Hydroxylamine (BioDeep_00000004394)
Secondary id: BioDeep_00000405556
human metabolite Endogenous blood metabolite
代谢物信息卡片
Hydroxylamine-1-hydrochloride
化学式: H3NO (33.0215)
中文名称: 羟胺 溶液, 羟胺
谱图信息:
最多检出来源 Homo sapiens(not specific) 50%
分子结构信息
SMILES: NO
InChI: InChI=1S/H3NO/c1-2/h2H,1H2
描述信息
Hydroxylamine is a reactive chemical with formula NH2OH. It can be considered a hybrid of ammonia and water due to parallels it shares with each. At room temperature pure NH2OH is ordinarily a white, unstable crystalline, hygroscopic compound; Hydroxylamine is a reactive chemical with formula NH2OH. It can be considered a hybrid of ammonia and water due to parallels it shares with each. At room temperature pure NH2OH is ordinarily a white, unstable crystalline, hygroscopic compound; however it is almost always encountered as an aqueous solution.; NH2OH is an intermediate in biological nitrification. The oxidation of NH3 is mediated by hydroxylamine oxidoreductase (HAO).; however it is almost always encountered as an aqueous solution.; A colorless inorganic compound (HONH2) used in organic synthesis and as a reducing agent, due to its ability to donate nitric oxide.; Hydroxylamine may explode on heating. It is an irritant to the respiratory tract, skin, eyes, and other mucous membranes. It may be absorbed through the skin, is harmful if swallowed, and is a possible mutagen.; NH2OH is an intermediate in the biological nitrification. The oxidation of NH3 is mediated by HAO (hydroxylamine oxidoreductase). Hydroxylamine is found in gram bean and mung bean.
Hydroxylamine is a reactive chemical with formula NH2OH. It can be considered a hybrid of ammonia and water due to parallels it shares with each. At room temperature pure NH2OH is ordinarily a white, unstable crystalline, hygroscopic compound; however it is almost always encountered as an aqueous solution. A colorless inorganic compound (HONH2) used in organic synthesis and as a reducing agent, due to its ability to donate nitric oxide. Hydroxylamine may explode on heating. It is an irritant to the respiratory tract, skin, eyes, and other mucous membranes. It may be absorbed through the skin, is harmful if swallowed, and is a possible mutagen. NH2OH is an intermediate in the biological nitrification. The oxidation of NH3 is mediated by HAO (hydroxylamine oxidoreductase).
同义名列表
20 个代谢物同义名
Hydroxylamine-1-hydrochloride; Hydrochloride, hydroxylamine; Hydroxylamine hydrochloride; Dihydridohydroxidonitrogen; Hydroxyamine hydrochloride; Chloride, hydroxylammonium; Hydroxylammonium chloride; Oxammonium hydrochloride; Hydroxylamine chloride; (1) Hydroxylamine; hydroxylamine; Hydroxylamin; HYDROXYAMINE; Oxammonium; Oxyammonia; Nitroxide; [NH2OH]; H2NHO; NH2OH; Hydroxylamine
数据库引用编号
22 个数据库交叉引用编号
- ChEBI: CHEBI:15429
- KEGG: C00192
- PubChem: 787
- HMDB: HMDB0003338
- ChEMBL: CHEMBL1191361
- Wikipedia: Hydroxylamine
- MeSH: Hydroxylamine
- MetaCyc: HYDROXYLAMINE
- KNApSAcK: C00053330
- foodb: FDB007499
- chemspider: 766
- CAS: 13408-29-2
- CAS: 11104-93-1
- CAS: 11129-69-4
- CAS: 7803-49-8
- PMhub: MS000016817
- PubChem: 3492
- PDB-CCD: HOA
- 3DMET: B01184
- NIKKAJI: J941E
- RefMet: Hydroxylamine
- KNApSAcK: 15429
分类词条
相关代谢途径
Reactome(0)
BioCyc(52)
- superpathway of anaerobic energy metabolism (invertebrates)
