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Merck
CN

D1797

all-cis-7,10,13,16,19-Docosapentaenoic acid

synthetic, ≥97%

Synonym(s):

Clupanodonic acid

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About This Item

Empirical Formula (Hill Notation):
C22H34O2
CAS Number:
24880-45-3
Molecular Weight:
330.50
MDL number:
MFCD00156103
UNSPSC Code:
12352211
PubChem Substance ID:
24893546
NACRES:
NA.25

Key Documents

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biological source

synthetic

Quality Level

100

Assay

≥97%

form

liquid

functional group

carboxylic acid

lipid type

unsaturated FAs

shipped in

ambient

storage temp.

−20°C

SMILES string

CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCCC(O)=O

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-

InChI key

YUFFSWGQGVEMMI-JLNKQSITSA-N

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Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ6572
MKCX1872
MKCT6959
MKCV2044
MKCT1213

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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
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
B S Mohammed et al.
The Biochemical journal, 326 ( Pt 2), 425-430 (1997-09-18)
It is now established that fatty acid 7,10,13,16-22:4 is metabolized into 4,7,10,13,16-22:5 as follows: 7,10,13,16-22:4-->9,12,15, 18-24:4-->6,9,12,15,18-24:5-->4,7,10,13,16-22:5. Neither C24 fatty acid was esterified to 1-acyl-sn-glycero-3-phosphocholine (1-acyl-GPC) by microsomes, whereas the rates of esterification of 4, 7,10,13,16-22:5, 7,10,13,16-22:4 and 5,8,11,14-20:4 were respectively
Yanzhong Feng et al.
Frontiers in immunology, 11, 599735-599735 (2020-11-17)
Ulva prolifera extract contains a variety of functional active substances. Whether these substances had any beneficial effects on the small intestine of weaned piglets under oxidative stress remained unknown. We explored the effects of U. prolifera extract on oxidative stress
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