1-Naphthol (BioDeep_00000002138)
Secondary id: BioDeep_00000868150
human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite
代谢物信息卡片
化学式: C10H8O (144.0575118)
中文名称: 萘酚, 1-萘酚
谱图信息:
最多检出来源 Homo sapiens(blood) 0.17%
分子结构信息
SMILES: C1=CC=C2C(=C1)C=CC=C2O
InChI: InChI=1S/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H
描述信息
1-Naphthol, or ?-naphthol, is a colorless crystalline solid with the formula C10H7OH. It is an isomer of 2-naphthol differing by the location of the hydroxyl group on naphthalene. The naphthols are naphthalene homologues of phenol, with the hydroxyl group being more reactive than in the phenols. Both isomers are soluble in simple alcohols, ethers, and chloroform. They can be used in the production of dyes and in organic synthesis.; 1-naphthol (1N) is a metabolite of carbaryl and naphthalene that is an intermediate in Metabolism of xenobiotics by cytochrome P450. It is generated by spontaneous reaction from (1R,2S)-Naphthalene epoxide then is it converted to 1,4-Dihydroxynaphthalene. Although 1-Naphthol is not persistent in the body, a single urine sample may adequately predict exposure over several months to chlorpyrifos, which is a broad-spectrum organophosphate insecticide. In adult men, TCPY and 1N were associated with reduced testosterone levels (PMID: 16357596, 15579421). Naphthalen-1-ol is found in black walnut.
1-naphthol (1N) is a metabolite of carbaryl and naphthalene that is an intermediate in Metabolism of xenobiotics by cytochrome P450. It is generated by spontaneous reaction from (1R,2S)-Naphthalene epoxide then is it converted to 1,4-Dihydroxynaphthalene. Although 1-Naphthol is not persistent in the body, a single urine sample may adequately predict exposure over several months to chlorpyrifos, which is a broad-spectrum organophosphate insecticide. In adult men, TCPY and 1N were associated with reduced testosterone levels (PMID:16357596, 15579421).
CONFIDENCE standard compound; INTERNAL_ID 1136; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8253; ORIGINAL_PRECURSOR_SCAN_NO 8251
CONFIDENCE standard compound; INTERNAL_ID 1136; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9487; ORIGINAL_PRECURSOR_SCAN_NO 9486
CONFIDENCE standard compound; INTERNAL_ID 1136; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8287; ORIGINAL_PRECURSOR_SCAN_NO 8285
ORIGINAL_PRECURSOR_SCAN_NO 9486; CONFIDENCE standard compound; INTERNAL_ID 1136; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9487
CONFIDENCE standard compound; INTERNAL_ID 1136; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4807; ORIGINAL_PRECURSOR_SCAN_NO 4806
CONFIDENCE standard compound; INTERNAL_ID 1136; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4732; ORIGINAL_PRECURSOR_SCAN_NO 4731
CONFIDENCE standard compound; INTERNAL_ID 1136; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9506; ORIGINAL_PRECURSOR_SCAN_NO 9505
CONFIDENCE standard compound; INTERNAL_ID 1136; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4804; ORIGINAL_PRECURSOR_SCAN_NO 4799
CONFIDENCE standard compound; INTERNAL_ID 1136; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4717; ORIGINAL_PRECURSOR_SCAN_NO 4715
CONFIDENCE standard compound; INTERNAL_ID 1136; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8261; ORIGINAL_PRECURSOR_SCAN_NO 8259
CONFIDENCE standard compound; INTERNAL_ID 1136; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4771; ORIGINAL_PRECURSOR_SCAN_NO 4767
CONFIDENCE standard compound; INTERNAL_ID 1136; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8267; ORIGINAL_PRECURSOR_SCAN_NO 8265
CONFIDENCE standard compound; INTERNAL_ID 1136; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4779; ORIGINAL_PRECURSOR_SCAN_NO 4777
CONFIDENCE standard compound; INTERNAL_ID 46
1-naphthol is an excited state proton transfer (ESPT) fluorescent molecular probe.
