3-Јodotironamin

3-Јodotironamin
	4-[4-(2-Amino-etil)-2-jodo-fenoksi]-fenol
Drugi nazivi	T1AM
Identifikacija
CAS registarski broj	712349-95-6
ChemSpider	8126125
Jmol-3D slike	Slika 1; Slika 2
SMILES
	OC1=CC=C(OC2=C(I)C=C(CCN)C=C2)C=C1 Ic2cc(ccc2Oc1ccc(O)cc1)CCN
InChI
	InChI=1S/C14H14INO2/c15-13-9-10(7-8-16)1-6-14(13)18-12-4-2-11(17)3-5-12/h1-6,9,17H,7-8,16H2 ; Kod: XIINYOJWNGOUPF-UHFFFAOYSA-N InChI=1/C14H14INO2/c15-13-9-10(7-8-16)1-6-14(13)18-12-4-2-11(17)3-5-12/h1-6,9,17H,7-8,16H2; Kod: XIINYOJWNGOUPF-UHFFFAOYAJ
Svojstva
Molekulska formula	C14H14INO2
Molarna masa	355,17 g/mol
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

3-Jodotironamin (T₁AM) je endogeni tironamin. T₁AM je ligand visokog afiniteta za trag amin-asocirani receptor TAAR1 (TAR1, TA1), nedavno otkriveni G protein spregnuti receptor.^[2]^[3] T₁AM je najpotentniji TAAR1 agonist do sada otkriven.^[4] Aktivacija TAAR1 receptora T₁AM ligandom dovodi do produkcije velikih količina cAMP-a. Taj efekat je spregnut sa sniženjem telesne temperature i srčanog izlaza.^[5] T₁AM je deo signalnog puta koji moduliše srčanu funkciju.^[6]

Reference

↑ 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
↑ Scanlan T, Suchland K, Hart M, Chiellini G, Huang Y, Kruzich P, Frascarelli S, Crossley D, Bunzow J, Ronca-Testoni S, Lin E, Hatton D, Zucchi R, Grandy D (2004). „3-Iodothyronamine is an endogenous and rapid-acting derivative of thyroid hormone”. Nat. Med. 10 (6): 638–42. DOI:10.1038/nm1051. PMID 15146179.
↑ Hart M, Suchland K, Miyakawa M, Bunzow J, Grandy D, Scanlan T (2006). „Trace amine-associated receptor agonists: synthesis and evaluation of thyronamines and related analogues”. J. Med. Chem. 49 (3): 1101–12. DOI:10.1021/jm0505718. PMID 16451074.
↑ Wu SY, Green WL, Huang WS, Hays MT, Chopra IJ (2005). „Alternate Pathways of Thyroid Hormone Metabolism”. Thyroid 15 (8): 943–958. DOI:10.1089/thy.2005.15.943. PMID 16131336.
↑ „New compound may act to keep thyroid activity in check”. Pristupljeno 30. 5. 2008.
↑ Chiellini G, Frascarelli S, Ghelardoni S, Carnicelli V, Tobias SC, Debarber A, Brogioni S, Ronca-Testoni S, Cerbai E, Grandy DK, Scanlan TS, Zucchi R. (2007). „Cardiac effects of 3-iodothyronamine: a new aminergic system modulating cardiac function”. The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 21 (7): 1597–608. DOI:10.1096/fj.06-7474com. PMID 17284482.

Povezano

Spoljašnje veze

Portal Hemija

MeSH 3-iodothyronamine

[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

[2] Scanlan T, Suchland K, Hart M, Chiellini G, Huang Y, Kruzich P, Frascarelli S, Crossley D, Bunzow J, Ronca-Testoni S, Lin E, Hatton D, Zucchi R, Grandy D (2004). „3-Iodothyronamine is an endogenous and rapid-acting derivative of thyroid hormone”. Nat. Med. 10 (6): 638–42. DOI:10.1038/nm1051. PMID 15146179.

[3] Hart M, Suchland K, Miyakawa M, Bunzow J, Grandy D, Scanlan T (2006). „Trace amine-associated receptor agonists: synthesis and evaluation of thyronamines and related analogues”. J. Med. Chem. 49 (3): 1101–12. DOI:10.1021/jm0505718. PMID 16451074.

[Wu-4] Wu SY, Green WL, Huang WS, Hays MT, Chopra IJ (2005). „Alternate Pathways of Thyroid Hormone Metabolism”. Thyroid 15 (8): 943–958. DOI:10.1089/thy.2005.15.943. PMID 16131336.

[5] „New compound may act to keep thyroid activity in check”. Pristupljeno 30. 5. 2008.

[6] Chiellini G, Frascarelli S, Ghelardoni S, Carnicelli V, Tobias SC, Debarber A, Brogioni S, Ronca-Testoni S, Cerbai E, Grandy DK, Scanlan TS, Zucchi R. (2007). „Cardiac effects of 3-iodothyronamine: a new aminergic system modulating cardiac function”. The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 21 (7): 1597–608. DOI:10.1096/fj.06-7474com. PMID 17284482.

[1]

[2]

[3]

[4]

[5]

[6]

p r u Neurotransmiteri
Aminokiseline	Alanin • Aspartat • Cikloserin • DMG • GABA • Glutamat • Glicin • Hipotaurin • Kinurenska kiselina (Transtorin) • NAAG (Spaglumska kiselina) • NMG (Sarkozin) • Serin • Taurin • TMG (Betain)
Endokanabinoidi	2-AG • 2-AGE (Noladin etar) • AEA (Anandamid) • NADA • OAE (Virodhamin) • Oleamid
Gasotransmiteri	Ugljen-monoksid • Vodonik-sulfid • Azot-monoksid • Azotsuboksid
Monoamini	Dopamin • Epinefrin (Adrenalin) • Melatonin • NAS (Normelatonin) • Norepinefrin (Noradrenalin) • Serotonin (5-HT)
Purini	Adenozin • ADP • AMP • ATP
Trag amini	3-ITA • 5-MeO-DMT • Bufotenin • DMT • NMT • Oktopamin • Fenetilamin • Sinefrin • Tironamin • Triptamin • Tiramin
Drugi	1,4-BD • Acetilholin • GBL • GHB • Histamin
Vidi isto Neuropeptidi