In vitro stability and metabolism of salvinorin A in rat plasma. - Wikidata - wikimedia - TriplyDB

In vitro stability and metabolism of salvinorin A in rat plasma.

In vitro stability and metabolism of salvinorin A in rat plasma.

http://www.wikidata.org/entity/Q46091354

about

Here today, gone tomorrow…and back again? A review of herbal marijuana alternatives (K2, Spice), synthetic cathinones (bath salts), kratom, Salvia divinorum, methoxetamine, and piperazines Neuropharmacology of the naturally occurring kappa-opioid hallucinogen salvinorin A Real-time bioluminescence imaging of glycans on live cells.New drugs of abuse.Salvinorin A produces cerebrovasodilation through activation of nitric oxide synthase, κ receptor, and adenosine triphosphate-sensitive potassium channel.Salvinorin A and derivatives: protection from metabolism does not prolong short-term, whole-brain residence.LC-MS/MS quantification of salvinorin A from biological fluids.Salvia divinorum: from Mazatec medicinal and hallucinogenic plant to emerging recreational drug.Hansen solubility parameters for assay method optimization of simvastatin, ramipril, atenolol, hydrochlorothiazide and aspirin in human plasma using liquid chromatography with tandem mass spectrometry.In vitro stability and metabolism of O2', O3', O5'-tri-acetyl-N6-(3-hydroxylaniline) adenosine in rat, dog and human plasma: chemical hydrolysis and role of plasma esterases.Validation of a Rapid and Sensitive UPLC-MS-MS Method Coupled with Protein Precipitation for the Simultaneous Determination of Seven Pyrethroids in 100 µL of Rat Plasma by Using Ammonium Adduct as Precursor Ion.Utility of the carboxylesterase inhibitor bis-para-nitrophenylphosphate (BNPP) in the plasma unbound fraction determination for a hydrolytically unstable amide derivative and agonist of the TGR5 receptor.Addressing Structural Flexibility at the A-Ring on Salvinorin A: Discovery of a Potent Kappa-Opioid Agonist with Enhanced Metabolic Stability.Semisynthesis and Kappa-Opioid Receptor Activity of Derivatives of Columbin, a Furanolactone Diterpene.Analysis of Salvinorin A in urine using microextraction in packed syringe and GC-MS/MS.The elimination of MTC-220, a novel anti-tumor agent of conjugate of paclitaxel and muramyl dipeptide analogue, in rats.The C-2 derivatives of salvinorin A, ethoxymethyl ether Sal B and β-tetrahydropyran Sal B, have anti-cocaine properties with minimal side effects.Conversion and pharmacokinetics profiles of a novel pro-drug of 3-n-butylphthalide, potassium 2-(1-hydroxypentyl)-benzoate, in rats and dogs.Modular Approach to pseudo-Neoclerodanes as Designer κ-Opioid Ligands.

P2860

Q24631675-91F882DE-BC49-4861-AD15-98E4A1B9DC67 Q30467220-87E1171F-944A-4759-9063-366D3879C51B Q33932166-DBAC3801-D888-4906-9E4D-6A06D32D2841 Q34451886-9E9D7E80-A699-456C-9D46-A8F8DA108649 Q36069379-4A01CA54-F1DB-40A3-8E1C-9CF33132D950 Q37349384-60BB11CD-B327-4D55-A5D1-9107F624CAAE Q37451366-794795F0-4C7C-4CC4-9547-4A94B1BED89A Q38116484-49CD639B-4A81-4EA5-8AE1-67E22C494E9C Q38655367-69FB5D3C-FB79-4659-B593-8EF15DFF1703 Q39761375-D08AE860-8B35-4F46-9D64-F32D7EE36530 Q42751400-C87F1952-DED6-4B07-8FAF-CD46BB13739B Q43125212-7907A588-B1C4-4B81-98CC-A33B61389C05 Q44344643-B94A4730-19E9-47F4-A7CC-295E7EFB2301 Q44347299-38E66647-3CFF-4E77-B74C-7D674776F506 Q46178251-0D8FA99A-14FE-4B99-A1E5-9879ECEE98E9 Q46831381-43F4E5B8-A4EF-44B1-A672-53D340B20822 Q47878237-78A68DA3-CE44-4EC2-8412-9506AEBD4434 Q48113763-46A5C7F0-4A78-4815-8F81-4B147ABB715A Q50591898-B9B4752C-5117-4BC9-8632-EC1D5AC015A8

P2860

In vitro stability and metabolism of salvinorin A in rat plasma.

http://www.wikidata.org/entity/Q46091354

description

2009 nî lūn-bûn

@nan

2009年の論文

@ja

2009年学术文章

@wuu

2009年学术文章

@zh

2009年学术文章

@zh-cn

2009年学术文章

@zh-hans

2009年学术文章

@zh-my

2009年学术文章

@zh-sg

2009年學術文章

@yue

2009年學術文章

@zh-hant

name

In vitro stability and metabolism of salvinorin A in rat plasma.

