Pinostrobin (BioDeep_00000003823)

 

Secondary id: BioDeep_00000843596

natural product PANOMIX_OTCML-2023


代谢物信息卡片


(2R)-5-hydroxy-7-methoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one

化学式: C16H14O4 (270.0892)
中文名称: 松属素-7-甲醚, 球松素
谱图信息: 最多检出来源 Viridiplantae(plant) 16.49%

分子结构信息

SMILES: C1(OC)=CC2OC(C3C=CC=CC=3)CC(=O)C=2C(O)=C1
InChI: InChI=1S/C16H14O4/c1-19-11-7-12(17)16-13(18)9-14(20-15(16)8-11)10-5-3-2-4-6-10/h2-8,14,17H,9H2,1H3

描述信息

A monohydroxyflavanone that is (2S)-flavanone substituted by a hydroxy group at position 5 and a methoxy group at position 7 respectively.
Pinostrobin is a natural product found in Uvaria chamae, Zuccagnia punctata, and other organisms with data available.

同义名列表

16 个代谢物同义名

5-hydroxy-7-methoxy-2-phenylchroman-4-one; 5-Hydroxy-7-methoxyflavanone; Pinocembrin-7-methyl ether; Pinostrobin; (2R)-5-hydroxy-7-methoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one; (S)-2,3-Dihydro-5-hydroxy-7-methoxy-2-phenyl-4-benzopyrone; 5-hydroxy-7-methoxy-2-phenyl-2,3-dihydro-4H-chromen-4-one; 5-hydroxy-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one; ( inverted exclamation markA)-Pinostrobin; (+/-)-Pinostrobin, >=99.0\\% (TLC); Chloroformic acidN-amyl ester; ORJDDOBAOGKRJV-UHFFFAOYSA-N; (+/-)-Pinostrobin; ()-Pinostrobin; (S)-2,3-Dihydro-5-hydroxy-7-methoxy-2-phenyl-4H-1-benzopyran-4-one; Pinostrobin



数据库引用编号

40 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(1)

代谢反应

49 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(1)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(48)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

