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Callicarpa maingayi

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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 UUID6440269690b2e943309466
Scientific name Callicarpa maingayi
Authority King & Gamble
First published in Bull. Misc. Inform. Kew 1908: 106 (1908)

Description Top

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Callicarpa maingayi, also known as beautyberry, is a plant species belonging to the Lamiaceae family. It is native to Malaysia and Singapore, where it can be found growing in various habitats. This plant is known for its attractive purple berries, which are often used in traditional medicine and as a decorative element in gardens. It is also a popular choice for landscaping due to its low maintenance and ability to attract birds and butterflies. Callicarpa maingayi is a unique and beautiful addition to the flora of Malaysia and Singapore.

Synonyms Top

No known synonyms.

Common names Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000770045
Tropicos 50215783
KEW urn:lsid:ipni.org:names:861398-1
The Plant List kew-30877
Open Tree Of Life 900370
NCBI Taxonomy 536998
IUCN Red List 31820
IPNI 861398-1
iNaturalist 190099
GBIF 5609496
Freebase /m/02x8pwd
EOL 5386804
Wikipedia Callicarpa_maingayi
CMAUP NPO550

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
Green synthesis of silver nanoparticles using Ocimum sanctum Linn. and its antibacterial activity against multidrug resistant Acinetobacter baumannii Gautam D, Dolma KG, Khandelwal B, Gupta M, Singh M, Mahboob T, Teotia A, Thota P, Bhattacharya J, Goyal R, M.R. Oliveira S, Pereira MD, Wiart C, Wilairatana P, Eawsakul K, Rahmatullah M, Saravanabhavan SS, Nissapatorn V PeerJ 28-Jul-2023
PMCID:PMC10389072
doi:10.7717/peerj.15590
PMID:37529215
Antimicrobial Applications of Green Synthesized Bimetallic Nanoparticles from Ocimum basilicum More PR, Zannella C, Folliero V, Foglia F, Troisi R, Vergara A, Franci G, De Filippis A, Galdiero M Pharmaceutics 14-Nov-2022
PMCID:PMC9695082
doi:10.3390/pharmaceutics14112457
PMID:36432648
Evaluation of two different Cannabis sativa L. extracts as antioxidant and neuroprotective agents Cásedas G, Moliner C, Maggi F, Mazzara E, López V Front Pharmacol 13-Sep-2022
PMCID:PMC9513154
doi:10.3389/fphar.2022.1009868
PMID:36176449
Nano-Drug Delivery Systems Entrapping Natural Bioactive Compounds for Cancer: Recent Progress and Future Challenges Chavda VP, Patel AB, Mistry KJ, Suthar SF, Wu ZX, Chen ZS, Hou K Front Oncol 29-Mar-2022
PMCID:PMC9004605
doi:10.3389/fonc.2022.867655
PMID:35425710
Plant Terpenoids as the Promising Source of Cholinesterase Inhibitors for Anti-AD Therapy Lai Shi Min S, Liew SY, Chear NJ, Goh BH, Tan WN, Khaw KY Biology (Basel) 14-Feb-2022
PMCID:PMC8869317
doi:10.3390/biology11020307
PMID:35205173
Silver Nanoparticle Production Mediated by Vitis vinifera Cane Extract: Characterization and Antibacterial Activity Evaluation Michailidu J, Maťátková O, Kolouchová I, Masák J, Čejková A Plants (Basel) 05-Feb-2022
PMCID:PMC8840298
doi:10.3390/plants11030443
PMID:35161424
An overview of the phytosynthesis of various metal nanoparticles Tiwari S, Verma SK, Bhagat P, Yadav S, Sharma R, Aseri GK, Sohal JS, Sharma D, Dwivedi UK, Singh R, Singh D, Khare N 3 Biotech 29-Oct-2021
PMCID:PMC8556431
doi:10.1007/s13205-021-03014-0
PMID:34790502
Green synthesis of silver nanoparticles with algae and the importance of capping agents in the process Chugh D, Viswamalya VS, Das B J Genet Eng Biotechnol 24-Aug-2021
PMCID:PMC8385017
doi:10.1186/s43141-021-00228-w
PMID:34427807
Antimicrobial Synergy of Silver-Platinum Nanohybrids With Antibiotics Ranpariya B, Salunke G, Karmakar S, Babiya K, Sutar S, Kadoo N, Kumbhakar P, Ghosh S Front Microbiol 01-Feb-2021
PMCID:PMC7882503
doi:10.3389/fmicb.2020.610968
PMID:33597929
Metal nanoparticles fabricated by green chemistry using natural extracts: biosynthesis, mechanisms, and applications El-Seedi HR, El-Shabasy RM, Khalifa SA, Saeed A, Shah A, Shah R, Iftikhar FJ, Abdel-Daim MM, Omri A, Hajrahand NH, Sabir JS, Zou X, Halabi MF, Sarhan W, Guo W RSC Adv 08-Aug-2019
PMCID:PMC9069627
doi:10.1039/c9ra02225b
PMID:35527869
Optimisation of nitrate reductase enzyme activity to synthesise silver nanoparticles Khodashenas B, Ghorbani HR IET Nanobiotechnol 01-Jun-2016
PMCID:PMC8676541
doi:10.1049/iet-nbt.2015.0062
PMID:27256897
Isolation and Structure of Maingayic Acid, a Piscicidal Constituent of<i>Callicarpa maingayi</i> Chikao Nishino, Kazuyoshi Kawazu, Tetsuo Mitsui Oxford University Press (OUP) 13-Apr-2016
doi:10.1080/00021369.1971.10860157
Plant-Mediated Synthesis of Silver Nanoparticles: Their Characteristic Properties and Therapeutic Applications Chung IM, Park I, Seung-Hyun K, Thiruvengadam M, Rajakumar G Nanoscale Res Lett 28-Jan-2016
PMCID:PMC4731379
doi:10.1186/s11671-016-1257-4
PMID:26821160
Green and energy-efficient methods for the production of metallic nanoparticles Naghdi M, Taheran M, Brar SK, Verma M, Surampalli RY, Valero JR Beilstein J Nanotechnol 10-Dec-2015
PMCID:PMC4685792
doi:10.3762/bjnano.6.243
PMID:26734527
Biosynthesis of metallic nanoparticles using plant derivatives and their new avenues in pharmacological applications – An updated report Kuppusamy P, Yusoff MM, Maniam GP, Govindan N Saudi Pharm J 08-Dec-2014
PMCID:PMC4908060
doi:10.1016/j.jsps.2014.11.013
PMID:27330378

