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Tetracyclin

Erythromycin is active against gram-positive and certain gram-negative bacteria, also against Rickettsia and spirochaetes. It is used for patients who are allergic to or do not respond to treatment with penicillins or tetracyclines. [Pg.162]

M.p. 296 C. Accepts an electron from suitable donors forming a radical anion. Used for colorimetric determination of free radical precursors, replacement of Mn02 in aluminium solid electrolytic capacitors, construction of heat-sensitive resistors and ion-specific electrodes and for inducing radical polymerizations. The charge transfer complexes it forms with certain donors behave electrically like metals with anisotropic conductivity. Like tetracyanoethylene it belongs to a class of compounds called rr-acids. tetracyclines An important group of antibiotics isolated from Streptomyces spp., having structures based on a naphthacene skeleton. Tetracycline, the parent compound, has the structure ... [Pg.389]

The 7-chloro-derivative, the first of the group to be isolated (1948) is known as chlortetracy-cline. The 5-hydroxy-derivative is oxytetracy-dine. More recently introduced tetracyclines are 6-demethyl-7-chlorotetracycline and 5-hydroxy-6-deoxy-6-methyienetetracycline. [Pg.390]

Tetracyclines are broad-spectrum antibiotics. effective against Gram-positive and Gram-negative bacteria, also against Rickettsiae (typhus fever) and certain other organisms. [Pg.390]

Figure 7-15 shows the time evolution of the temperature, total energy, and potential energy for a 300 ps simulation of the tetracycline repressor dimer in its induced (i.e., hgand-bound) form. Starting from the X-ray structure of the monomer in a complex with one molecule of tetracycline and a magnesium ion (protein database... [Pg.369]

Figure 7-16. Superimpasition of the X-ray structure of the tetracycline repressor class D dimer (dark, protein database entry 2TRT) with the calculated geometrical average of a 3 ns MD simulation (light trace). Only the protein backbone C trace Is shown, The secondary structure elements and the tertiary structure are almost perfectly reproduced and maintained throughout the whole production phase of the calculation,... Figure 7-16. Superimpasition of the X-ray structure of the tetracycline repressor class D dimer (dark, protein database entry 2TRT) with the calculated geometrical average of a 3 ns MD simulation (light trace). Only the protein backbone C trace Is shown, The secondary structure elements and the tertiary structure are almost perfectly reproduced and maintained throughout the whole production phase of the calculation,...
Tetracyclines are produced by various Streptomyces strains and are extensively applied in human and veterinary medicine. They display a broad spectrum of antimicrobial activity in combination with low toxicity and can be applied orally. The most commonly prescribed tetracycline drugs are tetracycline itself and oxytetracycline, an oxygenated derivative, which are directly isolated from fermentation liquors, and doxycycline whose partial synthesis from oxy-... [Pg.316]

The numbering system of tetracyclines is used for synthetic intennediates. [Pg.318]


See other pages where Tetracyclin is mentioned: [Pg.37]    [Pg.321]    [Pg.389]    [Pg.372]    [Pg.64]    [Pg.245]    [Pg.299]    [Pg.311]    [Pg.316]    [Pg.317]    [Pg.317]    [Pg.317]    [Pg.318]    [Pg.318]    [Pg.952]    [Pg.895]    [Pg.10]    [Pg.19]    [Pg.19]    [Pg.56]    [Pg.56]    [Pg.60]    [Pg.60]    [Pg.65]    [Pg.78]    [Pg.121]    [Pg.135]    [Pg.188]    [Pg.193]    [Pg.196]    [Pg.204]    [Pg.206]    [Pg.237]    [Pg.284]   
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See also in sourсe #XX -- [ Pg.193 ]

See also in sourсe #XX -- [ Pg.3 ]




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6- membered tetracycline synthesis

