3,3,4,5,5,7-Hexahydroxyflavylium (BioDeep_00001868620)

Main id: BioDeep_00000003579

 


代谢物信息卡片


3,3,4,5,5,7-Hexahydroxyflavylium

化学式: C15H11O7+ (303.0505)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O
InChI: InChI=1S/C15H10O7/c16-7-3-9(17)8-5-12(20)15(22-13(8)4-7)6-1-10(18)14(21)11(19)2-6/h1-5H,(H5-,16,17,18,19,20,21)/p+1

描述信息

同义名列表

2 个代谢物同义名

3,3,4,5,5,7-Hexahydroxyflavylium; Delphinidin



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(1)

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)

66 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 16 AKT1, ANG, BCL2, CASP3, CAT, CCND1, EGFR, ERBB2, MAPK14, MAPK8, MAPK9, MTOR, PIK3CA, PTGS2, RELA, VEGFA
Peripheral membrane protein 2 MTOR, PTGS2
Endosome membrane 2 EGFR, ERBB2
Endoplasmic reticulum membrane 5 BCL2, EGFR, HMOX1, MTOR, PTGS2
Nucleus 15 AKT1, ANG, BCL2, CASP3, CCND1, EGFR, ERBB2, HMOX1, JUND, MAPK14, MAPK8, MAPK9, MTOR, RELA, VEGFA
cytosol 14 AKT1, ANG, BCL2, CASP3, CAT, CCND1, ERBB2, HMOX1, MAPK14, MAPK8, MAPK9, MTOR, PIK3CA, RELA
dendrite 1 MTOR
phagocytic vesicle 1 MTOR
centrosome 1 CCND1
nucleoplasm 11 AKT1, CASP3, CCND1, ERBB2, HMOX1, JUND, MAPK14, MAPK8, MAPK9, MTOR, RELA
RNA polymerase II transcription regulator complex 1 JUND
Cell membrane 4 AKT1, EGFR, ERBB2, TNF
Cytoplasmic side 2 HMOX1, MTOR
lamellipodium 2 AKT1, PIK3CA
ruffle membrane 2 EGFR, ERBB2
Early endosome membrane 1 EGFR
Golgi apparatus membrane 1 MTOR
Synapse 1 MAPK8
cell cortex 1 AKT1
cell junction 1 EGFR
cell surface 3 EGFR, TNF, VEGFA
glutamatergic synapse 5 AKT1, CASP3, EGFR, MAPK14, RELA
Golgi apparatus 1 VEGFA
Golgi membrane 3 EGFR, INS, MTOR
growth cone 1 ANG
lysosomal membrane 1 MTOR
neuromuscular junction 1 ERBB2
neuronal cell body 3 ANG, CASP3, TNF
postsynapse 1 AKT1
presynaptic membrane 1 ERBB2
Lysosome 1 MTOR
endosome 1 EGFR
plasma membrane 6 AKT1, EGFR, ERBB2, MAPK9, PIK3CA, TNF
Membrane 8 AKT1, BCL2, CAT, EGFR, ERBB2, HMOX1, MTOR, VEGFA
apical plasma membrane 2 EGFR, ERBB2
axon 1 MAPK8
basolateral plasma membrane 2 EGFR, ERBB2
caveola 1 PTGS2
extracellular exosome 1 CAT
Lysosome membrane 1 MTOR
endoplasmic reticulum 4 BCL2, HMOX1, PTGS2, VEGFA
extracellular space 6 ANG, EGFR, HMOX1, INS, TNF, VEGFA
perinuclear region of cytoplasm 4 EGFR, ERBB2, HMOX1, PIK3CA
Schaffer collateral - CA1 synapse 1 MAPK9
adherens junction 1 VEGFA
bicellular tight junction 1 CCND1
intercalated disc 1 PIK3CA
mitochondrion 4 BCL2, CAT, MAPK14, MAPK9
protein-containing complex 5 AKT1, BCL2, CAT, EGFR, PTGS2
intracellular membrane-bounded organelle 1 CAT
Microsome membrane 2 MTOR, PTGS2
postsynaptic density 1 CASP3
TORC1 complex 1 MTOR
TORC2 complex 1 MTOR
Single-pass type I membrane protein 2 EGFR, ERBB2
Secreted 3 ANG, INS, VEGFA
extracellular region 7 ANG, CAT, ERBB2, INS, MAPK14, TNF, VEGFA
Mitochondrion outer membrane 2 BCL2, MTOR
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 3 BCL2, HMOX1, MTOR
