362
50
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T77584 |
Tubulin inhibitor 35
Tubulin IN 35 |
Apoptosis; Microtubule Associated; Topoisomerase | Apoptosis; Cytoskeletal Signaling; DNA Damage/DNA Repair |
Tubulin inhibitor 35 (Tubulin IN 35) 是一种有效的拓扑异构酶 I 和微管蛋白聚合 的双重抑制剂,具有抗肿瘤活性,对 MGC-803 和 RKO 细胞株的迁移和侵袭有抑制作用,中断细胞周期,诱导凋亡 (apoptosis)。 | |||
T13224 |
Tubulin inhibitor 6
iHAP1 |
Microtubule Associated | Cytoskeletal Signaling |
Tubulin inhibitor 6 (iHAP1) 是一种微管蛋白抑制剂,抑制微管蛋白聚合,IC50为 0.87 μM。它抑制多种癌细胞系,抑制 K562 细胞生长,IC50为 840 nM。 | |||
T9812 |
Tubulin inhibitor 24
|
Microtubule Associated | Cytoskeletal Signaling |
Tubulin inhibitor 24 是一种 tubulin 抑制剂,可以抑制微管蛋白聚合,以浓度依赖性方式诱导细胞周期停滞在 G2/M 期, 具有抗肿瘤活性且无明显毒性。 | |||
T67935 |
Tubulin inhibitor 11
|
Apoptosis; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
Tubulin inhibitor 11 是一种口服活性的有效微管蛋白抑制剂。它通过靶向秋水仙碱结合位点,抑制tubulin聚合,进而促进有丝分裂阻断和apoptosis。 | |||
T77651 |
Tubulin polymerization-IN-47
|
Microtubule Associated | Cytoskeletal Signaling |
Tubulin polymerization-IN-47 是一种 tubulin 聚合抑制剂和有丝分裂抑制剂,具有抗肿瘤活性,对神经母细胞瘤癌细胞增殖具有抑制作用,对 Chp-134 和 Kelly 细胞系的IC50 分别为 7 和 12 nM。Tubulin polymerization-IN-47 是治疗肝癌、结肠癌、肺癌和乳腺癌的候选化合物。 | |||
T77647 |
Tubulin polymerization-IN-43
|
Apoptosis; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
Tubulin polymerization-IN-43 是一种微管蛋白聚合 (tubulin polymerization) 抑制剂。Tubulin polymerization-IN-43 具有多种作用,通过靶向 Colchicine 位点破坏细胞微管网络,促进白血病细胞的细胞周期停滞在 G2/M 期和细胞凋亡 (apoptosis)。Tubulin polymerization-IN-43 具有抗血管生成活性。 | |||
T13226 |
Tubulin inhibitor 8
|
Microtubule Associated | Cytoskeletal Signaling |
Tubulin inhibitor 8是管蛋白和多种癌症细胞系的抑制剂,对管蛋白聚合和K562细胞生长具有抑制作用 ,IC50分别为0.73μM 和14nM。 | |||
T78701 |
Tubulin inhibitor 32
|
Apoptosis | Apoptosis |
Tubulin inhibitor 32是一种口服活性的新型微管抑制剂,具有抗增殖和抗肿瘤活性,可抑制微管聚合,可诱导细胞凋亡及在G2/M期引起细胞周期停滞。 | |||
T77728 |
Tubulin polymerization-IN-55
|
Microtubule Associated | Cytoskeletal Signaling |
Tubulin polymerization-IN-55 是一种高效的 Tubulin Polymerization 抑制剂,具有潜在的抗血管生成和抗肿瘤活性,对 A549、K562、HepG2、MDA-MB-231 和 HFL-1 显示出抗增殖作用。 | |||
T13225 | Tubulin inhibitor 7 | Microtubule Associated | Cytoskeletal Signaling |
Tubulin inhibitor 7 is an inhibitor of tubulin and a potent inhibitor of multiple cancer cell lines (tubulin polymerization (IC50: 0.52 μM), K562 cell growth (IC50: 11 nM)). | |||
T13227 | Tubulin inhibitor 1 | Microtubule Associated | Cytoskeletal Signaling |
Tubulin inhibitor 1 is an inhibitor of tubulin, inhibits tubulin polymerization, with potent anti-tumor activity, induces cellular apoptosis causes and cellular mitotic arrest in the G2/M phase. | |||
