AI3-28796 (BioDeep_00000862066)

Main id: BioDeep_00000276193

 

PANOMIX_OTCML-2023


代谢物信息卡片


InChI=1\C9H10O4\c1-12-7-3-6(5-10)4-8(13-2)9(7)11\h3-5,11H,1-2H

化学式: C9H10O4 (182.057906)
中文名称: 丁香醛
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: COC1=CC(=CC(=C1O)OC)C=O
InChI: InChI=1S/C9H10O4/c1-12-7-3-6(5-10)4-8(13-2)9(7)11/h3-5,11H,1-2H3

描述信息

Syringaldehyde is a polyphenolic compound belonging to the group of flavonoids and is found in different plant species like Manihot esculenta and Magnolia officinalis[1]. Syringaldehyde moderately inhibits COX-2 activity with an IC50 of 3.5 μg/mL[2]. Anti-hyperglycemic and anti-inflammatory activities[1].
Syringaldehyde is a polyphenolic compound belonging to the group of flavonoids and is found in different plant species like Manihot esculenta and Magnolia officinalis[1]. Syringaldehyde moderately inhibits COX-2 activity with an IC50 of 3.5 μg/mL[2]. Anti-hyperglycemic and anti-inflammatory activities[1].

同义名列表

27 个代谢物同义名

InChI=1\C9H10O4\c1-12-7-3-6(5-10)4-8(13-2)9(7)11\h3-5,11H,1-2H; 4-Hydroksy-3,5-dwumetoksybenzaldehyd [Polish]; 4-08-00-02718 (Beilstein Handbook Reference); 3,5-Dimethoxy-4-hydroxybenzene carbonal; Benzaldehyde, 3,5-dimethoxy-4-hydroxy-; Benzaldehyde, 4-hydroxy-3,5-dimethoxy-; 4-hydroxy-3,5-dimethoxy-benzaldehyde; 4-Hydroxy-3,5-dimethoxybenzaldehyde; 3,5-Dimethoxy-4-hydroxybenzaldehyde; Gallaldehyde 3,5-dimethyl ether; Syringic aldehyde; Syringylaldehyde; EINECS 205-167-5; Syringealdehyde; W404926_ALDRICH; Syringaldehyde; S7602_ALDRICH; ZINC00152926; 86220_FLUKA; AIDS-340410; BRN 0784514; AIDS340410; SBB007558; NSC 41153; AI3-28796; 134-96-3; NSC41153



数据库引用编号

5 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)

