Bulbophyllum vaginatum

Details Top

Internal ID UUID644017075fdf5717973259
Scientific name Bulbophyllum vaginatum
Authority Rchb.f.
First published in Ann. Bot. Syst. 6: 261 (1861)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Bulbophyllum vaginatum is cultivated primarily as an ornamental epiphytic orchid. It is offered by specialty orchid nurseries and through online horticultural retailers. The plant is traded as a living specimen, usually sold in pots or mounted on cork or tree fern. It is also distributed among orchid societies and collectors. The commercial product is the live plant, sometimes propagated through division or tissue culture for the ornamental market.

Scientific uses:
Molecular phylogenetic studies have included B. vaginatum to resolve relationships within Bulbophyllum and the broader Orchidaceae. Its DNA sequences are deposited in GenBank (e.g., accession numbers XXXXX). The species has been used as a representative of epiphytic orchids in comparative genomics and barcoding projects. It is also listed in the Orchidaceae database for community resources and reference genomes.

Properties relevant to use:
The species displays typical epiphytic growth; it forms small pseudobulbs that store water, enabling tolerance of periodic drought. Its inflorescences arise from the base of the pseudobulbs, bearing several small, fragrant flowers with a labellum specialized for pollinator attraction. These morphological traits make it suitable for greenhouse cultivation under controlled humidity and airflow. The plant propagates vegetatively via division of pseudobulbs and can be reproduced through in‑vitro tissue culture, which is common in orchid horticulture.

Standards and regulation:
Bulbophyllum vaginatum, like all members of Orchidaceae, is listed in CITES Appendix II, requiring export permits for commercial trade. National regulations in many countries (e.g., the U.S. Endangered Species Act, the EU Wildlife Trade Regulation) further control import and export of the species. Orchid nurseries must comply with CITES documentation and any national phytosanitary requirements.

Sustainability and sourcing:
Wild collection of B. vaginatum is limited; most commercial material is cultivated in controlled environments. Sustainable cultivation practices involve controlled propagation from nursery stock to reduce pressure on wild populations. When trade does occur, it should adhere to CITES permits and local licensing to ensure harvested specimens are legally sourced and that populations are not adversely affected.

Synonyms Top

Scientific name Authority First published in
Phyllorkis vaginata Kuntze Revis. Gen. Pl. 2: 677 (1891)
Bulbophyllum whiteanum J.J.Sm. Bull. Jard. Bot. Buitenzorg , sér. 2, 8: 29 (1912)
Cirrhopetalum caudatum Wight Icon. Pl. Ind. Orient. 5: t. 1658 (1851)
Cirrhopetalum stramineum Teijsm. & Binn. Natuurk. Tijdschr. Ned.-Indië 24: 310 (1862)
Cirrhopetalum vaginatum Lindl. Gen. Sp. Orchid. Pl. : 59 (1830)
Cirrhopetalum whiteanum Rolfe Bull. Misc. Inform. Kew 1895: 7 (1895)

Common names Top

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Language Common/alternative name
Chinese 鞘石豆兰

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indo-China
      • Thailand
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Maluku
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000647111
Tropicos 23507380
KEW urn:lsid:ipni.org:names:620417-1
The Plant List kew-27678
Open Tree Of Life 502278
NCBI Taxonomy 1138424
IPNI 620417-1
iNaturalist 372049
GBIF 2846303
Freebase /m/065_152
EOL 992216
Wikipedia Bulbophyllum_vaginatum

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
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
Cytotoxic Phenanthrene, Dihydrophenanthrene, and Dihydrostilbene Derivatives and Other Aromatic Compounds from Combretum laxum Bisoli E, Freire TV, Yoshida NC, Garcez WS, Queiróz LM, Matos MD, Perdomo RT, Garcez FR Molecules 10-Jul-2020
PMCID:PMC7397156
doi:10.3390/molecules25143154
PMID:32664233
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
Availability of orchid mycorrhizal fungi on roadside trees in a tropical urban landscape Izuddin M, Srivathsan A, Lee AL, Yam TW, Webb EL Sci Rep 20-Dec-2019
PMCID:PMC6925147
doi:10.1038/s41598-019-56049-y
PMID:31863015
CAM plasticity in epiphytic tropical orchid species responding to environmental stress Tay S, He J, Yam TW Bot Stud 13-May-2019
PMCID:PMC6513927
doi:10.1186/s40529-019-0255-0
PMID:31087187
Genus: Calanthe to Cyrtosia Teoh ES Medicinal Orchids of Asia 05-Nov-2015
PMCID:PMC7123092
doi:10.1007/978-3-319-24274-3_9
A biphenanthrene and a phenanthro[4,3-b]furan from the orchid Bulbophyllum vaginatum. Leong YW, Harrison LJ J Nat Prod 01-Sep-2004
doi:10.1021/NP049909B
PMID:15387671
Phenanthrenes, dihydrophenanthrenes and bibenzyls from the orchid bulbophyllum vaginatum Yuan-Wah Leong, Chiang-Cheong Kang, Leslie J. Harrison, Andrew D. Powell Elsevier BV 23-Apr-2003
doi:10.1016/S0031-9422(96)00387-1
Phenanthrene and other aromatic constituents of Bulbophyllum vaginatum Yuan-Wah Leong, Leslie J Harrison, Andrew D Powell Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00687-6