- superpathway of L-lysine, L-threonine and L-methionine biosynthesis I
- aspartate superpathway
- trans-4-hydroxy-L-proline degradation II
- L-lysine biosynthesis I
- canavanine degradation
- superpathway of L-arginine, putrescine, and 4-aminobutanoate degradation
- L-arginine degradation X (arginine monooxygenase pathway)
- superpathway of L-arginine and L-ornithine degradation
- methanol and methylamine oxidation to formaldehyde
- superpathway of C1 compounds oxidation to CO2
- superpathway of trimethylamine degradation
- superpathway of coenzyme A biosynthesis I (bacteria)
- formaldehyde assimilation I (serine pathway)
- methylamine degradation II
- methylamine degradation I
- superpathay of heme b biosynthesis from glutamate
- CMP-N-acetylneuraminate biosynthesis II (bacteria)
- superpathway of CMP-sialic acids biosynthesis
- tetrapyrrole biosynthesis I (from glutamate)
- superpathway of proto- and siroheme biosynthesis
- superpathway of L-lysine degradation
- L-lysine fermentation to acetate and butanoate
- NADH to cytochrome bo oxidase electron transfer I
- NADH to cytochrome bd oxidase electron transfer I
- ammonia oxidation I (aerobic)
- protein S-nitrosylation and denitrosylation
- ammonia oxidation III
- ammonia oxidation IV (autotrophic ammonia oxidizers)
- nitrifier denitrification
- lysine degradation I (saccharopine pathway)
- L-lysine degradation V
- L-lysine degradation XI (mammalian)
- L-lysine degradation IX
- superpathway of adenosine nucleotides de novo biosynthesis I
- superpathway of purine nucleotides de novo biosynthesis I
- anaerobic energy metabolism (invertebrates, cytosol)
- superpathway of penicillin, cephalosporin and cephamycin biosynthesis
- deacetylcephalosporin C biosynthesis
- trans-4-hydroxy-L-proline degradation I
- superpathway of L-methionine salvage and degradation
- adenosine nucleotides de novo biosynthesis
- succinate to cytochrome bo oxidase electron transfer
- NADH to cytochrome bo oxidase electron transfer II
- D-lactate to cytochrome bo oxidase electron transfer
- glycerol-3-phosphate to cytochrome bo oxidase electron transfer
- proline to cytochrome bo oxidase electron transfer
- pyruvate to cytochrome bo oxidase electron transfer
- nitrite reduction (hemoglobin)
- NADH to cytochrome bd oxidase electron transfer II
- succinate to cytochrome bd oxidase electron transfer
- ammonia oxidation II (anaerobic)
PlantCyc(3)
代谢反应
42 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(13)
- ammonia oxidation IV (autotrophic ammonia oxidizers):
A(H2) + O2 + ammonia ⟶ A + H2O + hydroxylamine - ammonia oxidation I (aerobic):
A(H2) + O2 + ammonia ⟶ A + H2O + hydroxylamine - nitrifier denitrification:
A(H2) + O2 + ammonia ⟶ A + H2O + hydroxylamine - protein S-nitrosylation and denitrosylation:
O2 + a [protein]-L-cysteine + nitric oxide ⟶ H+ + a [protein] 3-nitrosothio-L-alanine + superoxide - nitrite reduction (hemoglobin):
OH- + a ferrihemoglobin + ammonium ⟶ H+ + a ferrohemoglobin + hydroxylamine - protein S-nitrosylation and denitrosylation:
H2O + NAD+ + ammonium ⟶ H+ + NADH + hydroxylamine - ammonia oxidation III:
A(H2) + O2 + ammonia ⟶ A + H2O + hydroxylamine - protein S-nitrosylation and denitrosylation:
