Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Mukkanti Amere"'
Publikováno v:
In Journal of Organometallic Chemistry 2002 649(2):209-213
Autor:
Pranamee Sarma, Esther Martinez-Martinez, Ramesh Gujjar, Pierre-Yves Desprez, Mukkanti Amere, Jonathon Judkins, Eiman Elwakeel, Sean D. McAllister, Rumi Kawamura, Ryuichi Murase, Eric Singer, Anu Mahadevan, Sonali Dayal, Arash Pakdel
Publikováno v:
British Journal of Pharmacology. 171:4464-4477
Background and Purpose The psychoactive cannabinoid Δ9-tetrahydrocannabinol (THC) and the non-psychoactive cannabinoid cannabidiol (CBD) can both reduce cancer progression, each through distinct anti-tumour pathways. Our goal was to discover a compo
Autor:
Mauro Maccarrone, Bėla Horváth, Mohanraj Rajesh, Rachel Y. Gao, Anu Mahadevan, Sandor Batkai, Roger G. Pertwee, Lisa Anne Gauson, Mukkanti Amere, Partha Mukhopadhyay, Aron H. Lichtman, Natalia Battista, Pal Pacher
Publikováno v:
British Journal of Pharmacology. 165:2450-2461
BACKGROUND AND PURPOSE Activation of cannabinoid CB2 receptors protects against various forms of ischaemia-reperfusion (I/R) injury. Δ8-Tetrahydrocannabivarin (Δ8-THCV) is a synthetic analogue of the plant cannabinoid Δ9-tetrahydrocannabivarin, wh
Autor:
Ryuichi, Murase, Rumi, Kawamura, Eric, Singer, Arash, Pakdel, Pranamee, Sarma, Jonathon, Judkins, Eiman, Elwakeel, Sonali, Dayal, Esther, Martinez-Martinez, Mukkanti, Amere, Ramesh, Gujjar, Anu, Mahadevan, Pierre-Yves, Desprez, Sean D, McAllister
Publikováno v:
British journal of pharmacology. 171(19)
The psychoactive cannabinoid Δ(9) -tetrahydrocannabinol (THC) and the non-psychoactive cannabinoid cannabidiol (CBD) can both reduce cancer progression, each through distinct anti-tumour pathways. Our goal was to discover a compound that could effic
Publikováno v:
Translational stroke research. 3(3)
We reported previously that both a cannabinoid receptor 2 (CB2R) agonist and a cannabinoid receptor 1 (CB1R) antagonist were protective in the treatment of transient middle cerebral artery occlusion/reperfusion injury (MCAO/R) and that they acted in
Publikováno v:
ChemInform. 40
The enantioselective decarboxylative protonation (EDP) of malonic or acetoacetic acid derivatives is a synthetic methodology by which the chirality of the product is generated during the enol/enolate protonation step. Although EDP is a century-old re
Publikováno v:
European Journal of Organic Chemistry
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2008, 2008 (33), pp.5493-5506. ⟨10.1002/ejoc.200800759⟩
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2008, 2008 (33), pp.5493-5506. ⟨10.1002/ejoc.200800759⟩
The enantioselective decarboxylative protonation (EDP) of malonic or acetoacetic acid derivatives is a synthetic methodology by which the chirality of the product is generated during the enol/enolate protonation step. Although EDP is a century-old re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49345cc4b0ebe64d215203a34a127850
https://hal-normandie-univ.archives-ouvertes.fr/hal-02327983
https://hal-normandie-univ.archives-ouvertes.fr/hal-02327983
Publikováno v:
ChemInform. 38
Thiourea derived cinchona alkaloids promote the asymmetric decarboxylative protonation of cyclic, acyclic, or bicyclic alpha-aminomalonate hemiesters under mild and metal-free conditions to afford enantioenriched aminoesters in high yields and enanti
Publikováno v:
Synfacts. 2007:0984-0984
Publikováno v:
Organic Letters; Jul2007, Vol. 9 Issue 14, p2621-2624, 4p