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
3-Galloylshikimic acid 10449030 Click to see C1C(C(C(C=C1C(=O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O 326.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(4aS,7S,8S,8aR)-8-[2-(furan-3-yl)ethyl]-4,7,8-trimethyl-1,2,5,6,7,8a-hexahydronaphthalene-4a-carboxylic acid 162941813 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C)C(=O)O 316.40 unknown https://doi.org/10.1080/00021369.1971.10860157
8-[2-(Furan-3-yl)ethyl]-4,7,8-trimethyl-1,2,5,6,7,8a-hexahydronaphthalene-4a-carboxylic acid 12312682 Click to see CC1CCC2(C(C1(C)CCC3=COC=C3)CCC=C2C)C(=O)O 316.40 unknown https://doi.org/10.1080/00021369.1971.10860157
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-1,3-dihydroxy-4,5-bis[(3,4,5-trihydroxybenzoyl)oxy]cyclohexane-1-carboxylic acid 13270012 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O 496.40 unknown via CMAUP database
3,4-Di-O-galloylquinic acid 460895 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O 496.40 unknown via CMAUP database
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-4-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-4-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 101228664 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C(C(=CC(=C56)O)O)C7C(C(OC8=CC(=CC(=C78)O)O)C9=CC(=C(C=C9)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1155.00 unknown via CMAUP database
Procyanidin B3 146798 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin C2 11182062 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Leucocianidol 440833 Click to see C1=CC(=C(C=C1C2C(C(C3=C(C=C(C=C3O2)O)O)O)O)O)O 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(-)-Gallocatechin 9882981 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Delphinidin 3-O-glucoside cation 443650 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 465.40 unknown via CMAUP database
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
3',5'-Dimethoxy-4',7-dihydroxy-5-(beta-D-glucopyranosyloxy)-3-[(6-O-acetyl-beta-D-glucopyranosyl)oxy]flavylium 101918997 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C([O+]=C3C=C(C=C(C3=C2)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC(=C(C(=C5)OC)O)OC)O)O)O 697.60 unknown via CMAUP database
Cyanin 441688 Click to see C1=CC(=C(C=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 611.50 unknown via CMAUP database
Malvin 441765 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 655.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 12304323 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
kaempferol 3-O-beta-L-glucopyranoside 9911508 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Quercetin 3-O-(6''-galloyl)-beta-D-galactopyranoside 5491814 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O 616.50 unknown via CMAUP database
Quercetin 3-O-(6''-galloyl)-beta-D-glucopyranoside 9830456 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O 616.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
(1R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylic acid 102004656 Click to see C1C(C2=C(C1=O)OC(=O)C3=CC(=C(C(=C32)O)O)O)C(=O)O 292.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
(2R,3R,4S,5R,6R)-6-(((3,4,5-Trihydroxybenzoyl)oxy)methyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetrakis(3,4,5-trihydroxybenzoate) 9876301 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown via CMAUP database
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown via CMAUP database
NP-003686 73178 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 788.60 unknown via CMAUP database
Pentagalloylglucose 65238 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
1,2-Di-O-galloyl-4,6-O-(S)-hexahydroxydiphenoyl-beta-D-glucopyranose 101259865 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown via CMAUP database
3-O-digalloyl-1,2,4,6-tetra-O-beta-D-galloylglucose 16164119 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 1092.80 unknown via CMAUP database
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown via CMAUP database
Geraniin 3001497 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 952.60 unknown via CMAUP database
Xcxwmhrrisfuff-xngpzlstsa- 21636130 Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C9C(C(COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O9)O)O)O)O)O)O)OC8OC(=O)C1=CC(=C(C(=C1)O)O)O)OC5=O)O)O)O)O)O)O 1110.80 unknown via CMAUP database

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