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ChemicalBook--->CAS DataBase List--->32988-50-4

32988-50-4

32988-50-4 Structure

32988-50-4 Structure
IdentificationBack Directory
[Name]

viomycin
[CAS]

32988-50-4
[Synonyms]

Viocin
viomycin
Vioactane
FLORIMYCIN
Coliomycin
Vinacetin A
Tuberactinomycin B
viomycin USP/EP/BP
Glycine, 3-amino-N-[(3S)-3,6-diamino-1-oxohexyl]-L-alanyl-L-seryl-L-seryl-(2Z)-3-[(aminocarbonyl)amino]-2,3-didehydroalanyl-2-[(4R,6S)-2-amino-1,4,5,6-tetrahydro-6-hydroxy-4-pyrimidinyl]-, (5→13)-lactam, (2S)-
(S)-3,6-Diamino-N-((3S,9S,12S,15S,Z)3((2R,4S)-6-amino-4-hydroxy-1,2,3,4-tetrahydropyridin-2-yl)-9,12-bis(hydroxymethyl)-2,5,8,11,14-pentaoxo-6-(ureidomethylene)-1,4,7,10,13-pentaazacyclohexadecan-15-yl)hexanamidedisulfate
[EINECS(EC#)]

251-323-0
[Molecular Formula]

C25H43N13O10
[MDL Number]

MFCD01741621
[MOL File]

32988-50-4.mol
[Molecular Weight]

685.696
Chemical PropertiesBack Directory
[Melting point ]

280 °C
[Boiling point ]

695.81°C (rough estimate)
[density ]

1.3613 (rough estimate)
[refractive index ]

1.6700 (estimate)
[storage temp. ]

Store at -20°C
[solubility ]

Water (Slightly)
[form ]

Powder
[pka]

pKa 8.2 (Uncertain);10.3 (Uncertain)
[Water Solubility ]

Soluble to 75 mM in water
[Stability:]

Hygroscopic
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P264-P270-P301+P312-P330-P501
Hazard InformationBack Directory
[Description]

Viomycin was found independently in 1951, in the culture broth of Streptomyces puniceus by Pfizer Research Laboratories and in that of S. floridae by Parke Davis Co. It shows strong activity against Mycobacterium species and moderate activity against gram-positive and gram-negative bacteria. Viomycin has been used by intramuscular administration to treat tuberculosis, but because of its ototoxicity and renal toxicity it is being replaced by more active and less toxic drugs, such as enviomycin and other antituberculotic antibiotics.
[Originator]

Vinactane,Ciba,US ,1953
[Uses]

Viomycin is a basic peptide antibiotic, which is an effective agent against multidrug-resistant tuberculosis.
[Definition]

ChEBI: A cyclic peptide antibiotic produced by the actinomycete Streptomyces puniceus, used in the treatment of tuberculosis.
[Indications]

Viomycin is a complex polypeptide antibiotic that is active against MDR strains of tuberculosis. Cross-resistance between viomycin and kanamycin is less frequent than between viomycin and capreomycin.
[Manufacturing Process]

Viomycin is produced by inoculating a nutrient medium with a viable strain of the organism Actinomyces vinaceus. A method for the production of viomycin is set forth in US Patent 2,663,445 comprising inoculating a medium containing soy peptone, beef extract, dextrose, sodium chloride and a silicone antifoaming agent with a spore suspension of Actinomyces vinaceus and incubating the inoculated medium for 120 hours at a temperature of 26°C while passing sterile air through the medium at a rate of 500 ml per liter of medium per minute.
[Brand name]

Viocin Sulfate (Pfizer).
[Therapeutic Function]

Antitubercular
[Biological Activity]

Member of the tuberactinomycin family of antibiotics . Inhibits group I intron splicing and prokaryotic protein synthesis. Freezes bacterial ribosomes in either the pre- or post-translational state. Facilitates trans -cleavage of the Neurospora VS ribozyme.
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