Benzoic acid (BioDeep_00000000313)

 

Secondary id: BioDeep_00000403049

natural product human metabolite PANOMIX_OTCML-2023 blood metabolite Chemicals and Drugs


代谢物信息卡片


ScavengePore(TM) benzoic acid, macroporous, 40-70 mesh, extent of labeling: 0.5-1.5 mmol per g loading

化学式: C7H6O2 (122.0367776)
中文名称: 苯甲酸
谱图信息: 最多检出来源 Homo sapiens(blood) 0.03%

Reviewed

Last reviewed on 2024-06-28.

Cite this Page

Benzoic acid. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/benzoic_acid (retrieved 2024-09-17) (BioDeep RN: BioDeep_00000000313). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: c1ccc(cc1)C(=O)O
InChI: InChI=1/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9)/f/h8H

描述信息

Benzoic acid appears as a white crystalline solid. Slightly soluble in water. The primary hazard is the potential for environmental damage if released. Immediate steps should be taken to limit spread to the environment. Used to make other chemicals, as a food preservative, and for other uses.
Benzoic acid is a compound comprising a benzene ring core carrying a carboxylic acid substituent. It has a role as an antimicrobial food preservative, an EC 3.1.1.3 (triacylglycerol lipase) inhibitor, an EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitor, a plant metabolite, a human xenobiotic metabolite, an algal metabolite and a drug allergen. It is a conjugate acid of a benzoate.
A fungistatic compound that is widely used as a food preservative. It is conjugated to GLYCINE in the liver and excreted as hippuric acid. As the sodium salt form, sodium benzoate is used as a treatment for urea cycle disorders due to its ability to bind amino acids. This leads to excretion of these amino acids and a decrease in ammonia levels. Recent research shows that sodium benzoate may be beneficial as an add-on therapy (1 gram/day) in schizophrenia. Total Positive and Negative Syndrome Scale scores dropped by 21\\\\\% compared to placebo.
Benzoic acid is a Nitrogen Binding Agent. The mechanism of action of benzoic acid is as an Ammonium Ion Binding Activity.
Benzoic acid, C6H5COOH, is a colourless crystalline solid and the simplest aromatic carboxylic acid. Benzoic acid occurs naturally free and bound as benzoic acid esters in many plant and animal species. Appreciable amounts have been found in most berries (around 0.05\\\\\%). Cranberries contain as much as 300-1300 mg free benzoic acid per kg fruit. Benzoic acid is a fungistatic compound that is widely used as a food preservative. It often is conjugated to glycine in the liver and excreted as hippuric acid. Benzoic acid is a byproduct of phenylalanine metabolism in bacteria. It is also produced when gut bacteria process polyphenols (from ingested fruits or beverages).
A fungistatic compound that is widely used as a food preservative. It is conjugated to GLYCINE in the liver and excreted as hippuric acid.
See also: Salicylic Acid (active moiety of); Benzoyl Peroxide (active moiety of); Sodium Benzoate (active moiety of) ... View More ...
Widespread in plants especies in essential oils and fruits, mostly in esterified formand is also present in butter, cooked meats, pork fat, white wine, black and green tea, mushroom and Bourbon vanilla. It is used in foodstuffs as antimicrobial and flavouring agent and as preservative. In practical food preservation, the Na salt of benzoic acid is the most widely used form (see MDQ71-S). The antimicrobial activity comprises a wide range of microorganisms, particularly yeasts and moulds. Undissociated benzoic acid is more effective than dissociated, thus the preservative action is more efficient in acidic foodstuffs. Typical usage levels are 500-2000 ppm. Benzoic acid is found in many foods, some of which are animal foods, common grape, lovage, and fruits.
Benzoic acid, C6H5COOH, is a colourless crystalline solid and the simplest aromatic carboxylic acid. Benzoic acid occurs naturally free and bound as benzoic acid esters in many plant and animal species. Appreciable amounts have been found in most berries (around 0.05\\\\\%). Cranberries contain as much as 300-1300 mg free benzoic acid per kg fruit. Benzoic acid is a fungistatic compound that is widely used as a food preservative. It often is conjugated to glycine in the liver and excreted as hippuric acid. Benzoic acid is a byproduct of phenylalanine metabolism in bacteria. It is also produced when gut bacteria process polyphenols (from ingested fruits or beverages). It can be found in Serratia (PMID:23061754).

