Rosmarinic acid (BioDeep_00000000016)

 

Secondary id: BioDeep_00000017211, BioDeep_00000419325, BioDeep_00000869763

human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite BioNovoGene_Lab2019 natural product


代谢物信息卡片


(2R)-3-(3,4-dihydroxyphenyl)-2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxypropanoic acid

化学式: C18H16O8 (360.0845)
中文名称: 罗丹酚酸, 酪萨维, 肉桂醇甙, 迷迭香酸
谱图信息: 最多检出来源 Viridiplantae(plant) 16.23%

Reviewed

Last reviewed on 2024-11-05.

Cite this Page

Rosmarinic acid. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/rosmarinic_acid (retrieved 2024-12-22) (BioDeep RN: BioDeep_00000000016). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: c1(c(ccc(c1)/C=C/C(=O)O[C@H](Cc1cc(c(cc1)O)O)C(=O)O)O)O
InChI: InChI=1S/C18H16O8/c19-12-4-1-10(7-14(12)21)3-6-17(23)26-16(18(24)25)9-11-2-5-13(20)15(22)8-11/h1-8,16,19-22H,9H2,(H,24,25)/b6-3+/t16-/m0/s1

描述信息

Rosmarinic acid is an ester of caffeic acid and 3,4-dihydroxyphenyllactic acid. It is commonly found in species of the Boraginaceae and the subfamily Nepetoideae of the Lamiaceae. It is a red-orange powder that is slightly soluble in water, but well soluble is most organic solvents. Rosmarinic acid is one of the polyphenolic substances contained in culinary herbs such as perilla (Perilla frutescens L.), rosemary (Rosmarinus officinalis L.), sage (Salvia officinalis L.), mint (Mentha arvense L.), and basil (Ocimum basilicum L.). These herbs are commonly grown in the garden as kitchen herbs, and while used to add flavor in cooking, are also known to have several potent physiological effects (PMID: 12482446, 15120569). BioTransformer predicts that rosmarinic acid is a product of methylrosmarinic acid metabolism via a hydrolysis-of-carboxylic-acid-ester-pattern1 reaction occurring in humans and human gut microbiota and catalyzed by the liver carboxylesterase 1 (P23141) enzyme (PMID: 30612223).
(R)-rosmarinic acid is a stereoisomer of rosmarinic acid having (R)-configuration. It has a role as a plant metabolite and a geroprotector. It is a conjugate acid of a (R)-rosmarinate. It is an enantiomer of a (S)-rosmarinic acid.
Rosmarinic acid is a natural product found in Dimetia scandens, Scrophularia scorodonia, and other organisms with data available.
See also: Rosemary Oil (part of); Comfrey Root (part of); Holy basil leaf (part of) ... View More ...
D004791 - Enzyme Inhibitors > D011480 - Protease Inhibitors > D015842 - Serine Proteinase Inhibitors
D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents
D006401 - Hematologic Agents > D010975 - Platelet Aggregation Inhibitors
Isolated from rosemary, mint, sage, thyme, lemon balm and other plants
D002491 - Central Nervous System Agents > D000700 - Analgesics
A stereoisomer of rosmarinic acid having (R)-configuration.
D020011 - Protective Agents > D000975 - Antioxidants
D000893 - Anti-Inflammatory Agents
D018501 - Antirheumatic Agents
Acquisition and generation of the data is financially supported in part by CREST/JST.
Rosmarinic acid is a widespread phenolic ester compound in the plants. Rosmarinic acid inhibits MAO-A, MAO-B and COMT enzymes with IC50s of 50.1, 184.6 and 26.7 μM, respectively.
Rosmarinic acid is a widespread phenolic ester compound in the plants. Rosmarinic acid inhibits MAO-A, MAO-B and COMT enzymes with IC50s of 50.1, 184.6 and 26.7 μM, respectively.

