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内部出版物
在“
Elsevier电子期刊
”中,
命中:
658
条,耗时:小于0.01 秒
1.
Transformation of aryl
carboxamides
into 1,3-dioxo-1,3-dihydroisobenzofuran-4-
carboxamides
作者:
Benjamin Prek
;
Jure Bezen&scaron
;
ek
;
Marta Počkaj
;
Branko Stanovnik
;
branko.stanovnik@fkkt.uni-lj.si
关键词:
Enaminones
;
Carboxamides
;
Aroylacetamidines
;
(E)-N-(1-(dimethylamino)ethylidene)-
carboxamides
;
1
;
3-Dioxo-1
;
3-dihydroisobenzofuran-4-
carboxamides
刊名:Tetrahedron
出版年:2017
2.
Synthesis, biological evaluation, docking study and ulcerogenicity profiling of some novel quinoline-2-
carboxamides
as dual COXs/LOX inhibitors endowed with anti-inflammatory activity
作者:
Mostafa H. Abdelrahman
a
;
Bahaa G.M. Youssif
b
;
c
;
bgyoussif@ju.edu.sa
;
Mohamed A. abdelgawad
c
;
d
;
Ahmed H. Abdelazeem
e
;
f
;
Hussein M. Ibrahim
g
;
h
;
Abd El Ghany A. Moustafa
h
;
i
;
Laurent Treamblu
j
;
Syed Nasir Abbas Bukhari
c
;
snab_hussaini@yahoo.com
关键词:
Quinoline-2-
carboxamides
;
COXs
;
LOX
;
Docking
;
Anti-inflammatory
刊名:European Journal of Medicinal Chemistry
出版年:2017
3.
Crystal structures, binding interactions, and ADME evaluation of brain penetrant N-substituted indazole-5-
carboxamides
as subnanomolar, selective monoamine oxidase B and dual MAO-A/B inhibitors
作者:
Nikolay T. Tzvetkov
a
;
ntzvetkov@ntzlab.com
;
Hans-Georg Stammler
b
;
Beate Neumann
b
;
Silvia Hristova
c
;
Liudmil Antonov
c
;
Marcus Gastreich
d
关键词:
ADME
;
MAO inhibitors
;
Molecular modeling
;
Indazole-5-
carboxamides
;
Parkinson's disease
;
X-ray
刊名:European Journal of Medicinal Chemistry
出版年:2017
4.
Structure-activity relationship study and discovery of indazole 3-
carboxamides
as calcium-release activated calcium channel blockers
作者:
Sha Bai
a
;
Masazumi Nagai
a
;
Steffi K. Koerner
a
;
Aristidis Veves
b
;
Lijun Sun
a
;
lsun1@bidmc.harvard.edu
关键词:
Mast cell
;
Inflammation
;
Calcium channel blockers
;
Indazole-3-
carboxamides
刊名:Bioorganic & Medicinal Chemistry Letters
出版年:2017
5.
Sonochemistry in organocatalytic enamine-azide [3+2] cycloadditions: A rapid alternative for the synthesis of 1,2,3-triazoyl
carboxamides
作者:
Daiane M. Xavier
a
;
daianedamotta@yahoo.com.br" class="auth_mail" title="E-mail the corresponding author
;
Bruna S. Goldani
a
;
goldanibruna@gmail.com" class="auth_mail" title="E-mail the corresponding author
;
Natá
;
lia Seus
a
;
natyseus@gmail.com" class="auth_mail" title="E-mail the corresponding author
;
Raquel G. Jacob
a
;
raquel.jacob@ufpel.edu.br" class="auth_mail" title="E-mail the corresponding author
;
Thiago Barcellos
b
;
tbsilva6@ucs.br" class="auth_mail" title="E-mail the corresponding author
;
Má
;
rcio W. Paixã
;
o
c
;
mwpaixao@ufscar.br" class="auth_mail" title="E-mail the corresponding author
;
Rafael Luque
d
;
q62alsor@uco.es" class="auth_mail" title="E-mail the corresponding author
;
Diego Alves
a
;
diego.alves@ufpel.edu.br" class="auth_mail" title="E-mail the corresponding author
关键词:
Sonochemistry
;
Cycloadditions
;
Organocatalysis
;
1
2 ;
3-Triazoles
;
Carboxamides
刊名:Ultrasonics Sonochemistry
出版年:2017
6.
