Myriocin

For research use only. Not for therapeutic Use.

  • CAT Number: R056414
  • CAS Number: 35891-70-4
  • Molecular Formula: C21H39NO6
  • Molecular Weight: 401.54
  • Purity: ≥95%
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Myriocin(Cat No.:R056414)is a potent, selective inhibitor of serine palmitoyltransferase (SPT), the key enzyme in sphingolipid biosynthesis. By inhibiting SPT, Myriocin reduces the production of sphingosine-1-phosphate (S1P) and other sphingolipids, which play crucial roles in cell growth, survival, and inflammation. This makes Myriocin valuable in studying sphingolipid metabolism and its involvement in various diseases, including cancer, neurodegenerative disorders, and autoimmune conditions. It is commonly used in research to explore the therapeutic potential of modulating sphingolipid pathways for the treatment of these diseases.


Catalog Number R056414
CAS Number 35891-70-4
Synonyms

(2S,3R,4R,6E)-2-Amino-3,4-dihydroxy-2-(hydroxymethyl)-14-oxo-6-eicosenoic Acid; [2S-(2R*,3S*,4S*,6E)]-2-Amino-3,4-dihydroxy-2-(hydroxymethyl)-14-oxo-6-eicosenoic Acid; (+)-Myriocin; ISP-I; NSC 177379; Thermozymocidin; (2S,3R,4R)-(E)-2-Amino-3,4-dih

Molecular Formula C21H39NO6
Purity ≥95%
Target HCV
Solubility Soluble in DMSO
Storage Store at -20°C
IUPAC Name (E,2S,3R,4R)-2-amino-3,4-dihydroxy-2-(hydroxymethyl)-14-oxoicos-6-enoic acid
InChI InChI=1S/C21H39NO6/c1-2-3-4-10-13-17(24)14-11-8-6-5-7-9-12-15-18(25)19(26)21(22,16-23)20(27)28/h9,12,18-19,23,25-26H,2-8,10-11,13-16,22H2,1H3,(H,27,28)/b12-9+/t18-,19+,21+/m1/s1
InChIKey ZZIKIHCNFWXKDY-GNTQXERDSA-N
SMILES CCCCCCC(=O)CCCCCC/C=C/C[C@H]([C@@H]([C@@](CO)(C(=O)O)N)O)O
Reference

Myriocin, a new antifungal antibiotic from Myriococcum albomyces. Kluepfel D. J. Antibiot. 1972, 25, 109.<br/><br/>Serine palmitoyltransferase is the primary target of a sphingosine-like immunosuppressant, ISP-1/myriocin. Miyake Y. et al. , Biochem. Biophys. Res. Commun. 1995, 211, 396. <br/><br/>Fungal metabolites. Part 12. Potent immunosuppressant, 14-deoxomyriocin, (2S,3R,4R)-(E)-2-amino-3,4-dihydroxy-2-hydroxymethyleicos-6-enoic acid and structure-activity relationships of myriocin derivatives. Fujita T. et al. , J. Biol. Chem. 2005, 280, 10284.</span></p>

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