AI3-20480 (BioDeep_00000860134)

Main id: BioDeep_00000017372

 

PANOMIX_OTCML-2023


代谢物信息卡片


Myricyl alcohol (VAN)

化学式: C30H62O (438.48)
中文名称: 三十烷醇, 三十醇
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO
InChI: InChI=1S/C30H62O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31/h31H,2-30H2,1H3

描述信息

同义名列表

24 个代谢物同义名

Myricyl alcohol (VAN); 1-Hydroxytriacontane; Triacontyl alcohol; Melissyl alcohol; EINECS 209-794-5; Triacontan-1-ol; Myricyl alcohol; 1-​Triacontanol; 1-Triacontanol; n-Triacontanol; Triacontanol-1; 237809_ALDRICH; LMFA05000006; triacontanol; CHEBI:28409; T3777_SIGMA; NSC 402492; NSC 405588; NSC402492; AI3-20480; NSC405588; 593-50-0; C08392; Triacontan-1-ol



数据库引用编号

13 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)

102 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。

亚细胞结构定位 关联基因列表
Cytoplasm 11 ANG, ATF7, CASP3, CAT, MARVELD1, NLRP3, PTGS1, PTGS2, PYCARD, TLR4, TYR
Peripheral membrane protein 2 PTGS1, PTGS2
Endosome membrane 1 TLR4
Endoplasmic reticulum membrane 3 HMGCR, PTGS1, PTGS2
Nucleus 6 ANG, ATF7, CASP3, MARVELD1, NLRP3, PYCARD
cytosol 7 ANG, CASP3, CAT, GPT, LIPE, NLRP3, PYCARD
nucleoplasm 4 ATF7, CASP3, CD2, PYCARD
RNA polymerase II transcription regulator complex 1 ATF7
Cell membrane 6 CD2, CLDN1, LIPE, MARVELD1, TLR4, TNF
Multi-pass membrane protein 4 ATP4A, CLDN1, HMGCR, MARVELD1
Golgi apparatus membrane 2 NLRP3, PYCARD
cell surface 3 CD2, TLR4, TNF
glutamatergic synapse 1 CASP3
Golgi apparatus 2 CD2, PTGS1
Golgi membrane 3 INS, NLRP3, PYCARD
growth cone 1 ANG
neuronal cell body 4 ANG, CASP3, PYCARD, TNF
Cytoplasm, cytosol 2 LIPE, NLRP3
Lysosome 1 TYR
plasma membrane 7 ATP4A, CD2, CD7, CLDN1, MARVELD1, TLR4, TNF
Membrane 9 ATP4A, CAT, CD7, CLDN1, HMGCR, LIPE, MARVELD1, NLRP3, TLR4
apical plasma membrane 2 ATP4A, CLDN1
basolateral plasma membrane 1 CLDN1
caveola 2 LIPE, PTGS2
extracellular exosome 3 CAT, GPT, PTGS1
endoplasmic reticulum 4 HMGCR, NLRP3, PTGS2, PYCARD
extracellular space 4 ANG, ATP4A, INS, TNF
perinuclear region of cytoplasm 2 TLR4, TYR
Cell junction, tight junction 1 CLDN1
bicellular tight junction 1 CLDN1
mitochondrion 3 CAT, NLRP3, PYCARD
protein-containing complex 5 CAT, CD2, CLDN1, PTGS2, PYCARD
intracellular membrane-bounded organelle 3 CAT, PTGS1, TYR
Microsome membrane 2 PTGS1, PTGS2
postsynaptic density 1 CASP3
Single-pass type I membrane protein 3 CD2, TLR4, TYR
Secreted 3 ANG, INS, NLRP3
extracellular region 7 ANG, CAT, CD2, INS, NLRP3, PYCARD, TNF
cytoplasmic side of plasma membrane 1 CD2
mitochondrial matrix 1 CAT
photoreceptor outer segment 1 PTGS1
external side of plasma membrane 3 CD2, TLR4, TNF
actin cytoskeleton 1 ANG
nucleolus 2 ANG, PYCARD
Melanosome membrane 1 TYR
Early endosome 1 TLR4
cell-cell junction 1 CD2
Golgi-associated vesicle 1 TYR
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
Apical cell membrane 1 ATP4A
Membrane raft 1 TNF
Cytoplasm, cytoskeleton 1 MARVELD1
focal adhesion 1 CAT
microtubule 1 PYCARD
Peroxisome 1 CAT
basement membrane 1 ANG
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 2 CAT, HMGCR
lateral plasma membrane 1 CLDN1
Cytoplasm, cytoskeleton, microtubule organizing center 1 NLRP3
Inflammasome 2 NLRP3, PYCARD
interphase microtubule organizing center 1 NLRP3
NLRP3 inflammasome complex 2 NLRP3, PYCARD