410 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 13 AIMP2, ALB, ANXA5, BCL2, CASP3, CAT, CYP2C19, NQO1, PIK3CA, PPARG, PTGS1, PTGS2, TYR
Peripheral membrane protein 3 ANXA5, PTGS1, PTGS2
Endoplasmic reticulum membrane 6 BCL2, CYP19A1, CYP2C19, HMOX1, PTGS1, PTGS2
Nucleus 8 AIMP2, ALB, BCL2, CASP3, GABPA, HMOX1, NQO1, PPARG
cytosol 10 AIMP2, ALB, ANXA5, BCL2, CASP3, CAT, HMOX1, NQO1, PIK3CA, PPARG
dendrite 1 NQO1
centrosome 1 ALB
nucleoplasm 5 CASP3, GABPA, HMOX1, PPARG, SCNN1G
RNA polymerase II transcription regulator complex 1 PPARG
Cell membrane 1 TNF
Cytoplasmic side 1 HMOX1
lamellipodium 1 PIK3CA
Multi-pass membrane protein 2 CYP19A1, SCNN1G
Synapse 1 NQO1
cell surface 1 TNF
glutamatergic synapse 1 CASP3
Golgi apparatus 2 ALB, PTGS1
neuronal cell body 3 CASP3, NQO1, TNF
sarcolemma 1 ANXA5
Cytoplasm, cytosol 2 AIMP2, NQO1
Lysosome 1 TYR
plasma membrane 4 CYP2C19, PIK3CA, SCNN1G, TNF
Membrane 7 AIMP2, ANXA5, BCL2, CAT, CYP19A1, HMOX1, NQO1
apical plasma membrane 1 SCNN1G
caveola 1 PTGS2
extracellular exosome 5 ALB, ANXA5, CAT, PTGS1, SCNN1G
endoplasmic reticulum 5 ALB, BCL2, CYP19A1, HMOX1, PTGS2
extracellular space 5 ALB, HMOX1, IL10, IL6, TNF
perinuclear region of cytoplasm 4 HMOX1, PIK3CA, PPARG, TYR
intercalated disc 1 PIK3CA
mitochondrion 2 BCL2, CAT
protein-containing complex 4 ALB, BCL2, CAT, PTGS2
intracellular membrane-bounded organelle 5 CAT, CYP2C19, PPARG, PTGS1, TYR
Microsome membrane 3 CYP19A1, PTGS1, PTGS2
postsynaptic density 1 CASP3
Single-pass type I membrane protein 1 TYR
Secreted 3 ALB, IL10, IL6
extracellular region 6 ALB, ANXA5, CAT, IL10, IL6, TNF
Mitochondrion outer membrane 1 BCL2
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 2 BCL2, HMOX1
mitochondrial matrix 1 CAT
anchoring junction 1 ALB
photoreceptor outer segment 1 PTGS1
Nucleus membrane 1 BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 1 BCL2
external side of plasma membrane 3 ANXA5, SCNN1G, TNF
Melanosome membrane 1 TYR
Golgi-associated vesicle 1 TYR
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
Apical cell membrane 1 SCNN1G
Membrane raft 1 TNF
pore complex 1 BCL2
focal adhesion 2 ANXA5, CAT
Peroxisome 1 CAT
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
collagen-containing extracellular matrix 1 ANXA5
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
receptor complex 1 PPARG
Zymogen granule membrane 1 ANXA5
neuron projection 2 PTGS1, PTGS2
ciliary basal body 1 ALB
chromatin 2 GABPA, PPARG
phagocytic cup 1 TNF
centriole 1 ALB
spindle pole 1 ALB
blood microparticle 1 ALB
Endomembrane system 1 PTGS1
sodium channel complex 1 SCNN1G
Melanosome 1 TYR
myelin sheath 1 BCL2
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 1 CAT
endoplasmic reticulum lumen 3 ALB, IL6, PTGS2
platelet alpha granule lumen 1 ALB
phosphatidylinositol 3-kinase complex 1 PIK3CA
phosphatidylinositol 3-kinase complex, class IA 1 PIK3CA
Single-pass type IV membrane protein 1 HMOX1
vesicle membrane 1 ANXA5
death-inducing signaling complex 1 CASP3
aminoacyl-tRNA synthetase multienzyme complex 1 AIMP2
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
catalase complex 1 CAT
interleukin-6 receptor complex 1 IL6
endothelial microparticle 1 ANXA5
BAD-BCL-2 complex 1 BCL2
phosphatidylinositol 3-kinase complex, class IB 1 PIK3CA
ciliary transition fiber 1 ALB
