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1

Chopra, Deepak, T. P. Mohan, K. S. Sreedhar, and T. N. Guru Row. "4-Fluoro-3-phenoxybenzoic acid." Acta Crystallographica Section E Structure Reports Online 61, no. 10 (2005): o3228—o3229. http://dx.doi.org/10.1107/s160053680502831x.

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2

Kondo, Miwa, Hiroko Kikumoto, Thomas G. Osimitz, Samuel M. Cohen, Brian G. Lake, and Tomoya Yamada. "An Evaluation of the Human Relevance of the Liver Tumors Observed in Female Mice Treated With Permethrin Based on Mode of Action." Toxicological Sciences 175, no. 1 (2020): 50–63. http://dx.doi.org/10.1093/toxsci/kfaa017.

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Abstract In 2-year studies, the nongenotoxic pyrethroid insecticide permethrin produced hepatocellular tumors in CD-1 mice but not in Wistar rats. Recently, we demonstrated that the mode of action (MOA) for mouse liver tumor formation by permethrin involves activation of the peroxisome proliferator-activated receptor alpha (PPARα), resulting in a mitogenic effect. In the present study, the effects of permethrin and 2 major permethrin metabolites, namely 3-phenoxybenzoic acid and trans-dichlorochrysanthemic acid, on cytochrome P450 mRNA levels and cell proliferation (determined as replicative D
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3

Popov, Yu V., V. S. Lobasenko, A. K. Novikova, A. I. Yakovlev, and T. A. Chernykhova. "SYNTHESIS OF NEW 3-PHENOXYBENZOIC ACID DERIVATIVES." Izvestia Volgograd State Technical University, no. 12 (2022): 78–82. http://dx.doi.org/10.35211/1990-5297-2022-12-271-78-82.

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4

LOBASENKO, V. S., YU A. BARYSHEVA, and A. I. YAKOVLEV. "SYNTHESIS OF 2-(3-PHENOXYPHENYL)ALKYLYLIMIDAZOLINES." IZVESTIA VOLGOGRAD STATE TECHNICAL UNIVERSITY, no. 5(288) (May 2024): 57–59. http://dx.doi.org/10.35211/1990-5297-2024-5-288-57-59.

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5

Jackson, Victoria J., Yuliana Yosaatmadja, Jack U. Flanagan, and Christopher J. Squire. "Structure of AKR1C3 with 3-phenoxybenzoic acid bound." Acta Crystallographica Section F Structural Biology and Crystallization Communications 68, no. 4 (2012): 409–13. http://dx.doi.org/10.1107/s1744309112009049.

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6

Chen, Shaohua, Wei Hu, Ying Xiao, Yinyue Deng, Jianwen Jia, and Meiying Hu. "Degradation of 3-Phenoxybenzoic Acid by a Bacillus sp." PLoS ONE 7, no. 11 (2012): e50456. http://dx.doi.org/10.1371/journal.pone.0050456.

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7

Spasov, A. A., Yu V. Popov, V. S. Lobasenko, et al. "Synthesis and pharmacological activity of 3-phenoxybenzoic acid derivatives." Russian Journal of Bioorganic Chemistry 43, no. 2 (2017): 163–69. http://dx.doi.org/10.1134/s1068162017020145.

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8

Akhtar, M. Hurriayoun, S. Mahadevan, and Faye Russell. "Cleavage of 3-phenoxybenzoic acid by chicken microsomal preparations." Journal of Environmental Science and Health, Part B 28, no. 5 (1993): 527–43. http://dx.doi.org/10.1080/03601239309372840.

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9

Spasov, A. A., V. S. Lobasenko, V. A. Kosolapov, et al. "Synthesis and Pharmacological Activity of 3-Phenoxybenzoic Acid Derivatives." Pharmaceutical Chemistry Journal 54, no. 3 (2020): 229–35. http://dx.doi.org/10.1007/s11094-020-02185-z.

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10

BURKE, ALISON B., PETER MILLBURN, and KEITH R. HUCKLE. "The metabolism of 3-phenoxybenzoic acid and of benzoic acid in fish." Biochemical Society Transactions 16, no. 1 (1988): 24–25. http://dx.doi.org/10.1042/bst0160024.

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11

Akhtar, M. Humayoun, S. Mahadevan, and Alenka Paquet. "Comparative metabolism of deltamethrin and 3-phenoxybenzoic acid in chickens." Journal of Environmental Science and Health, Part B 29, no. 3 (1994): 369–94. http://dx.doi.org/10.1080/03601239409372886.