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
Cell projection, ruffle 1 TLR4
ruffle 1 TLR4
receptor complex 1 TLR4
neuron projection 2 PTGS1, PTGS2
chromatin 1 ATF7
phagocytic cup 2 TLR4, TNF
Chromosome 1 ANG
cytoskeleton 1 MARVELD1
[Isoform 5]: Cytoplasm 1 ATF7
Nucleus, nucleolus 1 ANG
Chromosome, telomere 1 ATF7
chromosome, telomeric region 1 ATF7
Basolateral cell membrane 1 CLDN1
Endomembrane system 2 NLRP3, PTGS1
endosome lumen 1 INS
Lipid droplet 1 LIPE
Membrane, caveola 1 LIPE
microtubule organizing center 1 NLRP3
Nucleus, nucleoplasm 1 ATF7
Melanosome 1 TYR
Cytoplasm, Stress granule 1 ANG
cytoplasmic stress granule 1 ANG
Peroxisome membrane 1 HMGCR
lipopolysaccharide receptor complex 1 TLR4
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 3 CAT, INS, PYCARD
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 INS, PTGS2
endocytic vesicle 1 ANG
transport vesicle 1 INS
tight junction 1 CLDN1
azurophil granule lumen 1 PYCARD
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
AIM2 inflammasome complex 1 PYCARD
IkappaB kinase complex 1 PYCARD
death-inducing signaling complex 1 CASP3
canonical inflammasome complex 1 PYCARD
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
angiogenin-PRI complex 1 ANG
catalase complex 1 CAT
potassium:proton exchanging ATPase complex 1 ATP4A
NLRP1 inflammasome complex 1 PYCARD
NLRP6 inflammasome complex 1 PYCARD
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Tunisha Verma, Savita Bhardwaj, Ali Raza, Ivica Djalovic, Pv Vara Prasad, Dhriti Kapoor. Mitigation of salt stress in Indian mustard (Brassica juncea L.) by the application of triacontanol and hydrogen sulfide. Plant signaling & behavior. 2023 12; 18(1):2189371. doi: 10.1080/15592324.2023.2189371. [PMID: 36934336]
  • 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]
  • Izabela Weremczuk-Jeżyna, Katarzyna Hnatuszko-Konka, Liwia Lebelt, Dorota G Piotrowska, Izabela Grzegorczyk-Karolak. The Effect of the Stress-Signalling Mediator Triacontanol on Biochemical and Physiological Modifications in Dracocephalum forrestii Culture. International journal of molecular sciences. 2022 Dec; 23(23):. doi: 10.3390/ijms232315147. [PMID: 36499476]
  • Shakil Ahmed, Maria Ahmad, Rehana Sardar, Muhammad Amir Ismail. Triacontanol priming as a smart strategy to attenuate lead toxicity in Brassica oleracea L. International journal of phytoremediation. 2022 Nov; ?(?):1-16. doi: 10.1080/15226514.2022.2143478. [PMID: 36384370]
  • Giovanni Mian, Nicola Belfiore, Rita Musetti, Diego Tomasi, Pierpaolo Cantone, Lorenzo Lovat, Stefania Lupinelli, Lucilla Iacumin, Emilio Celotti, Fabrizio Golinelli. Effect of a triacontanol-rich biostimulant on the ripening dynamic and wine must technological parameters in Vitis vinifera cv. 'Ribolla Gialla'. Plant physiology and biochemistry : PPB. 2022 Oct; 188(?):60-69. doi: 10.1016/j.plaphy.2022.07.032. [PMID: 35987022]
  • Rehana Sardar, Shakil Ahmed, Muhammad Akbar, Nasim Ahmad Yasin, Guihua Li. Alleviation of cadmium phytotoxicity in triacontanol treated Coriandrum sativum L. by modulation of physiochemical attributes, oxidative stress biomarkers and antioxidative system. Chemosphere. 2022 May; 295(?):133924. doi: 10.1016/j.chemosphere.2022.133924. [PMID: 35149022]
