225
36
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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]. | |||
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。 | |||
T61940 | Tubulin polymerization-IN-4 | ||
Tubulin polymerization-IN-4 是有效的微管蛋白聚合体 (tubulin polymerization) 抑制剂(IC50=4.6 μM)。Tubulin polymerization-IN-4 可以破坏微管蛋白聚合,将细胞周期阻滞在G2/M 期,诱导细胞凋亡 (apoptosis),抑制细胞的克隆发生和迁移。Tubulin polymerization-IN-4还可以破坏血管系统。 | |||
T62040 |
Tubulin polymerization-IN-30
|
||
Tubulin polymerization-IN-30 (compound 6e) 是有效的微管蛋白聚合 (Tubulin polymerization) 抑制剂,可破坏细胞内微管组织,将细胞周期阻滞在 G2/M 期。Tubulin polymerization-IN-30 对 HeLa、SGC-7901和A549 等肿瘤细胞系具有良好的抗肿瘤活性,其IC50分别为 0.403、 2.16和2.21 μM。 | |||
T63849 | Tubulin polymerization-IN-34 | ||
Tubulin polymerization-IN-34 是 [1,2] 恶唑异吲哚微管蛋白聚合的抑制剂,能够高度选择边缘区淋巴瘤 VL51 细胞系。 | |||
T60735 | Tubulin polymerization-IN-22 | ||
Tubulin aggregation-IN-22 抑制细胞周期在 G2/M 期,并且诱导细胞凋亡。Tubulin aggregation-IN-22 是一种微管蛋白聚合抑制剂 (IC50 = 8.1 μM)。 | |||
T61482 | Tubulin polymerization-IN-13 | ||
Tubulin polymerization-IN-13 (Compound 4f) is a potent inhibitor of tubulin polymerization, with an IC50 value of 0.37 μM. It displays significant anti-proliferative effects against cancer cells, inducing apoptosis and exhibiting potential antivascular activity [1]. | |||
T60936 | Tubulin polymerization-IN-24 | ||
Tubulin aggregation-IN-24 (compound HMBA) 是一种有效的微管蛋白聚合抑制剂,可提高 GTP 水解速率并抑制微管组装。Tubulin aggregation-IN-24 诱导细胞凋亡和细胞周期停滞在 G2/M 期。Tubulin aggregation-IN-24 抑制乳腺癌细胞 MCF-7 的增殖。 | |||
T79532 |
Tubulin polymerization-IN-44
|
||
Tubulin polymerization-IN-44 (7w)为具高效性的微管蛋白聚合抑制剂,其IC50为0.21 μM。该化合物可诱发G2/M期阻塞并触发癌细胞凋亡(apoptosis),适用于肿瘤研究。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T62369 | Tubulin polymerization-IN-17 | ||
Tubulin aggregation-IN-17 (compound 23g) 是一种 tubulin 聚合的有效抑制剂。Tubulin aggregation-IN-17 具有微管蛋白解聚作用,能够诱导细胞凋亡并抑制迁移。Tubulin aggregation-IN-17 具有潜力进行癌症疾病的研究。 | |||
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]. | |||
T61129 |
Tubulin polymerization-IN-27
|
||
Tubulin polymerization-IN-27 (compound 5j) is an inhibitor of tubulin polymerization. It has the ability to halt the cell cycle specifically at the G2/M phase and also induce apoptosis [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。 | |||
T79429 |
Tubulin polymerization-IN-50
|
||
Tubulin polymerization-IN-50(compound 7n)是一种Tubulin polymerization抑制剂,其在SK-Mel-28细胞中的IC50值为5.05 μM,能够诱导(cell cycle)阻滞在G2/M期。 | |||
T80922 |
Tubulin polymerization-IN-56
|
||
Tubulin polymerization-IN-56(compound 8l),一种吲唑衍生的微管蛋白聚合抑制剂,通过与秋水仙碱位点的相互作用,能够引发细胞周期停滞与细胞凋亡。该化合物还能降低细胞迁移并在体内更有效地抑制肿瘤生长。 | |||
T72169 |
Tubulin polymerization-IN-40
|
||
Tubulin polymerization-IN-40为基于吖啶的微管蛋白聚合抑制剂,IC50值为1.5 μM,能在G2/M期阻滞癌细胞并诱导细胞凋亡,同时显示出抗癌活性与免疫增强作用。 | |||
T79645 |
Tubulin polymerization-IN-48
|
||
Tubulin polymerization-IN-48 (Compound 4k) 是一种中等强度破坏微管网络的微管蛋白聚合抑制剂。其对神经母细胞瘤癌细胞增殖的抑制效果显著,Chp-134 细胞系和 Kelly 细胞系的IC50值分别为79 nM和165 nM。 | |||
