leucoline (BioDeep_00001867678)
Main id: BioDeep_00000003482
代谢物信息卡片
QUINOLINE
化学式: C9H7N (129.0578462)
中文名称: 喹啉
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1=CC=C2C(=C1)C=CC=N2
InChI: InChI=1S/C9H7N/c1-2-6-9-8(4-1)5-3-7-10-9/h1-7H
数据库引用编号
17 个数据库交叉引用编号
- ChEBI: CHEBI:17362
- KEGG: C06413
- KEGGdrug: D97671
- PubChem: 7047
- ChEMBL: CHEMBL14474
- CAS: 15793-87-0
- CAS: 15793-82-5
- CAS: 31177-31-8
- CAS: 15793-85-8
- CAS: 15793-84-7
- CAS: 15793-83-6
- CAS: 15793-86-9
- CAS: 91-22-5
- PubChem: 8648
- KNApSAcK: C00026478
- 3DMET: B00959
- NIKKAJI: J3.922E
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
5 个相关的物种来源信息
- 28974 - Averrhoa carambola: 10.1021/JF00062A009
- 671128 - Gymnodinium nagasakiense: 10.1016/0031-9422(92)80160-G
- 225107 - Karenia mikimotoi: 10.1016/0031-9422(92)80160-G
- 292239 - Mentha arvensis: 10.1021/JF00021A034
- 43879 - Peganum harmala: 10.1007/BF00563655
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：
- PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。
文献列表
- Francis Kayamba, Teboho Malimabe, Idowu Kehinde Ademola, Ofentse Jacob Pooe, Narva Deshwar Kushwaha, Mavela Mahlalela, Robyn L van Zyl, Michelle Gordon, Pertunia T Mudau, Tawanda Zininga, Addmore Shonhai, Vincent O Nyamori, Rajshekhar Karpoormath. Design and synthesis of quinoline-pyrimidine inspired hybrids as potential plasmodial inhibitors.
European journal of medicinal chemistry.
2021 May; 217(?):113330. doi:
10.1016/j.ejmech.2021.113330. [PMID: 33744688] - Letícia C Assis, Alexandre A de Castro, João P A de Jesus, Eugenie Nepovimova, Kamil Kuca, Teodorico C Ramalho, Felipe A La Porta. Computational evidence for nitro derivatives of quinoline and quinoline N-oxide as low-cost alternative for the treatment of SARS-CoV-2 infection.
Scientific reports.
2021 03; 11(1):6397. doi:
10.1038/s41598-021-85280-9. [PMID: 33737545] - Ruoyu He, Bingyong Xu, Li Ping, Xiaoqing Lv. Structural optimization towards promising β-methyl-4-acrylamido quinoline derivatives as PI3K/mTOR dual inhibitors for anti-cancer therapy: The in vitro and in vivo biological evaluation.
European journal of medicinal chemistry.
2021 Mar; 214(?):113249. doi:
10.1016/j.ejmech.2021.113249. [PMID: 33561608] - Paul Awolade, Nosipho Cele, Oluwakemi Ebenezer, Nagaraju Kerru, Lalitha Gummidi, Liang Gu, Gabriella Palma, Mandeep Kaur, Parvesh Singh. Synthesis of 1H-1,2,3-Triazole-Linked Quinoline-Isatin Molecular Hybrids as Anti-Breast Cancer and Anti-Methicillin-Resistant Staphylococcus aureus (MRSA) Agents.
Anti-cancer agents in medicinal chemistry.
2021; 21(10):1228-1239. doi:
10.2174/1871520620666200929153138. [PMID: 32990543] - Prem Prakash Kushwaha, Atul Kumar Singh, Kumari Sunita Prajapati, Mohd Shuaib, Shaimaa Fayez, Gerhard Bringmann, Shashank Kumar. Induction of apoptosis in breast cancer cells by naphthylisoquinoline alkaloids.
Toxicology and applied pharmacology.