同义名列表

74 个代谢物同义名

BENZENEPROPANOIC ACID, .ALPHA.-(((2E)-3-(3,4-DIHYDROXYPHENYL)-1-OXO-2-PROPEN-1-YL)OXY)-3,4-DIHYDROXY-, (.ALPHA.R)-; Benzenepropanoic acid, .alpha.-[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-3,4-dihydroxy-, (.alpha.R)-; BENZENEPROPANOIC ACID, .ALPHA.-(((2E)-3-(3,4-DIHYDROXYPHENYL)-1-OXO-2-PROPENYL)OXY)-3,4-DIHYDROXY-, (.ALPHA.R)-; BENZENEPROPANOIC ACID, alpha-(((2E)-3-(3,4-DIHYDROXYPHENYL)-1-OXO-2-PROPEN-1-YL)OXY)-3,4-DIHYDROXY-, (alphaR)-; BENZENEPROPANOIC ACID, alpha-(((2E)-3-(3,4-DIHYDROXYPHENYL)-1-OXO-2-PROPENYL)OXY)-3,4-DIHYDROXY-, (alphaR)-; Benzenepropanoic acid, .alpha.-((3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl)oxy)-3,4-dihydroxy-, (R-(E))-; Benzenepropanoic acid, alpha-((3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl)oxy)-3,4-dihydroxy-, (R-(E))-; Benzenepropanoic acid,a-[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-3,4-dihydroxy-,(aR)-; [R-(+)]-?-[[3-(3,4-Dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-3,4-dihydroxybenzenepropanoic acid; (2r)-3-(3,4-Dihydroxyphenyl)-2-{[(2e)-3-(3,4-Dihydroxyphenyl)prop-2-Enoyl]oxy}propanoic Acid; Benzenepropanoic acid, alpha-((3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl)oxy)-3,4-dihydroxy-; (2R)-3-(3,4-dihydroxyphenyl)-2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-propanoic acid; (2R)-3-(3,4-dihydroxyphenyl)-2-[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid; (2R)-3-(3,4-dihydroxyphenyl)-2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxypropanoic acid; (2R)-3-(3,4-dihydroxyphenyl)-2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxypropanoicacid; alpha-(((3,4-Dihydroxyphenyl)-1-oxo-2-propenyl)oxy)-3,4-dihydroxy-benzenepropanoic acid; (2R)-3-(3,4-DIHYDROXYPHENYL)-2-{[3-(3,4-DIHYDROXYPHENYL)PROP-2-ENOYL]OXY}PROPANOIC ACID; alpha-(((3,4-Dihydroxyphenyl)-1-oxo-2-propenyl)oxy)-3,4-dihydroxybenzenepropanoic acid; 3-(3,4-dihydroxyphenyl)-2-((2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyloxy)propanoic acid; (R,E)-3-(3,4-dihydroxyphenyl)-2-((3-(3,4-dihydroxyphenyl)acryloyl)oxy)propanoic acid; (R,E)-3-(3,4-dihydroxyphenyl)-2-((3-(3,4-dihydroxyphenyl)acryloyl)oxy)propanoicacid; (R,E)-3-(3,4-dihydroxyphenyl)-2-(3-(3,4-dihydroxyphenyl)acryloyloxy)propanoic acid; 3-(3,4-DIHYDROXYPHENYL)ACRYLIC ACID-1-CARBOXY-2-(3,4-DIHYDROXYPHENYL)ETHYL ESTER; CINNAMIC ACID, 3,4-DIHYDROXY-, 2-ESTER with 3-(3,4-DIHYDROXYPHENYL)LACTIC ACID; 3,4-Dihydroxycinnamic acid (R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethyl ester; 3,4-Dihydroxycinnamic acid 2-ester with 3-(3,4-dihydroxyphenyl)lactic acid; R-(+)-2-(3,4-Dihydroxycinnamoyloxy)-3-(3,4-dihydroxyphenyl)propionic acid; Rosmarinic acid, United States Pharmacopeia (USP) Reference Standard; (R)-O-(3,4-Dihydroxycinnamoyl)-3-(3,4- dihydroxyphenyl)lactic acid; (R)-O-(3,4-Dihydroxycinnamoyl)-3-(3,4-dihydroxyphenyl)lactic acid; Rosmarinic acid, >=98\\% (HPLC), from Rosemarinus officinalis L.; Rosmarinic acid, European Pharmacopoeia (EP) Reference Standard; Rosmarinic acid, primary pharmaceutical reference standard; ROSMARINIC ACID (CONSTITUENT OF HOLY BASIL LEAF) [DSC]; (2R)-O-caffeoyl-3-(3,4-dihydroxyphenyl)lactic acid; ROSMARINIC ACID (CONSTITUENT OF HOLY BASIL LEAF); ROSMARINIC ACID (CONSTITUENT OF ROSEMARY) [DSC]; (2R)-O-Caffeoyl-3-(3,4-dihydroxyphenyl)lactate; ROSMARINIC ACID (CONSTITUENT OF ROSEMARY); 93B6A3BF-927D-4C59-8A49-29BDBC87C194; rosmarinic acid, (R-(E))-isomer; DOUMFZQKYFQNTF-WUTVXBCWSA-N; Rosmarinic acid racemate; ROSMARINIC ACID [USP-RS]; ROSMARINIC ACID (USP-RS); ROSMARINIC ACID [INCI]; ROSMARINIC ACID [HSDB]; Rosmarinic acid, 96\\%; trans-Rosmarinic acid; ROSMARINIC ACID [MI]; (R)-rosmarinic acid; (Z)-Rosmarinic acid; Rosmarinic acid, 2; (R)-Rosmarinate; Labiatenic acid; Rosmarinic acid; Rosmarimic acid; Rosmarinic-acid; UNII-MQE6XG29YI; Rosemaric acid; Rosmarinicacid; Labiatic acid; MEGxp0_000163; Rosemary acid; ORISTRACT ROA; ACon1_001068; Rosmarinate; MQE6XG29YI; Rosmarinic; RM 21A; RM-21A; (S)-rosmarinic acid; Rosmarinic acid; Rosmarinate



