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Drimiopsis maculata

Drimiopsis maculata - 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 UUID644025fe368b7413854420
Scientific name Drimiopsis maculata
Authority Lindl. & Paxton
First published in Paxton's Fl. Gard. 2: 73 (1851)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ledebouria petiolata J.C.Manning & Goldblatt Edinburgh J. Bot. 60: 561 (2003 publ. 2004)
Drimia petiolata K.Koch & C.D.Bouché Index Seminum (B, Berolinensis) 1861(App.): 3 (1861)
Drimiopsis minor Baker Refug. Bot. 3: t. 192 (1870)

Common names Top

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Language Common/alternative name
Chinese 阔叶麻点百合

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
  • Africa
    • East Tropical Africa
      • Tanzania
    • Macaronesia
      • Canary Islands
    • South Tropical Africa
      • Mozambique
    • Southern Africa
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000766226
Tropicos 18403047
KEW urn:lsid:ipni.org:names:534585-1
The Plant List kew-305089
Open Tree Of Life 807075
NCBI Taxonomy 81747
IPNI 534585-1
iNaturalist 343937
GBIF 2776471
Freebase /m/011q95z4
EPPO DYIMA
EOL 1087789
USDA GRIN 14683
Wikipedia Drimiopsis_maculata

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
Spiro-Flavonoids in Nature: A Critical Review of Structural Diversity and Bioactivity Pecio Ł, Pecio S, Mroczek T, Oleszek W Molecules 14-Jul-2023
PMCID:PMC10385819
doi:10.3390/molecules28145420
PMID:37513292
Xanthones: Biosynthesis and Trafficking in Plants, Fungi and Lichens Badiali C, Petruccelli V, Brasili E, Pasqua G Plants (Basel) 04-Feb-2023
PMCID:PMC9967055
doi:10.3390/plants12040694
PMID:36840041
A Global Overview of Diversity and Phylogeny of the Rust Genus Uromyces Gautam AK, Avasthi S, Verma RK, Sushma, Niranjan M, Devadatha B, Jayawardena RS, Suwannarach N, Karunarathna SC J Fungi (Basel) 14-Jun-2022
PMCID:PMC9224716
doi:10.3390/jof8060633
PMID:35736116
Total Synthesis of Naturally Occurring 5,7,8-Trioxygenated Homoisoflavonoids Kwon S, Lee S, Heo M, Lee B, Fei X, Corson TW, Seo SY ACS Omega 06-May-2020
PMCID:PMC7241036
doi:10.1021/acsomega.0c00932
PMID:32455225
Nor-Lignans: Occurrence in Plants and Biological Activities—A Review Frezza C, Venditti A, Toniolo C, De Vita D, Franceschin M, Ventrone A, Tomassini L, Foddai S, Guiso M, Nicoletti M, Serafini M, Bianco A Molecules 03-Jan-2020
PMCID:PMC6983269
doi:10.3390/molecules25010197
PMID:31947789
Lanostane-Type Triterpenoids from Scilla scilloides and Structure Revision of Drimiopsin D Ren FC, Wang LX, Yu Q, Jiang XJ, Wang F Nat Prod Bioprospect 12-Oct-2015
PMCID:PMC4607680
doi:10.1007/s13659-015-0076-0
PMID:26458926
Comparative analysis of plant use in peri-urban domestic gardens of the Limpopo Province, South Africa Mosina GK, Maroyi A, Potgieter MJ J Ethnobiol Ethnomed 04-Apr-2014
PMCID:PMC3977957
doi:10.1186/1746-4269-10-35
PMID:24708756
Inferences of biogeographical histories within subfamily Hyacinthoideae using S-DIVA and Bayesian binary MCMC analysis implemented in RASP (Reconstruct Ancestral State in Phylogenies) Ali SS, Yu Y, Pfosser M, Wetschnig W Ann Bot 27-Oct-2011
PMCID:PMC3241591
doi:10.1093/aob/mcr274
PMID:22039008
Vascular myorelaxing activity of isolates from South African Hyacinthaceae partly mediated by activation of soluble guanylyl cyclase in rat aortic ring preparations. Fusi F, Ferrara A, Koorbanally C, Crouch NR, Mulholland DA, Sgaragli G J Pharm Pharmacol 01-Apr-2008
doi:10.1211/JPP.60.4.0012
PMID:18380922
Norlignans and homoisoflavanones from two South African Drimiopsis species (Hyacinthaceae: Hyacinthoideae) Chantal Koorbanally, Dulcie A. Mulholland, Neil R. Crouch Elsevier BV 07-Apr-2006
doi:10.1016/J.BSE.2005.12.011
Coincident isolation of a novel homoisoflavonoid from Resnova humifusa and Eucomis montana (Hyacinthoideae: Hyacinthaceae) Neil A. Koorbanally, Neil R. Crouch, Avinash Harilal, Bavani Pillay, Dulcie A. Mulholland Elsevier BV 24-Nov-2005
doi:10.1016/J.BSE.2005.08.003
First Nuclear DNA Amounts in more than 300 Angiosperms ZONNEVELD BJ, LEITCH IJ, BENNETT MD Ann Bot 19-May-2005
PMCID:PMC4246870
doi:10.1093/aob/mci170
PMID:15905300
Anti-inflammatory activity and QSAR studies of compounds isolated from Hyacinthaceae species and Tachiadenus longiflorus Griseb. (Gentianaceae). du Toit K, Elgorashi EE, Malan SF, Drewes SE, van Staden J, Crouch NR, Mulholland DA Bioorg Med Chem 01-Apr-2005
doi:10.1016/J.BMC.2005.01.036
PMID:15755657
Xanthones from Drimiopsis maculata. Mulholland DA, Koorbanally C, Crouch NR, Sandor P J Nat Prod 01-Oct-2004
doi:10.1021/NP040076Z
PMID:15497949

