Methcathinone is a substrate for the serotonin uptake transporter. - Wikidata - awgldk - TriplyDB

Methcathinone is a substrate for the serotonin uptake transporter.

Methcathinone is a substrate for the serotonin uptake transporter.

http://www.wikidata.org/entity/Q40615026

about

The designer methcathinone analogs, mephedrone and methylone, are substrates for monoamine transporters in brain tissue Mephedrone, an abused psychoactive component of 'bath salts' and methamphetamine congener, does not cause neurotoxicity to dopamine nerve endings of the striatum Clinical characteristics of mephedrone toxicity reported to the U.K. National Poisons Information Service Pharmacological characterization of designer cathinones in vitro Neurotoxicity following chronic intravenous use of "Russian cocktail".Instability of the ecstasy market and a new kid on the block: mephedrone.Neurotoxicity Induced by Mephedrone: An up-to-date Review.Mephedrone does not damage dopamine nerve endings of the striatum, but enhances the neurotoxicity of methamphetamine, amphetamine, and MDMA Pharmacological examination of trifluoromethyl ring-substituted methcathinone analogs Cathinone derivatives: a review of their chemistry, pharmacology and toxicology.An overview of recent developments in the analytical detection of new psychoactive substances (NPSs).Neurotoxicology of Synthetic Cathinone Analogs.Fatal Intoxication with α-PVP, a Synthetic Cathinone Derivative.

P2860

Q24615008-8BBAAD9F-56D2-47DD-BA4F-8E2A6DD95744 Q24621938-DD653A7F-EDC4-4268-BD64-FCE1698FC8E4 Q24629270-E420C98D-8DD2-409C-98AC-7AF2B9DDC4C3 Q28273207-E464BBE4-1B33-4026-859B-4CBF297F70A2 Q31161897-A218438D-9BA8-4A93-BA3B-42BD3248F41D Q34136889-703E07FB-E63D-4DD5-A50A-1F5D48F54CA7 Q34546425-58AD0D5F-EDED-40C1-A633-8E0DF410EADB Q36703786-C01D9688-F185-4957-B589-A92B17A72648 Q36851442-CF8C5CA9-4C18-4CD1-BA9F-E7916DB10C7F Q37900939-88123DDB-BA36-4F2E-9CF5-55A64BFCD07E Q38510888-065F3058-F8D5-4FF5-AD9A-61B6B0C5511B Q38983638-C84106FE-9D38-4EB9-AFAE-4733599F7EB7 Q48380075-FDE08797-5EE7-4D3F-9959-64444F7019CA

P2860

Methcathinone is a substrate for the serotonin uptake transporter.

http://www.wikidata.org/entity/Q40615026

description

2003 nî lūn-bûn

@nan

2003年の論文

@ja

2003年論文

@yue

2003年論文

@zh-hant

2003年論文

@zh-hk

2003年論文

@zh-mo

2003年論文

@zh-tw

2003年论文

@wuu

2003年论文

@zh

2003年论文

@zh-cn

name

Methcathinone is a substrate for the serotonin uptake transporter.

@en

type

label

Methcathinone is a substrate for the serotonin uptake transporter.

@en

prefLabel

Methcathinone is a substrate for the serotonin uptake transporter.

@en

P1433

Q40615026-E09CB1E4-B55F-49D9-9953-E4F916CD76F2

P1476

Q40615026-428ED521-C03B-4BF6-BDBB-7E27710DD8FF

P2093

Q40615026-211DDEE5-A51F-47E4-8ACC-00F93ABA38B7

Q40615026-A0784279-50F5-424D-83BB-0BF9F69357E9

P2860

Q40615026-0E92E1E9-ECE5-4C59-8D2F-9B03FC1679B7

Q40615026-1630A70C-28EE-4B38-8657-6FAF550B5E82

Q40615026-2559872D-0396-4349-882B-3D2B992B2F3D

Q40615026-35B211F2-3957-4B7B-84B0-ECF5000FC42B

Q40615026-5AE3B173-A403-4782-93B8-64C0747AB2FB

Q40615026-5D67AF0B-CF49-4027-952E-C7C86F669CE2

Q40615026-6F1D8748-9D35-4E20-8472-A6B581CA777D

Q40615026-74C3F71F-16CC-4954-9D8F-0A5CC139BD94

Q40615026-80069642-CC2D-4216-A15C-3E8FC9C4D04D

Q40615026-942A3DA8-0990-4899-A633-2DFC09D90726

P304

Q40615026-8FED747F-774E-45B3-BA10-C7714638E4EE

P31

Q40615026-11355E92-28F7-4219-9093-A7DD997431B6

P356

Q40615026-1A9A085D-BD9B-4C51-A86E-DAED3D5A9E87

P433

Q40615026-8FC3F5FC-4305-486F-913C-8DEC64696E88

P478

Q40615026-DEB0CC09-EFB5-4095-ADF0-C2DD47E321DA

P577

Q40615026-8EB5E72C-9319-441B-A273-188162A7C855

P5875

Q40615026-E9B3B77E-5804-4B38-82E2-CD56D1014C98

P698

Q40615026-94B29D37-CE92-4072-A7BA-A98783CD44EC

P356

J.1600-0773.2003.PTO930504.X

P1433

Basic and Clinical Pharmacology and Toxicology

P1476

Methcathinone is a substrate for the serotonin uptake transporter.

@en

P2093

Kevin F Foley

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

Nicholas V Cozzi

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

P2860

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

Inhibition of plasma membrane monoamine transporters by beta-ketoamphetamines

p-methylthioamphetamine is a potent new non-neurotoxic serotonin-releasing agent

Cocaine-stimulus generalization to two new designer drugs: methcathinone and 4-methylaminorex

Methcathinone: a new and potent amphetamine-like agent

Effects of 5-HT-releasing agents on the extracellullar hippocampal 5-HT of rats. Implications for the development of novel antidepressants with a short onset of action.

p-Methylthioamphetamine and 1-(m-chlorophenyl)piperazine, two non-neurotoxic 5-HT releasers in vivo, differ from neurotoxic amphetamine derivatives in their mode of action at 5-HT nerve endings in vitro.

Intravenous self-injection of methcathinone in the baboon.

Dopamine uptake by the human platelet: effects of dopamine receptor agonists.

Methcathione ("cat"): an enantiomeric potency comparison.

P304

219-225

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

P31

scholarly article

P356

10.1046/J.1600-0773.2003.PTO930504.X

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

P433

5

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

P478

93

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

P577

2003-11-01T00:00:00Z

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

P5875

6766238

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

P698

14629733

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