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                同义名:
                    
                        
                            
                                (±)-10-HCPT; Hydroxycamptothecine
                            
                        
                    
                
                
                
                    
                     
                
            
(±)-10-Hydroxycamptothecin是一种拓扑异构酶I抑制剂,具有抗癌活性,能影响组蛋白H1和H3的磷酸化。
 HazMat Fee +
 HazMat Fee + There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.
| Type | HazMat fee for 500 gram (Estimated) | 
| Excepted Quantity | USD 0.00 | 
| Limited Quantity | USD 15-60 | 
| Inaccessible (Haz class 6.1), Domestic | USD 80+ | 
| Inaccessible (Haz class 6.1), International | USD 150+ | 
| Accessible (Haz class 3, 4, 5 or 8), Domestic | USD 100+ | 
| Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ | 
 
                                 
                                
                            

| 规格 | 价格 | 会员价 | 库存 | 数量 | |||
|---|---|---|---|---|---|---|---|
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| 产品名称 | Topo I ↓ ↑ | Topo II ↓ ↑ | Topo IV ↓ ↑ | Topoisomerase ↓ ↑ | 其他靶点 | 纯度 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Ellagic acid | ✔ | 98% | |||||||||||||||||
| β-Lapachone | ✔ | 99%+ | |||||||||||||||||
| (s)-10-hydroxycamptothecin | ✔ | 98+% | |||||||||||||||||
| Camptothecin | ++ Topo I, IC50: 0.68 μM | 98% | |||||||||||||||||
| Betulinic acid | ++ Eukaryotic topoisomerase I, IC50: 5 μM | 98% | |||||||||||||||||
| Topotecan | ++++ Topo I (DU-145 Luc cells), IC50: 2 nM Topo I (MCF-7 Luc cells), IC50: 13 nM | 98% | |||||||||||||||||
| Irinotecan HCl Trihydrate | ✔ | 98% | |||||||||||||||||
| SN-38 | ✔ | 98% | |||||||||||||||||
| Levofloxacin hydrate | ✔ | 98% | |||||||||||||||||
| Dexrazoxane | ✔ | 99%+ | |||||||||||||||||
| Ofloxacin | ✔ | 98+% | |||||||||||||||||
| Enoxacin | ✔ | 99%+ | |||||||||||||||||
| Flumequine | + Topo II, IC50: 15 μM | 98% | |||||||||||||||||
| Levofloxacin | ✔ | 97% | |||||||||||||||||
| Etoposide | ✔ | 98% | |||||||||||||||||
| Pefloxacin mesylate dihydrate | ✔ | 99.5% | |||||||||||||||||
| Marbofloxacin | ✔ | 98+% | |||||||||||||||||
| Voreloxin HCl | ✔ | 98% | |||||||||||||||||
| Mitoxantrone 2HCl | ✔ | PKC | 98% | ||||||||||||||||
| Nalidixic acid | ✔ | 98% | |||||||||||||||||
| Doxorubicin | ✔ | 97% | |||||||||||||||||
| Novobiocin sodium | ✔ | 95% | |||||||||||||||||
| Amonafide | ✔ | 99%+ | |||||||||||||||||
| Pirarubicin | ✔ | 98%+ | |||||||||||||||||
| Idarubicin HCl | +++ Topo II (MCF-7 cells), IC50: 3.3 ng/mL | 99%+ | |||||||||||||||||
| Genistein | ✔ | EGFR | 98% | ||||||||||||||||
| Teniposide | ✔ | 98% | |||||||||||||||||
| Moxifloxacin | ✔ | 98% | |||||||||||||||||
| Ciprofloxacin | ✔ | 98% | |||||||||||||||||
| Clinafloxacin | ✔ | 99% | |||||||||||||||||
| Gatifloxacin | ✔ | 98% | |||||||||||||||||
| Daunorubicin HCl | +++ DNA synthesis, Ki: 20 nM | 98% | |||||||||||||||||
