Identification | Back Directory | [Name]
lymecycline | [CAS]
992-21-2 | [Synonyms]
Armyl Tertamyl Tetramyl Mucomycin Tetralisal Tetralysal Lymecycline Vebicyclysal Lymecycline (85%) lymecycline USP/EP/BP N-lysinomethyltetracycline Tetracyclinemethylene lysine Tetracycline-L-methylenelysine N6-[[(4S)-4β-(Dimethylamino)-1,4,4aβ,5,5aβ,6,11,12a-octahydro-3,6α,10,12,12aβ-pentahydroxy-6-methyl-1,11-dioxonaphthacen-2-yl]carbonylaminomethyl]-L-lysine (+)-N-(5-Amino-5-carboxypentylaminomethyl)-4-dimethylamino-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxonaphthacene-2-carboxamide L-Lysine, N6-[[[[(4S,4aS,5aS,6S,12aS)-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenyl]carbonyl]amino]methyl]- (S)-2-amino-6-((((4S,4aS,5aS,6S,12aS)-4-(dimethylamino)-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamido)methyl)amino)hexanoic acid | [EINECS(EC#)]
213-592-2 | [Molecular Formula]
C29H38N4O10 | [MOL File]
992-21-2.mol | [Molecular Weight]
602.637 |
Chemical Properties | Back Directory | [Appearance]
Yellow, hygroscopic powder. | [Melting point ]
192.5°C | [Boiling point ]
648.97°C (rough estimate) | [density ]
1.53 | [refractive index ]
1.5500 (estimate) | [solubility ]
Very soluble in water, slightly soluble in ethanol (96 per cent), practically insoluble in methylene chloride. | [pka]
2.50±0.24(Predicted) |
Hazard Information | Back Directory | [Chemical Properties]
Yellow, hygroscopic powder. | [Uses]
Labelled Lymecycline. A semi-synthetic antibiotic related to Tetracycline (T291400). Antibacterial. | [Definition]
ChEBI: A tetracycline-based broad-spectrum antibiotic. It is approximately 5000 times more soluble than tetracycline base and is unique amongst tetracyclines in that it is absorbed by the "active transport" process across the intestinal wall. | [Originator]
Armyl,Armour Pharm. | [Manufacturing Process]
Amido-N-(lysinomethyl)tetracycline hydrochloride: To 18.3 g of L-lysine hydrochloride dissolved in 100 ml of water is added 10
ml of 37% aqueous solution of formaldehyde. To the resultant mixture is
added 44.0 g of anhydrous tetracycline dissolved in 500 ml of tetrahydrofuran.
After thorough mixing the product forms over a period of about 15 min as an
oily layer which after separation from the aqueous phase is added dropwise to
3 L of stirred isopropyl alcohol. The product after recovery by filtration, is
reslurried with acetone, filtered and dried at 65°C at reduced pressure. The product thus obtained has a bioassay of 500 mcg/mg (K. pneumonlae
oxytetracyoline assay). | [Therapeutic Function]
Antibiotic | [Pharmaceutical Applications]
2-N-lysinomethyl-tetracycline. A water-soluble prodrug of
tetracycline available for oral administration.
Its antimicrobial activity is due to the tetracycline content. It
is lipophilic, rapidly absorbed from the gastrointestinal tract and
widely distributed. Concentrations around 1 mg/kg have been
found in maxillary sinus tissue some 3 h after administration
of a conventional dose. The half-life is 7–14 h. Approximately
30% of an orally administered dose is excreted as active drug in
the urine, where it achieves concentrations of 300 mg/L.
Its untoward effects and clinical uses are those of tetracycline,
although it is claimed to be better tolerated. | [Clinical Use]
Antibacterial agent:
Also used for treatment of acne | [Drug interactions]
Molecular weight (daltons) 602.6
% Protein binding Approx 25-60
% Excreted unchanged in urine 25
Volume of distribution (L/kg) Approx 1.3-1.7
Half-life - normal/ESRF (hrs) 10 / Increased | [Metabolism]
The tetracyclines are excreted in the urine and in the
faeces. Renal clearance is by glomerular filtration.
Up to 60% of an intravenous dose, and up to 55% of an
oral dose, is eliminated unchanged in the urine. Usually
between 40% and 70% of a dose is excreted in the urine;
urinary excretion is increased if urine is alkalinised. |
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SVR Drugs Pvt Ltd
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Company Name: |
Kopran Ltd
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www.kopran.com |
Company Name: |
LGM Pharma
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1-(800)-881-8210 |
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www.lgmpharma.com |
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