7-OH-DPAT
7-OH-DPAT | |||
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IUPAC ime |
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Naziv po klasifikaciji | 7-(Dipropilamino)-5,6,7,8-tetrahidronaftalen-2-ol[1] | ||
Identifikacija | |||
Abrevijacija | 7-OH-DPAT | ||
CAS registarski broj | 74938-11-7 ![]() | ||
PubChem[2][3] | 1219, 6603867 (R), 23928184 (S) | ||
ChemSpider[4] | 1182 ![]() ![]() | ||
MeSH | 7-Hydroxy-2-N,N-dipropylaminotetralin | ||
ChEMBL[5] | CHEMBL285755 ![]() | ||
Jmol-3D slike | Slika 1 Slika 2 | ||
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Svojstva | |||
Molekulska formula | C16H25NO | ||
Molarna masa | 247.38 g mol−1 | ||
log P | 3,653 | ||
pKa | 10,389 | ||
Baznost (pKb) | 3,608 | ||
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala | |||
Infobox references |
7-OH-DPAT je sintetičko jedinjenje koje deluje kao agonist dopaminskog receptora sa umerenom selektivnošću za D3 receptorski podtip,[6][7][8] i sa niskim afinitetom za serotoninske receptore, za razliku od njegovog strukturnog izomera 8-OH-DPAT.[9][10][11]
Reference
- ↑ 1,0 1,1 „7-hydroxy-2-N,N-dipropylaminotetralin - PubChem Public Chemical Database”. The PubChem Project. USA: National Center for Biotechnology Information.
- ↑ 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
- ↑ 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
- ↑ Mulder TB, de Vries JB, Dijkstra D, Wiechers JW, Grol CJ, Horn AS (November 1987). „Further in vitro and in vivo studies with the putative presynaptic dopamine agonist N,N-dipropyl-7-hydroxy-2-aminotetralin”. Naunyn-Schmiedeberg's Archives of Pharmacology 336 (5): 494–501. PMID 2830544.
- ↑ Lévesque D, Diaz J, Pilon C, Martres MP, Giros B, Souil E, Schott D, Morgat JL, Schwartz JC, Sokoloff P (September 1992). „Identification, characterization, and localization of the dopamine D3 receptor in rat brain using 7-[3Hhydroxy-N,N-di-n-propyl-2-aminotetralin”]. Proceedings of the National Academy of Sciences of the United States of America 89 (17): 8155–9. DOI:10.1073/pnas.89.17.8155. PMC 49875. PMID 1518841.
- ↑ Lévesque D (August 1996). „Aminotetralin drugs and D3 receptor functions. What may partially selective D3 receptor ligands tell us about dopamine D3 receptor functions?”. Biochemical Pharmacology 52 (4): 511–8. DOI:10.1016/0006-2952(96)00239-0. PMID 8759022.
- ↑ Arvidsson LE, Johansson AM, Hacksell U, Nilsson JL, Svensson K, Hjorth S, Magnusson T, Carlsson A, Andersson B, Wikström H (November 1987). „(+)-cis-8-Hydroxy-1-methyl-2-(di-n-propylamino)tetralin: a potent and highly stereoselective 5-hydroxytryptamine receptor agonist”. Journal of Medicinal Chemistry 30 (11): 2105–9. DOI:10.1021/jm00394a029. PMID 2959776.
- ↑ Malmberg A, Nordvall G, Johansson AM, Mohell N, Hacksell U (August 1994). „Molecular basis for the binding of 2-aminotetralins to human dopamine D2A and D3 receptors”. Molecular Pharmacology 46 (2): 299–312. PMID 8078492.
- ↑ Eltayb A, Lindblom S, Oerther S, Ahlenius S (July 2001). „Additive hypothermic effects of the 5-HT1A receptor agonist 8-OH-DPAT and the dopamine D2/3 receptor agonist 7-OH-DPAT in the rat”. Acta Physiologica Scandinavica 172 (3): 205–9. DOI:10.1046/j.1365-201x.2001.00858.x. PMID 11472307.