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
> Lignans, neolignans and related compounds
Hinokiresinol 5377291 Click to see C=CC(C=CC1=CC=C(C=C1)O)C2=CC=C(C=C2)O 252.31 unknown https://doi.org/10.1016/J.BSE.2005.12.011
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3-Dihydroxy-2,6-dimethoxy-8-methylxanthen-9-one 11231920 Click to see CC1=CC(=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 302.28 unknown https://doi.org/10.1021/NP040076Z
1,3,6-Trihydroxy-2,4-dimethoxy-8-methylxanthen-9-one 11220848 Click to see CC1=CC(=CC2=C1C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)O 318.28 unknown https://doi.org/10.1021/NP040076Z
1,3,6-Trihydroxy-4-methoxy-8-methylxanthen-9-one 11437683 Click to see CC1=CC(=CC2=C1C(=O)C3=C(O2)C(=C(C=C3O)O)OC)O 288.25 unknown https://doi.org/10.1021/NP040076Z
1,3,6-Trihydroxy-4,5-dimethoxy-8-methylxanthen-9-one 11483958 Click to see CC1=CC(=C(C2=C1C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O 318.28 unknown https://doi.org/10.1021/NP040076Z
1,4,6-Trihydroxy-3-methoxy-8-methylxanthen-9-one 86002886 Click to see CC1=CC(=CC2=C1C(=O)C3=C(O2)C(=C(C=C3O)OC)O)O 288.25 unknown https://doi.org/10.1021/NP040076Z
1,6-Dihydroxy-2,3,4-trimethoxy-8-methylxanthen-9-one 11186597 Click to see CC1=CC(=CC2=C1C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O 332.30 unknown https://doi.org/10.1021/NP040076Z
Drimiopsin C 11254733 Click to see CC1=CC(=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 288.25 unknown https://doi.org/10.1021/NP040076Z
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3R)-5,6-dihydroxy-3-[(4-hydroxyphenyl)methyl]-7-methoxy-2,3-dihydrochromen-4-one 122182392 Click to see COC1=C(C(=C2C(=C1)OCC(C2=O)CC3=CC=C(C=C3)O)O)O 316.30 unknown https://doi.org/10.1016/J.BMC.2005.01.036
https://doi.org/10.1016/J.BSE.2005.12.011
https://doi.org/10.1211/JPP.60.4.0012
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
(3R)-3',5-dihydroxy-4',7-dimethoxyspiro[2H-chromene-3,7'-bicyclo[4.2.0]octa-1,3,5-triene]-4-one 162984745 Click to see COC1=CC(=C2C(=C1)OCC3(C2=O)CC4=CC(=C(C=C34)OC)O)O 328.30 unknown https://doi.org/10.1016/J.BMC.2005.01.036
https://doi.org/10.1211/JPP.60.4.0012
(3R)-3',5,7-trihydroxy-4'-methoxyspiro[2H-chromene-3,7'-bicyclo[4.2.0]octa-1,3,5-triene]-4-one 122182400 Click to see COC1=C(C=C2CC3(C2=C1)COC4=CC(=CC(=C4C3=O)O)O)O 314.29 unknown https://doi.org/10.1016/J.BMC.2005.01.036
https://doi.org/10.1016/J.BSE.2005.08.003
https://doi.org/10.1211/JPP.60.4.0012

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