  • Mubeen Sarwar, Sumreen Anjum, Muhammad Waqar Alam, Qurban Ali, C M Ayyub, Muhammad Saleem Haider, M Irfan Ashraf, Wajid Mahboob. Triacontanol regulates morphological traits and enzymatic activities of salinity affected hot pepper plants. Scientific reports. 2022 03; 12(1):3736. doi: 10.1038/s41598-022-06516-w. [PMID: 35260596]
  • Aarifa Nabi, Tariq Aftab, M Masroor, A Khan, M Naeem. Exogenous triacontanol provides tolerance against arsenic-induced toxicity by scavenging ROS and improving morphology and physiological activities of Mentha arvensis L. Environmental pollution (Barking, Essex : 1987). 2022 Feb; 295(?):118609. doi: 10.1016/j.envpol.2021.118609. [PMID: 34896400]
  • H Faiz, O Khan, I Ali, T Hussain, S T Haider, T Siddique, M Liaquat, A Noor, R W Khan, S Ashraf, S Rashid, A Noreen, S Asghar, Q S Anjum. Foliar application of triacontanol ameliorates heat stress through regulation of the antioxidant defense system and improves yield of eggplant. Brazilian journal of biology = Revista brasleira de biologia. 2022; 84(?):e253696. doi: 10.1590/1519-6984.253696. [PMID: 35043836]
  • Mubeen Sarwar, Sumreen Anjum, Qurban Ali, Muhammad Waqar Alam, Muhammad Saleem Haider, Wajid Mehboob. Triacontanol modulates salt stress tolerance in cucumber by altering the physiological and biochemical status of plant cells. Scientific reports. 2021 12; 11(1):24504. doi: 10.1038/s41598-021-04174-y. [PMID: 34969963]
  • Javed Ahmad, Arlene A Ali, Asma A Al-Huqail, M Irfan Qureshi. Triacontanol attenuates drought-induced oxidative stress in Brassica juncea L. by regulating lignification genes, calcium metabolism and the antioxidant system. Plant physiology and biochemistry : PPB. 2021 Sep; 166(?):985-998. doi: 10.1016/j.plaphy.2021.07.009. [PMID: 34265697]
  • Basmah M Alharbi, Awatif Mahfouz Abdulmajeed, Heba Hassan. Biochemical and Molecular Effects Induced by Triacontanol in Acquired Tolerance of Rice to Drought Stress. Genes. 2021 07; 12(8):. doi: 10.3390/genes12081119. [PMID: 34440293]
  • Mirka Macel, Isabella G S Visschers, Janny L Peters, Nicole M van Dam, Rob M de Graaf. High Concentrations of Very Long Chain Leaf Wax Alkanes of Thrips Susceptible Pepper Accessions (Capsicum spp). Journal of chemical ecology. 2020 Dec; 46(11-12):1082-1089. doi: 10.1007/s10886-020-01226-x. [PMID: 33089351]
  • S A Shoba, I V Gorepekin, G N Fedotov, T A Gracheva. Plant Growth Hormones Increase the Stimulation Efficiency of Seedlings Development for Spring Wheat Seeds upon Pre-sowing Treatment. Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections. 2020 Jul; 493(1):128-131. doi: 10.1134/s0012496620040080. [PMID: 32894427]
  • Yimeng Zhou, Ning Li, Zhixia Qiu, Xiaoyu Lu, Min Fang, Xijing Chen, Lili Ren, Guangji Wang, Pingkai Ouyang. Superior anti-neoplastic activities of triacontanol-PEG conjugate: synthesis, characterization and biological evaluations. Drug delivery. 2018 Nov; 25(1):1546-1559. doi: 10.1080/10717544.2018.1477864. [PMID: 30022695]
  • Stefania Sut, Clizia Franceschi, Gregorio Peron, Gabriele Poloniato, Stefano Dall'Acqua. Development and Validation of an HPLC-ELSD Method for the Quantification of 1-Triacontanol in Solid and Liquid Samples. Molecules (Basel, Switzerland). 2018 Oct; 23(11):. doi: 10.3390/molecules23112775. [PMID: 30373135]