217 个相关的物种来源信息

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

  • Tanvi Sahni, Sunita Sharma, Diksha Verma, Harleen Kaur, Sachin Kumar. Exploration of novel syringic esters as antifungal agent against phytopathogenic fungi of maize: Structure-activity studies. Journal of basic microbiology. 2023 Nov; 63(11):1265-1278. doi: 10.1002/jobm.202300040. [PMID: 37236164]
  • Sumayya Shahzad, Somaiya Mateen, Tasneem Kausar, Syed Shariq Naeem, Asif Hasan, Minhal Abidi, Shahid M Nayeem, Abul Faiz Faizy, Shagufta Moin. Effect of syringic acid and syringaldehyde on oxidative stress and inflammatory status in peripheral blood mononuclear cells from patients of myocardial infarction. Naunyn-Schmiedeberg's archives of pharmacology. 2020 04; 393(4):691-704. doi: 10.1007/s00210-019-01768-2. [PMID: 31822939]
  • Simone K Huber, Georg Höfner, Klaus T Wanner. Application of the concept of oxime library screening by mass spectrometry (MS) binding assays to pyrrolidine-3-carboxylic acid derivatives as potential inhibitors of γ-aminobutyric acid transporter 1 (GAT1). Bioorganic & medicinal chemistry. 2019 07; 27(13):2753-2763. doi: 10.1016/j.bmc.2019.05.001. [PMID: 31097402]
  • Sumayya Shahzad, Somaiya Mateen, P M Mubeena Mariyath, Syed Shariq Naeem, Kafil Akhtar, Waseem Rizvi, Shagufta Moin. Protective effect of syringaldehyde on biomolecular oxidation, inflammation and histopathological alterations in isoproterenol induced cardiotoxicity in rats. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2018 Dec; 108(?):625-633. doi: 10.1016/j.biopha.2018.09.055. [PMID: 30245462]
  • Tobias J Hauke, Thomas Wein, Georg Höfner, Klaus T Wanner. Novel Allosteric Ligands of γ-Aminobutyric Acid Transporter 1 (GAT1) by MS Based Screening of Pseudostatic Hydrazone Libraries. Journal of medicinal chemistry. 2018 11; 61(22):10310-10332. doi: 10.1021/acs.jmedchem.8b01602. [PMID: 30376325]
  • Yulin Ren, Gerardo D Anaya-Eugenio, Austin A Czarnecki, Tran Ngoc Ninh, Chunhua Yuan, Hee-Byung Chai, Djaja D Soejarto, Joanna E Burdette, Esperanza J Carcache de Blanco, A Douglas Kinghorn. Cytotoxic and NF-κB and mitochondrial transmembrane potential inhibitory pentacyclic triterpenoids from Syzygium corticosum and their semi-synthetic derivatives. Bioorganic & medicinal chemistry. 2018 08; 26(15):4452-4460. doi: 10.1016/j.bmc.2018.07.025. [PMID: 30057155]
  • Kar Mun Goh, Matthew Dickinson, Christina V Supramaniam. Morphological and transcript changes in the biosynthesis of lignin in oil palm (Elaeis guineensis) during Ganoderma boninense infections in vitro. Physiologia plantarum. 2018 Mar; 162(3):274-289. doi: 10.1111/ppl.12645. [PMID: 28940509]
  • Rong-Rong You, Xue-Qing Chen, Dan-Dan He, Chang-Gao Huang, Yang Jin, Shi-Hui Qian, Jian-Ming Ju, Jun-Ting Fan. [Chemical constituents from petroleum ether fraction of Swertia chirayita and their activities in vitro]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2017 Oct; 42(19):3764-3769. doi: 10.19540/j.cnki.cjcmm.20170807.003. [PMID: 29235293]
  • Se-Yong Kim, Eun-Ju Yang, Youn Kyoung Son, Joo-Hong Yeo, Kyung-Sik Song. Enhanced anti-oxidative effect of fermented Korean mistletoe is originated from an increase in the contents of caffeic acid and lyoniresinol. Food & function. 2016 May; 7(5):2270-7. doi: 10.1039/c6fo00138f. [PMID: 27072079]
  • Ting Jiang, Hui Qiao, Zhaojuan Zheng, Qiulu Chu, Xin Li, Qiang Yong, Jia Ouyang. Lactic Acid Production from Pretreated Hydrolysates of Corn Stover by a Newly Developed Bacillus coagulans Strain. PloS one. 2016; 11(2):e0149101. doi: 10.1371/journal.pone.0149101. [PMID: 26863012]
  • Yong Zhao, Chang-An Geng, Chang-Li Sun, Yun-Bao Ma, Xiao-Yan Huang, Tuan-Wu Cao, Kang He, Hao Wang, Xue-Mei Zhang, Ji-Jun Chen. Polyacetylenes and anti-hepatitis B virus active constituents from Artemisia capillaris. Fitoterapia. 2014 Jun; 95(?):187-93. doi: 10.1016/j.fitote.2014.03.017. [PMID: 24685503]