mitochondrial matrix 1 CAT
transcription regulator complex 2 JUND, RELA
Nucleus membrane 2 BCL2, CCND1
Bcl-2 family protein complex 1 BCL2
nuclear membrane 3 BCL2, CCND1, EGFR
external side of plasma membrane 1 TNF
Secreted, extracellular space, extracellular matrix 1 VEGFA
actin cytoskeleton 1 ANG
cytoplasmic vesicle 1 ERBB2
microtubule cytoskeleton 1 AKT1
nucleolus 1 ANG
Early endosome 1 ERBB2
cell-cell junction 1 AKT1
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
vesicle 1 AKT1
Cell projection, ruffle membrane 1 ERBB2
Cytoplasm, perinuclear region 1 ERBB2
Membrane raft 2 EGFR, TNF
pore complex 1 BCL2
focal adhesion 2 CAT, EGFR
spindle 1 AKT1
extracellular matrix 1 VEGFA
Peroxisome 1 CAT
basement membrane 1 ANG
intracellular vesicle 1 EGFR
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
Nucleus, PML body 1 MTOR
PML body 1 MTOR
Mitochondrion intermembrane space 1 AKT1
mitochondrial intermembrane space 1 AKT1
secretory granule 1 VEGFA
nuclear speck 2 MAPK14, MAPK9
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
receptor complex 2 EGFR, ERBB2
neuron projection 1 PTGS2
ciliary basal body 1 AKT1
chromatin 2 JUND, RELA
phagocytic cup 1 TNF
Chromosome 1 ANG
Nucleus, nucleolus 1 ANG
spindle pole 1 MAPK14
nuclear envelope 1 MTOR
Endomembrane system 1 MTOR
endosome lumen 1 INS
Cytoplasm, Stress granule 1 ANG
cytoplasmic stress granule 1 ANG
myelin sheath 2 BCL2, ERBB2
basal plasma membrane 2 EGFR, ERBB2
synaptic membrane 1 EGFR
ficolin-1-rich granule lumen 2 CAT, MAPK14
secretory granule lumen 3 CAT, INS, MAPK14
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 INS, PTGS2
transcription repressor complex 2 CCND1, JUND
platelet alpha granule lumen 1 VEGFA
phosphatidylinositol 3-kinase complex 1 PIK3CA
phosphatidylinositol 3-kinase complex, class IA 1 PIK3CA
endocytic vesicle 1 ANG
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
Single-pass type IV membrane protein 1 HMOX1
semaphorin receptor complex 1 ERBB2
clathrin-coated endocytic vesicle membrane 1 EGFR
basal dendrite 1 MAPK8
death-inducing signaling complex 1 CASP3
[Isoform 1]: Cell membrane 1 ERBB2
Cytoplasmic vesicle, phagosome 1 MTOR
cyclin-dependent protein kinase holoenzyme complex 1 CCND1
multivesicular body, internal vesicle lumen 1 EGFR
Shc-EGFR complex 1 EGFR
transcription factor AP-1 complex 1 JUND
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
angiogenin-PRI complex 1 ANG
catalase complex 1 CAT
ERBB3:ERBB2 complex 1 ERBB2
BAD-BCL-2 complex 1 BCL2
cyclin D1-CDK4 complex 1 CCND1
[N-VEGF]: Cytoplasm 1 VEGFA
[VEGFA]: Secreted 1 VEGFA
[Isoform L-VEGF189]: Endoplasmic reticulum 1 VEGFA
[Isoform VEGF121]: Secreted 1 VEGFA
[Isoform VEGF165]: Secreted 1 VEGFA
VEGF-A complex 1 VEGFA
NF-kappaB p50/p65 complex 1 RELA
NF-kappaB complex 1 RELA
cyclin D1-CDK6 complex 1 CCND1
phosphatidylinositol 3-kinase complex, class IB 1 PIK3CA