数据库引用编号

44 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)

249 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, CASP1, CASP3, ELANE, HMGB1, MAPK8, PIK3CA, PRKAA2, PTGS2, TLR4, TYR
Peripheral membrane protein 4 ACHE, CYP1B1, HMGB1, PTGS2
Endosome membrane 1 TLR4
Endoplasmic reticulum membrane 2 CYP1B1, PTGS2
Nucleus 6 ACHE, ANG, CASP3, HMGB1, MAPK8, PRKAA2
cytosol 8 ANG, CASP1, CASP3, ELANE, MAPK8, PIK3CA, PRKAA2, TAT
dendrite 1 PRKAA2
phagocytic vesicle 1 ELANE
nucleoplasm 4 CASP3, HMGB1, MAPK8, PRKAA2
Cell membrane 4 ACHE, CASP1, HMGB1, TLR4
lamellipodium 1 PIK3CA
Synapse 2 ACHE, MAPK8
cell surface 4 ACHE, ELANE, HMGB1, TLR4
glutamatergic synapse 1 CASP3
Golgi apparatus 2 ACHE, PRKAA2
Golgi membrane 1 INS
growth cone 1 ANG
lysosomal membrane 1 GAA
neuromuscular junction 1 ACHE
neuronal cell body 3 ANG, CASP3, PRKAA2
Lysosome 2 GAA, TYR
endosome 1 HMGB1
plasma membrane 8 ACHE, BCHE, CASP1, GAA, HMGB1, IGHE, PIK3CA, TLR4
Membrane 5 ACHE, CYP1B1, GAA, PRKAA2, TLR4
axon 2 MAPK8, PRKAA2
caveola 1 PTGS2
extracellular exosome 2 ELANE, GAA
Lysosome membrane 1 GAA
endoplasmic reticulum 2 HMGB1, PTGS2
extracellular space 9 ACHE, ANG, BCHE, CCL2, ELANE, HMGB1, IGHE, IL4, INS
lysosomal lumen 1 GAA
perinuclear region of cytoplasm 4 ACHE, PIK3CA, TLR4, TYR
intercalated disc 1 PIK3CA
mitochondrion 1 CYP1B1
protein-containing complex 2 CASP1, PTGS2
intracellular membrane-bounded organelle 3 CYP1B1, GAA, TYR
Microsome membrane 2 CYP1B1, PTGS2
postsynaptic density 1 CASP3
Single-pass type I membrane protein 3 IGHE, TLR4, TYR
Secreted 8 ACHE, ANG, BCHE, CCL2, GAA, HMGB1, IL4, INS
extracellular region 10 ACHE, ANG, BCHE, CCL2, ELANE, GAA, HMGB1, IGHE, IL4, INS
Extracellular side 2 ACHE, HMGB1
external side of plasma membrane 1 TLR4
actin cytoskeleton 1 ANG
nucleolus 2 ANG, CASP1
Melanosome membrane 1 TYR
Early endosome 1 TLR4
Golgi-associated vesicle 1 TYR
microtubule 1 CASP1
basement membrane 2 ACHE, ANG
collagen-containing extracellular matrix 1 ELANE
secretory granule 1 ELANE
nuclear speck 1 PRKAA2
NLRP3 inflammasome complex 1 CASP1
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 1 PTGS2
IgE immunoglobulin complex 1 IGHE
phagocytic cup 1 TLR4
Chromosome 2 ANG, HMGB1
Nucleus, nucleolus 1 ANG
blood microparticle 1 BCHE
Lipid-anchor, GPI-anchor 1 ACHE
[Isoform 2]: Cell membrane 1 IGHE
endosome lumen 1 INS
tertiary granule membrane 1 GAA
Melanosome 1 TYR
Cytoplasm, Stress granule 1 ANG
cytoplasmic stress granule 2 ANG, PRKAA2
side of membrane 1 ACHE
lipopolysaccharide receptor complex 1 TLR4
ficolin-1-rich granule lumen 1 HMGB1
secretory granule lumen 2 HMGB1, INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 3 BCHE, INS, PTGS2
transcription repressor complex 2 ELANE, HMGB1
phosphatidylinositol 3-kinase complex 1 PIK3CA
phosphatidylinositol 3-kinase complex, class IA 1 PIK3CA
specific granule lumen 1 ELANE
endocytic vesicle 1 ANG
transport vesicle 1 INS
azurophil granule membrane 1 GAA
azurophil granule lumen 1 ELANE
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
nuclear envelope lumen 1 BCHE
AIM2 inflammasome complex 1 CASP1
endoplasmic reticulum-Golgi intermediate compartment 1 HMGB1
synaptic cleft 1 ACHE
ficolin-1-rich granule membrane 1 GAA
basal dendrite 1 MAPK8
death-inducing signaling complex 1 CASP3
canonical inflammasome complex 1 CASP1
nucleotide-activated protein kinase complex 1 PRKAA2
condensed chromosome 1 HMGB1
Cytoplasmic vesicle, phagosome 1 ELANE
[Isoform 3]: Cell membrane 1 IGHE
[Isoform 1]: Secreted 1 IGHE
IgE B cell receptor complex 1 IGHE
immunoglobulin complex, circulating 1 IGHE
angiogenin-PRI complex 1 ANG
alphav-beta3 integrin-HMGB1 complex 1 HMGB1
autolysosome lumen 1 GAA
[Isoform H]: Cell membrane 1 ACHE
IPAF inflammasome complex 1 CASP1
NLRP1 inflammasome complex 1 CASP1
protease inhibitor complex 1 CASP1
phosphatidylinositol 3-kinase complex, class IB 1 PIK3CA