Benzoic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=65-85-0 (retrieved 2024-06-28) (CAS RN: 65-85-0). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Benzoic acid is an aromatic alcohol existing naturally in many plants and is a common additive to food, drinks, cosmetics and other products. It acts as preservatives through inhibiting both bacteria and fungi.
Benzoic acid is an aromatic alcohol existing naturally in many plants and is a common additive to food, drinks, cosmetics and other products. It acts as preservatives through inhibiting both bacteria and fungi.

同义名列表

162 个代谢物同义名

ScavengePore(TM) benzoic acid, macroporous, 40-70 mesh, extent of labeling: 0.5-1.5 mmol per g loading; Benzoic acid, puriss. p.a., ACS reagent, reag. Ph. Eur., >=99.9\\% (alkalimetric); Benzoic acid, Pharmaceutical Secondary Standard; Certified Reference Material; Benzoic acid, United States Pharmacopeia (USP) Reference Standard; Benzoic acid, European Pharmacopoeia (EP) Reference Standard; Benzoic acid, Standard for quantitative NMR, TraceCERT(R); Benzoic acid, NIST(R) SRM(R) 39j, calorimetric standard; METHYLAMINOLEVULINATE HYDROCHLORIDE IMPURITY I [EP]; HYDROUS BENZOYL PEROXIDE IMPURITY B [EP IMPURITY]; InChI=1/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9; Benzoic acid, puriss. p.a., ACS reagent, 99.9\\%; GLYCOPYRRONIUM BROMIDE IMPURITY D [EP IMPURITY]; Benzoic Acid Zone Refined (number of passes:20); METRONIDAZOLE BENZOATE IMPURITY C [EP IMPURITY]; Benzoic acid, meets USP testing specifications; Benzoic acid, purified by sublimation, >=99\\%; Benzoic acid, Vetec(TM) reagent grade, 98\\%; Benzoic acid, tested according to Ph.Eur.; Benzoic acid, SAJ special grade, >=99.5\\%; Kendall brand OF benzoic acid sodium salt; Benzoic acid, natural, >=99.5\\%, FCC, FG; Benzoic acid, SAJ first grade, >=99.5\\%; MEFENAMIC ACID IMPURITY D [EP IMPURITY]; 0BE368DC-6DE6-4927-AECF-E4BB2968A4A0; Benzoic acid, ACS reagent, >=99.5\\%; Benzoic acid, ReagentPlus(R), 99\\%; Benzoic acid, analytical standard; TIAPROFENIC ACID IMPURITY D [EP]; Benzoic acid, >=99.5\\%, FCC, FG; Benzoic acid, USP, 99.5-100.5\\%; ACIDUM BENZOICUM [WHO-IP LATIN]; 31 - Preservatives in Mascara; BENZOIC ACID (USP MONOGRAPH); BENZOIC ACID [USP MONOGRAPH]; BENZOIC ACID (EP MONOGRAPH); 