(2S,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol (BioDeep_00000000835)

Main id: BioDeep_00000619422

 

human metabolite PANOMIX_OTCML-2023 blood metabolite natural product


代谢物信息卡片


Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, endo-(.+/-.)-

化学式: C10H18O (154.1358)
中文名称: 异龙脑, (1S)-1,7,7-三甲基双环[2.2.1]庚烷-2-醇, 龙脑, （-）-冰片, (-)-冰片, 异冰片, DL-异冰片醇
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1(C2CCC1(C(C2)O)C)C
InChI: InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3

描述信息

Borneol appears as a white colored lump-solid with a sharp camphor-like odor. Burns readily. Slightly denser than water and insoluble in water. Used to make perfumes.
Borneol is a bornane monoterpenoid that is 1,7,7-trimethylbicyclo[2.2.1]heptane substituted by a hydroxy group at position 2. It has a role as a volatile oil component and a metabolite.
Isoborneol is a natural product found in Xylopia sericea, Eupatorium capillifolium, and other organisms with data available.
Both Borneol and Isoborneol and their acetates and formates are used as flavouring agents. 2-Bornanol is found in turmeric.
Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1)[1][2].
Isoborneol ((±)-Isoborneol) is a monoterpenoid alcohol present in the essential oils of numerous medicinal plants and has antioxidant and antiviral properties. Isoborneol is a potent inhibitor of herpes simplex virus type 1 (HSV-1)[1][2].

同义名列表

48 个代谢物同义名

Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-, endo-(.+/-.)-; (2S,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol; 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol, exo- #; Endo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol; exo-1,7,7-Trimethylbicyclo(2.2.1)-2-heptanol; Bicyclo(2.2.1)heptan-2-ol, 1,7,7-trimethyl-; 1,7,7-trimethyl-bicyclo[2.2.1]heptan-6-ol; 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol; 4,7,7-trimethylbicyclo[2.2.1]heptan-3-ol; 1,7,7-Trimethylbicyclo(2.2.1)heptan-2-ol; isoborneol, (endo-(+-))-isomer; 1,7,7-trimethylnorbornan-2-ol; isoborneol, (1S-endo)-isomer; isoborneol, (1R-endo)-isomer; isoborneol, (1S-exo)-isomer; isoborneol, (1R-exo)-isomer; isoborneol, (endo)-isomer; isoborneol, (exo)-isomer; Borneol and Isoborneol; Endo-2-hydroxycamphane; (+/-)-Isoborneol; Endo-2-camphanol; Sumatra camphor; exo-2-Camphanol; endo-2-Bornanol; exo-2-Bornanol; Borneo camphor; Bornyl alcohol; DL-Isoborneol; DL-2-Bornanol; Borneol, exo-; (+/-)-borneol; BORNEOL, (L); L(-)-Borneol; (-)-Borneol; 2-Bornanol; DL-Borneol; isoborneol; borneol; Bingpia; baros; (-)-Borneol; (±)-Isoborneol; Borneol; Borneol; (1S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol; (-)-Borneol; Isoborneol



数据库引用编号

27 个数据库交叉引用编号

分类词条

相关代谢途径

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代谢反应

0 个相关的代谢反应过程信息。

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Plant Reactome(0)

