Leucol (BioDeep_00000861968)

Main id: BioDeep_00000003482

 

BioNovoGene_Lab2019


代谢物信息卡片


InChI=1\C9H7N\c1-2-6-9-8(4-1)5-3-7-10-9\h1-7

化学式: C9H7N (129.0578)
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

18 个数据库交叉引用编号

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)

7 个相关的物种来源信息

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。

亚细胞结构定位 关联基因列表
Cytoplasm 13 ABCB1, AKT1, ALOX5, ANXA5, BCL2, BIRC5, CASP3, EGFR, MTOR, PIK3CA, PTGS2, TNK1, TUBB4B
Peripheral membrane protein 7 ACHE, ALOX5, ANXA5, CYP1B1, MTOR, PTGS2, TNK1
Endosome membrane 1 EGFR
Endoplasmic reticulum membrane 5 BCL2, CYP1B1, EGFR, MTOR, PTGS2
Nucleus 10 ACHE, AKT1, BCL2, BIRC5, CASP3, EGFR, MET, MTOR, PARP1, TUBB4B
cytosol 10 AKT1, ALOX5, ANXA5, BCL2, BIRC5, CASP3, MTOR, PARP1, PIK3CA, TUBB4B
dendrite 1 MTOR
nuclear body 2 MET, PARP1
phagocytic vesicle 1 MTOR
nucleoplasm 8 AKT1, ALOX5, BIRC5, CASP3, CD2, MET, MTOR, PARP1
Cell membrane 5 ABCB1, ACHE, AKT1, CD2, EGFR
Cytoplasmic side 1 MTOR
lamellipodium 2 AKT1, PIK3CA
ruffle membrane 1 EGFR
Early endosome membrane 1 EGFR
Multi-pass membrane protein 1 ABCB1
Golgi apparatus membrane 1 MTOR
Synapse 1 ACHE
cell cortex 1 AKT1
cell junction 1 EGFR
cell surface 5 ABCB1, ACHE, CD2, EGFR, MET
glutamatergic synapse 3 AKT1, CASP3, EGFR
Golgi apparatus 2 ACHE, CD2
Golgi membrane 2 EGFR, MTOR
lysosomal membrane 2 GAA, MTOR
neuromuscular junction 1 ACHE
neuronal cell body 1 CASP3
postsynapse 2 AKT1, MET
sarcolemma 1 ANXA5
Cytoplasm, cytosol 2 ALOX5, PARP1
Lysosome 2 GAA, MTOR
endosome 1 EGFR
plasma membrane 10 ABCB1, ACHE, AKT1, BCHE, CD2, EGFR, GAA, MET, PIK3CA, TNK1
Membrane 12 ABCB1, ACHE, AKT1, ANXA5, BCL2, CYP1B1, EGFR, GAA, MET, MTOR, PARP1, TNK1
apical plasma membrane 2 ABCB1, EGFR
basolateral plasma membrane 1 EGFR
caveola 1 PTGS2
extracellular exosome 4 ABCB1, ANXA5, GAA, TUBB4B
Lysosome membrane 2 GAA, MTOR
endoplasmic reticulum 2 BCL2, PTGS2
extracellular space 4 ACHE, ALOX5, BCHE, EGFR
lysosomal lumen 1 GAA
perinuclear region of cytoplasm 4 ACHE, ALOX5, EGFR, PIK3CA
intercalated disc 1 PIK3CA
mitochondrion 3 BCL2, CYP1B1, PARP1
protein-containing complex 7 AKT1, BCL2, BIRC5, CD2, EGFR, PARP1, PTGS2
intracellular membrane-bounded organelle 2 CYP1B1, GAA
Microsome membrane 3 CYP1B1, MTOR, PTGS2
postsynaptic density 1 CASP3
TORC1 complex 1 MTOR
TORC2 complex 1 MTOR
Single-pass type I membrane protein 2 CD2, EGFR
Secreted 3 ACHE, BCHE, GAA
extracellular region 8 ACHE, ALOX5, ANXA5, BCHE, CD2, GAA, MET, TUBB4B
cytoplasmic side of plasma membrane 1 CD2
Mitochondrion outer membrane 2 BCL2, MTOR
Single-pass membrane protein 2 BCL2, MET
mitochondrial outer membrane 2 BCL2, MTOR
Extracellular side 1 ACHE
transcription regulator complex 1 PARP1
Nucleus membrane 2 ALOX5, BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 3 ALOX5, BCL2, EGFR
external side of plasma membrane 2 ANXA5, CD2
Extracellular vesicle 1 TUBB4B
microtubule cytoskeleton 3 AKT1, BIRC5, TUBB4B
