Scopoletin (BioDeep_00000000004)

 

Secondary id: BioDeep_00000397986, BioDeep_00000859325

natural product human metabolite PANOMIX_OTCML-2023 Chemicals and Drugs


代谢物信息卡片


7-hydroxy-6-methoxy-2H-chromen-2-one

化学式: C10H8O4 (192.0423)
中文名称: 东莨菪内酯, 东莨菪亭, 东莨菪素, 莨菪亭
谱图信息: 最多检出来源 Viridiplantae(plant) 21.63%

Reviewed

Last reviewed on 2024-07-12.

Cite this Page

Scopoletin. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/scopoletin (retrieved 2024-12-22) (BioDeep RN: BioDeep_00000000004). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: COc(c1)c(O)cc(O2)c(C=CC(=O)2)1
InChI: InChI=1/C10H8O4/c1-13-9-4-6-2-3-10(12)14-8(6)5-7(9)11/h2-5,11H,1H3

描述信息

Scopoletin is a hydroxycoumarin that is umbelliferone bearing a methoxy substituent at position 6. It has a role as a plant growth regulator and a plant metabolite. It is functionally related to an umbelliferone.
Scopoletin is a natural product found in Ficus auriculata, Haplophyllum cappadocicum, and other organisms with data available.
Scopoletin is a coumarin compound found in several plants including those in the genus Scopolia and the genus Brunfelsia, as well as chicory (Cichorium), redstem wormwood (Artemisia scoparia), stinging nettle (Urtica dioica), passion flower (Passiflora), noni (Morinda citrifolia fruit) and European black nightshade (Solanum nigrum) that is comprised of umbelliferone with a methoxy group substituent at position 6. Scopoletin is used to standardize and establish pharmacokinetic properties for products derived from the plants that produce it, such as noni extract. Although the mechanism(s) of action have not yet been established, this agent has potential antineoplastic, antidopaminergic, antioxidant, anti-inflammatory and anticholinesterase effects.
Plant growth factor derived from the root of Scopolia carniolica or Scopolia japonica.
See also: Arnica montana Flower (part of); Lycium barbarum fruit (part of); Viburnum opulus root (part of).
Isolated from Angelica acutiloba (Dong Dang Gui). Scopoletin is found in many foods, some of which are lambsquarters, lemon, sunflower, and sherry.
Scopoletin is found in anise. Scopoletin is isolated from Angelica acutiloba (Dong Dang Gui
A hydroxycoumarin that is umbelliferone bearing a methoxy substituent at position 6.
Acquisition and generation of the data is financially supported in part by CREST/JST.
[Raw Data] CBA72_Scopoletin_pos_20eV.txt
[Raw Data] CBA72_Scopoletin_pos_40eV.txt
[Raw Data] CBA72_Scopoletin_neg_30eV.txt
[Raw Data] CBA72_Scopoletin_neg_50eV.txt
[Raw Data] CBA72_Scopoletin_pos_50eV.txt
[Raw Data] CBA72_Scopoletin_pos_10eV.txt
[Raw Data] CBA72_Scopoletin_neg_40eV.txt
[Raw Data] CBA72_Scopoletin_neg_10eV.txt
[Raw Data] CBA72_Scopoletin_pos_30eV.txt
[Raw Data] CBA72_Scopoletin_neg_20eV.txt

Scopoletin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=92-61-5 (retrieved 2024-07-12) (CAS RN: 92-61-5). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Scopoletin is an inhibitor of acetylcholinesterase (AChE).
Scopoletin is an inhibitor of acetylcholinesterase (AChE).