6-Deoxy tetracycline

7-Substituted fused ring tetracycline

7-Substituted fused ring tetracycline compounds

Achromycin - Tetracycline

Acitretin Tetracyclines

Adverse drug reactions tetracyclines

Amphoteric drugs tetracyclines

Antacids with tetracyclines

Antiarrhythmics tetracyclines

Antibacterial drug tetracyclines

Antibacterials tetracyclines

Antibiotic compounds tetracyclines

Antibiotics tetracycline

Antibiotics, detection tetracyclines

Antimicrobial agents/therapy tetracyclines

Antimicrobial therapy tetracyclines

Antimicrobials tetracyclines

Bacterial pneumonia tetracyclines

Biosynthesis of tetracyclines

Bismuth compounds Tetracyclines

Bismuth subcitrate/metronidazole tetracycline

Bismuth subsalicylate/metronidazole/tetracycline

Bone, tetracyclines affecting

Calcium complexing with tetracyclines

Calcium compounds Tetracyclines

Central nervous system tetracyclines

Chemistry and Synthesis of Tetracyclines

Chloramphenicol and tetracycline

Chlortetra cycline Tetracycline

Cholestyramine with tetracyclines

Colestipol Tetracycline

Deposit, tetracycline

Didanosine Tetracyclines

Drug discovery tetracyclines

Drug resistance tetracyclines

Efflux proteins tetracycline resistance

Efflux proteins tetracyclines

Electrospun tetracycline hydrochloride drug

Environmental tetracyclines

Epi-Tetracycline

Epimerization of tetracyclines

Ergot derivatives Tetracyclines

Ergotamine Tetracycline

Europium tetracycline

Ferrous sulfate Tetracycline

Foods: Dairy products Tetracyclines

Foods: Milk Tetracycline

General Characteristics of the Tetracyclines

Gram-positive/negative bacteria tetracyclines

Halofantrine Tetracycline

Halogenated tetracyclines

Hormonal) Tetracycline

Interactions tetracycline/calcium

Iron compounds Tetracyclines

Isotretinoin Tetracycline

Kaolin Tetracycline

Look up the names of both individual drugs and their drug groups to access full information Tetracycline

Magnesium compounds Tetracyclines

Magnesium sulfate Tetracycline

Mefloquine Tetracycline

Metformin Tetracyclines

Methoxyflurane Tetracycline

Metoclopramide Tetracycline

Microbial infections tetracycline

NSAIDs) Tetracycline

Natural product synthesis Tetracyclin

Natural tetracyclines

Nephrotoxicity tetracyclines

Newer tetracyclines

Of tetracycline

Oxy tetracycline

PAGE Tetracyclines

Panmycin - Tetracycline

Parent tetracyclines

Pectin Tetracycline

Penicillins Tetracyclines

Pharmaceuticals Tetracyclines)