  • S C Kuo, H H Chung, C H Huang, J T Cheng. Decrease of hyperglycemia by syringaldehyde in diabetic rats. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme. 2014 Jan; 46(1):8-13. doi: 10.1055/s-0033-1351274. [PMID: 23918689]
  • Haitang Liu, Huiren Hu, M Sarwar Jahan, Yonghao Ni. Furfural formation from the pre-hydrolysis liquor of a hardwood kraft-based dissolving pulp production process. Bioresource technology. 2013 Mar; 131(?):315-20. doi: 10.1016/j.biortech.2012.12.158. [PMID: 23360707]
  • Yue-Ming Zuo, Zhong-Li Zhang, Ya-Qin Yang, Guang-Ming Luo, Cai-Jun Cai, Yan-Yan Wang. [Study on the chemical components of Gardenia jasminoides]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2013 Feb; 36(2):225-7. doi: . [PMID: 23901647]
  • Chia-Hsin Huang, Mei-Fen Chen, Hsien-Hui Chung, Juei-Tang Cheng. Antihyperglycemic effect of syringaldehyde in streptozotocin-induced diabetic rats. Journal of natural products. 2012 Aug; 75(8):1465-8. doi: 10.1021/np3003723. [PMID: 22880723]
  • Yves Barrière, Valérie Méchin, Bruno Lefevre, Stéphane Maltese. QTLs for agronomic and cell wall traits in a maize RIL progeny derived from a cross between an old Minnesota13 line and a modern Iodent line. TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik. 2012 Aug; 125(3):531-49. doi: 10.1007/s00122-012-1851-5. [PMID: 22437492]
  • Harleen Kaur, Kamel Shaker, Nicolas Heinzel, John Ralph, Ivan Gális, Ian T Baldwin. Environmental stresses of field growth allow cinnamyl alcohol dehydrogenase-deficient Nicotiana attenuata plants to compensate for their structural deficiencies. Plant physiology. 2012 Aug; 159(4):1545-70. doi: 10.1104/pp.112.196717. [PMID: 22645069]
  • Lifeng Han, Lina Ji, Mavis Boakye-Yiadom, Wei Li, Xinbo Song, Xiumei Gao. Preparative isolation and purification of four compounds from Cistanches deserticola Y.C. Ma by high-speed counter-current chromatography. Molecules (Basel, Switzerland). 2012 Jul; 17(7):8276-84. doi: 10.3390/molecules17078276. [PMID: 22781440]
  • Siseon Lee, Ajay Kalanjana Monnappa, Robert J Mitchell. Biological activities of lignin hydrolysate-related compounds. BMB reports. 2012 May; 45(5):265-74. doi: 10.5483/bmbrep.2012.45.5.265. [PMID: 22617449]
  • Ademir E do Vale, Jorge M David, Edlene O dos Santos, Juceni P David, Lidercia C R C e Silva, Marcus V Bahia, Hugo N Brandão. An unusual caffeic acid derived bicyclic [2.2.2] octane lignan and other constituents from Cordia rufescens. Phytochemistry. 2012 Apr; 76(?):158-61. doi: 10.1016/j.phytochem.2011.09.019. [PMID: 22248687]
  • Naowarat Kongkum, Patoomratana Tuchinda, Manat Pohmakotr, Vichai Reutrakul, Pawinee Piyachaturawat, Surawat Jariyawat, Kanoknetr Suksen, Chalobon Yoosook, Jitra Kasisit, Chanita Napaswad. DNA topoisomerase IIα inhibitory and anti-HIV-1 flavones from leaves and twigs of Gardenia carinata. Fitoterapia. 2012 Mar; 83(2):368-72. doi: 10.1016/j.fitote.2011.11.015. [PMID: 22155186]
  • Thomas Arnold, Christopher Mealey, Hannah Leahey, A Whitman Miller, Jason M Hall-Spencer, Marco Milazzo, Kelly Maers. Ocean acidification and the loss of phenolic substances in marine plants. PloS one. 2012; 7(4):e35107. doi: 10.1371/journal.pone.0035107. [PMID: 22558120]
  • Hari Prasad Devkota, Masato Watanabe, Takashi Watanabe, Shoji Yahara. Phenolic compounds from the aerial parts of Diplomorpha canescens. Chemical & pharmaceutical bulletin. 2012; 60(4):554-6. doi: 10.1248/cpb.60.554. [PMID: 22466741]
  • Bo Yi, Lifei Hu, Wenli Mei, Kaibing Zhou, Hui Wang, Ying Luo, Xiaoyi Wei, Haofu Dai. Antioxidant phenolic compounds of cassava (Manihot esculenta) from Hainan. Molecules (Basel, Switzerland). 2011 Dec; 16(12):10157-67. doi: 10.3390/molecules161210157. [PMID: 22157579]
