/beta-catenin; Porcupine | Cytoskeletal Signaling; Stem Cells |
IWP-O1 是 Porcn 抑制剂,在 L-Wnt-STF 细胞中的 EC50值为 80 pM。它能够抑制 Wnt 蛋白分泌,可以抑制 HeLa 细胞中 Dvl2/3 和 LRP6 磷酸化。 | |||
T25969 |
Poloxin-2
Poloxin2,Poloxin 2 |
PLK | Cell Cycle/Checkpoint |
Poloxin-2 是一种具有有效性和选择性的 Plk1 PBD 抑制剂,具有抗肿瘤活性,可降低HeLa细胞中Plk1的蛋白水平。 | |||
T8903 |
Retro-2
Retro 2,2-{[(5-methyl-2-thienyl)methylene]amino} |
Others; Virus Protease; Parasite; Autophagy | Autophagy; Microbiology/Virology; Others |
Retro-2 (2-{[(5-methyl-2-thienyl)methylene]amino}) 是一种植物毒素蓖麻毒素抑制剂,它保护 HeLa 细胞免受蓖麻毒素、Stx1 和 Stx2 的侵害,选择性地阻断早期内体蛋白质-高尔基体界面处的逆行毒素运输。 | |||
T8623 |
TMIFRY8XAG
4,4,-二(4-氟苯)氯丁烷,1,1'-(4-CHLOROBUTYLIDENE)BIS(4-FLUOROBENZENE),4-oxo-1,4-dihydroquinoline-2-carboxylic acid |
Others | Others |
TMIFRY8XAG (4-oxo-1,4-dihydroquinoline-2-carboxylic acid) 是 Zerumbone 的衍生物,对 HeLa 癌细胞具有潜在的抗肿瘤作用。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11363 |
Ganoderic acid F
|
Others | Others |
Ganoderic acid F 是一种灵芝酸。它具有抗肿瘤和抗转移的活性,与抑制血管生成和涉及细胞增殖和细胞死亡,致癌作用,氧化应激,钙信号传导和内质网应激的蛋白质改变等机制相关。 | |||
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。 | |||
T5S1133 |
Ganoderic acid D
灵芝酸D,灵芝酸 D |
Apoptosis; Sirtuin | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair |
Ganoderic acid D 是高度氧化的四环三萜,是灵芝的主要活性成分,可诱导 HeLa 人宫颈癌细胞凋亡。它上调 SIRT3的蛋白质表达并通过 SIRT3 诱导脱乙酰化的亲环蛋白 D 。它抑制结肠癌细胞的能量重编程,包括结肠癌细胞中的葡萄糖摄取,乳酸、丙酮酸和乙酰辅酶的产生。 | |||
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。 | |||
T6427 |
Butein
2’,3,4,4’-tetrahydroxy Chalcone,紫铆因 |
Apoptosis; EGFR; Others; PDE; Autophagy | Angiogenesis; Apoptosis; Autophagy; JAK/STAT signaling; Metabolism; Others; Tyrosine Kinase/Adaptors |
Butein (2’,3,4,4’-tetrahydroxy Chalcone) 是一种 cAMP 特异性PDE 抑制剂,也是蛋白酪氨酸激酶抑制剂,还是一种SIRT1激活剂。它通过 AKT 和 ERK/p38 MAPK 通路,靶向 FoxO3a 使 HeLa 细胞对 Cisplatin 敏感。 | |||
T13475 |
β-Aminopropionitrile
3-氨基丙腈,3-Aminopropionitrile,BAPN |
Others; Endogenous Metabolite | Metabolism; Others |
β-Aminopropionitrile (3-Aminopropionitrile) 是赖氨酰氧化酶的特异性抑制剂。 | |||
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。 | |||
T3673 |
Mollugin
大叶茜草素,Rubimaillin |
HER; JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells; Tyrosine Kinase/Adaptors |
Mollugin (Rubimaillin) 是Rubia cordifolia L.中主要的生物活性成分。它能通过 p38-Smad 信号通路增强 BMP-2 的成骨作用。它通过抑制 TNF-α 诱导的 NF-κB 激活起抗癌疗效。 | |||
T14046 |
Anandamide
花生四烯酸乙醇胺,(5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)icosa-5,8,11,14-tetraenamide |
Cannabinoid Receptor; Endogenous Metabolite | GPCR/G Protein; Metabolism |
Anandamide ((5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)icosa-5,8,11,14-tetraenamide) 是一种免疫调节剂,通过大麻素受体 CB1 和 CB2 起作用,还通过中枢神经系统中的其他靶点起作用,如 GPR18/GPR55。 | |||
TN1915 |
Matairesinol 4′-O-β-D-glucopyranoside