O2 + a [protein]-L-cysteine + nitric oxide ⟶ H+ + a [protein] 3-nitrosothio-L-alanine + superoxide - protein S-nitrosylation and denitrosylation:
O2 + a [protein]-L-cysteine + nitric oxide ⟶ H+ + a [protein] 3-nitrosothio-L-alanine + superoxide - ammonia oxidation III:
A(H2) + O2 + ammonia ⟶ A + H2O + hydroxylamine - ammonia oxidation I (aerobic):
A(H2) + O2 + ammonia ⟶ A + H2O + hydroxylamine - ammonia oxidation IV (autotrophic ammonia oxidizers):
A(H2) + O2 + ammonia ⟶ A + H2O + hydroxylamine - ammonia oxidation I (aerobic):
A(H2) + O2 + ammonia ⟶ A + H2O + hydroxylamine
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(29)
- nitrite reduction (hemoglobin):
a ferrihemoglobin + hydroxylamine ⟶ H+ + a ferrohemoglobin + nitric oxide - nitrite reduction (hemoglobin):
OH- + a ferrihemoglobin + nitric oxide ⟶ H+ + a ferrohemoglobin + nitrite - nitrite reduction (hemoglobin):
a ferrihemoglobin + hydroxylamine ⟶ H+ + a ferrohemoglobin + nitric oxide - nitrite reduction (hemoglobin):
OH- + a ferrihemoglobin + nitric oxide ⟶ H+ + a ferrohemoglobin + nitrite - nitrite reduction (hemoglobin):
a ferrihemoglobin + hydroxylamine ⟶ H+ + a ferrohemoglobin + nitric oxide - nitrite reduction (hemoglobin):
OH- + a ferrihemoglobin + nitric oxide ⟶ H+ + a ferrohemoglobin + nitrite - nitrite reduction (hemoglobin):
OH- + a ferrihemoglobin + nitric oxide ⟶ H+ + a ferrohemoglobin + nitrite - nitrite reduction (hemoglobin):
a ferrihemoglobin + hydroxylamine ⟶ H+ + a ferrohemoglobin + nitric oxide - nitrite reduction (hemoglobin):
OH- + a ferrihemoglobin + nitric oxide ⟶ H+ + a ferrohemoglobin + nitrite - nitrite reduction (hemoglobin):
OH- + a ferrihemoglobin + nitric oxide ⟶ H+ + a ferrohemoglobin + nitrite - nitrite reduction (hemoglobin):
a ferrihemoglobin + hydroxylamine ⟶ H+ + a ferrohemoglobin + nitric oxide - nitrite reduction (hemoglobin):
OH- + a ferrihemoglobin + nitric oxide ⟶ H+ + a ferrohemoglobin + nitrite - nitrite reduction (hemoglobin):
a ferrihemoglobin + hydroxylamine ⟶ H+ + a ferrohemoglobin + nitric oxide - nitrite reduction (hemoglobin):
OH- + a ferrihemoglobin + nitric oxide ⟶ H+ + a ferrohemoglobin + nitrite - nitrite reduction (hemoglobin):
a ferrihemoglobin + hydroxylamine ⟶ H+ + a ferrohemoglobin + nitric oxide - nitrite reduction (hemoglobin):
a ferrihemoglobin + hydroxylamine ⟶ H+ + a ferrohemoglobin + nitric oxide - nitrite reduction (hemoglobin):
a ferrihemoglobin + hydroxylamine ⟶ H+ + a ferrohemoglobin + nitric oxide - nitrite reduction (hemoglobin):
OH- + a ferrihemoglobin + nitric oxide ⟶ H+ + a ferrohemoglobin + nitrite - nitrite reduction (hemoglobin):
OH- + a ferrihemoglobin + nitric oxide ⟶ H+ + a ferrohemoglobin + nitrite - nitrite reduction (hemoglobin):
a ferrihemoglobin + hydroxylamine ⟶ H+ + a ferrohemoglobin + nitric oxide - nitrite reduction (hemoglobin):
a ferrihemoglobin + hydroxylamine ⟶ H+ + a ferrohemoglobin + nitric oxide - nitrite reduction (hemoglobin):
OH- + a ferrihemoglobin + nitric oxide ⟶ H+ + a ferrohemoglobin + nitrite - nitrite reduction (hemoglobin):
OH- + a ferrihemoglobin + nitric oxide ⟶ H+ + a ferrohemoglobin + nitrite - nitrite reduction (hemoglobin):
a ferrihemoglobin + hydroxylamine ⟶ H+ + a ferrohemoglobin + nitric oxide - nitrite reduction (hemoglobin):
OH- + a ferrihemoglobin + nitric oxide ⟶ H+ + a ferrohemoglobin + nitrite - nitrite reduction (hemoglobin):
