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この商品について
実験式(ヒル表記法):
C22H34O2
CAS番号:
分子量:
330.50
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352211
MDL number:
製品名
all-cis-7,10,13,16,19-ドコサペンタエン酸, synthetic, ≥97%
InChI
1S/C22H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h3-4,6-7,9-10,12-13,15-16H,2,5,8,11,14,17-21H2,1H3,(H,23,24)/b4-3-,7-6-,10-9-,13-12-,16-15-
SMILES string
CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(O)=O
InChI key
YUFFSWGQGVEMMI-JLNKQSITSA-N
biological source
synthetic
assay
≥97%
form
liquid
functional group
carboxylic acid
lipid type
unsaturated FAs
shipped in
ambient
storage temp.
−20°C
Quality Level
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関連するカテゴリー
保管分類
10 - Combustible liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
D1797-VAR: + D1797-10MG-PW: + D1797-5MG: + D1797-1MG: + D1797-10MG: + D1797-BULK:
jan
Jan Philipp Schuchardt et al.
Prostaglandins, leukotrienes, and essential fatty acids, 121, 76-87 (2017-06-28)
EPA and DHA cause different physiological effects, which are in many cases mediated via their oxidative metabolites (oxylipins). However, metabolism studies investigating the effect of either EPA or DHA on comprehensive oxylipin patterns are lacking. The short and long term
A M Eltweri et al.
Clinical nutrition (Edinburgh, Scotland), 36(3), 768-774 (2016-06-28)
It has been demonstrated that short term intravenous (IV) administration of omega-3 polyunsaturated fatty acids (PUFAs) is more effective than oral supplementation at promoting incorporation of the bioactive omega-3 PUFAs eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) into plasma, blood
Additional data from our study on fatty acids variations during lactation: correlations between n-3 and n-6 PUFAs in human colostrum, transitional, and mature milk.
Carolina Moltó-Puigmartí et al.
Clinical nutrition (Edinburgh, Scotland), 30(3), 402-403 (2011-04-08)
Yuko Yonezawa et al.
International journal of molecular medicine, 18(4), 583-588 (2006-09-12)
We reported previously that unsaturated linear-chain fatty acids of the cis-configuration with a C18-hydrocarbon chain such as linoleic acid (cis-9, 12-octadecadienoic acid, C18:2) could potently inhibit the activity of mammalian DNA polymerases (Biochim Biophys Acta 1308: 256-262, 1996). In this
A Voss et al.
The Journal of biological chemistry, 266(30), 19995-20000 (1991-10-25)
The hypothesis that the last step in the biosynthesis of 4,7,10,13,16,19-22:6 from linolenate is catalyzed by an acyl-CoA-dependent 4-desaturase has never been evaluated by direct experimentation. When rat liver microsomes were incubated with [1-14C]7,10,13,16,19-22:5, under conditions where linoleate was readily
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