T61472 |
Tubulin inhibitor 18
|
||
Tubulin inhibitor 18 (compound 5j) is a highly potent chalcone compound that effectively inhibits tubulin. Its unique molecular structure renders Tubulin inhibitor 18 as a promising candidate for cancer research [1]. | |||
T72445 |
Tubulin inhibitor 30
|
||
Tubulin inhibitor 30 是一种 tubulin 组合抑制剂,IC50为 0.52 μM。Tubulin inhibitor 30 可以诱导 ferroptosis。 | |||
T62445 | Tubulin inhibitor 22 | ||
Tubulin inhibitor 22 (compound 4c) 是一种 tubulin 的有效抑制剂,表现出抗血管生成和抗癌活性。Tubulin inhibitor 22 能够将 MGC-803 细胞的细胞周期阻滞在 G2/M 期。Tubulin inhibitor 22 剂量依赖性地通过线粒体功能障碍引起 Caspase 诱导的 MGC-803 细胞凋亡 (apoptosis)。 | |||
T60026 |
KIF18A-IN-2
|
Microtubule Associated | Cytoskeletal Signaling |
KIF18A-IN-2 是有丝分裂驱动蛋白 Kif18A 的抑制剂,IC50 为 28 nM,可用于染色体不稳定性相关漏洞的研究。 | |||
T61545 | Tubulin inhibitor 28 | ||
Tubulin inhibitor 28 (compound 2g) 是一种有效的微管抑制剂,IC50值为 1.2 μM。Tubulin inhibitor 28 对 MCF-7 细胞具有抗增殖活性。 | |||
T60793 |
Tubulin inhibitor 26
|
||
Tubulin inhibitor 26 (compound 3c) 是一种吲唑衍生物,是微管蛋白抑制剂,对 HepG2、HCT116、SW620、HT29 和 A549 癌细胞系具有显著的低纳摩尔效力。Tubulin inhibitor 26 抑制G2/M 期肿瘤细胞,并且诱导细胞凋亡。Tubulin inhibitor 26 在体内抑制肿瘤生长,并且不影响小鼠体重。 | |||
T61242 |
Tubulin inhibitor 12
|
||
Tubulin inhibitor 12 (Hit 9) is a recently developed compound with potent inhibitory effects on tubulin (IC50 = 25.3 μM). This compound exhibits noteworthy anti-tumor and anti-proliferative activities, making it a promising candidate for the treatment of cancer [1]. | |||
T73832 | Tubulin inhibitor 21 | ||
Tubulin inhibitor 21 (compound 6f) 为基于查尔酮与褪黑激素混合的有效tubulin抑制剂。该化合物对SW480细胞展现显著的细胞毒性活性(IC50=0.26 μM),对非恶性细胞的毒性较低。 | |||
T15236 |
Entasobulin
|
Microtubule Associated | Cytoskeletal Signaling |
Entasobulin 是一种 β-微管蛋白聚合的抑制剂,具有潜在的抗癌活性。 | |||
T78772 |
Tubulin inhibitor 37
|
||
Tubulin inhibitor 37(化合物 12)作为Tubulin抑制剂,对Tubulin聚合表现出显著的抑制作用(IC50=1.3 µM)。此外,该化合物在人肿瘤细胞系上展现抗增殖潜力,因此对癌症研究颇具价值。 | |||
T60402 | Tubulin inhibitor 14 | ||
Tubulin inhibitor 14 是一种有效的 NQO2(醌氧化还原酶 2)抑制剂,IC50 为 1.0 μM,也抑制微管蛋白聚合和内皮细胞毛细管样管的形成。Tubulin inhibitor 14 是一种微管去稳定剂,具有潜在的肿瘤选择性以及抗血管生成和血管破坏的功能[1]。 | |||
T78917 | Tubulin inhibitor 33 | ||
Tubulin inhibitor 33为一种抗微管蛋白聚合化合物,其抑制作用表现为剂量依赖性,具有9.05 μM的IC50。该化合物不仅具备抗肿瘤活性,还能诱导细胞凋亡(apoptosis),在抗肿瘤研究领域有应用潜力。 | |||
T78771 |
Tubulin inhibitor 36
|
||
Tubulin inhibitor 36 (Compound 10) 是新型高效微管蛋白抑制剂,可阻止微管蛋白聚合并诱发细胞凋亡,IC50值为1.5±0.1 μM。该化合物在抗有丝分裂中表现出显著活性,并对胶质母细胞瘤(GBM)细胞线有效,适用于胶质母细胞瘤(GBM)的抗肿瘤研究。 | |||
T78773 |
Tubulin inhibitor 38
|
||
Tubulin inhibitor 38(化合物14)是一款强效的四唑基微管蛋白抑制剂,能够显著抑制细胞增殖。以100 nM浓度作用24小时后,该抑制剂能够引起有丝分裂停滞,特别是在G2/M期细胞周期阶段,进而诱导细胞凋亡。在HeLa、MCF7和U87 MG细胞系中,Tubulin inhibitor 38展现了较高的细胞毒性及选择性。 | |||