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986 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 14 ABCB1, AKT1, BCL2, CASP3, HIF1A, MAPK14, MAPK8, MARVELD1, MTOR, NOS3, PTGS2, RB1, TJP1, VEGFA
Peripheral membrane protein 4 GORASP1, MTOR, PTGS2, TJP1
Endoplasmic reticulum membrane 4 BCL2, MTOR, PTGS2, TRPM8
Nucleus 12 AKT1, BCL2, CASP3, HIF1A, MAPK14, MAPK8, MARVELD1, MTOR, NOS3, RB1, TJP1, VEGFA
cytosol 10 AKT1, BCL2, CASP3, HIF1A, MAPK14, MAPK8, MTOR, NOS3, RB1, TJP1
dendrite 1 MTOR
nuclear body 1 HIF1A
phagocytic vesicle 1 MTOR
nucleoplasm 8 AKT1, CASP3, HIF1A, MAPK14, MAPK8, MTOR, NOS3, RB1
RNA polymerase II transcription regulator complex 1 HIF1A
Cell membrane 7 ABCB1, AKT1, CLDN5, MARVELD1, TJP1, TNF, TRPM8
Cytoplasmic side 3 GORASP1, MTOR, TJP1
lamellipodium 1 AKT1
Multi-pass membrane protein 4 ABCB1, CLDN5, MARVELD1, TRPM8
Golgi apparatus membrane 2 GORASP1, MTOR
Synapse 1 MAPK8
cell cortex 1 AKT1
cell junction 2 CLDN5, TJP1
cell surface 3 ABCB1, TNF, VEGFA
glutamatergic synapse 3 AKT1, CASP3, MAPK14
Golgi apparatus 3 GORASP1, NOS3, VEGFA
Golgi membrane 3 GORASP1, MTOR, NOS3
lysosomal membrane 1 MTOR
mitochondrial inner membrane 1 BDH1
neuronal cell body 2 CASP3, TNF
postsynapse 1 AKT1
Lysosome 1 MTOR
plasma membrane 8 ABCB1, AKT1, CLDN5, MARVELD1, NOS3, TJP1, TNF, TRPM8
Membrane 9 ABCB1, AKT1, BCL2, BDH1, CLDN5, MARVELD1, MTOR, TRPM8, VEGFA
apical plasma membrane 2 ABCB1, TJP1
axon 1 MAPK8
basolateral plasma membrane 1 TJP1
caveola 2 NOS3, PTGS2
extracellular exosome 1 ABCB1
Lysosome membrane 1 MTOR
endoplasmic reticulum 3 BCL2, PTGS2, VEGFA
extracellular space 3 IL6, TNF, VEGFA
perinuclear region of cytoplasm 1 NOS3
Cell junction, tight junction 2 CLDN5, TJP1
adherens junction 2 TJP1, VEGFA
apicolateral plasma membrane 2 CLDN5, TJP1
bicellular tight junction 2 CLDN5, TJP1
gap junction 1 TJP1
intercalated disc 1 TJP1
intercellular canaliculus 1 TJP1
mitochondrion 4 BCL2, BDH1, MAPK14, TJP1
protein-containing complex 5 AKT1, BCL2, HIF1A, PTGS2, TJP1
intracellular membrane-bounded organelle 1 BDH1
Microsome membrane 2 MTOR, PTGS2
postsynaptic density 1 CASP3
TORC1 complex 1 MTOR
TORC2 complex 1 MTOR
Secreted 2 IL6, VEGFA
extracellular region 4 IL6, MAPK14, TNF, VEGFA
Mitochondrion outer membrane 2 BCL2, MTOR
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 2 BCL2, MTOR
Mitochondrion matrix 1 BDH1
mitochondrial matrix 1 BDH1
motile cilium 1 HIF1A
