推薦產品
生物源
synthetic
品質等級
等級
FG
Halal
Kosher
agency
meets purity specifications of JECFA
法律遵循
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117
化驗
≥98%
mp
>300 °C (lit.)
應用
flavors and fragrances
文件
see Safety & Documentation for available documents
食物過敏原
no known allergens
感官的
odorless
SMILES 字串
NCCS(O)(=O)=O
InChI
1S/C2H7NO3S/c3-1-2-7(4,5)6/h1-3H2,(H,4,5,6)
InChI 密鑰
XOAAWQZATWQOTB-UHFFFAOYSA-N
尋找類似的產品？ 前往 產品比較指南
一般說明
Taurine is a sulfur-containing amino acid mainly found in animal tissues. In mammals, it is reported to play an important role in the normal development of fetuses and neonates. Taurine is also one of the key ingredients in energy drinks.
應用
- Efficacy of taurine-enhanced enteral nutrition in improving the outcomes of critically ill patients: A systematic review and meta-analysis.: This meta-analysis evaluates the effectiveness of taurine-enhanced enteral nutrition in critically ill patients. The results indicate that taurine supplementation significantly improves patient outcomes, including reduced inflammation and enhanced recovery rates (Zhang et al., 2024).
- Taurine reduces the risk for metabolic syndrome: a systematic review and meta-analysis of randomized controlled trials.: This systematic review and meta-analysis demonstrate that taurine supplementation can significantly reduce the risk of metabolic syndrome. The findings support taurine′s potential as a therapeutic agent in managing metabolic health and preventing related diseases (Tzang et al., 2024).
生化／生理作用
甘氨酸受体的非选择性内源激动剂。在某些细胞中调节细胞凋亡的条件必需磺化氨基酸；在许多新陈代谢活动中起作用；是蛋氨酸和半胱氨酸的代谢产物。
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 2
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
客戶也查看了
Safety issues associated with commercially available energy drinks.
Clauson KA, et al.
Journal of the American Pharmaceutical Association, 48(3), e55-e67 (2008)
Taurine supplementation to a low protein diet during foetal and early postnatal life restores a normal proliferation and apoptosis of rat pancreatic islets.
Boujendar S, et al.
Diabetologia, 45(6), 856-866 (2002)
Tsutomu Suzuki et al.
Wiley interdisciplinary reviews. RNA, 2(3), 376-386 (2011-10-01)
Mitochondrial DNA mutations that cause mitochondrial dysfunction are responsible for a wide spectrum of human diseases, referred to as mitochondrial diseases. Pathogenic point mutations are found frequently in genes encoding mitochondrial (mt) tRNAs, indicating that impaired functioning of mutant mt
M Axelson et al.
Hepatology (Baltimore, Md.), 31(6), 1305-1312 (2000-05-29)
The biosynthesis of bile acids by primary cultures of normal human hepatocytes has been investigated. A general and sensitive method for the isolation and analysis of sterols and bile acids was used, based on anion exchange chromatography and gas chromatography-mass
Marlene Wewalka et al.
The Journal of clinical endocrinology and metabolism, 99(4), 1442-1451 (2014-01-18)
Bile acids (BAs) are newly recognized signaling molecules in glucose and energy homeostasis. Differences in BA profiles with type 2 diabetes mellitus (T2D) remain incompletely understood. The objective of the study was to assess serum BA composition in impaired glucose-tolerant
我們的科學家團隊在所有研究領域都有豐富的經驗，包括生命科學、材料科學、化學合成、色譜、分析等.
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