2020 12; 409(?):115297. doi:
10.1016/j.taap.2020.115297. [PMID: 33091442] - Jiawei Zuo, Shi-Meng Wang, Xia Jiang, Mengxin Cao, Ziwen Zhang, Tianlu Shi, Hua-Li Qin, Wenjian Tang. Design, synthesis and biological evaluation of novel arylpropionic esters for the treatment of acute kidney injury.
Bioorganic chemistry.
2020 12; 105(?):104455. doi:
10.1016/j.bioorg.2020.104455. [PMID: 33197847] - Bünyamin Aygün, Burak Alaylar, Kadir Turhan, Erdem Şakar, Mehmet Karadayı, Mohammed Ibrahim Abu Al-Sayyed, Emel Pelit, Medine Güllüce, Abdulhalik Karabulut, Zuhal Turgut, Bünyamin Alım. Investigation of neutron and gamma radiation protective characteristics of synthesized quinoline derivatives.
International journal of radiation biology.
2020 11; 96(11):1423-1434. doi:
10.1080/09553002.2020.1811421. [PMID: 32813583] - Abdul Rahim, Yohei Saito, Shuichi Fukuyoshi, Katsunori Miyake, Masuo Goto, Chin-Ho Chen, Gemini Alam, Kuo-Hsiung Lee, Kyoko Nakagawa-Goto. Paliasanines A-E, 3,4-Methylenedioxyquinoline Alkaloids Fused with a Phenyl-14-oxabicyclo[3.2.1]octane Unit from Melochia umbellata var. deglabrata.
Journal of natural products.
2020 10; 83(10):2931-2939. doi:
10.1021/acs.jnatprod.0c00454. [PMID: 32946697] - Lian-Shun Feng, Zhi Xu, Le Chang, Chuan Li, Xiao-Fei Yan, Chuan Gao, Chao Ding, Feng Zhao, Feng Shi, Xiang Wu. Hybrid molecules with potential in vitro antiplasmodial and in vivo antimalarial activity against drug-resistant Plasmodium falciparum.
Medicinal research reviews.
2020 05; 40(3):931-971. doi:
10.1002/med.21643. [PMID: 31692025] - Cristiane Luchese, Anelise Barth, Gabriel Pereira da Costa, Diego Alves, Diogo La Rosa Novo, Márcia Foster Mesko, Ethel Antunes Wilhelm. Role of 7-chloro-4-(phenylselanyl) quinoline as an anti-aging drug fighting oxidative damage in different tissues of aged rats.
Experimental gerontology.
2020 02; 130(?):110804. doi:
10.1016/j.exger.2019.110804. [PMID: 31811892] - Elaine Torres Suarez, Diana Susana Granados-Falla, Sara María Robledo, Javier Murillo, Yulieth Upegui, Gabriela Delgado. Antileishmanial activity of synthetic analogs of the naturally occurring quinolone alkaloid N-methyl-8-methoxyflindersin.
PloS one.
2020; 15(12):e0243392. doi:
10.1371/journal.pone.0243392. [PMID: 33370295] - Brijesh Rathi, Prakasha Kempaiah. Bioactive Chemical Entities: Pre-clinical and Clinical Aspects - Part-II.
Current topics in medicinal chemistry.
2020 ; 20(8):606. doi:
10.2174/156802662008200331074457. [PMID: 32362271] - Esengul Karahisar, Osman Tugay, Ilkay Erdogan Orhan, Fatma Sezer Senol Deniz, Simon Vlad Luca, Krystyna Skalicka-Wozniak, Mustafa Sahin. Metabolite Profiling by Hyphenated Liquid Chromatographic Mass Spectrometric Technique (HPLC-DAD-ESI-Q-TOF-MS/MS) and Neurobiological Potential of Haplophyllum sahinii and H. vulcanicum Extracts.
Chemistry & biodiversity.
2019 Sep; 16(9):e1900333. doi:
10.1002/cbdv.201900333. [PMID: 31365785] - Doris Natalia Rosado-Solano, Mario Alberto Barón-Rodríguez, Pedro Luis Sanabria Florez, Luz Karime Luna-Parada, Carlos Eduardo Puerto-Galvis, Andrés Felipe Zorro-González, Vladimir V Kouznetsov, Leonor Yamile Vargas-Méndez. Synthesis, Biological Evaluation and In Silico Computational Studies of 7-Chloro-4-(1H-1,2,3-triazol-1-yl)quinoline Derivatives: Search for New Controlling Agents against Spodoptera frugiperda (Lepidoptera: Noctuidae) Larvae.