Nucleus membrane 1 BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 1 BCL2
external side of plasma membrane 2 TNF, TRPM8
Secreted, extracellular space, extracellular matrix 1 VEGFA
microtubule cytoskeleton 1 AKT1
axon cytoplasm 1 HIF1A
Cytoplasm, P-body 1 NOS3
P-body 1 NOS3
apical part of cell 1 TJP1
cell-cell junction 2 AKT1, CLDN5
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
vesicle 1 AKT1
Apical cell membrane 1 ABCB1
Mitochondrion inner membrane 1 BDH1
Membrane raft 2 TNF, TRPM8
pore complex 1 BCL2
Cytoplasm, cytoskeleton 1 MARVELD1
spindle 2 AKT1, RB1
cis-Golgi network 1 GORASP1
extracellular matrix 1 VEGFA
Nucleus, PML body 1 MTOR
PML body 2 MTOR, RB1
Mitochondrion intermembrane space 1 AKT1
mitochondrial intermembrane space 1 AKT1
secretory granule 1 VEGFA
lateral plasma membrane 1 CLDN5
nuclear speck 2 HIF1A, MAPK14
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
neuron projection 1 PTGS2
ciliary basal body 1 AKT1
chromatin 2 HIF1A, RB1
cell projection 1 TJP1
phagocytic cup 1 TNF
cytoskeleton 2 MARVELD1, NOS3
Cell projection, podosome 1 TJP1
podosome 1 TJP1
spindle pole 1 MAPK14
nuclear envelope 1 MTOR
Endomembrane system 1 MTOR
Cytoplasm, Stress granule 1 NOS3
cytoplasmic stress granule 1 NOS3
Nucleus speckle 1 HIF1A
euchromatin 1 HIF1A
myelin sheath 1 BCL2
plasma membrane raft 1 TRPM8
ficolin-1-rich granule lumen 1 MAPK14
secretory granule lumen 1 MAPK14
endoplasmic reticulum lumen 2 IL6, PTGS2
platelet alpha granule lumen 1 VEGFA
endocytic vesicle membrane 1 NOS3
paranode region of axon 1 CLDN5
Schmidt-Lanterman incisure 1 CLDN5
tight junction 2 CLDN5, TJP1
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 GORASP1
SWI/SNF complex 1 RB1
Golgi apparatus, cis-Golgi network membrane 1 GORASP1
external side of apical plasma membrane 1 ABCB1
basal dendrite 1 MAPK8
death-inducing signaling complex 1 CASP3
apical junction complex 1 TJP1
Cytoplasmic vesicle, phagosome 1 MTOR
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
interleukin-6 receptor complex 1 IL6
chromatin lock complex 1 RB1
Rb-E2F complex 1 RB1
BAD-BCL-2 complex 1 BCL2
[N-VEGF]: Cytoplasm 1 VEGFA
[VEGFA]: Secreted 1 VEGFA
[Isoform L-VEGF189]: Endoplasmic reticulum 1 VEGFA
[Isoform VEGF121]: Secreted 1 VEGFA
[Isoform VEGF165]: Secreted 1 VEGFA
VEGF-A complex 1 VEGFA
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF
matrix side of mitochondrial inner membrane 1 BDH1


