Dendrobium crepidatum - Unknown
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Internal ID UUID644037c2d7636343790641
Scientific name Dendrobium crepidatum
Authority Lindl. & Paxton
First published in Paxton's Fl. Gard. 1: 63 (1850)

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Synonyms Top

Scientific name Authority First published in
Callista crepidata Kuntze Revis. Gen. Pl. 2: 654 (1891)
Callista lawiana (Lindl.) Kuntze Revis. Gen. Pl. 2: 655 (1891)
Dendrobium actinomorphum Blatt. & Hallb. J. Indian Bot. 2: 50 (1921)
Dendrobium lawanum Lindl. J. Proc. Linn. Soc., Bot. 3: 10 (1858)
Dendrochilum roseum Dalzell Hooker's J. Bot. Kew Gard. Misc. 4: 291 (1852)
Callista laviana Kuntze Revis. Gen. Pl. 2: 655 (1891)

Common names Top

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Language Common/alternative name
English shoe-lipped dendrobium
English shoe-lip dendrobium
Vietnamese Đại hoàng thảo
Chinese 束花石斛
Chinese 玫瑰石斛

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
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • West Himalaya
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000938878
Tropicos 50177066
KEW urn:lsid:ipni.org:names:627186-1
The Plant List kew-57500
Open Tree Of Life 868828
NCBI Taxonomy 154289
IPNI 627186-1
iNaturalist 967895
GBIF 5317107
Freebase /m/065_v8t
EOL 1093934
USDA GRIN 13493
Wikipedia Dendrobium_crepidatum
CMAUP NPO6381

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
A Promising Natural Anticancer Compound Derived from Gymnoascus dankaliensis Jafer FN, Al-Laaeiby A Arch Razi Inst 30-Apr-2023
PMCID:PMC10314247
doi:10.22092/ARI.2022.359717.2459
PMID:37396737
Orchid Micropropagation Using Conventional Semi-Solid and Temporary Immersion Systems: A Review Nongdam P, Beleski DG, Tikendra L, Dey A, Varte V, EL Merzougui S, Pereira VM, Barros PR, Vendrame WA Plants (Basel) 02-Mar-2023
PMCID:PMC10005664
doi:10.3390/plants12051136
PMID:36904000
Micromorphology of Labellum in Selected Dendrobium Sw. (Orchidaceae, Dendrobieae) Burzacka-Hinz A, Narajczyk M, Dudek M, Szlachetko DL Int J Mol Sci 24-Aug-2022
PMCID:PMC9455781
doi:10.3390/ijms23179578
PMID:36076976
Can natural products modulate cytokine storm in SARS-CoV2 patients? Abou Baker DH Biotechnol Rep (Amst) 09-Jun-2022
PMCID:PMC9181898
doi:10.1016/j.btre.2022.e00749
PMID:35702395
A Walk Through the Maze of Secondary Metabolism in Orchids: A Transcriptomic Approach Ghai D, Kaur A, Kahlon PS, Pawar SV, Sembi JK Front Plant Sci 29-Apr-2022
PMCID:PMC9100589
doi:10.3389/fpls.2022.837563
PMID:35574139
Natural Enantiomers: Occurrence, Biogenesis and Biological Properties Yu JH, Yu ZP, Capon RJ, Zhang H Molecules 14-Feb-2022
PMCID:PMC8880303
doi:10.3390/molecules27041279
PMID:35209066
Orchidaceae-Derived Anticancer Agents: A Review Śliwiński T, Kowalczyk T, Sitarek P, Kolanowska M Cancers (Basel) 31-Jan-2022
PMCID:PMC8833831
doi:10.3390/cancers14030754
PMID:35159021
Development, Identification, and Application of a Germplasm Specific SCAR Marker for Dendrobium officinale Kimura et Migo Zheng K, Cai Y, Chen W, Gao Y, Jin J, Wang H, Feng S, Lu J Front Plant Sci 14-May-2021
PMCID:PMC8160518
doi:10.3389/fpls.2021.669458
PMID:34054907
Identification, Biological Activities and Biosynthetic Pathway of Dendrobium Alkaloids Mou Z, Zhao Y, Ye F, Shi Y, Kennelly EJ, Chen S, Zhao D Front Pharmacol 20-Apr-2021
PMCID:PMC8096351
doi:10.3389/fphar.2021.605994
PMID:33959002
Traditional Uses and Pharmacologically Active Constituents of Dendrobium Plants for Dermatological Disorders: A Review Wang YH Nat Prod Bioprospect 20-Apr-2021
PMCID:PMC8390561
doi:10.1007/s13659-021-00305-0
PMID:33880726
Could natural products modulate early inflammatory responses, preventing acute respiratory distress syndrome in COVID-19-confirmed patients? Amaral-Machado L, Oliveira WN, Rodrigues VM, Albuquerque NA, Alencar ÉN, Egito ES Biomed Pharmacother 16-Dec-2020
PMCID:PMC7832252
doi:10.1016/j.biopha.2020.111143
PMID:33360048
Ethnobotanical study on wild edible plants used by three trans-boundary ethnic groups in Jiangcheng County, Pu’er, Southwest China Cao Y, Li R, Zhou S, Song L, Quan R, Hu H J Ethnobiol Ethnomed 27-Oct-2020
PMCID:PMC7590688
doi:10.1186/s13002-020-00420-1
PMID:33109239
Isolation and identification of beneficial orchid mycorrhizal fungi in Bletilla striata (Thunb.) Rchb.f.(Orchidaceae) Xi G, Shi J, Li J, Han Z Plant Signal Behav 08-Sep-2020
PMCID:PMC7671041
doi:10.1080/15592324.2020.1816644
PMID:32897833
Ethnopharmacological Potential of Aspilia africana for the Treatment of Inflammatory Diseases Okello D, Lee J, Kang Y Evid Based Complement Alternat Med 19-Jun-2020
PMCID:PMC7321516
doi:10.1155/2020/8091047
PMID:32733588
Crepidtumines A and B, Two Novel Indolizidine Alkaloids from Dendrobium crepidatum Xu X, Chen X, Yang R, Li Z, Zhou H, Bai Y, Yu M, Li B, Ding G Sci Rep 12-Jun-2020
PMCID:PMC7293321
doi:10.1038/s41598-020-66552-2
PMID:32533030