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Liyun Zhao, Liyuan Yao, Rui Chen, Jiani He, Tingting Lin, Silin Qiu, Guohua Chen, Hongfeng Chen, Sheng-Xiang Qiu. Pinosrtobin from plants and propolis against human coronavirus HCoV-OC43 by modulating host AHR/CYP1A1 pathway and lipid metabolism. Antiviral research. 2023 Mar; 212(?):105570. doi: 10.1016/j.antiviral.2023.105570. [PMID: 36863496]
  • Kanlayanee Tonum, Napason Chabang, Somsak Fongsupa, Suphat Chantawarin, Chutima Jiarpinitnun, Patoomrattana Tuchinda, Sunhapas Soodvilai. Pinostrobin inhibits renal CFTR-mediated Cl- secretion and retards cyst growth in cell-derived cyst and polycystic kidney disease rats. Journal of pharmacological sciences. 2022 Apr; 148(4):369-376. doi: 10.1016/j.jphs.2022.02.003. [PMID: 35300812]
  • Yvonne Jing Mei Liew, Yean Kee Lee, Norzulaani Khalid, Noorsaadah Abd Rahman, Boon Chin Tan. Cell-Free Expression of a Plant Membrane Protein BrPT2 From Boesenbergia Rotunda. Molecular biotechnology. 2021 Apr; 63(4):316-326. doi: 10.1007/s12033-021-00304-z. [PMID: 33565047]
  • Jamras Kanchanapiboon, Ubonphan Kongsa, Duangpen Pattamadilok, Sunisa Kamponchaidet, Detmontree Wachisunthon, Subhadhcha Poonsatha, Sasiwan Tuntoaw. Boesenbergia rotunda extract inhibits Candida albicans biofilm formation by pinostrobin and pinocembrin. Journal of ethnopharmacology. 2020 Oct; 261(?):113193. doi: 10.1016/j.jep.2020.113193. [PMID: 32730867]
  • Siwaporn Boonyasuppayakorn, Thanaphon Saelee, Peerapat Visitchanakun, Asada Leelahavanichkul, Kowit Hengphasatporn, Yasuteru Shigeta, Thao Nguyen Thanh Huynh, Justin Jang Hann Chu, Thanyada Rungrotmongkol, Warinthorn Chavasiri. Dibromopinocembrin and Dibromopinostrobin Are Potential Anti-Dengue Leads with Mild Animal Toxicity. Molecules (Basel, Switzerland). 2020 Sep; 25(18):. doi: 10.3390/molecules25184154. [PMID: 32932762]
  • Alvaro José Hernández Tasco, Román Yesid Ramírez Rueda, Carlos José Alvarez, Fabiana Terezinha Sartori, Ana Claudia B C Sacilotto, Izabel Yoko Ito, Walter Vichnewski, Marcos José Salvador. Antibacterial and antifungal properties of crude extracts and isolated compounds from Lychnophora markgravii. Natural product research. 2020 Mar; 34(6):863-867. doi: 10.1080/14786419.2018.1503263. [PMID: 30445853]
  • Kumju Youn, Mira Jun. Biological Evaluation and Docking Analysis of Potent BACE1 Inhibitors from Boesenbergia rotunda. Nutrients. 2019 Mar; 11(3):. doi: 10.3390/nu11030662. [PMID: 30893825]
  • Loretta Pobłocka-Olech, Iwona Inkielewicz-Stepniak, Mirosława Krauze-Baranowska. Anti-inflammatory and antioxidative effects of the buds from different species of Populus in human gingival fibroblast cells: Role of bioflavanones. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2019 Mar; 56(?):1-9. doi: 10.1016/j.phymed.2018.08.015. [PMID: 30668329]
  • Xiaoai He, Huichen Zhang, Xianrui Liang. Separation of six compounds from pigeon pea leaves by elution-extrusion counter-current chromatography. Journal of separation science. 2019 Mar; 42(6):1202-1209. doi: 10.1002/jssc.201801111. [PMID: 30653252]
  • Chuwen Li, Benqin Tang, Yu Feng, Fan Tang, Maggie Pui-Man Hoi, Ziren Su, Simon Ming-Yuen Lee. Pinostrobin Exerts Neuroprotective Actions in Neurotoxin-Induced Parkinson's Disease Models through Nrf2 Induction. Journal of agricultural and food chemistry. 2018 Aug; 66(31):8307-8318. doi: 10.1021/acs.jafc.8b02607. [PMID: 29961319]
