Arotinolol
(IUPAC ) ime
(RS )-5-(2[3-(tert -butilamino)-2-hidroksipropil]sulfanil 1,3-tiazol-4-il)tiofen-2-karboksamid
Klinički podaci
AHFS/Drugs.com
Internacionalno ime leka
Identifikatori
CAS broj
41287-43-8
ATC kod
nije dodeljen
PubChem [ 1] [ 2]
2239
ChemSpider [ 3]
2152
UNII
394E3P3B99 Y
KEGG [ 4]
D07465 Y
ChEMBL [ 5]
CHEMBL93298 Y
Hemijski podaci
Formula
C 15 H 21 N 3 O 2 S 3
Mol. masa
371,54 g/mol
SMILES
eMolekuli & PubHem
InChI
InChI=1S/C15H21N3O2S3/c1-15(2,3)17-6-9(19)7-21-14-18-10(8-22-14)11-4-5-12(23-11)13(16)20/h4-5,8-9,17,19H,6-7H2,1-3H3,(H2,16,20) Y Key: BHIAIPWSVYSKJS-UHFFFAOYSA-N Y
Farmakokinetički podaci
Bioraspoloživost
2 h
Poluvreme eliminacije
10 h
Farmakoinformacioni podaci
Trudnoća
?
Pravni status
℞ Prescription only
Način primene
Oralno
Arotinolol (Almarl ) je lek u klasi mešovitih alfa/beta blokatora .[ 6]
On se koristi za tretman visokog krvnog pritiska .[ 7] Predloženo je da se on može koristiti za treatman esencijalnog tremora .[ 8]
↑ 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
↑ Zhao J, Golozoubova V, Cannon B, Nedergaard J (July 2001). „Arotinolol is a weak partial agonist on beta 3-adrenergic receptors in brown adipocytes” . Can. J. Physiol. Pharmacol. 79 (7): 585–93. DOI :10.1139/cjpp-79-7-585 . PMID 11478592 .
↑ Wu H, Zhang Y, Huang J, et al. (September 2001). „Clinical trial of arotinolol in the treatment of hypertension: dippers vs. non-dippers” . Hypertens. Res. 24 (5): 605–10. DOI :10.1291/hypres.24.605 . PMID 11675958 . - Scholar search }}
↑ Lee KS, Kim JS, Kim JW, Lee WY, Jeon BS, Kim D (August 2003). „A multicenter randomized crossover multiple-dose comparison study of arotinolol and propranolol in essential tremor” . Parkinsonism Relat. Disord. 9 (6): 341–7. DOI :10.1016/S1353-8020(03)00029-4 . PMID 12853233 .
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.