文献列表

  • Yuqi Mei, Yan Chen, Haoyue Zhang, Wenxiang Fan, Longchan Liu, Ziying Wang, Jinyuan Wang, Linhong Fan, Aizhen Xiong, Li Yang, Zhengtao Wang. Borneol acts as an adjuvant agent to enhance the oral absorption of Panax notoginseng saponins in rats: Effect of optical configuration and compatibility ratios. Journal of ethnopharmacology. 2024 Sep; 331(?):118331. doi: 10.1016/j.jep.2024.118331. [PMID: 38734392]
  • Minyi Tian, Dan Xie, Yi Hong, Furong Ding, Xia Wu, Dongxin Tang. Anti-inflammatory effects and related mechanisms in vitro and in vivo of Hedychium coccineum rhizome essential oil. Journal of ethnopharmacology. 2024 Jun; 328(?):118103. doi: 10.1016/j.jep.2024.118103. [PMID: 38527573]
  • Xiaofeng Zhang, Fengjiao Deng, Xueqing Wang, Fanghan Liu, Yue Zhu, Bin Yu, Ming Ruan. Synergistic amelioration between Ligusticum striatum DC and borneol against cerebral ischemia by promoting astrocytes-mediated neurogenesis. Journal of ethnopharmacology. 2024 Jun; 327(?):118062. doi: 10.1016/j.jep.2024.118062. [PMID: 38492790]
  • Miao Luo, Jinfeng He, Liang Yin, Ping Zhan, Zhongqiu Zhao, Hui Xiong, Zhinan Mei. Borneol exerts its antipruritic effects by inhibiting TRPA1 and activating TRPM8. Journal of ethnopharmacology. 2024 Mar; 322(?):117581. doi: 10.1016/j.jep.2023.117581. [PMID: 38103845]
  • Peiwu Xie, Qiyi Yang, Jielian Chen, Tieyao Tu, Huiming Lian, Boxiang He, Yanling Cai. Unpredictable Chemical Diversity of Essential Oils in Cinnamomum burmanni (Lauraceae) Living Collections: Beyond Maternally Inherited Phylogenetic Relationships. Molecules (Basel, Switzerland). 2024 Mar; 29(6):. doi: 10.3390/molecules29061206. [PMID: 38542843]
  • Guodong Chen, Jialong Yang, An Wang, Jiapeng Deng, Kaitao Wang, Minle Ye, Qingyu Chen, Xinye Wang, Xinyu Wu, Dingsheng Lin. L-Borneol promotes skin flap survival by regulating HIF-1α/NF-κB pathway. Journal of ethnopharmacology. 2024 Mar; 321(?):117543. doi: 10.1016/j.jep.2023.117543. [PMID: 38056540]
  • Liang Fang, Junying Li, Hongyan Cheng, Huanhuan Liu, Caiyun Zhang. Dual fluorescence images, transport pathway, and blood-brain barrier penetration of B-Met-W/O/W SE. International journal of pharmaceutics. 2024 Jan; 652(?):123854. doi: 10.1016/j.ijpharm.2024.123854. [PMID: 38280499]
  • Dongyuan Wang, Dan Wang, Qipeng Jin, Xiaolong Wang. Suxiao Jiuxin Pill alleviates myocardial ischemia/reperfusion-induced autophagy via miR-193a-3p/ALKBH5 pathway. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2024 Jan; 125(?):155359. doi: 10.1016/j.phymed.2024.155359. [PMID: 38301300]
  • Yang Liu, Jia-Yu Cai, Yang Liu, Lu Zhang, Rui-Bo Guo, Xue-Tao Li, Ling-Yue Ma, Liang Kong. Borneol-modified docetaxel plus tetrandrine micelles for treatment of drug-resistant brain glioma. Drug development and industrial pharmacy. 2024 Jan; ?(?):1-15. doi: 10.1080/03639045.2024.2302886. [PMID: 38235554]
  • Tianyu Huang, Meng Lai, Zhenwei Lin, Ruiqi Luo, Xuezheng Xiang, Haozhe Xu, Ning Pan, Zhaojiang Zuo. Identification of algicidal monoterpenoids from four chemotypes of Cinnamomum camphora and their algicidal mechanisms on Microcystis aeruginosa. Environmental research. 2024 Jan; 241(?):117714. doi: 10.1016/j.envres.2023.117714. [PMID: 37989462]
  • Feng-Rui Li, Yang Yu, Yu-Meng Du, Liang Kong, Yang Liu, Jia-Hua Wang, Mu-Han Chen, Mo Liu, Zi-Xu Zhang, Xue-Tao Li, Rui-Jun Ju. Borneol-Modified Schisandrin B Micelles Cross the Blood-Brain Barrier To Treat Alzheimer's Disease in Aged Mice. ACS chemical neuroscience. 2024 Jan; ?(?):. doi: 10.1021/acschemneuro.3c00625. [PMID: 38214579]
  • Zhijie Zhao, Xiao Fan, Xinyu Li, Yuwei Qiu, Yunfeng Yi, Yuping Wei, Yong Wang. All-Natural Injectable Antibacterial Hydrogel Enabled by Chitosan and Borneol. Biomacromolecules. 2024 Jan; 25(1):134-142. doi: 10.1021/acs.biomac.3c00874. [PMID: 38145887]