Matairesinol 4'-O-beta-gentiobioside,罗汉松树脂酚-4'-O-Β-龙胆二糖苷,(3R-反式)-3-[[4-[(6-O-BETA-D-吡喃葡萄糖基-BETA-D-吡喃葡萄糖基)氧基]-3-甲氧基苯基]甲基]二氢-4-[(4-羟基-3-甲氧基苯基)甲基]-2(3H)-呋喃酮 |
Others | Others |
Matairesinol 4′-O-β-D-glucopyranoside 对 HeLa 细胞具有细胞毒活性(IC50:47.1 μM)。 | |||
TC0014 |
Trachelanthine
|
Others | Others |
Trachelanthine 是来自 Eupatorium fortunei 的天然产物。 | |||
TN5158 |
Trachelanthamine
|
Others | Others |
Trachelanthamine is a natural product from Eupatorium fortunei. | |||
TN4375 |
Kamebanin
|
Antifection | Microbiology/Virology |
Kamebanin 是一种天然二萜类化合物,具有抗菌活性。它对 HeLa 和 HL-60 细胞显示出有效的细胞毒活性。 | |||
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。 | |||
TN4618 |
N-trans-Sinapoyltyramine
|
Others | Others |
N-trans-Sinapoyltyramine 对 HeLa 人癌细胞系表现出强烈的选择性细胞毒性,IC50 值为 9.77 ± 1.25 μm。 | |||
T5738 |
7-Epi 10-desacetyl paclitaxel
10-Deacetyl-7-epipaclitaxel,7-Epi-10-deacetyltaxol,7-表-10-去乙酰基云南紫杉宁A |
Others; ADC Cytotoxin | Antibody-drug Conjugate/ADC Related; Others |
7-Epi 10-desacetyl paclitaxel (10-Deacetyl-7-epipaclitaxel) 是紫杉醇衍生物,对 HeLa 细胞具有细胞毒性(IC50:85 μM)。 | |||
TN7041 |
(-)-Epipodophyllotoxin
|
Apoptosis | Apoptosis |
(-)-Epipodophyllotoxin 是一种从八角莲中分离的癌细胞抗增殖剂,在 HeLa 细胞和 MCF-7 细胞中的GI50值分别为 0.36 和 0.24 μM。它可在体外抑制有丝分裂纺锤体组装。 | |||
TN3049 |
4-Methoxycinnamyl alcohol
|
Others | Others |
4-Methoxycinnamyl alcohol 对MCF-7、HeLa 和DU145癌症细胞系显示出毒性,IC50值分别为14.24、7.82和22.10μg/mL。4-methoxycinnamyl alcohol 是从Foeniculum vulgare 中分离出来的。4-Methoxycinnamyl alcohol 没有显示出凋亡作用,却在10μg/mL DNA 碎片研究显示48小时后发生了坏死。 | |||
TQ0170 |
Desacetylcinobufagin
Deacetylcinobufagin,去乙酰华蟾蜍精 |
Others | Others |
Desacetylcinobufagin (Deacetylcinobufagin) 是一种天然化合物,可用于微生物转化。 | |||
TN1916 |
Matairesinol
罗汉松树脂酚 |
ATPase; p38 MAPK; ROS | Immunology/Inflammation; MAPK; Membrane transporter/Ion channel |
Matairesinol has radical and superoxide scavenging activities,; it also has anti-angiogenic activity by suppressing mROS signaling , can decrease hypoxia-inducible factor-1α± in hypoxic HeLa cells. | |||
TN1393 |
(-)-Anonaine
番荔枝碱 |
Apoptosis; Antioxidant; Parasite; Antifungal | Apoptosis; Microbiology/Virology; oxidation-reduction |
(-)-Anonaine 可从木兰科和安妮科的几个物种中提取出来,具有抗疟、抗菌、抗真菌、抗氧化、抗癌、抗抑郁和血管舒张的活性。(-)-Anonaine 通过 Bax 和 caspase 依赖性途径诱导人类宫颈癌(HeLa)细胞的凋亡,诱导 DNA 损伤并抑制人类肺癌 h1299细胞的生长和迁移。 | |||
T3386 |
Kaempferitrin
Lespedin,Kaempferol,Lespenephryl,Lespenefril,Kaempferol 3,7-dirhamnoside,山奈苷 |
cell cycle arrest; Glucokinase; IGF-1R | Cell Cycle/Checkpoint; Metabolism; Tyrosine Kinase/Adaptors |
Kaempferitrin (Lespenephryl) 是天然黄酮苷类化合物,具有缓解疼痛、抗糖尿病、消炎、抗肿瘤和化疗作用,可激活胰岛素信号传导。 | |||
T3395 |
Timosaponin AIII
Filiferin B,知母皂苷 A-III,AneMarsaponin A3,Timosaponin A3 |
AChE; mTOR | Neuroscience; PI3K/Akt/mTOR signaling |
Timosaponin AIII (Timosaponin A3) 是一种乙酰胆碱酯酶活性抑制剂,其IC50=35.4 μM。 | |||
