1-Naftalenacetatna kiselina

1-Naftalenacetatna kiselina
	2-(1-Naftl)acetatna kiselina
Drugi nazivi	1-Naftalenacetatna kiselina; α-Naftalenacetatna kiselina; Naftilacetatna kiselina; NAA
Identifikacija
CAS registarski broj	86-87-3
PubChem	6862
ChemSpider	6601
DrugBank	DB01750
KEGG	D01558
ChEBI	32918
ChEMBL	CHEMBL428495
Jmol-3D slike	Slika 1
SMILES
	O=C(O)Cc2cccc1ccccc12
InChI
	InChI=1S/C12H10O2/c13-12(14)8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7H,8H2,(H,13,14) ; Kod: PRPINYUDVPFIRX-UHFFFAOYSA-N InChI=1/C12H10O2/c13-12(14)8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7H,8H2,(H,13,14); Kod: PRPINYUDVPFIRX-UHFFFAOYAF
Svojstva
Molekulska formula	C12H10O2
Molarna masa	186.21 g mol−1
Agregatno stanje	Beli prah
Tačka topljenja	135 °C
Rastvorljivost u vodi	0,38 g/L (17 °C)
pKa	4,24
Opasnost
Podaci o bezbednosti prilikom rukovanja (MSDS)	SIRI.org
Srodna jedinjenja
Srodna auksinske materije	Indol-3-acetatna kiselina
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

1-Naftalenacetatna kiselina (NAA) je organsko jedinjenje sa formulom C₁₀H₇CH₂CO₂H. Ova bezbojna čvrsta materija je rastvorna u organskim rastvaračima. Ova kiselina sadrži karboksilmetilnu grupu (CH₂CO₂H) sa naftalenom u 1-poziciji.

Use and regulation

NAA je sintetički biljni hormon iz auksinske familije i sastojak mnogih komercijalnih hortikulturnih produkata.^[7]

Reference

↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
↑ Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit
↑ Dippy, J. F. J.; Hughes, S. R. C.; Laxton, J. W. (1954). „Chemical Constitution and the Dissociation Constants of Monocarboxylic Acids. Part XIV. Monomethylcyclohexanecarboxylic Acids”. Journal of the Chemical Society (Resumed) 1954: 4102–4106. DOI:10.1039/JR9540004102.
↑ US patent 6800482, Šablon:Cite patent/authors, "Cultured cells of Australian laurel, Pittosporaceae and a method for culturing tissues by using said cultured cells", issued 5. 10. 2004.

Literatura

Tomlin, C.D.S., 2006. The Pesticide Manual, 14th ed. UK
V.A. Lozovaya, M.N. Markova, and I.A. Tarchevskii, Fiziol. Rast. (Moscow) 35, 1, 97 (1987)
A. Navalón, R. Blanc, J.L. Vilchez Determination of 1-naphthylacetic acid in commercial formulations and natural waters by solid-phase spectrofluorimetry Mikcrochim. Acta, 126 (1997), pp. 33–38
Q.M. Lu, L.H. Chen, M.H. Lu, G.N. Chen, L. Zhang Extraction and analysis of auxins in plants using dispersive liquid–liquid microextraction followed by high-performance liquid chromatography with fluorescence detection J. Agric. Food Chem., 58 (2010), pp. 2763–2770
W. Guan, P. Xu, K. Wang, Y. Song, H. Zhang Determination and study on dissipation of 1-naphthylacetic acid in garlic and soil using high performance liquid chromatography–tandem mass spectrometry College of Science, China Agricultural University, Beijing 100193, PR China
M.J. Benotti, F.P. Lee, R.A. Rieger, C.R. Iden, C.E. Heine, B.J. Brownawell HPLC/TOF-MS: an alternative to LC/MS/MS for sensitive and selective determination of polar organic contaminants in the aquatic environment Ferrer Imma, E.M. Thurman (Eds.), Liquid Chromatography/Mass Spectrometry, MS/MS and Time of Flight MS, American Chemical Society, New York (2003), pp. 109–127

Povezano

Vanjske veze

[1] Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit

[2] Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.

[3] Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit

[4] Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.

[5] Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit

[6] Dippy, J. F. J.; Hughes, S. R. C.; Laxton, J. W. (1954). „Chemical Constitution and the Dissociation Constants of Monocarboxylic Acids. Part XIV. Monomethylcyclohexanecarboxylic Acids”. Journal of the Chemical Society (Resumed) 1954: 4102–4106. DOI:10.1039/JR9540004102.

[7] US patent 6800482, Šablon:Cite patent/authors, "Cultured cells of Australian laurel, Pittosporaceae and a method for culturing tissues by using said cultured cells", issued 5. 10. 2004.

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