Zobrazeno 1 - 10
of 109
pro vyhledávání: '"V. Peyrou"'
Autor:
M. Barth, V. Peyrou, Frank Porreca, Jean-Louis Junien, Wenhong Guo, P. Dodey, D. Pruneau, Todd W. Vanderah, Jean-Michel Luccarini
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics. 318:195-205
The antinociceptive pharmacology of N -[[4-(4,5-dihydro-1 H -imidazol-2-yl)phenyl]methyl]-2-[2-[[(4-methoxy-2,6-dimethylphenyl) sulfonyl]methylamino]ethoxy]- N -methylacetamide fumarate (LF22-0542), a novel nonpeptidic B 1 antagonist, was characteriz
Publikováno v:
Blood Coagulation & Fibrinolysis. 8:175-184
This study was done to document further the mechanism of the antithrombotic effect of CY 216 after subcutaneous injection in the rabbit. We first measured the circulating anti-factor Xa and anti-thrombin activities expressed in either International U
Publikováno v:
Thrombosis and Haemostasis, 77(2), 312-316. Georg Thieme Verlag
Scopus-Elsevier
Scopus-Elsevier
SummaryRabbit being a common animal model to evaluate the antithrombotic effect of heparins, our purpose was to apply the heparin Standard Independent Unit (SIU) approach to rabbit plasma. To take into account the specificities of the enzymes we have
Autor:
S Saivin, A.M. Gabaig, Pierre Sie, Jean-Claude Lormeau, G Houin, Bernard Boneu, C. Caranobe, V. Peyrou, B. Crepon
Publikováno v:
Scopus-Elsevier
SummaryThis study compares some in vivo pharmacological properties of CY 216 and of its ACLM and BCLM components having a molecular weight above and below 5.4 kDa respectively. The anti-factor Xa/anti-thrombin ratio of these compounds determined in a
Autor:
L. Cointeaux, Boris Camuzat-Dedenis, P.M. Loiseau, Olivier Provot, V. Peyrou, J. Mayrargue, C. Bories, Jean-François Berrien
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 57(6)
Some perketals were synthesized by the Dussault procedure using simple bromides and 2-methoxyprop-2-yl hydroperoxide. Treatment with acetic acid gave the corresponding hydroperoxides. Both perketals and hydroperoxides were tested in vitro as trichomo
Autor:
B, Camuzat-Dedenis, O, Provot, L, Cointeaux, V, Peyrou, J F, Berrien, C, Bories, P M, Loiseau, J, Mayrargue, V, Perroux
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2001, 36 (10), pp.837-842. ⟨10.1016/S0223-5234(01)01278-8⟩
European Journal of Medicinal Chemistry, Elsevier, 2001, 36 (10), pp.837-842. ⟨10.1016/S0223-5234(01)01278-8⟩
Two series of three trioxanes and 18 disubstituted peroxides were synthesised and evaluated for their in vitro trichomonacidal activity against Trichomonas vaginalis . The most active compound, 2-methylprop-2-yl 2-methoxyeth-1-yl peroxide exhibited a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b41cfffc0c8772d97eeac7720ea6b885
https://hal.archives-ouvertes.fr/hal-02402911
https://hal.archives-ouvertes.fr/hal-02402911
Publikováno v:
Thrombosis and haemostasis. 79(2)
The effect of SR121566A, a new non-peptide GP IIb-IIIa antagonist was studied in vitro with regard to thrombin generation in platelet rich plasma and in vivo on stasis-induced venous thrombosis in the rabbit. SR121566A inhibited ADP-, arachidonic aci
Publikováno v:
Thrombosis and haemostasis. 77(2)
Rabbit being a common animal model to evaluate the antithrombotic effect of heparins, our purpose was to apply the heparin Standard Independent Unit (SIU) approach to rabbit plasma. To take into account the specificities of the enzymes we have measur
Autor:
V, Peyrou, J C, Lormeau, C, Caranobe, A M, Gabaig, B, Crepon, S, Saivin, G, Houin, P, Sié, B, Boneu
Publikováno v:
Thrombosis and haemostasis. 72(2)
This study compares some in vivo pharmacological properties of CY 216 and of its ACLM and BCLM components having a molecular weight above and below 5.4 kDa respectively. The anti-factor Xa/antithrombin ratio of these compounds determined in a rabbit
Autor:
Zhu C; Faculté Science et Ingénierie - Département de Chimie., Unsaturated molecules for physics, biology and chemistry group., Université Toulouse III - Paul Sabatier, 118 route de Narbonne, 31-062, Toulouse Cedex 09, France.; Key Laboratory of Functional Molecular Solids, Ministry of Education, and School of Chemistry and Materials Science, Anhui Normal University, Wuhu, 241002, China., Saquet A; LCC-CNRS, Université de Toulouse, CNRS, UPS, Toulouse, France., Maraval V; LCC-CNRS, Université de Toulouse, CNRS, UPS, Toulouse, France., Bijani C; LCC-CNRS, Université de Toulouse, CNRS, UPS, Toulouse, France., Cui X; Engineering Research Center of Molecular Medicine of Ministry of Education, Key Laboratory of Fujian Molecular Medicine, Key Laboratory of Xiamen Marine and Gene Drugs, School of Biomedical Sciences, Huaqiao University, Xiamen, 361021, China., Poater A; Institut de Química Computacional i Catàlisi, Departament de Química, Universitat de Girona, c/ Mª Aurèlia, Capmany 69, 17003, Girona, Catalonia, Spain., Chauvin R; Faculté Science et Ingénierie - Département de Chimie., Unsaturated molecules for physics, biology and chemistry group., Université Toulouse III - Paul Sabatier, 118 route de Narbonne, 31-062, Toulouse Cedex 09, France.; Engineering Research Center of Molecular Medicine of Ministry of Education, Key Laboratory of Fujian Molecular Medicine, Key Laboratory of Xiamen Marine and Gene Drugs, School of Biomedical Sciences, Huaqiao University, Xiamen, 361021, China.
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2024 May 08; Vol. 30 (26), pp. e202400451. Date of Electronic Publication: 2024 Mar 13.