Journal of agricultural and food chemistry.
2019 Aug; 67(33):9210-9219. doi:
10.1021/acs.jafc.9b01067. [PMID: 31390203] - Shanda de Freitas Couto, Stífani Machado Araujo, Vandreza Cardoso Bortolotto, Marcia Rósula Poetini, Franciane Cabral Pinheiro, Elize Aparecida Santos Musachio, Luana Barreto Meichtry, Manoela do Sacramento, Diego Alves, Diogo La Rosa Novo, Márcia Foster Mesko, Marina Prigol. 7-chloro-4-(phenylselanyl) quinoline prevents dopamine depletion in a Drosophila melanogaster model of Parkinson's-like disease.
Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS).
2019 Jul; 54(?):232-243. doi:
10.1016/j.jtemb.2018.10.015. [PMID: 30366679] - K N Vennila, Kuppanagounder P Elango. Understanding the binding of quinoline amines with human serum albumin by spectroscopic and induced fit docking methods.
Journal of biomolecular structure & dynamics.
2019 Jul; 37(11):2753-2765. doi:
10.1080/07391102.2018.1496141. [PMID: 30052140] - Marissa A Valentine-King, Katherine Cisneros, Margaret O James, Robert W Huigens, Mary B Brown. Turning the Tide against Antibiotic Resistance by Evaluating Novel, Halogenated Phenazine, Quinoline, and NH125 Compounds against Ureaplasma Species Clinical Isolates and Mycoplasma Type Strains.
Antimicrobial agents and chemotherapy.
2019 03; 63(3):. doi:
10.1128/aac.02265-18. [PMID: 30642935] - Qinyuan Lu, Chenyuan Zhang, Wenyi Wang, Biyue Yuan, Yongming Zhang, Bruce E Rittmann. Bioavailable electron donors leached from leaves accelerate biodegradation of pyridine and quinoline.
The Science of the total environment.
2019 Mar; 654(?):473-479. doi:
10.1016/j.scitotenv.2018.11.129. [PMID: 30447586] - Victor Zdorichenko, Romain Paumier, Thomas Whitmarsh-Everiss, Mark Roe, Brian Cox. The Synthesis of Waltherione F and Its Analogues with Modifications at the 2- and 3-Positions as Potential Antitrypanosomal Agents.
Chemistry (Weinheim an der Bergstrasse, Germany).
2019 Jan; 25(5):1286-1292. doi:
10.1002/chem.201804061. [PMID: 30398681] - Mohammad-Ali Sobhanifar, Baratali Mashkani, Mohammad Saadatmandzadeh, Hamid Reza Sadeghnia, Seyed Hadi Mousavi. Induction of cytotoxicity and apoptosis in FLT3 mutant expressing cells using novel pyrimido cyanoacrylates and quinoline derivatives.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
2018 Dec; 108(?):893-905. doi:
10.1016/j.biopha.2018.09.001. [PMID: 30372901] - Xiufang Zheng, Chungen Liang, Lisha Wang, Baoxia Wang, Yongfu Liu, Song Feng, Jim Zhen Wu, Lu Gao, Lichun Feng, Li Chen, Tao Guo, Hong C Shen, Hongying Yun. Discovery of Benzoazepinequinoline (BAQ) Derivatives as Novel, Potent, Orally Bioavailable Respiratory Syncytial Virus Fusion Inhibitors.
Journal of medicinal chemistry.
2018 11; 61(22):10228-10241. doi:
10.1021/acs.jmedchem.8b01394. [PMID: 30339388] - Yuan Chen, Xue-Rui Wei, Ru Sun, Yu-Jie Xu, Jian-Feng Ge. The fluorescent biomarkers for lipid droplets with quinolone-coumarin unit.
Organic & biomolecular chemistry.
