| 영문 | pyridoxine | 한글 | 피리독신 |
|---|---|---|---|
| 설명 | 비타민 B6라고도 부르며 pyridoxine, pyridoxal 및 pyridoxamine 세 가지의 화합물이 있다. 이들은 모두 체내에서 pyridoxal phosphate로 활성화되어 조효소로 작용한다. 이는 체내 아미노산 대사에 중요한 역할을 하는 조효소이다. 이 비타민이 결핍되면 다발성 말초신경염, 빈혈 및 피부병이 생긴다. |
||
| inj | injection; injury, injured, injurious |
|---|---|
| B6 | pyridoxine |
| PDD | pervasive developmental disorder; platinum diamminodichloride [cisplatin]; primary degenerative deme... |
| PNK | polynucleotide kinase; pyridoxine kinase |
| PNK(H) | pyridoxine kinase, high |
| PN | Pyridoxine |
|---|
| pyridoxine | <biochemistry> Member of the water soluble B vitamin group. Vitamin B6 or pyridoxine, is active in the metabolism of proteins, carbohydrates and fats. It is also a necessary part of haemoglobin synthesis. B6 deficiency results in retarded growth and a peripheral neuropathy. (27 Sep 1997) |
|---|---|
| pyridoxine 4-dehydrogenase | <enzyme> Chemical name: dehydrogenase, pyridoxol 4- Registry number: EC 1.1.1.65 Synonym: pyridoxine phosphate dehydrogenase, pyridoxal reductase (26 Jun 1999) |
| pyridoxine deficiency | A nutritional condition produced by a deficiency of pyridoxine in the diet, characterised by dermatitis, glossitis, cheilosis, and stomatitis. Marked deficiency causes irritability, weakness, depression, dizziness, peripheral neuropathy, and seizures. In infants and children typical manifestations are diarrhoea, anaemia, and seizures. Increasingly recognised as a cause is prolonged therapy with certain medications, among them isoniazid, cycloserine, and l-dopa. (12 Dec 1998) |
| pyridoxine dependency with seizure | An inherited disorder (autosomal recessive) apparently associated with deficient brain type I glutamate decarboxylase; seizures can be controlled with vitamin B6. (05 Mar 2000) |
| pyridoxine phosphate phosphatase | <enzyme> Involved in metabolism of vitamin b(6) Registry number: EC 3.1.3.- Synonym: pyridoxal phosphate phosphatase, pyridoxamine phosphate phosphatase, pyridoxal-p hydrolase, pyridoxamine-p hydrolase, vitamin b(6)-phosphate phosphatase (26 Jun 1999) |
| familial pyridoxine-responsive anaemia | A rare autosomal recessive hereditary hypochromic anaemia; autosomal trait, responsive to pyridoxine. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|