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Morfolini: Fenbutrazat • Morazon • Fendimetrazin • Fenmetrazin; Oksazolini: 4-Metilaminoreks (4-MAR, 4-MAX) • Aminoreks • Klominoreks • Ciklazodon • Fenozolon • Fluminoreks • Pemolin • Tozalinon; Fenetilamini (takođe amfetamini, katinoni, fentermini, itd): 2-Hidroksifenetilamin (2-OH-PEA) • 4-CAB • 4-Metilamfetamin (4-MA) • 4-Metilmetamfetamin (4-MMA) • Alfetamin • Amfekloral • Amfepentoreks • Amfepramon • Amfetamin (Dekstroamfetamin • Levoamfetamin) • Amfetaminil • β-Metilfenetilamin (β-Me-PEA) • Benzodioksolilbutanamin (BDB) • Benzodioksolilhidroksibutanamin (BOH) • Benzfetamin • Bufedron • Butilon • Katin • Katinon • Klobenzoreks • Klortermin • D-deprenil • Dimetoksiamfetamin (DMA) • Dimetoksimetamfetamin (DMMA) • Dimetilamfetamin • Dimetilkatinon (Dimetilpropion, metamfepramon) • Etkatinon (Etilpropion) • Etilamfetamin • Etilbenzodioksolilbutanamin (EBDB) • Etilon • Famprofazon • Fenetilin • Fenproporeks • Flefedron • Fludoreks • Furfenoreks • Hordenin • Lofofin (Homomiristicilamin) • Mefenoreks • Mefedron • Metamfetamin (Dezoksiefedrin, Metedrin; Dekstrometamfetamin • Levometamfetamin) • Metkatinon (Metilpropion) • Metedron • Metoksimetilenedioksiamfetamin (MMDA) • Metoksimetilendioksimetamfetamin (MMDMA) • Metilbenzodioksolilbutanamin (MBDB) • Metilendioksiamfetamin (MDA, tenamfetamin) • Metilendioksietilamfetamin (MDEA) • Metilendioksihidroksiamfetamin (MDOH) • Metilendioksimetamfetamin (MDMA) • Metilendioksimetilfenetilamin (MDMPEA, homarilamin) • Metilendioksifenetilamin (MDPEA, homopiperonilamin) • Metilon • Ortetamin • Parabromoamfetamin (PBA) • Parahloroamfetamin (PCA) • Parafluoroamfetamin (PFA) • Parafluorometamfetamin (PFMA) • Parahidroksiamfetamin (PHA) • Parajodoamfetamin (PIA) • Paredrin (Norfoledrin, Oksamfetamin) • Fenetilamin (PEA) • Foledrin • Fenprometamin • Prenilamin • Propilamfetamin • Tifloreks (Flutioreks) • Tiramin (TRA) • Ksilopropamin • Zilofuramin; Piperazini: 2,5-Dimetoksi-4-bromobenzilpiperazin (2C-B-BZP) • Benzilpiperazin (BZP) • Metoksifenilpiperazin (MeOPP, paraperazin) • Metilbenzilpiperazin (MBZP) • Metilendioksibenzilpiperazin (MDBZP, piperonilpiperazin); Drugi: 2-Amino-1,2-dihidronaftalen (2-ADN) • 2-Aminoindan (2-AI) • 2-Aminotetralin (2-AT) • 4-Benzilpiperidin (4-BP) • 5-IAI • Klofenciklan • Ciklopentamin • Cipenamin • Ciprodenat • Feprosidnin • Gilutensin • Heptaminol • Heksaciklonat • Indanilaminopropan (IAP) • Indanoreks • Izometepten • Metilheksanamin • Naftilaminopropan (NAP) • Oktodrin • Ftalimidopropiofenon • Propilheksedrin (Levopropilheksedrin) • Tuaminoheptan (Tuamin) |
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Hinazolinamini: SoRI-9804 • SoRI-20040 • SoRI-20041 |
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