同义名列表

74 个代谢物同义名

Scopoletin, United States Pharmacopeia (USP) Reference Standard; 2H-1-Benzopyran-2-one, 7-hydroxy-6-methoxy- (9CI); SCOPOLETIN (CONSTITUENT OF STINGING NETTLE) [DSC]; 5-18-03-00203 (Beilstein Handbook Reference); SCOPOLETIN (CONSTITUENT OF STINGING NETTLE); 2H-1-Benzopyran-2-one, 7-hydroxy-6-methoxy-; 7-Hydroxy-6-methoxy-2H-1-benzopyran-2-one; 7-hydroxy-6-methoxy-1-benzopyran-2-one; 7-Hydroxy-6-methoxy-2H-chromen-2-one #; 0B4B9FAA-686D-4977-AA08-65F8E4F1977C; 7-Hydroxy-6-methoxy-2H-chromen-2-one; 6-methoxy-7-oxidanyl-chromen-2-one; 7-hydroxy-6-methoxy-chromen-2-one; Gelseminic acid; 7-hydroxy-6-methoxychromen-2-one; Scopoletin, analytical standard; COUMARIN, 7-HYDROXY-6-METHOXY-; 7-hydroxy 6-methoxy coumarine; 7-hydroxy-6-methoxy-coumarin; 7-Hydroxy-5-methoxycoumarin; 7-Hydroxy-6-methoxycoumarin; 6-Methoxy-7-hydroxycoumarin; Aesculetin 6-methyl ether; Esculetin 6-methyl ether; Esculetin-6-methyl ether; 6-Methoxyumbelliferone; .beta.-Methylesculetin; beta -methylesculetin; beta-Methylesculetin; 6-O-Methylesculetin; SCOPOLETIN [USP-RS]; SCOPOLETIN (USP-RS); |A-Methylaesculetin; b-Methylaesculetin; Scopoletin, >=99\\%; Acid, Chrysotropic; Prestwick2_000962; 6-Methylesculetin; Chrysotropic Acid; Prestwick3_000962; Prestwick0_000962; Chrysatropic acid; Prestwick1_000962; Spectrum4_001054; Acid, Gelseminic; Spectrum2_001207; Spectrum5_000654; Spectrum3_001532; SCOPOLETIN [MI]; Gelseminic acid; UNII-KLF1HS0SXJ; Methylesculetin; BPBio1_001061; DivK1c_000720; Baogongteng B; MEGxp0_001192; KBio3_002444; ACon1_000143; KBio1_000720; NCI60_003834; IDI1_000720; Escopoletin; Scopoletine; CAS-92-61-5; KLF1HS0SXJ; Scopoletol; Scopoletin; Murrayetin; COPOLETIN; Buxuletin; T83; Chrysatropic acid; Scopoletin; Scopoletin



数据库引用编号

41 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(6)

PlantCyc(7)

代谢反应

339 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(9)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(330)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