T60459 | Tubulin inhibitor 15 | ||
Tubulin inhibitor 15 是有效的微管蛋白抑制剂,具有抗增殖活性。Tubulin inhibitor 15 在 HepG2 细胞中表现出细胞毒性。 | |||
T60460 | Tubulin inhibitor 16 | ||
Tubulin inhibitor 16 是有效的微管蛋白抑制剂,具有抗增殖活性。Tubulin inhibitor 16 在 HepG2 细胞中表现出细胞毒性。 | |||
T62922 |
Tubulin inhibitor 25
|
||
Tubulin inhibitor 25 是一种微管蛋白 (tubulin) 的有效抑制剂 (IC50: 0.98 μM),能够显著抑制 HT29 细胞。Tubulin inhibitor 25 对细胞迁移和微管形成具有抑制作用,有助于抗血管生成。 | |||
T62332 | Tubulin inhibitor 13 | ||
Tubulin inhibitor 13 (E27) 是一种有效的tubulin抑制剂,其对tubulin聚合的抑制IC50值为16.1 μM。该化合物不仅可以抑制癌细胞迁移和侵袭,还能诱导apoptosis,显示出抗癌活性。 | |||
T78761 |
Tubulin inhibitor 34
|
||
Tubulin inhibitor 34 (compound b5) 为抗癌效果显著之化学药物,能够阻断微管蛋白(tubulin)聚合,促使G2/M期细胞周期停滞及细胞凋亡(apoptosis),并展现出明显的抗血管生成与抗肿瘤活性。 | |||
T72449 |
Tubulin inhibitor 31
|
||
Tubulin inhibitor 31, 以IC50值4 µM的效力,是一种高效的微管蛋白(Tubulin)抑制剂,具有显著的抗增殖活性,并能抑制HUVEC的迁移。 | |||
T62498 |
Tubulin polymerization-IN-20
|
||
Tubulin aggregation-IN-20 (compound 11) 是一种有效的 tubulin 聚合抑制剂。Tubulin aggregation-IN-20 具有潜力进行乳腺癌和耐药结肠癌的研究。 | |||
T63836 |
Tubulin polymerization-IN-7
|
||
Tubulin aggregation-IN-7 是有效的 tubulin 聚合抑制剂,对癌症疾病表现出研究潜力。 | |||
T61084 |
Tubulin polymerization-IN-37
|
||
Tubulin polymerization-IN-37 is a potent inhibitor (IC50: 2.3 μΜ) of tubulin polymerization by binding specifically to the colchicine site of tubulin and preventing colchicine binding. It has potential applications in cancer research, notably for lymphomas [1]. | |||
T62971 |
Tubulin polymerization-IN-16
|
||
Tubulin aggregation-IN-16 (compound 5g) 是一种有效的 tubulin 聚合抑制剂。Tubulin aggregation-IN-16 对癌细胞有效 (IC50: 0.084-0.221 μM)。Tubulin aggregation-IN-16 能有效地破坏微管/管蛋白的动态,诱导 SGC-7901 细胞的细胞周期阻滞在 G2/M 期。 | |||
T62206 |
Tubulin polymerization-IN-19
|
||
Tubulin aggregation-IN-19 (compound 4) 是一种有效 tubulin 聚合抑制剂,对乳腺癌和耐药结肠癌表现出研究潜力。 | |||
T61524 |
Tubulin/HDAC-IN-1
|
||
Tubulin/HDAC-IN-1 is a compound that functions as a dual inhibitor for tubulin and HDAC-IN-1. It achieves this by interacting with tubulin through CH/π interaction and with HDAC8 through hydrogen bond interaction. This compound effectively inhibits tubulin polymerization and selectively targets HDAC8 with an IC50 of 150 nM. Additionally, Tubulin/HDAC-IN-1 demonstrates cytotoxicity against various human cancer cells, induces cell cycle arrest in the G2/M phase, and triggers cell apoptosis. This c... | |||
T79887 |
Tubulin polymerization-IN-49
|
||
Tubulin polymerization-IN-49 (compound 12d) 是一种抑制微管蛋白聚合的有效化合物。它通过结合到微管蛋白的秋水仙碱位点来抑制其聚合。此外,Tubulin polymerization-IN-49 能够诱导细胞周期在 G2/M 期停滞并触发细胞凋亡,表现出对抗癌的活性,能够预防肿瘤的生成及抑制肿瘤增殖和血管生成。 | |||
