| 词条 | Dipivefrine |
| 释义 |
| Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 460793250 | IUPAC_name = [2-(2,2-Dimethylpropanoyloxy)-4-(1-hydroxy-2-methylamino-ethyl)-phenyl] 2,2-dimethylpropanoate | image = Dipivefrine.svg | tradename = Propine, Pivalephrine | Drugs.com = {{drugs.com|international|dipivefrine}} | MedlinePlus = a686005 | pregnancy_US = B | legal_status = Rx-only | routes_of_administration = Eye drops | bioavailability = | metabolism = | elimination_half-life = | IUPHAR_ligand = 7166 | CAS_number_Ref = {{cascite|correct|??}} | CAS_number = 52365-63-6 | ATC_prefix = S01 | ATC_suffix = EA02 | ATC_supplemental = | PubChem = 3105 | DrugBank_Ref = {{drugbankcite|correct|drugbank}} | DrugBank = DB00449 | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 2994 | UNII_Ref = {{fdacite|correct|FDA}} | UNII = 8Q1PVL543G | KEGG_Ref = {{keggcite|correct|kegg}} | KEGG = D02349 | ChEBI_Ref = {{ebicite|correct|EBI}} | ChEBI = 4646 | ChEMBL_Ref = {{ebicite|changed|EBI}} | ChEMBL = 1201262 | synonyms = Dipivefrin | C=19 | H=29 | N=1 | O=5 | molecular_weight = 351.437 g/mol | smiles = O=C(Oc1cc(ccc1OC(=O)C(C)(C)C)C(O)CNC)C(C)(C)C | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 1S/C19H29NO5/c1-18(2,3)16(22)24-14-9-8-12(13(21)11-20-7)10-15(14)25-17(23)19(4,5)6/h8-10,13,20-21H,11H2,1-7H3 | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = OCUJLLGVOUDECM-UHFFFAOYSA-N }}Dipivefrine (INN) or dipivefrin (USAN), trade name Propine among others, is a prodrug of epinephrine, and is used to treat open-angle glaucoma.[1][2] It is available{{citation needed|date=January 2017}} as a 0.1% ophthalmic solution. It is no longer available in the United States.[3] ContraindicationsUse in narrow-angle glaucoma may be dangerous because it could make the eye susceptible to an attack of angle closure,[2] causing an increase in pressure and pain, and possibly loss of vision. Side effectsThe most common side effects of dipivefrine are burning, stinging and other irritations of the eye. Possible, but uncommon, side effects are those of epinephrine: tachycardia (fast heartbeat), hypertension (high blood pressure) and arrhythmias (irregular heartbeat).[2] PharmacologyDipivefrine penetrates the cornea and is then hydrolysed to epinephrine by esterase enzymes. It increases outflow of the aqueous humour and also reduces its formation (mediated by its action on α1 and α2 receptors), thus reducing pressure inside the eye. It also increases the conductivity of trabecular filtering cells (a β2 receptor mediated action). It is preferred to epinephrine because it is longer acting, more consistent in its action and better tolerated.[1] References1. ^1 {{cite book|title=Essentials of Medical Pharmacology|publisher=Jaypee Brothers Medical Publishers(P) Ltd.|isbn=81-8061-187-6|page=88|author=KD Tripari|edition=5}} {{Opthalmologicals}}2. ^1 2 Dipivefrin {{Drugs.com|pro|dipivefrin}}. 3. ^{{cite journal | author=Zhang L, Weizer JS, Musch DC | title= Perioperative medications for preventing temporarily increased intraocular pressure after laser trabeculoplasty | journal= Cochrane Database Syst Rev | volume= 2 | pages= CD010746 | date= 2017 | pmid= 28231380 | doi= 10.1002/14651858.CD010746.pub2 | pmc=5477062}} 4 : Prodrugs|Pivalates|Catecholamines|Alcohols |
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