Английская Википедия:Deoxypyridinoline

Материал из Онлайн справочника
Версия от 12:59, 26 февраля 2024; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{Chembox | ImageFile = Deoxypyridinoline.svg | ImageSize = 250 | SystematicName = (2''R'')-6-<nowiki/>{3-[(3''S'')-3-Amino-3-carboxypropyl]-4-[(2''S'')-2-amino-3-carboxyethyl]-5-hydroxypyridin-1-ium-1-yl}hexanoate |Section1={{Chembox Identifiers | CASNo = 83462-55-9 | CASNo_Ref = {{cascite|correct|CAS}} | UNII_Ref = {{fdacite|correct|FDA}} | UNII = GXI9WV7IP9 | PubChem = 105071 | Chem...»)
(разн.) ← Предыдущая версия | Текущая версия (разн.) | Следующая версия → (разн.)
Перейти к навигацииПерейти к поиску

Шаблон:Chembox


Deoxypyridinoline, also called D-Pyrilinks, Pyrilinks-D, or deoxyPYD, is one of two pyridinium cross-links that provide structural stiffness to type I collagen found in bones.[1] It is excreted unmetabolized in urine and is a specific marker of bone resorption and osteoclastic activity. It is measured in urine tests and is used along with other bone markers such as alkaline phosphatase, osteocalcin, and N-terminal telopeptide to diagnose bone diseases such as postmenopausal osteoporosis, bone metastasis, and Paget's disease, furthermore, it has been useful in monitoring treatments that contain bone-active agents such as estrogens and bisphosphonates. [1]

Certain studies have attempted to generate a standardization of Deoxypyridinoline via an individual molar absorptivity value at acid and neutrality pH. The result was 5160 and 5290 L mol−1 cm−1 respectively.[2]

References

Шаблон:Reflist