T62121 | Tubulin polymerization-IN-3 | ||
Tubulin polymerization-IN-3 是一种有效的微管蛋白聚合抑制剂 (IC50: 3.84 μM),能够诱导结肠癌细胞凋亡。 | |||
T1753 |
D-64131
|
Microtubule Associated | Cytoskeletal Signaling |
D64131 是一种微管蛋白聚合抑制剂,IC50 值为 0.53 μM。它具有抗丝分裂活性,可用于癌症研究。 | |||
T63120 |
Tubulin inhibitor 23
|
||
Tubulin inhibitor 23 是一种 Tubulin 的有效抑制剂 (IC50: 4.8 μM)。Tubulin inhibitor 23 以剂量依赖性方式表现出抗血管生成作用,并可诱导细胞凋亡。Tubulin inhibitor 23 具有潜力进行白血病的研究。 | |||
T60436 | Tubulin inhibitor 17 | ||
Tubulin inhibitor 17 (Compound 3b) 是微管蛋白聚合抑制剂(IC50 = 12.38 μM)。Tubulin inhibitor 17 显示出抗癌活性并且诱导细胞凋亡。 | |||
T60755 | Tubulin inhibitor 20 | ||
Tubulin inhibitor 20 (compound 1) 作为tubulin 的有效抑制剂,显示出癌症研究的潜力。 | |||
T61190 | Tubulin inhibitor 27 | ||
Tubulin inhibitor 27 (DYT-1) 是一种微管蛋白聚集 (tubulin polymerisation) 抑制剂,IC50为 25.6 μM。Tubulin inhibitor 27 具有抗血管生成活性和抗肿瘤活性。 | |||
T60568 |
Tubulin inhibitor 29
|
||
Tubulin inhibitor 29 (compound 3c) 是一种有效的微管抑制剂,可抑制微管聚合并与秋水仙碱位点结合 (IC 50 = 1.2 μM)。Tubulin inhibitor 29 具有抗增殖作用,对人乳腺癌细胞 MCF-7 细胞的 IC50值为 7.5 μM。 | |||
T61459 | Tubulin inhibitor 19 | ||
Tubulin inhibitor 19 (compound 9b) is a potent indole chalcone compound that exhibits strong inhibitory activity against tubulin. Its potential in cancer research makes it valuable for studying cancer diseases [1]. | |||
T9504 |
MAP4343
|
Microtubule Associated | Cytoskeletal Signaling |
MAP4343 是孕烯醇酮的 3-甲基醚衍生物。它在体外与微管相关蛋白 2 (MAP2) 结合并刺激微管蛋白聚合,从而增强神经突延伸和保护神经元免受神经毒剂的侵害。 | |||
T62058 |
αβ-Tubulin-IN-1
|
||
αβ-Tubulin-IN-1 是有效且具有口服活性的αβ-Tubulin 抑制剂。αβ-Tubulin-IN-1 将细胞周期阻滞在 G2/M 期并诱导细胞凋亡 (apoptosis)。αβ-Tubulin-IN-1 抑制肿瘤细胞迁移和转移。αβ-Tubulin-IN-1 具有显著的抗肿瘤功效。 | |||
T61069 | Tubulin polymerization-IN-15 | ||
Tubulin polymerization-IN-15 (compound 4) is a highly effective inhibitor of tubulin polymerization, with significant potential in cancer research [1]. | |||
T60758 |
Tubulin polymerization-IN-36
|
||
Tubulin polymerization-IN-36 可用于癌症研究,例如淋巴癌。Tubulin polymerization-IN-36 结合微管蛋白的秋水仙碱位点并且抑制秋水碱结合,是一种微管蛋白聚合的抑制剂,IC50值为 2.8 μM。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2773 |
Vindoline
文朵灵,文多灵 |
Microtubule Associated | Cytoskeletal Signaling |
Vindoline 是从长春花叶片中提取的一种生物碱,通过抑制微管组装而表现出抗有丝分裂活性。 | |||
T36850 |
Curvulin
|
Microtubule Associated | Cytoskeletal Signaling |
Curvulin 是一种植物毒素,可以抑制微管组装,也可以抑制 iNOS 的表达。 | |||
T8188 |
Podophyllotoxone
|
Others; Microtubule Associated | Cytoskeletal Signaling; Others |
Podophyllotoxone 是从八角莲根中分离得到的一种天然产物,能抑制微管蛋白聚合,具有抗癌活性。 | |||
T3S0209 |
Vincristine
|
ERK; p38 MAPK; NF-κB; Akt; JNK; mTOR | Cytoskeletal Signaling; MAPK; NF-κB; PI3K/Akt/mTOR signaling |
