L-BOAA (BioDeep_00001867474)

Main id: BioDeep_00000000206

 

PANOMIX_OTCML-2023


代谢物信息卡片


N-Oxalyl-L-alpha-beta-diaminopropionic acid (BOAA,ODAP)

化学式: C5H8N2O5 (176.0433)
中文名称: 三七素
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C(C(C(=O)O)N)NC(=O)C(=O)O
InChI: InChI=1S/C5H8N2O5/c6-2(4(9)10)1-7-3(8)5(11)12/h2H,1,6H2,(H,7,8)(H,9,10)(H,11,12)/t2-/m0/s1

描述信息

N(3)-oxalyl-L-2,3-diaminopropionic acid is an N(beta)-acyl-L-2,3-diaminopropionic acid in which the acyl group is oxalyl. It is functionally related to a propionic acid. It is a conjugate acid of a N(3)-(carboxylatoformyl)-L-2,3-diaminopropionate(1-).
Dencichin is a natural product found in Lathyrus latifolius and Lathyrus sativus with data available.
See also: Panax notoginseng root (part of).
Dencichin is a non-protein amino acid originally extracted from Panax notoginseng, and can inhibit HIF-prolyl hydroxylase-2 (PHD-2) activity.

同义名列表

58 个代谢物同义名

N-Oxalyl-L-alpha-beta-diaminopropionic acid (BOAA,ODAP); (2S)-2-amino-3-[(carboxycarbonyl)amino]propanoic acid; (2S)-2-amino-3-((carboxycarbonyl)amino)propanoic acid; beta-N-oxalyl-l-alpha,beta-diaminopropanoic acid; (S)-beta-Oxalyl-alpha,beta-diaminopropionic acid; beta-N-Oxalyl-L-alpha,beta-diaminopropionic acid; beta-N-Oxalo-L-alpha,beta-diaminopropionic acid; (2S)-2-amino-3-(carboxyformamido)propanoic acid; beta-N-Oxalo-L-alpha,eta-diaminopropionic acid; (S)-2-Amino-3-(carboxyformamido)propanoic acid; beta-N-Oxalyl-L-alpha,beta-diaminopropionate; L-alpha-Amino-beta-oxalylaminopropionic acid; oxalyldiaminopropionic acid, (L-Ala)-isomer; OXAMIC ACID, (2-AMINO-2-CARBOXYETHYL)-, L-; (2S)-2-amino-3-(oxaloamino)propanoic acid; N(3)-oxalyl-L-2,3-diaminopropionic acid; (2-amino-2-carboxymethyl)-L-oxamic acid; (2-Amino-2-carboxyethyl)-L-oxamic acid; 3-N-Oxalyl-L-2,3-diaminopropanoic acid; L-Alanine, 3-((carboxycarbonyl)amino)-; 3-N-Oxalyl-L-2,3-diaminopropionic acid; 3-amino-N-(carboxycarbonyl)-DL-alanine; 3-((CARBOXYCARBONYL)AMINO)ALANINE, L-; 3-N-OXALYL-L-2,3-DIAMINOPROPANOICACID; beta-N-oxalylaminoalanine, (L)-isomer; L-3-Oxalylamino-2-aminopropionic acid; 3-[(Carboxycarbonyl)amino]-L-alanine; 3-((Carboxycarbonyl)amino)-L-alanine; 3-oxalylamino-2-aminopropionic acid; 2-oxalylamino-3-aminopropionic acid; 3-amino-N-(carboxycarbonyl)alanine; 3-(Carboxycarbonylamino)-L-alanine; N3-Oxalyl-L-2,3-diaminopropanoate; 3-[(carboxycarbonyl)amino]alanine; Neurotoxin (Lathyrus sativus); N.BETA.-OXALYLAMINO-L-ALANINE; carboxycarbonyl-aminoalanine; beta-N-oxalylamino-L-alanine; oxalyldiaminopropionic acid; Nbeta-Oxalylamino-L-alanine; beta-N-oxalylaminoalanine; beta-ODAP, >=98\\% (HPLC); 3-(Oxaloamino)alanine; lathyrus neurotoxin; oxalylaminoalanine; UNII-O8VT5BZ48B; dencichin, DL-; L-Dencichin; | cent-odap; O8VT5BZ48B; dencichine; beta-ODAP; Dencichin; Ox-Dapro; L-BOAA; ODAP; BOAA; 3-(Carboxycarbonylamino)-L-alanine