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12

Katagi, Toshiyuki. "Photodegradation of 3-phenoxybenzoic acid in water and on solid surfaces." Journal of Agricultural and Food Chemistry 40, no. 7 (1992): 1269–74. http://dx.doi.org/10.1021/jf00019a038.

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13

Hardt, Jochen. "Ibuprofen interference in the determination of 3-phenoxybenzoic acid in urine." Fresenius’ Journal of Analytical Chemistry 371, no. 6 (2001): 787–90. http://dx.doi.org/10.1007/s002160100928.

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14

Imhof, D. A., C. J. Logan, and P. F. Dodds. "Synthesis op 3-phenoxybenzoic acid-containing lipids via the monoacylglycerol pathway." Biochemical Pharmacology 34, no. 16 (1985): 3009–10. http://dx.doi.org/10.1016/0006-2952(85)90033-4.

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15

Chen, Hongping, Xinlu Wang, Pingxiang Liu, et al. "Determination of Three Typical Metabolites of Pyrethroid Pesticides in Tea Using a Modified QuEChERS Sample Preparation by Ultra-High Performance Liquid Chromatography Tandem Mass Spectrometry." Foods 10, no. 1 (2021): 189. http://dx.doi.org/10.3390/foods10010189.

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Pyrethroid pesticides are widely used on tea plants, and their residues of high frequency and concentration have received great attention. Until recently, the residues of typical metabolites of pyrethroid pesticides in tea were unknown. Herein, a modified “quick, easy, cheap, effective, rugged and safe” (QuEChERS) method for the determination of three typical metabolites of pyrethroid pesticides in tea, using ultra performance liquid chromatography tandem mass spectrometry, was developed. The mixture of florisil, octadecylsilane, and graphite carbon black was employed as modified QuEChERS adso
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16

Ishimatsu, Ryoichi, Shinichi Shimizu, Surat Hongsibsong, et al. "Enzyme-linked immunosorbent assay based on light absorption of enzymatically generated aniline oligomer: Flow injection analysis for 3-phenoxybenzoic acid with anti-3-phenoxybenzoic acid monoclonal antibody." Talanta 218 (October 2020): 121102. http://dx.doi.org/10.1016/j.talanta.2020.121102.

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17

López-Gálvez, Nicolás, Rietta Wagoner, Paloma Beamer, Jill de Zapien, and Cecilia Rosales. "Migrant Farmworkers’ Exposure to Pesticides in Sonora, Mexico." International Journal of Environmental Research and Public Health 15, no. 12 (2018): 2651. http://dx.doi.org/10.3390/ijerph15122651.

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Expanding agribusiness in Sonora, a state in Northern Mexico, has increased the demand for temporary migrant agricultural workers. Sonora is one of the top states in Mexico for pesticide utilization. We conducted an exploratory study to evaluate exposure to organophosphate (OP) and pyrethroid pesticides among migrant farmworkers. A sample of 20 migrant farmworkers was recruited from a large commercial grape farm during the harvest season. We administered a questionnaire on work activities, exposure characteristics, and socio-demographics. We collected urine samples to quantify pesticide metabo
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18

Morgan, Marsha, Paul Jones, Jon Sobus, and Dana Boyd Barr. "Predictors of Urinary 3-Phenoxybenzoic Acid Levels in 50 North Carolina Adults." International Journal of Environmental Research and Public Health 13, no. 11 (2016): 1172. http://dx.doi.org/10.3390/ijerph13111172.

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19

Jo, Hye Mi, Mina Ha, and Won Jin Lee. "Urinary concentration of 3-phenoxybenzoic acid in elementary students in South Korea." Environmental Health and Toxicology 30 (October 13, 2015): e2015009. http://dx.doi.org/10.5620/eht.e2015009.

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20

Akhtar, M. H., and S. Mahadevan. "Diphenyl ether cleavage of 3-phenoxybenzoic acid by chicken kidney microsomal preparations." Drug Metabolism and Disposition 20, no. 3 (1992): 356–59. https://doi.org/10.1016/s0090-9556(25)08576-9.

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21

Richards, Jaben, Zhijiang Lu, Qiuguo Fu, Daniel Schlenk, and Jay Gan. "Conversion of Pyrethroid Insecticides to 3-Phenoxybenzoic Acid on Urban Hard Surfaces." Environmental Science & Technology Letters 4, no. 12 (2017): 546–50. http://dx.doi.org/10.1021/acs.estlett.7b00466.

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22

Smpokou, Evangelia-Theano, Marvin González-Quiroz, Carla Martins, et al. "Environmental exposures in young adults with declining kidney function in a population at risk of Mesoamerican nephropathy." Occupational and Environmental Medicine 76, no. 12 (2019): 920–26. http://dx.doi.org/10.1136/oemed-2019-105772.

