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20830-81-3
  • names:

    Daunorubicin

  • CAS號:

    20830-81-3

    MDL Number: MFCD00866340
  • MF(分子式): C27H29NO10 MW(分子量): 527.52
  • EINECS:244-069-7 Reaxys Number:No data available
  • Pubchem ID:30323 Brand:BIOFOUNT
柔紅霉素
柔紅霉素(20830-81-3,Daunorubicin)屬于第一代蒽環(huán)類抗腫瘤抗生素,又稱正定霉素,柔毛霉素,紅比霉素,紅保霉素,佐柔比星,紅比脘,被廣泛應用于腫瘤的臨床治療Chemicalbook。其作用機制在于細胞的核酸合成過程,能直接與DNA結合,阻礙DNA合成和依賴DNA的RNA合成反應,對RNA的影響尤為明顯,并可選擇性作用于嘌呤核苷。
貨品編碼 規(guī)格 純度 價格 (¥) 現(xiàn)價(¥) 特價(¥) 庫存描述 數(shù)量 總計 (¥)
YZM000922-50mg 50mg 99.9% ¥ 1620.00 ¥ 1620.00 Backorder
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0.00
YZM000922-10mg 10mg 99.9% ¥ 502.00 ¥ 502.00 Backorder
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中文別名 柔紅霉素(20830-81-3,Daunorubicin),道諾霉素雜質(zhì),柔紅比星雜質(zhì),紅保霉素,紅比霉素,紅衛(wèi)霉素,柔毛霉素
英文別名 Daunorubicin,20830-81-3,Daunomycin,Acetyladriamycin,Leukaemomycin C
CAS號 20830-81-3
Inchi InChI=1S/C27H29NO10/c1-10-22(30)14(28)7-17(37-10)38-16-9-27(35,11(2)29)8-13-19(16)26(34)21-20(24(13)32)23(31)12-5-4-6-15(36-3)18(12)25(21)33/h4-6,10,14,16-17,22,30,32,34-35H,7-9,28H2,1-3H3/t10-,14-,16-,17-,22+,27-/m0/s1
InchiKey STQGQHZAVUOBTE-VGBVRHCVSA-N
分子式 Formula C27H29NO10
分子量 Molecular Weight 527.52
溶解度Solubility
性狀 紅色結晶性或無定形粉末
儲藏條件 Storage conditions 庫房通風低溫干燥; 輕裝輕卸、與氧化劑和酸類分開存放

柔紅霉素(20830-81-3,Daunorubicin)毒性測試:
生物 測試類型 路線 報告劑量(標準化劑量) 影響 來源
human LDLo oral 6 mg/kg (6 mg/kg) CARDIAC: OTHER CHANGES Toxicology of Drugs and Chemicals, Deichmann, W.B., New York, Academic Press, Inc., 1969, -(521), 1969
rat LD50 oral 336 mg/kg (336 mg/kg)   Yakkyoku. Pharmacy., 25(573), 1974
rat LD50 intraperitoneal 20 mg/kg (20 mg/kg)   Advances in Teratology., 3(181), 1968
rat LD50 subcutaneous 33200 ug/kg (33.200000000000003 mg/kg)   Yakkyoku. Pharmacy., 25(573), 1974
rat LD50 intravenous 13 mg/kg (13 mg/kg) BLOOD: OTHER CHANGES; SKIN AND APPENDAGES (SKIN): HAIR: OTHER National Cancer Institute Report., -(304), 1967

柔紅霉素(20830-81-3,Daunorubicin)實驗注意事項:
1.實驗前需戴好防護眼鏡,穿戴防護服和口罩,佩戴手套,避免與皮膚接觸。
2.實驗過程中如遇到有毒或者刺激性物質(zhì)及有害物質(zhì)產(chǎn)生,必要時實驗操作需要手套箱內(nèi)完成以免對實驗人員造成傷害
3.實驗后產(chǎn)生的廢棄物需分類存儲,并交于專業(yè)生物廢氣物處理公司處理,以免造成環(huán)境污染

Daunorubicin(20830-81-3) Experimental considerations:
1. Wear protective glasses, protective clothing and masks, gloves, and avoid contact with the skin during the experiment.
2. The waste generated after the experiment needs to be stored separately, and handed over to a professional biological waste gas treatment company to avoid environmental pollution.