  • Wan-Yun Gao, Pei-Yi Chen, Shih-Fen Chen, Ming-Jiuan Wu, Heng-Yuan Chang, Jui-Hung Yen. Pinostrobin Inhibits Proprotein Convertase Subtilisin/Kexin-type 9 (PCSK9) Gene Expression through the Modulation of FoxO3a Protein in HepG2 Cells. Journal of agricultural and food chemistry. 2018 Jun; 66(24):6083-6093. doi: 10.1021/acs.jafc.8b02559. [PMID: 29862818]
  • Piotr Kuś, Igor Jerković, Martina Jakovljević, Stela Jokić. Extraction of bioactive phenolics from black poplar (Populus nigra L.) buds by supercritical CO2 and its optimization by response surface methodology. Journal of pharmaceutical and biomedical analysis. 2018 Apr; 152(?):128-136. doi: 10.1016/j.jpba.2018.01.046. [PMID: 29414004]
  • Chengbo Gu, Linan Fu, Xiaohan Yuan, Zhiguo Liu. Promoting Effect of Pinostrobin on the Proliferation, Differentiation, and Mineralization of Murine Pre-osteoblastic MC3T3-E1 Cells. Molecules (Basel, Switzerland). 2017 Oct; 22(10):. doi: 10.3390/molecules22101735. [PMID: 29035339]
  • Shengnan Tan, Zhimin Dong, Jiashuo Zhang, Thomas Efferth, Yujie Fu, Xin Hua. Cytochrome P450 reaction phenotyping and inhibition and induction studies of pinostrobin in human liver microsomes and hepatocytes. Biomedical chromatography : BMC. 2017 Jun; 31(6):. doi: 10.1002/bmc.3888. [PMID: 28111763]
  • Yelin Kang, Bong-Gyu Kim, Sunghoon Kim, Youngshim Lee, Youngdae Yoon. Inhibitory potential of flavonoids on PtdIns(3,4,5)P3 binding with the phosphoinositide-dependent kinase 1 pleckstrin homology domain. Bioorganic & medicinal chemistry letters. 2017 02; 27(3):420-426. doi: 10.1016/j.bmcl.2016.12.051. [PMID: 28049590]
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  • Neeraj K Patel, Gaurav Jaiswal, Kamlesh K Bhutani. A review on biological sources, chemistry and pharmacological activities of pinostrobin. Natural product research. 2016 Sep; 30(18):2017-27. doi: 10.1080/14786419.2015.1107556. [PMID: 26653796]
  • Isabel Gómez-Betancur, Jaime Andrés Pereañez, Arley Camilo Patiño, Dora Benjumea. Inhibitory effect of pinostrobin from Renealmia alpinia, on the enzymatic and biological activities of a PLA2. International journal of biological macromolecules. 2016 Aug; 89(?):35-42. doi: 10.1016/j.ijbiomac.2016.04.042. [PMID: 27109758]
  • Jason Q D Goodger, Samiddhi L Seneratne, Dean Nicolle, Ian E Woodrow. Foliar Essential Oil Glands of Eucalyptus Subgenus Eucalyptus (Myrtaceae) Are a Rich Source of Flavonoids and Related Non-Volatile Constituents. PloS one. 2016; 11(3):e0151432. doi: 10.1371/journal.pone.0151432. [PMID: 26977933]
  • Jintawee Kicuntod, Wasinee Khuntawee, Peter Wolschann, Piamsook Pongsawasdi, Warinthorn Chavasiri, Nawee Kungwan, Thanyada Rungrotmongkol. Inclusion complexation of pinostrobin with various cyclodextrin derivatives. Journal of molecular graphics & modelling. 2016 Jan; 63(?):91-8. doi: 10.1016/j.jmgm.2015.11.005. [PMID: 26709752]
  • Francisca Palomares-Alonso, Irma Susana Rojas-Tomé, Victorino Juárez Rocha, Guadalupe Palencia Hernández, Angélica González-Maciel, Andrea Ramos-Morales, Rosalba Santiago-Reyes, Iliana Elvira González-Hernández, Helgi Jung-Cook. Cysticidal activity of extracts and isolated compounds from Teloxys graveolens: In vitro and in vivo studies. Experimental parasitology. 2015 Sep; 156(?):79-86. doi: 10.1016/j.exppara.2015.06.001. [PMID: 26072200]
