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                同义名:
                    
                        
                            
                                NSC 241240; CBDCA
                            
                        
                    
                
                
                
                    
                     
                
            
Carboplatin (NSC 241240)通过与DNA结合,阻碍DNA合成,从而阻碍复制和转录过程,最终导致细胞死亡。Carboplatin是从顺铂(CDDP)衍生出来的,是一种有效的抗癌剂。
 
                                 
                                
                            

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| 产品名称 | DNA synthesis ↓ ↑ | helicase ↓ ↑ | RdRp ↓ ↑ | ribonucleotide reductase ↓ ↑ | tRNA synthetase ↓ ↑ | YB-1 ↓ ↑ | 其他靶点 | 纯度 | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Fexinidazole | ✔ | 98% | |||||||||||||||||
| Daptomycin | ✔ | 98% | |||||||||||||||||
| Blasticidin S·HCl | ✔ | 98% | |||||||||||||||||
| Metronidazole | ✔ | 98% | |||||||||||||||||
| Daunorubicin HCl | +++ DNA synthesis, Ki: 20 nM | 98% | |||||||||||||||||
| Triglycidyl isocyanurate | ✔ | p53 | 98+% | ||||||||||||||||
| Nedaplatin | ✔ | 99%+ | |||||||||||||||||
| Oxolinic acid | ✔ | 98+% | |||||||||||||||||
| Bendamustine | ✔ | 98+% | |||||||||||||||||
| Trifluridine | ✔ | 98% | |||||||||||||||||
| Robinetin | ✔ | 99%+ | |||||||||||||||||
| Carboplatin | ✔ | 99% | |||||||||||||||||
| Cidofovir | ✔ | 99% | |||||||||||||||||
| Cisplatin | ✔ | 99% | |||||||||||||||||
| Cytarabine | ++++ DNA synthesis, IC50: 16 nM | 98% | |||||||||||||||||
| Acelarin | ++++ DNA synthesis, EC50: 0.2 nM | 99%+ | |||||||||||||||||
| Oxaliplatin | ✔ | 98% | |||||||||||||||||
| YK-4-279 | ✔ | 99%+ | |||||||||||||||||
| ML216 | + BLM636-1298, IC50: 0.97 μM BLMfull-length, IC50: 2.98 μM | 99%+ | |||||||||||||||||
| RK-33 | ✔ | 98% | |||||||||||||||||
| Brr2-IN-3 | ✔ | 99%+ | |||||||||||||||||
| Phen-DC3 Trifluoromethanesulfonate | ✔ | 95% | |||||||||||||||||
| Favipiravir | ✔ | 99% | |||||||||||||||||
| Suramin sodium salt | ++ RdRp, IC50: 0.26 μM | 99%+ | |||||||||||||||||
| Clofarabine | ++ Ribonucleotide reductase, IC50: 65 nM | 97% | |||||||||||||||||
| Didox | ✔ | 98% | |||||||||||||||||
| (E)-3-AP | ✔ | 99% | |||||||||||||||||
| Halofuginone | +++ prolyl-tRNA synthetase, Ki: 18.3nM | 99%+ | |||||||||||||||||
| BC-LI-0186 | +++ Leucyl-tRNA synthetase, Kd: 42.1 nM Leucyl-tRNA synthetase, IC50: 46.11 nM | 98% | |||||||||||||||||
| SU056 | + YB-1, IC50: 1.73 μM | 98% | |||||||||||||||||
| 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。 | |||||||||||||||||||
| 靶点 | 
 | 
| 描述 | Carboplatinum is the second generation platinum anticancer drug with nonspecific cell cycle and similar effect to alkylating agent. A decrease in carboplatinum hemotoxicity was detected in experiments on C57B1 mice treated with the drug in combination with indralin (urgent radioprotector). Carboplatinum in a dose of 125 mg/kg, injected intraperitoneally, caused 80-100% death; the median term of death was 6 days (3-17)[3]. S. typhimurium A1-R and CAR (Carboplatinum) moderately inhibited tumor growth compared to the untreated group on day 15 (P < 0.001 and P < 0.001, respectively). S. typhimurium A1-R combined with CAR inhibited the tumor growth significantly more compared to S. typhimurium A1-R monotherapy or CAR monotherapy on day 15 (P = 0.004 and P = 0.001, respectively)[4]. In vitro synergistic efficacy of MK-2206 when combined with carboplatinum and paclitaxel in the three cell lines examined. Efficacy was dose dependent[5]. Sequential therapy with carboplatin plus paclitaxel followed by topotecan, all given at standard doses, is feasible and provides favorable response rates[6]. | 
| Administration | Dosage | Frequency | Description | References | ||
| Nude mice | Breast cancer dormancy model | Intraperitoneal injection | 2 mg/kg | Administered on days 3 and 5, duration of 7 days | KMT2B and KMT2D KD BCCs showed significantly reduced metastasis to the brain, indicating that targeting H3K4 can reduce brain metastasis. | Cell Commun Signal. 2024 Feb 12;22(1):119. | 
| Nude mice | OVCAR5 xenograft model | Intraperitoneal injection | 50 mg/kg | Once a week for 4 weeks | To evaluate the effect of PFK158 in combination with carboplatin, results showed that PFK158 combined with carboplatin significantly inhibited tumor growth and metastasis | J Exp Clin Cancer Res. 2021 Jun 3;40(1):182. | 
| BALB/c nude mice | IGROV1 xenograft tumor model | Intraperitoneal injection | 20 mg/kg or 60 mg/kg | Every 2 days for 2 weeks | Carboplatin treatment significantly increased SENP1 expression in IGROV1 xenograft tumors | Cell Death Dis. 2021 Apr 1;12(4):341 | 
| 细胞系 | 浓度 | 检测类型 | 检测时间 | 活性说明 | 数据源 | 
| 3AO | Growth Inhibition Assay | 72 h | IC50=63.4 μM | 25520132 | |
| 4T1 | Growth Inhibition Assay | IC50=84.62 ± 30.05 μM μM | 25277461 | ||
| A2780 | Growth Inhibition Assay | 72 h | IC50=145.7 μM | 25520132 | |
| A2780 | Growth Inhibition Assay | IC50=14.0 ± 1.4 μM | 24209693 | ||
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 2.69mL 0.54mL 0.27mL | 13.47mL 2.69mL 1.35mL | 26.94mL 5.39mL 2.69mL | |
| CAS号 | 41575-94-4 | 
| 分子式 | C6H12N2O4Pt | 
| 分子量 | 371.25 | 
| SMILES Code | O=C1C2(CCC2)C(O[Pt]O1)=O.N.N | 
| MDL No. | MFCD00070464 | 
| 别名 | NSC 241240; CBDCA; Ribocarbo; Platinwas; Paraplatine; JM-8 | 
| 运输 | 蓝冰 | 
| InChI Key | VSRXQHXAPYXROS-UHFFFAOYSA-N | 
| Pubchem ID | 426756 | 
| 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,2-8°C | 
| 溶解方案 | H2O: 10 mg/mL(26.94 mM),配合低频超声,并水浴加热至45℃助溶 
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