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DESIGN, SYNTHESIS, PHARMACOLOGICAL AND MOLECULAR MODELING EVALUATION OF NOVEL PYRAZOLO PYRIMIDINE DERIVATIVES AS HUMAN A3 ADENOSINE RECEPTOR ANTAGONISTS

机译：新型吡唑并嘧啶衍生物作为人类A3腺苷受体拮抗剂的设计，合成，药理和分子建模评价

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GOPALAKRISHNAN VENKATESAN;
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1. Fluorosulfonyl- and bis-(beta-chloroethyl)amino-phenylamino functionalized pyrazolo(4,3-e)1,2,4-triazolo(1,5-c)pyrimidine derivatives: irreversible antagonists at the human A3 adenosine receptor and molecular modeling studies. [J] . Baraldi PG, Cacciari B, Moro S, Journal of Medicinal Chemistry . 2001,第17期

机译：氟磺酰基-和双-（β-氯乙基）氨基-苯氨基官能化的吡唑并（4,3-e）1,2,4-三唑并（1,5-c）嘧啶衍生物：人类A3腺苷受体的不可逆拮抗剂和分子模型学习。
2. Design, synthesis, and biological evaluation of C9- and C2-substituted pyrazolo(4,3-e)-1,2,4-triazolo(1,5-c)pyrimidines as new A2A and A3 adenosine receptors antagonists. [J] . Baraldi PG, Fruttarolo F, Tabrizi MA, Journal of Medicinal Chemistry . 2003,第7期

机译：作为新的A2A和A3腺苷受体拮抗剂的C9和C2取代的吡唑并（4,3-e）-1,2,4-三唑并（1,5-c）嘧啶的设计，合成和生物学评估。
3. Exploring the 7-oxo-thiazolo[5,4-d]pyrimidine core for the design of new human adenosine A(3) receptor antagonists. Synthesis, molecular modeling studies and pharmacological evaluation [J] . Varano Flavia, Catarzi Daniela, Squarcialupi Lucia, European Journal of Medicinal Chemistry: Chimie Therapeutique . 2015,第Null期

机译：探索7-氧代噻唑并[5,4-d]嘧啶核用于设计新的人腺苷A（3）受体拮抗剂。合成，分子建模研究和药理评价
4. QSAR Analysis of Human Adenosine A3 Receptor Antagonists [C] . QIAO Kang, ZENG Ling-Xiao, JIN Hong-Wei, International conference of molecular simulations and applied informatics technologies . 2012

机译：人腺苷A3受体拮抗剂的QSAR分析
5. Design and synthesis of adenosine receptor antagonist bioconjugates as anti-tumor immunotherapies. [D] . Thomas, Rhiannon. 2011

机译：设计和合成腺苷受体拮抗剂生物共轭物作为抗肿瘤免疫疗法。
6. Design and Synthesis of 26-Disubstituted-4′-Selenoadenosine-5′-NN-Dimethyluronamide Derivatives as Human A3 Adenosine Receptor Antagonists [O] . Hongseok Choi, Kenneth A. Jacobson, Jinha Yu, 2021

机译：设计和合成26-二取代-4-硒诺诺酸氨-5-NN-二甲基磺酰胺衍生物作为人A3腺苷受体拮抗剂
7. DESIGN, SYNTHESIS, PHARMACOLOGICAL AND MOLECULAR MODELING EVALUATIONS OF NEW PYRAZOLO-TRIAZOLO-PYRIMIDINE DERIVATIVES AS HUMAN A3 ADENOSINE RECEPTOR ANTAGONISTS [O] . CHEONG SIEW LEE 2011

机译：新型吡唑并三唑并嘧啶衍生物作为人类A3腺苷受体拮抗剂的设计，合成，药理和分子建模评价

DESIGN, SYNTHESIS, PHARMACOLOGICAL AND MOLECULAR MODELING EVALUATION OF NOVEL PYRAZOLO PYRIMIDINE DERIVATIVES AS HUMAN A3 ADENOSINE RECEPTOR ANTAGONISTS

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