1969 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 15 AKR1B1, AKT1, ANG, BCL2, CASP3, CAT, EGFR, MAPK14, NFE2L2, PIK3CA, PRKAA2, PTGS2, TP53, TYR, VEGFA
Peripheral membrane protein 3 ACHE, CYP1B1, PTGS2
Endosome membrane 1 EGFR
Endoplasmic reticulum membrane 4 BCL2, CYP1B1, EGFR, PTGS2
Nucleus 11 ACHE, AKT1, ANG, BCL2, CASP3, EGFR, MAPK14, NFE2L2, PRKAA2, TP53, VEGFA
cytosol 11 AKR1B1, AKT1, ANG, BCL2, CASP3, CAT, MAPK14, NFE2L2, PIK3CA, PRKAA2, TP53
dendrite 1 PRKAA2
centrosome 2 NFE2L2, TP53
nucleoplasm 7 AKR1B1, AKT1, CASP3, MAPK14, NFE2L2, PRKAA2, TP53
RNA polymerase II transcription regulator complex 1 NFE2L2
Cell membrane 4 ACHE, AKT1, EGFR, TNF
lamellipodium 2 AKT1, PIK3CA
ruffle membrane 1 EGFR
Early endosome membrane 1 EGFR
Synapse 1 ACHE
cell cortex 1 AKT1
cell junction 1 EGFR
cell surface 4 ACHE, EGFR, TNF, VEGFA
glutamatergic synapse 4 AKT1, CASP3, EGFR, MAPK14
Golgi apparatus 4 ACHE, NFE2L2, PRKAA2, VEGFA
Golgi membrane 2 EGFR, INS
growth cone 1 ANG
neuromuscular junction 1 ACHE
neuronal cell body 4 ANG, CASP3, PRKAA2, TNF
postsynapse 1 AKT1
Cytoplasm, cytosol 1 NFE2L2
Lysosome 1 TYR
endosome 1 EGFR
plasma membrane 6 ACHE, AKT1, EGFR, NFE2L2, PIK3CA, TNF
Membrane 9 ACHE, AKT1, BCL2, CAT, CYP1B1, EGFR, PRKAA2, TP53, VEGFA
apical plasma membrane 1 EGFR
axon 1 PRKAA2
basolateral plasma membrane 1 EGFR
caveola 1 PTGS2
extracellular exosome 2 AKR1B1, CAT
endoplasmic reticulum 4 BCL2, PTGS2, TP53, VEGFA
extracellular space 8 ACHE, AKR1B1, ANG, EGFR, IL6, INS, TNF, VEGFA
perinuclear region of cytoplasm 4 ACHE, EGFR, PIK3CA, TYR
adherens junction 1 VEGFA
intercalated disc 1 PIK3CA
mitochondrion 6 AKR1B1, BCL2, CAT, CYP1B1, MAPK14, TP53
protein-containing complex 6 AKT1, BCL2, CAT, EGFR, PTGS2, TP53
intracellular membrane-bounded organelle 3 CAT, CYP1B1, TYR
Microsome membrane 2 CYP1B1, PTGS2
postsynaptic density 1 CASP3
Single-pass type I membrane protein 2 EGFR, TYR
Secreted 5 ACHE, ANG, IL6, INS, VEGFA
extracellular region 8 ACHE, ANG, CAT, IL6, INS, MAPK14, TNF, VEGFA
Mitochondrion outer membrane 1 BCL2
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 1 BCL2
Mitochondrion matrix 1 TP53
mitochondrial matrix 2 CAT, TP53
Extracellular side 1 ACHE
transcription regulator complex 1 TP53
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 1 TP53
Nucleus membrane 1 BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 2 BCL2, EGFR
external side of plasma membrane 1 TNF
Secreted, extracellular space, extracellular matrix 1 VEGFA
actin cytoskeleton 1 ANG
microtubule cytoskeleton 1 AKT1
nucleolus 2 ANG, TP53
Melanosome membrane 1 TYR
cell-cell junction 1 AKT1
Golgi-associated vesicle 1 TYR
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
vesicle 1 AKT1
Membrane raft 2 EGFR, TNF
pore complex 1 BCL2
Cytoplasm, cytoskeleton 1 TP53
focal adhesion 2 CAT, EGFR
spindle 1 AKT1
extracellular matrix 1 VEGFA
Peroxisome 1 CAT
basement membrane 2 ACHE, ANG
intracellular vesicle 1 EGFR
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
Nucleus, PML body 1 TP53
PML body 1 TP53
Mitochondrion intermembrane space 1 AKT1
mitochondrial intermembrane space 1 AKT1
secretory granule 1 VEGFA
nuclear speck 2 MAPK14, PRKAA2
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
receptor complex 1 EGFR
neuron projection 1 PTGS2
ciliary basal body 1 AKT1
chromatin 2 NFE2L2, TP53
mediator complex 1 NFE2L2
phagocytic cup 1 TNF
Chromosome 1 ANG
Nucleus, nucleolus 1 ANG
spindle pole 1 MAPK14
Lipid-anchor, GPI-anchor 1 ACHE
site of double-strand break 1 TP53
endosome lumen 1 INS
Melanosome 1 TYR
Cytoplasm, Stress granule 1 ANG
cytoplasmic stress granule 2 ANG, PRKAA2