T62477 |
Tubulin polymerization-IN-18
|
||
Tubulin aggregation-IN-18 (compound 3) 是一种有效的 tubulin 聚合抑制剂,具有潜力进行乳腺癌和耐药结肠癌的研究。 | |||
T62135 |
Tubulin polymerization-IN-25
|
||
Tubulin polymerization-IN-25 是一种选择性的、双重 tubulin polymerization (IC50: 1.11 μM) 和 farnesyl transferase (FTase) (IC50: 0.39 μM) 抑制剂。Tubulin polymerization-IN-25 对癌细胞表现出细胞毒性,能够阻断细胞增殖。 | |||
T60902 | Tubulin polymerization-IN-31 | ||
Tubulin polymerization-IN-31 (Compound 4c) 具有抗癌活性,并诱导癌细胞凋亡。Tubulin polymerization-IN-31 是微管蛋白聚合的抑制剂,IC50 值为 3.64 μM。 | |||
T79766 |
Tubulin polymerization-IN-52
|
||
Tubulin polymerization-IN-52 (compound SC23)是一种tubulin聚合抑制剂,具有2.9 μM的IC50值。 | |||
T61600 | Tubulin polymerization-IN-10 | ||
Tubulin polymerization-IN-10 is a highly potent inhibitor of tubulin polymerization, exhibiting an IC50 value of 4.25±0.75 μM. It possesses significant anti-tumor properties [1]. | |||
T79268 | Tubulin polymerization-IN-42 | ||
Tubulin polymerization-IN-42(compound 10j)是一种具有抗癌活性的吲哚取代呋喃酮类微管蛋白聚合抑制剂。 | |||
T61532 | Tubulin polymerization-IN-6 | ||
Tubulin polymerization-IN-6 (compound 5f) is a potent inhibitor of tubulin polymerization, with an IC50 of 1.09 μM. It not only inhibits cell migration and tube formation but also has anti-angiogenic properties. Additionally, Tubulin polymerization-IN-6 has been found to effectively hinder tumor growth in HT29 xenograft Balb/c nude mice [1]. | |||
T63580 |
Tubulin polymerization-IN-21
|
||
Tubulin polymerization-IN-21 是微管蛋白聚合抑制剂,能够破坏细胞完整性和影响葡萄糖代谢,具有抗癌作用。 | |||
T63111 | Tubulin polymerization-IN-33 | ||
Tubulin polymerization-IN-33 是一种 [1,2] 恶唑洛异吲哚微管蛋白聚合的抑制剂,能够较好的抗 NCI 系列癌细胞的增殖。 | |||
T62349 |
Tubulin polymerization-IN-8
|
||
Tubulin aggregation-IN-8 (compound IIc) 是一种有效的tubulin 聚合抑制剂。Tubulin aggregation-IN-8 浓度依赖性地导致 HCT116 肿瘤细胞 G2/M 期细胞周期停滞,并显示显着抑制微管蛋白聚合,IC50值为 12.7 μM。Tubulin aggregation-IN-8 具有研究癌症疾病的潜力。 | |||
T80923 | Tubulin polymerization-IN-53 | ||
Tubulin polymerization-IN-53 是一种β-tubulin聚合的抑制剂,能够阻断细胞周期于G2/M阶段。对MDA-MB-231细胞系显示出抗增殖作用,其IC50为3.24 μM。 | |||
T60802 | Tubulin polymerization-IN-2 | ||
Tubulin polymerization-IN-2 为针对β-微管蛋白的强效抗癌分子,IC50 值为0.92 μM。该分子在多种细胞系中,包括白血病、非小细胞肺癌、肾癌、前列腺癌及乳腺癌细胞中展现出显著的抑制效果。 | |||
T72167 |
Tubulin polymerization-IN-39
|
||
Tubulin polymerization-IN-39,一种以IC50为4.9μM抑制微管蛋白聚合,通过占据秋水仙碱结合位点来实现其作用。此外,Tubulin polymerization-IN-39能有效抑制癌细胞增殖。 | |||
T62693 |
Tubulin polymerization-IN-29
|
||
Tubulin polymerization-IN-29 是一种有效的微管蛋白聚合抑制剂,显示出有效的抗增殖效果。Tubulin polymerization-IN-29 能够诱导 HeLa 细胞的细胞周期阻滞在 G2/M 期。 | |||
T62217 | Tubulin polymerization-IN-9 | ||
Tubulin polymerization-IN-9 是一种微管蛋白 (tubulin) 的有效抑制剂 (IC50: 1.82 μM)。Tubulin polymerization-IN-9 能够将 K562 细胞的细胞周期停滞在 G2/M 期,并诱导其凋亡 (apoptosis) 及线粒体去极化。Tubulin polymerization-IN-9 表现出强大的抗血管和抗肿瘤作用。 | |||
T63611 | Tubulin polymerization-IN-32 | ||
Tubulin polymerization-IN-32 是微管蛋白 (tubulin) 聚合抑制剂,能够抑制癌细胞增殖,可用于研究淋巴瘤等癌症。 | |||