27 - Preservatives in Cream; BENZOIC ACID [EP MONOGRAPH]; Benzoic acid, p.a., 99.5\\%; Benzoic acid (7CI,8CI,9CI); benzene-2-carboxylic acid; Benzoic acid-2,3,4,5,6-d5; BENZOIC ACID [GREEN BOOK]; Benzoic-2,3,4,5,6-d5 acid; Benzoic acid, ACS reagent; Kyselina benzoova [Czech]; Benzoic acid, AR, >=99\\%; Acide benzoique [French]; Acido benzoico [Italian]; Benzoic acid, LR, >=99\\%; Benzoic acid sodium salt; Aromatic carboxylic acid; benzene carboxylic acid; Benzoic acid (JP17/USP); Benzoic acid [USAN:JAN]; BENZOICUM ACIDUM [HPUS]; benzenecarboxylic acid; Benzoic acid [USP:JAN]; Benzoic acid (USP:JAN); Benzoic acid (natural); Phenylcarboxylic acid; BENZOIC ACID (USP-RS); Benzoesaeure [German]; BENZOIC ACID [WHO-IP]; BENZOIC ACID [WHO-DD]; BENZOIC ACID [USP-RS]; Benzenemethanoic acid; BENZOIC ACID (MART.); BENZOIC ACID [MART.]; Aromatic carboxylate; BENZOIC ACID [VANDF]; Benzenemethonic acid; Sodium benzoic acid; BENZOIC ACID [FHFI]; Benzoate, Potassium; BENZOIC ACID [HSDB]; BENZOIC ACID [INCI]; Rheumatism Diarrhea; Benzoic-3,5-d2 Acid; Benzoic acid, tech.; Potassium Benzoate; Benzeneformic acid; BENZOIC ACID [JAN]; Benzenecarboxylate; BENZOIC ACID [FCC]; BENZOIC-4-D1 ACID; BENZOIC ACID [II]; BENZOIC ACID [MI]; phenylformic acid; Benzenemethanoate; Phenylcarboxylate; BENZOIC ACID (II); Kyselina benzoova; benzenecarboxylic; Benzoic acid (TN); Benzoicum acidum; Acidum benzoicum; Benzoic Acid,(S); Provita Equiband; Benzoesaeure GV; UNII-8SKN0B0MIM; Acide benzoique; Benzoesaeure GK; CARBOXYLBENZENE; Sodium Benzoate; BENZOICACID-D5; DRACYCLIC ACID; Benzeneformate; DIACYCLIC ACID; Benzoate (VAN); Menno-florades; Carboxybenzene; Acido benzoico; Salvo, liquid; phenylcarboxy; Dracylic acid; Solvo, powder; benzoic- acid; Phenylformate; Diacylic acid; Acid, Benzoic; ProvitaCombat; Aromatic acid; Oracylic acid; Eyelids Wipes; Salvo liquid; benzoic aicd; Retarder BAX; Tox21_202403; Benzoesaeure; Solvo powder; Tox21_300180; Salvo powder; Benzoic Acid; Benzoicum Ac; benzoic-acid; Retarded BA; Retarder BA; bezoic acid; HA 1 (acid); Unisept BZA; CAS-65-85-0; SAMPL4, O1; 8SKN0B0MIM; Vevovitall; AI3-03710; Diacylate; Dracylate; Tenn-Plas; WLN: QVR; AI3-0310; Retardex; Tennplas; benzoate; Ucephan; Benzoic; 1kqb; e210; 1gyx; HA 1; B A; Benzoic acid; Benzoic acid