Vincristine 与微管蛋白结合并抑制微管的形成,从而抑制癌细胞的有丝分裂。 Vincristine 可用作微管去稳定剂,用于研究治疗血液系统癌症,如白血病和淋巴瘤以及儿童肉瘤的相关研究。 | |||
T1121 |
Podofilox
鬼臼毒素,Podophyllotoxin,(+)-Shikonin |
Microtubule Associated; Topoisomerase | Cytoskeletal Signaling; DNA Damage/DNA Repair |
Podofilox ((+)-Shikonin) 是从八角莲中分离的一种木脂素,是微管组装和 DNA 拓扑异构酶 II 抑制剂。它对皮肤和粘膜有很强的刺激性,具有角质溶解作用,可用于治疗疣和角化病,具有潜在的抗肿瘤特性。 | |||
TN2256 |
Taccalonolide B
根薯酮内酯B,根薯酮内酯 B |
Microtubule Associated | Cytoskeletal Signaling |
Taccalonolide B 是从广西裂果薯中分离得到的一种微管稳定剂,具有抗肿瘤活性。它抑制 SK-OV-3 细胞的生长,IC50 为 208 nM,在体外对过表达 P-糖蛋白 (Pgp) 和多药耐药蛋白 (MRP7) 的细胞系有效。 | |||
TN2190 |
Scoulerine
|
Apoptosis; Beta-Secretase; BACE; Parasite | Apoptosis; Microbiology/Virology; Neuroscience |
Scoulerine 是抗有丝分裂化合物。它抑制细胞增殖,阻止细胞周期,并诱导癌细胞凋亡。它也是BACE1(淀粉样前体蛋白裂解酶 1) 的抑制剂。 | |||
TN2254 |
Taccalonolide A
根薯酮内酯A,根薯酮内酯 A |
Apoptosis; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
Taccalonolide A 是从水田七根茎中分离得到的一种类固醇,具有细胞毒性和抗疟活性。它在体外对过表达 p 糖蛋白、多药耐药蛋白 7 细胞系有抑制作用,抑制 SK-OV-3 细胞生长的 IC50值为 622 nM。它是微管稳定剂,能引起 G2-M 期滞留、Bcl-2 磷酸化,并引发细胞凋亡。 | |||
TN1087 |
Deoxypodophyllotoxin
脱氧鬼臼毒素,去氧鬼臼毒素 |
Apoptosis; Microtubule Associated; Autophagy | Apoptosis; Autophagy; Cytoskeletal Signaling |
Deoxypodophyllotoxin 是从桃儿七根茎分离的一种木酚素,是鬼臼毒素衍生物,具有抗有丝分裂和抗病毒特性。它是血管生成抑制剂,作为靶向微管药物,在肿瘤学中具有重大影响。它引起 DRG 神经元细胞内 Ca2+浓度增加,诱导细胞自噬和凋亡。 | |||
T0320 |
Colchicine
秋水仙碱,秋水仙素,Colcin,Colchineos,Colchisol |
Apoptosis; Microtubule Associated; Autophagy | Apoptosis; Autophagy; Cytoskeletal Signaling |
Colchicine (Colcin) 属于天然产物,是一种微管聚合的抑制剂 (IC50=3 nM),通过与微管蛋白结合来阻断微管的聚合。Colchicine 可以被用于治疗通风和风湿病。 | |||
T2217 |
Cephalomannine
Baccatin III,三尖杉宁碱 |
Microtubule Associated | Cytoskeletal Signaling |
Cephalomannine (Baccatin III) 是一种从云南红豆杉中提取的紫杉醇衍生物,具有抗肿瘤活性,可用于癌症研究。 | |||
T0968 |
Paclitaxel
Taxol,紫杉醇,NSC 125973 |
Apoptosis; Microtubule Associated; Autophagy | Apoptosis; Autophagy; Cytoskeletal Signaling |
Paclitaxel (Taxol) 属于天然产物,是一种微管聚合物稳定剂。Paclitaxel 具有抗肿瘤活性;通过诱导有丝分裂停滞、细胞凋亡、细胞自噬等,导致细胞死亡。 | |||
T6490 |
Epothilone A
埃博霉素 A,epothile,Epo A |
Apoptosis; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
Epothilone A (Epo A) 是紫杉醇和管蛋白聚合物结合的一种竞争性抑制剂,其Ki 值为 0.6-1.4 μM。 | |||
T16016 |
Maytansinol
美登醇,Ansamitocin P-0 |
Apoptosis; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
Maytansinol (Ansamitocin P-0) 在体外抑制微管组装并导致微管分解。它与辐射联用,用于果蝇和人类癌细胞。 | |||
T6272 |
Fosbretabulin Disodium
Combretastatin A4 Phosphate,CA 4DP,CA 4P,福他布林,Combretastatin A4 disodium phosphate,Fosbretabulin (Combretastatin A4 Phosphate (CA4P)) Disodium |
Apoptosis; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
