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Internal ID UUID6440083a56bfe903225589
Scientific name Bulbophyllum kwangtungense
Authority Schltr.
First published in Repert. Spec. Nov. Regni Veg. 19: 381 (1924)

Description Top

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Bulbophyllum kwangtungense is a type of orchid belonging to the Bulbophyllum genus. This orchid species contains three unique chemicals, cumulatin, densiflorol A, and plicatol B, which can be extracted from the plant. These chemicals have potential uses in various industries and add to the overall value of this orchid species.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 广东石豆兰
Chinese 广石豆兰

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-0000525354
Tropicos 50026322
KEW urn:lsid:ipni.org:names:619255-1
The Plant List kew-26279
Open Tree Of Life 217245
NCBI Taxonomy 1185425
IPNI 619255-1
iNaturalist 848667
GBIF 2844327
Freebase /m/07kft0x
EOL 249532
Wikipedia Bulbophyllum_kwangtungense

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
Ethnobotanical study on herbal tea drinks in Guangxi, China Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C J Ethnobiol Ethnomed 31-Mar-2023
PMCID:PMC10064729
doi:10.1186/s13002-023-00579-3
PMID:37004116
Ethnobotany, Phytochemistry, Biological Activities, and Health-Promoting Effects of the Genus Bulbophyllum Sharifi-Rad J, Quispe C, Bouyahya A, El Menyiy N, El Omari N, Shahinozzaman M, Ara Haque Ovey M, Koirala N, Panthi M, Ertani A, Nicola S, Lapava N, Herrera-Bravo J, Salazar LA, Changan S, Kumar M, Calina D Evid Based Complement Alternat Med 07-Mar-2022
PMCID:PMC8920616
doi:10.1155/2022/6727609
PMID:35295925
Chemical Composition and Cytotoxic Activity of the Essential Oil and Oleoresins of In Vitro Micropropagated Ansellia africana Lindl: A Vulnerable Medicinal Orchid of Africa Saleh-E-In MM, Bhattacharyya P, Van Staden J Molecules 28-Jul-2021
PMCID:PMC8347246
doi:10.3390/molecules26154556
PMID:34361724
Total Synthesis of Oxepin and Dihydrooxepin Containing Natural Products Sokol KR, Magauer T Synthesis (Stuttg) 24-Jun-2021
PMCID:PMC7612190
doi:10.1055/s-0037-1610776
PMID:35001983
Comparative Cytotoxic Activity of Wild Harvested Stems and In Vitro-Raised Protocorms of Dendrobium chryseum Rolfe in Human Cervical Carcinoma and Glioblastoma Cell Lines Pant B, Joshi PR, Maharjan S, Thakuri LS, Pradhan S, Shah S, Wagner SH, Pant B Adv Pharmacol Pharm Sci 06-Jan-2021
PMCID:PMC7808824
doi:10.1155/2021/8839728
PMID:33506210
Dactylorhiza hatagirea (D. Don) Soo: A Critically Endangered Perennial Orchid from the North-West Himalayas Wani IA, Kumar V, Verma S, Tasleem Jan A, Rather IA Plants (Basel) 25-Nov-2020
PMCID:PMC7760081
doi:10.3390/plants9121644
PMID:33255646
Bibenzyls and bisbybenzyls of bryophytic origin as promising source of novel therapeutics: pharmacology, synthesis and structure-activity Nandy S, Dey A Daru 15-Aug-2020
PMCID:PMC7429097
doi:10.1007/s40199-020-00341-0
PMID:32803687
Cytotoxic effect of selected wild orchids on two different human cancer cell lines Joshi PR, Paudel MR, Chand MB, Pradhan S, Pant KK, Joshi GP, Bohara M, Wagner SH, Pant B, Pant B Heliyon 17-May-2020
PMCID:PMC7235618
doi:10.1016/j.heliyon.2020.e03991
PMID:32455176
Vascular Epiphytic Medicinal Plants as Sources of Therapeutic Agents: Their Ethnopharmacological Uses, Chemical Composition, and Biological Activities Nugraha AS, Triatmoko B, Wangchuk P, Keller PA Biomolecules 24-Jan-2020
PMCID:PMC7072150
doi:10.3390/biom10020181
PMID:31991657
Distribution of vascular epiphytes along a tropical elevational gradient: disentangling abiotic and biotic determinants Ding Y, Liu G, Zang R, Zhang J, Lu X, Huang J Sci Rep 22-Jan-2016
PMCID:PMC4726354
doi:10.1038/srep19706
PMID:26796667
Secondary Metabolites of Plants Teoh ES Medicinal Orchids of Asia 05-Nov-2015
PMCID:PMC7123774
doi:10.1007/978-3-319-24274-3_5
New Short Strategy for the Synthesis of the Dibenz[b,f]oxepin Scaffold Moreno DR, Giorgi G, Salas CO, Tapia RA Molecules 29-Nov-2013
PMCID:PMC6270238
doi:10.3390/molecules181214797
PMID:24352054
RECENT SYNTHETIC DEVELOPMENTS AND APPLICATIONS OF THE ULLMANN REACTION. A REVIEW Lin H, Sun D Org Prep Proced Int 16-Aug-2013
PMCID:PMC3819134
doi:10.1080/00304948.2013.816208
PMID:24223434
New dihydrodibenzoxepins from Bulbophyllum kwangtungense. Wu B, He S, Pan YJ Planta Med 01-Oct-2006
doi:10.1055/S-2006-947200
PMID:16981129

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 / Phenanthrenes and derivatives / Phenanthrols
Moscatin 194774 Click to see COC1=C2C(=CC(=C1)O)C=CC3=C2C(=CC=C3)O 240.25 unknown https://doi.org/10.1055/S-2006-947200
> Organoheterocyclic compounds / Benzoxepines / Dibenzoxepines
13-Methoxy-2,15,17-trioxatetracyclo[9.7.0.03,8.014,18]octadeca-1(18),3(8),4,6,11,13-hexaen-4-ol 86044945 Click to see COC1=C2C(=C3C(=C1)CCC4=C(O3)C(=CC=C4)O)OCO2 286.28 unknown https://doi.org/10.1055/S-2006-947200
13-Methoxy-2,15,17-trioxatetracyclo[9.7.0.03,8.014,18]octadeca-1(18),3(8),4,6,11,13-hexaen-5-ol 162909936 Click to see COC1=C2C(=C3C(=C1)CCC4=C(O3)C=C(C=C4)O)OCO2 286.28 unknown https://doi.org/10.1055/S-2006-947200
13-Methoxy-2,15,17-trioxatetracyclo[9.7.0.03,8.014,18]octadeca-1(18),3(8),4,6,11,13-hexaen-6-ol 11818504 Click to see COC1=C2C(=C3C(=C1)CCC4=C(O3)C=CC(=C4)O)OCO2 286.28 unknown https://doi.org/10.1055/S-2006-947200
> Phenylpropanoids and polyketides / Stilbenes
3-[2-(1,3-Benzodioxol-5-yl)ethyl]-5-methoxyphenol 637412 Click to see COC1=CC(=CC(=C1)O)CCC2=CC3=C(C=C2)OCO3 272.29 unknown https://doi.org/10.1055/S-2006-947200
3-O-Methylgigantol 10108163 Click to see COC1=C(C=C(C=C1)CCC2=CC(=CC(=C2)OC)O)OC 288.34 unknown https://doi.org/10.1055/S-2006-947200

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