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André Erdling - Research Outputs - Lund University

CGRP and its receptors are found in areas of the central and peripheral nervous system that are important for the transmission of Telcagepant. Telcagepant ( INN) (code name MK-0974) is a calcitonin gene-related peptide receptor antagonist which was an investigational drug for the acute treatment and prevention of migraine, developed by Merck & Co.. In the acute treatment of migraine, it was found to have equal potency to rizatriptan and zolmitriptan. MK-0974(Telcagepant) is a highly potent, selective, and orally bioavailable CGRP receptor antagonist with Ki values of 0.77 nM and 1.2 nM for human and rhesus CGRP receptors respectively; displays >1500-fold lower affinity for the canine and rat receptors.;IC50 value: 0.77/1.2 nM(Human and rhesus CGRP) [1];Target: CGRP receptor;In vitro: MK-0974 is a potent antagonist of the human (K(i) = 0.77 nM) and rhesus (K(i) = 1.2 nM) CGRP receptors but displays >1500-fold lower affinity for the canine English: Chemical structure of telcagepant—an antimigraine drug. Date: 18 February 2009: Source: Own work: Author: Anypodetos This vector image was Telcagepant CAS Number: 781649-09-0: Molecular Weight: 566.523: Density: 1.5±0.1 g/cm3: Boiling Point: N/A: Molecular Formula: C 26 H 27 F 5 N 6 O 3: Melting Point: N/A: MSDS: N/A Flash Point: N/A The Vertex CGRP program was focused on identifying potent, orally bioavailable CGRP receptor antagonists that, in contrast to olcegepant and telcagepant, would be CNS-penetrant.

Telcagepant structure

MK-0974(Telcagepant) is a highly potent, selective, and orally bioavailable CGRP receptor antagonist with Ki values of 0.77 nM and 1.2 nM for human and rhesus CGRP receptors respectively; displays >1500-fold lower affinity for the canine and rat receptors.;IC50 value: 0.77/1.2 nM(Human and rhesus CGRP) [1];Target: CGRP receptor;In vitro: MK-0974 is a potent antagonist of the human (K(i) = 0.77 nM) and rhesus (K(i) = 1.2 nM) CGRP receptors but displays >1500-fold lower affinity for the canine English: Chemical structure of telcagepant—an antimigraine drug. Date: 18 February 2009: Source: Own work: Author: Anypodetos This vector image was Telcagepant CAS Number: 781649-09-0: Molecular Weight: 566.523: Density: 1.5±0.1 g/cm3: Boiling Point: N/A: Molecular Formula: C 26 H 27 F 5 N 6 O 3: Melting Point: N/A: MSDS: N/A Flash Point: N/A The Vertex CGRP program was focused on identifying potent, orally bioavailable CGRP receptor antagonists that, in contrast to olcegepant and telcagepant, would be CNS-penetrant. 159 Starting from truncated analogs of olcegepant, they identified 165 (Fig. 36, K i = 280 nM) and optimized this flexible lead structure by incorporating conformational constraints.

781649-09-0 - CGDZXLJGHVKVIE-DNVCBOLYSA-N - Telcagepant [USAN:INN] - Similar structures search, synonyms, formulas, resource links, and other chemical information. 953077-35-5 - VESUVMGLUABQCA-LEVQAPRMSA-M - Telcagepant potassium [USAN] - Similar structures search, synonyms, formulas, resource links, and other chemical information.

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TELCAGEPANT D42O649ALL Investigational Source: NCT00442936: Phase 3 Migraine (2007 TELCAGEPANT MK 0974 pubchem.compound:11319053 chemidplus:781649-09-0 drugbank:12228 chembl:CHEMBL236593 Drug Info: ChemblDrugs ChemblInteractions TTD DrugBank (0 MK-0974 (Telcagepant) is a potent and selective antagonist of the human and rhesus CGRP receptors. Structure General Activity Publications Application Names 8: Classification Identifiers 7: Related Substances 3: TELCAGEPANT POTASSIUM L303VER2NG 2011-07-20 · Two additional reports show somewhat conflicting data on the efficacy of telcagepant. 9,10 This first report shows that 27% of patients respond to telcagepant whereas 33% of Sumatriptan patients respond and 40% of rizatriptan respond to being pain free after 2 h. 9 The second report, however, looked at the response rates of individuals that respond to triptans and those that do not.