Fosbretabulin Disodium (CA 4P) 是一种微管蛋白去稳定剂,是 Combretastatin A4 前药,可选择性靶向内皮细胞,诱导新生肿瘤新血管消退,减少肿瘤血流量并引起中央肿瘤坏死。 | |||
T1668 |
Vinblastine sulfate
硫酸长春碱,NSC49842,Vincaleukoblastine sulfate salt |
Microtubule Associated; AChR; Autophagy | Autophagy; Cytoskeletal Signaling; Neuroscience |
Vinblastine sulfate (Vincaleukoblastine sulfate salt) 是对各种癌症类型有细胞毒性的生物碱。 它可以抑制微管的形成,也可以抑制 nAChR,IC50值为8.9 μM。 | |||
T3S2372 |
7-epi-Taxol
7-Epitaxol,7-表紫杉醇,7-epi-Paclitaxel |
Others; Microtubule Associated | Cytoskeletal Signaling; Others |
7-epi-Taxol (7-Epitaxol) 是在细胞中发现的紫杉醇的主要衍生物,在抑制细胞增殖、微管解离和诱导微管聚合等方面与紫杉醇作用相当。 | |||
T21351 |
Maytansine
NSC-153858,NSC153858,Maitansina,NSC 153858,Maitansine,美坦新 |
Microtubule Associated; Antibiotic | Cytoskeletal Signaling; Microbiology/Virology |
Maytansine (NSC-153858) 是从变叶美登木中分离的一种高效微管靶向天然产物,可诱导有丝分裂阻滞并在亚纳摩尔浓度杀死肿瘤细胞。 | |||
T1270 |
Vincristine sulfate
Leurocristine,22-Oxovincaleukoblastine sulfate,Leurocristine sulfate,硫酸长春新碱 |
Apoptosis; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
Vincristine sulfate (Leurocristine sulfate) 是一种抗肿瘤长春花生物碱。在细胞周期的 S 期不可逆地与微管(Ki: 85 nM) 和纺锤体蛋白结合,并干扰有丝分裂纺锤体的形成。 | |||
T19720 |
Colcemid
C 12669,C-12669,NSC-3096,Kolchicin,C12669,Demecolcine |
Microtubule Associated | Cytoskeletal Signaling |
Colcemid (NSC-3096) 是一种微管聚合抑制剂,可诱导细胞凋亡,可用于肿瘤和胚胎克隆的研究。 | |||
T1034 |
Docetaxel
多西他赛,NSC 628503,RP-56976,多烯紫杉醇 |
Apoptosis; Microtubule Associated; Endogenous Metabolite | Apoptosis; Cytoskeletal Signaling; Metabolism |
Docetaxel (RP-56976) 是紫杉醇的半合成类似物,是一种微管解聚抑制剂 (IC50=0.2 μM)。Docetaxel 可以减弱 bcl-2 和 bcl-xL 基因表达的影响,具有诱导凋亡、抗肿瘤活性。 | |||
T2220 |
2-Methoxyestradiol
2-甲氧雌二醇,二甲氧基雌二醇,NSC-659853,2-MeOE2,2-ME2 |
Apoptosis; Reactive Oxygen Species; Microtubule Associated; Endogenous Metabolite; HIF; Autophagy | Angiogenesis; Apoptosis; Autophagy; Chromatin/Epigenetic; Cytoskeletal Signaling; Immunology/Inflammation; Metabolism; NF-κB |
2-Methoxyestradiol (2-ME2) 是一种口服生物可利用的雌二醇代谢物,具有抗肿瘤活性。它通过减少内皮细胞增殖和诱导内皮细胞凋亡来抑制血管生成,也可破坏微管的稳定。它可诱导半胱天冬酶活化,导致细胞周期停滞在 G2 期、DNA 断裂和细胞凋亡。 | |||
TP1180 |
Dolastatin 10
尾海兔素10,NSC 376128,DLS 10 |
Microtubule Associated | Cytoskeletal Signaling |
Dolastatin 10 (DLS 10) 是一种多肽,可以抑制微管蛋白聚合,显示除抗有丝分裂的活性。 | |||
T6212 |
Combretastatin A4
CA4,康普瑞汀,Z)-3,4,5,4',-四甲氧基-3'-羟基二苯乙烯,CRC 87-09 |
Microtubule Associated | Cytoskeletal Signaling |
Combretastatin A4 (CA4) 是一种微管靶向剂,可结合 β-tubulin,Kd 值为 0.4 μM。 | |||
T22455 |
Vindesine sulfate
DVA,Desacetylvinblastine amide,硫酸长春地辛,DAVA,Desacetyl Vinblastine amide,VDS |
Others | Others |
Vindesine sulfate (Desacetyl Vinblastine amide) 是一种长春花生物碱,它是长春碱的合成衍生物,与有丝分裂纺锤体的微管蛋白结合,导致微管结晶和有丝分裂停滞或细胞死亡。 | |||
