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Daunorubicin (hydrochloride)

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    Daunorubicin (hydro<wbr>chloride)
  • Daunorubicin (hydro<wbr>chloride)
Cat No: 14159
Cayman

Daunorubicin is an antitumor antibiotic.{22542} At 0.2-1μM, daunorubicin induces apoptosis in mature monocytic U937 and myelocytic HL-60 acute myeloid leukemia (AML) cells. However, immature AML cells (CD 34+-KG1a, -KG1, or -HEL cells) appear resistan...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 8S-acetyl-10S-[(3-amino-2,3,6-trideoxy-?-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-5,12-naphthacenedione, monohydrochloride
Correlated keywords:
  • RP13057 NDC00824155 00824155 NDC0082 U 937 HL60 CD34 CD34+ KG 1a KG 1 MEKK SEK MEKK1SEK1 MEKK1SEK1JNK AP1
Product Overview:
Daunorubicin is an antitumor antibiotic.{22542} At 0.2-1μM, daunorubicin induces apoptosis in mature monocytic U937 and myelocytic HL-60 acute myeloid leukemia (AML) cells. However, immature AML cells (CD 34+-KG1a, -KG1, or -HEL cells) appear resistant to apoptosis at similar concentrations.{22542} In mature AML cells, daunorubicin has been shown to trigger a reactive oxygen species-dependent sphingomyelin-ceramide pathway that activates the MEKK1-SEK1-JNK cascade leading to enhanced DNA binding activity of the transcription factor AP-1.{22542,5396}
Size 5 mg
Shipping dry ice
CAS Number 23541-50-6
Molecular Formula C27H29NO10 • HCl
SMILES COC1=C(C(C(C(O)=C([C@@H](O[C@@]2([H])C[C@H](N)[C@H](O)[C@H](C)O2)C[C@@](C(C)=O)(O)C3)C3=C4O)=C4C5=O)=O)C5=CC=C1.Cl
Molecular Weight 564
Formulation A crystalline solid
Purity ≥98%
Custom Code 2907.29
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

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ISO Guide 34:2009

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