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Mosla scabra

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fe3b48f29d556724668
Scientific name Mosla scabra
Authority (Thunb.) C.Y.Wu & H.W.Li
First published in Acta Phytotax. Sin. 12: 230 (1974)

Description Top

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Synonyms Top

Scientific name Authority First published in
Mosla lanceolata (Benth.) Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 20: 459 (1875)
Mosla punctata (Thunb.) Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 20: 460 (1875)
Mosla punctulata Nakai Bot. Mag. (Tokyo) 42: 475 (1928)
Ocimum punctatum Thunb. ex Murray Syst. Veg., ed. 14 (J. A. Murray). 545. 1784 [May-Jun 1784]
Ocimum punctulatum J.F.Gmel. Syst. Nat. ed. 13[bis] : 917 (1792)
Ocimum scabrum Thunb. Trans. Linn. Soc. London 2: 338 (1794)
Orthodon lanceolatus Kudô Mem. Fac. Sci. Taihoku Imp. Univ. 2: 80 (1929)
Orthodon punctatus Kudô Mem. Fac. Sci. Taihoku Imp. Univ. 2: 80 (1929)
Orthodon punctulatus (J.F.Gmel.) Ohwi Acta Phytotax. Geobot. 4: 68 (1935)
Orthodon scaber (Thunb.) Hand.-Mazz. Symb. Sin. 7: 933 (1936)
Perilla lanceolata Benth. Prodr. 12: 164 (1848)

Common names Top

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Language Common/alternative name
Chinese 北风头上一枝香
Chinese 石荠苎（石荠宁）
Chinese 野蕾香
Chinese 野苏叶
Chinese 野升麻
Chinese 蜻蜓花
Chinese 紫花草
Chinese 母鸡窝
Chinese 月斑草
Chinese 斑点荠苎
Chinese 小苏金
Chinese 土香茹草
Chinese 叶进根
Chinese 野薄荷
Chinese 不脸草
Chinese 石荠苧
Chinese 石荠宁
Chinese 干汗草
Chinese 石薺薴
Chinese 石荠苎
Chinese 水苋菜
Chinese 痱子草
Chinese 野棉花
Chinese 野荆芥
Chinese 沙虫药
Chinese 土荆芥

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000246375
Tropicos 17603553
KEW urn:lsid:ipni.org:names:452218-1
The Plant List kew-130206
Open Tree Of Life 6082015
NCBI Taxonomy 1898873
IPNI 452218-1
iNaturalist 447036
GBIF 3904978
EOL 2893997
USDA GRIN 407928