TN2755 |
2-Desoxy-4-epi-pulchellin
|
Anti-infection | Microbiology/Virology |
2-Desoxy-4-epi-pulchellin 是分离自 Polygonum hydropiper 的二氯甲烷可溶部分的一种化合物。 | |||
T6213 |
Vinorelbine ditartrate
Vinorelbine Tartrate,Nor-5'-anhydrovinblastine ditartrate,KW-2307,Navelbine tartrate,长春瑞滨酒石酸盐,酒石酸长春瑞滨 |
Microtubule Associated; Autophagy | Autophagy; Cytoskeletal Signaling |
Vinorelbine ditartrate (KW-2307)是一种抗有丝分裂剂,能够抑制 Hela 细胞的增殖,IC50值为 1.25 nM。 | |||
T3002 |
Piperine
胡椒碱,1-Piperoylpiperidine,Bioperine |
P450; Endogenous Metabolite; P-gp; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Piperine (Bioperine) 是从胡椒中分离的一种生物碱,可以抑制P-糖蛋白和 CYP3A4 的活性,在HeLa 细胞中的IC50值为61.94±0.054 μg/mL。它已用于研究治疗多发性骨髓瘤和吞咽障碍的试验。 | |||
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。 | |||
T1879 |
3-Methyladenine
3-MA,3-甲基腺嘌呤,NSC 66389 |
Mitophagy; PI3K; Endogenous Metabolite; Autophagy | Autophagy; Metabolism; PI3K/Akt/mTOR signaling |
3-Methyladenine (3-MA) 是一种 PI3K 抑制剂,选择性抑制 IB 类 PI3Kγ (IC50=60 μM) 和 III 类 VPS34 (IC50=25 μM)。3-Methyladenine 具有自噬抑制活性。 | |||
T0190 |
Vinorelbine
长春瑞宾,KW-2307 base |
Microtubule Associated | Cytoskeletal Signaling |
Vinorelbine (KW-2307 base) 是一种半合成的长春花生物碱。它与微管蛋白结合并阻止有丝分裂纺锤体的形成,导致中期肿瘤细胞生长停滞。 | |||
T0122 |
Bergenin
Cuscutin,Bengenin,岩白菜素 |
Apoptosis; IL Receptor; Virus Protease; TNF; NF-κB; Antibacterial; NOD; Autophagy; Antifungal | Apoptosis; Autophagy; Immunology/Inflammation; Microbiology/Virology; NF-κB |
Bergenin (Bengenin) 是一种在许多药用植物中发现的多酚,有细胞保护和抗氧化作用。它还具有广泛的保肝、抗炎、抗肿瘤、抗病毒、抗真菌以及免疫调节作用。 | |||
TN6569 | cis-Moschamine | ||
cis-Moschamine exerts antitumour effects on HeLa, MCF7 and A431 cells. | |||
TN5287 |
3β,5α-Dihydroxyergosta-7,22-dien-6-one
|
||
3β,5α-Dihydroxy-(22E,24R)-ergosta-7,22-dien-6-one exhibits strong or moderate cytotoxic activities against MCF-7, A549, Hela and KB cell lines with IC50 values 4.98 (MCF-7), 1.95 (A549), 0.68(Hela), and 1.50 uM (KB), respectively. | |||
T83481 |
1,1′-Disinomenine
|
||
1,1'-Disinomenine,一种从Sinomenium acutum茎部分离得到的生物碱,对A549和Hela细胞表现出较弱的抑制效果。 | |||
T35234 |
Yadanzioside B
|
||
Yadanzioside B 是提取自鸦胆子的苦木素苷类化合物。Yadanzioside B 能够抑制HeLa细胞中的蛋白质合成,但对体外翻译几乎没有影响。 | |||
TN3619 |
Cedrusin
|
PARP; Caspase | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Proteases/Proteasome |
Cedrusin shows a cytotoxic effect on A375 and HeLa cells. | |||
TN3837 |
Desmethoxycentaureidin
|
Others | Others |
Desmethoxycentaureidin shows high inhibitory activity against HeLa cell growth (GI50 9 microM). | |||
TN7405 |
Ganolucidic acid E
|
Others | Others |
Ganolucidic acid E effectively suppresses the proliferation of three human cancer cell lines: Caco-2 (colon cancer), HepG2 (hepatocellular carcinoma), and HeLa (cervical cancer). | |||
