Luteolinidin (BioDeep_00000004005)
Secondary id: BioDeep_00000270761, BioDeep_00000615541, BioDeep_00001869202
human metabolite PANOMIX_OTCML-2023 Endogenous PANOMIX-Anthocyanidin natural product
代谢物信息卡片
化学式: C15H11O5+ (271.0606)
中文名称: 木犀草定氯化物, 木犀草素
谱图信息:
最多检出来源 Viridiplantae(plant) 12.73%
分子结构信息
SMILES: C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2)O)O)O)O
InChI: InChI=1S/C15H10O5/c16-9-6-12(18)10-2-4-14(20-15(10)7-9)8-1-3-11(17)13(19)5-8/h1-7H,(H3-,16,17,18,19)/p+1
描述信息
Luteolinidin is found in corn. Luteolinidin is a chemical compound belonging to the 3-deoxyanthocyanidins and that can be found in Sorghum bicolor
Luteolinidin is a chemical compound belonging to the 3-deoxyanthocyanidins and that can be found in Sorghum bicolor.
同义名列表
数据库引用编号
18 个数据库交叉引用编号
- ChEBI: CHEBI:6584
- KEGG: C08652
- PubChem: 441701
- HMDB: HMDB0029249
- ChEMBL: CHEMBL1275834
- Wikipedia: Luteolinidin
- MetaCyc: CPD-11945
- KNApSAcK: C00006611
- foodb: FDB000078
- chemspider: 390308
- CAS: 16975-93-2
- CAS: 1154-78-5
- PubChem: 10845
- 3DMET: B02302
- NIKKAJI: J244.826B
- RefMet: Luteolinidin
- KNApSAcK: 6584
- LOTUS: LTS0102344
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
代谢反应
82 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(1)
- luteolinidin 5-O-glucoside biosynthesis:
UDP-α-D-glucose + luteolinidin ⟶ H+ + UDP + luteolinidin 5-O-glucoside
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(81)
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
2-oxoglutarate + H+ + O2 + luteoforol ⟶ CO2 + H2O + luteolinidin + succinate
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
- luteolinidin 5-O-glucoside biosynthesis:
NADP+ + luteoforol ⟶ (2S)-eriodictyol + H+ + NADPH
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
27 个相关的物种来源信息
- 15314 - Andropogon: LTS0102344
- 79826 - Bothriochloa: LTS0102344
- 106883 - Bothriochloa insculpta: 10.1038/2131033A0
- 106883 - Bothriochloa insculpta: LTS0102344
- 2759 - Eukaryota: LTS0102344
- 26122 - Gesneriaceae: LTS0102344
- 9606 - Homo sapiens: -
- 42078 - Hyparrhenia: LTS0102344
- 106890 - Hyparrhenia filipendula: 10.1038/2131033A0
- 106890 - Hyparrhenia filipendula: LTS0102344
- 42079 - Hyparrhenia hirta: 10.1038/2131033A0
- 42079 - Hyparrhenia hirta: LTS0102344
- 80368 - Imperata: LTS0102344
- 80369 - Imperata cylindrica: 10.1038/2131033A0
- 80369 - Imperata cylindrica: LTS0102344
- 4447 - Liliopsida: LTS0102344
- 3398 - Magnoliopsida: LTS0102344
- 4479 - Poaceae: LTS0102344
- 48789 - Sinningia: LTS0102344
- 189007 - Sinningia cardinalis: 10.1016/0031-9422(88)84093-7
- 189007 - Sinningia cardinalis: LTS0102344
- 35493 - Streptophyta: LTS0102344
- 66042 - Themeda: LTS0102344
- 106636 - Themeda triandra: 10.1038/2131033A0
- 106636 - Themeda triandra: LTS0102344
- 58023 - Tracheophyta: LTS0102344
- 33090 - Viridiplantae: LTS0102344
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
- Yuki Yagishita, Mai Mihara, Yoshiumi Kohno, Masashi Shibata. Photochromic Properties of 3-Deoxyanthocyanidin Pigments in Nontoxic Solvents.
Journal of food science.
2016 Dec; 81(12):E2950-E2955. doi:
10.1111/1750-3841.13548
. [PMID: 27925261] - Daniel A Abugri, William H Witola, Jesse M Jaynes, Nashar Toufic. In vitro activity of Sorghum bicolor extracts, 3-deoxyanthocyanidins, against Toxoplasma gondii.
Experimental parasitology.
