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32886-15-0

32886-15-0 Structure

32886-15-0 Structure
IdentificationBack Directory
[Name]

Neoenactin M1
[CAS]

32886-15-0
[Synonyms]

G-26146
Brn 2394950
Neoenactin M1
L-2-Amino-N-(14-methyl-3,10-dioxopentadecyl)hydracrylohydroxamic acid
(2S)-2-Amino-N,3-dihydroxy-N-(14-methyl-3,10-dioxopentadecyl)propanamide
Hydracrylohydroxamic acid, 2-amino-N-(14-methyl-3,10-dioxopentadecyl)-, L-
Propanamide, 2-amino-N,3-dihydroxy-N-(14-methyl-3,10-dioxopentadecyl)-, (S)-
[Molecular Formula]

C19H36N2O5
[MDL Number]

MFCD01722759
[MOL File]

32886-15-0.mol
[Molecular Weight]

372.502
Chemical PropertiesBack Directory
[Boiling point ]

578.1±60.0 °C(Predicted)
[density ]

1.094±0.06 g/cm3(Predicted)
[pka]

8.46±0.50(Predicted)
Hazard InformationBack Directory
[Uses]

Lipoxamycin is an antifungal antibiotic and a potent serine palmitoyltransferase inhibitor with an IC50 of 21 nM[1][2].
[in vivo]

Lipoxamycin is highly toxic in mice when applied subeutaneously or topically. Toxicity may be mechanism based, since studies with a Chinese hamster ovary cell mutant have shown that the serine palmitoyltransferase is an essential enzymein mammalian cells[1].

[References]

[1] S M Mandala, et al. Inhibition of Serine Palmitoyl-Transferase Activity by Lipoxamycin. J Antibiot (Tokyo). 1994 Mar;47(3):376-9. DOI:10.7164/antibiotics.47.376
[2] H A Whaley. The Structure of Lipoxamycin, a Novel Antifungal Antibiotic. J Am Chem Soc. 1971 Jul 28;93(15):3767-9. DOI:10.1021/ja00744a036
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