| Epirubicin HCl | ✔ | 99%+ | |||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| 描述 | 10-Hydroxycamptothecin (HCPT) is an inhibitor of topoisomerase I and can affect phosphorylation of histone H1 and H3 with anticancer activity. It can be isolated from camptotheca acuminate. Gel electrophoresis found that HCPT had a selectively inhibitory effect on the phosphorylation of histone H1 and H3, but less effect on the other kinds of histones. In vivo, HCPT also exhibited a suppressive effect on histone H1 and H3 phosphorylation[1]. After treatment with HCPT at differentiation-inducing concentrations 5-20 mg/L for 6 d, Hep G2 cells were mainly arrested at G2/M phase and the PCNA expression rate was lower than that of control cells. When Hep G2 cells grew in a medium containing HCPT 5 mg/L for 6 d, the p53 expression level markedly increased in comparison with the control cells. The telomerase activity did not change in Hep G2 cells treated with HCPT 5-20 mg/L for 8 d[2]. HCPT exhibited adverse effects on mouse oocyte maturation and quality, and MT (Melatonin) administration alleviated the negative influence of HCPT[3]. | 
| Concentration | Treated Time | Description | References | |
| LO2 cells | 100 μM | 48 h | Evaluate the cytotoxicity of HpYss on normal LO2 cells, with an IC50 significantly lower than free HCPT. | Bioact Mater. 2021 Jul 24;9:120-133. | 
| A549 cells | 100 μM | 48 h | Evaluate the cytotoxicity of HpYss on A549 cells, with an IC50 similar to free HCPT. | Bioact Mater. 2021 Jul 24;9:120-133. | 
| PC-3 cells | 100 μM | 48 h | Evaluate the cytotoxicity of HpYss on PC-3 cells, with an IC50 similar to free HCPT. | Bioact Mater. 2021 Jul 24;9:120-133. | 
| HeLa cells | 100 μM | 48 h | Evaluate the cytotoxicity of HpYss on HeLa cells, with an IC50 significantly lower than free HCPT. | Bioact Mater. 2021 Jul 24;9:120-133. | 
| MCF-7 cells | 100 μM | 48 h | Evaluate the cytotoxicity of HpYss on MCF-7 cells, with an IC50 significantly lower than free HCPT. | Bioact Mater. 2021 Jul 24;9:120-133. | 
| HepG2 cells | 100 μM | 48 h | Evaluate the cytotoxicity of HpYss on HepG2 cells, with an IC50 of 80 nM, significantly lower than other control groups. | Bioact Mater. 2021 Jul 24;9:120-133. | 
| Administration | Dosage | Frequency | Description | References | ||
| BALB/c nude mice | HepG2 xenograft model | Intravenous injection | 3 mg/kg HCPT-equivalent | Once every three days, total three times | Evaluate the antitumor efficacy of HpYss in HepG2 xenograft model, significantly inhibiting tumor growth. | Bioact Mater. 2021 Jul 24;9:120-133. | 
| BALB/c nude mice | Orthotopic glioma model | Tail intravenous injection | 5 mg/kg HCPT | Administered at Days 7, 9, 12, 15, 18 and 21 | To evaluate the anti-glioma effect of HCPT-M-CA-NPs in the glioma model, the results showed that the median survival time of the HCPT-M-CA-NPs group (25.5 days) was significantly longer than that of the free HCPT group (17.0 days) and the HCPT-CA-NPs group (22.0 days). | Acta Pharm Sin B. 2019 Jul;9(4):843-857 | 
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 2.74mL 0.55mL 0.27mL | 13.72mL 2.74mL 1.37mL | 27.45mL 5.49mL 2.74mL | |
| CAS号 | 64439-81-2 | 
| 分子式 | C20H16N2O5 | 
| 分子量 | 364.35 | 
| SMILES Code | O=C1C(O)(CC)C2=C(CO1)C(N3CC4=CC5=CC(O)=CC=C5N=C4C3=C2)=O | 
| MDL No. | MFCD09027971 | 
| 别名 | (±)-10-HCPT; Hydroxycamptothecine; 10-Hydroxycamptothecin | 
| 运输 | 蓝冰 | 
| InChI Key | HAWSQZCWOQZXHI-UHFFFAOYSA-N | 
| Pubchem ID | 4330531 | 
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, inert atmosphere, store in freezer, under -20°C | 
| 溶解方案 | DMSO: 25 mg/mL(68.62 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶 
 
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