  • Farid Khallouki, Roswitha Haubner, Cornelia M Ulrich, Robert W Owen. Ethnobotanical survey, chemical composition, and antioxidant capacity of methanolic extract of the root bark of Annona cuneata Oliv. Journal of medicinal food. 2011 Nov; 14(11):1397-402. doi: 10.1089/jmf.2010.0228. [PMID: 21870939]
  • Huang-Hui Chen, Wenchang Chiang, Jang-Yang Chang, Ya-Lin Chien, Ching-Kuo Lee, Ko-Jiunn Liu, Yen-Ting Cheng, Ting-Fang Chen, Yueh-Hsiung Kuo, Ching-Chuan Kuo. Antimutagenic constituents of adlay (Coix lachryma-jobi L. var. ma-yuen Stapf) with potential cancer chemopreventive activity. Journal of agricultural and food chemistry. 2011 Jun; 59(12):6444-52. doi: 10.1021/jf200539r. [PMID: 21561091]
  • Jong H Kim, Kathleen L Chan, Noreen Mahoney, Bruce C Campbell. Antifungal activity of redox-active benzaldehydes that target cellular antioxidation. Annals of clinical microbiology and antimicrobials. 2011 May; 10(?):23. doi: 10.1186/1476-0711-10-23. [PMID: 21627838]
  • João C Gasparetto, Thais M Guimarães de Francisco, Francinete R Campos, Roberto Pontarolo. Development and validation of two methods based on high-performance liquid chromatography-tandem mass spectrometry for determining 1,2-benzopyrone, dihydrocoumarin, o-coumaric acid, syringaldehyde and kaurenoic acid in guaco extracts and pharmaceutical preparations. Journal of separation science. 2011 Apr; 34(7):740-8. doi: 10.1002/jssc.201000792. [PMID: 21374810]
  • Ying Zhang, Yi Yuan, Baosong Cui, Shuai Li. [Study on chemical constituents from ethyl acetate extract of Myricaria bracteata]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2011 Apr; 36(8):1019-23. doi: . [PMID: 21809576]
  • Ursula Kües, Martin Rühl. Multiple multi-copper oxidase gene families in basidiomycetes - what for?. Current genomics. 2011 Apr; 12(2):72-94. doi: 10.2174/138920211795564377. [PMID: 21966246]
  • Ani Tejirian, Feng Xu. Inhibition of enzymatic cellulolysis by phenolic compounds. Enzyme and microbial technology. 2011 Mar; 48(3):239-47. doi: 10.1016/j.enzmictec.2010.11.004. [PMID: 22112906]
  • Magdalena Zuk, Anna Kulma, Lucyna Dymińska, Katarzyna Szołtysek, Anna Prescha, Jerzy Hanuza, Jan Szopa. Flavonoid engineering of flax potentiate its biotechnological application. BMC biotechnology. 2011 Jan; 11(?):10. doi: 10.1186/1472-6750-11-10. [PMID: 21276227]
  • Liya Li, Navindra P Seeram. Maple syrup phytochemicals include lignans, coumarins, a stilbene, and other previously unreported antioxidant phenolic compounds. Journal of agricultural and food chemistry. 2010 Nov; 58(22):11673-9. doi: 10.1021/jf1033398. [PMID: 21033720]
  • Carmen Gayoso, Federico Pomar, Esther Novo-Uzal, Fuencisla Merino, Oskar Martínez de Ilárduya. The Ve-mediated resistance response of the tomato to Verticillium dahliae involves H2O2, peroxidase and lignins and drives PAL gene expression. BMC plant biology. 2010 Oct; 10(?):232. doi: 10.1186/1471-2229-10-232. [PMID: 20977727]
  • Juan José Villaverde, Alberto De Vega, Pablo Ligero, Carmen S R Freire, Carlos Pascoal Neto, Armando J D Silvestre. Miscanthus x giganteus bark organosolv fractionation: fate of lipophilic components and formation of valuable phenolic byproducts. Journal of agricultural and food chemistry. 2010 Jul; 58(14):8279-85. doi: 10.1021/jf101174x. [PMID: 20593898]
  • Huiyuan Zhai, Chenyang Li, Sheng'an Tang, Hongquan Duan. [Phenol constituents of Pachysandra terminalis and their antioxidant activity]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2010 Jul; 35(14):1820-3. doi: 10.4268/cjcmm20101411. [PMID: 20939276]