  • Shevin R Feroz, Rumana A Sumi, Sri N A Malek, Saad Tayyab. A comparative analysis on the binding characteristics of various mammalian albumins towards a multitherapeutic agent, pinostrobin. Experimental animals. 2015; 64(2):101-8. doi: 10.1538/expanim.14-0053. [PMID: 25519455]
  • Casey L Sayre, Samaa Alrushaid, Stephanie E Martinez, Hope D Anderson, Neal M Davies. Pre-Clinical Pharmacokinetic and Pharmacodynamic Characterization of Selected Chiral Flavonoids: Pinocembrin and Pinostrobin. Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques. 2015; 18(4):368-95. doi: 10.18433/j3bk5t. [PMID: 26626242]
  • Isabel Gómez-Betancur, Dora Benjumea, Arley Patiño, Nora Jiménez, Edison Osorio. Inhibition of the toxic effects of Bothrops asper venom by pinostrobin, a flavanone isolated from Renealmia alpinia (Rottb.) MAAS. Journal of ethnopharmacology. 2014 Sep; 155(3):1609-15. doi: 10.1016/j.jep.2014.08.002. [PMID: 25138354]
  • Neeraj K Patel, Kamlesh K Bhutani. Pinostrobin and Cajanus lactone isolated from Cajanus cajan (L.) leaves inhibits TNF-α and IL-1β production: in vitro and in vivo experimentation. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2014 Jun; 21(7):946-53. doi: 10.1016/j.phymed.2014.02.011. [PMID: 24680612]
  • Sha-Sha Tian, Fu-Sheng Jiang, Kun Zhang, Xue-Xin Zhu, Bo Jin, Jin-Jian Lu, Zhi-Shan Ding. Flavonoids from the leaves of Carya cathayensis Sarg. inhibit vascular endothelial growth factor-induced angiogenesis. Fitoterapia. 2014 Jan; 92(?):34-40. doi: 10.1016/j.fitote.2013.09.016. [PMID: 24096161]
  • A K Sariev, D A Abaimov, M V Tankevich, D I Prokhorov, S M Adekenov, L I Arystan, R D Seĭfulla. [Experimental study of pinostrobine oxime biotransformation]. Eksperimental'naia i klinicheskaia farmakologiia. 2014; 77(8):39-44. doi: NULL. [PMID: 25335390]
  • Chul Lee, Jin Woo Lee, Qinghao Jin, Dae Sik Jang, Sung-Joon Lee, Dongho Lee, Jin Tae Hong, Youngsoo Kim, Mi Kyeong Lee, Bang Yeon Hwang. Inhibitory constituents of the heartwood of Dalbergia odorifera on nitric oxide production in RAW 264.7 macrophages. Bioorganic & medicinal chemistry letters. 2013 Jul; 23(14):4263-6. doi: 10.1016/j.bmcl.2013.04.032. [PMID: 23743282]
  • Harry Alvarez-Ospina, Isabel Rivero Cruz, Georgina Duarte, Robert Bye, Rachel Mata. HPLC determination of the major active flavonoids and GC-MS analysis of volatile components of Dysphania graveolens (Amaranthaceae). Phytochemical analysis : PCA. 2013 May; 24(3):248-54. doi: 10.1002/pca.2405. [PMID: 23037638]
  • Casey L Sayre, Yangmiao Zhang, Stephanie E Martinez, Jody K Takemoto, Neal M Davies. Stereospecific analytical method development and preliminary in vivo pharmacokinetic characterization of pinostrobin in the rat. Biomedical chromatography : BMC. 2013 May; 27(5):548-50. doi: 10.1002/bmc.2834. [PMID: 23070926]
  • Shevin R Feroz, Saharuddin B Mohamad, Zarith S D Bakri, Sri N A Malek, Saad Tayyab. Probing the interaction of a therapeutic flavonoid, pinostrobin with human serum albumin: multiple spectroscopic and molecular modeling investigations. PloS one. 2013; 8(10):e76067. doi: 10.1371/journal.pone.0076067. [PMID: 24116089]
  • David R Katerere, Alexander I Gray, Robert J Nash, Roger D Waigh. Phytochemical and antimicrobial investigations of stilbenoids and flavonoids isolated from three species of Combretaceae. Fitoterapia. 2012 Jul; 83(5):932-40. doi: 10.1016/j.fitote.2012.04.011. [PMID: 22546149]
