Leu-enkefalin

Leu-enkefalin
	(2R)-2-[[(2R)-2-[[2-[[2-[[(2R)-2-amino-3-; (4-hydroxyphenyl)propanoyl]amino]acetyl]; amino]acetyl]amino]-3-phenylpropanoyl]; amino]-4-methylpentanoic acid
Identifikacija
CAS registarski broj	58822-25-6
PubChem	10415290
ChemSpider	21106451
IUPHAR ligand	1613
Jmol-3D slike	Slika 1
SMILES
	Oc2ccc(C[C@H](N)C(=O)NCC(=O)NCC(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CC(C)C)C(O)=O)cc2
InChI
	InChI=1S/C28H37N5O7/c1-17(2)12-23(28(39)40)33-27(38)22(14-18-6-4-3-5-7-18)32-25(36)16-30-24(35)15-31-26(37)21(29)13-19-8-10-20(34)11-9-19/h3-11,17,21-23,34H,12-16,29H2,1-2H3,(H,30,35)(H,31,37)(H,32,36)(H,33,38)(H,39,40)/t21-,22+,23-/m0/s1 ; Kod: URLZCHNOLZSCCA-ZRBLBEILSA-N InChI=1/C28H37N5O7/c1-17(2)12-23(28(39)40)33-27(38)22(14-18-6-4-3-5-7-18)32-25(36)16-30-24(35)15-31-26(37)21(29)13-19-8-10-20(34)11-9-19/h3-11,17,21-23,34H,12-16,29H2,1-2H3,(H,30,35)(H,31,37)(H,32,36)(H,33,38)(H,39,40)/t21-,22+,23-/m0/s1; Kod: URLZCHNOLZSCCA-ZRBLBEILBT
Svojstva
Molekulska formula	C28H37N5O7
Molarna masa	555.62268 g/mol
	; ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Leu-enkefalin je endogenni opioidni peptidni neurotransmiter koji se prirodno javlja u mozgu mnogih životinja, uključujući čoveka.^[4]^[5] On je jedna od dve forme enkefalina. Druga forma je met-enkefalin. Za tirozinski ostatak u poziciji 1 se smatra da je analogan sa 3-hidroksilnom grupom morfina.

Leu-enkefalin je peptid sa sekvencom: Tyr - Gly - Gly - Phe - Leu. On proizvodi farmakološke efekte na mi i delta opioidnim receptorima, mada ima veću potentnost na delta receptoru.

Literatura

↑ 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
↑ Dudás B, Merchenthaler I (2003). „Topography and associations of leu-enkephalin and luteinizing hormone-releasing hormone neuronal systems in the human diencephalon”. J Clin Endocrinol Metab. 88 (4): 1842-8.
↑ Khachaturian, Henry Lewis, Michael E. Watson, Stanley J. (2006). Immunocytochemical studies with antisera against Leu-enkephalin and an enkephalin-precursor fragment (BAM-22P) in the rat brain. Elsevier. DOI:10.1016/0024-3205(82)90233-8. PMID 6759829.

Spoljašnje veze

Portal Hemija

[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] Dudás B, Merchenthaler I (2003). „Topography and associations of leu-enkephalin and luteinizing hormone-releasing hormone neuronal systems in the human diencephalon”. J Clin Endocrinol Metab. 88 (4): 1842-8.

[5] Khachaturian, Henry Lewis, Michael E. Watson, Stanley J. (2006). Immunocytochemical studies with antisera against Leu-enkephalin and an enkephalin-precursor fragment (BAM-22P) in the rat brain. Elsevier. DOI:10.1016/0024-3205(82)90233-8. PMID 6759829.

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