  • Luting Lin, Jingming Luo, Zeng Wang, Xinjun Cai. Borneol promotes autophagic degradation of HIF-1α and enhances chemotherapy sensitivity in malignant glioma. PeerJ. 2024; 12(?):e16691. doi: 10.7717/peerj.16691. [PMID: 38188151]
  • Qian Xie, Danni Lu, Jianmei Yuan, Mihong Ren, Yong Li, Jiajun Wang, Rong Ma, Jian Wang. l-borneol promotes neurovascular unit protection in the subacute phase of transient middle cerebral artery occlusion rats: p38-MAPK pathway activation, anti-inflammatory, and anti-apoptotic effect. Phytotherapy research : PTR. 2023 Sep; 37(9):4166-4184. doi: 10.1002/ptr.7878. [PMID: 37310024]
  • Xiaojing Lin, Linxuan Huang, Huilin Liang, Chen Hou, Xuli Ling, Yuanxia Chen, Peng Yang, Qingwen Wu, Haiying Zhao, Sirong Wu, Ruoting Zhan, Dongming Ma, Jinfen Yang. Genome-wide identification and functional characterization of borneol dehydrogenases in Wurfbainia villosa. Planta. 2023 Aug; 258(4):69. doi: 10.1007/s00425-023-04221-0. [PMID: 37608037]
  • Rong Ma, Danni Lu, Jian Wang, Qian Xie, Jialiang Guo. Comparison of pharmacological activity and safety of different stereochemical configurations of borneol: L-borneol, D-borneol, and synthetic borneol. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2023 Jun; 164(?):114668. doi: 10.1016/j.biopha.2023.114668. [PMID: 37321057]
  • Weifeng Tian, Dongmei He, Jingjing Liu, Feiyu Chen, Wenjie Zhang, Jinsheng Hu, Shu Wang. Topical borneol relieves nonhistaminergic pruritus via targeting TRPA1 and TRPM8 channels in peripheral nerve terminals of mice. European journal of pharmacology. 2023 Jun; 953(?):175833. doi: 10.1016/j.ejphar.2023.175833. [PMID: 37290679]
  • 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]
  • Zhiyong Xu, Junhui Chen, Ruifeng Shang, Fan Yang, Chuanqi Xie, Yunfei Liu, Xuefang Wen, Jianping Fu, Wei Xiong, Lei Wu. The Mosquito Larvicidal Activity of Lignans from Branches of Cinnamomum camphora chvar. Borneol. Molecules (Basel, Switzerland). 2023 Apr; 28(9):. doi: 10.3390/molecules28093769. [PMID: 37175177]
  • Huang Ding, Xiao-Ping Huang, Xiao-Dan Liu, Yan-Ling Li, San Tang, Hai-Long Xiong, Mei-Ting Huang, Ying Li, Cai-Xia Liu, Wei Zhang, Chang-Qing Deng. Effects of borneol combined with astragaloside IV and Panax notoginseng saponins regulation of microglia polarization to promote neurogenesis after cerebral ischaemia. The Journal of pharmacy and pharmacology. 2023 Apr; ?(?):. doi: 10.1093/jpp/rgad033. [PMID: 37185938]
  • Dongli Qi, Huihui Li, Chunxia Liang, Peijin Peng, Zhen Yang, Yanquan Gao, Ziwei Li, Qingqing Zhang, Zhidong Liu. Herb-drug interaction of Xingnaojing injection and Edaravone via pharmacokinetics, mixed inhibition of UGTs, and molecular docking. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2023 Apr; 112(?):154696. doi: 10.1016/j.phymed.2023.154696. [PMID: 36764095]
  • Yu Wang, Xiao-Yun Qiu, Jia-Ying Liu, Bei Tan, Fei Wang, Min-Juan Sun, Xu-Hong Jiang, Xu-Ming Ji, Ceng-Lin Xu, Yi Wang, Zhong Chen. (+)-Borneol enantiomer ameliorates epileptic seizure via decreasing the excitability of glutamatergic transmission. Acta pharmacologica Sinica. 2023 Mar; ?(?):. doi: 10.1038/s41401-023-01075-w. [PMID: 36973542]
  • Dan-Ni Lu, Qian Xie, Zhuo Xu, Jian-Mei Yuan, Rong Ma, Jian Wang. [Protective effects of three kinds of borneol on different brain regions in acute cerebral ischemia/reperfusion model rats]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2023 Mar; 48(5):1289-1299. doi: 10.19540/j.cnki.cjcmm.20221025.406. [PMID: 37005813]