T63725 | Tubulin polymerization-IN-35 | ||
Tubulin polymerization-IN-35 是 [1,2] 恶唑异吲哚微管蛋白聚合的抑制剂,能够高度选择性作用于边缘区淋巴瘤 VL51 细胞系。 | |||
T61880 |
Tubulin polymerization-IN-26
|
||
Tubulin polymerization-IN-26 (compound 12h) is a chemical compound that inhibits the polymerization of microtubulin. It achieves this by binding to the colchicine binding site of microtubulin, with an IC50 value of 4.64 μM. Additionally, Tubulin polymerization-IN-26 has the ability to induce apoptosis and inhibit cell metastasis or migration. Due to these properties, it holds potential as a valuable compound for researching lung cancer [1]. | |||
T80924 | Tubulin polymerization-IN-51 | ||
Tubulin polymerization-IN-51(compound 7u)是抑制SK-Mel-28细胞微管蛋白聚合的化合物,IC50介于2.55至17.89μM。该化合物适用于癌症研究。 | |||
T60600 | Tubulin polymerization-IN-14 | ||
Tubulin polymerization-IN-14 (Compound 20a) 是一种微管蛋白聚合抑制剂(IC 50 = 3.15 μM) ,具有强大的抗血管和抗癌活性,包括诱导癌细胞凋亡。 | |||
T79341 |
Tubulin polymerization-IN-45
|
||
Tubulin polymerization-IN-45 是针对微管蛋白的靶向抑制剂,通过与微管蛋白秋水仙碱结合位点相结合,能够诱导肝细胞癌细胞 (HCC) 发生细胞凋亡 (apoptosis)。 | |||
T79629 |
Tubulin polymerization-IN-46
|
||
Tubulin polymerization-IN-46(compound 9q)是一种微管蛋白抑制剂,能够阻断微管蛋白聚合并诱发细胞凋亡。该化合物通过抑制有丝分裂,导致MCF-7细胞在G2/M期停滞,对MCF-7乳腺癌细胞展现出抗增殖效果,其IC50值为10 nM。 | |||
T2164 |
Wiskostatin
|
Others | Others |
Wiskostatin 是神经元 Wiskott-Aldrich 综合征蛋白介导的肌动蛋白聚合的选择性抑制剂,能够不可逆的使细胞 ATP 水平快速下降。 | |||
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。 | |||
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。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8211 |
(±)-Decursinol
紫花前胡醇,3',4'-dihydro-3'-hydroxy-Xanthyletin |
Others; Antibacterial | Microbiology/Virology; Others |
(±)-Decursinol (3',4'-dihydro-3'-hydroxy-Xanthyletin) 是来自当归的一种 FtsZ 抑制剂,抑制 B. anthracis 的 FtsZ 聚合,IC50为 102 μM。 | |||
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。 | |||
T4821 |
Tetrahydro-2H-pyran-2-one
δ-Valerolactone,δ-Valeryllactone,delta-戊内酯,2-Oxotetrahydropyran |
Others; Endogenous Metabolite | Metabolism; Others |
Tetrahydro-2H-pyran-2-one (δ-Valerolactone) 是内源性代谢产物的一种。 | |||
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。 | |||
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。 | |||
T5791 |
Fructo-oligosaccharide DP7/GF6
Fructoheptasaccharide,蔗果七糖 |
Others | Others |
Fructo-oligosaccharide DP7/GF6 (Fructoheptasaccharide) 属于一种聚果糖,聚合度 (DP=7)。其中 Fructo-oligosaccharides (FOS) 由 6 个果糖单元通过 (2→1)-β-糖苷键连接,并在非还原性末端具有 1 个 D-葡萄糖单元。 | |||
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。 | |||
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。 | |||
T13864 |
Resolvin D1
RvD1 |
Apoptosis | Apoptosis |
Resolvin D1 (RvD1) 是一种内源性促进炎症消解介质,可通过调节肌动蛋白聚合阻断促进炎症的中性粒细胞迁移,减少 TNF-α 介导的炎症在巨噬细胞中的作用,并增强巨噬细胞对凋亡细胞的吞噬作用。 | |||
T7916 |
4-Acetamidobenzenesulfonyl azide
|
Others | Others |
4-Acetamidobenzenesulfonyl azide 用于各种科学研究应用,包括药物、肽和其他生物活性分子的合成,也被用作聚合反应和聚合物合成中的催化剂。 | |||
TN2401 |
Ethyl glucoside
