Chemistry:Terguride

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Short description: Chemical compound
Terguride
Terguride.png
Clinical data
Trade namesTeluron
Other namesDironyl; Mysalfon; trans-Dihydrolisuride; Transdihydrolisuride; TDHL; SH-406; VUFB-6638; ZK-31224; N,N-Diethyl-N'-[(8α)-6-methylergolin-8-yl]urea
AHFS/Drugs.comInternational Drug Names
Routes of
administration		Oral
ATC code
Legal status
Legal status
  • In general: ℞ (Prescription only)
Identifiers
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
Chemical and physical data
FormulaC20H28N4O
Molar mass340.471 g·mol−1
3D model (JSmol)
  (verify)


Pharmacology

Pharmacodynamics

Terguride acts as an agonist of the dopamine D2 receptor and as an antagonist of the serotonin 5-HT2A and 5-HT2B receptors, among other actions.[citation needed]

As an antagonist of the 5-HT2B receptor, terguride is not associated with cardiac valvulopathy.[1]

Activities of terguride at various sites[2][3][4][5]
Site Affinity (Ki [nM]) Efficacy (Emax [%]) Action
D1 28 ? ?
D2S 0.81 39 Partial agonist
D2L 1.1 0 Silent antagonist
D3 1.0 36 Partial agonist
D4 8.1 0 Silent antagonist
D5 23 ? ?
5-HT1A 3.5 71 Partial agonist
5-HT1B 257 37 Partial agonist
5-HT1D 16 62 Partial agonist
5-HT2A 4.8 49 Partial agonist
5-HT2B 7.1 0 Silent antagonist
5-HT2C 48 0 Silent antagonist
5-HT7 8–42 ? ?
α1A 3.5 0 Silent antagonist
α1B 35 ? ?
α1D 3.9 ? ?
α2A 0.30 0 Silent antagonist
α2B 0.45 0 Silent antagonist
α2C 0.76 0 Silent antagonist
α2D 1.5 ? ?
β1 661 ? ?
β2 20 ? ?
H1 339 ? ?
M1 >10,000 ? ?
Notes: All receptors are human except α2D-adrenergic, which is rat (no human counterpart), and 5-HT7, which was guinea pig.[2][5]

Research

Serotonin stimulates the proliferation of pulmonary artery smooth muscle cells, and induces fibrosis in the wall of pulmonary arteries. Together, this causes vascular remodeling and narrowing of the pulmonary arteries. These changes result in increased vascular resistance and PAH. Due to the potential anti-proliferative and anti-fibrotic activity of terguride, this potential medicine could offer the hope of achieving reversal of pulmonary artery vascular remodeling and attenuation of disease progression.[6] In May 2008, terguride was granted orphan drug status for the treatment of pulmonary arterial hypertension.[7] In May 2010 Pfizer purchased worldwide rights for the drug.[8] However, development was discontinued in 2011.

References

  1. ↑ "Ergotamine and nicergoline - facts and myths". Pharmacol Rep 67 (2): 360–3. April 2015. doi:10.1016/j.pharep.2014.10.010. PMID 25712664. 
  2. ↑ 2.0 2.1 "Differential actions of antiparkinson agents at multiple classes of monoaminergic receptor. I. A multivariate analysis of the binding profiles of 14 drugs at 21 native and cloned human receptor subtypes". J Pharmacol Exp Ther 303 (2): 791–804. November 2002. doi:10.1124/jpet.102.039867. PMID 12388666. 
  3. ↑ "Differential actions of antiparkinson agents at multiple classes of monoaminergic receptor. II. Agonist and antagonist properties at subtypes of dopamine D(2)-like receptor and alpha(1)/alpha(2)-adrenoceptor". J Pharmacol Exp Ther 303 (2): 805–14. November 2002. doi:10.1124/jpet.102.039875. PMID 12388667. 
  4. ↑ "Differential actions of antiparkinson agents at multiple classes of monoaminergic receptor. III. Agonist and antagonist properties at serotonin, 5-HT(1) and 5-HT(2), receptor subtypes". J Pharmacol Exp Ther 303 (2): 815–22. November 2002. doi:10.1124/jpet.102.039883. PMID 12388668. 
  5. ↑ 5.0 5.1 "PDSP Database - UNC". https://pdsp.unc.edu/databases/pdsp.php?testFreeRadio=testFreeRadio&testLigand=Terguride&doQuery=Submit+Query. 
  6. ↑ "5-HT2B receptor antagonists inhibit fibrosis and protect from RV heart failure". BioMed Research International 2015: 438403. 2015. doi:10.1155/2015/438403. PMID 25667920. 
  7. ↑ Presseportal (Swiss press portal, in German)
  8. ↑ "TheDay.com 5/10/2010". http://www.theday.com/article/20100513/BIZ02/305139376/1044. 



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