T82982 |
Aplyronine C
|
||
Aplyronine C是一种抗肿瘤活性化合物,对HeLa-S3细胞表现出细胞毒性,其IC50为2.9 nM,适用于癌症研究。 | |||
TN6399 |
1-(3',5'-dimethoxy)phenyl-2-[4''-O-beta-D-glucopyranosyl (6->1)-O-alpha-L-rhamnopyranosyl]phenylethane
|
||
1-(3',5'-dimethoxy)phenyl-2-[4''-O-β-D-glucopyranosyl (6→1)-O-α-L-rhamnopyranosyl]phenylethane showed cytotoxic activities to Hela and hep2 cell lines. | |||
TN5212 |
Uvedalin
|
Others | Others |
Uvedalin shows cytotoxicity against HeLa, HL-60, and Murine B16-F10 melanoma cell lines. | |||
T82983 |
Aplyronine B
|
||
Aplyronine B是一种具有抗肿瘤活性的活性化合物,对HeLa-S3细胞表现出细胞毒性,IC50值为2.9 nM,适用于癌症研究。 | |||
TN5336 |
9-Oxo-10,11-dehydroageraphorone
4,7(11)-Cadinadiene-3,8-dione,DTD,7,11-Dehydro-8-oxoageraphorone,泽兰二酮 |
||
9-Oxo-10,11-dehydroageraphorone has acaricidal activity. It induces hepatotoxicity and cholestasis in rats. 9-Oxo-10,11-dehydroageraphorone also effectively inhibits the proliferation of HeLa cells by arresting the cell cycle transition from S to G2/M pha | |||
T79991 |
Condurango glycoside A
|
Others | Others |
Condurango glycoside A 作为p53激活剂,能够促进ROS的生成并且上调p53的表达。此外,Condurango glycoside A 还能够诱导HeLa细胞发生与DNA损伤相关的凋亡及过早老化。 | |||
TN2964 | 3'-Methylflavokawin | Others | Others |
3'-Methylflavokawin shows cytotoxicity against HeLa cells, the IC 50 value comparable to xanthohumol (8.2-19.2 microM). | |||
TN5574 |
Heudelotinone
|
||
Heudelotinone shows cytotoxicity against three cancer cell lines A549, Hela, and SMMC-7721( IC50 values of 16.04, 10.67 and 21.68 uM , respectively). | |||
T37444 |
Aranorosin
|
Others | Others |
Aranorosin is a fungal metabolite originally isolated from P. roseus. It has antimicrobial activity against B. subtilis, A. niger, and C. albicans when used at a concentration of 1 mg/ml. Aranorosin also reduces viability in apoptosis-resistant HeLa/Bcl-2 cells. | |||
TN1776 |
Isocucurbitacin B
|
Others | Others |
Isocucurbitacin B 对 HeLa 和 HT-29 人类癌细胞具有显着的抑制活性,IC50 值范围为 0.93 至 9.73uM。 | |||
T81602 |
Ophiopogonin R
|
||
Ophiopogonin R (compound 3),一种甾体皂苷,源自麦冬的分离纯化。该化合物对包括HepG2、HLE、BEL7402、BEL7403和Hela在内的五种人类肿瘤细胞系均未显示细胞毒性。 | |||
TN5093 |
Taiwanhomoflavone A
|
COX | Immunology/Inflammation; Neuroscience |
Taiwanhomoflavone A is cytotoxic with ED50 values of 3.4, 1.0, 2.0 and 2.5 microg/ml, respectively, against KB epidermoid carcinoma of nasopharynx, COLO-205 colon carcinoma, Hepa-3B hepatoma, and Hela cervix tumor cells. | |||
TN2142 |
Resibufagin
|
Others | Others |
Resibufagin shows strong cytotoxic activity against HeLa cell line. | |||
------------------------ 更多 ------------------------ |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-01332 |
Ferrochelatase Protein, Human, Recombinant (His & Myc)