side of membrane 1 ACHE
germ cell nucleus 1 TP53
replication fork 1 TP53
myelin sheath 1 BCL2
basal plasma membrane 1 EGFR
synaptic membrane 1 EGFR
ficolin-1-rich granule lumen 2 CAT, MAPK14
secretory granule lumen 3 CAT, INS, MAPK14
Golgi lumen 1 INS
endoplasmic reticulum lumen 3 IL6, INS, PTGS2
nuclear matrix 1 TP53
transcription repressor complex 1 TP53
platelet alpha granule lumen 1 VEGFA
phosphatidylinositol 3-kinase complex 1 PIK3CA
phosphatidylinositol 3-kinase complex, class IA 1 PIK3CA
endocytic vesicle 1 ANG
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
clathrin-coated endocytic vesicle membrane 1 EGFR
[Isoform 1]: Nucleus 1 TP53
synaptic cleft 1 ACHE
protein-DNA complex 1 NFE2L2
death-inducing signaling complex 1 CASP3
nucleotide-activated protein kinase complex 1 PRKAA2
multivesicular body, internal vesicle lumen 1 EGFR
Shc-EGFR complex 1 EGFR
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
angiogenin-PRI complex 1 ANG
catalase complex 1 CAT
interleukin-6 receptor complex 1 IL6
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
[Isoform H]: Cell membrane 1 ACHE
phosphatidylinositol 3-kinase complex, class IB 1 PIK3CA
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • M Salihu, L G Hassan, U Z Faruq, A J Yusuf. Deciphering the interactions of scopoletin and scopolin from Catunaregam nilotica roots against Naja nigricollis phospholipase A2 enzyme. Toxicon : official journal of the International Society on Toxinology. 2024 May; 243(?):107732. doi: 10.1016/j.toxicon.2024.107732. [PMID: 38642905]
  • Sourav Kundu, Sitara Ghosh, Bidya Dhar Sahu. Scopoletin alleviates high glucose-induced toxicity in human renal proximal tubular cells via inhibition of oxidative damage, epithelial-mesenchymal transition, and fibrogenesis. Molecular biology reports. 2024 May; 51(1):620. doi: 10.1007/s11033-024-09579-2. [PMID: 38709349]
  • Jing Wang, Peitao Chen, Tengfei Zhao, Xianhui Huang, Jikai Zong, Qingqing Luo, Chao Peng, Xiaoyan Wu, Fei Qiu, Dongchao Zhao, Lien Xiang, Yan Zhang, Chunxian Yang, Fangyuan Zhang, Zhihua Liao, Yufan Fu, Junlan Zeng. Biosynthesis of Scopoletin in Sweet Potato Confers Resistance against Fusarium oxysporum. Journal of agricultural and food chemistry. 2024 Apr; 72(14):7749-7764. doi: 10.1021/acs.jafc.3c09389. [PMID: 38537104]
  • Hong Zhou, Yeshuang Ning, Yufan Jian, Miao Zhang, Matthana Klakong, Fuyou Guo, Qingyi Shao, Yanhong Li, Pinglong Yang, Zongquan Li, Liang Yang, Shili Li, Wei Ding. Functional analysis of a down-regulated transcription factor-SoxNeuroA gene involved in the acaricidal mechanism of scopoletin against spider mites. Pest management science. 2023 Nov; ?(?):. doi: 10.1002/ps.7892. [PMID: 37986233]
  • Na Song, Jinsong Wu. Synergistic induction of phytoalexins in Nicotiana attenuata by JA and ethylene signaling mediated by NaWRKY70. Journal of experimental botany. 2023 Oct; ?(?):. doi: 10.1093/jxb/erad415. [PMID: 37870145]
  • Vincent Lebot, Floriane Lawac, Ismaël Muñoz-Cuervo, Pierre-Edouard Mercier, Laurent Legendre. Metabolite fingerprinting of cassava (Manihot esculenta Crantz) landraces assessed for post-harvest physiological deterioration (PPD). Food chemistry. 2023 Sep; 421(?):136217. doi: 10.1016/j.foodchem.2023.136217. [PMID: 37121018]
  • Swati Sharma, Vishal Sharma, Sunil Taneja, Alka Bhatia, Aishwarya Anand, Amol N Patil, Dibyajyoti Banerjee. Scopoletin a potential phytochemical therapy for antitubercular treatment drug induced liver injury (ATT-DILI) model in Wistar rats. Journal of complementary & integrative medicine. 2023 Sep; ?(?):. doi: 10.1515/jcim-2023-0168. [PMID: 37732506]