migrän - Wikidocumentaries

Telcagepant ( INN) (code name MK-0974) is a calcitonin gene-related peptide receptor antagonist which was an investigational drug for the acute treatment and prevention of migraine, developed by Merck & Co.. In the acute treatment of migraine, it was found to have equal potency to rizatriptan and zolmitriptan. MK-0974(Telcagepant) is a highly potent, selective, and orally bioavailable CGRP receptor antagonist with Ki values of 0.77 nM and 1.2 nM for human and rhesus CGRP receptors respectively; displays >1500-fold lower affinity for the canine and rat receptors.;IC50 value: 0.77/1.2 nM(Human and rhesus CGRP) [1];Target: CGRP receptor;In vitro: MK-0974 is a potent antagonist of the human (K(i) = 0.77 nM) and rhesus (K(i) = 1.2 nM) CGRP receptors but displays >1500-fold lower affinity for the canine English: Chemical structure of telcagepant—an antimigraine drug. Date: 18 February 2009: Source: Own work: Author: Anypodetos This vector image was Telcagepant CAS Number: 781649-09-0: Molecular Weight: 566.523: Density: 1.5±0.1 g/cm3: Boiling Point: N/A: Molecular Formula: C 26 H 27 F 5 N 6 O 3: Melting Point: N/A: MSDS: N/A Flash Point: N/A The Vertex CGRP program was focused on identifying potent, orally bioavailable CGRP receptor antagonists that, in contrast to olcegepant and telcagepant, would be CNS-penetrant. 159 Starting from truncated analogs of olcegepant, they identified 165 (Fig. 36, K i = 280 nM) and optimized this flexible lead structure by incorporating conformational constraints. Telcagepant (MK-0974) displays saturable binding to SK-N-MC membranes with a K D of 1.9 nM and B max of 479 fmol/mg protein. Telcagepant (MK-0974) also displays saturable binding to rhesus cerebellum homogenate with a K D of 1.3 nM and B max of 20 fmol/mg.
1 hg i dl

Telcagepant. Molecular Formula C 26 H 27 F 5 N 6 O 3; Average mass 566.523 Da; Monoisotopic mass 566.206482 Da; ChemSpider ID 9494017 Telcagepant; Usage on sh.wikipedia.org Telkagepant; Usage on sr.wikipedia.org Telkagepant; Usage on vi.wikipedia.org Telcagepant Telcagepant CAS Number: 781649-09-0: Molecular Weight: 566.523: Density: 1.5±0.1 g/cm3: Boiling Point: N/A: Molecular Formula: C 26 H 27 F 5 N 6 O 3: Melting Point: N/A: MSDS: N/A Flash Point: N/A Telcagepant (100) is a calcitonin gene-related peptide (CGRP) receptor antagonist which entered clinical trials for the treatment of acute migraine (Fig. 20, Table 22).

Structure and pharmacology of telcagepant The CGRP family of receptors mediate their physiological eﬀ ects through the joining of CLR and RAMP1, which are needed for G-protein signal transduction via the receptor component-protein.15 Initial high-throughput screening resulted in identiﬁ cation of a potent and orally bioavailable Importance of the field: Calcitonin gene-related peptide (CGRP) receptor antagonists have recently come to attention with the development of olcegepant and telcagepant for the treatment of migraine. The availability of high-affinity, non-peptide antagonists opens the way for trials of these compounds in other conditions where CGRP antagonism might be useful, such as septic shock and inhibition Overexpression of hRAMP1 increases CGRP signalling by changing the maximal response or ligand sensitivity, depending on tissue type. Furthermore, telcagepant inhibited transgenic hRAMP1 CGRP receptors, but the degree of inhibition suggests that the transgenic mice are only partially humanized or bot … Calcitonin gene-related peptide (CGRP) is a potent neuropeptide whose agonist interaction with the CGRP receptor (CGRP-R) in the periphery promotes vasodilation, neurogenic inflammation and trigeminovascular sensory activation. This process is implicated in the cause of migraine headaches, and CGRP- … Examples of structuralism differ based on the field they are associated with.
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Migrän – Wikipedia

Recently, an orally bio available CGRP receptor antagonist, telcagepant. Unraveling the aflatoxin− FAPY conundrum: structural basis for differential of the (3R,6S)-3-Amino-6-(2,3-difluorophenyl)azepan-2-one of Telcagepant Jan 31, 2017 Telcagepant structure.svg. Telcagepant, MK-0974.

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doi: 10.1111/bph.13783.

781649-09-0 - CGDZXLJGHVKVIE-DNVCBOLYSA-N - Telcagepant [USAN:INN] - Similar structures search, synonyms, formulas, resource links, and other chemical information. Structure, properties, spectra, suppliers and links for: Telcagepant potassium, 953077-35-5. Telcagepant, also known as MK0974, is a calcitonin gene-related peptide receptor antagonist under development for the acute treatment and prevention of migraine. MedKoo Biosciences, Inc. Leading supplier of anticancer chemical reagents and kinase inhibitors Telcagepant (MK-0974) is a novel calcitonin gene-related peptide (CGRP) receptor antagonist currently undergoing clinical trials for migraine (). MK-0974 is currently being studied in phase III clinical trials.