2016 May; 164(?):12-9. doi:
10.1016/j.exppara.2016.02.001
. [PMID: 26855040] - Hiroshi Mizuno, Takayuki Yazawa, Shigemitsu Kasuga, Yuji Sawada, Jun Ogata, Tsuyu Ando, Hiroyuki Kanamori, Jun-ichi Yonemaru, Jianzhong Wu, Masami Yokota Hirai, Takashi Matsumoto, Hiroyuki Kawahigashi. Expression level of a flavonoid 3'-hydroxylase gene determines pathogen-induced color variation in sorghum.
BMC research notes.
2014 Oct; 7(?):761. doi:
10.1186/1756-0500-7-761
. [PMID: 25346182] - Marie-Annette Carbonneau, Moctar Cisse, Nathalie Mora-Soumille, Sofiane Dairi, Maxence Rosa, Françoise Michel, Céline Lauret, Jean-Paul Cristol, Olivier Dangles. Antioxidant properties of 3-deoxyanthocyanidins and polyphenolic extracts from Côte d'Ivoire's red and white sorghums assessed by ORAC and in vitro LDL oxidisability tests.
Food chemistry.
2014 Feb; 145(?):701-9. doi:
10.1016/j.foodchem.2013.07.025
. [PMID: 24128534] - Carloalberto Petti, Rekha Kushwaha, Mizuki Tateno, Anne Elizabeth Harman-Ware, Mark Crocker, Joseph Awika, Seth Debolt. Mutagenesis breeding for increased 3-deoxyanthocyanidin accumulation in leaves of Sorghum bicolor (L.) Moench: a source of natural food pigment.
Journal of agricultural and food chemistry.
2014 Feb; 62(6):1227-32. doi:
10.1021/jf405324j
. [PMID: 24460064] - Sanjeev Kumar, Satyendra Gautam, Arun Sharma. Identification of antimutagenic properties of anthocyanins and other polyphenols from rose (Rosa centifolia) petals and tea.
Journal of food science.
2013 Jun; 78(6):H948-54. doi:
10.1111/1750-3841.12135
. [PMID: 23627876] - Mandeep Sharma, Chenglin Chai, Kengo Morohashi, Erich Grotewold, Maurice E Snook, Surinder Chopra. Expression of flavonoid 3'-hydroxylase is controlled by P1, the regulator of 3-deoxyflavonoid biosynthesis in maize.
BMC plant biology.
2012 Nov; 12(?):196. doi:
10.1186/1471-2229-12-196
. [PMID: 23113982] - Katja Zuther, Jörg Kahnt, Jan Utermark, Julia Imkampe, Simon Uhse, Jan Schirawski. Host specificity of Sporisorium reilianum is tightly linked to generation of the phytoalexin luteolinidin by Sorghum bicolor.
Molecular plant-microbe interactions : MPMI.
2012 Sep; 25(9):1230-7. doi:
10.1094/mpmi-12-11-0314
. [PMID: 22670753] - A P Polycarpe Kayodé, M J Rob Nout, Anita R Linnemann, Joseph D Hounhouigan, Emmerich Berghofer, Susanne Siebenhandl-Ehn. Uncommonly high levels of 3-deoxyanthocyanidins and antioxidant capacity in the leaf sheaths of dye sorghum.
Journal of agricultural and food chemistry.
2011 Feb; 59(4):1178-84. doi:
10.1021/jf103963t
. [PMID: 21322653] - Yegang Du, Hung Chu, Mingfu Wang, Ivan K Chu, Clive Lo. Identification of flavone phytoalexins and a pathogen-inducible flavone synthase II gene (SbFNSII) in sorghum.
Journal of experimental botany.
2010 Feb; 61(4):983-94. doi:
10.1093/jxb/erp364
. [PMID: 20007684] - Michael F Cohen, Yasuko Sakihama, Yojiro C Takagi, Toshio Ichiba, Hideo Yamasaki. Synergistic effect of deoxyanthocyanins from symbiotic fern Azolla spp. on hrmA gene induction in the cyanobacterium Nostoc punctiforme.
Molecular plant-microbe interactions : MPMI.
2002 Sep; 15(9):875-82. doi:
10.1094/mpmi.2002.15.9.875
. [PMID: 12236594] - E E Swinny. A novel acetylated 3-deoxyanthocyanidin laminaribioside from the fern Blechnum novae-zelandiae.
Zeitschrift fur Naturforschung. C, Journal of biosciences.
2001 Mar; 56(3-4):177-80. doi:
10.1515/znc-2001-3-402
. [PMID: 11371005]