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Indoramin

Introduction

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| C=22 | H=25 | N=3 | O=1 | molecular_weight = 347.454 g/mol | smiles = O=C(c1ccccc1)NC4CCN(CCc3c2ccccc2nc3)CC4 | InChI = 1/C22H25N3O/c26-22(17-6-2-1-3-7-17)24-19-11-14-25(15-12-19)13-10-18-16-23-21-9-5-4-8-20(18)21/h1-9,16,19,23H,10-15H2,(H,24,26) | InChIKey = JXZZEXZZKAWDSP-UHFFFAOYAC | StdInChI_Ref =  ☑Y | StdInChI = 1S/C22H25N3O/c26-22(17-6-2-1-3-7-17)24-19-11-14-25(15-12-19)13-10-18-16-23-21-9-5-4-8-20(18)21/h1-9,16,19,23H,10-15H2,(H,24,26) | StdInChIKey_Ref =  ☑Y | StdInChIKey = JXZZEXZZKAWDSP-UHFFFAOYSA-N }}

Overview

Overview

Indoramin (trade names Baratol and Doralese) is a piperidine antiadrenergic agent.

It is an alpha-1 selective adrenoceptor antagonist[1] with direct myocardial depression action; therefore, it results in no reflex tachycardia. It is also used in benign prostatic hyperplasia (BPH).[2]

It is commonly synthesized from tryptophol.[3]

Dosage

Dosage

Indoramin is commonly prescribed as 20mg tablets when used in BPH.[4]

Side Effects

Side Effects

Drowsiness, dizziness, dry mouth, nasal congestion, headache, fatigue, weight gain, hypotension, postural hypotension, depression, problems with ejaculation, diarrhoea, nausea, increased need to pass urine, and palpitations.[5]

References

References

  1. ↑ Pierce V, Shepperson NB, Todd MH, Waterfall JF (February 1986). “Investigation into the cardioregulatory properties of the alpha 1-adrenoceptor blocker indoramin”. Br. J. Pharmacol. 87 (2): 433–441. doi:10.1111/j.1476-5381.1986.tb10834.x. PMC 1916533. PMID 3955309.
  2. ↑ “Indoramin 20mg tablets”. Medicines.org.uk. April 20, 2011. Retrieved September 30, 2012.
  3. ↑ Ullman’s encyclopedia of Industrial Chemistry, Sixth Edition, 2002.
  4. ↑ “Indoramin hydrochloride”. National Health Service (UK). Retrieved September 30, 2012.
  5. ↑ “Indoramin 20mg tablets”. Medicines.org.uk. Retrieved September 30, 2012.

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