数据库引用编号

48 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(3)

BioCyc(0)

PlantCyc(6)

代谢反应

385 个相关的代谢反应过程信息。

Reactome(66)

BioCyc(1)

WikiPathways(3)

Plant Reactome(3)

INOH(0)

PlantCyc(311)

COVID-19 Disease Map(1)

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。



文献列表

  • Yanan Lu, Xue Han. Therapeutic Implications of Phenolic Acids for Ameliorating Inflammatory Bowel Disease. Nutrients. 2024 Apr; 16(9):. doi: 10.3390/nu16091347. [PMID: 38732594]
  • Emily M Catania, Nicole M Dubs, Shejal Soumen, Todd J Barkman. The mutational road not taken: using Ancestral Sequence Resurrection to evaluate the evolution of plant enzyme substrate preferences. Genome biology and evolution. 2024 Jan; ?(?):. doi: 10.1093/gbe/evae016. [PMID: 38290535]
  • Tomoaki Yamaguchi, Keita Shibata, Keiji Hasumi, Koji Nobe. Potent Efficacy of 3-Amino-4-hydroxy Benzoic Acid, a Small Molecule Having Anti-fibrotic Activity, in a Mouse Model of Non-alcoholic Steatohepatitis. Biological & pharmaceutical bulletin. 2024; 47(2):434-442. doi: 10.1248/bpb.b23-00771. [PMID: 38369342]
  • Eleonora Barilli, Pierluigi Reveglia, Francisco J Agudo-Jurado, Vanessa Cañete García, Alessio Cimmino, Antonio Evidente, Diego Rubiales. Comparative Analysis of Secondary Metabolites Produced by Ascochyta fabae under In Vitro Conditions and Their Phytotoxicity on the Primary Host, Vicia faba, and Related Legume Crops. Toxins. 2023 Dec; 15(12):. doi: 10.3390/toxins15120693. [PMID: 38133197]
  • Yangyang Chen, Xiao Wu, Xiaohua Wang, Yubo Yuan, Kaijie Qi, Shaoling Zhang, Hao Yin. PusALDH1 gene confers high levels of volatile aroma accumulation in both pear and tomato fruits. Journal of plant physiology. 2023 Nov; 290(?):154101. doi: 10.1016/j.jplph.2023.154101. [PMID: 37806175]
  • Bijie Hu, Yiran Zheng, Jiaxing Lv, Jing Zhang, Yan Dong. Proteomic analysis of the faba bean-wheat intercropping system in controlling the occurrence of faba bean fusarium wilt due to stress caused by Fusarium oxysporum f. sp. fabae and benzoic acid. BMC plant biology. 2023 Oct; 23(1):472. doi: 10.1186/s12870-023-04481-8. [PMID: 37803265]
  • . Insecticidal activity and physiopathological effects of Cotula cinerea crude extract against Culex pipiens. Tropical biomedicine. 2023 Jun; 40(2):241-249. doi: 10.47665/tb.40.2.016. [PMID: 37650412]
  • Adam Yasgar, Danielle Bougie, Richard T Eastman, Ruili Huang, Misha Itkin, Jennifer Kouznetsova, Caitlin Lynch, Crystal McKnight, Mitch Miller, Deborah K Ngan, Tyler Peryea, Pranav Shah, Paul Shinn, Menghang Xia, Xin Xu, Alexey V Zakharov, Anton Simeonov. Quantitative Bioactivity Signatures of Dietary Supplements and Natural Products. ACS pharmacology & translational science. 2023 May; 6(5):683-701. doi: 10.1021/acsptsci.2c00194. [PMID: 37200814]
  • Congcong Chen, Junshen Tian, Xiaoxia Gao, Xuemei Qin, Guanhua Du, Yuzhi Zhou. An integrated strategy to study the combination mechanisms of Bupleurum chinense DC and Paeonia lactiflora Pall for treating depression based on correlation analysis between serum chemical components profiles and endogenous metabolites profiles. Journal of ethnopharmacology. 2023 Apr; 305(?):116068. doi: 10.1016/j.jep.2022.116068. [PMID: 36574791]
