Therapeutic Targets Database
BIDD Pharmainformatics Databases


TTD Drug ID: DAP000305

Drug Information
SynonymsPrestwick1_000382; AC1L1DIZ; SPBio_002484; Lopac0_000193; CHEBI:3082; BSPBio_000563; CHEMBL423; DB00195; Betazolol; Prestwick3_000382; ALO-1401-02; D07526; Kerlone; L000125; Betaxolol (TN); (.+/-.)-1-[p-[2-(Cyclopropylmethoxy)ethyl]phenoxy]-3-(isopropylamino)-2-propanol; 1-(isopropylamino)-3-[p-(cyclopropylmethoxyethyl)phenoxy]-2-propanol; SL 75212; CID2369; UNII-O0ZR1R6RZ2; 1-[(4-{2-[(cyclopropylmethyl)oxy]ethyl}phenyl)oxy]-3-[(1-methylethyl)amino]propan-2-ol; Prestwick0_000382; Betaxolol HCL; Prestwick2_000382; C06849; HMS2089I07; AC-1115; NCGC00024863-04; Betaxolol (INN); MolPort-003-845-027; 63659-18-7; LS-122005; 2-Propanol, 1-(4-(2-(cyclopropylmethoxy)ethyl)phenoxy)-3-((1-methylethyl)amino)-; C18H29NO3; 1-[4-[2-(cyclopropylmethoxy)ethyl]phenoxy]-3-(propan-2-ylamino)propan-2-ol; betaxolol; NCGC00024863-03; Betaxololum; 1-{4-[2-(cyclopropylmethoxy)ethyl]phenoxy}-3-(propan-2-ylamino)propan-2-ol; NCGC00015159-08; KERLEDEX; Betaxololum [INN-Latin]; Betaxolol [INN:BAN]; 1-(4-(2-(Cyclopropylmethoxy)ethyl)phenoxy)-3-((1-methylethyl)amino)-2-propanol; BRD-A02759312-003-03-9; BPBio1_000621; SL-75212; 63659-19-8 (hydrochloride)
Trade NameBetoptic; Betoptic S; Lokren; Kerlone
CompanyLorex Pharmaceuticals
[ICD9: 401   ICD10: I10, I11, I12, I13, I15]
Approved    [1]

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Therapeutic ClassAntihypertensive Agents
CAS NumberCAS 63659-18-7
PubChem Compound IDCID 2369.
PubChem Substance IDSID 9067.
SuperDrug ATC IDC07AB05; S01ED02
SuperDrug CAS ID063659187;
TargetBeta-1 adrenergic receptorAntagonist[2][3]
Ref 1Natural products as sources of new drugs over the last 25 years. J Nat Prod. 2007 Mar;70(3):461-77. Epub 2007 Feb 20. To Reference
Ref 2beta-adrenergic enhancement of brain kynurenic acid production mediated via cAMP-related protein kinase A signaling. Prog Neuropsychopharmacol Biol Psychiatry. 2009 Apr 30;33(3):519-29. Epub 2009 Feb 12. To Reference
Ref 3Betaxolol, a beta(1)-adrenoceptor antagonist, reduces Na(+) influx into cortical synaptosomes by direct interaction with Na(+) channels: comparison with other beta-adrenoceptor antagonists. Br J Pharmacol. 2000 Jun;130(4):759-66. To Reference


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