Phenoxybenzamine

Phenoxybenzamine

Clinical data
Trade names	Dibenzyline
AHFS/Drugs.com	Monograph
MedlinePlus	a682059
Pregnancy category	AU: B2
Routes of administration	Oral
ATC code	C04AX02 (WHO)
Pharmacokinetic data
Elimination half-life	24 hours
Identifiers
IUPAC name (RS)-N-Benzyl-N-(2-chloroethyl)-1-phenoxypropan-2-amine
CAS Number	59-96-1 Y
PubChem CID	4768
IUPHAR/BPS	7268
DrugBank	DB00925 Y
ChemSpider	4604 Y
UNII	0TTZ664R7Z
KEGG	D08358 Y
ChEMBL	ChEMBL753 Y
CompTox Dashboard (EPA)	DTXSID0023458
ECHA InfoCard	100.000.406
Chemical and physical data
Formula	C18H22ClNO
Molar mass	303.83 g·mol−1
3D model (JSmol)	Interactive image
Chirality	Racemic mixture
SMILES ClCCN(C(COc1ccccc1)C)Cc2ccccc2
InChI InChI=1S/C18H22ClNO/c1-16(15-21-18-10-6-3-7-11-18)20(13-12-19)14-17-8-4-2-5-9-17/h2-11,16H,12-15H2,1H3 Y Key:QZVCTJOXCFMACW-UHFFFAOYSA-N Y
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Phenoxybenzamine (PBZ, marketed under the trade names Dibenzyline and Dibenyline) is a non-selective, irreversible alpha blocker.

Uses

It is used in the treatment of hypertension, and specifically that caused by pheochromocytoma. It has a slower onset and a longer-lasting effect compared with other alpha blockers.

It was also the first alpha blocker to be used for treatment of benign prostatic hyperplasia, although it is currently seldom used for that indication due to unfavourable side effects.

It has been used in the treatment of hypoplastic left heart syndrome.

It is also used in complex regional pain syndrome (CRPS) type 1 due to its antiadrenergic effects. It has shown to be beneficial if used in the first 3 months of the CRPS diagnosis.

Investigational

Phenoxybenzamine has long been known to block ejaculation without affecting semen quality or ability to achieve orgasm, which could make it an effective male contraceptive. This effect is completely reversible, and is believed to be the result of alpha-1 adrenoceptor blockade in the longitudinal muscles of the vas deferens. A dose of 20 mg/day results in aspermia due to reversible paralyzing effects on the vas deferens, ampulla, and ejaculatory ducts. Due to these actions, phenoxybenzamine is also useful for the treatment of premature ejaculation in men.

Pharmacology

Phenoxybenzamine is used as an anti-hypertensive due to its efficacy in reducing the vasoconstriction caused by epinephrine (adrenaline) and norepinephrine. Phenoxybenzamine forms a permanent covalent bond with adrenergic receptors. Based on known information about the structures of these receptors, it likely involves attack by the cysteine at position 3.36 in transmembrane helix 3 to form a stable linkage. Thus, it remains permanently bound to the receptor, preventing adrenaline and noradrenaline from binding. This causes vasodilation in blood vessels, due to its antagonistic effect at the alpha-1 adrenoceptor found in the walls of blood vessels, resulting in a drop in blood pressure. A side effect of phenoxybenzamine is reflex tachycardia.

As a non-selective alpha receptor antagonist, it will also affect both the postsynaptic alpha 1 and presynaptic alpha 2 receptors in the nervous system, and so reduce sympathetic activity. This results in further vasodilation, pupil constriction, an increase in GI tract motility and secretions, and glycogen synthesis.

Clinically, non-selective alpha antagonists block alpha receptors (but do not differentiate between alpha-1 and alpha-2). They are used as antihypertensives because they block alpha-receptor-mediated vasoconstriction. The block on alpha-2 receptors further potentiates beta-effects, increasing cardiac output.

Phenoxybenzamine has a long-lasting action, binding covalently to the alpha receptors. Its only current clinical use is in preparing patients with pheochromocytoma for surgery; its irreversible antagonism and the resultant depression in the maximum of the agonist dose-response curve are desirable in a situation where surgical manipulation of the tumour may release a large bolus of pressor amine into the circulation. Typically, phenoxybenzamine is not used in the long term, as new receptors are made to upregulate alpha stimulation. The main limiting side-effects of alpha antagonists is that the baroreceptor reflex is disrupted and thus this can cause postural hypotension.

Phenoxybenzamine also has irreversible antagonist/weak partial agonist properties at the serotonin 5-HT_2A receptor. Due to its 5-HT_2A receptor antagonism, phenoxybenzamine is useful in the treatment of carcinoid tumor, a neoplasm that secretes large amounts of serotonin and causes diarrhea, bronchoconstriction, and flushing.

Stereoisomerism

Phenoxybenzamine contains a stereocenter, so there are two enantiomers, the (R)- and the (S)-forms. All commercial preparations contain the drug as racemate.

Enantiomers of phenoxybenzamine
(R)-Phenoxybenzamine CAS number: 71799-91-2	(S)-Phenoxybenzamine CAS number: 71799-90-1

See also

• Ketanserin
• Pindobind
• Phentolamine

External links

• Media related to Phenoxybenzamine at Wikimedia Commons