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Sergio R Zúñiga-Hernández, Trinidad García-Iglesias, Monserrat Macías-Carballo, Alejandro Pérez-Larios, Yanet Karina Gutiérrez-Mercado, Gabriela Camargo-Hernández, Christian Martin Rodríguez-Razón. Targets and Effects of Common Biocompounds of Hibiscus sabdariffa (Delphinidin-3-Sambubiosid, Quercetin, and Hibiscus Acid) in Different Pathways of Human Cells According to a Bioinformatic Assay. Nutrients. 2024 Feb; 16(4):. doi: 10.3390/nu16040566. [PMID: 38398890]
  • Juliana Gimenez Casagrande, Marcelo Macedo Rogero, Dalila Cunha de Oliveira, Bruna J Quintanilha, Vinícius Cooper Capetini, Edson Naoto Makiyama, Bruna Roberta Oliveira Neves, Carlos Eduardo da Silva Gonçalves, Sumara de Freitas, Neuza Mariko Aymoto Hassimotto, Ricardo Ambrósio Fock. Effects of grape juice intake on the cell migration properties in overweight women: Modulation mechanisms of cell migration in vitro by delphinidin-3-O-glucoside. Food research international (Ottawa, Ont.). 2024 Feb; 178(?):113873. doi: 10.1016/j.foodres.2023.113873. [PMID: 38309895]
  • Naymul Karim, Shiyu Liu, Ahmed K Rashwan, Jiahong Xie, Jianling Mo, Ahmed I Osman, David W Rooney, Wei Chen. Green synthesis of nanolipo-fibersomes using Nutriose® FB 06 for delphinidin-3-O-sambubioside delivery: Characterization, physicochemical properties, and application. International journal of biological macromolecules. 2023 Aug; 247(?):125839. doi: 10.1016/j.ijbiomac.2023.125839. [PMID: 37454997]
  • Dario E Iglesias, Eleonora Cremonini, Shelly N Hester, Steven M Wood, Mark Bartlett, Cesar G Fraga, Patricia I Oteiza. Cyanidin and delphinidin restore colon physiology in high fat diet-fed mice: Involvement of TLR-4 and redox-regulated signaling. Free radical biology & medicine. 2022 08; 188(?):71-82. doi: 10.1016/j.freeradbiomed.2022.06.006. [PMID: 35691508]
  • Edward Valera-Vera, Chantal Reigada, Melisa Sayé, Fabio A Digirolamo, Facundo Galceran, Mariana R Miranda, Claudio A Pereira. Trypanocidal activity of the anthocyanidin delphinidin, a non-competitive inhibitor of arginine kinase. Natural product research. 2022 Jun; 36(12):3153-3157. doi: 10.1080/14786419.2021.1947270. [PMID: 34219561]
  • John Bradley Morris, Brandon D Tonnis, Ming Li Wang, Uttam Bhattarai. Genetic Diversity for Quercetin, Myricetin, Cyanidin, and Delphinidin Concentrations in 38 Blackeye Pea (Vigna unguiculata L. Walp.) Genotypes for Potential Use as a Functional Health Vegetable. Journal of dietary supplements. 2022 May; ?(?):1-16. doi: 10.1080/19390211.2022.2077881. [PMID: 35615864]
  • Eleonora Cremonini, Dario E Iglesias, Karen E Matsukuma, Shelly N Hester, Steven M Wood, Mark Bartlett, Cesar G Fraga, Patricia I Oteiza. Supplementation with cyanidin and delphinidin mitigates high fat diet-induced endotoxemia and associated liver inflammation in mice. Food & function. 2022 Jan; 13(2):781-794. doi: 10.1039/d1fo03108b. [PMID: 34981106]
