ISOQUINOLINE (BioDeep_00001867984)

Main id: BioDeep_00000002906

 

natural product


代谢物信息卡片


ISOQUINOLINE

化学式: C9H7N (129.0578)
中文名称: 异喹啉
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC=C2C=NC=CC2=C1
InChI: InChI=1S/C9H7N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-7H

描述信息

同义名列表

3 个代谢物同义名

ISOQUINOLINE; Isoquinoline; Isoquinoline



数据库引用编号

14 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)

11 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, BCL2, BDNF, CASP3, MAPK14, MYLK, NFE2L2, PIK3CA, PRKX, PTGS2, TUBB4B, XDH
Peripheral membrane protein 3 ACHE, HSD17B6, PTGS2
Endoplasmic reticulum membrane 2 BCL2, PTGS2
Nucleus 9 ACHE, AKT1, BCL2, CASP3, MAPK14, NFE2L2, PARP1, PRKX, TUBB4B
cytosol 11 AKT1, BCL2, CASP3, MAPK14, MYLK, NFE2L2, PARP1, PIK3CA, PRKCQ, TUBB4B, XDH
dendrite 2 BDNF, DRD2
nuclear body 1 PARP1
centrosome 1 NFE2L2
nucleoplasm 7 AKT1, CASP3, CD2, MAPK14, NFE2L2, PARP1, PRKX
RNA polymerase II transcription regulator complex 1 NFE2L2
Cell membrane 5 ABCB1, ACHE, AKT1, CD2, DRD2
Cleavage furrow 1 MYLK
lamellipodium 3 AKT1, MYLK, PIK3CA
Early endosome membrane 1 HSD17B6
Multi-pass membrane protein 2 ABCB1, DRD2
Golgi apparatus membrane 1 DRD2
Synapse 3 ACHE, DRD2, MYLK
cell cortex 1 AKT1
cell surface 3 ABCB1, ACHE, CD2
glutamatergic synapse 4 AKT1, CASP3, DRD2, MAPK14
Golgi apparatus 3 ACHE, CD2, NFE2L2
Golgi membrane 1 DRD2
neuromuscular junction 1 ACHE
neuronal cell body 1 CASP3
postsynapse 1 AKT1
presynaptic membrane 1 DRD2
synaptic vesicle 1 BDNF
Cytoplasm, cytosol 2 NFE2L2, PARP1
acrosomal vesicle 1 DRD2
plasma membrane 10 ABCB1, ACHE, AKT1, BCHE, CD2, DRD2, MYLK, NFE2L2, PIK3CA, PRKCQ
synaptic vesicle membrane 1 DRD2
Membrane 6 ABCB1, ACHE, AKT1, BCL2, BDNF, PARP1
apical plasma membrane 1 ABCB1
axon 2 BDNF, DRD2
caveola 1 PTGS2
extracellular exosome 2 ABCB1, TUBB4B
Lumenal side 1 HSD17B6
endoplasmic reticulum 3 BCL2, HSD17B6, PTGS2
extracellular space 4 ACHE, BCHE, BDNF, XDH
perinuclear region of cytoplasm 3 ACHE, BDNF, PIK3CA
intercalated disc 1 PIK3CA
mitochondrion 3 BCL2, MAPK14, PARP1
protein-containing complex 5 AKT1, BCL2, CD2, PARP1, PTGS2
intracellular membrane-bounded organelle 1 HSD17B6
Microsome membrane 2 HSD17B6, PTGS2
postsynaptic density 1 CASP3
Single-pass type I membrane protein 1 CD2
Secreted 3 ACHE, BCHE, BDNF
extracellular region 6 ACHE, BCHE, BDNF, CD2, MAPK14, TUBB4B
cytoplasmic side of plasma membrane 1 CD2
Mitochondrion outer membrane 1 BCL2
