1-Aminociklopropan-1-karboksilna kiselina

1-Aminociklopropan-1-karboksilna kiselina
Nazivi
	Drugi nazivi 1-Aminociklopropankarboksilna kiselina
Identifikacija
CAS broj	22059-21-8 ;
3D model (Jmol)	: interaktivna slika; interaktivna slika;
Abrevijacija	ACC
ChEBI	CHEBI:58360 ;
ChemSpider	520 ;
DrugBank	DB02085 ;
ECHA InfoCard	100.108.227
KEGG	C01234 ;
PubChem C ID	535;
	SMILES : C(O)(=O)C1(CC1)(N); O=C(O)C1(N)CC1; ; ; ; ;
Svojstva
Hemijska formula	C4H7NO2
Molarna masa	101,1
	Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa).
	verifikuj (šta je ?)
	Reference infokutije

1-Aminociklopropan-1-karboksilna kiselina (ACC) je disupstituisana ciklična alfa-aminokiselina u kojoj je tročlani ciklopropanski prsten kondenzovan sa C(alfa)-atomom aminokiseline.

ACC ima značajnu ulogu u biosintezi biljnog hormona etilena.^[5]^[6] Ova kiselina se sintetiše posredstvom enzima ACC synthase ( EC 4.4.1.14) iz metionina i konvertuje se u etilen posredstvom ACC oksidaze (EC 1.14.17.4).^[7]

ACC takođe nefiziološki parcijalni agonist NMDA receptora sisara.^[8]

Reference

^ Caspi R, Foerster H, Fulcher CA, Hopkinson R, Ingraham J, Kaipa P, Krummenacker M, Paley S, Pick J, Rhee SY, Tissier C, Zhang P, Karp PD (2006). „MetaCyc: a multiorganism database of metabolic pathways and enzymes”. Nucleic Acids Res. 34 (Database issue): D511—6. PMC 1347490  . PMID 16381923. doi:10.1093/nar/gkj128.
^ 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.
^ 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. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди
^ 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.
^ Yang S, Hoffman N (1984). „Ethylene biosynthesis and its regulation in higher plants”. Annu. Rev. Plant Physiol. 35: 155—189. doi:10.1146/annurev.pp.35.060184.001103.
^ Kende H (1993). „Ethylene biosynthesis”. Annu. Rev. Plant Physiol. 44: 283—307. doi:10.1146/annurev.pp.44.060193.001435.
^ Kende H (1989). „Enzymes of Ethylene Biosynthesis”. Plant Physiol. 91 (1): 1—4. PMC 1061940  . PMID 16666977. doi:10.1104/pp.91.1.1.
^ Inanobe A, Furukawa H, Gouaux E (2005). „Mechanism of partial agonist action at the NR1 subunit of NMDA receptors”. Neuron. 47 (1): 71—84. PMID 15996549. doi:10.1016/j.neuron.2005.05.022.

[pmid16381923-1] Caspi R, Foerster H, Fulcher CA, Hopkinson R, Ingraham J, Kaipa P, Krummenacker M, Paley S, Pick J, Rhee SY, Tissier C, Zhang P, Karp PD (2006). „MetaCyc: a multiorganism database of metabolic pathways and enzymes”. Nucleic Acids Res. 34 (Database issue): D511—6. PMC 1347490  . PMID 16381923. doi:10.1093/nar/gkj128.

[2] 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.

[3] 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. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди

[4] 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.

[Yang_1984-5] Yang S, Hoffman N (1984). „Ethylene biosynthesis and its regulation in higher plants”. Annu. Rev. Plant Physiol. 35: 155—189. doi:10.1146/annurev.pp.35.060184.001103.

[Kende_1993-6] Kende H (1993). „Ethylene biosynthesis”. Annu. Rev. Plant Physiol. 44: 283—307. doi:10.1146/annurev.pp.44.060193.001435.

[Kende_1989-7] Kende H (1989). „Enzymes of Ethylene Biosynthesis”. Plant Physiol. 91 (1): 1—4. PMC 1061940  . PMID 16666977. doi:10.1104/pp.91.1.1.

[pmid15996549-8] Inanobe A, Furukawa H, Gouaux E (2005). „Mechanism of partial agonist action at the NR1 subunit of NMDA receptors”. Neuron. 47 (1): 71—84. PMID 15996549. doi:10.1016/j.neuron.2005.05.022.

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