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Phleomycin
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Phleomycin

CAS: 11006-33-0

Ref. 3D-AP106412

5mgTo inquire
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Estimated delivery in United States, on Monday 25 Nov 2024

Product Information

Name:
Phleomycin
Synonyms:
  • 2'-{5-acetyl-15-(6-amino-2-{3-amino-1-[(2,3-diamino-3-oxopropyl)amino]-3-oxopropyl}-5-methylpyrimidin-4-yl)-13-[{[(2R,3S,4S,5S,6S)-3-{[(2S,3R,4R,5S)-4-carbamoyl-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)-3-methyltetrahydro-2H-pyran-2-yl]oxy}(1H-imidazol-5-yl)methyl]-9-hydroxy-8,10-dimethyl-4,7,12,15-tetraoxo-3,6,11,14-tetraazapentadec-1-yl}-4',5'-dihydro-2,4'-bi-1,3-thiazole-4-carboxamide (non-preferred name)
  • Phleomycin Streptomyces verticillus
Description:

Phleomycin is an antibiotic that is used to treat various types of infections caused by opportunistic fungi, such as Aspergillus, Candida, and Cryptococcus. Phleomycin inhibits the nuclear factor kappa-light-chain-enhancer (NF-κB), which is a transcription factor that plays a crucial role in the expression of genes involved with cell proliferation and differentiation. It binds to DNA near the NF-κB binding site and prevents it from binding to DNA. This inhibition causes decreased synthesis of proteins that are responsible for cell proliferation and differentiation. Phleomycin also has carcinogenic potential in mice and may cause chromosomal aberrations in cells. The high resistance observed in some fungal species may be due to its ability to form homologous pairs with dna.
Phleomycin is synthesized from erythromycin through a series of chemical reactions involving acetylation, oxidation, acetylation again, and finally cle

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
1,326.38 g/mol
Formula:
C51H75N17O21S2
Purity:
Min. 95%
MDL:
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EINECS:
Merck:
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Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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