数据库引用编号

15 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)

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 10 AXIN2, CA1, CASP3, CAT, FOLH1, GLUL, HIF1A, NFATC1, SMAD7, VEGFA
Peripheral membrane protein 1 AOC1
Endoplasmic reticulum membrane 1 SLC7A11
Nucleus 9 AXIN2, CASP3, FOS, GLRX, GLUL, HIF1A, NFATC1, SMAD7, VEGFA
autophagosome 1 MAP1LC3A
cytosol 13 AXIN2, CA1, CASP3, CAT, FOS, GLRX, GLUL, GSR, HIF1A, MAP1LC3A, NFATC1, PRKCQ, SMAD7
nuclear body 2 HIF1A, NFATC1
centrosome 2 AXIN2, SMAD7
nucleoplasm 6 CASP3, CD2, FOS, HIF1A, NFATC1, SMAD7
RNA polymerase II transcription regulator complex 2 FOS, HIF1A
Cell membrane 6 AOC1, CD2, FOLH1, GLUL, GRID1, SLC7A11
Lipid-anchor 2 GLUL, MAP1LC3A
Multi-pass membrane protein 2 GRID1, SLC7A11
cell surface 4 CD2, FOLH1, SLC7A11, VEGFA
glutamatergic synapse 3 CASP3, GRID1, MAP1LC3A
Golgi apparatus 2 CD2, VEGFA
neuronal cell body 1 CASP3
Cytoplasm, cytosol 1 GLUL
plasma membrane 9 AOC1, AXIN2, CD2, FOLH1, GLUL, GRID1, PRKCQ, SLC7A11, SMAD7
Membrane 4 CAT, FOLH1, SLC7A11, VEGFA
basolateral plasma membrane 1 SLC7A11
extracellular exosome 8 AOC1, CA1, CAT, FOLH1, GLRX, GLUL, GRID1, GSR
endoplasmic reticulum 3 FOS, GLUL, VEGFA
extracellular space 2 AOC1, VEGFA
perinuclear region of cytoplasm 1 NFATC1
adherens junction 1 VEGFA
bicellular tight junction 1 AOC1
mitochondrion 3 CAT, GLUL, GSR
protein-containing complex 4 CAT, CD2, HIF1A, SMAD7
intracellular membrane-bounded organelle 2 CAT, MAP1LC3A
postsynaptic density 1 CASP3
Single-pass type I membrane protein 2 CD2, SLC7A11
Secreted 1 VEGFA
extracellular region 4 AOC1, CAT, CD2, VEGFA
cytoplasmic side of plasma membrane 1 CD2
mitochondrial matrix 2 CAT, GSR
Extracellular side 1 AOC1
transcription regulator complex 1 NFATC1
centriolar satellite 1 PRKCQ
motile cilium 1 HIF1A
external side of plasma membrane 2 CD2, GSR
Secreted, extracellular space, extracellular matrix 1 VEGFA
beta-catenin destruction complex 1 AXIN2
axon cytoplasm 1 HIF1A
sarcoplasm 1 NFATC1
apical part of cell 1 SLC7A11
cell-cell junction 1 CD2
Single-pass type II membrane protein 1 FOLH1
postsynaptic membrane 1 GRID1
Cytoplasm, cytoskeleton 1 MAP1LC3A
focal adhesion 1 CAT
microtubule 1 MAP1LC3A
GABA-ergic synapse 1 GRID1
extracellular matrix 1 VEGFA
Peroxisome 2 AOC1, CAT
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
secretory granule 1 VEGFA
lateral plasma membrane 1 SLC7A11
nuclear speck 1 HIF1A
Postsynaptic cell membrane 1 GRID1
Late endosome 1 MAP1LC3A
chromatin 4 FOS, HIF1A, NFATC1, SMAD7
Cytoplasmic vesicle, autophagosome membrane 1 MAP1LC3A
autophagosome membrane 1 MAP1LC3A
Secreted, extracellular space 1 AOC1
brush border membrane 1 SLC7A11
Basolateral cell membrane 1 SLC7A11
Cell projection, microvillus membrane 1 SLC7A11
microvillus membrane 1 SLC7A11
organelle membrane 1 MAP1LC3A
fibrillar center 1 SMAD7
Endomembrane system 1 MAP1LC3A
Nucleus speckle 1 HIF1A
euchromatin 1 HIF1A
cell body 1 GLUL
Microsome 1 GLUL
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 1 CAT
nuclear matrix 1 FOS
platelet alpha granule lumen 1 VEGFA
specific granule lumen 1 AOC1
postsynaptic density membrane 1 GRID1
immunological synapse 1 PRKCQ
aggresome 1 PRKCQ
heteromeric SMAD protein complex 1 SMAD7
protein-DNA complex 1 FOS
death-inducing signaling complex 1 CASP3
astrocyte projection 1 SLC7A11
glial cell projection 1 GLUL
transcription factor AP-1 complex 1 FOS
Autolysosome 1 MAP1LC3A
catalase complex 1 CAT
[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
[Isoform PSMA']: Cytoplasm 1 FOLH1