  • Xiaoyu Lu, Min Fang, Yu Dai, Yue Yang, Ali Fan, Jiaqiu Xu, Zhiying Qin, Yang Lu, Di Zhao, Xijing Chen, Ning Li. Quantification of triacontanol and its PEGylated prodrug in rat plasma by GC-MS/MS: Application to a pre-clinical pharmacokinetic study. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2018 Jul; 1089(?):8-15. doi: 10.1016/j.jchromb.2018.04.037. [PMID: 29738967]
  • Elham Asadi Karam, Viviana Maresca, Sergio Sorbo, Batool Keramat, Adriana Basile. Effects of triacontanol on ascorbate-glutathione cycle in Brassica napus L. exposed to cadmium-induced oxidative stress. Ecotoxicology and environmental safety. 2017 Oct; 144(?):268-274. doi: 10.1016/j.ecoenv.2017.06.035. [PMID: 28633105]
  • Kan Chen, Chang-Qian Wang, Yu-Qi Fan, Zhi-Hua Han, Yue Wang, Lin Gao, Hua-Su Zeng. [Lipid-lowering effect of seven traditional Chinese medicine monomers in zebrafish system]. Sheng li xue bao : [Acta physiologica Sinica]. 2017 Feb; 69(1):55-60. doi: . [PMID: 28217808]
  • Muhammad Waqas, Raheem Shahzad, Abdul Latif Khan, Sajjad Asaf, Yoon-Ha Kim, Sang-Mo Kang, Saqib Bilal, Muhammad Hamayun, In-Jung Lee. Salvaging effect of triacontanol on plant growth, thermotolerance, macro-nutrient content, amino acid concentration and modulation of defense hormonal levels under heat stress. Plant physiology and biochemistry : PPB. 2016 Feb; 99(?):118-25. doi: 10.1016/j.plaphy.2015.12.012. [PMID: 26744997]
  • Divya Pulivarthi, Kelly Marie Steinberg, Lianet Monzote, Abel Piñón, William N Setzer. Antileishmanial Activity of Compounds Isolated from Sassafras albidum. Natural product communications. 2015 Jul; 10(7):1229-30. doi: . [PMID: 26411017]
  • Chunfeng Wang, Ali Fan, Xiaojie Zhu, Yang Lu, Shuhua Deng, Wenchao Gao, Wei Zhang, Qi Liu, Xijing Chen. Trace quantification of 1-triacontanol in beagle plasma by GC-MS/MS and its application to a pharmacokinetic study. Biomedical chromatography : BMC. 2015 May; 29(5):749-55. doi: 10.1002/bmc.3351. [PMID: 25331188]
  • Chunfeng Wang, Ali Fan, Shuhua Deng, Wenchao Gao, Wei Zhang, Wei Yang, Xiaojie Zhu, Yang Lu, Xijing Chen. Investigation on pharmacokinetics, tissue distribution and excretion of 1-triacontanol in rats by gas chromatography-tandem mass spectrometry (GC-MS/MS). Xenobiotica; the fate of foreign compounds in biological systems. 2015 Jan; 45(1):71-8. doi: 10.3109/00498254.2014.943334. [PMID: 25080280]
  • Sugey López-Martínez, Gabriel Navarrete-Vázquez, Samuel Estrada-Soto, Ismael León-Rivera, María Yolanda Rios. Chemical constituents of the hemiparasitic plant Phoradendron brachystachyum DC Nutt (Viscaceae). Natural product research. 2013; 27(2):130-6. doi: 10.1080/14786419.2012.662646. [PMID: 22360797]
  • M K Akitha Devi, G Sakthivelu, P Giridhar, G A Ravishankar. Protocol for augmented shoot organogenesis in selected variety of soybean [Glycine max L. (Merr.)]. Indian journal of experimental biology. 2012 Oct; 50(10):729-34. doi: . [PMID: 23214267]
  • Veeramuthu Duraipandiyan, Naif Abdullah Al-Harbi, Savarimuthu Ignacimuthu, Chinnasamy Muthukumar. Antimicrobial activity of sesquiterpene lactones isolated from traditional medicinal plant, Costus speciosus (Koen ex.Retz.) Sm. BMC complementary and alternative medicine. 2012 Mar; 12(?):13. doi: 10.1186/1472-6882-12-13. [PMID: 22397713]