  • Xuan Ni, Xiaoyu Yin, Chelimuge Qi, Chunyu Liu, Hao Chen, Yini Zhou, Wuliji Ao, Shuyin Bao, Jiangdong Xue, Jingfeng Yang, Wu Dong. Cardiotoxicity of (-)-borneol, (+)-borneol, and isoborneol in zebrafish embryos is associated with Na+ /K+ -ATPase and Ca2+ -ATPase inhibition. Journal of applied toxicology : JAT. 2023 Mar; 43(3):373-386. doi: 10.1002/jat.4388. [PMID: 36062847]
  • Wenting Su, Congyan Liu, Xi Jiang, Yanli Lv, Qin Chen, Jiachen Shi, Huangqin Zhang, Qiuling Ma, Chang Ge, Fei Kong, Xiaoqi Li, Yuping Liu, Yan Chen, Ding Qu. An intravitreal-injectable hydrogel depot doped borneol-decorated dual-drug-coloaded microemulsions for long-lasting retina delivery and synergistic therapy of wAMD. Journal of nanobiotechnology. 2023 Mar; 21(1):71. doi: 10.1186/s12951-023-01829-y. [PMID: 36859261]
  • Yu Long, Songyu Liu, Jinyan Wan, Yulu Zhang, Dan Li, Shuang Yu, Ai Shi, Nan Li, Fei He. Brain targeted borneol-baicalin liposome improves blood-brain barrier integrity after cerebral ischemia-reperfusion injury via inhibiting HIF-1α/VEGF/eNOS/NO signal pathway. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2023 Feb; 160(?):114240. doi: 10.1016/j.biopha.2023.114240. [PMID: 36731339]
  • Marwa Chraibi, Mouhcine Fadil, Abdellah Farah, Nesrine Benkhaira, Sara Lebrazi, Kawtar Fikri-Benbrahim. Simplex-centroid design as innovative approach in the optimization of antimicrobial effect of Thymus satureioides, Myrtus communis and Artemisia herba alba essential oils against Escherichia coli, Staphylococcus aureus and Candidatropicalis. Experimental parasitology. 2023 Jan; 247(?):108472. doi: 10.1016/j.exppara.2023.108472. [PMID: 36693583]
  • Zerui Yang, Ting Zhan, Chunzhu Xie, Song Huang, Xiasheng Zheng. Genome-wide analyzation and functional characterization on the TPS family provide insight into the biosynthesis of mono-terpenes in the camphor tree. Plant physiology and biochemistry : PPB. 2023 Jan; 196(?):55-64. doi: 10.1016/j.plaphy.2023.01.039. [PMID: 36696798]
  • Ting Zhang, Yongjie Zheng, Chao Fu, Haikuan Yang, Xinliang Liu, Fengying Qiu, Xindong Wang, Zongde Wang. Chemical Variation and Environmental Influence on Essential Oil of Cinnamomum camphora. Molecules (Basel, Switzerland). 2023 Jan; 28(3):. doi: 10.3390/molecules28030973. [PMID: 36770639]
  • Yuqi Mei, Linnan Li, Linghong Fan, Wenxiang Fan, Longchan Liu, Fangli Zhang, Zhizhi Hu, Kang Wang, Li Yang, Zhengtao Wang. The history, stereochemistry, ethnopharmacology and quality assessment of borneol. Journal of ethnopharmacology. 2023 Jan; 300(?):115697. doi: 10.1016/j.jep.2022.115697. [PMID: 36087846]
  • Abdellatif Alami, Abdelhakim El Ouali Lalami, Saoussan Annemer, Fouad El-Akhal, Yassine Ez Zoubi, Abdellah Farah. Chemical Composition and Larvicidal Properties of Essential Oils from Wild and Cultivated Artemisia campestris L., an Endemic Plant in Morocco. TheScientificWorldJournal. 2023; 2023(?):5748133. doi: 10.1155/2023/5748133. [PMID: 37849964]
  • L Liu, Y Yang, F Yang, Y Lin, K Liu, X Wang, Y Zhang. A mechanistic investigation about hepatoxic effects of borneol using zebrafish. Human & experimental toxicology. 2023 Jan; 42(?):9603271221149011. doi: 10.1177/09603271221149011. [PMID: 36594174]
  • Ayelign M Adal, Elaheh Najafianashrafi, Lukman S Sarker, Soheil S Mahmoud. Cloning, functional characterization and evaluating potential in metabolic engineering for lavender ( +)-bornyl diphosphate synthase. Plant molecular biology. 2023 Jan; 111(1-2):117-130. doi: 10.1007/s11103-022-01315-3. [PMID: 36271988]
  • Wenzhe Yang, Xue Pan, Peng Zhang, Xue Yang, Huashi Guan, Huan Dou, Qian Lu. Defeating Melanoma Through a Nano-Enabled Revision of Hypoxic and Immunosuppressive Tumor Microenvironment. International journal of nanomedicine. 2023; 18(?):3711-3725. doi: 10.2147/ijn.s414882. [PMID: 37435153]
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