货号:A130952
同义名:
盐酸阿霉素
/ Hydroxydaunorubicin hydrochloride; Doxorubicin (hydrochloride)
Doxorubicin HCl is an antibiotic agent that inhibits DNA topoisomerase II and induces DNA damage and apoptosis in tumor cells.
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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+% | |||||||||||||||||
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。 |
产品名称 | Autophagy ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SBI-0206965 |
+++
ULK1, IC50: 108 nM ULK2, IC50: 711 nM |
95% | |||||||||||||||||
Hydroxychloroquine sulfate | ✔ | 99% | |||||||||||||||||
Valproic acid sodium | ✔ | HDAC | 97% | ||||||||||||||||
PFK-015 |
++
PFKFB3, IC50: 207 nM |
99%+ | |||||||||||||||||
MRT68921 HCl |
++++
ULK1, IC50: 2.9 nM ULK2, IC50: 1.1 nM |
99%+ | |||||||||||||||||
ROC-325 | ✔ | 99%+ | |||||||||||||||||
Autophinib |
+++
Autophagy, IC50: 40 nM |
99% | |||||||||||||||||
Lys05 | ✔ | 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 | Doxorubicin hydrochloride, a potent chemotherapeutic agent and cytotoxic anthracycline antibiotic, inhibits human DNA topoisomerase I and II with IC50 values of 0.8 µM and 2.67 µM, respectively. It diminishes the basal phosphorylation of AMPK and acetyl-CoA carboxylase, leading to the induction of apoptosis and autophagy[1][2][3]. |
细胞系 | 浓度 | 检测类型 | 检测时间 | 活性说明 | 数据源 |
16HBE | 10 μM | Growth Inhibition Assay | 72 h | GI50=0.18 μM | 24650643 |
1A9 | Cytotoxic Assay | ED50=0.02 μM | 17591444 | ||
2008/MRP1 | Cytotoxic Assay | 5 d | IC50=0.577 μM | 19725578 | |
2008/P | Cytotoxic Assay | 5 d | IC50=0.063 μM | 19725578 | |
Animal study | Doxorubicin hydrochloride, in animal studies, is utilized to develop models of heart failure. When administered alone, neither Doxorubicin at a dosage of 2 mg/kg nor Zoledronic acid at 100 μg/kg significantly reduces the final tumor volume compared to saline treatment. However, mice receiving a combined treatment of Doxorubicin and Zoledronic acid show significantly smaller final tumor volumes than those treated with Doxorubicin alone[6].Administering Doxorubicin (ranging from 4% to 20% concentration; via a single intrastriatal injection) demonstrates neurotoxic effects in Sprague-Dawley mice[7].Doxorubicin can be attached to gold nanoparticles (Au NPs) through pH-sensitive bonds in acidic environments, enhancing its ability to cross the blood-brain barrier. The maximum absorption wavelength for this conjugation is 528 nm[9]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
1.72mL 0.34mL 0.17mL |
8.62mL 1.72mL 0.86mL |
17.24mL 3.45mL 1.72mL |
CAS号 | 25316-40-9 |
分子式 | C27H30ClNO11 |
分子量 | 579.98 |
SMILES Code | COC1=CC=CC2=C1C(C3=C(C(O)=C4C[C@](O)(C[C@@H](C4=C3O)O[C@H]5C[C@@H]([C@@H]([C@@H](O5)C)O)N)C(CO)=O)C2=O)=O.[H]Cl |
MDL No. | MFCD00077757 |
别名 | 盐酸阿霉素 ;Hydroxydaunorubicin hydrochloride; Doxorubicin (hydrochloride); DOX; Hydroxydaunorubicin HCl; NSC 123127; Adriamycin; Doxorubicin HCl |
运输 | 蓝冰 |
InChI Key | MWWSFMDVAYGXBV-RUELKSSGSA-N |
Pubchem ID | 443939 |
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 |
动物实验配方 |
PO 0.5% CMC-Na 50 mg/mL suspension |