文献列表

  • Mohsen Mardani, Katalin Badakné, Ildikó Szedljak, Csilla Sörös, Jamshid Farmani. Lipophilized rosmarinic acid: Impact of alkyl type and food matrix on antioxidant activity, and optimized enzymatic production. Food chemistry. 2024 Sep; 452(?):139518. doi: 10.1016/j.foodchem.2024.139518. [PMID: 38713983]
  • Łukasz Sęczyk, Elvyra Jariene, Danuta Sugier, Barbara Kołodziej. Effects of the dose of administration, co-antioxidants, food matrix, and digestion-related factors on the in vitro bioaccessibility of rosmarinic acid - A model study. Food chemistry. 2024 Aug; 449(?):139201. doi: 10.1016/j.foodchem.2024.139201. [PMID: 38599104]
  • Guanwen Xie, Xiuzai Zou, Zishan Liang, Ke Zhang, Duan Wu, Honglei Jin, Hongbin Wang, Qi Shen. GBF family member PfGBF3 and NAC family member PfNAC2 regulate rosmarinic acid biosynthesis under high light. Plant physiology. 2024 Jun; 195(2):1728-1744. doi: 10.1093/plphys/kiae036. [PMID: 38441888]
  • Guilian Zhang, Yuee Sun, Najeeb Ullah, Deepak Kasote, Longyi Zhu, Hui Liu, Ling Xu. Changes in secondary metabolites contents and stress responses in Salvia miltiorrhiza via ScWRKY35 overexpression: Insights from a wild relative Salvia castanea. Plant physiology and biochemistry : PPB. 2024 Jun; 211(?):108671. doi: 10.1016/j.plaphy.2024.108671. [PMID: 38703500]
  • Sara Motyka, Agnieszka Szopa, Sergio J Ochatt. Distinction of chia varieties in vivo and in vitro based on the flow cytometry and rosmarinic acid production. Applied microbiology and biotechnology. 2024 May; 108(1):337. doi: 10.1007/s00253-024-13171-w. [PMID: 38767664]
  • Mei Ling Ng, Amin Malik Shah Abdul Majid, Siew Mei Yee, V Natesan, Mohamed Khadeer Ahamed Basheer, Ashok Gnanasekaran, Fouad Saleih Resq Al-Suede, Christopher Parish, Meena Dalal, Long Chiau Ming, Mansoureh Nazari V, Shamsuddin Sultan Khan, Siti Balkees Stn Hameed Sultan, K Govind Babu, Aman Shah Abdul Majid, Mohamed Amir Shah Abdul Aziz. A phase II randomized, double-blind, placebo-controlled study of Nuvastatic (C50SEW505OESA), a standardized rosmarinic acid-rich polymolecular botanical extract formulation to reduce cancer-related fatigue in patients with solid tumors. Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer. 2024 May; 32(6):331. doi: 10.1007/s00520-024-08536-w. [PMID: 38710920]
  • Natticha Sumneang, Komsak Pintha, Sarawut Kongkarnka, Maitree Suttajit, Napapan Kangwan. Protective Effect of Perilla Seed Meal and Perilla Seed Extract against Dextran Sulfate Sodium-Induced Ulcerative Colitis through Suppressing Inflammatory Cytokines in Mice. Molecules (Basel, Switzerland). 2024 Apr; 29(9):. doi: 10.3390/molecules29091940. [PMID: 38731431]
  • Mona H Soliman, Suliman M S Alghanem, Ibtisam M Alsudays, Abdullah Alaklabi, Basmah M Alharbi, Hadba Al-Amrah, Ehab Azab, Ghalia S H Alnusairi. Co-application of titanium nanoparticles and melatonin effectively lowered chromium toxicity in lemon balm (Melissa officinalis L.) through modifying biochemical characteristics. Environmental science and pollution research international. 2024 Apr; 31(17):25258-25272. doi: 10.1007/s11356-024-32771-7. [PMID: 38468007]