  • Jean P Dzoyem, Antoine H L Nkuete, Victor Kuete, Michel F Tala, Hippolyte K Wabo, Santosh K Guru, Vikrant S Rajput, Akash Sharma, Pierre Tane, Inshad A Khan, Anil K Saxena, Hartmut Laatsch, Ning-Hua Tan. Cytotoxicity and antimicrobial activity of the methanol extract and compounds from Polygonum limbatum. Planta medica. 2012 May; 78(8):787-92. doi: 10.1055/s-0031-1298431. [PMID: 22495442]
  • Davide Bertelli, Giulia Papotti, Laura Bortolotti, Gian Luigi Marcazzan, Maria Plessi. ¹H-NMR simultaneous identification of health-relevant compounds in propolis extracts. Phytochemical analysis : PCA. 2012 May; 23(3):260-6. doi: 10.1002/pca.1352. [PMID: 21853496]
  • Mirza Bojić, Željko Debeljak, Marica Medić-Šarić, Maja Tomičić. Interference of selected flavonoid aglycons in platelet aggregation assays. Clinical chemistry and laboratory medicine. 2012 Feb; 50(8):1403-8. doi: 10.1515/cclm-2011-0960. [PMID: 22868805]
  • Keivan Zandi, Boon-Teong Teoh, Sing-Sin Sam, Pooi-Fong Wong, Mohd Rais Mustafa, Sazaly Abubakar. Antiviral activity of four types of bioflavonoid against dengue virus type-2. Virology journal. 2011 Dec; 8(?):560. doi: 10.1186/1743-422x-8-560. [PMID: 22201648]
  • Xin Hua, Yu-Jie Fu, Yuan-Gang Zu, Lin Zhang, Wei Wang, Meng Luo. Determination of pinostrobin in rat plasma by LC-MS/MS: application to pharmacokinetics. Journal of pharmaceutical and biomedical analysis. 2011 Dec; 56(4):841-5. doi: 10.1016/j.jpba.2011.07.038. [PMID: 21840667]
  • Siddig Ibrahim Abdelwahab, Syam Mohan, Mahmmod Ameen Abdulla, Mohd Aspollah Sukari, Ahmad Bustamam Abdul, Manal Mohamed Elhassan Taha, Suvitha Syam, Syahida Ahmad, Ka-Heng Lee. The methanolic extract of Boesenbergia rotunda (L.) Mansf. and its major compound pinostrobin induces anti-ulcerogenic property in vivo: possible involvement of indirect antioxidant action. Journal of ethnopharmacology. 2011 Sep; 137(2):963-70. doi: 10.1016/j.jep.2011.07.010. [PMID: 21771650]
  • Tran Thi Thanh Thuy, Tran Duc Quan, Nguyen Thi Hoang Anh, Tran Van Sung. A new hydrochalcone from Miliusa sinensis. Natural product research. 2011 Aug; 25(14):1361-5. doi: 10.1080/14786419.2011.569505. [PMID: 21859261]
  • De-lin Wu, Shi-yun Chen, Jing-song Liu, Chuan-shan Jin, Feng-qing Xu. [Chemical constituents of Carya cathayensis and their antitumor bioactivity]. Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials. 2011 Jul; 34(7):1055-7. doi: ". [PMID: 22066397]
  • Monika Barbarić, Katarina Mišković, Mirza Bojić, Mirela Baus Lončar, Asja Smolčić-Bubalo, Zeljko Debeljak, Marica Medić-Šarić. Chemical composition of the ethanolic propolis extracts and its effect on HeLa cells. Journal of ethnopharmacology. 2011 Jun; 135(3):772-8. doi: 10.1016/j.jep.2011.04.015. [PMID: 21515353]
  • Nan Wu, Yu Kong, Yuangang Zu, Yujie Fu, Zhiguo Liu, Ronghua Meng, Xia Liu, Thomas Efferth. Activity investigation of pinostrobin towards herpes simplex virus-1 as determined by atomic force microscopy. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2011 Jan; 18(2-3):110-8. doi: 10.1016/j.phymed.2010.07.001. [PMID: 20739162]
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  • Russell A Nicholson, Laurence S David, Rui Le Pan, Xin Min Liu. Pinostrobin from Cajanus cajan (L.) Millsp. inhibits sodium channel-activated depolarization of mouse brain synaptoneurosomes. Fitoterapia. 2010 Oct; 81(7):826-9. doi: 10.1016/j.fitote.2010.05.005. [PMID: 20472040]
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