a ferrihemoglobin + hydroxylamine ⟶ H+ + a ferrohemoglobin + nitric oxide - nitrite reduction (hemoglobin):
a ferrihemoglobin + hydroxylamine ⟶ H+ + a ferrohemoglobin + nitric oxide - nitrite reduction (hemoglobin):
a ferrihemoglobin + hydroxylamine ⟶ H+ + a ferrohemoglobin + nitric oxide - nitrite reduction (hemoglobin):
OH- + a ferrihemoglobin + nitric oxide ⟶ H+ + a ferrohemoglobin + nitrite
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
9 个相关的物种来源信息
- 3702 - Arabidopsis thaliana:
- 3055 - Chlamydomonas reinhardtii: 10.1111/TPJ.12747
- 9606 - Homo sapiens: -
- 645164 - Lotus burttii: 10.1111/J.1365-3040.2010.02266.X
- 47247 - Lotus corniculatus: 10.1111/J.1365-3040.2010.02266.X
- 264956 - Lotus filicaulis: 10.1111/J.1365-3040.2010.02266.X
- 34305 - Lotus japonicus:
- 347996 - Lotus tenuis: 10.1111/J.1365-3040.2010.02266.X
- 28901 - Salmonella enterica: 10.1021/ACS.JPROTEOME.0C00281
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
- Manman Zhang, Tengxia He, Qifeng Wu, Mengping Chen, Xiwen Liang. Hydroxylamine supplementation accelerated the rates of cell growth, aerobic denitrification and nitrous oxide emission of Pseudomonas taiwanensis EN-F2.
Journal of environmental management.
2024 May; 358(?):120826. doi:
10.1016/j.jenvman.2024.120826. [PMID: 38608579] - Bingsen Zhang, Yan Yu, Bennett W Fox, Yinong Liu, Venkatesh P Thirumalaikumar, Aleksandra Skirycz, Hening Lin, Frank C Schroeder. Amino acid and protein specificity of protein fatty acylation in C. elegans.
Proceedings of the National Academy of Sciences of the United States of America.
2024 Jan; 121(5):e2307515121. doi:
10.1073/pnas.2307515121. [PMID: 38252833] - Yukie Akutsu, Takaaki Fujiwara, Rintaro Suzuki, Yuki Nishigaya, Toshimasa Yamazaki. Juglone, a plant-derived 1,4-naphthoquinone, binds to hydroxylamine oxidoreductase and inhibits the electron transfer to cytochrome c554.
Applied and environmental microbiology.
2023 Dec; 89(12):e0129123. doi:
10.1128/aem.01291-23. [PMID: 38009977] - Mengping Chen, Tengxia He, Xiwen Liang, Cerong Wang, Chunxia Zheng. Efficient transformation of hydroxylamine from wastewater after supplementation with sodium carbonate or calcium bicarbonate.
Ecotoxicology and environmental safety.
2023 Nov; 266(?):115603. doi:
10.1016/j.ecoenv.2023.115603. [PMID: 37856986] - E V Dmitrieva, A Z Temerdashev, M O Zorina, Yu-Qi Feng, P N Nesterenko. Solid-phase analytical derivatization as a tool for the quantification of steroid hormones in human urine with HPLC-Q-ToF detection.
Journal of pharmaceutical and biomedical analysis.
2022 May; 214(?):114736. doi:
10.1016/j.jpba.2022.114736. [PMID: 35338944] - Manman Zhang, Tengxia He, Mengping Chen, Qifeng Wu. Ammonium and hydroxylamine can be preferentially removed during simultaneous nitrification and denitrification by Pseudomonas taiwanensis EN-F2.
Bioresource technology.
2022 Apr; 350(?):126912. doi:
10.1016/j.biortech.2022.126912. [PMID: 35231598] - Shi-Lei Wang, Yu Wang, Lei Wu, Yuan-Yuan Cai, Zi-Chao Wang, Raphael N Alolga, Lian-Wen Qi, Bin Li, Feng-Qing Huang. Paired Derivatization Approach with H/D-Labeled Hydroxylamine Reagents for Sensitive and Accurate Analysis of Monosaccharides by Liquid Chromatography Tandem Mass Spectrometry.
