产品名称
视黄醇(维生素A)棕榈酸酯 CRM, United States Pharmacopeia (USP) Reference Standard
InChI
1S/C36H60O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-25-35(37)38-30-28-32(3)23-20-22-31(2)26-27-34-33(4)24-21-29-36(34,5)6/h20,22-23,26-28H,7-19,21,24-25,29-30H2,1-6H3/b23-20+,27-26+,31-22+,32-28+
SMILES string
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/COC(CCCCCCCCCCCCCCC)=O)C(C)(C)CCC1
InChI key
VYGQUTWHTHXGQB-FFHKNEKCSA-N
grade
pharmaceutical primary standard
API family
retinyl compounds
manufacturer/tradename
USP
application(s)
pharmaceutical (small molecule)
format
neat
storage temp.
2-8°C
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Analysis Note
这些产品仅供测试和分析使用。它们不适用于人类或动物的给药，不可用于诊断、治疗或治愈任何疾病。
Biochem/physiol Actions
评论：维生素 A 代谢。
General description
本品按现行药典规定交付。所有为支持本产品而提供的信息，包括 SDS 和任何产品信息小册子，均由药典颁发机构制定和发布。
如需进一步的信息和支持，请访问现行药典网站。
如需进一步的信息和支持，请访问现行药典网站。
Other Notes
可能适用相应的销售限制。
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Repr. 1B
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 2
flash_point_f
381.2 °F
flash_point_c
194.00 °C
Vitamin A
USP43-NF38: United States Pharmacopeia and National Formulary
United States Pharmacopeia, 44(2), 4632-4632 (2019)
Vitamin A Assay
USP43-NF38: United States Pharmacopeia and National Formulary
United States Pharmacopeia, 38(6), 6801-6801 (2014)
Shaikh Meshbahuddin Ahmad et al.
Contemporary clinical trials, 39(2), 269-279 (2014-10-02)
In recent years, neonatal vitamin A supplementation is considered as an essential infant-survival intervention but the evidence is not conclusive. This randomized controlled clinical trial was conducted to evaluate the effect of vitamin A on immune competence in early infancy.
Hans L Mooij et al.
Journal of lipid research, 56(3), 665-673 (2015-01-09)
Elevated nonfasting TG-rich lipoprotein levels are a risk factor for CVD. To further evaluate the relevance of LDL-receptor (LDLr) pathway and heparan sulfate proteoglycans (HSPGs) in TG homeostasis, we analyzed fasting and postprandial TG levels in mice bearing combined heterozygous
Xiaofeng Liao et al.
PloS one, 10(3), e0118176-e0118176 (2015-03-17)
Roles of all-trans-retinoic acid (tRA), a metabolite of vitamin A (VA), in both tolerogenic and immunogenic responses are documented. However, how tRA affects the development of systemic autoimmunity is poorly understood. Here we demonstrate that tRA have paradoxical effects on
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