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Strophioblachia fimbricalyx

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fede46bef5005798802
Scientific name Strophioblachia fimbricalyx
Authority Boerl.
First published in Handl. Fl. Ned. Ind. 3: 236 (1900)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Strophioblachia fimbricalyx var. cordifolia (Airy Shaw) H.S.Kiu Guihaia 19: 195 (1999)
Strophioblachia fimbricalyx var. efimbriata Airy Shaw Kew Bull. 25: 544 (1971)
Strophioblachia glandulosa Pax Pflanzenr. , IV, 147, III: 360 (1911)
Strophioblachia glandulosa var. cordifolia Airy Shaw Kew Bull. 25: 545 (1971)
Strophioblachia glandulosa var. tonkinensis Gagnep. Fl. Indo-Chine 5: 410. 1926
Blachia glandulosa Pierre ex Pax Pflanzenr. , IV, 147, III: 36 (1911)

Common names Top

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Language Common/alternative name
Chinese 宿萼木
Chinese 宿萼木叶

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
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indo-China
      • Cambodia
      • Thailand
      • Vietnam
    • Malesia
      • Philippines
      • Sulawesi

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000317363
Tropicos 50077356
KEW urn:lsid:ipni.org:names:356629-1
The Plant List kew-198307
Open Tree Of Life 788214
NCBI Taxonomy 179702
IUCN Red List 156218377
IPNI 356629-1
iNaturalist 628133
GBIF 3063337
EOL 1150030

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
Feeding Postures and Substrate Use of François’ Langurs (Trachypithecus francoisi) in the Limestone Forest of Southwest China Lu S, Lin N, Huang A, Tong D, Liang Y, Li Y, Lu C Animals (Basel) 08-Feb-2024
PMCID:PMC10886065
doi:10.3390/ani14040565
PMID:38396533
Leaf nitrogen and phosphorus resorption efficiencies are related to drought resistance across woody species in a Chinese savanna Zhang SB, Song Y, Wen HD, Chen YJ Tree Physiol 15-Dec-2023
PMCID:PMC10849754
doi:10.1093/treephys/tpad149
PMID:38102768
Trade-offs between xylem hydraulic efficiency and mechanical strength in Chinese evergreen and deciduous savanna species Zhang SB, Wen GJ, Qu YY, Yang LY, Song Y Tree Physiol 14-Feb-2022
PMCID:PMC9272745
doi:10.1093/treephys/tpac017
PMID:35157087
Tropical deciduous forest in Yunnan, southwestern China: Implications for geological and climatic histories from a little-known forest formation Zhu H, Ashton P, Gu B, Zhou S, Tan Y Plant Divers 16-Jan-2021
PMCID:PMC8720685
doi:10.1016/j.pld.2021.01.001
PMID:35024513
Antiplasmodial natural products: an update Tajuddeen N, Van Heerden FR Malar J 05-Dec-2019
PMCID:PMC6896759
doi:10.1186/s12936-019-3026-1
PMID:31805944
Antimalarial Activity of Plant Metabolites Pan WH, Xu XY, Shi N, Tsang SW, Zhang HJ Int J Mol Sci 06-May-2018
PMCID:PMC5983777
doi:10.3390/ijms19051382
PMID:29734792
Bioactive compounds from the roots of Strophioblachia fimbricalyx. Seephonkai P, Pyne SG, Willis AC, Lie W J Nat Prod 26-Jul-2013
doi:10.1021/NP400268D
PMID:23806014
Cytotoxic and antiplasmodial compounds from the roots of Strophioblachia fimbricalyx. Seephonkai P, Sangdee A, Bunchalee P, Pyne SG J Nat Prod 01-Oct-2009
doi:10.1021/NP900352N
PMID:19778068
The complete nucleotide sequence of the cassava (Manihot esculenta) chloroplast genome and the evolution of atpF in Malpighiales: RNA editing and multiple losses of a group II intron Daniell H, Wurdack KJ, Kanagaraj A, Lee SB, Saski C, Jansen RK Theor Appl Genet 24-Jan-2008
PMCID:PMC2587239
doi:10.1007/s00122-007-0706-y
PMID:18214421

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 / Naphthalenes
4,6,9-Trimethoxyphenanthropolone 44557155 Click to see 324.40 unknown https://doi.org/10.1021/NP900352N
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
(3R,16R)-11-hydroxy-7,16,22,26-tetramethoxy-8,14,14,19,25-pentamethyl-2,17-dioxaheptacyclo[16.12.0.03,16.04,13.05,10.020,29.023,28]triaconta-1(18),4,6,8,10,12,19,21,23(28),24,26,29-dodecaen-15-one 71746632 Click to see 608.70 unknown https://doi.org/10.1021/NP400268D
(3R,16S)-11-hydroxy-7,16,22,26-tetramethoxy-8,14,14,19,25-pentamethyl-2,17-dioxaheptacyclo[16.12.0.03,16.04,13.05,10.020,29.023,28]triaconta-1(18),4,6,8,10,12,19,21,23(28),24,26,29-dodecaen-15-one 71746633 Click to see CC1=CC2=C(C=C1OC)C3=CC4=C(C(=C3C=C2OC)C)OC5(C(O4)C6=C7C=C(C(=CC7=C(C=C6C(C5=O)(C)C)O)C)OC)OC 608.70 unknown https://doi.org/10.1021/NP400268D
1,1,7-Trimethyl-3,6-dimethoxy-9-hydroxyphenanthrene-2(1H)-one 44557096 Click to see CC1=CC2=C(C=C3C(=C2C=C1OC)C=C(C(=O)C3(C)C)OC)O 312.40 unknown https://doi.org/10.1021/NP900352N
4-[(3,6-Dimethoxy-1,1,7-trimethyl-2-oxo-9-phenanthryl)oxy]-8-methoxy-3,3,7-trimethyl-cyclopenta[a]naphthalene-2,5-dione 71623988 Click to see CC1=CC2=C(C=C1OC)C3=CC(=O)C(C3=C(C2=O)OC4=C5C=C(C(=CC5=C6C=C(C(=O)C(C6=C4)(C)C)OC)OC)C)(C)C 578.60 unknown https://doi.org/10.1021/NP400268D
Trigonostemone 14731300 Click to see 326.40 unknown https://doi.org/10.1021/NP900352N
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
3,6,9-Trimethoxyphenanthropolone 44557154 Click to see 324.40 unknown https://doi.org/10.1021/NP900352N
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(1S,2S,4R,6S,7R,8R,9R,10R,13R,14R)-7,8-dihydroxy-2,8,10,13,18,18-hexamethyl-6-(2-methylprop-1-enyl)-16-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-oxapentacyclo[11.8.0.02,10.04,9.014,19]henicosa-15,19-diene-12,17-dione 6325480 Click to see 660.80 unknown https://doi.org/10.1021/NP400268D
> Organoheterocyclic compounds / Naphthofurans
Naphtho[1,2-c]furan-1(3H)-one, 3-hydroxy-5,8-dimethoxy-3,7-dimethyl- 71746813 Click to see 288.29 unknown https://doi.org/10.1021/NP400268D
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
6-Hydroxy-9-methoxy-4,4,8-trimethyl-benzo[h]isochromene-1,3-dione 71746809 Click to see CC1=CC2=C(C=C3C(=C2C=C1OC)C(=O)OC(=O)C3(C)C)O 300.30 unknown https://doi.org/10.1021/NP400268D

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