Phenformin Tetracycline

Photosensitivity from tetracyclines

Photosensitivity, tetracyclines causing

Polyketides tetracyclines

Pregnancy tetracyclines

Primidone Tetracycline

Protein synthesis, antibacterial drug tetracyclines

Pseudomonas aeruginosa tetracyclines

Quinapril Tetracycline

Quinine with tetracycline

Quinine-tetracycline

Resistance tetracyclines

Resistance to tetracyclines

Retinoids Tetracyclines

Ribosomes, tetracyclines

Risperidone tetracycline

SSRIs) Tetracyclines

Second generation tetracycline

Selective toxicity tetracyclines

Semisynthetic drugs tetracyclines

Semisynthetic tetracyclines

Skin toxicity tetracyclines

Sodium bicarbonate Tetracycline

Staphylococci tetracyclines

Staphylococcus aureus tetracycline-resistant

Streptomyces aureofaciens [Tetracyclines

Streptomyces rimosus, tetracyclines

Subject tetracyclines

Sucralfate Tetracycline

Sumycin - Tetracycline

Teclinazets - Tetracycline

Teeth, tetracycline staining

TetA, tetracycline resistance

Tetracyclin antibiotics

Tetracyclin synthesis

Tetracycline ( hci

Tetracycline 6-demethyl

Tetracycline 6-deoxy-5-hydroxy

Tetracycline 7-chloro-,

Tetracycline Alcohol

Tetracycline Aminophylline

Tetracycline Antacids

Tetracycline Atovaquone

Tetracycline Benzylpenicillin

Tetracycline Bismuth subsalicylate

Tetracycline Carbamazepine

Tetracycline Cimetidine

Tetracycline Coffee

Tetracycline Contraceptives, hormonal

Tetracycline Dicumarol

Tetracycline Digoxin

Tetracycline Ethanol

Tetracycline Ethinylestradiol

Tetracycline Foods

Tetracycline HCL

Tetracycline INDEX

Tetracycline Lymecycline

Tetracycline Magnesium hydroxide

Tetracycline Methotrexate

Tetracycline Milk

Tetracycline Orange juice

Tetracycline Phenobarbital

Tetracycline Phenytoin

Tetracycline Phosphate Complex

Tetracycline Rolitetracycline

Tetracycline Theophylline

Tetracycline Warfarin

Tetracycline adverse effects

Tetracycline adverse reaction

Tetracycline agents

Tetracycline allergy

Tetracycline analogs

Tetracycline analysis

Tetracycline antibiotics isolation

Tetracycline antimicrobial activity

Tetracycline biochemical effects

Tetracycline case

Tetracycline chemical structure

Tetracycline chemistry

Tetracycline classification

Tetracycline cleanup

Tetracycline confirmation

Tetracycline contraindications

Tetracycline derivatives

Tetracycline detection

Tetracycline detection chromatographic methods

Tetracycline development

Tetracycline diarrhea with

Tetracycline dosage

Tetracycline dosing

Tetracycline drug interactions

Tetracycline drugs

Tetracycline drugs absorption

Tetracycline drugs administration

Tetracycline epimers

Tetracycline excretion

Tetracycline formula

Tetracycline gastrointestinal effects

Tetracycline gene modification

Tetracycline group

Tetracycline hepatotoxicity

Tetracycline hydrochloric acid

Tetracycline hydrochloride

Tetracycline hydrochloride ointment

Tetracycline hypersensitivity reactions

Tetracycline in pneumonia

Tetracycline in syphilis

Tetracycline in urinary tract infections

Tetracycline inducible

Tetracycline interaction with other drugs

Tetracycline liquid chromatographic methods

Tetracycline liquid chromatography-mass spectrometry

Tetracycline local application

Tetracycline metabolites

Tetracycline metabolites 4-aminoanhydrochlortetracycline

Tetracycline metabolites 4-oxoanhydrochlortetracycline

Tetracycline metabolites 4-oxochlortetracycline

Tetracycline metabolites 4-oxodehydrochlortetracycline

Tetracycline metabolites anhydrochlortetracycline

Tetracycline metabolites chloraureovocidin

Tetracycline metabolites chloro-A-C-diquinone

Tetracycline metabolites chlorpretetramide

Tetracycline metabolites chlortetramide-blue

Tetracycline metabolites chlortetramide-green

Tetracycline metabolites dehydrochlortetracycline

Tetracycline metabolites methylchlorpretetramide

Tetracycline metabolites methylchlortetramide-blue

Tetracycline metabolites methylhydroxychlorpretetramide

Tetracycline metal chelate affinity

Tetracycline metal chelate affinity chromatography

Tetracycline methods

Tetracycline mycoplasma infections

Tetracycline operator

Tetracycline oral administration

Tetracycline outdated

Tetracycline oxygenation

Tetracycline pancreatitis with

Tetracycline parenteral administration

Tetracycline pharmacokinetics

Tetracycline phototoxicity

Tetracycline physicochemical properties

Tetracycline renal insufficiency and

Tetracycline repressor

Tetracycline resistance genes

Tetracycline resistant genes

Tetracycline skeleton

Tetracycline skin eruptions with