@en

In vitro stability and metabolism of salvinorin A in rat plasma.

@nl

type

label

In vitro stability and metabolism of salvinorin A in rat plasma.

@en

In vitro stability and metabolism of salvinorin A in rat plasma.

@nl

prefLabel

In vitro stability and metabolism of salvinorin A in rat plasma.

@en

In vitro stability and metabolism of salvinorin A in rat plasma.

@nl

P1433

Q46091354-F7964A64-E0A2-4629-B8E7-B130D34F5960

P1476

Q46091354-6649E934-1B83-4992-BF8D-56C21F9CF20D

P2093

Q46091354-0FB54A79-B655-4DD7-9B0B-0828914D47CA

Q46091354-13F2D1CB-BBE3-4D4D-9155-254ED012DF75

Q46091354-626FA0AA-A38D-4332-8B63-2E260A3F62C1

Q46091354-BF20939D-B4F4-4114-8073-A912B8E8D5C4

Q46091354-DA717B09-82BD-4AED-8FE2-A18995337366

Q46091354-E6F47CC8-429F-4C7B-B8B8-750C4E81D0C0

P2860

Q46091354-040045AD-C1D1-4B49-8F76-B2D67297B6A3

Q46091354-19963228-F866-4649-BB49-56EAD657F01C

Q46091354-363EF190-7246-47FA-9600-B9112BC46C2B

Q46091354-36B5A5F5-78C0-46B0-A4B1-4EA786E0A903

Q46091354-5627D321-8F8F-4F75-B331-9BE7BFDA650C

Q46091354-65E67842-8632-41F7-A433-0650E39EC0F1

Q46091354-7C908B8F-F26A-4D1A-9611-9A20857EB305

Q46091354-7E8E02E1-0FEE-4956-833A-D9A0182A9F10

Q46091354-8FEF1E08-3287-4CD0-8BB4-C14FB746BF1B

Q46091354-A7535877-FFDE-4A26-9FAA-3330B551E044

P304

Q46091354-57FAC040-1B92-4650-9DD0-605E9728D473

P31

Q46091354-8B4B9FD8-4BE5-44FD-829B-779D067E7DBF

P356

Q46091354-08F12393-7F22-4616-BF68-469582AD97E9

P407

Q46091354-BC90FA6C-1122-4E04-9634-9F3924A31513

P433

Q46091354-DDD28124-4A8D-4666-8A71-4A64A6F9F642

P478

Q46091354-61485147-E622-4779-8A74-D68D0E5C55C2

P577

Q46091354-49DC5EAF-5389-45B1-A00C-02B9C7DE64E4

P5875

Q46091354-EC540B98-B8D2-49FB-BB69-7CB8C914589E

P698

Q46091354-38485865-5F7F-4A55-A34E-93D471ABAB82

P356

00498250902769967

P1433

P1476

In vitro stability and metabolism of salvinorin A in rat plasma.

@en

P2093

H Inoue

http://www.w3.org/2001/XMLSchema#string

H Miyaguchi

http://www.w3.org/2001/XMLSchema#string

K Kuwayama

http://www.w3.org/2001/XMLSchema#string

K Tsujikawa

http://www.w3.org/2001/XMLSchema#string

T Kanamori

http://www.w3.org/2001/XMLSchema#string

Y T Iwata

http://www.w3.org/2001/XMLSchema#string

P2860

Salvinorin A: a potent naturally occurring nonnitrogenous kappa opioid selective agonist

Involvement of human blood arylesterases and liver microsomal carboxylesterases in nafamostat hydrolysis

Salvinorin A, an active component of the hallucinogenic sage salvia divinorum is a highly efficacious kappa-opioid receptor agonist: structural and functional considerations

Human carboxylesterase isozymes: catalytic properties and rational drug design

Ethnopharmacology of ska María Pastora (Salvia divinorum, Epling and Játiva-M.)

Determination of Salvinorin A in body fluids by high performance liquid chromatography-atmospheric pressure chemical ionization.

Lactonase and lactonizing activities of human serum paraoxonase (PON1) and rabbit serum PON3.

Salvia divinorum and salvinorin A: new pharmacologic findings.

A facile method for the preparation of deuterium labeled salvinorin A: synthesis of [2,2,2-2H3]-salvinorin A.

Determination of salvinorins and divinatorins in Salvia divinorum leaves by liquid chromatography/multistage mass spectrometry.

P304

391-398

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1080/00498250902769967

http://www.w3.org/2001/XMLSchema#string

P407

P433

5

http://www.w3.org/2001/XMLSchema#string

P478

39

http://www.w3.org/2001/XMLSchema#string

P577

2009-05-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

24195322

http://www.w3.org/2001/XMLSchema#string

P698

19280383

http://www.w3.org/2001/XMLSchema#string