β-D-Glucopyranoside, ethyl,Ethyl D-glucoside |
Others | Others |
Ethyl glucoside (β-D-Glucopyranoside, ethyl) 是一种用于水基钻井液的页岩抑制剂,是酶催化区域选择性内酯开环聚合的多功能引发剂,是一种存在于 Sisyrinchium palmifolium 的天然化合物。 | |||
T8154 |
Fructo-oligosaccharide DP9/GF8
Fructo-oligosaccharide DP9 / GF8,蔗果九糖 |
Others | Others |
Fructo-oligosaccharide DP9/GF8 (Fructo-oligosaccharide DP9 / GF8) 是一种低聚果糖(FOS),其聚合度DP=9。低聚果糖(FOS)由 8 个果糖单元通过 (2→1)-β-糖苷键连接,并在非还原性末端具有 1 个 D-葡萄糖单元。 | |||
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。 | |||
TN2376 |
Fructo-oligosaccharide DP8/GF7
蔗果八糖,Fructo-oligosaccharide DP8 / GF7 |
Others | Others |
Fructo-oligosaccharide DP8/GF7 (Fructo-oligosaccharide DP8 / GF7) 是一种聚果糖,聚合度(DP=8)。Fructo-oligosaccharides 由 7 个果糖单元通过 (2→1)-β-糖苷键连接,并在非还原性末端具有 1 个 D-葡萄糖单元。 | |||
T4840 |
3-Hydroxybenzoic acid
|
Others; Endogenous Metabolite | Metabolism; Others |
3-Hydroxybenzoic acid 是内源性代谢产物的一种。 | |||
T5S1981 |
alpha-Cyperone
(+)-α-Cyperone,α-香附酮,α-Cyperone |
Others; Endogenous Metabolite | Metabolism; Others |
alpha-Cyperone (α-Cyperone) 与 IL-6, Cox-2, Cdc42, Nck-2, Rac1 的表达下调相关,从而能够抑制炎症反应。 | |||
T35609 |
19-O-Acetylchaetoglobosin A
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19-O-Acetylchaetoglobosin A is a fungal metabolite originally isolated fromC. globosumthat has actin polymerization inhibitory and cytotoxic activities.1,2It inhibits actin polymerization in a cell-free assay when used at a concentration of 2 μM.219-O-Acetylchaetoglobosin A (3.2, 10, and 32 μg/ml) is cytotoxic to HeLa cervical cancer cells.1 1.Umeda, M., Ohtsubo, K., Saito, M., et al.Cytotoxicity of new cytochalasans from Chaetomium globosumExperientia31(4)435-438(1975) 2.Sekita, S., Yoshihira, ... | |||
T82369 |
Fructo-oligosaccharide DP14
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Fructo-oligosaccharide DP14为从Atractylodes lancea中提取的寡糖。 | |||
T10928 |
Cytochalasin A
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HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Cytochalasin A is a cell-permeable fungal toxin and is an oxidized derivative of cytochalasin B. Cytochalasin A is an inhibitor of HIV-1 protease (IC50 = 3 μM), inhibits actin polymerization and interferes with microtubule assembly by reacting with sulfhy | |||
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。 | |||
T19328 |
Fructo-oligosaccharide DP11/GF10
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Others | Others |
Fructo-oligosaccharide DP11/GF10 is a fructooligosaccharide (FOS) compound with a degree of polymerization (DP) equal to 11. FOS consists of 10 fructose units connected by (2→1)-β-glycosidic bonds, with a single D-glucosyl unit present at the non-reducing end. | |||
TN2358 |
Fructo-oligosaccharide DP10/GF9
蔗果十糖,Fructo-oligosaccharide DP10/GF9 |
Others | Others |
