Phentolamine: Difference between revisions

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Phentolamine
Clinical data
Trade names	Regitine
AHFS/Drugs.com	Micromedex Detailed Consumer Information
Pregnancy; category	C (U.S.);
Routes of; administration	Usually IV or IM
ATC code	C04AB01 (WHO) V03AB36 (WHO);
Pharmacokinetic data
Metabolism	Hepatic
Elimination half-life	19 minutes
Identifiers
	IUPAC name 3-[(4,5-dihydro-1H-imidazol-2-ylmethyl)(4-methylphenyl)amino]phenol;
CAS Number	50-60-2 ;
PubChem CID	5775;
IUPHAR/BPS	502;
DrugBank	DB00692 ;
ChemSpider	5571 ;
UNII	Z468598HBV;
KEGG	D08362 ;
ChEBI	CHEBI:8081 ;
ChEMBL	ChEMBL597 ;
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	C17H19N3O
Molar mass	281.352 g/mol
3D model (JSmol)	Interactive image;
	SMILES Oc3cc(N(c1ccc(cc1)C)CC/2=N/CCN\2)ccc3;
	InChI InChI=1S/C17H19N3O/c1-13-5-7-14(8-6-13)20(12-17-18-9-10-19-17)15-3-2-4-16(21)11-15/h2-8,11,21H,9-10,12H2,1H3,(H,18,19) ; Key:MRBDMNSDAVCSSF-UHFFFAOYSA-N ;
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VisualWikitext

Revision as of 02:04, 25 July 2014

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Phentolamine (Regitine) is a reversible^[1] nonselective alpha-adrenergic antagonist.^[2]

Mechanism

Its primary action is vasodilation due to α₁ blockade.^[3]

It also can lead to reflex tachycardia because of hypotension and α₂ inhibition, which increases sympathetic tone.^[4]

Uses

The primary application for phentolamine is for the control of hypertensive emergencies, most notably due to pheochromocytoma. ^[5]

It also has usefulness in the treatment of cocaine-induced cardiovascular complications, where one would generally avoid Beta-blockers (e.g. metoprolol), as they can cause unopposed alpha-adrenergic mediated coronary vasoconstriction, worsening myocardial ischemia and hypertension. It is important to note that phentolamine is not a first-line agent for this indication. Phentolamine should only be given to patients who do not fully respond to benzodiazepines, nitroglycerin, and calcium channel blockers. ^[6]^[7]

When given by injection it causes blood vessels to expand, thereby increasing blood flow. When injected into the penis (intracavernosal), it increases blood flow to the penis, which results in an erection.^[8]

It may be stored in crash carts to counteract severe peripheral vasoconstriction secondary to extravasation of peripherally placed vasopressor infusions, typically of norepinephrine. Epinephrine infusions are less vasoconstrictive than norepinephrine as they primarily stimulate beta receptor more than alpha receptors, but the effect remains dose dependent.

Phentolamine also has diagnostic and therapeutic roles in complex regional pain syndrome (reflex sympathetic dystrophy).^[9]

Phentolamine has recently been introduced in the dental field as a local anesthetic reversal agent. Distributed by Septodont, OraVerse is a Phentolamine Mesylate injection designed to reverse the local vasoconstrictor properties used in many local anesthetics to prolong anesthesia.^[10] OraVerse has been shown to accelerate the reversal of the lingering soft-tissue numbness associated with the widely used anesthetic-vasoconstrictor combinations.^[11]

Chemistry

Phentolamine can be synthesized by alkylation of 3-(4-methylanilino)phenol using 2-chloromethylimidazoline:^[12]^[13]

References

↑ Jewell, John R.; Longworth, David L.; Stoller, James K.; Casey, David (2003). The Cleveland Clinic internal medicine case reviews. Hagerstown, MD: Lippincott Williams & Wilkins. p. 32. ISBN 0-7817-4266-8.
↑ Phentolamine at the US National Library of Medicine Medical Subject Headings (MeSH)
↑ Brock G. Oral phentolamine (Vasomax). Drugs Today (Barcelona). 2000 Feb-Mar;36(2-3):121-4.
↑ Shen, Howard (2008). Illustrated Pharmacology Memory Cards: PharMnemonics. Minireview. p. 14. ISBN 1-59541-101-1.
↑ Tuncel M, Ram VC. Hypertensive emergencies. Etiology and management. American Journal of Cardiovascular Drugs. 2003;3(1):21-31.
↑ Hollander JE, Henry TD. Evaluation and management of the patient who has cocaine-associated chest pain. Cardiology Clinics. 2006 Feb;24(1):103-14.
↑ Chan GM, Sharma R, Price D, Hoffman RS, Nelson LS. Phentolamine Therapy for Cocaine-Association Acute Coronary Syndrome (CAACS). Journal of Medical Toxicology. 2006 Sep;2(3):108-11.
↑ Bella AJ, Brock GB. Intracavernous pharmacotherapy for erectile dysfunction. Endocrine. 2004 Mar-Apr;23(2-3):149-55.
↑ Rowbotham MC. Pharmacologic management of complex regional pain syndrome. Clinical Journal of Pain. 2006 Jun;22(5):425-9.
↑ http://www.novalar.com/oraverse-dental-specialty-pharmaceutical
↑ Malamed S. What's new in local anaesthesia? Society For The Advancement Of Anaesthesia In Dentistry Digest. 2009 Jan;25:4-14.
↑ K. Miescher, A. Marxer, E. Urech, Template:US Patent (1950)
↑ E. Urech, A. Marxer, K. Miescher, Helv. Chim. Acta, 33, 1386 (1950)

