serw-MX  [xml]  
 


    
 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.875 Tyrosinemias .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.100 Amino Acid Metabolism, Inborn Errors .
C16.320.565.100.880 Tyrosinemias .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.875 Tyrosinemias .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.875 Tyrosinemias .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.100 Amino Acid Metabolism, Inborn Errors .
C18.452.648.100.880 Tyrosinemias .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.875 Tyrosinemias .
D02 Organic Chemicals .
D02.092 Amines .
D02.092.211 Biogenic Amines .
D02.092.211.215 Biogenic Monoamines .
D02.092.211.215.811 Tyramine .
D04 Polycyclic Compounds .
D04.345 Macrocyclic Compounds .
D04.345.566 Peptides, Cyclic .
D04.345.566.850 Tyrothricin .
D04.345.566.850.920 Tyrocidine .
D08 Enzymes and Coenzymes .
D08.811 Enzymes .
D08.811.682 Oxidoreductases .
D08.811.682.690 Oxygenases .
D08.811.682.690.708 Mixed Function Oxygenases .
D08.811.682.690.708.125 Catechol Oxidase .
D08.811.682.690.708.125.500 Monophenol Monooxygenase .
D12 Amino Acids, Peptides, and Proteins .
D12.125 Amino Acids .
D12.125.072 Amino Acids, Cyclic .
D12.125.072.050 Amino Acids, Aromatic .
D12.125.072.050.875 Tyrosine .
D12.644 Peptides .
D12.644.641 Peptides, Cyclic .
D12.644.641.850 Tyrothricin .
D12.644.641.850.920 Tyrocidine .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Tyrocidine .
Brevicidin .
Rapicidin .
Tyrocidines .
An antibiotic mixture produced by Bacillus brevis which may be separated into three components, tyrocidines A, B, and C. It is the major constituent (40-60 per cent) of tyrothricin, gramicidin accounting for the remaining 10-20 per cent active material. It is a topical antimicrobial agent, that is very toxic parenterally. .
1.00
086
 
Tyrosine .
L-Tyrosine .
Tyrosine, L-isomer .
para-Tyrosine .
L Tyrosine .
Tyrosine, L isomer .
para Tyrosine .
A non-essential amino acid. In animals it is synthesized from PHENYLALANINE. It is also the precursor of EPINEPHRINE; THYROID HORMONES; and melanin. .
0.66
6439313
 
Tyrothricin .
Codétricine .
Dermotricine .
Hydrotricine .
Martricin .
Tyroderm .
Tyrosur .
A polypeptide antibiotic mixture obtained from Bacillus brevis. It consists of a mixture of three tyrocidines (60%) and several gramicidins (20%) and is very toxic to blood, liver, kidneys, meninges, and the olfactory apparatus. It is used topically. .
0.61
1491
 