  • Zhiyong Zhang, Yan Pan, Yan Zhao, Mudan Ren, Yarui Li, Guifang Lu, Kaichun Wu, Shuixiang He. Delphinidin modulates JAK/STAT3 and MAPKinase signaling to induce apoptosis in HCT116 cells. Environmental toxicology. 2021 Aug; 36(8):1557-1566. doi: 10.1002/tox.23152. [PMID: 33955636]
  • Nguyen Minh Thuy, Vo Quang Minh, Tran Chi Ben, My Tuyen Thi Nguyen, Ho Thi Ngan Ha, Ngo Van Tai. Identification of Anthocyanin Compounds in Butterfly Pea Flowers (Clitoria ternatea L.) by Ultra Performance Liquid Chromatography/Ultraviolet Coupled to Mass Spectrometry. Molecules (Basel, Switzerland). 2021 Jul; 26(15):. doi: 10.3390/molecules26154539. [PMID: 34361692]
  • Reine-Solange Sauer, Ivo Krummenacher, Ezgi Eylül Bankoglu, Shaobing Yang, Beatrice Oehler, Friedrich Schöppler, Milad Mohammadi, Paul Güntzel, Adel Ben-Kraiem, Ulrike Holzgrabe, Helga Stopper, Jens A Broscheit, Holger Braunschweig, Norbert Roewer, Alexander Brack, Heike L Rittner. Stabilization of Delphinidin in Complex with Sulfobutylether-β-Cyclodextrin Allows for Antinociception in Inflammatory Pain. Antioxidants & redox signaling. 2021 06; 34(16):1260-1279. doi: 10.1089/ars.2019.7957. [PMID: 32977733]
  • Qunfeng Zhang, Jianhui Hu, Meiya Liu, Yuanzhi Shi, Ric C H De Vos, Jianyun Ruan. Stimulated biosynthesis of delphinidin-related anthocyanins in tea shoots reducing the quality of green tea in summer. Journal of the science of food and agriculture. 2020 Mar; 100(4):1505-1514. doi: 10.1002/jsfa.10158. [PMID: 31756273]
  • Abu Hazafa, Khalil-Ur- Rehman, Nazish Jahan, Zara Jabeen. The Role of Polyphenol (Flavonoids) Compounds in the Treatment of Cancer Cells. Nutrition and cancer. 2020; 72(3):386-397. doi: 10.1080/01635581.2019.1637006. [PMID: 31287738]
  • Candice Mazewski, Morgan Sanha Kim, Elvira Gonzalez de Mejia. Anthocyanins, delphinidin-3-O-glucoside and cyanidin-3-O-glucoside, inhibit immune checkpoints in human colorectal cancer cells in vitro and in silico. Scientific reports. 2019 08; 9(1):11560. doi: 10.1038/s41598-019-47903-0. [PMID: 31399602]
  • Ana Solopova, Amanda Y van Tilburg, Alexandre Foito, J William Allwood, Derek Stewart, Saulius Kulakauskas, Oscar P Kuipers. Engineering Lactococcus lactis for the production of unusual anthocyanins using tea as substrate. Metabolic engineering. 2019 07; 54(?):160-169. doi: 10.1016/j.ymben.2019.04.002. [PMID: 30978503]
  • Hadzic Maida, Haveric Sanin, Haveric Anja, Lojo-Kadric Naida, Galic Borivoj, Jasmin Ramic, Pojskic Lejla. Bioflavonoids protect cells against halogenated boroxine-induced genotoxic damage by upregulation of hTERT expression. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2019 May; 74(5-6):125-129. doi: 10.1515/znc-2018-0132. [PMID: 30864408]
  • Ye Tian, Oskar Laaksonen, Heta Haikonen, Anita Vanag, Huma Ejaz, Kaisa Linderborg, Saila Karhu, Baoru Yang. Compositional Diversity among Blackcurrant ( Ribes nigrum) Cultivars Originating from European Countries. Journal of agricultural and food chemistry. 2019 May; 67(19):5621-5633. doi: 10.1021/acs.jafc.9b00033. [PMID: 31013088]
