所有图片(1)
别名:
2-氨基乙磺酸
线性分子式:
NH2CH2CH2SO3H
CAS号:
分子量:
125.15
Beilstein:
1751215
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24
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等级
pharmaceutical primary standard
API类
taurine
制造商/商品名称
USP
mp
>300 °C (lit.)
应用
pharmaceutical (small molecule)
格式
neat
储存温度
2-8°C
SMILES字符串
NCCS(O)(=O)=O
InChI
1S/C2H7NO3S/c3-1-2-7(4,5)6/h1-3H2,(H,4,5,6)
InChI key
XOAAWQZATWQOTB-UHFFFAOYSA-N
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一般描述
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.
应用
Taurine USP reference standard, intended for use in specified quality tests and assays as specified in the USP compendia.
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。
分析说明
These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.
其他说明
Sales restrictions may apply.
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
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Proceedings of the National Academy of Sciences of the United States of America, 112(2), 388-393 (2014-12-31)
Intradiol aromatic ring-cleaving dioxygenases use an active site, nonheme Fe(3+) to activate O2 and catecholic substrates for reaction. The inability of Fe(3+) to directly bind O2 presents a mechanistic conundrum. The reaction mechanism of protocatechuate 3,4-dioxygenase is investigated here using
Allan D Rasmussen et al.
Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie, 67(1), 13-20 (2014-12-03)
The overall purpose of this study was to establish a model that may be used for examining the effect of Vigabatrin-induced retinal toxicity in pigmented rats, and subsequently examine the possible effects of taurine on the retinal toxicity. In the
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Journal of cardiovascular pharmacology, 64(1), 60-68 (2014-04-08)
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