2018 11; 16(41):7619-7625. doi:
10.1039/c8ob02047g. [PMID: 30280167] - Wentao Liu, Wenfang Qin, Xiaobei Wang, Fei Xue, Xiao-Yu Liu, Yong Qin. Bioinspired Synthesis of (+)-Cinchonidine Using Cascade Reactions.
Angewandte Chemie (International ed. in English).
2018 09; 57(38):12299-12302. doi:
10.1002/anie.201804848. [PMID: 30084528] - Thomas Lindner, Anastasia Loktev, Annette Altmann, Frederik Giesel, Clemens Kratochwil, Jürgen Debus, Dirk Jäger, Walter Mier, Uwe Haberkorn. Development of Quinoline-Based Theranostic Ligands for the Targeting of Fibroblast Activation Protein.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine.
2018 09; 59(9):1415-1422. doi:
10.2967/jnumed.118.210443. [PMID: 29626119] - Satoshi Yamaori, Noriyuki Araki, Mio Shionoiri, Kurumi Ikehata, Shinobu Kamijo, Shigeru Ohmori, Kazuhito Watanabe. A Specific Probe Substrate for Evaluation of CYP4A11 Activity in Human Tissue Microsomes and a Highly Selective CYP4A11 Inhibitor: Luciferin-4A and Epalrestat.
The Journal of pharmacology and experimental therapeutics.
2018 09; 366(3):446-457. doi:
10.1124/jpet.118.249557. [PMID: 29976573] - Dieudonné Tshitenge Tshitenge, Doris Feineis, Virima Mudogo, Marcel Kaiser, Reto Brun, Ean-Jeong Seo, Thomas Efferth, Gerhard Bringmann. Mbandakamine-Type Naphthylisoquinoline Dimers and Related Alkaloids from the Central African Liana Ancistrocladus ealaensis with Antiparasitic and Antileukemic Activities.
Journal of natural products.
2018 04; 81(4):918-933. doi:
10.1021/acs.jnatprod.7b01041. [PMID: 29560715] - Rohitesh Kumar, Sandra Duffy, Vicky M Avery, Anthony R Carroll, Rohan A Davis. Microthecaline A, a Quinoline Serrulatane Alkaloid from the Roots of the Australian Desert Plant Eremophila microtheca.
Journal of natural products.
2018 04; 81(4):1079-1083. doi:
10.1021/acs.jnatprod.7b00992. [PMID: 29533611] - Ane G Vogt, Guilherme T Voss, Renata L de Oliveira, Jaini J Paltian, Luis F B Duarte, Diego Alves, Cristiano R Jesse, Silvane S Roman, Juliano A Roehrs, Ethel A Wilhelm, Cristiane Luchese. Organoselenium group is critical for antioxidant activity of 7-chloro-4-phenylselenyl-quinoline.
Chemico-biological interactions.
2018 Feb; 282(?):7-12. doi:
10.1016/j.cbi.2018.01.003. [PMID: 29317251] - Jonathan L Wagner, Emyr Jones, Asel Sartbaeva, Sean A Davis, Laura Torrente-Murciano, Christopher J Chuck, Valeska P Ting. Zeolite Y supported nickel phosphide catalysts for the hydrodenitrogenation of quinoline as a proxy for crude bio-oils from hydrothermal liquefaction of microalgae.
Dalton transactions (Cambridge, England : 2003).
2018 Jan; 47(4):1189-1201. doi:
10.1039/c7dt03318d. [PMID: 29292457] - Iram Parveen, Naseem Ahmed, Danish Idrees, Parvez Khan, Md Imtaiyaz Hassan. Synthesis, estrogen receptor binding affinity and molecular docking of pyrimidine-piperazine-chromene and -quinoline conjugates.
Bioorganic & medicinal chemistry letters.
2017 09; 27(18):4493-4499. doi:
10.1016/j.bmcl.2017.07.077. [PMID: 28797797] - Ethel A Wilhelm, Ana Teresinha Ferreira, Mikaela P Pinz, Angélica S Dos Reis, Ane G Vogt, Andre L Stein, Gilson Zeni, Cristiane Luchese. Antioxidant effect of quinoline derivatives containing or not selenium: Relationship with antinociceptive action quinolines are antioxidant and antinociceptive.