  • Yanfang Liu, Jianhua Zhang, Xiaohong Yang, Jiangmin Wang, Yangang Li, Peng Zhang, Jin Mao, Qingmei Huang, Hao Tang. Diversity in flower colorations of Ranunculus asiaticus L. revealed by anthocyanin biosynthesis pathway in view of gene composition, gene expression patterns, and color phenotype. Environmental science and pollution research international. 2019 May; 26(14):13785-13794. doi: 10.1007/s11356-018-2779-3. [PMID: 30145754]
  • Liga Saulite, Kaspars Jekabsons, Maris Klavins, Ruta Muceniece, Una Riekstina. Effects of malvidin, cyanidin and delphinidin on human adipose mesenchymal stem cell differentiation into adipocytes, chondrocytes and osteocytes. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2019 Feb; 53(?):86-95. doi: 10.1016/j.phymed.2018.09.029. [PMID: 30668416]
  • Megan Stevens, Christopher R Neal, Elena C Craciun, Maria Dronca, Steven J Harper, Sebastian Oltean. The natural drug DIAVIT is protective in a type II mouse model of diabetic nephropathy. PloS one. 2019; 14(3):e0212910. doi: 10.1371/journal.pone.0212910. [PMID: 30865689]
  • Christiane Schön, Roland Wacker, Antje Micka, Jasmin Steudle, Stefanie Lang, Bernd Bonnländer. Bioavailability Study of Maqui Berry Extract in Healthy Subjects. Nutrients. 2018 Nov; 10(11):. doi: 10.3390/nu10111720. [PMID: 30423989]
  • Ezgi Eyluel Bankoglu, Jens Broscheit, Theresa Arnaudov, Norbert Roewer, Helga Stopper. Protective effects of tricetinidin against oxidative stress inducers in rat kidney cells: A comparison with delphinidin and standard antioxidants. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2018 Nov; 121(?):549-557. doi: 10.1016/j.fct.2018.09.058. [PMID: 30266311]
  • Eliza Łata, Agnieszka Fulczyk, Teresa Kowalska, Mieczysław Sajewicz. Vulnerability of anthocyanins to the components of a thin-layer chromatographic system and comprehensive screening of anthocyanes in alimentary products. Journal of chromatography. A. 2018 Oct; 1572(?):137-144. doi: 10.1016/j.chroma.2018.08.040. [PMID: 30150119]
  • Elena Daveri, Eleonora Cremonini, Angela Mastaloudis, Shelly N Hester, Steven M Wood, Andrew L Waterhouse, Mauri Anderson, Cesar G Fraga, Patricia I Oteiza. Cyanidin and delphinidin modulate inflammation and altered redox signaling improving insulin resistance in high fat-fed mice. Redox biology. 2018 09; 18(?):16-24. doi: 10.1016/j.redox.2018.05.012. [PMID: 29890336]
  • Marcela Parra-Vargas, Ana Sandoval-Rodriguez, Roberto Rodriguez-Echevarria, Jose Alfredo Dominguez-Rosales, Arturo Santos-Garcia, Juan Armendariz-Borunda. Delphinidin Ameliorates Hepatic Triglyceride Accumulation in Human HepG2 Cells, but Not in Diet-Induced Obese Mice. Nutrients. 2018 Aug; 10(8):. doi: 10.3390/nu10081060. [PMID: 30103390]