1-naphthol is an excited state proton transfer (ESPT) fluorescent molecular probe.
同义名列表
35 个代谢物同义名
1-Naphthol, 1-(14)C-labeled; 1-Naphthol, 2-(13)C-labeled; 1-Naphthol, potassium salt; α-Hydroxynaphthalene; 1-Naphthol, lithium salt; α-Naphthyl alcohol; alpha-Hydroxynaphthalene; 1-Naphthol, sodium salt; alpha-Naphthyl alcohol; 1-Hydroxynaphthalene; Α-hydroxynaphthalene; a-Hydroxynaphthalene; Durafur developer D; 1-Naphthol, ion(1+); 1-Naphthyl alcohol; α-Naphthol; naphthalen-1-ol; BASF ursol ern; alpha-Naphthol; 1-Naphthalenol; Naphthyl-1-ol; Fouramine ern; Fourrine ern; Tertral ern; Fourrine 99; 1-NAPHTHOL; Α-naphthol; a-Naphthol; Naphthol-1; Ursol ern; naphthol; furro ER; Zoba ern; nako TRB; NSC 9586
数据库引用编号
34 个数据库交叉引用编号
- ChEBI: CHEBI:10319
- KEGG: C11714
- PubChem: 7005
- HMDB: HMDB0012138
- Metlin: METLIN62807
- ChEMBL: CHEMBL122617
- Wikipedia: 1-Naphthol
- MetaCyc: NAPHTHOL
- foodb: FDB005841
- chemspider: 6739
- CAS: 50356-21-3
- CAS: 1321-67-1
- CAS: 90-15-3
- MoNA: LU113601
- MoNA: UA004601
- MoNA: LU113653
- MoNA: LU113604
- MoNA: LU113655
- MoNA: LU113606
- MoNA: LU113603
- MoNA: LU113652
- MoNA: UA004603
- MoNA: LU113605
- MoNA: LU113654
- MoNA: UA004604
- MoNA: LU113651
- MoNA: LU113656
- MoNA: LU113602
- PMhub: MS000001918
- PubChem: 13879
- PDB-CCD: 1NP
- NIKKAJI: J3.911J
- RefMet: 1-Naphthol
- medchemexpress: HY-Y1309
分类词条
相关代谢途径
Reactome(0)
PlantCyc(0)
代谢反应
64 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(2)
- phenolic malonylglucosides biosynthesis:
2-naphthol glucoside + malonyl-CoA ⟶ 2-naphthol 6'-O-malonylglucoside + coenzyme A
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(61)
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol glucoside + malonyl-CoA ⟶ 2-naphthol 6'-O-malonylglucoside + coenzyme A
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol glucoside + malonyl-CoA ⟶ 2-naphthol 6'-O-malonylglucoside + coenzyme A
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
- phenolic malonylglucosides biosynthesis:
2-naphthol glucoside + malonyl-CoA ⟶ 2-naphthol 6'-O-malonylglucoside + coenzyme A
- phenolic malonylglucosides biosynthesis:
2-naphthol + UDP-α-D-glucose ⟶ 2-naphthol glucoside + H+ + UDP
COVID-19 Disease Map(0)
PathBank(1)
- Phenolic Malonylglucosides Biosynthesis:
2-Naphthol + Uridine diphosphate glucose ⟶ 2-naphthol glucoside + Hydrogen Ion + Uridine 5'-diphosphate
PharmGKB(0)
4 个相关的物种来源信息
- 81733 - Hemerocallis minor: -
- 9606 - Homo sapiens: -
- 16719 - Juglans nigra: 10.1080/10412905.1992.9698128
- 137174 - Selaginella sinensis: 10.1007/S10600-012-0230-4
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
- Najjapak Sooksawat, Duangrat Inthorn, Apisit Chittawanij, Alisa Vangnai, Pornpimol Kongtip, Susan Woskie. Phytoextraction Potential of Sunn Hemp, Sunflower, and Marigold for Carbaryl Contamination: Hydroponic Experiment.