Tag:柔紅霉素(20830-81-3,Daunorubicin),柔紅霉素試劑,柔紅霉素抑制劑,柔紅霉素的純度,柔紅霉素的作用,柔紅霉素的用途,柔紅霉素的效果,柔紅霉素的使用,柔紅霉素的合成,柔紅霉素的生產(chǎn),柔紅霉素的MSDS,柔紅霉素COA,柔紅霉素的外觀
產(chǎn)品說明 柔紅霉素(20830-81-3,Daunorubicin)是具有有效抗腫瘤活性的DNA拓撲異構酶II的抑制劑.
IntroductionDaunorubicin (20830-81-3,柔紅霉素) is atopoisomerase IIinhibitor with potent antineoplastic activities.
Application1Daunorubicin (20830-81-3,柔紅霉素) inhibitesDNA and RNA synthesisin sensitive and resistant Ehrlich ascites tumor cells.
Application2
Application3
1. Adsorptive Stripping Voltammetric Determination of Low Levels of Daunorubicin
Joseph Wang,* Meng Shan Lin and Vince Villa. ANALYST, SEPTEMBER 1987, VOL. 112
The anthracycline antibiotic daunorubicin is a widely used anticancer drug, owing to its clinical efficacy against a wide range of malignancies. This drug was the first compound to show therapeutic effects in the treatment of leukaemia in man. The cytotoxic activity of daunorubicin against cancerous cells is hampered by dose-related cardiotoxic effects. Conse-quently, a highly sensitive analytical method is essential for the evaluation and administration of this drug. Various analytical methods have been employed for this purpose, including fluorescence, radioimmunoassayn and liquid chromatographic techniques. The complex redox activity of daunorubicin, and related anthracycline antibiotics, was investigated by Rao et aZ. who discussed the redox process in relation to the antineoplastic activity of these drugs. Anthracycline antibiotics contain two electroactive moieties: a reducible quinone group and an oxidisable hydroquinone centre. The reduction of the quinone group was used for polarographic measurements of the structurally similar anthracycline, Adriamycin, down to micromolar concentrations and for measuring the binding of anthracyclines to DNA. Trace amounts of daunorubicin have not yet been determined by voltammetric procedures.
Daunorubicin/Cytarabine Liposome: A Review in Acute Myeloid Leukaemia
Disposition of Liposomal Daunorubicin During Cotreatment with Cytarabine in Patients with Leukaemia
Distribution of anticancer antibiotic daunomycin in the rat heart and kidney revealed by immunocytochemistry using monoclonal antibodies
Pharmacokinetics of liposomal daunorubicin (DaunoXome) during a phase I-II study in children with relapsed acute lymphoblastic leukaemia
Overview on in vitro and in vivo investigations of nanocomposite based cancer diagnosis and therapeutics
A. P. Subramanian, S. K. Jaganathan* and Eko Supriyanto. RSC Adv.,2015, 5, 72638–72652
Nanocomposite made of nano Fe3O4 and polylactide nanofibers loaded with daunorubicin to cause the induction of cell death of leukemia cancer cells was reported. The number of viable cells decreased when treated with the daunorubicin loaded nanocomposite. The cellular uptake was demonstrated by the inter-cellular green fluorescence emitted by the daunorubicin drug. The cell inhibition with the 9.93 *10-7 and 1.99 * 10-6 mol L-1 daunorubicin concentrations in the presence of Fe3O4 nanoparticles or PLA nanofibers produced no significant di?erence fromthat of the cell treated with daunorubicin alone. However, for daunorubicin concentrations at 9.93 * 10-7 and 1.99 * 10-6 mol L-1, the inhibition rates increased to 31% and 46% for the cell system cultured with daunorubicin and Fe3O4–PLA. Chen et al. developed a poly(lactic acid) (PLA) based nanocomposites for targeted drug delivery of daunorubicin to the leukemia K562 cells.
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