  • Alexander Beesley, Sebastian F Beyer, Verena Wanders, Sophie Levecque, Sandra Bredenbruch, Samer S Habash, A Sylvia S Schleker, Jochem Gätgens, Marco Oldiges, Holger Schultheiss, Uwe Conrath, Caspar J G Langenbach. Engineered coumarin accumulation reduces mycotoxin-induced oxidative stress and disease susceptibility. Plant biotechnology journal. 2023 Aug; ?(?):. doi: 10.1111/pbi.14144. [PMID: 37578146]
  • Nishit D Patel, Samir G Patel, Amit A Patel, Manan A Raval. Estimation of Scopoletin from Roots of Argyreia nervosa (Burm. fill.) Bojer Using a Validated HPLC-Fluorescence Method Optimized Using the Design of Experiment Approach. Journal of AOAC International. 2023 Jul; 106(4):992-1002. doi: 10.1093/jaoacint/qsad018. [PMID: 36707989]
  • Qinggang Yin, Tianze Wu, Ranran Gao, Lan Wu, Yuhua Shi, Xingwen Wang, Mengyue Wang, Zhichao Xu, Yueliang Zhao, Xiaojia Su, Yanyan Su, Xiaoyan Han, Ling Yuan, Li Xiang, Shilin Chen. Multi-omics reveal key enzymes involved in the formation of phenylpropanoid glucosides in Artemisia annua. Plant physiology and biochemistry : PPB. 2023 Jun; 201(?):107795. doi: 10.1016/j.plaphy.2023.107795. [PMID: 37301186]
  • Kripa Shankar Nainawat, Sarita Singh, Karishma Agarwal, Hina Iqbal, Poonam Rani, Divya Bhatt, Sana Khan, Debabrata Chanda, Dnyaneshwar Umrao Bawankule, Sudeep Tandon, Feroz Khan, Anil Kumar Gupta, Atul Gupta. Synthesis of 6-alkoxy and 6-hydroxy-alkyl amine derivatives of braylin as vasorelaxing agents. Bioorganic & medicinal chemistry letters. 2023 06; 89(?):129311. doi: 10.1016/j.bmcl.2023.129311. [PMID: 37149230]
  • Jieren Liao, Guangxin Sun, Elisabeth Kurze, Wieland Steinchen, Timothy D Hoffmann, Chuankui Song, Zhiwei Zou, Thomas Hoffmann, Wilfried G Schwab. Subfunctionalization of a monolignol to a phytoalexin glucosyltransferase is accompanied by substrate inhibition. Plant communications. 2023 05; 4(3):100506. doi: 10.1016/j.xplc.2022.100506. [PMID: 36566353]
  • Siqi Liu, Pengmin Ding, Mengjiao Wu, Zhihao Zhu, Jiayue Tao, Jing Wang, Zhe Xue, Rufeng Wang. Screening quality markers (Q-markers) of Xiaoer Chaige Tuire Oral Liquid by in vitro sequential metabolism and in vivo biopharmaceutical analysis. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2023 Apr; 116(?):154844. doi: 10.1016/j.phymed.2023.154844. [PMID: 37163902]
  • Kunpeng Yu, Cheng Peng, Yanling Lin, Lijun Li, Hui Ni, Qingbiao Li. [Expression of β-glucosidase An-bgl3 from Aspergillus niger for conversion of scopolin]. Sheng wu gong cheng xue bao = Chinese journal of biotechnology. 2023 Mar; 39(3):1232-1246. doi: 10.13345/j.cjb.220709. [PMID: 36994584]
  • Yifan Sun, Guangxi Ren, Qijin Shi, Hongyu Zhu, Na Zhou, Xianghe Kong, Dan Jiang, Chunsheng Liu. Identification of a Novel Coumarins Biosynthetic Pathway in the Endophytic Fungus Fusarium oxysporum GU-7 with Antioxidant Activity. Applied and environmental microbiology. 2023 01; 89(1):e0160122. doi: 10.1128/aem.01601-22. [PMID: 36598487]
  • Zhong Wang, Lanxin Ma, Pingping Liu, Zhaopeng Luo, Zefeng Li, Mingzhu Wu, Xin Xu, Wenxuan Pu, Pingjun Huang, Jun Yang. Transcription factor NtWRKY33a modulates the biosynthesis of polyphenols by targeting NtMYB4 and NtHCT genes in tobacco. Plant science : an international journal of experimental plant biology. 2023 Jan; 326(?):111522. doi: 10.1016/j.plantsci.2022.111522. [PMID: 36332766]
  • Israt Jahan, Shahenur Alam Sakib, Najmul Alam, Mohuya Majumder, Sanjida Sharmin, A S M Ali Reza. Pharmacological insights into Chukrasia velutina bark: Experimental and computer-aided approaches. Animal models and experimental medicine. 2022 12; 5(4):377-388. doi: 10.1002/ame2.12268. [PMID: 36047481]
