Microtubule/Tubulin
Microtubule/Tubulin(微管/微管蛋白)
Microtubule is the cylindrical and filamentous structure that required for cell shape, migration, cilia and flagella mobility etc. Tubulin is the major component of microtubules.
Microtubule/Tubulin 相关产品(248)
- GC38480Vat-Cit-PAB-Monomethyl Dolastatin 10CAS: 1415329-13-3
Vat-Cit-PAB-Monomethyl Dolastatin 10 是抗体-药物偶联物的一部分,由 Monomethyl Dolastatin 10 (一种有效的微管蛋白抑制剂) 和 ADC linker Vat-Cit-PAB 连接而成。
- GC38564DeoxypodophyllotoxinCAS: 19186-35-7纯度: >99.50%
A flavolignan with diverse biological activities
- GC39177Valecobulin hydrochlorideCAS: 1240321-53-2纯度: >98.50%
Valecobulin hydrochloride (CKD-516 hydrochloride) 是 S516 的缬氨酸前体药和血管阻断剂 (VDA), 是一种强效的、β-微管蛋白聚合抑制剂,对小鼠和人类的实体肿瘤具有显著的抗肿瘤活性。
- GC39486DCLK1-IN-1CAS: 2222635-15-4纯度: >98.00%
DCLK1-IN-1是DCLK1和DCLK2的高选择性抑制剂,在KINOMEscan结合试验中对DCLK1和DCLK2的IC 50 分别为9.5nM和31nM。在ATP激酶实验中的IC 50 分别为57nM和103nM。
- GC39558Tubulin inhibitor 6CAS: 105925-39-1纯度: >99.50%
An inhibitor of tubulin polymerization and a PP2A activator
- GC39798ScoulerineCAS: 6451-73-6纯度: >99.00%
A benzylisoquinoline alkaloid with diverse biological activities
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC38456 | Pironetin | 151519-02-7 | - | |
An inhibitor of microtubule assembly | ||||
| GC38460 | DM4-SPDP | 2245698-48-8 | - | |
DM4-SPDP 是由连接桥 SPDP 和 毒性分子 DM4 连接而成的,可用来制备抗体偶联药物。DM4 是抑制细胞分裂的抗微管蛋剂。SPDP 是一种短链交联剂,可通过 NHS-酯和吡啶基二硫醇反应性基团与半胱氨酸巯基形成可裂解的 (可还原的) 二硫键,实现胺与巯基的结合。 | ||||
| GC38468 | DM4-SMe | 796073-68-2 | >98.00% | |
DM4-SMe 是抗体-美登素偶联物 (AMC) 的代谢产物,是一种微管蛋白 (tubulin) 抑制剂,还是一种抗体-药物偶联物 (ADCs) 的细胞毒性部分,可通过二硫键或稳定的硫醚键与抗体连接。DM4-SMe 抑制 KB 细胞的增殖,IC50 值为 0.026 nM。 | ||||
| GC38480 | Vat-Cit-PAB-Monomethyl Dolastatin 10 | 1415329-13-3 | - | |
Vat-Cit-PAB-Monomethyl Dolastatin 10 是抗体-药物偶联物的一部分,由 Monomethyl Dolastatin 10 (一种有效的微管蛋白抑制剂) 和 ADC linker Vat-Cit-PAB 连接而成。 | ||||
| GC38564 | Deoxypodophyllotoxin | 19186-35-7 | >99.50% | |
A flavolignan with diverse biological activities | ||||
| GC38945 | S516 | 1016543-77-3 | >98.00% | |
S516 (Compound 22) 是 CKD-516 的活性代谢产物,是一种有效的微管蛋白聚合抑制剂,其 IC50 值为 4.29 μM。S516 具有显著的抗肿瘤活性。 | ||||
| GC39177 | Valecobulin hydrochloride | 1240321-53-2 | >98.50% | |
Valecobulin hydrochloride (CKD-516 hydrochloride) 是 S516 的缬氨酸前体药和血管阻断剂 (VDA), 是一种强效的、β-微管蛋白聚合抑制剂,对小鼠和人类的实体肿瘤具有显著的抗肿瘤活性。 | ||||
| GC39483 | BO-264 | 2408648-20-2 | >99.50% | |
A TACC3 inhibitor | ||||
| GC39486 | DCLK1-IN-1 | 2222635-15-4 | >98.00% | |
DCLK1-IN-1是DCLK1和DCLK2的高选择性抑制剂,在KINOMEscan结合试验中对DCLK1和DCLK2的IC 50 分别为9.5nM和31nM。在ATP激酶实验中的IC 50 分别为57nM和103nM。 | ||||
| GC39558 | Tubulin inhibitor 6 | 105925-39-1 | >99.50% | |
An inhibitor of tubulin polymerization and a PP2A activator | ||||
| GC39798 | Scoulerine | 6451-73-6 | >99.00% | |
A benzylisoquinoline alkaloid with diverse biological activities | ||||
| GC40482 | Curvulin | 19054-27-4 | >98.00% | |
An inhibitor of microtubule assembly | ||||
| GC40663 | Corynecin V | 40958-12-1 | >98.00% | |
A chloramphenicol-like bacterial metabolite | ||||
| GC40664 | Colcemid | 477-30-5 | >98.00% / >99.00% / >99.50% | |
Colcemid是一种细胞骨架抑制剂,可以在哺乳动物细胞或卵母细胞中诱导G2/M期的有丝分裂停滞或囊泡破裂(GVBD)期的减数分裂停滞。 | ||||
| GC40890 | CAY10701 | 1616967-52-2 | >98.00% | |
CAY10701 is a 7-deazahypoxanthine analog that prevents microtubule formation, blocking the proliferation of HeLa and MCF-7 cells (GI50s = 22 and 38 nM, respectively). | ||||
| GC41272 | Lateropyrone | 93752-78-4 | >99.00% | |
A fungal metabolite | ||||
| GC41304 | Deoxybrevianamide E | 34610-68-9 | >99.00% | |
A fungal metabolite | ||||
| GC41520 | Lachnone A | 903892-99-9 | >95.00% | |
A fungal metabolite | ||||
| GC41564 | MPT0B014 | 1215208-59-5 | >98.00% | |
An inhibitor of tubulin polymerization | ||||
| GC42610 | 7-hydroxy Pestalotin | 41164-59-4 | >99.00% | |
A fungal metabolite | ||||
| GC42942 | bis-ANS (potassium salt) | 65664-81-5 | >98.00% / >95.00% | |
一种高亲和力非共价外源荧光染料 | ||||
| GC43300 | Combretastatin A1 | 109971-63-3 | >98.00% | |
An inhibitor of microtubule assembly | ||||
| GC43315 | Corynecin IV | 40958-11-0 | >99.00% | |
A chloramphenicol-like bacterial metabolite | ||||
| GC43469 | Diminutol | 361431-33-6 | >98.00% | |
An NQO1 inhibitor | ||||