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 1 BCL2
Extracellular side 1 ACHE
transcription regulator complex 1 PARP1
centriolar satellite 1 PRKCQ
ciliary membrane 1 DRD2
Nucleus membrane 1 BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 1 BCL2
external side of plasma membrane 1 CD2
Extracellular vesicle 1 TUBB4B
actin cytoskeleton 1 MYLK
dendritic spine 1 DRD2
perikaryon 1 DRD2
microtubule cytoskeleton 2 AKT1, TUBB4B
nucleolus 1 PARP1
cell-cell junction 2 AKT1, CD2
vesicle 1 AKT1
postsynaptic membrane 1 DRD2
Apical cell membrane 1 ABCB1
Cell projection, lamellipodium 1 MYLK
pore complex 1 BCL2
Cytoplasm, cytoskeleton 1 TUBB4B
microtubule 1 TUBB4B
spindle 1 AKT1
GABA-ergic synapse 1 DRD2
Peroxisome 1 XDH
basement membrane 1 ACHE
sarcoplasmic reticulum 1 XDH
Mitochondrion intermembrane space 1 AKT1
mitochondrial intermembrane space 1 AKT1
lateral plasma membrane 1 DRD2
nuclear speck 1 MAPK14
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
neuron projection 1 PTGS2
ciliary basal body 1 AKT1
cilium 1 DRD2
chromatin 2 NFE2L2, PARP1
mediator complex 1 NFE2L2
mitotic spindle 1 TUBB4B
Chromosome 1 PARP1
cytoskeleton 1 TUBB4B
Nucleus, nucleolus 1 PARP1
spindle pole 1 MAPK14
nuclear replication fork 1 PARP1
chromosome, telomeric region 1 PARP1
blood microparticle 1 BCHE
non-motile cilium 1 DRD2
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 2 DRD2, TUBB4B
nuclear envelope 1 PARP1
axonemal microtubule 1 TUBB4B
side of membrane 1 ACHE
myelin sheath 1 BCL2
stress fiber 1 MYLK
ficolin-1-rich granule lumen 1 MAPK14
secretory granule lumen 1 MAPK14
endoplasmic reticulum lumen 3 BCHE, BDNF, PTGS2
axon terminus 1 DRD2
phosphatidylinositol 3-kinase complex 1 PIK3CA
phosphatidylinositol 3-kinase complex, class IA 1 PIK3CA
endocytic vesicle 1 DRD2
azurophil granule lumen 1 TUBB4B
immunological synapse 1 PRKCQ
aggresome 1 PRKCQ
nuclear envelope lumen 1 BCHE
Cytoplasm, cytoskeleton, stress fiber 1 MYLK
synaptic cleft 1 ACHE
protein-DNA complex 2 NFE2L2, PARP1
external side of apical plasma membrane 1 ABCB1
death-inducing signaling complex 1 CASP3
dopaminergic synapse 1 DRD2
site of DNA damage 1 PARP1
[Poly [ADP-ribose] polymerase 1, processed N-terminus]: Chromosome 1 PARP1
[Poly [ADP-ribose] polymerase 1, processed C-terminus]: Cytoplasm 1 PARP1
BAD-BCL-2 complex 1 BCL2
G protein-coupled receptor complex 1 DRD2
[Isoform H]: Cell membrane 1 ACHE
[Neurotrophic factor BDNF precursor form]: Secreted 1 BDNF
phosphatidylinositol 3-kinase complex, class IB 1 PIK3CA