Ferrochelatase, mitochondrial,Heme synthase,Protohe... |
Human | E. coli |
Catalyzes the ferrous insertion into protoporphyrin IX. Ferrochelatase Protein, Human, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 49.6 kDa and the accession number is P22830. | |||
TMPH-00265 |
Ferrochelatase, mitochondrial Protein, Bovine, Recombinant (His & Myc & SUMO)
Ferrochelatase, mitochondrial,Protoheme ferro-lyase... |
Bovine | E. coli |
Catalyzes the ferrous insertion into protoporphyrin IX. Ferrochelatase, mitochondrial Protein, Bovine, Recombinant (His & Myc & SUMO) is expressed in E. coli expression system with N-10xHis-SUMO and C-Mycd tag. The predicted molecular weight is 58.1 kDa and the accession number is P22600. | |||
TMPY-00570 |
Alkaline Phosphatase/PLAP Protein, Human, Recombinant (His)
ALPI,PALP,PLAP,PLAP-1,alkaline phosphatase, placental,IAP,AL... |
Human | P. pastoris (Yeast) |
Most importantly, placental alkaline phosphatase (ALPP), an ectoenzyme that locates on cell surface with catalytic domains outside the plasma membrane and is overexpressed on many cancer cells, dephosphorylate the d-tyrosine phosphates on the surface of the magnetic nanoparticle and enable the magnetic nanoparticles to adhere selectively to the cancer cells, such as HeLa cells. Placental alkaline phosphatase (PLAP), encoded by the ALPP gene, is produced by the fetal side of the placenta. | |||
TMPY-02521 |
HIST3H2A Protein, Human, Recombinant
histone cluster 3, H2a,MGC3165 |
Human | E. coli |
Histones are a complex family of highly conserved basic proteins responsible for packaging chromosomal DNA into nucleosomes. There are subtype diversities: H1, H2A, H2B, and H3 or H4. It has become more and more evident that histone modifications are key players in the regulation of chromatin states and dynamics as well as in gene expression. Therefore, histone modifications and the enzymatic machinery that set them are crucial regulators that can control cellular proliferation, differentiation,... | |||
TMPH-00604 |
CDTA Protein, E. coli, Recombinant (His)
Cytolethal distending toxin subunit A,CDTA,CDT A |
E. coli | E. coli |
CDTs are cytotoxins which induce host cell distension, growth arrest in G2/M phase, nucleus swelling, and chromatin fragmentation in HeLa cells. CdtA, along with CdtC, probably forms a heterodimeric subunit required for the delivery of CdtB. | |||
TMPH-03026 |
CARDS Protein, Mycoplasma pneumoniae, Recombinant (His & Myc)
ADP-ribosylating toxin CARDS,CARDX TX,ADP-ribosyltransferase... |
Mycoplasma pneumoniae | E. coli |
