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Merck
모든 사진(2)

주요 문서

D1515

Sigma-Aldrich

Doxorubicin hydrochloride

98.0-102.0% (HPLC)

동의어(들):

Adriamycin, DOX, Hydroxydaunorubicin hydrochloride

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About This Item

실험식(Hill 표기법):
C27H29NO11 · HCl
CAS Number:
Molecular Weight:
579.98
Beilstein:
4229251
EC Number:
MDL number:
UNSPSC 코드:
51281818
PubChem Substance ID:
NACRES:
NA.76

가격 및 재고 정보를 현재 이용할 수 없음

생물학적 소스

synthetic (organic)

Quality Level

분석

98.0-102.0% (HPLC)

양식

powder

mp

216 °C (dec.) (lit.)

solubility

water: 50.0-52.0 mg/mL, clear, orange to red

항생제 활성 스펙트럼

viruses

동작 모드

DNA synthesis | interferes

저장 온도

2-8°C

SMILES string

Cl[H].COc1cccc2C(=O)c3c(O)c4C[C@](O)(C[C@H](O[C@H]5C[C@H](N)[C@H](O)[C@H](C)O5)c4c(O)c3C(=O)c12)C(=O)CO

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일반 설명

Doxorubicin hydrochloride (DOX) is an anthracycline antibiotic isolated from Streptomyces peucetius var. caesius.[1][2] The water soluble anti-cancer agent DOX[3] is a hydroxy derivative of daunorubicin.[4]

Doxorubicin also leads to the generation of reactive oxygen species (ROS), which further damage DNA, proteins, and membranes. It exerts cytotoxic, antitumor, anticancer, and antineoplastic activity and finds application in cancer, metabolomics, cell biology, and biochemical research.[4]

애플리케이션

Doxorubicin hydrochloride has been used:
  • in cell viability assays[5]
  • MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) assay[6]
  • as a drug in polymeric PLGA-based microparticulate drug delivery[7]
  • to develop doxorubicin-resistant HepG2 cells (HepG2-DR) and K562 cells (K562-DR)[8]

생화학적/생리학적 작용

Naturally fluorescent anthracycline antibiotic, anticancer drug. Doxorubicin is a substrate of MRP1 which was first cloned from a DOX-resistant lung cancer cell line. Fluorescent property has been exploited for the measurement of drug efflux pump activities as well as resolving the important question of intracellular localization of various multidrug resistance proteins and the role of subcellular organelles (Golgi and lysosome) in the sequestration of drugs and its implication in drug resistant phenotypes.
Substrate of MRP1; used for measurement of drug efflux pump activities. Doxorubicin hydrochloride (DOX) inhibits topoisomerase II by intercalating between base pairs and by inducing strand breaks, resulting in the inhibition of nucleic acid and protein synthesis.[1] It also contributes to the formation of free radicals for the disruption of membrane lipids and DNA strands.[1]

특징 및 장점

  • High-quality antibiotic suitable for multiple research applications
  • Ideal for Cell Biology, Metabolomics, and Biochemical research.

제조 메모

Soluble in water and in isotonic sodium chloride solution, slightly soluble in methanol. Practically insoluble in chloroform, ether, and in other organic solvents.

저장 및 안정성

Tightly closed. Dry. Keep in a well -ventilated place. Keep locked up or in an area accessible

기타 정보

For additional information on our range of Biochemicals, please complete this form.
Keep container tightly closed in a dry and well-ventilated place. Moisture sensitive. Light sensitive.

관련 제품

제품 번호
설명
가격

호환 제품

픽토그램

Health hazardExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral - Carc. 1B - Muta. 1B - Repr. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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시험 성적서(COA)

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이 제품을 이미 가지고 계십니까?

문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Poly (ethylene glycol)-conjugated multi-walled carbon nanotubes as an efficient drug carrier for overcoming multidrug resistance
Cheng J, et al.
Toxicology and Applied Pharmacology, 250(2), 184-193 (2011)
Current Pharmaceutical Design (1999)
The release behavior of doxorubicin hydrochloride from medicated fibers prepared by emulsion-electrospinning
Xu X, et al.
European Journal of Pharmaceutics and Biopharmaceutics, 70(1), 165-170 (2008)
Consumers Guide to Cancer Drugs (2004)
In vitro study of anticancer drug doxorubicin in PLGA-based microparticles
Lin R, et al.
Biomaterials, 26(21), 4476-4485 (2005)

문서

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