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Cinnamomum bejolghota

Cinnamomum bejolghota - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID6440112b222ce958915475
Scientific name Cinnamomum bejolghota
Authority (Buch.-Ham.) Sweet
First published in Hort. Brit. : 344 (1826)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cinnamomum van-houttei Lukman. Nomencl. Icon. Cannel. 12 1889
Laurus bejolghota Buch.-Ham. Trans. Linn. Soc. London 13: 559 (1822)

Common names Top

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Language Common/alternative name
Burmese လုလင်ကျော်ပင်
Thai สมุลแว้ง
Chinese 抱木
Chinese 鈍葉桂
Chinese 鸭母楠
Chinese 鸭母桂
Chinese 香桂楠
Chinese 青樟木
Chinese 老母猪桂皮
Chinese 老母楠
Chinese 梅宗英龙
Chinese 土桂皮
Chinese 山玉桂
Chinese 山桂楠
Chinese 钝叶樟
Chinese 山桂
Chinese 奉楠
Chinese 钝叶桂
Chinese 大叶山桂
Chinese 野桂皮
Chinese 假桂皮

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Cinnamomum bejolghota var. bejolghota Unknown
Cinnamomum bejolghota var. jarainum Baruah & S.C.Nath Nordic J. Bot. 21: 572 (2001 publ. 2002)
Cinnamomum bejolghota var. pubescens Grierson & D.G.Long Notes Roy. Bot. Gard. Edinburgh 40: 128 (1982)

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 South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • Nepal
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000604917
Tropicos 17806426
KEW urn:lsid:ipni.org:names:463310-1
The Plant List kew-2721146
Open Tree Of Life 864871
Observations.org 457204
NCBI Taxonomy 397101
IUCN Red List 145301455
IPNI 463310-1
GBIF 7304259
Elurikkus 585600
USDA GRIN 424788

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
Therapeutic potential of Thai herbal formula for cognitive impairment: A metabolomics approach for Comprehensive Insights Akarasereenont P, Pattanapholkornsakul S, Limsuvan S, Mamaethong D, Booranasubkajorn S, Pakaprot N, Tripatara P, Pilakasiri K Heliyon 16-Mar-2024
PMCID:PMC10981045
doi:10.1016/j.heliyon.2024.e28027
PMID:38560220
Three-tiered authentication of herbal traditional Chinese medicine ingredients used in women’s health provides progressive qualitative and quantitative insight Mück F, Scotti F, Mauvisseau Q, Thorbek BL, Wangensteen H, de Boer HJ Front Pharmacol 05-Feb-2024
PMCID:PMC10875096
doi:10.3389/fphar.2024.1353434
PMID:38375033
The interaction of Suk-Saiyasna remedy with GABAA and CB1 receptor-targeting drugs: Enhancing hypnotic and sedative effects in in vivo models Damjuti W, Thitikornpong W, Saengow S, Thanusuwannasak T, Fuangfoo T, Boonruab J J Adv Pharm Technol Res 15-Jan-2024
PMCID:PMC10880918
doi:10.4103/JAPTR.JAPTR_355_23
PMID:38389972
Antibacterial and Antifungal Terpenes from the Medicinal Angiosperms of Asia and the Pacific: Haystacks and Gold Needles Wiart C, Kathirvalu G, Raju CS, Nissapatorn V, Rahmatullah M, Paul AK, Rajagopal M, Sathiya Seelan JS, Rusdi NA, Lanting S, Sulaiman M Molecules 04-May-2023
PMCID:PMC10180233
doi:10.3390/molecules28093873
PMID:37175283
Endophytic species of Induratia from coffee and carqueja plants from Brazil and its potential for the biological control of toxicogenic fungi on coffee beans by means of antimicrobial volatiles Gomes AA, Paes SA, Ferreira AP, Pinho DB, de Lourdes Cardeal Z, Menezes HC, Cardoso PG, Pereira OL Braz J Microbiol 04-Jan-2023
PMCID:PMC9944607
doi:10.1007/s42770-022-00887-y
PMID:36598751
Insecticidal Activity of Essential Oils against Mealybug Pests (Hemiptera: Pseudococcidae): A Systematic Review and Meta-Analysis Avila MD, Achimón F, Brito VD, Aguilar R, Pizzolitto RP, Zunino MP, Peschiutta ML Plants (Basel) 26-Dec-2022
PMCID:PMC9824342
doi:10.3390/plants12010109
PMID:36616236
Siwalik plant megafossil diversity in the Eastern Himalayas: A review Khan MA, Mahato S, Spicer RA, Spicer TE, Ali A, Hazra T, Bera S Plant Divers 17-Dec-2022
PMCID:PMC10311196
doi:10.1016/j.pld.2022.12.003
PMID:37397603
Advancements and future prospective of DNA barcodes in the herbal drug industry Mahima K, Sunil Kumar KN, Rakhesh KV, Rajeswaran PS, Sharma A, Sathishkumar R Front Pharmacol 21-Oct-2022
PMCID:PMC9635000
doi:10.3389/fphar.2022.947512
PMID:36339543
Phylogeny and taxonomy of Cinnamomum (Lauraceae) Yang Z, Liu B, Yang Y, Ferguson DK Ecol Evol 01-Oct-2022
PMCID:PMC9526118
doi:10.1002/ece3.9378
PMID:36203627
Ethnomedicinal Practices and Traditional Medicinal Plants of Barak Valley, Assam: a systematic review Barbhuiya PA, Laskar AM, Mazumdar H, Dutta PP, Pathak MP, Dey BK, Sen S J Pharmacopuncture 30-Sep-2022
PMCID:PMC9510141
doi:10.3831/KPI.2022.25.3.149
PMID:36186100
Novel Approaches for Inhibiting the Indoor Allergen Der f 2 Excreted from House Dust Mites by Todomatsu Oil Produced from Woodland Residues Lin Y, Enyoh CE, Wang Q, Lu S, Zhang W, Xiao K, Zhou S, Kaneko T, Seguchi A, Wang W, Guo Y Int J Environ Res Public Health 31-Aug-2022
PMCID:PMC9517791
doi:10.3390/ijerph191710881
PMID:36078598
Phytochemical Classification of Medicinal Plants Used in the Treatment of Kidney Disease Based on Traditional Persian Medicine Rabizadeh F, Mirian MS, Doosti R, Kiani-Anbouhi R, Eftekhari E Evid Based Complement Alternat Med 31-Jul-2022
PMCID:PMC9357710
doi:10.1155/2022/8022599
PMID:35958915
Synbiotic Effects of Fermented Rice on Human Health and Wellness: A Natural Beverage That Boosts Immunity Fuloria S, Mehta J, Talukdar MP, Sekar M, Gan SH, Subramaniyan V, Rani NN, Begum MY, Chidambaram K, Nordin R, Maziz MN, Sathasivam KV, Lum PT, Fuloria NK Front Microbiol 13-Jul-2022
PMCID:PMC9325588
doi:10.3389/fmicb.2022.950913
PMID:35910609
Cinnamomum Species: Bridging Phytochemistry Knowledge, Pharmacological Properties and Toxicological Safety for Health Benefits Sharifi-Rad J, Dey A, Koirala N, Shaheen S, El Omari N, Salehi B, Goloshvili T, Cirone Silva NC, Bouyahya A, Vitalini S, Varoni EM, Martorell M, Abdolshahi A, Docea AO, Iriti M, Calina D, Les F, López V, Caruntu C Front Pharmacol 11-May-2021
PMCID:PMC8144503
doi:10.3389/fphar.2021.600139
PMID:34045956
Daldiniaeschsone A, a Rare Tricyclic Polyketide Having a Chromone Unit Fused to a δ-Lactone and Its Symmetrical Biphenyl Dimer, Daldiniaeschsone B, from an Endophytic Fungus Daldinia eschscholtzii SDBR-CMUNKC745 Wutthiwong N, Suthiphasilp V, Pintatum A, Suwannarach N, Kumla J, Lumyong S, Maneerat T, Charoensup R, Cheenpracha S, Limtharakul T, Pyne SG, Laphookhieo S J Fungi (Basel) 02-May-2021
PMCID:PMC8147462
doi:10.3390/jof7050358
PMID:34063266