  • Wei Jia, Xixuan Wu, Lin Shi. Naturally forming benzoic acid orientates perilipin to facilitate glyceride-type polyunsaturated fatty acid degradation via fermentation behavior. Journal of dairy science. 2023 Mar; 106(3):1650-1671. doi: 10.3168/jds.2022-22381. [PMID: 36710193]
  • Ranjita S Das, Vijay N Mohakar, Anupama Kumar. Valorization of potato peel waste: Recovery of p-hydroxy benzoic acid (antioxidant) through molecularly imprinted solid-phase extraction. Environmental science and pollution research international. 2023 Feb; 30(8):19860-19872. doi: 10.1007/s11356-022-23547-y. [PMID: 36241837]
  • Meng Li, Xinjie Wan, Xin He, Chunying Rong, Shubin Liu. Impacts of external fields on aromaticity and acidity of benzoic acid: a density functional theory, conceptual density functional theory and information-theoretic approach study. Physical chemistry chemical physics : PCCP. 2023 Jan; 25(3):2595-2605. doi: 10.1039/d2cp04557e. [PMID: 36602177]
  • Lars Hareng, Paul Schuster, Volker Haake, Tilman Walk, Michael Herold, Heike Laue, Andreas Natsch. Towards the mechanism of spermatotoxicity of p-tert-butyl-alpha-methylhydrocinnamic aldehyde: inhibition of late stage ex-vivo spermatogenesis in rat seminiferous tubule cultures by para-tert-butyl- benzoic acid. Archives of toxicology. 2023 01; 97(1):279-294. doi: 10.1007/s00204-022-03379-y. [PMID: 36173422]
  • Jinling Zhang, Wenbao Wang, Yanzhao Tian, Liwei Ma, Lin Zhou, Hao Sun, Yukun Ma, Huiling Hou, Xiaoli Wang, Jin Ye, Xiaobo Wang. Design, synthesis and biological evaluation of novel diosgenin-benzoic acid mustard hybrids with potential anti-proliferative activities in human hepatoma HepG2 cells. Journal of enzyme inhibition and medicinal chemistry. 2022 Dec; 37(1):1299-1314. doi: 10.1080/14756366.2022.2070161. [PMID: 35652316]
  • Suyoung Song, Eun Kyeong Jeon, Cher-Won Hwang. Characteristic Analysis of Soil-Isolated Bacillus velezensis HY-3479 and Its Antifungal Activity Against Phytopathogens. Current microbiology. 2022 Oct; 79(12):357. doi: 10.1007/s00284-022-03060-8. [PMID: 36251101]
  • Mona Isaq, Prathap Somu, Diptikanta Acharya, Levin Anbu Gomez, Jesse Joel Thathapudi, Yerappa Lakshmikanth Ramachandra, Sunitha Bommanahalli Rudraiah, Pooja Ravi, Padmalatha S Rai, Rosina Rosalin, Chandrappa Chinna Poojari, Yong Rok Lee. Phytochemical Screening and Bioactivity Studies of Endophytes Cladosporium sp. Isolated from the Endangered Plant Vateria Indica Using In Silico and In Vitro Analysis. Applied biochemistry and biotechnology. 2022 Oct; 194(10):4546-4569. doi: 10.1007/s12010-022-03933-5. [PMID: 35522363]
  • Qian Li, Sentai Liao, Daorui Pang, Erna Li, Tongxian Liu, Fan Liu, Yuxiao Zou. The transported active mulberry leaf phenolics inhibited adipogenesis through PPAR-γ and Leptin signaling pathway. Journal of food biochemistry. 2022 10; 46(10):e14270. doi: 10.1111/jfbc.14270. [PMID: 35702955]
  • Krishnan Raguvaran, Manickam Kalpana, Thulasiraman Manimegalai, Suresh Kalaivani, Palanisamy Devapriya, Nagarajan Siddharthan, Rengasamy Balakrishnan, Tamil Selvan Silambarasan, Rajan Maheswaran. Larvicidal, antioxidant and biotoxicity assessment of (2-(((2-ethyl-2 methylhexyl)oxy)carbonyl)benzoic acid isolated from Bacillus pumilus against Aedes aegypti, Anopheles stephensi and Culex quinquefasciatus. Archives of microbiology. 2022 Sep; 204(10):650. doi: 10.1007/s00203-022-03264-3. [PMID: 36173486]
