ChemicalBook--->CAS DataBase List--->16846-34-7

16846-34-7

16846-34-7 Structure

16846-34-7 Structure
IdentificationBack Directory
[Name]

Turimycin H-5
[CAS]

16846-34-7
[Synonyms]

LM-A1
Turimycin H-5
Kitasamycin A1
3-Deacetyljosamycin
Leucomycin V, 4B-(3-methylbutanoate)
Leucomycin V 4''-(3-methylbutanoate)
KitasaMycin A1, TuriMycin H5, LeucoMycin V 4-isovalerate
[Molecular Formula]

C40H67NO14
[MOL File]

16846-34-7.mol
[Molecular Weight]

785.96
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

solid
Hazard InformationBack Directory
[Uses]

Leucomycin A1 is a major metabolite from the leucomycin complex, a family of closely related macrocyclic lactone antibiotics produced by Streptomyces kitasatoensis, discovered in 1953. Leucomycin complex (kitasamycin) is used as an animal health product for control of Gram positive bacteria, Gram negative cocci, leptospira and mycoplasma. Little is known about the activity of individual analogues within the complex as their limited availability has restricted investigation.
[Definition]

ChEBI:Leucomycin A1 is a macrolide.
[Biological Activity]

leucomycin a1, a major metabolite extracted from the leucomycin complex, is a major macrocyclic lactone antibiotics produced by streptomyces kitasatoensis.leucomycin a1 is one of the more potent members of leucomycin complex. leucomycin complex (kitasamycin) is effective against a wide spectrum of pathogens, such as gram-positive bacteria, gram-negative cocci, mycoplasma, and leptospira. leucomycin complex has been used as an animal health product for control of gram positive bacteria, gram negative cocci, mycoplasma, and leptospira. until now, little is known about the activity of individual analogues within the complex. at a concentration of 1.56μg/ml, kitasamycin inhibited all isolates of diplococcus pneumonia [2]. each component of leucomycins potently inhibited the growth of gram-positive bacteria and showed not so strong activity against the gram-negative bacteria. each component showed the same tendency towards the antibacterial spectrum [3].
[storage]

Store at -20°C
[References]

[1] hata t, sano y, ohki n, et al. leucomycin, a new antibiotic[j]. the journal of antibiotics, 1953, 6(2): 87-89.
[2] balducci y, bodey g p. in vitro activity of kitasamycin against gram-positive cocci[j]. the journal of antibiotics, 1974, 27(7): 516-519.
[3] omura s, katagiri m, umezawa i, et al. structure-biological activities relationships among leucomycins and their derivatives[j]. the journal of antibiotics, 1968, 21(9): 532-538.
Safety DataBack Directory
[Toxicity]

LD50 intraperitoneal in mouse: 620mg/kg
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