文献列表

  • Erika Plazas, Mónica C Avila M, Diego R Muñoz, Luis E Cuca S. Natural isoquinoline alkaloids: Pharmacological features and multi-target potential for complex diseases. Pharmacological research. 2022 03; 177(?):106126. doi: 10.1016/j.phrs.2022.106126. [PMID: 35151857]
  • Emmanoel V Costa, Liviane do N Soares, Jamal da Silva Chaar, Valdenizia R Silva, Luciano de S Santos, Hector H F Koolen, Felipe M A da Silva, Josean F Tavares, Gokhan Zengin, Milena B P Soares, Daniel P Bezerra. Benzylated Dihydroflavones and Isoquinoline-Derived Alkaloids from the Bark of Diclinanona calycina (Annonaceae) and Their Cytotoxicities. Molecules (Basel, Switzerland). 2021 Jun; 26(12):. doi: 10.3390/molecules26123714. [PMID: 34207059]
  • Yang Huang, Tiejie Wang, Zhengjin Jiang. Fast analysis of alkaloids from different parts of Mahonia bealei (Fort.) Carr. studied for their anti-Alzheimer's activity using supercritical fluid chromatography. Journal of separation science. 2021 May; 44(9):2006-2014. doi: 10.1002/jssc.202001079. [PMID: 33650266]
  • Daniela Marasco, Caterina Vicidomini, Pawel Krupa, Federica Cioffi, Pham Dinh Quoc Huy, Mai Suan Li, Daniele Florio, Kerensa Broersen, Maria Francesca De Pandis, Giovanni N Roviello. Plant isoquinoline alkaloids as potential neurodrugs: A comparative study of the effects of benzo[c]phenanthridine and berberine-based compounds on β-amyloid aggregation. Chemico-biological interactions. 2021 Jan; 334(?):109300. doi: 10.1016/j.cbi.2020.109300. [PMID: 33098838]
  • Huan Xia, Yitong Liu, Guiyang Xia, Yi Liu, Sheng Lin, Lijia Guo. Novel Isoquinoline Alkaloid Litcubanine A - A Potential Anti-Inflammatory Candidate. Frontiers in immunology. 2021; 12(?):685556. doi: 10.3389/fimmu.2021.685556. [PMID: 34163484]
  • Jun-Yan Xiang, Yan-Yu Chi, Jin-Xin Han, Hongyu Xiang, Qiuhong Xie. The Toxicity and Attenuation Methods of Toxic Chinese Materia Medica for its Reasonable Application: A Review. The American journal of Chinese medicine. 2021; 49(1):41-67. doi: 10.1142/s0192415x21500038. [PMID: 33416023]
  • Lin-Hai Chen, Qing Zhang, Xin Xie, Fa-Jun Nan. Modulation of the G-Protein-Coupled Receptor 84 (GPR84) by Agonists and Antagonists. Journal of medicinal chemistry. 2020 12; 63(24):15399-15409. doi: 10.1021/acs.jmedchem.0c01378. [PMID: 33267584]
  • Zhihui Liu, Zhenru Mi, Panpan Wang, Sheng Chang, Na Han, Jun Yin. Two new alkaloids from the tubers of Corydalis ambigua subsp. amurensis and their anti-proliferative activity. Natural product research. 2020 Dec; 34(23):3305-3312. doi: 10.1080/14786419.2019.1566821. [PMID: 30908089]
  • Jing-Jing Xue, Chun-Yu Jiang, De-Li Zou, Bin-Jie Li, Jin-Cai Lu, Da-Hong Li, Bin Lin, Zhan-Lin Li, Hui-Ming Hua. Baicalensines A and B, Two Isoquinoline Alkaloids from the Roots of Thalictrum baicalense. Organic letters. 2020 10; 22(19):7439-7442. doi: 10.1021/acs.orglett.0c02444. [PMID: 32886519]
  • Ruifei Zhang, Qiang Guo, Edward J Kennelly, Chunlin Long, Xingyun Chai. Diverse alkaloids and biological activities of Fumaria (Papaveraceae): An ethnomedicinal group. Fitoterapia. 2020 Oct; 146(?):104697. doi: 10.1016/j.fitote.2020.104697. [PMID: 32739338]
