Juniperic acid

Juniperic acid
Names
	IUPAC name 16-Hydroxyhexadecanoic acid
	Other names 16-Hydroxypalmitic acid; omega-Hydroxypalmitic acid; ω-Hydroxypalmitic acid;
Identifiers
CAS Number	506-13-8;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:55328;
ChEMBL	ChEMBL4281719;
ChemSpider	10034;
ECHA InfoCard	100.007.299
EC Number	208-028-7;
KEGG	C18218;
PubChem CID	10466;
CompTox Dashboard (EPA)	DTXSID6060133 ;
	InChI InChI=1S/C16H32O3/c17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16(18)19/h17H,1-15H2,(H,18,19) Key: UGAGPNKCDRTDHP-UHFFFAOYSA-N;
	SMILES C(CCCCCCCC(=O)O)CCCCCCCO;
Properties
Chemical formula	C16H32O3
Molar mass	272.429 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Juniperic acid or 16-hydroxyhexadecanoic acid is an omega-hydroxy long-chain fatty acid that is palmitic acid which is substituted at position 16 by a hydroxy group. Palmitic acid is converted to juniperic acid by cytochrome P450 various enzymes,^[1] including CYP704B22.^[2]

Juniperic acid is a key monomer of cutin in the plant cuticle.^[3] It has a role as a plant metabolite.

References edit

^ Van Bogaert, Inge N. A.; Groeneboer, Sara; Saerens, Karen; Soetaert, Wim (2011). "The role of cytochrome P450 monooxygenases in microbial fatty acid metabolism". FEBS Journal. 278 (2): 206–221. doi:10.1111/j.1742-4658.2010.07949.x. PMID 21156025. S2CID 22920318.
^ Li, Hui; Pinot, Franck; Sauveplane, Vincent; Werck-Reichhart, Danièle; Diehl, Patrik; Schreiber, Lukas; Franke, Rochus; Zhang, Ping; Chen, Liang; Gao, Yawei; Liang, Wanqi; Zhang, Dabing (2010). "Cytochrome P450 Family Member CYP704B2 Catalyzes the ω -Hydroxylation of Fatty Acids and is Required for Anther Cutin Biosynthesis and Pollen Exine Formation in Rice". The Plant Cell. 22 (1): 173–190. doi:10.1105/tpc.109.070326. PMC 2828706. PMID 20086189.
^ "Metabocard for 16-Hydroxyhexadecanoic acid (HMDB0006294)". The Metabolomics Innovation Centre.

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

[1] Van Bogaert, Inge N. A.; Groeneboer, Sara; Saerens, Karen; Soetaert, Wim (2011). "The role of cytochrome P450 monooxygenases in microbial fatty acid metabolism". FEBS Journal. 278 (2): 206–221. doi:10.1111/j.1742-4658.2010.07949.x. PMID 21156025. S2CID 22920318.

[2] Li, Hui; Pinot, Franck; Sauveplane, Vincent; Werck-Reichhart, Danièle; Diehl, Patrik; Schreiber, Lukas; Franke, Rochus; Zhang, Ping; Chen, Liang; Gao, Yawei; Liang, Wanqi; Zhang, Dabing (2010). "Cytochrome P450 Family Member CYP704B2 Catalyzes the ω -Hydroxylation of Fatty Acids and is Required for Anther Cutin Biosynthesis and Pollen Exine Formation in Rice". The Plant Cell. 22 (1): 173–190. doi:10.1105/tpc.109.070326. PMC 2828706. PMID 20086189.

[3] "Metabocard for 16-Hydroxyhexadecanoic acid (HMDB0006294)". The Metabolomics Innovation Centre.

[1]

[2]

[3]

Names

IUPAC name 16-Hydroxyhexadecanoic acid
Other names 16-Hydroxypalmitic acid omega-Hydroxypalmitic acid ω-Hydroxypalmitic acid
Identifiers
CAS Number	506-13-8
3D model (JSmol)	Interactive image
ChEBI	CHEBI:55328
ChEMBL	ChEMBL4281719
ChemSpider	10034
ECHA InfoCard	100.007.299
EC Number	208-028-7
KEGG	C18218
PubChem CID	10466
CompTox Dashboard (EPA)	DTXSID6060133
InChI InChI=1S/C16H32O3/c17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16(18)19/h17H,1-15H2,(H,18,19) Key: UGAGPNKCDRTDHP-UHFFFAOYSA-N
SMILES C(CCCCCCCC(=O)O)CCCCCCCO
Properties
Chemical formula	C₁₆H₃₂O₃
Molar mass	272.429 g·mol⁻¹
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references