Anais da Academia Brasileira de Ciencias.
2017 May; 89(1 Suppl 0):457-467. doi:
10.1590/0001-3765201720160668. [PMID: 28538816] - Xiangjuan Ma, Lixia Bian, Jingfeng Ding, Yaping Wu, Huilong Xia, Jionghui Li. Electrochemical oxidation of quinoline aqueous solution on β-PbO2 anode and the evolution of phytotoxicity on duckweed.
Water science and technology : a journal of the International Association on Water Pollution Research.
2017 Apr; 75(7-8):1820-1829. doi:
10.2166/wst.2017.053. [PMID: 28452774] - Michael Luciano, Mohsen Erfanzadeh, Feifei Zhou, Hua Zhu, Tobias Bornhütter, Beate Röder, Quing Zhu, Christian Brückner. In vivo photoacoustic tumor tomography using a quinoline-annulated porphyrin as NIR molecular contrast agent.
Organic & biomolecular chemistry.
2017 Jan; 15(4):972-983. doi:
10.1039/c6ob02640k. [PMID: 28059409] - Panhong Zhang, Rong Jia, Yuxiu Zhang, Peili Shi, Tuanyao Chai. Quinoline-degrading strain Pseudomonas aeruginosa KDQ4 isolated from coking activated sludge is capable of the simultaneous removal of phenol in a dual substrate system.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering.
2016 Nov; 51(13):1139-48. doi:
10.1080/10934529.2016.1206377. [PMID: 27458688] - Anukool Vaishnav, Sarita Kumari, Shekhar Jain, Ajit Varma, Narendra Tuteja, Devendra Kumar Choudhary. PGPR-mediated expression of salt tolerance gene in soybean through volatiles under sodium nitroprusside.
Journal of basic microbiology.
2016 Nov; 56(11):1274-1288. doi:
10.1002/jobm.201600188. [PMID: 27439917] - Kakali Ghoshal, Sangita Das, Krishnendu Aich, Shyamaprosad Goswami, Subhankar Chowdhury, Maitree Bhattacharyya. A novel sensor to estimate the prevalence of hypochlorous (HOCl) toxicity in individuals with type 2 diabetes and dyslipidemia.
Clinica chimica acta; international journal of clinical chemistry.
2016 Jul; 458(?):144-53. doi:
10.1016/j.cca.2016.05.006. [PMID: 27178483] - Sunil Kumar, Melissa Birol, Andrew D Miranker. Foldamer scaffolds suggest distinct structures are associated with alternative gains-of-function in a preamyloid toxin.
Chemical communications (Cambridge, England).
2016 05; 52(38):6391-4. doi:
10.1039/c6cc01248e. [PMID: 27079937] - David J Good, Ruiling Hartley, Neil Mathias, John Crison, Giridhar Tirucherai, Peter Timmins, Munir Hussain, Raja Haddadin, Otilia Koo, Faranak Nikfar, Nga Kit Eliza Fung. Mitigation of Adverse Clinical Events of a Narrow Target Therapeutic Index Compound through Modified Release Formulation Design: An in Vitro, in Vivo, in Silico, and Clinical Pharmacokinetic Analysis.
Molecular pharmaceutics.
2015 Dec; 12(12):4434-44. doi:
10.1021/acs.molpharmaceut.5b00624. [PMID: 26536519] - Panzi Qiu, Xinyan Guo, Na Wang, Xiangji Kong, Hua He. [Simultaneous determination of ten antibiotics in pharmaceutical wastewater using ultra-high performance liquid chromatography-tandem mass spectrometry].
Se pu = Chinese journal of chromatography.
2015 Jul; 33(7):722-9. doi:
10.3724/sp.j.1123.2015.03039. [PMID: 26672201] - Da-Wei Wang, Hong-Yan Lin, Run-Jie Cao, Tao Chen, Feng-Xu Wu, Ge-Fei Hao, Qiong Chen, Wen-Chao Yang, Guang-Fu Yang. Synthesis and Herbicidal Activity of Triketone-Quinoline Hybrids as Novel 4-Hydroxyphenylpyruvate Dioxygenase Inhibitors.