  • Vijaya Ravinayagam, Ravindran Jaganathan, Sachdanandam Panchanadham, Shanthi Palanivelu. Potential Antioxidant Role of Tridham in Managing Oxidative Stress against Aflatoxin-B(1)-Induced Experimental Hepatocellular Carcinoma. International journal of hepatology. 2012; 2012(?):428373. doi: 10.1155/2012/428373. [PMID: 22518320]
  • Niranjan Das, Basudev Achari, Yoshihiro Harigaya, Biswanath Dinda. A new flavonol glucoside from the aerial parts of Sida glutinosa. Journal of Asian natural products research. 2011 Oct; 13(10):965-71. doi: 10.1080/10286020.2011.602343. [PMID: 21972814]
  • Sumayya Saied, Shazia Shah, Zulfiqar Ali, Ajmal Khan, Bishnu P Marasini, Muhammad Iqbal Choudhary. Chemical constituents of Cichorium intybus and their inhibitory effects against urease and alpha-chymotrypsin enzymes. Natural product communications. 2011 Aug; 6(8):1117-20. doi: . [PMID: 21922913]
  • Dong Min Jung, Mi Jin Lee, Suk Hoo Yoon, Mun Yhung Jung. A gas chromatography-tandem quadrupole mass spectrometric analysis of policosanols in commercial vegetable oils. Journal of food science. 2011 Aug; 76(6):C891-9. doi: 10.1111/j.1750-3841.2011.02232.x. [PMID: 22417487]
  • Wende Liu, Xiaoying Zhou, Guotian Li, Lei Li, Lingan Kong, Chenfang Wang, Haifeng Zhang, Jin-Rong Xu. Multiple plant surface signals are sensed by different mechanisms in the rice blast fungus for appressorium formation. PLoS pathogens. 2011 Jan; 7(1):e1001261. doi: 10.1371/journal.ppat.1001261. [PMID: 21283781]
  • Gerald S Pullman, Kylie Bucalo. Pine somatic embryogenesis using zygotic embryos as explants. Methods in molecular biology (Clifton, N.J.). 2011; 710(?):267-91. doi: 10.1007/978-1-61737-988-8_19. [PMID: 21207275]
  • V J Galani, B G Patel, N B Patel. Argyreia speciosa (Linn. f.) sweet: A comprehensive review. Pharmacognosy reviews. 2010 Jul; 4(8):172-8. doi: 10.4103/0973-7847.70913. [PMID: 22228958]
  • Priyono, Bruno Florin, Michel Rigoreau, Jean-Paul Ducos, Ucu Sumirat, Surip Mawardi, Charles Lambot, Pierre Broun, Vincent Pétiard, Teguh Wahyudi, Dominique Crouzillat. Somatic embryogenesis and vegetative cutting capacity are under distinct genetic control in Coffea canephora Pierre. Plant cell reports. 2010 Apr; 29(4):343-57. doi: 10.1007/s00299-010-0825-9. [PMID: 20145933]
  • Berit Ebert, Daniela Zöller, Alexander Erban, Ines Fehrle, Jürgen Hartmann, Annette Niehl, Joachim Kopka, Joachim Fisahn. Metabolic profiling of Arabidopsis thaliana epidermal cells. Journal of experimental botany. 2010 Mar; 61(5):1321-35. doi: 10.1093/jxb/erq002. [PMID: 20150518]
  • Nurhan T Dunford, Jeff Edwards. Nutritional bioactive components of wheat straw as affected by genotype and environment. Bioresource technology. 2010 Jan; 101(1):422-5. doi: 10.1016/j.biortech.2009.08.009. [PMID: 19716291]
  • Pinar Karacakaya, Nur Koçberber Kiliç, Ergin Duygu, Gönül Dönmez. Stimulation of reactive dye removal by cyanobacteria in media containing triacontanol hormone. Journal of hazardous materials. 2009 Dec; 172(2-3):1635-9. doi: 10.1016/j.jhazmat.2009.08.037. [PMID: 19740608]
  • Daniela Haim, Miriam Berríos, Alfonso Valenzuela, Luis A Videla. Trace quantification of 1-octacosanol and 1-triacontanol and their main metabolites in plasma by liquid-liquid extraction coupled with gas chromatography-mass spectrometry. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2009 Dec; 877(32):4154-8. doi: 10.1016/j.jchromb.2009.10.034. [PMID: 19931494]