  • Jia Sun, Jian Gou, Li-Qin Liu, Chun-Hua Liu, Jie Pan, Yue-Ting Li, Zi-Peng Gong. [Excretion of Cynanchum auriculatum extract in urine and feces of normal and functional dyspepsia rats]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2022 Dec; 47(23):6355-6364. doi: 10.19540/j.cnki.cjcmm.20220621.202. [PMID: 36604880]
  • Jia Sun, Li-Qin Liu, Jian Gou, Si-Ying Chen, Zi-Peng Gong, Ting Liu, Yong-Jun Li, Yuan Lu. [Differences in intestinal absorption characteristics of Cynanchum auriculatum extract based on in situ intestinal circulation perfusion model in two states]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2022 Dec; 47(23):6340-6347. doi: 10.19540/j.cnki.cjcmm.20220621.203. [PMID: 36604878]
  • Farah Naz, Mukesh Kumar, Tirthankar Koley, Priyanka Sharma, Muhammad Anzarul Haque, Arti Kapil, Manoj Kumar, Punit Kaur, Abdul Samath Ethayathulla. Screening of plant-based natural compounds as an inhibitor of FtsZ from Salmonella Typhi using the computational, biochemical and in vitro cell-based studies. International journal of biological macromolecules. 2022 Oct; 219(?):428-437. doi: 10.1016/j.ijbiomac.2022.07.241. [PMID: 35932806]
  • Joana L Rodrigues, Daniela Gomes, Lígia R Rodrigues. Challenges in the Heterologous Production of Furanocoumarins in Escherichia coli. Molecules (Basel, Switzerland). 2022 Oct; 27(21):. doi: 10.3390/molecules27217230. [PMID: 36364054]
  • Meiwei Zhao, Lan Ma, Na Song, Junbin Cheng, Zhengxiong Zhao, Jinsong Wu. The regulation of Alternaria alternata resistance by LRR-RK4 through ERF109, defensin19 and phytoalexin scopoletin in Nicotiana attenuata. Plant science : an international journal of experimental plant biology. 2022 Oct; 323(?):111414. doi: 10.1016/j.plantsci.2022.111414. [PMID: 35963495]
  • Théodora K Kowa, Olivia Jansen, Allison Ledoux, Lucia Mamede, Hippolyte K Wabo, Alembert T Tchinda, Gregory Genta-Jouve, Michel Frédérich. Bioassay-guided isolation of vilasinin-type limonoids and phenyl alkene from the leaves of Trichilia gilgiana and their antiplasmodial activities. Natural product research. 2022 Oct; 36(19):5039-5047. doi: 10.1080/14786419.2021.1920017. [PMID: 33951995]
  • Muqeet Wahid, Fatima Saqib, Muhammad Qamar, Zyta M Ziora. Antispasmodic activity of the ethanol extract of Citrullus lanatus seeds: Justifying ethnomedicinal use in Pakistan to treat asthma and diarrhea. Journal of ethnopharmacology. 2022 Sep; 295(?):115314. doi: 10.1016/j.jep.2022.115314. [PMID: 35490899]
  • Qiuxiang Ma, Jia Xu, Yancai Feng, Xiaoyun Wu, Xinlu Lu, Peng Zhang. Knockdown of p-Coumaroyl Shikimate/Quinate 3'-Hydroxylase Delays the Occurrence of Post-Harvest Physiological Deterioration in Cassava Storage Roots. International journal of molecular sciences. 2022 Aug; 23(16):. doi: 10.3390/ijms23169231. [PMID: 36012496]
  • Lucia Dwi Antika, Aprilia Nur Tasfiyati, Hikmat Hikmat, Abdi Wira Septama. Scopoletin: a review of its source, biosynthesis, methods of extraction, and pharmacological activities. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2022 Jul; 77(7-8):303-316. doi: 10.1515/znc-2021-0193. [PMID: 35218175]
  • Li-Qin Liu, Jing-Ya Zhang, Yuan Lu, Chun-Hua Liu, Jian Gou, Zhu-Jun Li, Ai-Min Wang, Jia Sun. [Intestinal absorption characteristics of root tuber of Cynanchum auriculatum extract in normal and functional dyspepsia model rats via everted intestine sac model]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2022 Jul; 47(14):3915-3922. doi: 10.19540/j.cnki.cjcmm.20220215.201. [PMID: 35850850]
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