Journal of agricultural and food chemistry.
2015 Jun; 63(23):5587-96. doi:
10.1021/acs.jafc.5b01530. [PMID: 26006257] - Jing Li, Wen-ying Li. [Screening of a Highly Efficient Quinoline-degrading Strain and Its Enhanced Biotreatment on Coking Waste Water].
Huan jing ke xue= Huanjing kexue.
2015 Apr; 36(4):1385-91. doi:
". [PMID: 26164916] - Peng Xu, Wencheng Ma, Hongjun Han, Baolin Hou, Shengyong Jia. Biodegradation and interaction of quinoline and glucose in dual substrates system.
Bulletin of environmental contamination and toxicology.
2015 Mar; 94(3):365-9. doi:
10.1007/s00128-014-1388-1. [PMID: 25283366] - Chunrong Wang, Mengru Zhang, Fanglin Cheng, Qi Geng. Biodegradation characterization and immobilized strains' potential for quinoline degradation by Brevundimonas sp. K4 isolated from activated sludge of coking wastewater.
Bioscience, biotechnology, and biochemistry.
2015; 79(1):164-70. doi:
10.1080/09168451.2014.952615. [PMID: 25175484] - Núbia Boechat, Maria de Lourdes G Ferreira, Luiz C S Pinheiro, Antônio M L Jesus, Milene M M Leite, Carlos C S Júnior, Anna C C Aguiar, Isabel M de Andrade, Antoniana U Krettli. New compounds hybrids 1h-1,2,3-triazole-quinoline against Plasmodium falciparum.
Chemical biology & drug design.
2014 Sep; 84(3):325-32. doi:
10.1111/cbdd.12321. [PMID: 24803084] - Reza Karimi Shervedani, Zeinab Rezvaninia, Hassan Sabzyan, Hassan Zali Boeini. Characterization of gold-thiol-8-hydroxyquinoline self-assembled monolayers for selective recognition of aluminum ion using voltammetry and electrochemical impedance spectroscopy.
Analytica chimica acta.
2014 May; 825(?):34-41. doi:
10.1016/j.aca.2014.03.041. [PMID: 24767148] - Ke Zhang, Zheng-yin Yang, Bao-dui Wang, Shao-Bo Sun, Ying-Dong Li, Tian-rong Li, Zeng-chen Liu, Jun-mei An. A highly selective chemosensor for Al3+ based on 2-oxo-quinoline-3-carbaldehyde Schiff-base.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.
2014 Apr; 124(?):59-63. doi:
10.1016/j.saa.2013.12.076. [PMID: 24463240] - Pinkesh G Sutariya, Alok Pandya, Anand Lodha, Shobhana K Menon. Fluorescence switch on-off-on receptor constructed of quinoline allied calix[4]arene for selective recognition of Cu2+ from blood serum and F- from industrial waste water.
The Analyst.
2013 May; 138(9):2531-5. doi:
10.1039/c3an00209h. [PMID: 23478482] - Hui Mao, Hong Yu, Jing Chen, Xuepin Liao. Biphasic catalysis using amphiphilic polyphenols-chelated noble metals as highly active and selective catalysts.
Scientific reports.
2013; 3(?):2226. doi:
10.1038/srep02226. [PMID: 23863916] - Pinkesh G Sutariya, Nishith R Modi, Alok Pandya, Bhoomika K Joshi, Kuldeep V Joshi, Shobhana K Menon. An ICT based 'turn on/off' quinoline armed calix[4]arene fluoroionophore: its sensing efficiency towards fluoride from waste water and Zn2+ from blood serum.
The Analyst.
2012 Dec; 137(23):5491-4. doi:
10.1039/c2an36247c. [PMID: 23047153] - Nahid Shahabadi, Maryam Maghsudi, Shohre Rouhani. Study on the interaction of food colourant quinoline yellow with bovine serum albumin by spectroscopic techniques.
Food chemistry.