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Ethane 6324 Click to see CC 30.07 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Arctigenin 64981 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
Arctiin 100528 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 534.60 unknown via CMAUP database
Matairesinoside 486612 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O 520.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S)-1alpha-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4,7alpha-dicarboxylic acid 4-beta-D-glucopyranosyl 7-methyl ester 101673970 Click to see COC(=O)C1CCC2C1C(OC=C2C(=O)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 566.50 unknown via CMAUP database
(1S)-1alpha-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4,7alpha-dicarboxylic acid 4-beta-D-glucopyranosyl ester 101673969 Click to see C1CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC4C(C(C(C(O4)CO)O)O)O)C(=O)O 552.50 unknown via CMAUP database
(1S)-1alpha-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4,7alpha-dicarboxylic acid 7-methyl ester 101673972 Click to see COC(=O)C1CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown via CMAUP database
(1S)-1alpha-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydrocyclopenta[c]pyran-4,7alpha-dicarboxylic acid dimethyl ester 101673971 Click to see COC(=O)C1CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O 418.40 unknown via CMAUP database
Adoxosidic acid 13892717 Click to see C1CC2C(C1CO)C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 376.36 unknown via CMAUP database
Forsythide 15559328 Click to see C1CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)C(=O)O 390.34 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Forsythoside F 6442994 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 756.70 unknown via CMAUP database
Forsythoside G 101231533 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(CO4)(CO)O)OC)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 770.70 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines / Phenylpiperidines
1-[(1S,4S,5S,6R,8S,9S,10R)-6,9-dihydroxy-6,10-dimethyl-9-phenyl-12-azatricyclo[6.3.1.04,12]dodecan-5-yl]ethanone 101306730 Click to see CC1CC2CCC3N2C(C1(C4=CC=CC=C4)O)CC(C3C(=O)C)(C)O 343.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.24-3757
Crepidin 573287 Click to see CC1CC2CCC3N2C(C1(C4=CC=CC=C4)O)CC(C3C(=O)C)(C)O 343.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.24-3757
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
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 via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
Dendrocrepin 615602 Click to see CC1CC2CCCN2C(C1(C3=CC=CC=C3)O)CC(=O)CC4C(C(CC5N4CCC5)C)(C6=CC=CC=C6)O 516.70 unknown https://doi.org/10.1016/S0040-4039(01)85839-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 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
Isoquercetin 5280804 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
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Crepidatin 14353469 Click to see COC1=CC(=CC(=C1OC)OC)CCC2=CC(=C(C=C2)O)OC 318.40 unknown https://doi.org/10.1016/S0031-9422(00)97904-4
https://doi.org/10.1016/0031-9422(93)85180-Y

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