  • Saima Muzammil, Yunsheng Wang, Muhammad Hussnain Siddique, Errum Zubair, Sumreen Hayat, Muhammad Zubair, Arpita Roy, Rabia Mumtaz, Muhammad Azeem, Talha Bin Emran, Muhammad Qasim Shahid. Polyphenolic Composition, Antioxidant, Antiproliferative and Antidiabetic Activities of Coronopus didymus Leaf Extracts. Molecules (Basel, Switzerland). 2022 Sep; 27(19):. doi: 10.3390/molecules27196263. [PMID: 36234800]
  • Umair Khurshid, Saeed Ahmad, Hammad Saleem, Arslan Hussain LodhI, Irfan Pervaiz, Mohsin Abbas Khan, Haroon Khan, Abdulwahab AlamrI, Mukhtar AnsarI, Marcello LocatellI, Muhammad Adeel Arshad, Muhammad Asif Wazir, Juwairiya Butt, Sirajudheen Anwar. Multifaced Assessment of Antioxidant Power, Phytochemical Metabolomics, In-Vitro Biological Potential and In-Silico Studies of Neurada procumbens L.: An Important Medicinal Plant. Molecules (Basel, Switzerland). 2022 Sep; 27(18):. doi: 10.3390/molecules27185849. [PMID: 36144585]
  • Roham Foroumadi, Maryam Baeeri, Sara Asgarian, Zahra Emamgholipour, Fereshteh Goli, Loghman Firoozpour, Mohammad Keykhaei, Mahdi Gholami, Ahmad R Dehpour, Mohammad Abdollahi, Alireza Foroumadi. Antidiabetic and neuroprotective effects of a novel repaglinide analog. Journal of biochemical and molecular toxicology. 2022 Sep; 36(9):e23125. doi: 10.1002/jbt.23125. [PMID: 35702883]
  • Dursun Kısa, Rizvan Imamoglu, Zafer Kaya, Tugba Taskin-Tok, Parham Taslimi. Turanecio hypochionaeus: Determination of Its Polyphenol Contents, and Bioactivities Potential Assisted with in Silico Studies. Chemistry & biodiversity. 2022 Sep; 19(9):e202200109. doi: 10.1002/cbdv.202200109. [PMID: 35983912]
  • Bret Cooper. The Detriment of Salicylic Acid to the Pseudomonas savastanoi pv. phaseolicola Proteome. Molecular plant-microbe interactions : MPMI. 2022 Sep; 35(9):814-824. doi: 10.1094/mpmi-05-22-0104-r. [PMID: 35612310]
  • Gabriele Soriano, Antonietta Siciliano, Mónica Fernández-Aparicio, Antonio Cala Peralta, Marco Masi, Antonio Moreno-Robles, Marco Guida, Alessio Cimmino. Iridoid Glycosides Isolated from Bellardia trixago Identified as Inhibitors of Orobanche cumana Radicle Growth. Toxins. 2022 08; 14(8):. doi: 10.3390/toxins14080559. [PMID: 36006221]
  • Xu Pang, Guo-Wei Cai, Meng-Yan Wang, Xiu-Fei Chen, Wen-Ni He, Wu-Li Zhao, Tao Zhang, Li-Yan Yu. Metabolites from the plant endophytic fungus Penicillium sp. CPCC 401423 and their cytotoxic activity against MIA PaCa-2 cells. Journal of Asian natural products research. 2022 Aug; ?(?):1-12. doi: 10.1080/10286020.2022.2104719. [PMID: 35920176]
  • Menghan Chen, Liqing Wang, Shuyan Xing, Yong Yang, Rong Rong. Rapid screening of neuraminidase inhibitors with the benzoic acid skeleton from Paeonia suffruticosa Andrews by solid-phase extraction with an enzyme activity switch combined with mass spectrometry analysis. Journal of chromatography. A. 2022 Aug; 1676(?):463213. doi: 10.1016/j.chroma.2022.463213. [PMID: 35717865]
  • Fatma A Farghaly, Hussein Kh Salam, Afaf M Hamada, Abeer A Radi. Alleviating excess boron stress in tomato calli by applying benzoic acid to various biochemical strategies. Plant physiology and biochemistry : PPB. 2022 Jul; 182(?):216-226. doi: 10.1016/j.plaphy.2022.04.019. [PMID: 35526419]