nucleolus 1 PARP1
midbody 1 BIRC5
cell-cell junction 2 AKT1, CD2
vesicle 1 AKT1
Apical cell membrane 1 ABCB1
Cytoplasm, perinuclear region 1 ALOX5
Membrane raft 1 EGFR
pore complex 1 BCL2
Cytoplasm, cytoskeleton 1 TUBB4B
Cytoplasm, cytoskeleton, spindle 1 BIRC5
focal adhesion 2 ANXA5, EGFR
microtubule 2 BIRC5, TUBB4B
spindle 2 AKT1, BIRC5
basement membrane 1 ACHE
intracellular vesicle 1 EGFR
Nucleus, PML body 1 MTOR
PML body 1 MTOR
Mitochondrion intermembrane space 1 AKT1
mitochondrial intermembrane space 1 AKT1
collagen-containing extracellular matrix 1 ANXA5
interphase microtubule organizing center 1 BIRC5
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
receptor complex 2 EGFR, MET
Zymogen granule membrane 1 ANXA5
neuron projection 1 PTGS2
ciliary basal body 1 AKT1
chromatin 1 PARP1
mitotic spindle 1 TUBB4B
Chromosome 2 BIRC5, PARP1
cytoskeleton 1 TUBB4B
centriole 1 BIRC5
Nucleus, nucleolus 1 PARP1
nuclear replication fork 1 PARP1
chromosome, telomeric region 1 PARP1
nuclear chromosome 1 BIRC5
blood microparticle 1 BCHE
Lipid-anchor, GPI-anchor 1 ACHE
site of double-strand break 1 PARP1
intercellular bridge 1 TUBB4B
Cytoplasm, cytoskeleton, flagellum axoneme 1 TUBB4B
sperm flagellum 1 TUBB4B
nuclear envelope 3 ALOX5, MTOR, PARP1
Nucleus envelope 1 ALOX5
Endomembrane system 1 MTOR
Chromosome, centromere 1 BIRC5
Chromosome, centromere, kinetochore 1 BIRC5
axonemal microtubule 1 TUBB4B
tertiary granule membrane 1 GAA
side of membrane 1 ACHE
myelin sheath 1 BCL2
basal plasma membrane 2 EGFR, MET
synaptic membrane 1 EGFR
ficolin-1-rich granule lumen 1 ALOX5
secretory granule lumen 1 ALOX5
endoplasmic reticulum lumen 2 BCHE, PTGS2
nuclear matrix 1 ALOX5
phosphatidylinositol 3-kinase complex 1 PIK3CA
phosphatidylinositol 3-kinase complex, class IA 1 PIK3CA
kinetochore 1 BIRC5
azurophil granule membrane 1 GAA
azurophil granule lumen 1 TUBB4B
Nucleus matrix 1 ALOX5
nuclear envelope lumen 2 ALOX5, BCHE
chromosome, centromeric region 1 BIRC5
vesicle membrane 1 ANXA5
clathrin-coated endocytic vesicle membrane 1 EGFR
chromosome passenger complex 1 BIRC5
cytoplasmic microtubule 1 BIRC5
synaptic cleft 1 ACHE
protein-DNA complex 1 PARP1
ficolin-1-rich granule membrane 1 GAA
spindle microtubule 1 BIRC5
survivin complex 1 BIRC5
external side of apical plasma membrane 1 ABCB1
death-inducing signaling complex 1 CASP3
Cytoplasmic vesicle, phagosome 1 MTOR
site of DNA damage 1 PARP1
multivesicular body, internal vesicle lumen 1 EGFR
Shc-EGFR complex 1 EGFR
endothelial microparticle 1 ANXA5
[Poly [ADP-ribose] polymerase 1, processed N-terminus]: Chromosome 1 PARP1
[Poly [ADP-ribose] polymerase 1, processed C-terminus]: Cytoplasm 1 PARP1
Nucleus intermembrane space 1 ALOX5
autolysosome lumen 1 GAA
BAD-BCL-2 complex 1 BCL2
[Isoform H]: Cell membrane 1 ACHE
phosphatidylinositol 3-kinase complex, class IB 1 PIK3CA


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]
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