Analytical chemistry.
2022 03; 94(8):3590-3599. doi:
10.1021/acs.analchem.1c04924. [PMID: 35171578] - Mengping Chen, Chenyu Ding, Tengxia He, Manman Zhang, Qifeng Wu. Efficient hydroxylamine removal through heterotrophic nitrification by novel bacterium Glutamicibacter arilaitensis EM-H8.
Chemosphere.
2022 Feb; 288(Pt 1):132475. doi:
10.1016/j.chemosphere.2021.132475. [PMID: 34624339] - Mark J Henderson, Kathleen A Trychta, Shyh-Ming Yang, Susanne Bäck, Adam Yasgar, Emily S Wires, Carina Danchik, Xiaokang Yan, Hideaki Yano, Lei Shi, Kuo-Jen Wu, Amy Q Wang, Dingyin Tao, Gergely Zahoránszky-Kőhalmi, Xin Hu, Xin Xu, David Maloney, Alexey V Zakharov, Ganesha Rai, Fumihiko Urano, Mikko Airavaara, Oksana Gavrilova, Ajit Jadhav, Yun Wang, Anton Simeonov, Brandon K Harvey. A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome.
Cell reports.
2021 04; 35(4):109040. doi:
10.1016/j.celrep.2021.109040. [PMID: 33910017] - Keita Saito, Shoko Okazaki, Yoko Tachibana, Kazunori Anzai, Toshihiko Ozawa, Keizo Takeshita. In vivo ESR imaging of redox status in mice after X-ray irradiation, measured by acyl-protected hydroxylamine probe, ACP.
Free radical biology & medicine.
2020 11; 160(?):596-603. doi:
10.1016/j.freeradbiomed.2020.08.028. [PMID: 32891759] - T Joshua Moore, Bhavya Sharma. Direct Surface Enhanced Raman Spectroscopic Detection of Cortisol at Physiological Concentrations.
Analytical chemistry.
2020 01; 92(2):2052-2057. doi:
10.1021/acs.analchem.9b04532. [PMID: 31874025] - Hossein Jahangirian, Bahram Saleh, Katayoon Kalantari, Roshanak Rafiee-Moghaddam, Bahareh Nikpey, Siavash Jahangirian, Thomas J Webster. Enzymatic Synthesis of Ricinoleyl Hydroxamic Acid Based on Commercial Castor Oil, Cytotoxicity Properties and Application as a New Anticancer Agent.
International journal of nanomedicine.
2020; 15(?):2935-2945. doi:
10.2147/ijn.s223796. [PMID: 32425525] - Nicole A Spiegelman, Xiaoyu Zhang, Hui Jing, Ji Cao, Ilana B Kotliar, Pornpun Aramsangtienchai, Miao Wang, Zhen Tong, Kelly M Rosch, Hening Lin. SIRT2 and Lysine Fatty Acylation Regulate the Activity of RalB and Cell Migration.
ACS chemical biology.
2019 09; 14(9):2014-2023. doi:
10.1021/acschembio.9b00492. [PMID: 31433161] - Quan V Vo, Mai Van Bay, Pham Cam Nam, Adam Mechler. Is Indolinonic Hydroxylamine a Promising Artificial Antioxidant?.
The journal of physical chemistry. B.
2019 09; 123(37):7777-7784. doi:
10.1021/acs.jpcb.9b05160. [PMID: 31462046] - Cho Rong Hong, William R Wilson, Kevin O Hicks. An Intratumor Pharmacokinetic/Pharmacodynamic Model for the Hypoxia-Activated Prodrug Evofosfamide (TH-302): Monotherapy Activity is Not Dependent on a Bystander Effect.
Neoplasia (New York, N.Y.).
2019 02; 21(2):159-171. doi:
10.1016/j.neo.2018.11.009. [PMID: 30591421] - Andrea Baschieri, Luca Valgimigli, Simone Gabbanini, Gino A DiLabio, Eduardo Romero-Montalvo, Riccardo Amorati. Extremely Fast Hydrogen Atom Transfer between Nitroxides and HOO· Radicals and Implication for Catalytic Coantioxidant Systems.