T1152 |
Albendazole
SKF-62979,阿苯达唑 |
HIF/HIF Prolyl-Hydroxylase; Microtubule Associated; Antibiotic; Parasite | Chromatin/Epigenetic; Cytoskeletal Signaling; Metabolism; Microbiology/Virology |
Albendazole (SKF-62979) 是一种广谱抗寄生虫剂,具有高效,低宿主毒性的特点。 它用于研究人类和动物的胃肠道寄生虫。 | |||
T5165 |
10-Deacetyltaxol
10-DAT,10-Desacetyl Paclitaxel,去乙酰紫衫醇,Deacetyltaxol,10-去乙酰紫杉醇,10-deacetyl-paclitaxel,Deacetyl Paclitaxel |
Others; Microtubule Associated | Cytoskeletal Signaling; Others |
10-Deacetyltaxol (10-DAT) 是从红豆杉中分离得到的一种紫杉醇衍生物,对人脑胶质细胞瘤和神经母细胞瘤细胞具有细胞毒性。它能促进微管蛋白的聚合,在体外抑制由钙离子诱导的微管解聚。 | |||
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。 | |||
T0186 |
Docetaxel trihydrate
RP-56976 (Trihydrate),RP56976 (NSC 628503) Trihydrate,多西他赛三水合物 |
Apoptosis; BCL; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
Docetaxel trihydrate (RP-56976 Trihydrate) 是一种抗肿瘤试剂,抑制微管解聚的IC50值为 0.2 μM。它是紫杉醇的半合成类似物,能减弱 bcl-2 和 bcl-xL 基因表达的影响。它阻滞G2/M 细胞周期,导致细胞凋亡。 | |||
T2937 |
4'-Demethylepipodophyllotoxin
4'-DMEP,4-Demethylepipodophyllotoxin,4'-脱甲基表鬼臼毒素,4'-去甲基表鬼臼毒素,DMEP,4'-O-demethylepipodophyllotoxin |
Microtubule Associated | Cytoskeletal Signaling |
4'-Demethylepipodophyllotoxin (DMEP) 是一种有效的微管组装抑制剂。 | |||
T2543 |
Cabazitaxel
XRP6258,卡巴他塞,RPR-116258A,TXD 258,taxoid XRP6258 |
Microtubule Associated; Autophagy | Autophagy; Cytoskeletal Signaling |
Cabazitaxel (taxoid XRP6258) 是一种紫杉烷类的抗肿瘤剂,可用于治疗多西他赛失败后的去势抵抗性转移性前列腺癌。 | |||
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。 | |||
T5749 |
10-Deacetyl-7-xylosyl paclitaxel
10-Deacetyl-7-xylosyltaxol,10-Deacetyltaxol 7-Xyloside,7-Xylosyl-10-deacetyltaxol,7-木糖甙-10-脱乙酰基紫杉醇,10-Deacetylpaclitaxel 7-Xyloside |
Others; Microtubule Associated | Cytoskeletal Signaling; Others |
10-Deacetyl-7-xylosyl paclitaxel (7-Xylosyl-10-deacetyltaxol) 是一种紫杉醇衍生物,具有改进的药理特性和更高的水溶性,用于治疗癌症。 | |||
TN6706 |
3-demethylcolchicine
3-去甲秋水仙碱,3-去甲基秋水仙碱 |
Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB |
3-Demethylcolchicine 是一种从金莲花中分离得到的天然产物,对纯化的牛脑微管蛋白的聚合有抑制作用。 | |||
T22262 |
Ansamitocin p-3
Maytansinol isobutyrate,Antibiotic C 15003P3,NSC292222 |
Microtubule Associated | Cytoskeletal Signaling |
Ansamitocin p-3 (Maytansinol isobutyrate) 是一种微管抑制剂,对微管蛋白聚合的 IC50 为 3.4 μM。 | |||
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。 | |||
T13653 |
Dihydrocephalomannine
|
Others | Others |
Dihydrocephalomannine is similar to paclitaxel, showing reduced cytotoxicity and tubulin binding. | |||
T28428 |
PM-060184
Plocabulin,PM 060184 |
||
PM-060184, a tubulin polymerisation inhibitor, is used potentially for the treatment of solid tumours and breast cancer. | |||