  • Qianyu Yue, Lili Xu, Guangqing Xiang, Xin Yu, Yuxin Yao. Characterization of Gene Expression Profile, Phenolic Composition, and Antioxidant Capacity in Red-Fleshed Grape Berries and Their Wines. Journal of agricultural and food chemistry. 2018 Jul; 66(27):7190-7199. doi: 10.1021/acs.jafc.8b01323. [PMID: 29920074]
  • Rocio González-Barrio, María Jesús Periago, Cristina Luna-Recio, Francisco Javier Garcia-Alonso, Inmaculada Navarro-González. Chemical composition of the edible flowers, pansy (Viola wittrockiana) and snapdragon (Antirrhinum majus) as new sources of bioactive compounds. Food chemistry. 2018 Jun; 252(?):373-380. doi: 10.1016/j.foodchem.2018.01.102. [PMID: 29478556]
  • Wenji Xu, Gangjun Luo, Fengyang Yu, Qingxiang Jia, Yang Zheng, Xiaoying Bi, Jiajun Lei. Characterization of anthocyanins in the hybrid progenies derived from Iris dichotoma and I. domestica by HPLC-DAD-ESI/MS analysis. Phytochemistry. 2018 Jun; 150(?):60-74. doi: 10.1016/j.phytochem.2018.03.003. [PMID: 29550699]
  • Pavel A Zykin, Elena A Andreeva, Anna N Lykholay, Natalia V Tsvetkova, Anatoly V Voylokov. Anthocyanin Composition and Content in Rye Plants with Different Grain Color. Molecules (Basel, Switzerland). 2018 Apr; 23(4):. doi: 10.3390/molecules23040948. [PMID: 29671758]
  • Hee Duk Oh, Duk Jun Yu, Sun Woo Chung, Sinath Chea, Hee Jae Lee. Abscisic acid stimulates anthocyanin accumulation in 'Jersey' highbush blueberry fruits during ripening. Food chemistry. 2018 Apr; 244(?):403-407. doi: 10.1016/j.foodchem.2017.10.051. [PMID: 29120800]
  • Wei-Ming Chai, Qian Huang, Mei-Zhen Lin, Chong Ou-Yang, Wen-Yang Huang, Ying-Xia Wang, Kai-Li Xu, Hui-Ling Feng. Condensed Tannins from Longan Bark as Inhibitor of Tyrosinase: Structure, Activity, and Mechanism. Journal of agricultural and food chemistry. 2018 Jan; 66(4):908-917. doi: 10.1021/acs.jafc.7b05481. [PMID: 29313327]
  • H Du, L Lai, F Wang, W Sun, L Zhang, X Li, L Wang, L Jiang, Y Zheng. Characterisation of flower colouration in 30 Rhododendron species via anthocyanin and flavonol identification and quantitative traits. Plant biology (Stuttgart, Germany). 2018 Jan; 20(1):121-129. doi: 10.1111/plb.12649. [PMID: 29054107]
  • Swathi Putta, Nagendra Sastry Yarla, Eswar Kumar K, Dhananjaya Bhadrapura Lakkappa, Mohammad A Kamal, Luciana Scotti, Marcus T Scotti, Ghulam Md Ashraf, B Sasi Bhusana Rao, Sarala Kumari D, Gorla V Reddy, Vadim V Tarasov, Sarat Babu Imandi, Gjumrakch Aliev. Preventive and Therapeutic Potentials of Anthocyanins in Diabetes and Associated Complications. Current medicinal chemistry. 2018; 25(39):5347-5371. doi: 10.2174/0929867325666171206101945. [PMID: 29210634]
  • Stefano Catola, Antonella Castagna, Marco Santin, Valentina Calvenzani, Katia Petroni, Andrea Mazzucato, Annamaria Ranieri. The dominant allele Aft induces a shift from flavonol to anthocyanin production in response to UV-B radiation in tomato fruit. Planta. 2017 Aug; 246(2):263-275. doi: 10.1007/s00425-017-2710-z. [PMID: 28516293]
