cemadotin free base
CAS No. 159776-69-9
cemadotin free base ( —— )
产品货号. M36342 CAS No. 159776-69-9
Cemadotin (LU103793) 是 Dolastatin 15 (HY-P1126) 的类似物,Dolastatin 15 是天然存在的细胞毒性肽。Cemadotin 阻止细胞有丝分裂,抑制微管 (tubulin) 的 Ki 为 1 μM。Cemadotin 可用于抗癌研究。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1910 | 有现货 |
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| 10MG | ¥2784 | 有现货 |
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| 25MG | ¥4278 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称cemadotin free base
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Cemadotin (LU103793) 是 Dolastatin 15 (HY-P1126) 的类似物,Dolastatin 15 是天然存在的细胞毒性肽。Cemadotin 阻止细胞有丝分裂,抑制微管 (tubulin) 的 Ki 为 1 μM。Cemadotin 可用于抗癌研究。
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产品描述Cemadotin (LU103793) is an analogue of Dolastatin 15 (HY-P1126) which is naturally occurring cytotoxic peptides. Cemadotin blocks cells at mitosis, and exhibits Ki value of 1 μM for inhibiting tubulin. Cemadotin can be used to research anticancer.
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体外实验Cemadotin (0-100 μM; 35 min) inhibits polymerization dose-dependently in Tubulin-treated Strongylocentrotus purpuratus.Cemadotin (0-1000 nM) preferentially suppresses the rate and extent of growing excursions of tubulin, and suppression is dependent upon the drug concentration.Cemadotin (0-1 μM) markedly increases the rescue frequency but had little effect on the catastrophe frequency.Cemadotin (400 pM~300 nM; 72 h) inhibits cancer cells HEK 293, F9 and HL60.Cell Proliferation Assay Cell Line:HEK 293, F9 and HL60 Concentration:400 pM~300 nM Incubation Time:72 h Result:Exhibited cytotoxicity against HEK 293, F9 and HL60 with IC50s of 0.7 nM, 14.8 nM and 0.5 nM, respectively.
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体内实验——
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同义词——
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通路Others
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靶点Other Targets
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受体Microtubule Associated
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研究领域——
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适应症——
化学信息
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CAS Number159776-69-9
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分子量640.86
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分子式C35H56N6O5
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纯度>98% (HPLC)
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溶解度——
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SMILESC([C@@H](N(C([C@@H](NC([C@H](C(C)C)N(C)C)=O)C(C)C)=O)C)[C@@H](C)C)(=O)N1[C@H](C(=O)N2[C@H](C(NCC3=CC=CC=C3)=O)CCC2)CCC1
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Jordan MA, et al. Suppression of microtubule dynamics by binding of cemadotin to tubulin: possible mechanism for its antitumor action. Biochemistry. 1998 Dec 15;37(50):17571-8.?
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