2012 Dec; 135(3):1836-41. doi:
10.1016/j.foodchem.2012.06.095. [PMID: 22953930] - Narendra Reddy Chereddy, Sathiah Thennarasu, Asit Baran Mandal. Incorporation of triazole into a quinoline-rhodamine conjugate imparts iron(III) selective complexation permitting detection at nanomolar levels.
Dalton transactions (Cambridge, England : 2003).
2012 Oct; 41(38):11753-9. doi:
10.1039/c2dt31316b. [PMID: 22903587] - Riyaz Ahmad Dar, Pradeep Kumar Brahman, Sweety Tiwari, Krishna Sadashiv Pitre. Electrochemical studies of quinine in surfactant media using hanging mercury drop electrode: a cyclic voltammetric study.
Colloids and surfaces. B, Biointerfaces.
2012 Oct; 98(?):72-9. doi:
10.1016/j.colsurfb.2012.04.035. [PMID: 22659207] - Ikarastika Rahayu Abdul Wahab, Nikki Siu Hai Wong, Fabio Boylan. Choisyaternatine, a new alkaloid isolated from Choisya ternata.
Planta medica.
2012 Sep; 78(14):1597-600. doi:
10.1055/s-0032-1315044. [PMID: 22815205] - Tomohiro Yoshida, Fumihiko Akahoshi, Hiroshi Sakashita, Shuji Sonda, Masahiro Takeuchi, Yoshihito Tanaka, Mika Nabeno, Hiroyuki Kishida, Ikuko Miyaguchi, Yoshiharu Hayashi. Fused bicyclic heteroarylpiperazine-substituted L-prolylthiazolidines as highly potent DPP-4 inhibitors lacking the electrophilic nitrile group.
Bioorganic & medicinal chemistry.
2012 Aug; 20(16):5033-41. doi:
10.1016/j.bmc.2012.06.033. [PMID: 22824762] - Sergey Kapishnikov, Allon Weiner, Eyal Shimoni, Peter Guttmann, Gerd Schneider, Noa Dahan-Pasternak, Ron Dzikowski, Leslie Leiserowitz, Michael Elbaum. Oriented nucleation of hemozoin at the digestive vacuole membrane in Plasmodium falciparum.
Proceedings of the National Academy of Sciences of the United States of America.
2012 Jul; 109(28):11188-93. doi:
10.1073/pnas.1118120109. [PMID: 22745164] - Victoria J Philbin, David J Dowling, Leighanne C Gallington, Guadalupe Cortés, Zhen Tan, Eugénie E Suter, Kevin W Chi, Ariel Shuckett, Liat Stoler-Barak, Mark Tomai, Richard L Miller, Keith Mansfield, Ofer Levy. Imidazoquinoline Toll-like receptor 8 agonists activate human newborn monocytes and dendritic cells through adenosine-refractory and caspase-1-dependent pathways.
The Journal of allergy and clinical immunology.
2012 Jul; 130(1):195-204.e9. doi:
10.1016/j.jaci.2012.02.042. [PMID: 22521247] - Rui-Fang Xie, Zhi-Cheng Li, Bo Gao, Zhi-Na Shi, Xin Zhou. Bufothionine, a possible effective component in cinobufocini injection for hepatocellular carcinoma.
Journal of ethnopharmacology.
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Bioorganic & medicinal chemistry letters.
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Drug metabolism and disposition: the biological fate of chemicals.
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Bioelectromagnetics.
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BMC genomics.
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The Journal of neuroscience : the official journal of the Society for Neuroscience.
2012 Mar; 32(12):4284-96. doi:
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Physiologia plantarum.
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Bioresource technology.
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Bioorganic & medicinal chemistry.
2012 Feb; 20(4):1388-95. doi:
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The Journal of biological chemistry.
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Natural product research.
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Frontiers in microbiology.
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Malaria research and treatment.
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Biological & pharmaceutical bulletin.
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International journal of molecular sciences.
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Toxicological sciences : an official journal of the Society of Toxicology.
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Analytical biochemistry.
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European journal of drug metabolism and pharmacokinetics.
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Bioorganic & medicinal chemistry letters.
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