UNIVERSITY OF LJUBLJANA FACULTY OF PHARMACY IVA HARI OPTIMIZACIJA STRUKTURNO ODVISNIH PARAMETROV PRI SKLOPLJENI MASNI SPEKTROMETRIJI ZA IZBRANE SINTEZNE KANABINOIDE TER NJIHOVA MODULACIJA IONSKIH KANALOV OPTIMISATION OF COMPOUND-DEPENDENT PARAMETERS IN THE TANDEM MASS SPECTROMETRY FOR SELECTED SYNTH

No abstract is available for this paper.

• Publication year

  2014

• Venue

  Unknown venue

• Publication date

  Unknown publication date

• Fields of study

  Not labeled

• Identifiers

  No identifiers available.

• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

• Structural basis for activation of voltage-gated cation channels.

  2013cited by this paper
• Cannabinoid receptor 1 suppresses transient receptor potential vanilloid 1-induced inflammatory responses to corneal injury.

  2013cited by this paper
• Identification and structural elucidation of four cannabimimetic compounds (RCS-4, AM-2201, JWH-203 and JWH-210) in seized products.

  2013cited by this paper
• TRP channels and analgesia.

  2013cited by this paper
• Synthetic cannabinoid intoxication: a case series and review.

  2013cited by this paper
• Qualitative confirmation of 9 synthetic cannabinoids and 20 metabolites in human urine using LC-MS/MS and library search.

  2013cited by this paper
• Herbal Marijuana Alternatives and Bath Salts—“Barely Legal” Toxic Highs

  2012cited by this paper
• AM-251 and rimonabant act as direct antagonists at mu-opioid receptors: implications for opioid/cannabinoid interaction studies.

  2012cited by this paper
• Cytochrome P450-Mediated Oxidative Metabolism of Abused Synthetic Cannabinoids Found in K2/Spice: Identification of Novel Cannabinoid Receptor Ligands

  2012cited by this paper
• LC-MS/MS method for the quantitation of metabolites of eight commonly-used synthetic cannabinoids in human urine--an Australian perspective.

  2012cited by this paper
• Analysis of 30 synthetic cannabinoids in serum by liquid chromatography-electrospray ionization tandem mass spectrometry after liquid-liquid extraction.

  2012cited by this paper
• Analysis of psychoactive and intoxicating substances in legal highs.

  2012cited by this paper
• Identification of the major urinary metabolites in man of seven synthetic cannabinoids of the aminoalkylindole type present as adulterants in 'herbal mixtures' using LC-MS/MS techniques.

  2012cited by this paper
• [Effect and occurrence of synthetic cannabinoids].

  2012cited by this paper
• Ultra high performance liquid chromatography-electrospray ionization-tandem mass spectrometry screening method for direct analysis of designer drugs, "spice" and stimulants in oral fluid.

  2012influential reference
• Inhibiting the breakdown of endogenous opioids and cannabinoids to alleviate pain

  2012cited by this paper
• Chromatography-mass spectrometry studies on the metabolism of synthetic cannabinoids JWH-018 and JWH-073, psychoactive components of smoking mixtures.

  2011cited by this paper
• Are voltage-gated sodium channels on the dorsal root ganglion involved in the development of neuropathic pain?

  2011cited by this paper
• Transient Receptor Potential Channels

  2011cited by this paper
• The transient receptor potential family of ion channels

  2011cited by this paper
• Transient receptor potential channels as therapeutic targets

  2011cited by this paper
• "Legal highs" - new players in the old drama.

  2011influential reference
• Development and validation of a liquid chromatography-tandem mass spectrometry method for the quantitation of synthetic cannabinoids of the aminoalkylindole type and methanandamide in serum and its application to forensic samples.

  2011cited by this paper
• Role of Cannabinoids in the Treatment of Pain and (Painful) Spasticity

  2010cited by this paper
• Cave Canalem: how endogenous ion channels may interfere with heterologous expression in Xenopus oocytes.

  2010cited by this paper
• Detection of JWH-018 metabolites in smoking mixture post-administration urine.

  2010cited by this paper
• Pharmacology of Vanilloid Transient Receptor Potential Cation Channels

  2009influential reference
• Introduction to Mass Spectrometry:: Instrumentation, Applications, and Strategies for Data Interpretation

  2009cited by this paper
• Voltage-gated potassium channels as therapeutic targets

  2009influential reference
• TRPV1, a key target in peripheral pain sensation: modulation by venoms and toxins

  2008influential reference
• The hERG K+ channel: target and antitarget strategies in drug development.

  2008cited by this paper
• Applications of LC-MS in Toxicology

  2007cited by this paper
• Cannabidiol – Recent Advances

  2007cited by this paper
• Cannabidiol is an allosteric modulator at mu- and delta-opioid receptors

  2006cited by this paper
• The cannabinoid WIN 55,212-2 inhibits transient receptor potential vanilloid 1 (TRPV1) and evokes peripheral antihyperalgesia via calcineurin.

  2006cited by this paper
• International Union of Pharmacology. XLVIII. Nomenclature and Structure-Function Relationships of Voltage-Gated Calcium Channels

  2005influential reference
• Pharmacological actions of cannabinoids.

  2005cited by this paper
• Agonistic Properties of Cannabidiol at 5-HT1a Receptors

  2005cited by this paper
• Sodium channel inhibition by anandamide and synthetic cannabimimetics in brain.

  2003influential reference
• Heterologous expression of ion channels.

  2003cited by this paper
• Analogs of WIN 62,577 define a second allosteric site on muscarinic receptors.

  2002cited by this paper
• International Union of Pharmacology. XXVII. Classification of Cannabinoid Receptors

  2002cited by this paper
• The Forensic Pharmacology of Drugs of Abuse

  2001cited by this paper
• Influence of the N-1 alkyl chain length of cannabimimetic indoles upon CB(1) and CB(2) receptor binding.

  2000cited by this paper
• Structure, function and pharmacology of voltage-gated sodium channels

  2000influential reference
• Pharmacology of voltage-gated and calcium-activated potassium channels.

  1999cited by this paper
• Design, synthesis and pharmacology of cannabimimetic indoles

  1994cited by this paper
• Both extracellular and transmembrane residues contribute to the species selectivity of the neurokinin-1 receptor antagonist WIN 51708.

  1994cited by this paper
• (R)-methanandamide: a chiral novel anandamide possessing higher potency and metabolic stability.

  1994cited by this paper
• Isolation, Structure, and Partial Synthesis of an Active Constituent of Hashish

  1964cited by this paper

• No citing papers are available for this paper.