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
The Extract of Scutellaria baicalensis Attenuates the Pattern Recognition Receptor Pathway Activation Induced by Influenza A Virus in Macrophages Yang M, Ma L, Su R, Guo R, Zhou N, Liu M, Wu J, Wang Y, Hao Y Viruses 08-Jul-2023
PMCID:PMC10384909
doi:10.3390/v15071524
PMID:37515209
Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK Int J Mol Sci 01-Jan-2023
PMCID:PMC9821772
doi:10.3390/ijms24010739
PMID:36614181
Ethnobotanical study of Hakka traditional medicine in Ganzhou, China and their antibacterial, antifungal, and cytotoxic assessments Hu H, Yang Y, Aissa A, Tekin V, Li J, Panda SK, Huang H, Luyten W BMC Complement Med Ther 19-Sep-2022
PMCID:PMC9484230
doi:10.1186/s12906-022-03712-z
PMID:36123737
Lignans from Mosla scabra Ameliorated Influenza A Virus-Induced Pneumonia via Inhibiting Macrophage Activation Cai W, Wu LR, Zhang SL Evid Based Complement Alternat Med 30-Jul-2022
PMCID:PMC9356792
doi:10.1155/2022/1688826
PMID:35942373
Mechanistic Understanding of Lung Inflammation: Recent Advances and Emerging Techniques Keskinidou C, Vassiliou AG, Dimopoulou I, Kotanidou A, Orfanos SE J Inflamm Res 15-Jun-2022
PMCID:PMC9207257
doi:10.2147/JIR.S282695
PMID:35734098
Anti-Inflammatory Mechanisms of Total Flavonoids from Mosla scabra against Influenza A Virus-Induced Pneumonia by Integrating Network Pharmacology and Experimental Verification Cai W, Zhang SL Evid Based Complement Alternat Med 08-Jun-2022
PMCID:PMC9200497
doi:10.1155/2022/2154485
PMID:35722153
Experimental and Clinical Studies on the Effects of Natural Products on Noxious Agents-Induced Lung Disorders, a Review Saadat S, Beigoli S, Khazdair MR, Amin F, Boskabady MH Front Nutr 18-May-2022
PMCID:PMC9158561
doi:10.3389/fnut.2022.867914
PMID:35662950
Nanotechnology Applications of Flavonoids for Viral Diseases Jannat K, Paul AK, Bondhon TA, Hasan A, Nawaz M, Jahan R, Mahboob T, Nissapatorn V, Wilairatana P, Pereira MD, Rahmatullah M Pharmaceutics 08-Nov-2021
PMCID:PMC8625292
doi:10.3390/pharmaceutics13111895
PMID:34834309
Plant-Based Natural Products and Extracts: Potential Source to Develop New Antiviral Drug Candidates Thomas E, Stewart LE, Darley BA, Pham AM, Esteban I, Panda SS Molecules 14-Oct-2021
PMCID:PMC8537559
doi:10.3390/molecules26206197
PMID:34684782
Pharmacologic Activities of Plant-Derived Natural Products on Respiratory Diseases and Inflammations Timalsina D, Pokhrel KP, Bhusal D Biomed Res Int 04-Oct-2021
PMCID:PMC8505070
doi:10.1155/2021/1636816
PMID:34646882
Ecological stoichiometric characteristics of soil-moss C, N, and P in restoration stages of karst rocky desertification Meng W, Dai Q, Ren Q, Tu N, Leng T PLoS One 30-Jun-2021
PMCID:PMC8244914
doi:10.1371/journal.pone.0252838
PMID:34191821
Important Flavonoids and Their Role as a Therapeutic Agent Ullah A, Munir S, Badshah SL, Khan N, Ghani L, Poulson BG, Emwas AH, Jaremko M Molecules 11-Nov-2020
PMCID:PMC7697716
doi:10.3390/molecules25225243
PMID:33187049
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986
Aquaporins as Targets of Dietary Bioactive Phytocompounds Tesse A, Grossini E, Tamma G, Brenner C, Portincasa P, Marinelli RA, Calamita G Front Mol Biosci 18-Apr-2018
PMCID:PMC5915544
doi:10.3389/fmolb.2018.00030
PMID:29721498
Ethnobotany of wild plants used for starting fermented beverages in Shui communities of southwest China Hong L, Zhuo J, Lei Q, Zhou J, Ahmed S, Wang C, Long Y, Li F, Long C J Ethnobiol Ethnomed 28-May-2015
PMCID:PMC4458060
doi:10.1186/s13002-015-0028-0
PMID:26017691

