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pro vyhledávání: '"Methyldopamine"'
Akademický článek
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Autor:
Satoshi Tahara, Mengcen Wang, Tomohiko Takayama, Dongyeop Kim, Yasuyuki Hashidoko, Yasuko Sakihama
Publikováno v:
Journal of Pesticide Science. 38:181-187
Cochliophilin A (5-hydroxy-6,7-methylenedioxyflavone, 1) and N-(E)-feruloyl-4-O-methyldopamine (2) are naturally occurring host-specific chemoattractants for Aphanomyces cochlioides zoospores. In a cross-competition assay, compound 1 (4 fmol) applied
Autor:
Sven N. Reske, Ehab Al-Momani, Christoph Solbach, Boris D. Zlatopolskiy, Hans-Juergen Machulla
Publikováno v:
Applied Radiation and Isotopes. 70:1475-1479
A rapid and efficient n.c.a. radiosynthesis of 6-[ 11 C]methyldopamine ([ 11 C]MeDA) using the Stille cross-coupling reaction as a key step was developed. The labeling conditions for the formation of the intermediate compound (protected [ 11 C]MeDA,
Publikováno v:
Neurochemistry International. 58:92-101
The neurotoxicity of MDMA or “Ecstasy” in rats is selectively serotonergic, while in mice it is both dopaminergic and serotonergic. MDMA metabolism may play a key role in this neurotoxicity. The function of serotonin and dopamine transporter and
Autor:
Md. Abdullahil Baki ., Kazi Abdus Salam, A. H. M. Khurshid Alam, Golam Sadik, Md. Moniruzzaman Manir ., Robiul Islam, Md. Aslam Hossain .
Publikováno v:
Pakistan Journal of Biological Sciences. 9:1052-1055
Autor:
Eduarda Fernandes, Félix Carvalho, Maria de Lourdes Bastos, Márcia Carvalho, Nuno Milhazes, Fernando Remião, Fernanda Borges
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
In the past decade, clinical evidence has increasingly shown that the liver is a target organ for 3,4-methylenedioxymethamphetamine (MDMA, "ecstasy") toxicity. The aims of the present in vitro study were: (1) to evaluate and compare the hepatotoxic e
Publikováno v:
Brain Research. 987:144-154
Administration of 3,4-methylenedioxymethamphetamine (MDMA) or 3,4-methylenedioxyamphetamine (MDA) to rats produces serotonergic nerve terminal degeneration. However, they are not neurotoxic when injected directly into the brain, suggesting the requir
Publikováno v:
Allergy. 69
Background: It is suggested that allergic immune activation, combined with a genetic predisposition, may contribute to the expression of aberrant social behaviour relevant to autism. We have previously shown that a food allergic response reduced soci
Publikováno v:
Chemical Research in Toxicology. 12:1150-1157
Direct injection of either 3,4-(+/-)-methylenedioxymethamphetamine (MDMA) or 3,4-(+/-)-methylenedioxyamphetamine (MDA) into the brain fails to reproduce the serotonergic neurotoxicity seen following peripheral administration. The serotonergic neuroto
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 51:1338-1341
The crystal structure analysis of 4-[2-(methylamino)ethyl]-1,2-benzenediol 1-(dihydrogenphospate) hydrochloride, C 9 H 15 NO 5 P + .Cl - , shows that the Cl- ion is an acceptor in a hydrogen-bonding system joining the ammonium cations in endless chai