位置：成果数据库 > 期刊 > 期刊详情页
Design, Synthesis, and Biological Evaluation of a Series of Benzo[de][1,7]naphthyridin-7(8H)-ones Be
  • ISSN号：0022-2623
  • 期刊名称：Journal of Medicinal Chemistry
  • 时间：2013.4.4
  • 页码：2885-2903
  • 相关项目：针对分子靶点的抗肿瘤药物发现及其机理研究
作者： Zhang, Ao|Chen, Chuan-Huizi|Chen, TianTian|Song, Zilan|He, Jin-Xue|Huan, Xia-Juan|Song, Shan-Shan|Liu, Qiufeng|Chen, Yi|
同期刊论文项目
针对分子靶点的抗肿瘤药物发现及其机理研究
期刊论文 65
同项目期刊论文
Fluevirosines A-C: A Biogenesis Inspired Example in the Discovery of New Bioactive Scaffolds from Fl
Transition metal-free one-pot synthesis of 2-substituted 3-carboxy-4-quinolone and chromone derivati
Discovery and bioactivity of 4-(2-arylpyrido[3 ';,2 ';:3,4]pyrrolo[1,2-f][1,2,4]-triazin-4-yl) morph
Multisubstituted quinoxalines and pyrido[2,3-d]pyrimidines: Synthesis and SAR study as tyrosine kina
Serratustones A and B Representing a New Dimerization Pattern of Two Types of Sesquiterpenoids from
Kv1.2 potassium channel inhibitors from Chukrasia tabularis
Feng JM, Miao ZH*, Jiang Y, Chen Y, Li JX, Tong LJ, Zhang J, Huang YR, Ding J*. The Conversion Betwe
Wang Y, Xu Z, Ai J, Peng X, Lin J, Ji Y, Geng M*, Long Y*. Investigation on the 1,6-naphthyridine mo
A pharmacological model reveals biased dependency on PI3K isoforms for tumor cell growth
Highly enantioselective conjugate addition of nitroalkanes to enones catalyzed by cinchona alkaloid
Synthesis of 1,7-dimethoxy-2-hydroxyxanthone, a natural product with potential activity on erectile
Synthesis and antitumor activity of 10-arylcamptothecin derivatives
Limonoids from the stems of Toona ciliata var. henryi (Meliaceae)
Cytotoxic sesquiterpenoids from Sarcandra glabra
Cytotoxic Diterpenoids from Sapium insigne
Inhibition of Chemokine (CXC Motif) Ligand 12/Chemokine (CXC Motif) Receptor 4 Axis (CXCL12/CXCR4)-m
D11, a novel glycosylated diphyllin derivative, exhibits potent anticancer activity by targeting top
Design of Cell-Permeable Stapled Peptides as HIV-1 Integrase Inhibitors
Characterization of a novel curcumin analog P1 as potent inhibitor of the NF-kappa B signaling pathw
Chukrasones A and B: Potential Kv1.2 Potassium Channel Blockers with New Skeletons from Chukrasia ta
Morusalbanol A, a neuro-protective Diels-Alder adduct with an unprecedented architecture from Morus
Extensive Crosstalk between O-GlcNAcylation and Phosphorylation Regulates Akt Signaling
Inhibition of tumor cell growth, proliferation and migration by X-387, a novel active-site inhibitor
PH006, a novel and selective Src kinase inhibitor, suppresses human breast cancer growth and metasta
Marine-Derived Angiogenesis Inhibitors for Cancer Therapy
Sysmatic combination screening reveals synergism between rapamycin and sunitinib against human lung
Organic carbonate from natural sources
Synthesis and revision of stereochemistry of rubescensin S
Daphnane-Type Diterpenoids from Trigonostemon howii
Design, synthesis and biological evaluation of substituted 11H-benzo[a] carbazole-5-carboxamides as
Potent HGF/c-Met Axis Inhibitors from Eucalyptus globulus: the Coupling of Phloroglucinol and Sesqui
Total Synthesis of Lathyranoic Acid A
Constituents of Trigonostemon heterophyllus
Ivorenolide A, an Unprecedented Immunosuppressive Macrolide from Khaya ivorensis: Structural Elucida
Structure-based optimization of the piperazino-containing 1,3-disubstituted ureas affording sub-nano
Pseudolaric acid B-driven phosphorylation of c-Jun impairs its role in stabilizing HIF-1alpha: a nov
Oligomannurarate sulfate sensitizes cancer cells to doxorubicin by inhibiting atypical activation of
Discovery of Novel 2-N-Aryl-Substituted Benzenesulfonamidoacetamides: Orally Bioavailable Tubulin Po
Chemical constituents from Brucea javanica
Novel 5-(benzyloxy)pyridin-2(1H)-one derivatives as potent c-Met inhibitors
MT119, a new planar-structured compound, targets the colchicine site of tubulin arresting mitosis an
Natural Product Triptolide Mediates Cancer Cell Death by Triggering CDK7-Dependent Degradation of RN
Repositioning HIV-1 Integrase Inhibitors for Cancer Therapeutics: 1,6-Naphthyridine-7-carboxamide as
O-Linked Triazolotriazines: Potent and Selective c-Met Inhibitors
The role of histone deacetylase 7 (HDAC7) in cancer cell proliferation: regulation on c-Myc
Angustimine and Angustifolimine: Two New Alkaloids from Daphniphyllum angustifolium
Synthesis toward the Lindenane-type Sesquiterpenoid Monomer of Chlorahololide A
蛋白酪氨酸激酶小分子抑制剂的研究新进展
基于配体结构的Grb2-SH2抑制剂的结构优化：更高的活性、更少的电荷、更低的肽性
人类可溶性环氧化物水解酶抑制剂的研究进展