文献列表

  • Dan Huang, Xin Wang, Wei-Bing Liu, Bang-Ce Ye. Remodeling metabolism of Corynebacterium glutamicum for high-level dencichine production. Bioresource technology. 2023 Nov; 388(?):129800. doi: 10.1016/j.biortech.2023.129800. [PMID: 37748563]
  • Yu Sui, Xiaojiang Duan, Jingming Zhang, Yingming Chu, Xing Yang. Synthesis and characterization of a novel 68Ga-labeled p-bromobenzyl lysine-urea-ODAP PSMA inhibitor. Bioorganic & medicinal chemistry letters. 2023 07; 91(?):129382. doi: 10.1016/j.bmcl.2023.129382. [PMID: 37348571]
  • Rym Boulfekhar, Leanne Ohlund, Kathrina Mae Kumaresan, Meriem Megoura, Thomas D Warkentin, Pompilia Ispas-Szabo, Lekha Sleno, Mircea Alexandru Mateescu. Diamine Oxidase as a Therapeutic Enzyme: Study of Germination from Vegetal Sources and Investigation of the Presence of β-N-Oxalyl-L-α,β-diaminopropionic Acid (β-ODAP) Using LC-MS/MS. International journal of molecular sciences. 2023 Feb; 24(5):. doi: 10.3390/ijms24054625. [PMID: 36902055]
  • Anne Edwards, Isaac Njaci, Abhimanyu Sarkar, Zhouqian Jiang, Gemy George Kaithakottil, Christopher Moore, Jitender Cheema, Clare E M Stevenson, Martin Rejzek, Petr Novák, Marielle Vigouroux, Martin Vickers, Roland H M Wouters, Pirita Paajanen, Burkhard Steuernagel, Jonathan D Moore, Janet Higgins, David Swarbreck, Stefan Martens, Colin Y Kim, Jing-Ke Weng, Sagadevan Mundree, Benjamin Kilian, Shiv Kumar, Matt Loose, Levi Yant, Jiří Macas, Trevor L Wang, Cathie Martin, Peter M F Emmrich. Genomics and biochemical analyses reveal a metabolon key to β-L-ODAP biosynthesis in Lathyrus sativus. Nature communications. 2023 Feb; 14(1):876. doi: 10.1038/s41467-023-36503-2. [PMID: 36797319]
  • Wenna Li, Zhao Zhou, Xianglai Li, Lin Ma, Qingyuan Guan, Guojun Zheng, Hao Liang, Yajun Yan, Xiaolin Shen, Jia Wang, Xinxiao Sun, Qipeng Yuan. Biosynthesis of plant hemostatic dencichine in Escherichia coli. Nature communications. 2022 09; 13(1):5492. doi: 10.1038/s41467-022-33255-3. [PMID: 36123371]
  • Moshe Goldsmith, Shiri Barad, Maor Knafo, Alon Savidor, Shifra Ben-Dor, Alexander Brandis, Tevie Mehlman, Yoav Peleg, Shira Albeck, Orly Dym, Efrat Ben-Zeev, Ranjit S Barbole, Asaph Aharoni, Ziv Reich. Identification and characterization of the key enzyme in the biosynthesis of the neurotoxin β-ODAP in grass pea. The Journal of biological chemistry. 2022 05; 298(5):101806. doi: 10.1016/j.jbc.2022.101806. [PMID: 35271851]
  • Zijiang Yang, Guanze Liu, Guanghui Zhang, Jing Yan, Yang Dong, Yingchun Lu, Wei Fan, Bing Hao, Yuan Lin, Ying Li, Xuejiao Li, Qingyan Tang, Guisheng Xiang, Simei He, Junwen Chen, Wei Chen, Zhongping Xu, Zichao Mao, Shengchang Duan, Shuangxia Jin, Shengchao Yang. The chromosome-scale high-quality genome assembly of Panax notoginseng provides insight into dencichine biosynthesis. Plant biotechnology journal. 2021 05; 19(5):869-871. doi: 10.1111/pbi.13558. [PMID: 33529371]
  • Chao Huang, Lijing Cheng, Xinyan Feng, Xiaojun Li, Lihua Wang. Dencichine ameliorates renal injury by improving oxidative stress, apoptosis and fibrosis in diabetic rats. Life sciences. 2020 Oct; 258(?):118146. doi: 10.1016/j.lfs.2020.118146. [PMID: 32721462]
