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Home > CAS No. Inquiry > 1405-87-4

1405-87-4

[CAS Name] Bacitracin

[Formula] C66H103N17O16S

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[CAS Name]Bacitracin
[Alias]Agfivin; Altracin; Ayfivin; Baciquent; Citracin; Penitracin; Topitracin; Zutracin; cyclo[N~6~-(N-{[2-(1-amino-2-methylbutyl)-4,5-dihydro-1,3-thiazol-4-yl]carbonyl}leucyl-alpha-glutamylisoleucyl)-N~2~-asparaginyllysylornithylisoleucylphenylalanylhistidyl-alpha-aspartyl]; (4R)-4-[[(2S)-2-[[2-[(1S)-1-amino-2-methyl-butyl]4,5-dihydrothiazole-5-carbonyl]amino]-4-methyl-pentanoyl]amino]-5-[[(1S)-1-[[(3S,6R,9S,12R,15S,18R,21S)-3-(2-amino-2-oxo-ethyl)-18-(3-aminopropyl)-12-benzyl-6-(carboxymethyl)-9-(3H-imidazol-4-ylmethyl)-2,5,8,11,14,17,20-heptaoxo-15-sec-butyl-1,4,7,10,13,16,19-heptazacyclopentacos-21-yl]carbamoyl]-2-methyl-butyl]amino]-5-oxo-pentanoic acid
[Number]1405-87-4
[EINECS]215-786-2
[Formula]C66H103N17O16S
[Molecular weight]1422.6933

[Melting point]221-225℃
[Boiling point]1755.5°C at 760 mmHg
[Density]0mmHg at 25°C
[Flash point]1015.5°C

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Beijing Global Biologicals Co.Ltd

Antibiotic Product Bacitracin

Specification:

Bacitracin is a mixture of related cyclic polypeptides produced by organisms of the licheniformis group ofBacillus subtilis var Tracy, isolation of which was first reported in 1945. These peptides disrupt both gram positive and gram negative bacteria by interfering with cell wall and peptidoglycan synthesis.

Bacitracin is used as a topical preparation (since it is toxic and has poor oral bioavailability). In terms of adverse reactions only, in comparison with bacitracin, white petrolatum possesses an equally low infection rate and minimal risk for induction of allergy.

The widespread use of bacitracin, even for minor wounds where it is not useful, contributes to antibiotic resistance. This widespread use has contributed to the emergence of MRSA bacteria,specifically the highly lethal ST8:USA300 strain.

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Beijing Global Biologicals Co.Ltd

Anti-fungi Product Lovastatin

Specification:

Lovastatin is an inhibitor of 3-hydroxy-3methylglutaryl-coenzyme A reductase (HMG-CoA reductase), an enzyme that catalyzes the conversion of HMG-CoA to mevalonate. Mevalonate is a required building block for cholesterol biosynthesis and lovastatin interferes with its production by acting as a reversible competitive inhibitor for HMG-CoA, which binds to the HMG-CoA reductase. Lovastatin, being inactive in the native form, the form in which it is administered, is hydrolysed to the β-hydroxy acid form in the body; this is the active form.

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