International journal of environmental research and public health.
2022 12; 19(24):. doi:
10.3390/ijerph192416482
. [PMID: 36554374] - Zi-Jian Chen, Hui-Ling Wu, Yu-Dong Shen, Hong Wang, Yi-Feng Zhang, Bruce Hammock, Zhen-Feng Li, Lin Luo, Hong-Tao Lei, Zhen-Lin Xu. Phosphate-triggered ratiometric fluoroimmunoassay based on nanobody-alkaline phosphatase fusion for sensitive detection of 1-naphthol for the exposure assessment of pesticide carbaryl.
Journal of hazardous materials.
2022 02; 424(Pt C):127411. doi:
10.1016/j.jhazmat.2021.127411
. [PMID: 34629198] - Zhiping Che, Song Zhang, Jiaxuan He, Di Sun, Xiaolong Guo, Yuanhao Li, Lina Zhu, Yihao Guo, Yibo Liu, Yuee Tian, Xiaobo Huang, Shengming Liu, Genqiang Chen. Combinatorial Synthesis of Sulfonate Derivatives of α/β-Naphthol as Anti- Oomycete Agents.
Combinatorial chemistry & high throughput screening.
2022; 25(12):2026-2032. doi:
10.2174/1386207325666220128120208
. [PMID: 35088660] - Max Petitjean, José Ramón Isasi. Chitosan, xanthan and locust bean gum matrices crosslinked with β-cyclodextrin as green sorbents of aromatic compounds.
International journal of biological macromolecules.
2021 Jun; 180(?):570-577. doi:
10.1016/j.ijbiomac.2021.03.098
. [PMID: 33753196] - Zi-Jian Chen, Xi-Xia Liu, Zhi-Li Xiao, Hui-Jun Fu, Yu-Ping Huang, Shu-Yi Huang, Yu-Dong Shen, Fan He, Xing-Xing Yang, Bruce Hammock, Zhen-Lin Xu. Production of a specific monoclonal antibody for 1-naphthol based on novel hapten strategy and development of an easy-to-use ELISA in urine samples.
Ecotoxicology and environmental safety.
2020 Jun; 196(?):110533. doi:
10.1016/j.ecoenv.2020.110533
. [PMID: 32247241] - Akito Takeuchi, Sadao Nakamura, Akira Namera, Tomoaki Kondo, Hiroyuki Onuki, Shinobu Yamamoto, Shingo Okamura, Osamu Nishinoiri, Yoko Endo, Hiroyuki Miyauchi, Ginji Endo. Simple and reliable method to simultaneously determine urinary 1- and 2-naphthol using in situ derivatization and gas chromatography-mass spectrometry for biological monitoring of naphthalene exposure in occupational health practice.
Journal of occupational health.
2020 Jan; 62(1):e12144. doi:
10.1002/1348-9585.12144
. [PMID: 32713100] - Katrin Klotz, Tobias Weiß, Melanie Zobel, Daniel Bury, Dietmar Breuer, Silke Werner, Kirsten Sucker, Wolfgang Zschiesche, Thomas Göen, Thomas Brüning, Hans Drexler. Validity of different biomonitoring parameters in human urine for the assessment of occupational exposure to naphthalene.
Archives of toxicology.
2019 08; 93(8):2185-2195. doi:
10.1007/s00204-019-02468-9
. [PMID: 31222524] - Dan Huang, Tiecheng Wang, Kecheng Zhu, Song Zhao, Yafang Shi, Mao Ye, Chuanyi Wang, Hanzhong Jia. Low-molecular-weight organic acids impede the degradation of naphthol in iron oxides/persulfate systems: Implications for research experiments in pure conditions.