  • Neena Srivastava, Sayadda Khatoon, A K S Rawat, Vartika Rai, Shanta Mehrotra. Chromatographic estimation of p-coumaric acid and triacontanol in an Ayurvedic root drug patala (Stereospermum suaveolens Roxb.). Journal of chromatographic science. 2009 Nov; 47(10):936-9. doi: 10.1093/chromsci/47.10.936. [PMID: 19930809]
  • Wendong Xu, Chenggen Zhu, Wei Cheng, Xiaona Fan, Xiaoguang Chen, Sen Yang, Ying Guo, Fei Ye, Jiangong Shi. Chemical Constituents of the Roots of Euphorbia micractina. Journal of natural products. 2009 Sep; 72(9):1620-6. doi: 10.1021/np900305j. [PMID: 19702283]
  • Anna Lytovchenko, Romina Beleggia, Nicolas Schauer, Tal Isaacson, Jan E Leuendorf, Hanjo Hellmann, Jocelyn Kc Rose, Alisdair R Fernie. Application of GC-MS for the detection of lipophilic compounds in diverse plant tissues. Plant methods. 2009 Apr; 5(?):4. doi: 10.1186/1746-4811-5-4. [PMID: 19393072]
  • G Sivakumar Swamy, Sivakumar G Swamy, K Ramanarayan, Laxmi S Inamdar, Sanjeev R Inamdar. Triacontanol and jasmonic acid differentially modulate the lipid organization as evidenced by the fluorescent probe behavior and 31P nuclear magnetic resonance shifts in model membranes. The Journal of membrane biology. 2009 Apr; 228(3):165-77. doi: 10.1007/s00232-009-9169-1. [PMID: 19418089]
  • An Liu, Lizhen Xu, Zhongmei Zou, Shilin Yang. [Studies on chemical constituents from leaves of Cassia alata]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2009 Apr; 34(7):861-3. doi: . [PMID: 19623982]
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  • Miao Wen, Reinhard Jetter. Composition of secondary alcohols, ketones, alkanediols, and ketols in Arabidopsis thaliana cuticular waxes. Journal of experimental botany. 2009; 60(6):1811-21. doi: 10.1093/jxb/erp061. [PMID: 19346242]
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  • Ravi K Upadhyay, Leena Rohatgi, Mukesh K Chaubey, Subhash C Jain. Ovipositional responses of the pulse beetle, Bruchus chinensis (Coleoptera: Bruchidae) to extracts and compounds of Capparis decidua. Journal of agricultural and food chemistry. 2006 Dec; 54(26):9747-51. doi: 10.1021/jf0608367. [PMID: 17177496]
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  • Hasenah Ali, P J Houghton, Amala Soumyanath. alpha-Amylase inhibitory activity of some Malaysian plants used to treat diabetes; with particular reference to Phyllanthus amarus. Journal of ethnopharmacology. 2006 Oct; 107(3):449-55. doi: 10.1016/j.jep.2006.04.004. [PMID: 16678367]
  • Nian-Yun Yang, Jin-Ao Duan, Ping Li, Shi-Hui Qian. Chemical constituents of Glechoma longituba. Yao xue xue bao = Acta pharmaceutica Sinica. 2006 May; 41(5):431-4. doi: . [PMID: 16848319]
  • Livy Williams, Maria C Coscarón, Pablo M Dellapé, Timberley M Roane. The shield-backed bug, Pachycoris stallii: description of immature stages, effect of maternal care on nymphs, and notes on life history. Journal of insect science (Online). 2005 Nov; 5(?):29. doi: 10.1093/jis/5.1.29. [PMID: 17119611]
  • Ill-Min Chung, Sang-Joon Hahn, Ateeque Ahmad. Confirmation of potential herbicidal agents in hulls of rice, Oryza sativa. Journal of chemical ecology. 2005 Jun; 31(6):1339-52. doi: 10.1007/s10886-005-5290-5. [PMID: 16222775]
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