相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Acridine Orange Encapsulated Mesoporous Manganese Dioxide Nanoparticles to Enhance Radiotherapy
Junzhi Liu et al.
BIOCONJUGATE CHEMISTRY (2020)
Synthesis and antiproliferative activity of new hybrids bearing neocryptolepine, acridine and α-aminophosphonate scaffolds
Abdullah A. S. Ahmed et al.
JOURNAL OF THE IRANIAN CHEMICAL SOCIETY (2020)
Negatively Charged Red-Emitting Acridine Dyes for Facile Reductive Amination, Separation, and Fluorescent Detection of Glycans
Maksim A. Fomin et al.
ANALYTICAL CHEMISTRY (2020)
Structural Basis for Targeting T:T Mismatch with Triaminotriazine-Acridine Conjugate Induces a U-Shaped Head-to-Head Four-Way Junction in CTG Repeat DNA
Ching-Ming Chien et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2020)
Application of the Povarov Reaction in Biaryls under Iron Catalysis for the General Synthesis of Dibenzo[a,c]Acridines
Baitan Chakraborty et al.
JOURNAL OF ORGANIC CHEMISTRY (2020)
Synthesis, Antiviral, Antibacterial, and Cytotoxicity Assessment of Some 3H-Benzo[a]imidazo[4,5-j]acridines and 3H-Benzo[a]pyrazolo[3,4-j]acridines
M. Faramarzi et al.
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY (2020)
Acridine Orange: A Review of Nove Applications for Surgical Cancer Imaging and Therapy
Vadim A. Byvaltsev et al.
FRONTIERS IN ONCOLOGY (2019)
Achieving Enhanced Thermally Activated Delayed Fluorescence Rates and Shortened Exciton Lifetimes by Constructing Intramolecular Hydrogen Bonding Channels
Liangying Wang et al.
ACS APPLIED MATERIALS & INTERFACES (2019)
Synthesis, chemiluminescence, and application of 2,4-disubstituted phenyl 10-methyl-10λ4-acridine-9-carboxylates
Manabu Nakazono et al.
DYES AND PIGMENTS (2019)
Catalyst-Free Synthesis of Xanthene and Pyrimidine-Fused Heterocyclic Derivatives at Water-Ethanol Medium and Their Antioxidant Properties
Reddi Mohan Naidu Kalla et al.
CHEMISTRYSELECT (2019)
Synthesis of 2-substituted indoles through cyclization and demethylation of 2-alkynyldimethylanilines by ethanol
Guangkuan Zhao et al.
GREEN CHEMISTRY (2019)
Synthesis and Antibacterial Activity of New N9-Substituted Acridine-9-amines
T. N. Kudryavtseva et al.
RUSSIAN JOURNAL OF GENERAL CHEMISTRY (2019)
Synthesis and Application of Acridine Derivatives
Songbuer et al.
CHINESE JOURNAL OF ORGANIC CHEMISTRY (2018)
Novel carbazolyl-substituted spiro[acridine-9,9 '-fluorene] derivatives as deep-blue emitting materials for OLED applications
Wei Sun et al.
DYES AND PIGMENTS (2018)
Ethanol: A Promising Green Solvent for the Deconstruction of Lignocellulose
Kubilay Tekin et al.
CHEMSUSCHEM (2018)
Synthesis of Novel Bis(thiazolylchromen-2-one) Derivatives Linked to Alkyl Spacer via Phenoxy Group
Mohamed Hosny et al.
JOURNAL OF HETEROCYCLIC CHEMISTRY (2018)
Spiro[4H-pyran-3,3-oxindoles] Derived from 1,2,3,4-tetrahydroquinolinePart 2
Mehdi M. Baradarani et al.
JOURNAL OF HETEROCYCLIC CHEMISTRY (2017)
Spiro[4H-pyran-3,3-oxindoles] Derived from 9,10-dihydroacridine
Mousa Alipour et al.
JOURNAL OF HETEROCYCLIC CHEMISTRY (2017)
Synthesis, characterization and antitumor activity of 2-methyl-9-substituted acridines
Rajesh Kumar et al.
ARABIAN JOURNAL OF CHEMISTRY (2017)
Recent developments in the synthesis and biological activity of acridine/acridone analogues
Monika Gensicka-Kowalewska et al.
RSC ADVANCES (2017)
Simple and efficient synthesis of 3,4-dihydropyrimidin-2(1H)-thiones utilizing L-proline nitrate as a proficient, recyclable and eco-friendly catalyst
Sandeep P. Bahekar et al.
JOURNAL OF SAUDI CHEMICAL SOCIETY (2017)
New spiro-acridines: DNA interaction, antiproliferative activity and inhibition of human DNA topoisomerases
Sinara Monica Vitalino de Almeida et al.
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES (2016)
Spiro[4H-pyran-3,3′-oxindoles] Derived from 1,2,3,4-Tetrahydroquinoline
Hosein Vahedi et al.
JOURNAL OF HETEROCYCLIC CHEMISTRY (2015)
Biomimetic One-Pot Route to Acridine Epoxides
Margarida Linhares et al.
JOURNAL OF ORGANIC CHEMISTRY (2015)
Solvent Effects on the Kinetic and Mechanism of N-Mannich Bases of 3-Hydrazonoindole-2-one
Tahani Saad Al-Garni et al.
ASIAN JOURNAL OF CHEMISTRY (2014)
Acridine and its derivatives: a patent review (2009-2013)
Bin Zhang et al.
EXPERT OPINION ON THERAPEUTIC PATENTS (2014)
Aqueous ethanol: a suitable medium for the diastereoselective Diels-Alder reaction mediated by chiral bases
Nitin A. Mirgane et al.
GREEN CHEMISTRY LETTERS AND REVIEWS (2011)
Acridine-N Peptide Conjugates Display Enhanced Affinity and Specificity for boxB RNA Targets
Xin Qi et al.
BIOCHEMISTRY (2010)
A review of aqueous organic reactions for the undergraduate teaching laboratory
Andrew P. Dicks
GREEN CHEMISTRY LETTERS AND REVIEWS (2009)
Synthesis and Modeling of acridine dyes as potential photosensitizers for dye-sensitized photovoltaic applications
Ravi Mosurkal et al.
JOURNAL OF MACROMOLECULAR SCIENCE PART A-PURE AND APPLIED CHEMISTRY (2006)
Synthesis and evaluation of acridine- and acridone-based anti-herpes agents with topoisomerase activity
John R. Goodell et al.
BIOORGANIC & MEDICINAL CHEMISTRY (2006)
Rational design, synthesis, and biological evaluation of bis(pyrimido[5,6,1-de]acridines) and bis(pyrazolo[3,4,5-kl]acridine-5-carboxamides) as new anticancer agents
I Antonini et al.
JOURNAL OF MEDICINAL CHEMISTRY (2004)
分享论文
