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Endomorphins and morphine limit anoxia-reoxygenation-induced brain mitochondrial dysfunction in the
ISSN号:0024-3205
期刊名称:Life Sciences
时间:0
页码:752-763
语言:英文
相关项目:不对称合成
作者:
Feng, Yun|Wang, Rui|Lin, Xin|Zhao, Qianyu|Li, Wei|Gao, Yanfeng|Lu, Yingwei|
同期刊论文项目
不对称合成
期刊论文 78
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The stimulative effects of endogenous opioids on endothelial cell proliferation, migration and angio
Low ligand loading, highly enantioselective addition of phenylacetylene to aromatic ketones catalyze
Utilization of combined chemical modifications to enhance the blood-brain barrier permeability and p
Abnormal modulation of cholinergic neurotransmission by endomorphin 1 and endomorphin 2 in isolated
A new type of ligand derived from N-terminal protected dipeptides in enantioselective addition of ph
Opioid receptor binding and antinociceptive activity of the analogues of endomorphin-2 and morphicep
Rat/mouse hemokinin-1, a mammalian tachykinin peptide, markedly potentiates the antinociceptive effe
Asymmetric addition of phenylacetylene to aldehydes catalyzed by beta-sulfonamide alcohol-titanium c
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Novel potent agonist [(pF)Phe(4),Aib(7) Aib(11),Arg(14),Lys(15)]N/OFQ-NH2 and antagonist [Nphe(1),(p
Thymopentin (TP5), an immunomodulatory peptide, suppresses proliferation and induces differentiation
In vivo inhibition of neuropeptide FF agonism by BIBP3226, an NPYY1 receptor antagonist
Endomorphin1 and endomorphin2, endogenous potent inhibitors of electrical field stimulation (EFS)-in
A novel, practical and green synthesis of Ag nanoparticles catalyst and its application in three-com
Asymmetric Aza-Mannich Addition of Oxazolones to N-Tosyl Aldimines: Synthesis of Chiral α-Disubstitu
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Highly Enantioselective 1,4-Addition of Diethyl Phosphite to Enones Using a Dinuclear Zn Catalyst
Computational study of the heterodimerization between mu and delta receptors
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Asymmetric Addition of Phenylacetylene to Aromatic Ketones Catalyzed by Zinc or Titanium Complexes w
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Doubly Stereocontrolled Asymmetric Aza-Henry Reaction with in situ Generation of N-Boc-Imines Cataly
Structure-activity study of endomorphin-2 analogs with C-terminal modifications by NMR spectroscopy
Cardiovascular responses to rat/mouse hemokinin-1, a mammalian tachykinin peptide: Systemic study in
Asymmetric addition of 1-ethynylcyclohexene to both aromatic and heteroaromatic ketones catalyzed by
Structure-activity study on the spatial arrangement of the third aromatic ring of endomorphins 1 and
Pharmacological effects of the dansylated neuropeptide FF analogues on body temperature and morphine
Melatonin attenuates the development of antinociceptive tolerance to delta-, but not to mu-opioid re
Highly enantioselective synthesis of gamma-hydroxy-alpha,beta-acetylenic esters catalyzed by a beta-
Conformational analysis of endomorphin-2 analogs with phenylalanine mimics by NMR and molecular mode
Cardiovascular responses to intrathecal administration of endomorphins in anesthetized rats
Effects of rat/mouse hemokinin-1, a mammalian tachykinin peptide, on the antinociceptive activity of
An enantioselective Michael addition of malonate to nitroalkenes catalyzed by low loading demethylqu
Mechanisms of relaxing response induced by rat/mouse hemokinin-1 in porcine coronary arteries: Roles
Antitumor effects, cell selectivity and structure-activity relationship of a novel antimicrobial pep
In vivo characterization of the effects of human hemokinin-1 and human hemokinin-1(4-11), mammalian
Neuropeptide FF receptors antagonist, RF9, attenuates opioid-evoked hypothermia in mice
Type 1 diabetes attenuates the modulatory effects of endomorphins on mouse colonic motility
DNA damage induced by caffeic acid phenyl ester in the presence of Cu(II) ions: Potential mechanism
Inhibition of neuropeptide FF (NPFF)-induced hypothermia and anti-morphine analgesia by RF9, a new s
Potent antitumor effects of a novel actinomycin D analog Leu(5) AMD
Water-soluble derivative of propolis mitigates scopolamine-induced learning and memory impairment in
Differential cardiovascular effects of synthetic peptides derived from endomorphin-1 in anesthetized
Caffeic acid phenethyl ester and its related compounds limit the functional alterations of the isola
Endomorphin-1 analogs with enhanced metabolic stability and systemic analgesic activity: Design, syn
In vitro and in vivo characterization of opioid activities of endomorphins analogs with novel constr
In vitro characterization of the effects of endomorphin 1 and 2, endogenous ligands for the mu-opioi
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