  • Yan-Hai Zhang, Yuan-Gui Yang, Lei Shi, Yan Jin, Zheng-Tao Wang. [Fingerprinting analysis of non-saponins from water-soluble part and determination of dencichine from Panax notoginseng, P. ginseng and P. quinquefolium based on liquid chromatography coupled with charged aerosol detection]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2020 Jul; 45(14):3475-3480. doi: 10.19540/j.cnki.cjcmm.20200403.202. [PMID: 32726064]
  • Suman, Yasmin Ahmad, Vikrant Nain. A convenient and robust protocol for preparation of ODAP-free Lathyrus sativus protein. Analytical biochemistry. 2020 02; 591(?):113544. doi: 10.1016/j.ab.2019.113544. [PMID: 31866288]
  • Peter M F Emmrich, Martin Rejzek, Lionel Hill, Paul Brett, Anne Edwards, Abhimanyu Sarkar, Rob A Field, Cathie Martin, Trevor L Wang. Linking a rapid throughput plate-assay with high-sensitivity stable-isotope label LCMS quantification permits the identification and characterisation of low β-L-ODAP grass pea lines. BMC plant biology. 2019 Nov; 19(1):489. doi: 10.1186/s12870-019-2091-5. [PMID: 31718544]
  • Kimino Minagawa, Shin-Ichi Yamada, Ayano Suzuki, Saeko Ta, Toshio Kumai, Fernand Lambein, Kuniko Kusama-Eguchi. Stress-related over-enhancement of the hypothalamic-pituitary-adrenal axis causes experimental neurolathyrism in rats. Environmental toxicology and pharmacology. 2019 Nov; 72(?):103245. doi: 10.1016/j.etap.2019.103245. [PMID: 31499324]
  • Veerababu Nagati, Monika Kallubai, Dinesh Kumar Chinthapalli, Rajagopal Subramanyam. Exploration of binding studies of β-oxalyldiamino propionic acid (β-ODAP), a non-protein amino acid with human serum albumin-biophysical and computational approach. Journal of biomolecular structure & dynamics. 2019 09; 37(15):3914-3922. doi: 10.1080/07391102.2018.1528181. [PMID: 30257618]
  • Jie Li, Pengcheng Qiu, Siwang Wang, Junsheng Wu, Qiaoyan He, Kaifeng Li, Lu Xu. β-N-Oxalyl-L-α,β-diaminopropionic acid from Panax notoginseng plays a major role in the treatment of type 2 diabetic nephropathy. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2019 Jun; 114(?):108801. doi: 10.1016/j.biopha.2019.108801. [PMID: 30928803]
  • Fengjuan Liu, Chengjin Jiao, Chunxiao Bi, Quanle Xu, Peng Chen, Adam L Heuberger, Hari B Krishnan. Metabolomics Approach To Understand Mechanisms of β-N-Oxalyl-l-α,β-diaminopropionic Acid (β-ODAP) Biosynthesis in Grass Pea (Lathyrus sativus L.). Journal of agricultural and food chemistry. 2017 Nov; 65(47):10206-10213. doi: 10.1021/acs.jafc.7b04037. [PMID: 29112818]
  • Li Jie, Qiu Pengcheng, He Qiaoyan, Bi Linlin, Zhang Meng, Wang Fang, Jia Min, Yan Li, Zhang Ya, Yang Qian, Wang Siwang. Dencichine ameliorates kidney injury in induced type II diabetic nephropathy via the TGF-β/Smad signalling pathway. European journal of pharmacology. 2017 Oct; 812(?):196-205. doi: 10.1016/j.ejphar.2017.06.024. [PMID: 28633927]
  • Quanle Xu, Fengjuan Liu, Peng Chen, Joseph M Jez, Hari B Krishnan. β-N-Oxalyl-l-α,β-diaminopropionic Acid (β-ODAP) Content in Lathyrus sativus: The Integration of Nitrogen and Sulfur Metabolism through β-Cyanoalanine Synthase. International journal of molecular sciences. 2017 Feb; 18(3):. doi: 10.3390/ijms18030526. [PMID: 28264526]
  • Rui-Yue Tan, Geng-Yan Xing, Guang-Ming Zhou, Feng-Min Li, Wen-Tao Hu, Fernand Lambein, Jun-Lan Xiong, Sheng-Xiang Zhang, Hai-Yan Kong, Hao Zhu, Zhi-Xiao Li, You-Cai Xiong. Plant toxin β-ODAP activates integrin β1 and focal adhesion: A critical pathway to cause neurolathyrism. Scientific reports. 2017 01; 7(?):40677. doi: 10.1038/srep40677. [PMID: 28094806]