TN5107 |
Taxcultine
|
Others | Others |
Taxcultine can actively promote tubulin assembly. | |||
T82241 | Halichondrin B | ||
Halichondrin B,源自海绵 Halichondria okadai,为非竞争性Vinca-alkaloid 微管蛋白结合抑制剂,微管蛋白聚合 IC50 值为1.2-1.4 μM,表现出抗肿瘤活性。 | |||
T82787 |
Calythropsin
|
||
Calythropsin是一种对有丝分裂产生微弱影响的细胞毒性查尔酮类化合物,该化合物可能还会影响微管蛋白的聚合。 | |||
T75521 | PM050489 | ||
PM050489 是一种有效的聚酮类微管/微管蛋白 (Microtubule/Tubulin) 抑制剂,可从马达加斯加海绵Lithoplocamia lithistoides 中分离。PM050489 抑制有丝分裂,IC50值为 26.4 nM。PM050489 具有抗肿瘤活性,能用于癌症研究。 | |||
T75646 | Moroidin | ||
Moroidin是一种双环八肽,隶属于荨麻疹科环肽科,有效抑制纯化的微管蛋白聚合,表现为微管蛋白聚合抑制剂。此外,Moroidin对包括A549人肺癌细胞在内的多种癌细胞显示出细胞毒性作用,能诱导细胞凋亡。 | |||
T13944 | Tubulysin M | Others | Others |
Tubulysin M is a natural product isolated from the myxobacterial species Archangium geophyra and Angiococcus disciformis, and is a highly cytotoxic peptide. Tubulysin M is a cytotoxic activity tubulysin that inhibits tubulin polymerization and leads to ce | |||
T13941 |
Tubulysin G
|
Others | Others |
Tubulysin G is a natural product isolated from the myxobacterial species Archangium geophyra and Angiococcus disciformis, and is a highly cytotoxic peptide. Tubulysin G is a cytotoxic activity tubulysin that inhibits tubulin polymerization and leads to ce | |||
T82857 |
Blestriarene B
(-)-Blestriarene B |
||
(-)-Blestriarene B 是一种从白芨(兰科)中分离得到的二苯乙烯类化合物,其通过抑制微管蛋白的聚合作用发挥效用。 | |||
T13940 |
Tubulysin F
|
Others | Others |
Tubulysin F is a natural product isolated from the myxobacterial species Archangium geophyra and Angiococcus disciformis, and is a highly cytotoxic peptide. Tubulysin F is a cytotoxic activity tubulysin that inhibits tubulin polymerization and leads to ce | |||
T13942 |
Tubulysin H
|
Others | Others |
Tubulysin H is a natural product isolated from the myxobacterial species Archangium geophyra and Angiococcus disciformis, and is a highly cytotoxic peptide. Tubulysin H is a cytotoxic activity tubulysin that inhibits tubulin polymerization and leads to ce | |||
T13943 |
Tubulysin I
|
Others | Others |
Tubulysin I is a natural product isolated from the myxobacterial species Archangium geophyra and Angiococcus disciformis, and is a highly cytotoxic peptide. Tubulysin I is a cytotoxic activity tubulysin which inhibits tubulin polymerization and leads to c | |||
T13228 |
Tubulysin D
|
Microtubule Associated | Cytoskeletal Signaling |
Tubulysin D is a tetrapeptide isolated from the myxobacterial species Archangium geophyra and Angiococcus disciformis, and displays potent antitumor activity. | |||
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