  • Tomohiro Itoh, Mariko Tsukane, Minako Koike, Chizu Nakamura, Kenji Ohguchi, Masafumi Ito, Yukihiro Akao, Seiichi Koshimizu, Yoshinori Nozawa, Toshiyuki Wakimoto, Haruo Nukaya, Yoshihide Suwa. Inhibitory effects of whisky congeners on IgE-mediated degranulation in rat basophilic leukemia RBL-2H3 cells and passive cutaneous anaphylaxis reaction in mice. Journal of agricultural and food chemistry. 2010 Jun; 58(12):7149-57. doi: 10.1021/jf100998c. [PMID: 20507065]
  • Silvia Forcat, Mark Bennett, Murray Grant, John W Mansfield. Rapid linkage of indole carboxylic acid to the plant cell wall identified as a component of basal defence in Arabidopsis against hrp mutant bacteria. Phytochemistry. 2010 Jun; 71(8-9):870-6. doi: 10.1016/j.phytochem.2010.03.010. [PMID: 20359727]
  • A Hymavathi, K Suresh Babu, V G M Naidu, S Rama Krishna, Prakash V Diwan, J Madhusudana Rao. Bioactivity-guided isolation of cytotoxic constituents from stem-bark of Premna tomentosa. Bioorganic & medicinal chemistry letters. 2009 Oct; 19(19):5727-31. doi: 10.1016/j.bmcl.2009.08.002. [PMID: 19700323]
  • Cuimin Hu, Xin Zhao, Jin Zhao, Siguo Wu, Zongbao K Zhao. Effects of biomass hydrolysis by-products on oleaginous yeast Rhodosporidium toruloides. Bioresource technology. 2009 Oct; 100(20):4843-7. doi: 10.1016/j.biortech.2009.04.041. [PMID: 19497736]
  • F Khallouki, W E Hull, R W Owen. Characterization of a rare triterpenoid and minor phenolic compounds in the root bark of Anisophyllea dichostyla R. Br. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2009 Aug; 47(8):2007-12. doi: 10.1016/j.fct.2009.05.018. [PMID: 19460411]
  • Ting Zhang, Hongqing Wang, Guanhua Du, Ruoyun Chen. [Study on chemical constituents from roots of Saussurea lappa]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2009 May; 34(10):1223-4. doi: . [PMID: 19673381]
  • Kumarasamy Murugesan, In-Hee Yang, Young-Mo Kim, Jong-Rok Jeon, Yoon-Seok Chang. Enhanced transformation of malachite green by laccase of Ganoderma lucidum in the presence of natural phenolic compounds. Applied microbiology and biotechnology. 2009 Feb; 82(2):341-50. doi: 10.1007/s00253-008-1819-1. [PMID: 19130052]
  • Chien-Chang Shen, Ching-Li Ni, Yuh-Chiang Shen, Yu-Ling Huang, Ching-Hsia Kuo, Tian-Shung Wu, Chien-Chih Chen. Phenolic constituents from the stem bark of Magnolia officinalis. Journal of natural products. 2009 Jan; 72(1):168-71. doi: 10.1021/np800494e. [PMID: 19086868]
  • Shuang Liang, Yun-Heng Shen, Jun-Mian Tian, Zhi-Jun Wu, Hui-Zi Jin, Wei-Dong Zhang, Shi-Kai Yan. Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production. Journal of natural products. 2008 Nov; 71(11):1902-5. doi: 10.1021/np8004166. [PMID: 18986199]
  • Pei Sun Loh, Axel E J Miller, Alison D Reeves, S Martyn Harvey, Julian Overnell. Optimised recovery of lignin-derived phenols in a Scottish fjord by the CuO oxidation method. Journal of environmental monitoring : JEM. 2008 Oct; 10(10):1187-94. doi: 10.1039/b808970a. [PMID: 19244642]
  • Naoko Tamaki, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Mitsunori Aramoto, Yoshio Takeda. Rearranged ent-kauranes from the stems of Tricalysia dubia and their biological activities. Journal of natural medicines. 2008 Jul; 62(3):314-20. doi: 10.1007/s11418-008-0248-x. [PMID: 18409065]
  • Jih-Jung Chen, Chang-Syun Yang, Chien-Fang Peng, Ih-Sheng Chen, Chang-Ling Miaw. Dihydroagarofuranoid sesquiterpenes, a lignan derivative, a benzenoid, and antitubercular constituents from the stem of Microtropis japonica. Journal of natural products. 2008 Jun; 71(6):1016-21. doi: 10.1021/np800097t. [PMID: 18471021]
  • M J B Juárez, A Zafra-Gómez, B Luzón-Toro, O A Ballesteros-García, A Navalón, J González, J L Vílchez. Gas chromatographic-mass spectrometric study of the degradation of phenolic compounds in wastewater olive oil by Azotobacter Chroococcum. Bioresource technology. 2008 May; 99(7):2392-8. doi: 10.1016/j.biortech.2007.05.010. [PMID: 17624767]