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
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R,3R,3'R)-2,2'-Bis(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-2H,2'H-4,8'-bichromene-3,3',5,5',7,7'-hexol 5320711 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 https://doi.org/10.1248/CPB.34.643
(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-4-[(2S,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 154497279 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 https://doi.org/10.1248/CPB.34.633
(2R,3R)-2-(3,4-dihydroxyphenyl)-6-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 13990894 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1248/CPB.34.633
(2R,3S)-2-(3,4-dihydroxyphenyl)-6-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 102266638 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1248/CPB.34.633
Endotelon 130556 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 https://doi.org/10.1248/CPB.34.643
ent-Epicatechin-(4alpha->6)-ent-epicatechin 13990892 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1248/CPB.34.643
Procyanidin A1 5089889 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown https://doi.org/10.1248/CPB.34.643
Procyanidin A2 124025 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown https://doi.org/10.1248/CPB.34.643
Procyanidin B1 11250133 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 https://doi.org/10.1248/CPB.34.643
Procyanidin B2, (+)- 122738 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 https://doi.org/10.1248/CPB.34.643
https://doi.org/10.1248/CPB.34.633
Procyanidin B5 124017 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1248/CPB.34.643
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1248/CPB.34.633
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 5-O-p-coumaroyl glycosides
[(2R,3S,4S,5R,6S)-6-[[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-5-yl]oxy]-3,4-dihydroxy-5-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 21637581 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(OC2OC3=CC(=CC4=C3CC(C(O4)C5=CC(=C(C=C5)O)O)O)O)COC(=O)C=CC6=CC=C(C=C6)O)O)O)O 774.70 unknown https://doi.org/10.1248/CPB.34.643
[6-[[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-5-yl]oxy]-3,4-dihydroxy-5-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 73818236 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(OC2OC3=CC(=CC4=C3CC(C(O4)C5=CC(=C(C=C5)O)O)O)O)COC(=O)C=CC6=CC=C(C=C6)O)O)O)O 774.70 unknown https://doi.org/10.1248/CPB.34.643

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