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Monochasma savateri

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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 UUID64404edc7c3dc383589545
Scientific name Monochasma savateri
Authority Franch. ex Maxim.
First published in Bull. Soc. Imp. Naturalistes Moscou 54(I): 39 (1879)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 白毛鹿茸草
Chinese 鹿茸草
Chinese 沙氏鹿茸草鹿茸草（绵毛鹿茸草、白毛鹿茸草）
Chinese 绵毛鹿茸草，沙氏鹿茸草
Chinese 沙氏鹿茸草

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001140112
Tropicos 29208444
KEW urn:lsid:ipni.org:names:806224-1
The Plant List tro-29208444
Open Tree Of Life 5536405
NCBI Taxonomy 1501483
iNaturalist 556429
GBIF 8052261
IPNI 806224-1

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
Genetic variation and structure of endemic and endangered wild celery (Kelussia odoratissima Mozaff.) quantified using novel microsatellite markers developed by next-generation sequencing Mahdavikia F, Ebadi MT, Shojaeiyan A, Ayyari M, Falahati-Anbaran M Front Plant Sci 04-Apr-2024
PMCID:PMC11024376
doi:10.3389/fpls.2024.1301936
Genetic diversity and population structure analysis of Paris polyphylla Sm. revealed by SSR marker Oliya BK, Maharjan L, Pant B Heliyon 17-Jul-2023
PMCID:PMC10395474
doi:10.1016/j.heliyon.2023.e18230
PMID:37539281
Ultrasound-Assisted Extraction of Verbascoside from Clerodendrum glandulosum Leaves for Analysis of Antioxidant and Antidiabetic Activities Khound P, Sarma H, Sarma PP, Jana UK, Devi R ACS Omega 31-May-2023
PMCID:PMC10268293
doi:10.1021/acsomega.3c00173
PMID:37323385
Genetic diversity of the wild ancient tea tree (Camellia taliensis) populations at different altitudes in Qianjiazhai Wang F, Cheng X, Cheng S, Li W, Huang X PLoS One 18-Apr-2023
PMCID:PMC10112783
doi:10.1371/journal.pone.0283189
PMID:37071624
Genomic and Epigenomic Mechanisms of the Interaction between Parasitic and Host Plants Ashapkin VV, Kutueva LI, Aleksandrushkina NI, Vanyushin BF, Teofanova DR, Zagorchev LI Int J Mol Sci 31-Jan-2023
PMCID:PMC9917227
doi:10.3390/ijms24032647
PMID:36768970
Identification of Competing Endogenous RNAs (ceRNAs) Network Associated with Drought Tolerance in Medicago truncatula with Rhizobium Symbiosis Jing J, Yang P, Wang Y, Qu Q, An J, Fu B, Hu X, Zhou Y, Hu T, Cao Y Int J Mol Sci 17-Nov-2022
PMCID:PMC9696283
doi:10.3390/ijms232214237
PMID:36430715
Molecular Characterization of Tinospora cordifolia (Willd.) Miers Using Novel g-SSR Markers and Their Comparison with EST-SSR and SCoT Markers for Genetic Diversity Study Paliwal R, Singh R, Choudhury DR, Tiwari G, Kumar A, Bhat KC, Singh R Genes (Basel) 05-Nov-2022
PMCID:PMC9690116
doi:10.3390/genes13112042
PMID:36360279
Analysis of the genetic diversity and population structure of Monochasma savatieri Franch. ex Maxim using novel EST-SSR markers Yang W, Bai Z, Wang F, Zou M, Wang X, Xie J, Zhang F BMC Genomics 16-Aug-2022
PMCID:PMC9382759
doi:10.1186/s12864-022-08832-x
PMID:35974306
Research Progress and Trends of Phenylethanoid Glycoside Delivery Systems Huang J, Zhao D, Cui C, Hao J, Zhang Z, Guo L Foods 07-Mar-2022
PMCID:PMC8909102
doi:10.3390/foods11050769
PMID:35267401
Traditional Chinese Medicine is an Alternative Therapeutic Option for Treatment of Pseudomonas aeruginosa Infections Pang Z, Zhu Q Front Pharmacol 27-Aug-2021
PMCID:PMC8429605
doi:10.3389/fphar.2021.737252
PMID:34512364
Integrated analyses of the transcriptome and small RNA of the hemiparasitic plant Monochasma savatieri before and after establishment of parasite-host association Chen L, Guo Q, Zhu Z, Wan H, Qin Y, Zhang H BMC Plant Biol 10-Feb-2021
PMCID:PMC7877053
doi:10.1186/s12870-021-02861-6
PMID:33568062
The changes of morphological and physiological characteristics in hemiparasitic Monochasma savatieri before and after attachment to the host plant Chen L, Zhu Z, Guo Q, Guo J, Huang Z, Zhang H PeerJ 19-Aug-2020
PMCID:PMC7443084
doi:10.7717/peerj.9780
PMID:32879807
Shoot organogenesis and somatic embryogenesis from leaf and root explants of Scaevolasericea Liang H, Xiong Y, Guo B, Yan H, Jian S, Ren H, Zhang X, Li Y, Zeng S, Wu K, Zheng F, Teixeira da Silva JA, Xiong Y, Ma G Sci Rep 09-Jul-2020
PMCID:PMC7347615
doi:10.1038/s41598-020-68084-1
PMID:32647162
Chinese Herbal Medicine Interventions in Neurological Disorder Therapeutics by Regulating Glutamate Signaling Liu Y, Wang S, Kan J, Zhang J, Zhou L, Huang Y, Zhang Y Curr Neuropharmacol 01-Apr-2020
PMCID:PMC7327939
doi:10.2174/1570159X17666191101125530
PMID:31686629
Application of Herbal Traditional Chinese Medicine in the Treatment of Acute Kidney Injury Li HD, Meng XM, Huang C, Zhang L, Lv XW, Li J Front Pharmacol 18-Apr-2019
PMCID:PMC6482429
doi:10.3389/fphar.2019.00376
PMID:31057404

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
6-Acetyloxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 14157899 Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C 418.40 unknown https://doi.org/10.1248/CPB.37.3153
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1248/CPB.37.3153
https://doi.org/10.1248/YAKUSHI1947.106.8_725
Bartsioside 14081907 Click to see C1C=C(C2C1C=COC2OC3C(C(C(C(O3)CO)O)O)O)CO 330.33 unknown https://doi.org/10.1248/YAKUSHI1947.106.8_725
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R)-2-[[(1R,2S,6S)-5-hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 138107792 Click to see C1=COC(C2C1C(C3C2(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O 362.33 unknown https://doi.org/10.1248/CPB.37.3153
https://doi.org/10.1248/YAKUSHI1947.106.8_725
Catalpol 91520 Click to see C1=COC(C2C1C(C3C2(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O 362.33 unknown https://doi.org/10.1248/CPB.37.3153
https://doi.org/10.1248/YAKUSHI1947.106.8_725
methyl (1S,4aS,7S,7aS)-7-hydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 101834770 Click to see COC(=O)C1=COC(C2C1CCC2O)OC3C(C(C(C(O3)CO)O)O)O 376.36 unknown https://doi.org/10.1248/CPB.37.3153
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1248/YAKUSHI1947.106.8_725
https://doi.org/10.1248/CPB.37.3153
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1248/YAKUSHI1947.106.8_725
https://doi.org/10.1248/CPB.37.3153

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