  • Kaho Hirai, Saiichiro Watanabe, Nozomi Nishijima, Kaoru Shibata, Akane Hase, Tsuyoshi Yamanaka, Masato Inazu. Molecular and Functional Analysis of Choline Transporters and Antitumor Effects of Choline Transporter-Like Protein 1 Inhibitors in Human Pancreatic Cancer Cells. International journal of molecular sciences. 2020 Jul; 21(15):. doi: 10.3390/ijms21155190. [PMID: 32707889]
  • Kwangho Song, Jae-Hyeon Oh, Min Young Lee, Seok-Geun Lee, In Jin Ha. Molecular Network-Guided Alkaloid Profiling of Aerial Parts of Papaver nudicaule L. Using LC-HRMS. Molecules (Basel, Switzerland). 2020 Jun; 25(11):. doi: 10.3390/molecules25112636. [PMID: 32517053]
  • Erika Plazas, Stefanie Hagenow, Monica Avila Murillo, Holger Stark, Luis Enrique Cuca. Isoquinoline alkaloids from the roots of Zanthoxylum rigidum as multi-target inhibitors of cholinesterase, monoamine oxidase A and Aβ1-42 aggregation. Bioorganic chemistry. 2020 05; 98(?):103722. doi: 10.1016/j.bioorg.2020.103722. [PMID: 32155491]
  • Mohamed A Tantawy, Farid M Sroor, Magda F Mohamed, Mostafa E El-Naggar, Fatma M Saleh, Hamdi M Hassaneen, Ismail A Abdelhamid. Molecular Docking Study, Cytotoxicity, Cell Cycle Arrest and Apoptotic Induction of Novel Chalcones Incorporating Thiadiazolyl Isoquinoline in Cervical Cancer. Anti-cancer agents in medicinal chemistry. 2020; 20(1):70-83. doi: 10.2174/1871520619666191024121116. [PMID: 31696811]
  • Shih-Yi Lee, Ling-Wei Hsin, Ming-Jai Su, Ching-Chia ChangChien, Hui-Chun Ku. A novel isoquinoline derivative exhibits anti-inflammatory properties and improves the outcomes of endotoxemia. Pharmacological reports : PR. 2019 Dec; 71(6):1281-1288. doi: 10.1016/j.pharep.2019.06.015. [PMID: 31683199]
  • Jerald J Nair, Johannes van Staden. Antiprotozoal alkaloid principles of the plant family Amaryllidaceae. Bioorganic & medicinal chemistry letters. 2019 10; 29(20):126642. doi: 10.1016/j.bmcl.2019.126642. [PMID: 31515186]
  • Anna Petruczynik, Tomasz Tuzimski, Tomasz Plech, Justyna Misiurek, Karolina Szalast, Grażyna Szymczak. Comparison of Anticancer Activity and HPLC-DAD Determination of Selected Isoquinoline Alkaloids from Thalictrum foetidum, Berberis sp. and Chelidonium majus Extracts. Molecules (Basel, Switzerland). 2019 Sep; 24(19):. doi: 10.3390/molecules24193417. [PMID: 31547046]
  • Cai-Feng Ding, Zhi Dai, Hao-Fei Yu, Xu-Dong Zhao, Xiao-Dong Luo. New aporphine alkaloids with selective cytotoxicity against glioma stem cells from Thalictrum foetidum. Chinese journal of natural medicines. 2019 Sep; 17(9):698-706. doi: 10.1016/s1875-5364(19)30084-6. [PMID: 31526505]
  • Zhong-Min Zhao, Xiao-Fei Shang, Raymond Kobla Lawoe, Ying-Qian Liu, Rui Zhou, Yu Sun, Yin-Fang Yan, Jun-Cai Li, Guan-Zhou Yang, Cheng-Jie Yang. Anti-phytopathogenic activity and the possible mechanisms of action of isoquinoline alkaloid sanguinarine. Pesticide biochemistry and physiology. 2019 Sep; 159(?):51-58. doi: 10.1016/j.pestbp.2019.05.015. [PMID: 31400784]