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ObjectivesThere is an epidemic of Mesoamerican nephropathy (MeN) in Central America, where sugarcane production is prominent. Numerous causes are proposed, but to date limited evidence supports any one hypothesis. A nested case–control study using biosamples from a rural, community-based follow-up study of 350 young adults from Northwest Nicaragua at risk of MeN was conducted with the aim of characterising the associations between urinary concentrations of metals, pesticides and mycotoxins from samples collected in the first 6 months and decline in kidney function over 2 years.MethodsUrine sam
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23

Wang, Xia, Bingnan He, Baida Kong та ін. "β-Cypermethrin and its metabolite 3-phenoxybenzoic acid exhibit immunotoxicity in murine macrophages". Acta Biochimica et Biophysica Sinica 49, № 12 (2017): 1083–91. http://dx.doi.org/10.1093/abbs/gmx111.

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24

Riederer, Anne M., Scott M. Bartell, Dana B. Barr, and P. Barry Ryan. "Diet and Nondiet Predictors of Urinary 3-Phenoxybenzoic Acid in NHANES 1999–2002." Environmental Health Perspectives 116, no. 8 (2008): 1015–22. http://dx.doi.org/10.1289/ehp.11082.

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25

Mikami, Nobuyoshi, Jun Yoshimura, Hideo Kaneko, Hirohiko Yamada, and Junshi Miyamoto. "Metabolism in rats of 3-phenoxybenzyl alcohol and 3-phenoxybenzoic acid glucoside conjugates formed in plants." Pesticide Science 16, no. 1 (1985): 33–45. http://dx.doi.org/10.1002/ps.2780160106.

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26

Chuang, Jane C., Jeanette M. Van Emon, Raquel M. Trejo, and Joyce Durnford. "Biological monitoring of 3-phenoxybenzoic acid in urine by an enzyme-linked immunosorbent assay." Talanta 83, no. 5 (2011): 1317–23. http://dx.doi.org/10.1016/j.talanta.2010.07.077.

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27

Tarazona, Jose V., Irene Cattaneo, Lars Niemann, et al. "A Tiered Approach for Assessing Individual and Combined Risk of Pyrethroids Using Human Biomonitoring Data." Toxics 10, no. 8 (2022): 451. http://dx.doi.org/10.3390/toxics10080451.

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Pyrethroids are a major insecticide class, suitable for biomonitoring in humans. Due to similarities in structure and metabolic pathways, urinary metabolites are common to various active substances. A tiered approach is proposed for risk assessment. Tier I was a conservative screening for overall pyrethroid exposure, based on phenoxybenzoic acid metabolites. Subsequently, probabilistic approaches and more specific metabolites were used for refining the risk estimates. Exposure was based on 95th percentiles from HBM4EU aligned studies (2014–2021) covering children in Belgium, Cyprus, France, Is
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28

Halden, Rolf U., Sandra M. Tepp, Barbara G. Halden, and Daryl F. Dwyer. "Degradation of 3-Phenoxybenzoic Acid in Soil byPseudomonas pseudoalcaligenes POB310(pPOB) and Two ModifiedPseudomonas Strains." Applied and Environmental Microbiology 65, no. 8 (1999): 3354–59. http://dx.doi.org/10.1128/aem.65.8.3354-3359.1999.

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ABSTRACT Pseudomonas pseudoalcaligenes POB310(pPOB) andPseudomonas sp. strains B13-D5(pD30.9) and B13-ST1(pPOB) were introduced into soil microcosms containing 3-phenoxybenzoic acid (3-POB) in order to evaluate and compare bacterial survival, degradation of 3-POB, and transfer of plasmids to a recipient bacterium. Strain POB310 was isolated for its ability to use 3-POB as a growth substrate; degradation is initiated by POB-dioxygenase, an enzyme encoded on pPOB. Strain B13-D5 contains pD30.9, a cloning vector harboring the genes encoding POB-dioxygenase; strain B13-ST1 contains pPOB. Degradati
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29

Baek, Jong-Beom, Christopher B. Lyons, and Loon-Seng Tan. "Grafting of Vapor-Grown Carbon Nanofibers via in-Situ Polycondensation of 3-Phenoxybenzoic Acid in Poly(phosphoric acid)." Macromolecules 37, no. 22 (2004): 8278–85. http://dx.doi.org/10.1021/ma048964o.