  • Lin Li, Cheng-xiao Wang, Yuan Qu, Xiu-ming Cui. [Content determination of dencichine in Panax Notoginseng by a reversed phase ion-pair chromatography]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2015 Oct; 40(20):4026-30. doi: ". [PMID: 27062822]
  • Jun-Lan Xiong, You-Cai Xiong, Xue Bai, Hai-Yan Kong, Rui-Yue Tan, Hao Zhu, Kadambot H M Siddique, Jian-Yong Wang, Neil C Turner. Genotypic Variation in the Concentration of β-N-Oxalyl-L-α,β-diaminopropionic Acid (β-ODAP) in Grass Pea (Lathyrus sativus L.) Seeds Is Associated with an Accumulation of Leaf and Pod β-ODAP during Vegetative and Reproductive Stages at Three Levels of Water Stress. Journal of agricultural and food chemistry. 2015 Jul; 63(27):6133-41. doi: 10.1021/acs.jafc.5b01729. [PMID: 26027639]
  • Ling-juan Yang, Cheng-jin Jiao, Er-quan Gao. [Determination of Dencichine and Its Isomer in Panax notoginseng by Pre-column Derivatization HPLC]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2015 Feb; 38(2):311-4. doi: ". [PMID: 26415407]
  • Bidisha Ghosh, Joy Mitra, Saikat Chakraborty, Jagannath Bhattacharyya, Anirban Chakraborty, Soumitra Kumar Sen, Muniasamy Neerathilingam. Simple Detection Methods for Antinutritive Factor β-ODAP Present in Lathyrus sativus L. by High Pressure Liquid Chromatography and Thin Layer Chromatography. PloS one. 2015; 10(11):e0140649. doi: 10.1371/journal.pone.0140649. [PMID: 26524073]
  • E Rivadeneyra-Domínguez, J F Rodríguez-Landa. Cycads and their association with certain neurodegenerative diseases. Neurologia (Barcelona, Spain). 2014 Nov; 29(9):517-22. doi: 10.1016/j.nrl.2013.03.005. [PMID: 23725821]
  • Ling-Fang Huang, Hai-Lian Shi, Bo Gao, Hui Wu, Li Yang, Xiao-Jun Wu, Zheng-Tao Wang. Decichine enhances hemostasis of activated platelets via AMPA receptors. Thrombosis research. 2014 May; 133(5):848-54. doi: 10.1016/j.thromres.2014.02.009. [PMID: 24630643]
  • Jun-Lan Xiong, Xue Bai, Asfa Batool, Hai-Yan Kong, Rui-Yue Tan, Ya-Fu Wang, Zhi-Xiao Li, You-Cai Xiong. [Ecological function and application of toxin beta-ODAP in grass pea (Lathyrus sativus)]. Ying yong sheng tai xue bao = The journal of applied ecology. 2014 Apr; 25(4):1197-205. doi: . [PMID: 25011318]
  • A Nur Onar, Behice Yavuz Erdoğan, Ilknur Ayan, Zeki Acar. Homoarginine, β-ODAP, and asparagine contents of grass pea landraces cultivated in Turkey. Food chemistry. 2014 Jan; 143(?):277-81. doi: 10.1016/j.foodchem.2013.07.051. [PMID: 24054240]
  • Maria Hoernke, Christian Schwieger, Andreas Kerth, Alfred Blume. Binding of cationic pentapeptides with modified side chain lengths to negatively charged lipid membranes: Complex interplay of electrostatic and hydrophobic interactions. Biochimica et biophysica acta. 2012 Jul; 1818(7):1663-72. doi: 10.1016/j.bbamem.2012.03.001. [PMID: 22433675]
  • Peter B Nunn, James R A Lyddiard, K P W Christopher Perera. Brain glutathione as a target for aetiological factors in neurolathyrism and konzo. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2011 Mar; 49(3):662-7. doi: 10.1016/j.fct.2010.08.037. [PMID: 20816718]
  • M Van Moorhem, F Lambein, L Leybaert. Unraveling the mechanism of β-N-oxalyl-α,β-diaminopropionic acid (β-ODAP) induced excitotoxicity and oxidative stress, relevance for neurolathyrism prevention. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2011 Mar; 49(3):550-5. doi: 10.1016/j.fct.2010.03.054. [PMID: 20510327]