  • Tian-Bao Wang, Ying He, Rui-Cheng Li, Yu-Xi Yu, Yu Liu, Zhong-Quan Qi. Rosmarinic acid mitigates acrylamide induced neurotoxicity via suppressing endoplasmic reticulum stress and inflammation in mouse hippocampus. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2024 Apr; 126(?):155448. doi: 10.1016/j.phymed.2024.155448. [PMID: 38394736]
  • Ke Zhang, Han Li, Jingjing Shi, Wenjing Liu, Yitao Wang, Pengfei Tu, Jun Li, Yuelin Song. Strategy strengthens structural identification through hyphenating full collision energy ramp-MS2 and full exciting energy ramp-MS3 spectra: An application for metabolites identification of rosmarinic acid. Analytica chimica acta. 2024 Apr; 1296(?):342346. doi: 10.1016/j.aca.2024.342346. [PMID: 38401935]
  • Jafar Fatahi Asl, Mehdi Goudarzi, Esrafil Mansouri, Hamed Shoghi. Rosmarinic Acid Protects the Testes of Rats against Cell Phone and Ultra-high Frequency Waves Induced Toxicity. Iranian journal of medical sciences. 2024 Apr; 49(4):237-246. doi: 10.30476/ijms.2023.97695.2952. [PMID: 38680223]
  • Hongtao Li, Meng Sun, Fuzhi Lei, Jinfeng Liu, Xixiang Chen, Yaqi Li, Ying Wang, Jiani Lu, Danmei Yu, Yueqiu Gao, Jianrong Xu, Hongzhuan Chen, Man Li, Zhigang Yi, Xiao He, Lili Chen. Methyl rosmarinate is an allosteric inhibitor of SARS-CoV-2 3 CL protease as a potential candidate against SARS-cov-2 infection. Antiviral research. 2024 Apr; 224(?):105841. doi: 10.1016/j.antiviral.2024.105841. [PMID: 38408645]
  • Maciej Jakobina, Jacek Łyczko, Antoni Szumny, Renata Galek. The influence of cultivation conditions on the formation of psychoactive salvinorin A, salvinorin B, rosmarinic acid and caffeic acid in Coleus scutellarioides. Scientific reports. 2024 03; 14(1):6693. doi: 10.1038/s41598-024-57399-y. [PMID: 38509159]
  • Zeinab Shariatmadari, Somayeh Zarezadeh, Hossein Riahi, Ali Akbar Ghotbi-Ravandi, Mehri Seyed Hashtroudi, Ensiyeh Shahroudi. Cyanobacterial elicitor enhances the biomass of Mentha piperita L. and improves the production of high-value rosmarinic acid under in vitro culture of apical meristem. BMC plant biology. 2024 Mar; 24(1):190. doi: 10.1186/s12870-024-04876-1. [PMID: 38486151]
  • Vasudeva Reddy Netala, Tianyu Hou, Siva Sankar Sana, Huizhen Li, Zhijun Zhang. Rosmarinic Acid-Rich Perilla frutescens Extract-Derived Silver Nanoparticles: A Green Synthesis Approach for Multifunctional Biomedical Applications including Antibacterial, Antioxidant, and Anticancer Activities. Molecules (Basel, Switzerland). 2024 Mar; 29(6):. doi: 10.3390/molecules29061250. [PMID: 38542889]
