Tertatolol
(IUPAC ) ime
(±)-1-(tert -butilamino)-3-(3,4-dihidro-2H -tiohromen-8-iloksi)propan-2-ol
Klinički podaci
AHFS/Drugs.com
Internacionalno ime leka
Identifikatori
CAS broj
34784-64-0
ATC kod
C07 AA16
PubChem [1] [2]
36920
UNII
9ZO341YQXP Y
KEGG [3]
D07182 Y
ChEMBL [4]
CHEMBL434200 Y
Hemijski podaci
Formula
C 16 H 25 N O 2 S
Mol. masa
295,44 g/mol
SMILES
eMolekuli & PubHem
InChI
InChI=1S/C16H25NO2S/c1-16(2,3)17-10-13(18)11-19-14-8-4-6-12-7-5-9-20-15(12)14/h4,6,8,13,17-18H,5,7,9-11H2,1-3H3 Y Key: HTWFXPCUFWKXOP-UHFFFAOYSA-N Y
Farmakoinformacioni podaci
Trudnoća
?
Pravni status
℞ Prescription only
Način primene
Oralno
Tertatolol (Artex , Artexal , Prenalex ) je lek u klasi beta blokatora . On se koristi za tretiranje visokog krvnog pritiska . Tertatolol je otkrila francuska farmaceutska kompanija Servijer i u prodaji je u Evropi .[5]
Tertatolol deluje kao antagonist 5-HT1A receptor , slično pindololu .[6] [7]
↑ 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 . http://www.sciencedirect.com/science/article/pii/S1359644610007737 . 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 .
↑ 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 . http://onlinelibrary.wiley.com/doi/10.1002/%28SICI%291097-0061%28200004%2917:1%3C48::AID-YEA2%3E3.0.CO;2-H/full .
↑ 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
↑ Swiss Pharmaceutical Society (2000). Index Nominum 2000: International Drug Directory (Book with CD-ROM) . Boca Raton: Medpharm Scientific Publishers. ISBN 3-88763-075-0 . http://books.google.com/books?id=5GpcTQD_L2oC&lpg=PA1002&pg=PA1002#v=onepage&q=&f=false .
↑ Jolas T, Haj-Dahmane S, Lanfumey L, et al. (May 1993). „(-)Tertatolol is a potent antagonist at pre- and postsynaptic serotonin 5-HT1A receptors in the rat brain”. Naunyn-Schmiedeberg's Archives of Pharmacology 347 (5): 453–63. PMID 7686633 .
↑ Soudijn, W.; Olivier, Berend; Wijngaarden, I. van (1997). Serotonin receptors and their ligands . Amsterdam: Elsevier. ISBN 0-444-82041-8 . http://books.google.com/books?id=lfo0hGqIex0C&lpg=PA37&pg=PA37#v=onepage&q=&f=false .
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Levonordefrin •
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Metoksamin •
Metildopa •
Midodrin •
Nafazolin •
Norepinefrin (Noradrenalin) •
Oktopamin •
Oksimetazolin •
Fenilefrin •
Fenilpropanolamin •
Pseudoefedrin •
Sinefrin •
Tetrahidrozolin Antagonisti :
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Atiprosin •
Benoksatian •
Buflomedil •
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CI-926 •
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DL-017 •
Domesticin •
Doksazosin •
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Fenspirid •
GYKI-12,743 •
GYKI-16,084 •
Indoramin •
Ketanserin •
L-765,314 •
Labetalol •
Mefendioksan •
Metazosin •
Monatepil •
Moksisilit (Timoksamin) •
Naftopidil •
Nantenin •
Neldazosin •
Nicergolin •
Niguldipin •
Pelanserin •
Fendioksan •
Fenoksibenzamin •
Fentolamin •
Piperoksan •
Prazosin •
Hinazosin •
Ritanserin •
RS-97,078 •
SGB-1,534 •
Silodosin •
SL-89.0591 •
Spiperon •
Talipeksol •
Tamsulosin •
Terazosin •
Tibalosin •
Tiodazosin •
Tipentosin •
Tolazolin •
Trimazosin •
Upidosin •
Urapidil •
Zolertin * Mnogi TCA , TeCA , antipsihotici , ergolini , i neki piperazini kao što su buspiron , trazodon , nefazodon , etoperidon , i mepiprazol takođe antagoniziraju α1 -adrenergičke receptore, što doprinosi njihovim nuspojavama.
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