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
2,4,5-Trimethoxybenzaldehyde 20525 Click to see COC1=CC(=C(C=C1C=O)OC)OC 196.20 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
> Benzenoids / Phenol ethers / Anisoles
alpha-Asarone 636822 Click to see CC=CC1=CC(=C(C=C1OC)OC)OC 208.25 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
Azaron 17903 Click to see CC=CC1=CC(=C(C=C1OC)OC)OC 208.25 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
> Lignans, neolignans and related compounds / Cyclobutane lignans
1-[(1R,2R)-2,3-dimethyl-4-(2,4,5-trimethoxyphenyl)cyclobutyl]-2,4,5-trimethoxybenzene 5318447 Click to see CC1C(C(C1C2=CC(=C(C=C2OC)OC)OC)C3=CC(=C(C=C3OC)OC)OC)C 416.50 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
1-[(1R,2S,3S,4R)-2,3-dimethyl-4-(2,4,5-trimethoxyphenyl)cyclobutyl]-2,4,5-trimethoxybenzene 10341859 Click to see CC1C(C(C1C2=CC(=C(C=C2OC)OC)OC)C3=CC(=C(C=C3OC)OC)OC)C 416.50 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
5-[(1S,2R,3S,4R)-2,3-dimethyl-4-(2,4,5-trimethoxyphenyl)cyclobutyl]-4,7-dimethoxy-1,3-benzodioxole 162973179 Click to see CC1C(C(C1C2=CC(=C(C=C2OC)OC)OC)C3=CC(=C4C(=C3OC)OCO4)OC)C 430.50 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
5-[(2R,3S)-2,3-dimethyl-4-(2,4,5-trimethoxyphenyl)cyclobutyl]-4,7-dimethoxy-1,3-benzodioxole 5319903 Click to see CC1C(C(C1C2=CC(=C(C=C2OC)OC)OC)C3=CC(=C4C(=C3OC)OCO4)OC)C 430.50 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
5-[2,3-Dimethyl-4-(2,4,5-trimethoxyphenyl)cyclobutyl]-4,7-dimethoxy-1,3-benzodioxole 78385329 Click to see CC1C(C(C1C2=CC(=C(C=C2OC)OC)OC)C3=CC(=C4C(=C3OC)OCO4)OC)C 430.50 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
6-[(1S,2R,3S,4R)-2,3-dimethyl-4-(2,4,5-trimethoxyphenyl)cyclobutyl]-4-methoxy-1,3-benzodioxole 162880150 Click to see CC1C(C(C1C2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C=C4OC)OC)OC)C 400.50 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
6-[(2R,3S)-2,3-dimethyl-4-(2,4,5-trimethoxyphenyl)cyclobutyl]-4-methoxy-1,3-benzodioxole 5319902 Click to see CC1C(C(C1C2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C=C4OC)OC)OC)C 400.50 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
6-[2,3-Dimethyl-4-(2,4,5-trimethoxyphenyl)cyclobutyl]-4-methoxy-1,3-benzodioxole 78385328 Click to see CC1C(C(C1C2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C=C4OC)OC)OC)C 400.50 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
Heterotropan 126324 Click to see CC1C(C(C1C2=CC(=C(C=C2OC)OC)OC)C3=CC(=C(C=C3OC)OC)OC)C 416.50 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
Magnosalin 10454589 Click to see CC1C(C(C1C2=CC(=C(C=C2OC)OC)OC)C3=CC(=C(C=C3OC)OC)OC)C 416.50 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/J.FITOTE.2009.12.005
https://doi.org/10.1016/S0031-9422(00)00105-9
Jacarandic acid 13653335 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
https://doi.org/10.1016/J.FITOTE.2009.12.005
> Organoheterocyclic compounds / Benzodioxoles
4,7-Dimethoxy-5-(1-propenyl)-1,3-benzodioxol 15559838 Click to see CC=CC1=CC(=C2C(=C1OC)OCO2)OC 222.24 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
4,7-Dimethoxy-5-(prop-1-en-1-yl)-2H-1,3-benzodioxole 53397165 Click to see CC=CC1=CC(=C2C(=C1OC)OCO2)OC 222.24 unknown https://doi.org/10.1016/S0031-9422(00)00105-9
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/J.FITOTE.2009.12.005
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown https://doi.org/10.1016/J.FITOTE.2009.12.005
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Mosloflavone 471722 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O)OC 298.29 unknown https://doi.org/10.1016/J.FITOTE.2009.12.005
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Hydroxy-7,8-dimethoxyflavone 188316 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=CC=C3)OC 298.29 unknown https://doi.org/10.1016/J.FITOTE.2009.12.005

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