Structure-based optimization of 1H-imidazole-2-
carboxamides
as Axl kinase inhibitors utilizing a Mer mutant surrogate
作者:
Walter Keung
a
;
walter.keung@takeda.com
;
Amogh Boloor
a
;
Jason Brown
a
;
Andre Kiryanov
a
;
Anthony Gangloff
a
;
J. David Lawson
b
;
Robert Skene
b
;
Isaac Hoffman
b
;
Josephine Atienza
c
;
Jason Kahana
c
;
Ron De Jong
c
;
Pamela Farrell
c
;
Deepika Balakrishna
c
;
Petro Halkowycz
c
关键词:
Axl
;
Mer
;
Structure design
;
Oncology design
;
Modeling
;
Crystallography
;
SBDD
刊名:Bioorganic & Medicinal Chemistry Letters
出版年:2017
7.
New pyridazinone-4-
carboxamides
as new cannabinoid receptor type-2 inverse agonists: Synthesis, pharmacological data and molecular docking
作者:
Giulio Ragusa
a
;
Marí
;
a Gó
;
mez-Cañ
;
as
b
;
c
;
d
;
Paula Morales
e
;
Carmen Rodrí
;
guez-Cueto
b
;
c
;
d
;
Marí
;
a R. Pazos
b
;
c
;
d
;
Battistina Asproni
a
;
Elena Cichero
f
;
Paola Fossa
f
;
Gerard A. Pinna
a
;
Nadine Jagerovic
e
;
Javier Ferná
;
ndez-Ruiz
b
;
c
;
d
;
Gabriele Murineddu
a
;
muri@uniss.it
关键词:
Scaffold hopping
;
Synthesis
;
Cannabinoid receptors
;
CB2 antagonism
;
ADME model
;
Docking studies
刊名:European Journal of Medicinal Chemistry
出版年:2017
8.
Linker-switch approach towards new ATP binding site inhibitors of DNA gyrase B
作者:
Marko Jukič
a
;
Janez Ila&scaron
;
a
;
Matjaž Brvar
b
;
Danijel Kikelj
a
;
Jožko Cesar
a
;
Marko Anderluh
a
;
marko.anderluh@ffa.uni-lj.si
关键词:
Antibiotics
;
Antibacterials
;
Inhibitor
;
DNA gyrase B
;
ATP binding site
;
Pyrrole-2-
carboxamides
;
Structure-based drug design
;
Ligand-based drug design
刊名:European Journal of Medicinal Chemistry
出版年:2017
9.
Design, synthesis and docking studies of novel 1,2-dihydro-4-hydroxy-2-oxoquinoline-3-carboxamide derivatives as a potential anti-proliferative agents
作者:
Saleha Banu
a
;
Rajitha Bollu
a
;
Rajashaker Bantu
a
;
Lingaiah Nagarapu
a
;
;
Sowjanya Polepalli
b
;
Nishant Jain
b
;
Radhika Vangala
c
;
Vijjulatha Manga
c
关键词:
Roquinimex
;
1
;
2-dihydro-4-hydroxy-2-oxoquinoline-3-
carboxamides
;
Piperazines
;
Anti-proliferative
;
Multiple sclerosis
;
Cell lines and molecular modeling
刊名:European Journal of Medicinal Chemistry
出版年:2017
10.
Synthesis and structure-activity studies of side chain analogues of the anti-tubercular agent, Q203
作者:
Sunhee Kang
a
;
d
;
Young Mi Kim
a
;
Ryang Yeo Kim
b
;
Min Jung Seo
a
;
Zaesung No
a
;
Kiyean Nam
c
;
Sanghee Kim
d
;
pennkim@snu.ac.kr
;
Jaeseung Kim
a
;
silanediol@gmail.com
关键词:
Tuberculosis
;
Imidazo[1
;
2-a]pyridine-3-carboxamide (IPA)
;
Pharmacokinetics
;
Structure-activity relationship (SAR)
;
Q203
刊名:European Journal of Medicinal Chemistry
出版年:2017
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