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lymecycline

lymecycline Structure
CAS No.
992-21-2
Chemical Name:
lymecycline
Synonyms
Tetralysal;Armyl;Tertamyl;Tetramyl;Mucomycin;Tetralisal;Lymecycline;Limeciclina;Vebicyclysal;Lymecycline (85%)
CBNumber:
CB2891297
Molecular Formula:
C29H38N4O10
Molecular Weight:
602.63
MOL File:
992-21-2.mol
MSDS File:
SDS
Modify Date:
2023/5/27 11:17:45

lymecycline Properties

Melting point 192.5°C
Boiling point 648.97°C (rough estimate)
Density 1.53
refractive index 1.5500 (estimate)
storage temp. Amber Vial, -86°C Freezer, Under inert atmosphere
solubility Very soluble in water, slightly soluble in ethanol (96 per cent), practically insoluble in methylene chloride.
form Solid
pka 2.50±0.24(Predicted)
color Yellow to Dark Brown
Stability Light Sensitive, Temperature Sensitive

SAFETY

Risk and Safety Statements

lymecycline Chemical Properties,Uses,Production

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.

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.

Drug interactions

Potentially hazardous interactions with other drugs
Anticoagulants: possibly enhanced anticoagulant effect of coumarins and phenindione.
Oestrogens: possibly reduce contraceptive effects of oestrogens (risk probably small).
Retinoids: possible increased risk of benign intracranial hypertension – avoid.

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.

lymecycline Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 62)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Vadivarhe Speciality Chemicals Limited +91-9028832204 +91-9028832204 Maharashtra, India 38 58 Inquiry
Kopran Ltd +91-9920289074 +91-9820220525 Maharashtra, India 21 58 Inquiry
SVR Drugs Pvt Ltd +91-9849004148 +91-9010204960 Hyderabad, India 29 58 Inquiry
REXIN Laboratories (Redson Group) +91-9898937773 +91-8866003844 Gujarat, India 11 58 Inquiry
Enaltec Labs Pvt Ltd +91-9167119247 +91-9167119247 Maharashtra, India 49 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
SynZeal Research Pvt Ltd +1 226-802-2078 Gujarat, India 6522 58 Inquiry
Shenzhen Nexconn Pharmatechs Ltd +86-755-89396905 +86-15013857715 China 10311 58 Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49392 58 Inquiry
N-lysinomethyltetracycline Armyl Mucomycin 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 Tetralisal (+)-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 Tertamyl Tetracycline-L-methylenelysine Tetramyl Vebicyclysal Lymecycline Tetracyclinemethylene lysine Lymecycline (85%) 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 lymecycline USP/EP/BP Limeciclina Tetralysal 992-21-2 C29H38N4O10 C29H30D8N4O10 Antibacterial Amines Intermediates & Fine Chemicals Pharmaceuticals Isotope Labelled Compounds