  • Boris Pejin, Ana Ciric, Jasmina Dimitric Markovic, Jasmina Glamoclija, Milos Nikolic, Marina Sokovic. An insight into anti-biofilm and anti-quorum sensing activities of the selected anthocyanidins: the case study of Pseudomonas aeruginosa PAO1. Natural product research. 2017 May; 31(10):1177-1180. doi: 10.1080/14786419.2016.1222386. [PMID: 27539815]
  • Yongbin Zhuang, Erin A Tripp. Genome-scale transcriptional study of hybrid effects and regulatory divergence in an F1 hybrid Ruellia (Wild Petunias: Acanthaceae) and its parents. BMC plant biology. 2017 01; 17(1):15. doi: 10.1186/s12870-016-0962-6. [PMID: 28095782]
  • Jean Christopher Chamcheu, Vaqar M Adhami, Stephane Esnault, Mario Sechi, Imtiaz A Siddiqui, Kenneth A Satyshur, Deeba N Syed, Shah-Jahan M Dodwad, Maria-Ines Chaves-Rodriquez, B Jack Longley, Gary S Wood, Hasan Mukhtar. Dual Inhibition of PI3K/Akt and mTOR by the Dietary Antioxidant, Delphinidin, Ameliorates Psoriatic Features In Vitro and in an Imiquimod-Induced Psoriasis-Like Disease in Mice. Antioxidants & redox signaling. 2017 01; 26(2):49-69. doi: 10.1089/ars.2016.6769. [PMID: 27393705]
  • Milica M Pantelić, Dragana Č Dabić Zagorac, Sonja M Davidović, Slavica R Todić, Zoran S Bešlić, Uroš M Gašić, Živoslav Lj Tešić, Maja M Natić. Identification and quantification of phenolic compounds in berry skin, pulp, and seeds in 13 grapevine varieties grown in Serbia. Food chemistry. 2016 Nov; 211(?):243-52. doi: 10.1016/j.foodchem.2016.05.051. [PMID: 27283628]
  • Mi-Hyeon Jeong, Hyeonseok Ko, Hyelin Jeon, Gi-Jun Sung, Soo-Yeon Park, Woo Jin Jun, Yoo-Hyun Lee, Jeongmin Lee, Sang-Wook Lee, Ho-Geun Yoon, Kyung-Chul Choi. Delphinidin induces apoptosis via cleaved HDAC3-mediated p53 acetylation and oligomerization in prostate cancer cells. Oncotarget. 2016 Aug; 7(35):56767-56780. doi: 10.18632/oncotarget.10790. [PMID: 27462923]
  • G Aichinger, G Pahlke, L J Nagel, W Berger, D Marko. Bilberry extract, its major polyphenolic compounds, and the soy isoflavone genistein antagonize the cytostatic drug erlotinib in human epithelial cells. Food & function. 2016 Aug; 7(8):3628-36. doi: 10.1039/c6fo00570e. [PMID: 27485636]
  • Motoki Murata, Reia Kosaka, Kana Kurihara, Shuya Yamashita, Hirofumi Tachibana. Delphinidin prevents disuse muscle atrophy and reduces stress-related gene expression. Bioscience, biotechnology, and biochemistry. 2016 Aug; 80(8):1636-40. doi: 10.1080/09168451.2016.1184560. [PMID: 27180787]
  • Baolu Cui, Zongli Hu, Yanjie Zhang, Jingtao Hu, Wencheng Yin, Ye Feng, Qiaoli Xie, Guoping Chen. Anthocyanins and flavonols are responsible for purple color of Lablab purpureus (L.) sweet pods. Plant physiology and biochemistry : PPB. 2016 Jun; 103(?):183-90. doi: 10.1016/j.plaphy.2016.03.011. [PMID: 26995313]
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