  • Yuan Tian, Wei Gui, Philip B Smith, Imhoi Koo, Iain A Murray, Margherita T Cantorna, Gary H Perdew, Andrew D Patterson. Isolation and Identification of Aryl Hydrocarbon Receptor Modulators in White Button Mushrooms (Agaricus bisporus). Journal of agricultural and food chemistry. 2019 Aug; 67(33):9286-9294. doi: 10.1021/acs.jafc.9b03212. [PMID: 31339733]
  • Wei Li, Guotong Wang, Jixing Lai, Shengkun Li. Multifunctional isoquinoline-oxazoline ligands of chemical and biological importance. Chemical communications (Cambridge, England). 2019 May; 55(42):5902-5905. doi: 10.1039/c9cc01790a. [PMID: 31045188]
  • Manju Bala, Shiv Kumar, Kunal Pratap, Praveen Kumar Verma, Yogendra Padwad, Bikram Singh. Bioactive isoquinoline alkaloids from Cissampelos pareira †. Natural product research. 2019 Mar; 33(5):622-627. doi: 10.1080/14786419.2017.1402319. [PMID: 29126362]
  • Chunshun Li, Ariel M Sarotti, Xiaohua Wu, Baojun Yang, James Turkson, Yongfei Chen, Qingsong Liu, Shugeng Cao. An Unusual Benzoisoquinoline-9-one Derivative and Other Related Compounds with Antiproliferative Activity from Hawaiian Endophytic Fungus Peyronellaea sp. FT431. Molecules (Basel, Switzerland). 2019 Jan; 24(1):. doi: 10.3390/molecules24010196. [PMID: 30621059]
  • Nick Barton, Máire Convery, Anthony W J Cooper, Kenneth Down, J Nicole Hamblin, Graham Inglis, Simon Peace, James Rowedder, Paul Rowland, Jonathan A Taylor, Natalie Wellaway. Discovery of Potent, Efficient, and Selective Inhibitors of Phosphoinositide 3-Kinase δ through a Deconstruction and Regrowth Approach. Journal of medicinal chemistry. 2018 12; 61(24):11061-11073. doi: 10.1021/acs.jmedchem.8b01556. [PMID: 30532965]
  • Shaimaa Fayez, Doris Feineis, Laurent Aké Assi, Marcel Kaiser, Reto Brun, Suresh Awale, Gerhard Bringmann. Ancistrobrevines E-J and related naphthylisoquinoline alkaloids from the West African liana Ancistrocladus abbreviatus with inhibitory activities against Plasmodium falciparum and PANC-1 human pancreatic cancer cells. Fitoterapia. 2018 Nov; 131(?):245-259. doi: 10.1016/j.fitote.2018.11.006. [PMID: 30419265]
  • Séverin Muyisa Kavatsurwa, Blaise Kimbadi Lombe, Doris Feineis, Dya Fita Dibwe, Vinesh Maharaj, Suresh Awale, Gerhard Bringmann. Ancistroyafungines A-D, 5,8'- and 5,1'-coupled naphthylisoquinoline alkaloids from a Congolese Ancistrocladus species, with antiausterity activities against human PANC-1 pancreatic cancer cells. Fitoterapia. 2018 Oct; 130(?):6-16. doi: 10.1016/j.fitote.2018.07.017. [PMID: 30059720]
  • Mao-Sheng Zhang, Yan Deng, Shao-Bin Fu, Da-Le Guo, Shi-Ji Xiao. Mahimbrine A, a Novel Isoquinoline Alkaloid Bearing a Benzotropolone Moiety from Mahonia imbricata. Molecules (Basel, Switzerland). 2018 Jun; 23(7):. doi: 10.3390/molecules23071539. [PMID: 29949909]