Journal of the American Chemical Society.
2018 08; 140(32):10354-10362. doi:
10.1021/jacs.8b06336. [PMID: 30022659] - Jagannathan Alagurajan, Navjot Singh Athwal, Mark S Hargrove. Steady-State Kinetics of Phytoglobin-Catalyzed Reduction of Hydroxylamine to Ammonium.
Biochemistry.
2018 08; 57(32):4824-4832. doi:
10.1021/acs.biochem.8b00586. [PMID: 30001111] - Dorottya Nagy-Szakal, Dinesh K Barupal, Bohyun Lee, Xiaoyu Che, Brent L Williams, Ellie J R Kahn, Joy E Ukaigwe, Lucinda Bateman, Nancy G Klimas, Anthony L Komaroff, Susan Levine, Jose G Montoya, Daniel L Peterson, Bruce Levin, Mady Hornig, Oliver Fiehn, W Ian Lipkin. Insights into myalgic encephalomyelitis/chronic fatigue syndrome phenotypes through comprehensive metabolomics.
Scientific reports.
2018 07; 8(1):10056. doi:
10.1038/s41598-018-28477-9. [PMID: 29968805] - Emmanuelle Thinon, Joseph P Fernandez, Henrik Molina, Howard C Hang. Selective Enrichment and Direct Analysis of Protein S-Palmitoylation Sites.
Journal of proteome research.
2018 05; 17(5):1907-1922. doi:
10.1021/acs.jproteome.8b00002. [PMID: 29575903] - Jinchao Zhang, Yunjie Huang, Jing Chen, Haining Zhu, Sidney W Whiteheart. Dynamic cycling of t-SNARE acylation regulates platelet exocytosis.
The Journal of biological chemistry.
2018 03; 293(10):3593-3606. doi:
10.1074/jbc.ra117.000140. [PMID: 29352103] - Natalia E Markina, Irina Yu Goryacheva, Alexey V Markin. Sample pretreatment and SERS-based detection of ceftriaxone in urine.
Analytical and bioanalytical chemistry.
2018 Mar; 410(8):2221-2227. doi:
10.1007/s00216-018-0888-y. [PMID: 29392377] - Yan-Feng Liang, Dong-Dong Zhang, Xiao-Jing Yu, Hong-Li Gao, Kai-Li Liu, Jie Qi, Hong-Bao Li, Qiu-Yue Yi, Wen-Sheng Chen, Wei Cui, Guo-Qing Zhu, Yu-Ming Kang. Hydrogen sulfide in paraventricular nucleus attenuates blood pressure by regulating oxidative stress and inflammatory cytokines in high salt-induced hypertension.
Toxicology letters.
2017 Mar; 270(?):62-71. doi:
10.1016/j.toxlet.2017.02.004. [PMID: 28185984] - Chloe Westley, Yun Xu, Baskaran Thilaganathan, Andrew J Carnell, Nicholas J Turner, Royston Goodacre. Absolute Quantification of Uric Acid in Human Urine Using Surface Enhanced Raman Scattering with the Standard Addition Method.
Analytical chemistry.
2017 02; 89(4):2472-2477. doi:
10.1021/acs.analchem.6b04588. [PMID: 28192933] - Li Sun, Yufang Lu, Fangwei Yu, Herbert J Kronzucker, Weiming Shi. Biological nitrification inhibition by rice root exudates and its relationship with nitrogen-use efficiency.
The New phytologist.
2016 Nov; 212(3):646-656. doi:
10.1111/nph.14057. [PMID: 27292630] - Renyi Peng, Zhiyuan Bian, Lina Zhou, Wei Cheng, Na Hai, Changquan Yang, Tao Yang, Xinyu Wang, Chongying Wang. Hydrogen sulfide enhances nitric oxide-induced tolerance of hypoxia in maize (Zea mays L.).
Plant cell reports.