Tetracycline stability

Tetracycline teratogenic effects

Tetracycline teratogenicity

Tetracycline tolerances

Tetracycline toxicity

Tetracycline transporter

Tetracycline ultrafiltration

Tetracycline with digoxin

Tetracycline with iron

Tetracycline with isotretinoin

Tetracycline with oral contraceptives

Tetracycline, 6-demethyl-6-deoxy

Tetracycline, biosynthetic pathway

Tetracycline, effect

Tetracycline, effect metabolism

Tetracycline, oxidation

Tetracycline, response

Tetracycline, structure

Tetracycline, synthesis

Tetracycline, topical application

Tetracycline-Specific Antibodies

Tetracycline-inducible VP-CAR transgenic mice

Tetracycline-resistant

Tetracycline-resistant bacteria

Tetracycline-specific efflux

Tetracyclines

Tetracyclines 13-oxidation inhibition

Tetracyclines Coumarins

Tetracyclines Dairy products

Tetracyclines Diuretics

Tetracyclines Metal-binding

Tetracyclines Sulfonylureas

Tetracyclines absorption

Tetracyclines action

Tetracyclines adsorption

Tetracyclines and Their 4-Epimers

Tetracyclines anhydrotetracycline

Tetracyclines antibacterial activity

Tetracyclines antimalarials

Tetracyclines aromatic polyketides

Tetracyclines bacterial infections

Tetracyclines bacterial resistance

Tetracyclines bacteriostatic action

Tetracyclines biliary excretion

Tetracyclines bioactivity

Tetracyclines bioavailability

Tetracyclines biosynthesis

Tetracyclines bone, accumulation

Tetracyclines calcium complexing

Tetracyclines chelating groups

Tetracyclines chemically modified

Tetracyclines chloro derivative

Tetracyclines chlortetracycline

Tetracyclines chromatography

Tetracyclines clinical aspects

Tetracyclines combination therapy

Tetracyclines commercially available

Tetracyclines cross-sensitivity

Tetracyclines demethylchlortetracycline

Tetracyclines derivatization

Tetracyclines description

Tetracyclines discovery

Tetracyclines distribution

Tetracyclines drug interactions/adverse effect

Tetracyclines drug-metal chelates

Tetracyclines efflux

Tetracyclines elimination

Tetracyclines environment

Tetracyclines epimerisation

Tetracyclines epimerization

Tetracyclines food interactions

Tetracyclines for anthrax

Tetracyclines for bacterial pneumonia

Tetracyclines for brucellosis

Tetracyclines for louse-borne typhus

Tetracyclines for rickettsioses

Tetracyclines for tularemia

Tetracyclines formulations

Tetracyclines from Streptomyces aureofacien

Tetracyclines gene switch

Tetracyclines hydrochloride salt solubility

Tetracyclines hyperpigmentation

Tetracyclines hypersensitivity

Tetracyclines immunoassay

Tetracyclines in agriculture

Tetracyclines in calf breeding

Tetracyclines in food additives

Tetracyclines in pig breeding

Tetracyclines in sheep breeding

Tetracyclines indications

Tetracyclines individual compounds

Tetracyclines infection site

Tetracyclines interactions

Tetracyclines isolation

Tetracyclines lipid solubility

Tetracyclines lipophilicity

Tetracyclines mechanism of action

Tetracyclines metal-binding properties

Tetracyclines oral bioavailability

Tetracyclines oxytetracycline

Tetracyclines pathway

Tetracyclines pharmaceutical preparations

Tetracyclines pharmacologic properties

Tetracyclines photosensitivity

Tetracyclines phototoxic reactions

Tetracyclines physicochemical methods

Tetracyclines plasma protein binding

Tetracyclines polyketide derivatives

Tetracyclines protein synthesis effects

Tetracyclines recent developments

Tetracyclines renal disease

Tetracyclines resistance mechanisms

Tetracyclines sample preparation

Tetracyclines selectivity, basis

Tetracyclines semisynthetic type

Tetracyclines skin tests

Tetracyclines solubility

Tetracyclines solubilization

Tetracyclines spectrophotometric methods

Tetracyclines stability constants

Tetracyclines structure-activity relationship

Tetracyclines table

Tetracyclines tetracycline-protein conjugates

Tetracyclines tetracycline-specific antibodies

Tetracyclines therapeutic applications

Tetracyclines therapeutic effects

Tetracyclines ulceration therapy

Tetracyclines urinary tract infections

Tetracyclines via conjugate addition of aryl cyanohydrin

Tetracyclines via oxyanion-accelerated rearrangement

Tetracyclines, Macrolides, and Lincosamides

Tetracyclines, history

Tetracyclines, infections

Tetracyclines, photodegradation

Tetracyclines, specific agents

Tetracyclines, specific agents tetracycline

Tetracyclins

The citrate and tetracycline transporters of E. coli

The tetracyclines

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