  • Kjell A Svensson, Beverly A Heinz, John M Schaus, James P Beck, Junliang Hao, Joseph H Krushinski, Matthew R Reinhard, Michael P Cohen, Sarah L Hellman, Brian G Getman, Xushan Wang, Michelle M Menezes, Deanna L Maren, Julie F Falcone, Wesley H Anderson, Rebecca A Wright, S Michelle Morin, Kelly L Knopp, Benjamin L Adams, Borys Rogovoy, Ilya Okun, Todd M Suter, Michael A Statnick, Donald R Gehlert, David L Nelson, Virginia L Lucaites, Renee Emkey, Neil W DeLapp, Todd R Wiernicki, Jeffrey W Cramer, Charles R Yang, Robert F Bruns. An Allosteric Potentiator of the Dopamine D1 Receptor Increases Locomotor Activity in Human D1 Knock-In Mice without Causing Stereotypy or Tachyphylaxis. The Journal of pharmacology and experimental therapeutics. 2017 Jan; 360(1):117-128. doi: 10.1124/jpet.116.236372. [PMID: 27811173]
  • Li-Hong Ye, Xi-De Liu, Jun Cao, Yan-Xu Chang, Mingrui An, Shu-Ling Wang, Jing-Jing Xu, Li-Qing Peng. Analysis of isoquinoline alkaloids using chitosan-assisted liquid-solid extraction followed by microemulsion liquid chromatography employing a sub-2-micron particle stationary phase. Electrophoresis. 2016 12; 37(23-24):3118-3125. doi: 10.1002/elps.201600114. [PMID: 27699822]
  • Le Quynh Lien, Tran My Linh, Vu Huong Giang, Nguyen Chi Mai, Nguyen Xuan Nhiem, Bui Huu Tai, Nguyen Thi Cuc, Hoang Le Tuan Anh, Ninh Khac Ban, Chau Van Minh, Phan Van Kiem. New naphthalene derivatives and isoquinoline alkaloids from Ancistrocladus cochinchinensis with their anti-proliferative activity on human cancer cells. Bioorganic & medicinal chemistry letters. 2016 08; 26(16):3913-7. doi: 10.1016/j.bmcl.2016.07.014. [PMID: 27423477]
  • Joshua A Baccile, Joseph E Spraker, Henry H Le, Eileen Brandenburger, Christian Gomez, Jin Woo Bok, Juliane Macheleidt, Axel A Brakhage, Dirk Hoffmeister, Nancy P Keller, Frank C Schroeder. Plant-like biosynthesis of isoquinoline alkaloids in Aspergillus fumigatus. Nature chemical biology. 2016 06; 12(6):419-24. doi: 10.1038/nchembio.2061. [PMID: 27065235]
  • Xianbao Deng, Lingping Zhu, Ting Fang, Sornkanok Vimolmangkang, Dong Yang, Collins Ogutu, Yanling Liu, Yuepeng Han. Analysis of Isoquinoline Alkaloid Composition and Wound-Induced Variation in Nelumbo Using HPLC-MS/MS. Journal of agricultural and food chemistry. 2016 Feb; 64(5):1130-6. doi: 10.1021/acs.jafc.5b06099. [PMID: 26800445]
  • Hengjia Ni, Yordan Martínez, Guiping Guan, Román Rodríguez, Dairon Más, Hanhui Peng, Manuel Valdivié Navarro, Gang Liu. Analysis of the Impact of Isoquinoline Alkaloids, Derived from Macleaya cordata Extract, on the Development and Innate Immune Response in Swine and Poultry. BioMed research international. 2016; 2016(?):1352146. doi: 10.1155/2016/1352146. [PMID: 28042566]
  • Kaisa A Salminen, Minna Rahnasto-Rilla, Raija Väänänen, Peter Imming, Achim Meyer, Aline Horling, Antti Poso, Tuomo Laitinen, Hannu Raunio, Maija Lahtela-Kakkonen. Time-Dependent Inhibition of CYP2C19 by Isoquinoline Alkaloids: In Vitro and In Silico Analysis. Drug metabolism and disposition: the biological fate of chemicals. 2015 Dec; 43(12):1891-904. doi: 10.1124/dmd.115.065755. [PMID: 26400396]