Fructo-oligosaccharide DP10/GF9 is a compound classified as a fructooligosaccharide (FOS) with a degree of polymerization (DP) of 10. FOS consists of a chain of 9 fructose units connected by (2→1)-β-glycosidic bonds, with a lone D-glucosyl unit located at the non-reducing end. | |||
T82787 |
Calythropsin
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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。 | |||
T82857 |
Blestriarene B
(-)-Blestriarene B |
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(-)-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。 | |||
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
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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 | |||
T13940 |
Tubulysin F
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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 | |||
T15721 |
Latrunculin A
LAT-A |
Others | Others |
Latrunculin A is a toxin isolated from the red sea sponge Latrunculia magnifica. Latrunculin A binds to actin monomers and it also inhibits polymerization of actin (Kds: 0.1, 0.4, 4.7 μM, and 0.19 μM for ATP-actin, ADP-Pi-actin, ADP-actin, and G-actin, re | |||
T19329 |
Fructo-oligosaccharide DP12/GF11
蔗果十二糖 |
Others | Others |
Fructo-oligosaccharide DP12/GF11 is a member of fructooligosaccharides (FOS) characterized by a degree of polymerization (DP) of 12. FOS compounds consist of 11 fructose units connected by (2→1)-β-glycosidic bonds, with a lone D-glucosyl unit located at the non-reducing end. | |||
T13942 |
Tubulysin H
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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
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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 | |||
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。 | |||
T20636 |
Latrunculin B
LAT-B,LATB,NSC 339663,NSC339663,NSC-339663,LAT B,INS115644 |
Antifungal | Microbiology/Virology |
Latrunculin B 是一种 来自红海海绵的生物碱,是一种肌动蛋白聚合 (actin polymerization) 抑制剂,具有抗真菌和抗原生动物活性。Latrunculin B 调节肺静脉电生理特征并减轻牵张性心律失常的发生,可用于研究青少年青光眼。 | |||
T73206 |
Wikstrol A
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Wikstrol A 是一种有效的抗真菌剂、抗有丝分裂剂和抗HIV-1剂。Wikstrol A 诱导稻瘟病菌菌丝体的形态变形,MMDC 值为 70.1 µM。Wikstrol 对微管聚合具有活性,IC50值为 131 µM。Wikstrol A 显示抗HIV-1活性,IC50值为 67.8 µM。 | |||
T78467 |
trans-10-Heptadecenoic acid
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trans-10-Heptadecenoic acid 是一种能在特定酶作用下参与生物合成与代谢过程的反式脂肪酸。在 2,4-二烯酰基-CoA 还原酶与 Delta3,Delta2-烯酰基-CoA 异构酶催化下,trans-10-Heptadecenoic acid 可合成聚羟基链烷酸酯。当缺乏 2,4-二烯酰基-CoA 还原酶时,该化合物则经由多功能酶 (MFE) 中的烯酰辅酶 A 水合酶 II 进行降解。此外,trans-10-Heptadecenoic acid 能通过还原酶依赖性与直接 MFE 依赖性途径引起细胞内的碳外流。 | |||
T11712 |
Jasplakinolide
Jaspamide,NSC-613009 |
Microtubule Associated; Antifungal | Cytoskeletal Signaling; Microbiology/Virology |
Jasplakinolide(Jaspamide) 是一种来自海洋海绵 (marine sponge) 的天然环状肽,是一种有效的肌动蛋白聚合反应 (actin polymerization) 诱导剂。Jasplakinolide 具有抗真菌和抗肿瘤活性,可以稳定先前存在的肌动蛋白丝。Jasplakinolide 与鬼笔环肽竞争性结合 F-肌动蛋白,对 F-肌动蛋白的 Kd 值为 15 nM。 |