Chemosphere.
2019 Jun; 225(?):1-8. doi:
10.1016/j.chemosphere.2019.02.127
. [PMID: 30852260] - Wenyong Hu, Xiaobo Min, Xinyu Li, Jingyi Liu, Haibin Yu, Yuan Yang, Jiachao Zhang, Lin Luo, Liyuan Chai, Yaoyu Zhou. Enhanced degradation of 1-naphthol in landfill leachate using Arthrobacter sp.
Environmental technology.
2019 Mar; 40(7):835-842. doi:
10.1080/09593330.2017.1408695
. [PMID: 29168925] - Emila Dziewirska, Michał Radwan, Bartosz Wielgomas, Anna Klimowska, Paweł Radwan, Paweł Kałużny, Wojciech Hanke, Maciej Słodki, Joanna Jurewicz. Human Semen Quality, Sperm DNA Damage, and the Level of Urinary Concentrations of 1N and TCPY, the Biomarkers of Nonpersistent Insecticides.
American journal of men's health.
2019 Jan; 13(1):1557988318816598. doi:
10.1177/1557988318816598
. [PMID: 30813854] - Nicholas A Lentini, Benjamin J Foust, Chia-Hung Christine Hsiao, Andrew J Wiemer, David F Wiemer. Phosphonamidate Prodrugs of a Butyrophilin Ligand Display Plasma Stability and Potent Vγ9 Vδ2 T Cell Stimulation.
Journal of medicinal chemistry.
2018 10; 61(19):8658-8669. doi:
10.1021/acs.jmedchem.8b00655
. [PMID: 30199251] - Kristin J Heaton, Alexis L Maule, Kristen W Smith, Ema G Rodrigues, Michael D McClean, Susan P Proctor. JP8 exposure and neurocognitive performance among US Air Force personnel.
Neurotoxicology.
2017 Sep; 62(?):170-180. doi:
10.1016/j.neuro.2017.07.001
. [PMID: 28687449] - T Berman, T Göen, L Novack, L Beacher, L Grinshpan, D Segev, K Tordjman. Urinary concentrations of organophosphate and carbamate pesticides in residents of a vegetarian community.
Environment international.
2016 Nov; 96(?):34-40. doi:
10.1016/j.envint.2016.08.027
. [PMID: 27588700] - Jitendriya Swain. Molecular level investigation on the interaction of pluronic F127 and human intestinal bile salts using excited state prototropism of 1-naphthol.
Journal of photochemistry and photobiology. B, Biology.
2016 Jul; 160(?):61-7. doi:
10.1016/j.jphotobiol.2016.03.039
. [PMID: 27093000] - Omayma Alshaarawy, Hosam A Elbaz, Michael E Andrew. The association of urinary polycyclic aromatic hydrocarbon biomarkers and cardiovascular disease in the US population.
Environment international.
2016 Apr; 89-90(?):174-8. doi:
10.1016/j.envint.2016.02.006
. [PMID: 26878282] - Phong K Thai, Amy L Heffernan, Leisa-Maree L Toms, Zheng Li, Antonia M Calafat, Peter Hobson, Sara Broomhall, Jochen F Mueller. Monitoring exposure to polycyclic aromatic hydrocarbons in an Australian population using pooled urine samples.
Environment international.
2016 Mar; 88(?):30-35. doi:
10.1016/j.envint.2015.11.019
. [PMID: 26700419] - Chieri Fujino, Yuki Tamura, Satoko Tange, Hiroyuki Nakajima, Seigo Sanoh, Yoko Watanabe, Naoto Uramaru, Hiroyuki Kojima, Kouichi Yoshinari, Shigeru Ohta, Shigeyuki Kitamura. Metabolism of methiocarb and carbaryl by rat and human livers and plasma, and effect on their PXR, CAR and PPARα activities.
The Journal of toxicological sciences.
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