Levobunolol
(IUPAC ) ime
(S )-5[3-(tert -butilamino)-2-hidroksipropil]oksi3,4-dihidronaftalen-1(2H )-on
Klinički podaci
Robne marke
Betagan
AHFS/Drugs.com
Monografija
MedlinePlus
a686011
Identifikatori
CAS broj
47141-42-4
ATC kod
S01 ED03
PubChem [ 1] [ 2] 39468
DrugBank
DB01210
ChemSpider [ 3] 36089
UNII
G6317AOI7K Y
KEGG [ 4] D08115 Y
ChEBI
CHEBI:6438 Y
ChEMBL [ 5] CHEMBL1201237 Y
Hemijski podaci
Formula
C 17 H 25 N O 3
Mol. masa
291,385 g/mol
SMILES
eMolekuli PubHem
InChI InChI=1S/C17H25NO3/c1-17(2,3)18-10-12(19)11-21-16-9-5-6-13-14(16)7-4-8-15(13)20/h5-6,9,12,18-19H,4,7-8,10-11H2,1-3H3/t12-/m0/s1 Y Y
Farmakokinetički podaci
Poluvreme eliminacije
20 sata
Farmakoinformacioni podaci
Trudnoća
?
Pravni status
℞ -only (SAD )
Način primene
Topikalno (kapi za oči )
Levobunolol (AK-Beta , Liquifilm , Betegan ) je neselektivni beta blokator . On se koristi topikalno za tretiranje glaukoma .
↑ 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 ↑ 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 . ↑ 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
Ishibashi T, Yokoi N, Kinoshita S (2003). „Comparison of the effects of topical levobunolol and timolol solution on the human ocular surface.”. Cornea 22 (8): 709–15. DOI :10.1097/00003226-200311000-00001 . PMID 14576520 . Ogasawara H, Yoshida A, Fujio N, Konno S, Ishiko S (1999). „[Effect of topical levobunolol on retinal, optic nerve head, and choroidal circulation in normal volunteers]”. Nippon Ganka Gakkai Zasshi 103 (7): 544–50. PMID 10443129 . Leung M, Grunwald J (1997). „Short-term effects of topical levobunolol on the human retinal circulation.”. Eye 11 (3): 371–6. DOI :10.1038/eye.1997.78 . PMID 9373479 .
Agonisti :
5-FNE •
6-FNE •
Amidefrin •
Anisodamin •
Anisodin •
Cirazolin •
Dipivefrin •
Dopamin •
Efedrin •
Epinefrin (Adrenalin) •
Etilefrin •
Etilnorepinefrin •
Indanidin •
Levonordefrin •
Metaraminol •
Metoksamin •
Metildopa •
Midodrin •
Nafazolin •
Norepinefrin (Noradrenalin) •
Oktopamin •
Oksimetazolin •
Fenilefrin •
Fenilpropanolamin •
Pseudoefedrin •
Sinefrin •
Tetrahidrozolin Antagonisti :
Abanohil •
Adimolol •
Ajmalicin •
Alfuzosin •
Amosulalol •
Arotinolol •
Atiprosin •
Benoksatian •
Buflomedil •
Bunazosin •
Karvedilol •
CI-926 •
Korinantin •
Dapiprazol •
DL-017 •
Domesticin •
Doksazosin •
Eugenodilol •
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.