  • Paraskevi Yfanti, Polyxeni Lazaridou, Vasiliki Boti, Dimitra Douma, Marilena E Lekka. Enrichment of Olive Oils with Natural Bioactive Compounds from Aromatic and Medicinal Herbs: Phytochemical Analysis and Antioxidant Potential. Molecules (Basel, Switzerland). 2024 Mar; 29(5):. doi: 10.3390/molecules29051141. [PMID: 38474654]
  • Łukasz Sęczyk, Barbara Kołodziej. Bioaccessibility of Rosmarinic Acid and Basil (Ocimum basilicum L.) Co-Compounds in a Simulated Digestion Model-The Influence of the Endogenous Plant Matrix, Dose of Administration and Physicochemical and Biochemical Digestion Environment. Molecules (Basel, Switzerland). 2024 Feb; 29(4):. doi: 10.3390/molecules29040901. [PMID: 38398652]
  • Jiuseng Zeng, Zhiqiang Xie, Li Chen, Xi Peng, Fei Luan, Jingwen Hu, Hongxiao Xie, Rong Liu, Nan Zeng. Rosmarinic acid alleviate CORT-induced depressive-like behavior by promoting neurogenesis and regulating BDNF/TrkB/PI3K signaling axis. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2024 Jan; 170(?):115994. doi: 10.1016/j.biopha.2023.115994. [PMID: 38070249]
  • Xiaoyu Li, Yali Lin, Yong Qin, Guiqi Han, Hai Wang, Zhuyun Yan. Beneficial endophytic fungi improve the yield and quality of Salvia miltiorrhiza by performing different ecological functions. PeerJ. 2024; 12(?):e16959. doi: 10.7717/peerj.16959. [PMID: 38406278]
  • Teng Ma, Jia-Qi Chen, Tie Yao, Bing-Yang Zhang, Feng Qiu. New depside and rosmarinic acid derivatives from Perilla frutescens and their anti-inflammatory activity. Journal of Asian natural products research. 2024 Jan; 26(1):69-77. doi: 10.1080/10286020.2024.2308794. [PMID: 38305031]
  • Urmi Rahman Rinik, Ji Eon Kim, Eunok Lee, Oran Kwon, Byung Hwa Jung. Development of simultaneous quantitative analytical method for three active components of Korean mint (Agastache rugosa (Fisch. & C.A.Mey.) Kuntze) extract in human plasma using ultra-high-performance liquid chromatography-tandem mass spectrometry. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2024 Jan; 1232(?):123957. doi: 10.1016/j.jchromb.2023.123957. [PMID: 38134516]
  • Qiong Ge, Zhewen Zhang, Zhiming Cao, Dan Wu, Changping Xu, Jianbiao Yao, Jian Gao, Yan Feng. Exploration of the in vitro Antiviral Effects and the Active Components of Changyanning Tablets Against Enterovirus 71. Drug design, development and therapy. 2024; 18(?):651-665. doi: 10.2147/dddt.s444625. [PMID: 38450095]
  • Herath Mudiyanselage Udari Lakmini Herath, Mei Jing Piao, Kyoung Ah Kang, Pincha Devage Sameera Madushan Fernando, Jin Won Hyun. Rosmarinic Acid Protects Skin Keratinocytes from Particulate Matter 2.5-Induced Apoptosis. International journal of medical sciences. 2024; 21(4):681-689. doi: 10.7150/ijms.90814. [PMID: 38464827]
  • Ambika Goswami, Adinpunya Mitra. Light spectra manipulation stimulates growth, specialized metabolites and nutritional quality in Anethum graveolens. Journal of photochemistry and photobiology. B, Biology. 2023 Dec; 249(?):112812. doi: 10.1016/j.jphotobiol.2023.112812. [PMID: 37972447]
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