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30

Popov, Yu V., T. K. Korchagina, V. S. Lobasenko, S. V. Anikeeva, and K. L. No. "PROCESS OF OBTAINING HYDROCHLORIDES OF IMMATES OF 3-PHENOXYBENZOIC ACID ON THE PINNER REACTION OPTIMIZATION." PROCEEDINGS OF UNIVERSITIES APPLIED CHEMISTRY AND BIOTECHNOLOGY 8, no. 2 (2018): 29–38. http://dx.doi.org/10.21285/2227-2925-2018-8-2-29-38.

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31

ASAKAWA, Fumiyuki, Fumihiko JITUNARI, Sigeru SUNA, JIN-OK Choi, Yoshiki MANABE, and Noriaki TAKEDA. "Determination of 3-Phenoxybenzoic Acid in Urine of Workers Exposed to Permethrin Using GC-MS." Sangyo Igaku 36, no. 5 (1994): 324–25. http://dx.doi.org/10.1539/joh1959.36.5_324.

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32

Kotova, Oxana, Valentina Utochnikova, Sergej Samoilenkov, and Natalia P. Kuzmina. "Thin Films of Tb(pobz)3 (Hpobz = 2-phenoxybenzoic acid): Reactive CVD and Optical Properties." ECS Transactions 25, no. 8 (2019): 1107–14. http://dx.doi.org/10.1149/1.3207713.

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33

Quistad, G. B., A. L. Saunders, W. S. Skinner, K. D. Collier, D. H. Sakai, and C. C. Reuter. "O-dephenylation and conjugation with benzoylornithine. New metabolic pathways for 3-phenoxybenzoic acid in chickens." Drug Metabolism and Disposition 16, no. 6 (1988): 818–22. https://doi.org/10.1016/s0090-9556(25)07042-4.

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34

Hirosawa, Naoko, Jun Ueyama, Takaaki Kondo, et al. "Effect of DDVP on urinary excretion levels of pyrethroid metabolite 3-phenoxybenzoic acid in rats." Toxicology Letters 203, no. 1 (2011): 28–32. http://dx.doi.org/10.1016/j.toxlet.2011.02.016.

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35

Ueyama, Jun, Akiko Kimata, Michihiro Kamijima, et al. "Urinary excretion of 3-phenoxybenzoic acid in middle-aged and elderly general population of Japan." Environmental Research 109, no. 2 (2009): 175–80. http://dx.doi.org/10.1016/j.envres.2008.09.006.

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36

Zhao, Jiayuan, Dongying Jia, Yuanlong Chi, and Kai Yao. "Co-metabolic enzymes and pathways of 3-phenoxybenzoic acid degradation by Aspergillus oryzae M-4." Ecotoxicology and Environmental Safety 189 (February 2020): 109953. http://dx.doi.org/10.1016/j.ecoenv.2019.109953.

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37

Fortes, C., S. Mastroeni, M. A. Pilla, G. Antonelli, L. Lunghini, and C. Aprea. "The relation between dietary habits and urinary levels of 3-phenoxybenzoic acid, a pyrethroid metabolite." Food and Chemical Toxicology 52 (February 2013): 91–96. http://dx.doi.org/10.1016/j.fct.2012.10.035.

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38

Zhao, Jiayuan, Xiaofeng Chen, Dongying Jia, and Kai Yao. "Identification of fungal enzymes involving 3-phenoxybenzoic acid degradation by using enzymes inhibitors and inducers." MethodsX 7 (2020): 100772. http://dx.doi.org/10.1016/j.mex.2019.100772.

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39

Hu, Kaidi, Jianlong Li, Tianye Zhao, et al. "Transcriptomic analysis reveals peripheral pathway in 3-phenoxybenzoic acid degradation by Aspergillus oryzae M-4." Journal of Environmental Management 325 (January 2023): 116626. http://dx.doi.org/10.1016/j.jenvman.2022.116626.

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40

Ahn, Ki Chang, Shirley J. Gee, Hee-Joo Kim, et al. "Immunochemical analysis of 3-phenoxybenzoic acid, a biomarker of forestry worker exposure to pyrethroid insecticides." Analytical and Bioanalytical Chemistry 401, no. 4 (2011): 1285–93. http://dx.doi.org/10.1007/s00216-011-5184-z.

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41

Pali, Madhavi, Candace R. S. Bever, Natalia Vasylieva, Bruce D. Hammock, and Ian I. Suni. "Impedance Detection of 3-Phenoxybenzoic Acid with a Noncompetitive Two-site Phage Anti-immunocomplex Assay." Electroanalysis 30, no. 11 (2018): 2653–59. http://dx.doi.org/10.1002/elan.201800457.