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
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1016/S0031-9422(98)00687-6
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
2,7-Phenanthrenediol, 9,10-dihydro-3,4,6-trimethoxy- 181637 Click to see 302.32 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
3,5-Dimethoxy-9,10-dihydrophenanthrene-2,7-diol 45267920 Click to see COC1=CC(=CC2=C1C3=CC(=C(C=C3CC2)O)OC)O 272.29 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
4-Methoxy-9,10-dihydrophenanthrene-2,3,6,7-tetrol 5319427 Click to see COC1=C2C(=CC(=C1O)O)CCC3=CC(=C(C=C32)O)O 274.27 unknown https://doi.org/10.1016/S0031-9422(98)00687-6
4-Methoxy-9,10-dihydrophenanthrene-2,3,7-triol 21159093 Click to see 258.27 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
4-Methoxy-9,10-Dihydrophenanthrene-2,7-Diol 11390848 Click to see 242.27 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
4,6-Dimethoxy-9,10-dihydrophenanthrene-2,3,7-triol 85708334 Click to see 288.29 unknown https://doi.org/10.1016/S0031-9422(98)00687-6
https://doi.org/10.1016/S0031-9422(96)00387-1
5-Methoxy-9,10-dihydrophenanthrene-2,3,7-triol 5319428 Click to see COC1=CC(=CC2=C1C3=CC(=C(C=C3CC2)O)O)O 258.27 unknown https://doi.org/10.1016/S0031-9422(98)00687-6
Erianthridin 10401022 Click to see COC1=C(C=C2CCC3=C(C2=C1OC)C=CC(=C3)O)O 272.29 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
2,5-Dihydroxy-4,9-dimethoxyphenanthrene 85708330 Click to see 270.28 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
2,7-Dihydroxy-4,6-dimethoxyphenanthrene 44572330 Click to see 270.28 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
2,7-Phenanthrenediol, 3,4,6-trimethoxy- 356766 Click to see 300.30 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
3,7-Dihydroxy-2,4-dimethoxyphenanthrene 10445823 Click to see 270.28 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
4-Methoxyphenanthrene-2,3,6,7-tetrol 5319479 Click to see 272.25 unknown https://doi.org/10.1016/S0031-9422(98)00687-6
4-Methoxyphenanthrene-2,3,7-triol 5319480 Click to see 256.25 unknown https://doi.org/10.1016/S0031-9422(98)00687-6
4,6-Dimethoxyphenanthrene-2,3,7-triol 85708339 Click to see 286.28 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
https://doi.org/10.1016/S0031-9422(98)00687-6
Fimbriol B 23900101 Click to see COC1=C2C(=CC(=C1O)O)C=CC3=C2C(=CC=C3)O 256.25 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
Flavanthrinin 14777892 Click to see 240.25 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
Nudol 158975 Click to see 270.28 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1016/S0031-9422(98)00687-6
Syringaresinol 100067 Click to see 418.40 unknown https://doi.org/10.1016/S0031-9422(98)00687-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3R)-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-9-methoxy-2,3,6,7-tetrahydronaphtho[2,1-g][1]benzofuran-5,11-diol 21589748 Click to see COC1=CC2=C(C(=C1)O)C3=C4C(=CC(=C3CC2)O)C(C(O4)C5=CC(=C(C(=C5)OC)O)OC)CO 466.50 unknown https://doi.org/10.1021/NP049909B
2-(4-Hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-9-methoxy-2,3,6,7-tetrahydronaphtho[2,1-g][1]benzofuran-5,11-diol 72967684 Click to see COC1=CC2=C(C(=C1)O)C3=C4C(=CC(=C3CC2)O)C(C(O4)C5=CC(=C(C(=C5)OC)O)OC)CO 466.50 unknown https://doi.org/10.1021/NP049909B
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1016/S0031-9422(98)00687-6
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1016/S0031-9422(98)00687-6
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1016/S0031-9422(98)00687-6
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Dihydroferulic Acid 14340 Click to see 196.20 unknown https://doi.org/10.1016/S0031-9422(98)00687-6
> Phenylpropanoids and polyketides / Stilbenes
batatasin III 10466989 Click to see COC1=CC(=CC(=C1)O)CCC2=CC(=CC=C2)O 244.28 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
Phenol, 4-[2-(3-hydroxy-5-methoxyphenyl)ethyl]-2-methoxy- 10221179 Click to see COC1=CC(=CC(=C1)O)CCC2=CC(=C(C=C2)O)OC 274.31 unknown https://doi.org/10.1016/S0031-9422(96)00387-1
Tristin 15736297 Click to see 260.28 unknown https://doi.org/10.1016/S0031-9422(98)00687-6
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
4,6-Dimethoxy-1-(2,3,7-trihydroxy-4,6-dimethoxyphenanthren-1-yl)phenanthrene-2,3,7-triol 11250035 Click to see COC1=C(C=C2C=CC3=C(C2=C1)C(=C(C(=C3C4=C(C(=C(C5=C4C=CC6=CC(=C(C=C65)OC)O)OC)O)O)O)O)OC)O 570.50 unknown https://doi.org/10.1021/NP049909B

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