Lymecycline drug data and news

Lymecycline drug data, resources, and news articles (when available). Onconews.org provides news on cancer research. This section, which includes profiles on medicines that may or not be cancer-related is in beta form. If things run smoothly we will be releasing a new format late in the summer of 2006.

Generic name Lymecycline
Brand Names/Synonyms AUREOMYCIN; Acronize; Acronize Pd; Aureocarmyl; Aureociclin; Aureociclina; Aureocina; Aureocycline; Aureomicina; Aureomycin Hydrochloride; Aureomycin Monohydrochloride; Aureomycin a-377; Aureomykoin; Aurofac; Aurofac 10; Auxeomycin; B-Aureo; Biomitsin; Biomitsin Hydrochloride; Biomycin; Biomycin A; Biomycin Hydrochloride; Biovetin; C4881; CHEMBANK901; CLTC; CTC; Centraureo; Chlorotetracycline; Chlorotetracycline Hydrochloride; Chlortetracyclin; Chlortetracycline; Chlortetracycline Hydrochloride; Chlortetracyclinium Chloride; Chrusomykine; Chrysomykine; Clorocipan; Duomycin; Flamycin; Isphamycin; Lymecycline; Orospray; Psittacin Hydrochloride; Tetra 5; Tetralysal; Tocopherex; U-6780
Indication For the treatment of bacterial infection including: Brucellosis; Mycoplasma infection; Trachoma; Chronic bronchitis; Acne vulgaris; Chlamydial infection
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Description Not Available
Pharmacology Lymecycline is a tetracycline antibiotic that is commonly prescribed by medical doctors for infections and to treat acne. It may also be used to treat urinary tract infections, gum disease, and other bacterial infections such as gonorrhea and chlamydia. Lymecycline is also used commonly as a prophylactic treatment for infection by Bacillus anthracis (anthrax). It is also effective against Yersinia pestis and malaria and is also prescribed for the treatment of Lyme disease. Lymecycline inhibits cell growth by inhibiting translation.
Mechanism Of Action Lymecycline inhibits cell growth by inhibiting translation. It binds to the 30S ribosomal subunit and prevents the amino-acyl tRNA from binding to the A site of the ribosome. The binding is reversible in nature. Lymecycline is lipophilic and can easily pass through the cell membrane or passively diffuses through porin channels in the bacterial membrane. Cells become resistant to Lymecycline by at least two mechanisms: efflux and ribosomal protection. In efflux, a resistance gene encodes a membrane protein that actively pumps Lymecycline out of the cell. This is the mechanism of action of the tetracycline resistance gene on the artificial plasmid pBR322. In ribosomal protection, a resistance gene encodes a protein which binds to the ribosome and prevents Lymecycline from acting on the ribosome.
Lymecycline News
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Dosage Forms Capsule
Drug_Category Antiprotozoals; Anti-bacterial Agents; ATC:J01AA04
Absorption Not Available
Interactions Drug Interactions: The absorption of lymecycline may be affected by the simultaneous administration of indigestion remedies, iron or zinc supplements. Oral contraceptives may be less effective while you are taking lymecycline.
Toxicity Not Available
Organisms Affected Enteric bacteria and other eubacteria
Chemical IUPAC Name 2-(amino-hydroxy-methylidene)-7-chloro-4-dimethylamino-6,10,11,12a-tetrahydroxy-6-methyl-4,4a,5,5a-tetrahydrotetracene-1,3,12-trione
Chemical Formula C22H23ClN2O8
Molecular Weight 478.879 g/mol
Smiles String CC1(C2CC3C(C(=O)C(=C(N)O)C(=O)C3(C(=O)C2=C(C4=C(C=CC(=C41)Cl)O)O)O)N(C)C)O
Melting Point Not Available
Water Solubility Not Available
State Solid
LogP/Hphobicity 0.315
Isoelectric Point Not Available
Biotransformation Not Available
Half Life Not Available
Protein Binding [%] Not Available
RxList Link Not Available>RXlist
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Drug Reference Not Available
Drug Type Approved Drug
Accession No APRD00565
CAS Registry Number 992-21-2
KEGG Compound ID Not Available
PubChem ID SID:605300
PharmGKB ID Not Available
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] Not Available

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