Tyrosinemias .
4-Hydroxyphenol Pyruvic Acid Oxidase Deficiency Disease .
4-Hydroxyphenylpyruvate Dioxygenase Deficiency .
4-Hydroxyphenylpyruvic Acid Oxidase Deficiency .
Deficiency Disease, 4-Hydroxyphenol Pyruvic Acid Oxidase .
Deficiency Disease, Fumarylacetoacetase .
Deficiency Disease, Tyrosine Transaminase .
Fumarylacetoacetase Deficiency .
Hepatorenal Tyrosinemia .
Hereditary Tyrosinemia, Type I .
Hereditary Tyrosinemia, Type II .
Hereditary Tyrosinemia, Type III .
Hereditary Tyrosinemias .
Hypertyrosinemia .
Hypertyrosinemia, Type I .
Keratosis Palmoplantaris with Corneal Dystrophy .
Oregon Type Tyrosinemia .
Richner-Hanhart Syndrome .
Richner-Hanhart Syndrome, Tyrosinosis, Oculocutaneous Type .
Tat Deficiency .
Tyrosine Aminotransferase Deficiency .
Tyrosine Transaminase Deficiency .
Tyrosinemia .
Tyrosinemia Type 1 .
Tyrosinemia, Type 2 .
Tyrosinemia, Type I .
Tyrosinemia, Type II .
Tyrosinemia, Type III .
Tyrosinemias, Hereditary .
Tyrosinosis, Oculocutaneous Type .
2 Tyrosinemias, Type .
4 Hydroxyphenol Pyruvic Acid Oxidase Deficiency Disease .
Deficiencies, 4-Hydroxyphenylpyruvate Dioxygenase .
Deficiencies, Fumarylacetoacetase .
Deficiencies, Tat .
Deficiency Disease, 4 Hydroxyphenol Pyruvic Acid Oxidase .
Deficiency Diseases, Fumarylacetoacetase .
Deficiency, 4-Hydroxyphenylpyruvate Dioxygenase .
Deficiency, Fumarylacetoacetase .
Deficiency, Tat .
Dioxygenase Deficiencies, 4-Hydroxyphenylpyruvate .
Dioxygenase Deficiency, 4-Hydroxyphenylpyruvate .
Disease, Fumarylacetoacetase Deficiency .
Diseases, Fumarylacetoacetase Deficiency .
Fumarylacetoacetase Deficiencies .
Fumarylacetoacetase Deficiency Diseases .
Hepatorenal Tyrosinemias .
Hereditary Tyrosinemia .
Hypertyrosinemias, Type I .
Oculocutaneous Type Tyrosinoses .
Oculocutaneous Type Tyrosinosis .
Richner Hanhart Syndrome .
Richner-Hanhart Syndromes .
Syndrome, Richner-Hanhart .
Syndromes, Richner-Hanhart .
Tat Deficiencies .
Type 2 Tyrosinemia .
Type 2 Tyrosinemias .
Type I Hypertyrosinemia .
Type I Hypertyrosinemias .
Type I Tyrosinemia .
Type I Tyrosinemias .
Type II Tyrosinemia .
Type II Tyrosinemias .
Type III Tyrosinemia .
Type III Tyrosinemias .
Type Tyrosinoses, Oculocutaneous .
Type Tyrosinosis, Oculocutaneous .
Tyrosinemia Type 1s .
Tyrosinemia, Hepatorenal .
Tyrosinemia, Hereditary .
Tyrosinemias, Hepatorenal .
Tyrosinemias, Type 2 .
Tyrosinemias, Type I .
Tyrosinemias, Type II .
Tyrosinemias, Type III .
Tyrosinoses, Oculocutaneous Type .
Fumarylacetoacetase Deficiency Disease .
Tyrosine Transaminase Deficiency Disease .
4 Hydroxyphenylpyruvate Dioxygenase Deficiency Disease .
A group of disorders which have in common elevations of tyrosine in the blood and urine secondary to an enzyme deficiency. Type I tyrosinemia features episodic weakness, self-mutilation, hepatic necrosis, renal tubular injury, and seizures and is caused by a deficiency of the enzyme fumarylacetoacetase. Type II tyrosinemia features INTELLECTUAL DISABILITY, painful corneal ulcers, and keratoses of the palms and plantar surfaces and is caused by a deficiency of the enzyme TYROSINE TRANSAMINASE. Type III tyrosinemia features INTELLECTUAL DISABILITY and is caused by a deficiency of the enzyme 4-HYDROXYPHENYLPYRUVATE DIOXYGENASE. (Menkes, Textbook of Child Neurology, 5th ed, pp42-3) .
0.58
11340
 
Monophenol Monooxygenase .
Cresolase .
Phenol Oxidase .
Phenoloxidase A .
Phenoloxidase B .
Monooxygenase, Monophenol .
Oxidase, Dopa .
Oxidase, Phenol .
Dopa Oxidase .
Phenoloxidase .
Tyrosinase .
An enzyme of the oxidoreductase class that catalyzes the reaction between L-tyrosine, L-dopa, and oxygen to yield L-dopa, dopaquinone, and water. It is a copper protein that acts also on catechols, catalyzing some of the same reactions as CATECHOL OXIDASE. EC 1.14.18.1. .
0.56
286223
 
Tyramine .
4-(2-Aminoethyl)phenol .
4-Hydroxyphenethylamine .
p-Tyramine .
para-Tyramine .
4 Hydroxyphenethylamine .
An indirect sympathomimetic that occurs naturally in cheese and other foods. Tyramine does not directly activate adrenergic receptors, but it can serve as a substrate for adrenergic uptake systems and MONOAMINE OXIDASE to prolong the actions of adrenergic transmitters. It also provokes transmitter release from adrenergic terminals and may be a neurotransmitter in some invertebrate nervous systems. .
0.54
104901