  • Peter K Cheplogoi, Dulcie A Mulholland, Philip H Coombes, Milijaona Randrianarivelojosia. An azole, an amide and a limonoid from Vepris uguenensis (Rutaceae). Phytochemistry. 2008 Apr; 69(6):1384-8. doi: 10.1016/j.phytochem.2007.12.013. [PMID: 18267321]
  • Saibal Kumar Das, K Anantha Reddy, K Mukkanti. Total synthesis of phenylpropanoid glycosides, grayanoside A and syringalide B, through a common intermediate. Carbohydrate research. 2007 Nov; 342(15):2309-15. doi: 10.1016/j.carres.2007.06.022. [PMID: 17637461]
  • M J Reigosa, E Malvido-Pazos. Phytotoxic effects of 21 plant secondary metabolites on Arabidopsis thaliana germination and root growth. Journal of chemical ecology. 2007 Jul; 33(7):1456-66. doi: 10.1007/s10886-007-9318-x. [PMID: 17577597]
  • Ana Gutiérrez, Jorge Rencoret, David Ibarra, Setefilla Molina, Susana Camarero, Javier Romero, José C Del Río, Angel T Martínez. Removal of lipophilic extractives from paper pulp by laccase and lignin-derived phenols as natural mediators. Environmental science & technology. 2007 Jun; 41(11):4124-9. doi: 10.1021/es062723+. [PMID: 17612200]
  • Riccardo Flamini, Antonio Dalla Vedova, Davide Cancian, Annarita Panighel, Mirko De Rosso. GC/MS-positive ion chemical ionization and MS/MS study of volatile benzene compounds in five different woods used in barrel making. Journal of mass spectrometry : JMS. 2007 May; 42(5):641-6. doi: 10.1002/jms.1193. [PMID: 17370248]
  • Noélia Duarte, Maria-José U Ferreira. Lagaspholones A and B: two new jatropholane-type diterpenes from Euphorbia lagascae. Organic letters. 2007 Feb; 9(3):489-92. doi: 10.1021/ol062854f. [PMID: 17249794]
  • Jih-Jung Chen, Chien-Fang Peng, Hung-Yi Huang, Ih-Sheng Chen. Benzopyrans, biphenyls and xanthones from the root of Garcinia linii and their activity against Mycobacterium tuberculosis. Planta medica. 2006 Apr; 72(5):473-7. doi: 10.1055/s-2005-916253. [PMID: 16557464]
  • Hui-Yan Zhou, Hui Zhang, Shi-Min Li. [Chemical constituents from leaves of Phyllostachys pubescens I]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2005 Dec; 30(24):1933-4. doi: ". [PMID: 16494028]
  • Fu-Chi Chen, Chien-Fang Peng, Ian-Lih Tsai, Ih-Sheng Chen. Antitubercular constituents from the stem wood of Cinnamomum kotoense. Journal of natural products. 2005 Sep; 68(9):1318-23. doi: 10.1021/np0580210. [PMID: 16180806]
  • Daniel R Cardoso, Luiz G Andrade-Sobrinho, Alexandre F Leite-Neto, Roni V Reche, William D Isique, Marcia M C Ferreira, Benedito S Lima-Neto, Douglas W Franco. Comparison between cachaça and rum using pattern recognition methods. Journal of agricultural and food chemistry. 2004 Jun; 52(11):3429-33. doi: 10.1021/jf035262+. [PMID: 15161210]
  • Maria Cantarella, Laura Cantarella, Alberto Gallifuoco, Agata Spera, Francesco Alfani. Effect of inhibitors released during steam-explosion treatment of poplar wood on subsequent enzymatic hydrolysis and SSF. Biotechnology progress. 2004 Jan; 20(1):200-6. doi: 10.1021/bp0257978. [PMID: 14763843]
  • Pei-cheng Zhang, Yan Wu, De-quan Yu. [Chemical constituents from the leaves of Dalbergia hainanensis]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2003 Jun; 28(6):527-30. doi: ". [PMID: 15015332]
  • H B Klinke, L Olsson, A B Thomsen, B K Ahring. Potential inhibitors from wet oxidation of wheat straw and their effect on ethanol production of Saccharomyces cerevisiae: wet oxidation and fermentation by yeast. Biotechnology and bioengineering. 2003 Mar; 81(6):738-47. doi: 10.1002/bit.10523. [PMID: 12529889]
  • F Pomar, F Merino, A Ros Barceló. O-4-Linked coniferyl and sinapyl aldehydes in lignifying cell walls are the main targets of the Wiesner (phloroglucinol-HCl) reaction. Protoplasma. 2002 Oct; 220(1-2):17-28. doi: 10.1007/s00709-002-0030-y. [PMID: 12417933]
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