  • C-J Jiao, J-L Jiang, C Li, L-M Ke, W Cheng, F-M Li, Z-X Li, C-Y Wang. β-ODAP accumulation could be related to low levels of superoxide anion and hydrogen peroxide in Lathyrus sativus L. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2011 Mar; 49(3):556-62. doi: 10.1016/j.fct.2010.05.054. [PMID: 20510333]
  • C-J Jiao, J-L Jiang, L-M Ke, W Cheng, F-M Li, Z-X Li, C-Y Wang. Factors affecting β-ODAP content in Lathyrus sativus and their possible physiological mechanisms. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2011 Mar; 49(3):543-9. doi: 10.1016/j.fct.2010.04.050. [PMID: 20510335]
  • Dirk Enneking. The nutritive value of grasspea (Lathyrus sativus) and allied species, their toxicity to animals and the role of malnutrition in neurolathyrism. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2011 Mar; 49(3):694-709. doi: 10.1016/j.fct.2010.11.029. [PMID: 21112364]
  • Kuniko Kusama-Eguchi, Yoshiko Yamazaki, Tadashi Ueda, Atsuhiro Suda, Yukari Hirayama, Fumio Ikegami, Kazuko Watanabe, Mike May, Fernand Lambein, Tadashi Kusama. Hind-limb paraparesis in a rat model for neurolathyrism associated with apoptosis and an impaired vascular endothelial growth factor system in the spinal cord. The Journal of comparative neurology. 2010 Mar; 518(6):928-42. doi: 10.1002/cne.22257. [PMID: 20058324]
  • Geeta Mishra, Rakesh Shukla, Mahdi Hasan, Subhash K Khanna, Mukul Das. Potentiation of neurotoxicity of Lathyrus sativus by manganese: alterations in blood-brain barrier permeability. Toxicology mechanisms and methods. 2009 May; 19(4):318-26. doi: 10.1080/15376510902758947. [PMID: 19778223]
  • George K Shinomol, Muralidhara. Differential induction of oxidative impairments in brain regions of male mice following subchronic consumption of Khesari dhal (Lathyrus sativus) and detoxified Khesari dhal. Neurotoxicology. 2007 Jul; 28(4):798-806. doi: 10.1016/j.neuro.2007.03.002. [PMID: 17451808]
  • Guo-Xiang Xie, Yun-Ping Qiu, Ming-Feng Qiu, Xian-Fu Gao, Yu-Min Liu, Wei Jia. Analysis of dencichine in Panax notoginseng by gas chromatography-mass spectrometry with ethyl chloroformate derivatization. Journal of pharmaceutical and biomedical analysis. 2007 Feb; 43(3):920-5. doi: 10.1016/j.jpba.2006.09.009. [PMID: 17029672]
  • Jing Zhu, San-kang Liu, Chun-mei Fu, Zhang-wan Li. [Analysis of dencichine by HPLC with pre-column derivatization]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2006 Nov; 31(22):1865-8. doi: ". [PMID: 17285985]
  • Jing Zhu, Xin Zhou, Hu Zheng, Zhangwan Li. Enantioselective determination of dencichine in rabbit plasma by high-performance liquid chromatography-electrospray mass spectrometry. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2006 Aug; 840(2):124-31. doi: 10.1016/j.jchromb.2006.04.041. [PMID: 16730243]
  • You-Cai Xiong, Geng-Mei Xing, Feng-Min Li, Shao-Ming Wang, Xian-Wei Fan, Zhi-Xiao Li, Ya-Fu Wang. Abscisic acid promotes accumulation of toxin ODAP in relation to free spermine level in grass pea seedlings (Lathyrus sativus L.). Plant physiology and biochemistry : PPB. 2006 Feb; 44(2-3):161-9. doi: 10.1016/j.plaphy.2006.03.002. [PMID: 16650769]
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