2016 Nov; 35(11):2325-2340. doi:
10.1007/s00299-016-2037-4. [PMID: 27516180] - Navjot Singh Athwal, Jagannathan Alagurajan, Amy H Andreotti, Mark S Hargrove. Role of Reversible Histidine Coordination in Hydroxylamine Reduction by Plant Hemoglobins (Phytoglobins).
Biochemistry.
2016 10; 55(41):5809-5817. doi:
10.1021/acs.biochem.6b00775. [PMID: 27661977] - Qien Li, Zhaofeng Wang, Yanning Zhao, Xiaochen Zhang, Shuaijun Zhang, Letao Bo, Yao Wang, Yingfeng Ding, Lizhe An. Putrescine protects hulless barley from damage due to UV-B stress via H2S- and H2O2-mediated signaling pathways.
Plant cell reports.
2016 May; 35(5):1155-68. doi:
10.1007/s00299-016-1952-8. [PMID: 26910861] - Kevin C Honeychurch, Joshua Brooks, John P Hart. Development of a voltammetric assay, using screen-printed electrodes, for clonazepam and its application to beverage and serum samples.
Talanta.
2016 Jan; 147(?):510-5. doi:
10.1016/j.talanta.2015.10.032. [PMID: 26592640] - Ravi Kant Bhatia, Shashi Kant Bhatia, Praveen Kumar Mehta, Tek Chand Bhalla. Bio-statistical enhancement of acyl transfer activity of amidase for biotransformation of N-substituted aromatic amides.
The Journal of general and applied microbiology.
2016; 62(2):90-7. doi:
10.2323/jgam.62.90. [PMID: 27118077] - Charles Darkoh, Cynthia Chappell, Christopher Gonzales, Pablo Okhuysen. A rapid and specific method for the detection of indole in complex biological samples.
Applied and environmental microbiology.
2015 Dec; 81(23):8093-7. doi:
10.1128/aem.02787-15. [PMID: 26386049] - Omar Alharbi, Yun Xu, Royston Goodacre. Detection and quantification of the opioid tramadol in urine using surface enhanced Raman scattering.
The Analyst.
2015 Sep; 140(17):5965-70. doi:
10.1039/c5an01177a. [PMID: 26194152] - Navjot Singh Athwal, Jagannathan Alagurajan, Ryan Sturms, D Bruce Fulton, Amy H Andreotti, Mark S Hargrove. Electron self-exchange in hemoglobins revealed by deutero-hemin substitution.
Journal of inorganic biochemistry.
2015 Sep; 150(?):139-47. doi:
10.1016/j.jinorgbio.2015.06.014. [PMID: 26141377] - Jie Xiong, Yongjie Yang, Guanfu Fu, Longxing Tao. Novel roles of hydrogen peroxide (H₂O₂) in regulating pectin synthesis and demethylesterification in the cell wall of rice (Oryza sativa) root tips.
The New phytologist.
2015 Apr; 206(1):118-126. doi:
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Synapse (New York, N.Y.).
2015 Mar; 69(3):128-38. doi:
10.1002/syn.21793. [PMID: 25482019] - Elisabeth Haller, Gerald Stübiger, Daniel Lafitte, Wolfgang Lindner, Michael Lämmerhofer. Chemical recognition of oxidation-specific epitopes in low-density lipoproteins by a nanoparticle based concept for trapping, enrichment, and liquid chromatography-tandem mass spectrometry analysis of oxidative stress biomarkers.
Analytical chemistry.
2014 Oct; 86(19):9954-61. doi:
10.1021/ac502855n. [PMID: 25219896] - Tomás Herraiz, Juan Galisteo. Naturally-occurring tetrahydro-β-carboline alkaloids derived from tryptophan are oxidized to bioactive β-carboline alkaloids by heme peroxidases.
Biochemical and biophysical research communications.
2014 Aug; 451(1):42-7. doi:
10.1016/j.bbrc.2014.07.047. [PMID: 25035927] - Jan T Kielstein, Hans-Gert Bernstein. The reversible part of cognitive impairment in chronic kidney disease: can mice help men break the TEMPOLimit?.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
2014 Mar; 29(3):476-8. doi:
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Neuroscience.
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