AmphotericinB

Modify Date: 2024-01-11 13:50:46

AmphotericinB Structure
AmphotericinB structure
Common Name AmphotericinB
CAS Number 36148-89-7 Molecular Weight 938.106
Density 1.3±0.1 g/cm3 Boiling Point 1102.6±65.0 °C at 760 mmHg
Molecular Formula C48H75NO17 Melting Point N/A
MSDS N/A Flash Point 620.6±34.3 °C

 Use of AmphotericinB


Amphotericin B methyl ester is the methyl ester derivative of the polyene antibiotic Amphotericin B (A634250). Amphotericin B methyl ester is the cholesterol-binding compound possesses significant antifungal activity. Amphotericin B methyl ester disrupts HIV-1 particle production and potently inhibits HIV-1 replication[1][2].

 Names

Name amphotericin B methyl ester
Synonym More Synonyms

 AmphotericinB Biological Activity

Description Amphotericin B methyl ester is the methyl ester derivative of the polyene antibiotic Amphotericin B (A634250). Amphotericin B methyl ester is the cholesterol-binding compound possesses significant antifungal activity. Amphotericin B methyl ester disrupts HIV-1 particle production and potently inhibits HIV-1 replication[1][2].
Related Catalog
In Vitro Amphotericin B methyl ester inhibits HIV-1 particle production with no significant effect on Gag binding to the plasma membrane, Gag association with lipid rafts, or Gag multimerization[1].
References

[1]. Waheed AA, et al. Inhibition of human immunodeficiency virus type 1 assembly and release by the cholesterol-binding compound amphotericin B methyl ester: evidence for Vpu dependence. J Virol. 2008 Oct;82(19):9776-81.

[2]. Keim GR, et al. Comparative toxicological studies of amphotericin B methyl ester and amphotericin B in mice, rats, and dogs. ntimicrob Agents Chemother. 1976 Oct;10(4):687-90.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 1102.6±65.0 °C at 760 mmHg
Molecular Formula C48H75NO17
Molecular Weight 938.106
Flash Point 620.6±34.3 °C
Exact Mass 937.503479
PSA 308.61000
LogP 1.63
Vapour Pressure 0.0±0.6 mmHg at 25°C
Index of Refraction 1.602

 Precursor & DownStream

Precursor  0

DownStream  1

 Synonyms

14,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylic acid, 33-[(3-amino-3,6-dideoxy-β-D-mannopyranosyl)oxy]-1,3,5,6,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-, methyl ester, (1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,19E,21E,23E,25E,27E,29E,31E,33R,35S,36R,37S)-
35-Deoxy Amphotericin B Methyl
methylamphotericin b
methyl (1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,19E,21E,23E,25E,27E,29E,31E,33R,35S,36R,37S)-33-[(3-amino-3,6-dideoxy-β-D-mannopyranosyl)oxy]-1,3,5,6,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-14,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylate
Methyl (1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,19E,21E,23E,25E,27E,29E,31E,33R,35S,36R,37S)-33-[(3-amino-3,6-dideoxy-β-D-mannopyranosyl)oxy]-1,3,5,6,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-14, 39-dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylate
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