Template:Peripheral vasodilators

[isbn0-7817-4266-8-1] Jewell, John R.; Longworth, David L.; Stoller, James K.; Casey, David (2003). The Cleveland Clinic internal medicine case reviews. Hagerstown, MD: Lippincott Williams & Wilkins. p. 32. ISBN 0-7817-4266-8.

[2] Phentolamine at the US National Library of Medicine Medical Subject Headings (MeSH)

[3] Brock G. Oral phentolamine (Vasomax). Drugs Today (Barcelona). 2000 Feb-Mar;36(2-3):121-4.

[pharmnemonics-4] Shen, Howard (2008). Illustrated Pharmacology Memory Cards: PharMnemonics. Minireview. p. 14. ISBN 1-59541-101-1.

[5] Tuncel M, Ram VC. Hypertensive emergencies. Etiology and management. American Journal of Cardiovascular Drugs. 2003;3(1):21-31.

[6] Hollander JE, Henry TD. Evaluation and management of the patient who has cocaine-associated chest pain. Cardiology Clinics. 2006 Feb;24(1):103-14.

[7] Chan GM, Sharma R, Price D, Hoffman RS, Nelson LS. Phentolamine Therapy for Cocaine-Association Acute Coronary Syndrome (CAACS). Journal of Medical Toxicology. 2006 Sep;2(3):108-11.

[8] Bella AJ, Brock GB. Intracavernous pharmacotherapy for erectile dysfunction. Endocrine. 2004 Mar-Apr;23(2-3):149-55.

[9] Rowbotham MC. Pharmacologic management of complex regional pain syndrome. Clinical Journal of Pain. 2006 Jun;22(5):425-9.

[10] ttp://www.novalar.com/oraverse-dental-specialty-pharmaceutical

[11] Malamed S. What's new in local anaesthesia? Society For The Advancement Of Anaesthesia In Dentistry Digest. 2009 Jan;25:4-14.

[12] K. Miescher, A. Marxer, E. Urech, Template:US Patent (1950)

[13] E. Urech, A. Marxer, K. Miescher, Helv. Chim. Acta, 33, 1386 (1950)

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@@ Line 52: / Line 52: @@
 | StdInChIKey = MRBDMNSDAVCSSF-UHFFFAOYSA-N
 }}
+__NOTOC__
+{{SI}}
+{{CMG}}
+==Overview==
 '''Phentolamine''' (Regitine) is a reversible<ref name="isbn0-7817-4266-8">{{cite book |author=Jewell, John R.; Longworth, David L.; Stoller, James K.; Casey, David |title=The Cleveland Clinic internal medicine case reviews |publisher=Lippincott Williams & Wilkins |location=Hagerstown, MD |year=2003 |isbn=0-7817-4266-8 |oclc= |doi= |accessdate= |page=32}}</ref> nonselective alpha-[[adrenergic antagonist]].<ref>{{MeshName|Phentolamine}}</ref>
@@ Line 74: / Line 80: @@
 ==Chemistry==
 Phentolamine can be synthesized by alkylation of 3-(4-methylanilino)phenol using 2-chloromethylimidazoline:<ref>K. Miescher, A. Marxer, E. Urech, {{US Patent|2503059}} (1950)</ref><ref>E. Urech, A. Marxer, K. Miescher, Helv. Chim. Acta, 33, 1386 (1950)</ref>
-:[[File:Phentolamine synthesis.png|400px|left]]{{clear left}}
 ==References==
@@ Line 82: / Line 86: @@
 {{Antihypertensives and diuretics}}
 {{Peripheral vasodilators}}
-{{Drugs for erectile dysfunction and PE}}
-{{Alpha blockers}}
 [[Category:Antihypertensive agents]]
+[[Category:Alpha blockers]]
+[[Category:Diuretics]]
+[[Category:Cardiovascular Drugs]]
+[[Category:Drug]]
 [[Category:Vasodilators]]
-[[Category:Imidazolines]]
-[[Category:Alpha blockers]]
-[[Category:Phenols]]
-[[Category:Anilines]]

v t e Antihypertensives (C02) and diuretics (C03)
Sympatholytic agents	Template:Navbox subgroup
Vasodilators	Diazoxide • hydrazinophthalazine (Hydralazine, Dihydralazine, Endralazine, Cadralazine) • Minoxidil • Nitroprusside • Phentolamine
Other antihypertensives	serotonin antagonist (Ketanserin) • endothelin receptor antagonist (Bosentan, Ambrisentan, Sitaxsentan) • MAOI (Pargyline) • THI (Metirosine)
Diuretics	Template:Navbox subgroup