  • Valery M Dembitsky, Tatyana A Gloriozova, Vladimir V Poroikov. Naturally occurring plant isoquinoline N-oxide alkaloids: their pharmacological and SAR activities. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2015 Jan; 22(1):183-202. doi: 10.1016/j.phymed.2014.11.002. [PMID: 25636889]
  • Tsvetelina Doncheva, Amgalan Solongo, Nadezhda Kostova, Yadamsuren Gerelt-Od, Dangaa Selenge, Stefan Philipov. Leptopyrine, new alkaloid from Leptopyrum fumarioides L. (Ranunculaceae). Natural product research. 2015; 29(9):853-6. doi: 10.1080/14786419.2014.991322. [PMID: 25529023]
  • Yali Chen, Min Li, Jianjun Liu, Qian Yan, Mei Zhong, Junxi Liu, Duolong Di, Jinxia Liu. Simultaneous determination of the content of isoquinoline alkaloids in Dicranostigma leptopodum (Maxim) Fedde and the effective fractionation of the alkaloids by high-performance liquid chromatography with diode array detection. Journal of separation science. 2015 Jan; 38(1):9-17. doi: 10.1002/jssc.201400905. [PMID: 25330407]
  • Hui-Liang Zou, Hong-Yu Li, Bai-Lian Liu, Guang-Xiong Zhou. A new cytotoxic benzophenanthridine isoquinoline alkaloid from the fruits of Macleaya cordata. Journal of Asian natural products research. 2015; 17(8):856-60. doi: 10.1080/10286020.2015.1016000. [PMID: 25761206]
  • Xuelong Yu, Xiaoli Gao, Zhixiang Zhu, Yuan Cao, Qian Zhang, Pengfei Tu, Xingyun Chai. Alkaloids from the tribe Bocconieae (papaveraceae): a chemical and biological review. Molecules (Basel, Switzerland). 2014 Aug; 19(9):13042-60. doi: 10.3390/molecules190913042. [PMID: 25157468]
  • Azeana Zahari, Foo Kit Cheah, Jamaludin Mohamad, Syazreen Nadia Sulaiman, Marc Litaudon, Kok Hoong Leong, Khalijah Awang. Antiplasmodial and antioxidant isoquinoline alkaloids from Dehaasia longipedicellata. Planta medica. 2014 May; 80(7):599-603. doi: 10.1055/s-0034-1368349. [PMID: 24723007]
  • Sayaree Dhar, Dipak Kumar Rana, Arunava Pal, Subhash Chandra Bhattacharya. Photobehavior and docking simulations of drug within macromolecules: binding of an antioxidative isoquinolindione to a serine protease and albumin proteins. Journal of photochemistry and photobiology. B, Biology. 2013 Dec; 129(?):69-77. doi: 10.1016/j.jphotobiol.2013.09.007. [PMID: 24177206]
  • Hong Zhao, H Dorota Halicka, Jiangwei Li, Zbigniew Darzynkiewicz. Berberine suppresses gero-conversion from cell cycle arrest to senescence. Aging. 2013 Aug; 5(8):623-36. doi: 10.18632/aging.100593. [PMID: 23974852]
  • Asama Mukherjee, Sushanta Dutta, Utpal Sanyal. Evaluation of antitumor efficacy and toxicity of novel 6-nitro-2-(3-chloropropyl)-1H-benz[de]isoquinoline-1,3-dione in vivo in mouse. Journal of cancer research and therapeutics. 2013 Jul; 9(3):442-6. doi: 10.4103/0973-1482.119332. [PMID: 24125980]
  • Robert Domitrović, Hrvoje Jakovac, Vanja Vasiljev Marchesi, Biljana Blažeković. Resolution of liver fibrosis by isoquinoline alkaloid berberine in CCl₄-intoxicated mice is mediated by suppression of oxidative stress and upregulation of MMP-2 expression. Journal of medicinal food. 2013 Jun; 16(6):518-28. doi: 10.1089/jmf.2012.0175. [PMID: 23734997]
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