  • Raúl Velasco-Azorsa, Reyna Zeferino-Díaz, José G Alvarado-Rodríguez, Heraclio López-Ruiz, Susana Rojas-Lima, Kinardo Flores-Castro, Ignacio Cid Del Prado-Vera, Raquel Alatorre-Rosas, Felipe Tut-Pech, María G Carrillo-Benítez, Eleuterio Burgueño-Tapia, J Martín Torres-Valencia. Nematicidal activity of furanoeremophilenes against Meloidogyne incognita and Nacobbus aberrans. Pest management science. 2022 Jun; 78(6):2571-2580. doi: 10.1002/ps.6888. [PMID: 35338557]
  • Yuya Kakumu, Thi Minh Tu Nguyen, Kosei Yamauchi, Tohru Mitsunaga. New benzoic acid and caffeoyl derivatives with anti-inflammatory activities isolated from leaves of Ilex kaushue. Natural product research. 2022 Jun; 36(12):3013-3021. doi: 10.1080/14786419.2021.1939334. [PMID: 34382490]
  • Lingqi Yue, Yongshen Li, Min Zhong, Xirong Chai, Puyan Zhao, Riming Huang, Yunyan Kang, Xian Yang. Benzoic Acid, Chlorine Dioxide, and 1-Methylcyclopropene Induce Flavonoid Metabolic Shifts in Postharvest Flowering Chinese Cabbage Revealed by High-Dimensional Analytical Data. International journal of molecular sciences. 2022 May; 23(11):. doi: 10.3390/ijms23116011. [PMID: 35682691]
  • Zhao-Yue Dong, Qing-Hong Zeng, Lin Wei, Xin Guo, Yan Sun, Fan-Cheng Meng, Guo-Wei Wang, Xiao-Zhong Lan, Zhi-Hua Liao, Min Chen. Berberisides A-D: three novel prenylated benzoic acid derivatives and a clerodane glycoside from Berberis tsarica aherndt. Natural product research. 2022 Apr; 36(8):1996-2001. doi: 10.1080/14786419.2020.1839460. [PMID: 33118393]
  • Nidal Jaradat, Ahmad Khasati, Maram Hawi, Mohammed Hawash, Suhaib Shekfeh, Mohammad Qneibi, Ahmad M Eid, Mohammad Arar, Mohammed T Qaoud. Antidiabetic, antioxidant, and anti-obesity effects of phenylthio-ethyl benzoate derivatives, and molecular docking study regarding α-amylase enzyme. Scientific reports. 2022 02; 12(1):3108. doi: 10.1038/s41598-022-07188-2. [PMID: 35210523]
  • Evren Caglar Eroglu, Umran Kucukgoz Gulec, Mehmet Ali Vardar, Semra Paydas. GC-MS based metabolite fingerprinting of serous ovarian carcinoma and benign ovarian tumor. European journal of mass spectrometry (Chichester, England). 2022 Feb; 28(1-2):12-24. doi: 10.1177/14690667221098520. [PMID: 35503418]
  • Wenbao Wang, Chuan Li, Zhe Chen, Jinling Zhang, Liwei Ma, Yanzhao Tian, Yukun Ma, Lina Guo, Xiaoli Wang, Jin Ye, Xiaobo Wang. Novel diosgenin-amino acid-benzoic acid mustard trihybrids exert antitumor effects via cell cycle arrest and apoptosis. The Journal of steroid biochemistry and molecular biology. 2022 02; 216(?):106038. doi: 10.1016/j.jsbmb.2021.106038. [PMID: 34861390]
  • Trung-Anh Le, Yong Guo, Jun-Nian Zhou, Jiaqi Yan, Hongbo Zhang, Tan-Phat Huynh. Synthesis, characterization and biocompatibility of guar gum-benzoic acid. International journal of biological macromolecules. 2022 Jan; 194(?):110-116. doi: 10.1016/j.ijbiomac.2021.11.180. [PMID: 34861275]
  • Xuemei Xiao, Ju Li, Jian Lyu, Linli Hu, Yue Wu, Zhongqi Tang, Jihua Yu, Alejandro Calderón-Urrea. Grafting-enhanced tolerance of cucumber to toxic stress is associated with regulation of phenolic and other aromatic acids metabolism. PeerJ. 2022; 10(?):e13521. doi: 10.7717/peerj.13521. [PMID: 35669966]
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