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42

Pali, Madhavi, and Ian I. Suni. "Impedance Detection of 3‐Phenoxybenzoic Acid Comparing Wholes Antibodies and Antibody Fragments for Biomolecular Recognition." Electroanalysis 30, no. 12 (2018): 2899–907. http://dx.doi.org/10.1002/elan.201800495.

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43

Tang, Jie, Qiong Hu, Bo Liu, et al. "Efficient biodegradation of 3-phenoxybenzoic acid and pyrethroid pesticides by the novel strain Klebsiella pneumoniae BPBA052." Canadian Journal of Microbiology 65, no. 11 (2019): 795–804. http://dx.doi.org/10.1139/cjm-2019-0183.

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A novel Klebsiella pneumoniae strain (BPBA052) capable of degrading 3-phenoxybenzoic acid (3-PBA) was isolated from soybean rhizosphere soil. The strain was obtained by screening after enrichment, isolation, and purification using 3-PBA as the sole carbon and energy source. It could degrade 96.37% of 3-PBA (100 mg/L) within 72 h, and its growth and 3-PBA degradation followed kinetics models of logistic growth (XBPBA052 = 0.0883 × e0.0947t / [1 − 0.0792 × (1 − 0.0883 × e0.0947t)]; μm = 0.0947 h–1, X0 = 0.0883, and Xm = 1.1145) and first-order degradation (CBPBA052 = 101.8194 × e–0.0403t, k = 0.
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44

Zhang, Jun, Zhi-Fei Lang, Jin-Wei Zheng, et al. "Sphingobium jiangsuense sp. nov., a 3-phenoxybenzoic acid-degrading bacterium isolated from a wastewater treatment system." International Journal of Systematic and Evolutionary Microbiology 62, Pt_4 (2012): 800–805. http://dx.doi.org/10.1099/ijs.0.029827-0.

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A non-sporulating, non-motile, catalase- and oxidase-positive, Gram-negative, rod-shaped bacterial strain, designated BA-3T, was isolated from activated sludge of a wastewater treatment facility. The strain was able to degrade about 95 % of 100 mg 3-phenoxybenzoic acid l−1 within 2 days of incubation. Growth occurred in the presence of 0–2 % (w/v) NaCl [optimum, 0.5 % (w/v) NaCl], at pH 5.5–9.0 (optimum, pH 7.0) and at 10–37 °C (optimum, 28 °C). Phylogenetic analysis based on 16S rRNA gene sequence comparisons revealed that strain BA-3T was a member of the genus Sphingobium ; it showed highest
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45

He, Jinxin, Mi Zhu, Xiaorong Chen, Shengrui Shi, Fang Tang, and Shaopeng Gu. "Multivalent nanobody–biotin amplified enzyme-linked immunosorbent assay for the environmental detection of 3-phenoxybenzoic acid." Analytical Methods 13, no. 43 (2021): 5247–53. http://dx.doi.org/10.1039/d1ay01491a.

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46

XIE, Wen-Jun, Jian-Min ZHOU, Huo-Yan WANG, and Xiao-Qin CHEN. "Effect of Nitrogen on the Degradation of Cypermethrin and Its Metabolite 3-Phenoxybenzoic Acid in Soil." Pedosphere 18, no. 5 (2008): 638–44. http://dx.doi.org/10.1016/s1002-0160(08)60058-2.

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47

Liu, Yuan, Aihua Wu, Jing Hu, et al. "Detection of 3-phenoxybenzoic acid in river water with a colloidal gold-based lateral flow immunoassay." Analytical Biochemistry 483 (August 2015): 7–11. http://dx.doi.org/10.1016/j.ab.2015.04.022.

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48

Jin-Ok, Choi, Fumihiko Jitsunari, Fumiyuki Asakawa, Shigeru Suna, Yoshiki Manabe, and Noriaki Takeda. "Study on biological monitoring of fenpropathrin exposure in application by utilizing urinary 3-phenoxybenzoic acid level." Environmental Health and Preventive Medicine 2, no. 4 (1998): 145–50. http://dx.doi.org/10.1007/bf02931692.

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49

Kuder, Reshma Shabnam, and Harold Philip Gundala. "Developmental toxicity of deltamethrin and 3-phenoxybenzoic acid in embryo–larval stages of zebrafish (Danio rerio)." Toxicology Mechanisms and Methods 28, no. 6 (2018): 415–22. http://dx.doi.org/10.1080/15376516.2018.1439131.

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50

Wang, He, Yanjie Wu, and Hongwei Song. "Synergistic effects of photonic crystal and gold nanostars for quantitative SERS detection of 3-Phenoxybenzoic acid." Applied Surface Science 476 (May 2019): 587–93. http://dx.doi.org/10.1016/j.apsusc.2019.01.061.

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