Acts as an ADP-ribosylating toxin, which may transfer the ADP-ribosyl group from NAD(+) to specific amino acids in target proteins. Elicits cytopathic effects in mammalian cells, such as disorganization and disruption of respiratory epithelial integrity in tracheal epithelium and vacuolization in the cytoplasm of CHO and HeLa cells. | |||
TMPJ-00546 |
EFNA1 Protein, Human, Recombinant (hFc)
TNFAIP4,LERK1,Tumor Necrosis Factor α-Induced Protein 4,Imme... |
Human | HEK293 Cells |
Ephrin-A1 is a member of the A-type ephrin family of cell surface proteins that function as ligands for the A-type Eph receptor tyrosine kinase family. Ephrin-A1 can be induced by TNF and IL1B. Its expression levels can be down-regulated in primary glioma tissues compared to the normal tissues. The soluble monomeric form is expressed in the glioblastoma multiforme (GBM) and breast cancer cells. Soluble Ephrin-A1 is necessary for the transformation of HeLa and SK-BR3 cells and participates in the... | |||
TMPY-02132 |
LYPLA2 Protein, Human, Recombinant (His)
APT-2,lysophospholipase II,DJ886K2.4,APT2 |
Human | E. coli |
Lysophospholipase II (LYPLA2, LPL-II, or LysoPLA II), also known as Acyl-protein thioesterase 2 (APT-2), belongs to the AB hydrolase 2 family. This enzyme has lysophospholipase activity and may hydrolyze fatty acids from S-acylated cysteine residues in proteins such as trimeric G alpha proteins or HRAS. Acyl-protein thioesterase 1 (APT-1) and Acyl-protein thioesterase 2 (APT-2) are cytosolic lysophospholipids hydrolyzing enzymes. The serum activity of APT-1 may play an important role in the dete... | |||
TMPY-03397 |
TPPP3 Protein, Human, Recombinant (His)
CGI-38,TPPP3,p25gamma,tubulin polymerization-promoting prote... |
Human | E. coli |
TPPP3, a member of the Tubulin polymerization-promoting protein family, is an intrinsically unstructured protein that induces tubulin polymerization. TPPP3 is a marker in the developing musculoskeletal system. In tendons, Tppp3 is expressed in cells at the circumference of the developing tendons, likely the progenitors of connective tissues that surround tendons: the tendon sheath, epitenon, and paratenon. Tppp3 is also expressed in forming synovial joints. The onset of Tppp3 expression in joint... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T69600 |
Spermidine-d6
|
||
Spermidine-d6 is intended for use as an internal standard for the quantification of spermidine by GC- or LC-MS. Spermidine is an endogenous polyamine. It is formed from putrescine by spermidine synthase. Spermidine (25 µM) inhibits the activity of the human inward-rectifying potassium channel Kir2.3 in a patch-clamp assay. It induces autophagy in HeLa cells when used at a concentration of 100 µM and increases the lifespan of D. melanogaster, yeast, and C. elegans. Spermidine (30 mM in the drinki... |