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Schizocarphus nervosus

Schizocarphus nervosus - 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 UUID64402225c0a4f364398088
Scientific name Schizocarphus nervosus
Authority (Burch.) van der Merwe
First published in Fl. Pl. South Africa 23: t. 904 (1943)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ornithogalum nervosum Burch. Trav. S. Africa 1: 537 (1822)
Schizocarphus rigidifolius (Kunth) van der Merwe Fl. Pl. South Africa 23: t. 905 (1943)
Schizocarphus gerrardii (Baker) van der Merwe Fl. Pl. South Africa 23: t. 906 (1943)
Schizocarphus acerosus (van der Merwe) van der Merwe Fl. Pl. South Africa 23: t. 904 (1943)
Scilla bakeriana Poelln. Ber. Deutsch. Bot. Ges. 61: 209 (1944)
Scilla eriospermoides Engl. & Gilg Kunene-Sambesi Exped. : 195 (1903)
Schizocarphus setiferus (Baker) Speta Phyton (Horn) 38: 120 (1998)
Schizocarphus hispidulus (Baker) Speta Phyton (Horn) 38: 120 (1998)
Scilla hispidula Baker Trans. Linn. Soc. London, Bot. 1(5): 248. 1878 [1880 publ. Jan 1878]
Scilla gerrardii Baker J. Linn. Soc., Bot. 13: 237 (1873)
Scilla setifera Baker Fl. Trop. Afr. 7: 549 (1898)
Scilla rigidifolia Kunth Enum. Pl. 4: 330 (1843)
Scilla pallidiflora Baker Refug. Bot. 3: t. 179 (1870)
Scilla nervosa (Burch.) J.P.Jessop J. S. African Bot. 36: 243 (1970)
Scilla pubescens Baker Bull. Herb. Boissier , sér. 2, 1: 853 (1901)
Urginea bragae Engl. Pflanzenw. Ost-Afrikas C (1895) 142.
Drimia dregeana Kunth Enum. Pl. 4: 340 (1843)
Scilla rigidifolia var. nervosa van der Merwe Fl. Pl. S. Africa 21: t. 821 1941
Scilla rigidifolia var. nervosa (Burch.) Baker J. Linn. Soc., Bot. 13: 242. 1873
Scilla rigidifolia var. gerrardii (Baker) Baker Fl. Cap. 6: 481. 1897
Scilla rigidifolia Baker
Scilla rigidifolia var. acerosa Hedw.

Common names Top

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Language Common/alternative name
Spanish schizocarphus

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
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Namibia
      • Northern Provinces
      • Swaziland
    • West-central Tropical Africa
      • Rwanda

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000734854
Tropicos 18402919
KEW urn:lsid:ipni.org:names:540594-1
The Plant List kew-287043
Open Tree Of Life 803256
NCBI Taxonomy 65770
IPNI 540594-1
iNaturalist 556790
GBIF 2771381
EPPO SLLNE
EOL 1082140
USDA GRIN 447327

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
Medicinal Plant Growth in Heavy Metals Contaminated Soils: Responses to Metal Stress and Induced Risks to Human Health Hlihor RM, Roșca M, Hagiu-Zaleschi L, Simion IM, Daraban GM, Stoleru V Toxics 27-Aug-2022
PMCID:PMC9504071
doi:10.3390/toxics10090499
PMID:36136464
Inhibitory mechanism of two homoisoflavonoids from Ophiopogon japonicus on tyrosinase activity: insight from spectroscopic analysis and molecular docking Wang L, Qin Y, Wang Y, Zhou Y, Liu B, Bai M, Tong X, Fang R, Huang X RSC Adv 22-Oct-2021
PMCID:PMC9042378
doi:10.1039/d1ra06091k
PMID:35497266
Isolation and Biological Characterization of Homoisoflavanoids and the Alkylamide N-p-Coumaroyltyramine from Crinum biflorum Rottb., an Amaryllidaceae Species Collected in Senegal Masi M, Koirala M, Delicato A, Di Lecce R, Merindol N, Ka S, Seck M, Tuzi A, Desgagne-Penix I, Calabrò V, Evidente A Biomolecules 31-Aug-2021
PMCID:PMC8466962
doi:10.3390/biom11091298
PMID:34572511
A Comprehensive Review on Chemotaxonomic and Phytochemical Aspects of Homoisoflavonoids, as Rare Flavonoid Derivatives Mottaghipisheh J, Stuppner H Int J Mol Sci 08-Mar-2021
PMCID:PMC7962952
doi:10.3390/ijms22052735
PMID:33800482
Stilbenoids: A Natural Arsenal against Bacterial Pathogens Mattio LM, Catinella G, Dallavalle S, Pinto A Antibiotics (Basel) 18-Jun-2020
PMCID:PMC7345618
doi:10.3390/antibiotics9060336
PMID:32570824
Antiangiogenic Activity and Cytotoxicity of Triterpenoids and Homoisoflavonoids from Massonia pustulata and Massonia bifolia. Schwikkard SL, Whitmore H, Corson TW, Sishtla K, Langat MK, Carew M, Mulholland DA Planta Med 28-Feb-2018
PMCID:PMC6467464
doi:10.1055/a-0577-5322
PMID:29490386
Antibacterial activity of crude extracts of some South African medicinal plants against multidrug resistant etiological agents of diarrhoea Bisi-Johnson MA, Obi CL, Samuel BB, Eloff JN, Okoh AI BMC Complement Altern Med 19-Jun-2017
PMCID:PMC5474864
doi:10.1186/s12906-017-1802-4
PMID:28629407
Virtualizing the p-ANAPL Library: A Step towards Drug Discovery from African Medicinal Plants Ntie-Kang F, Amoa Onguéné P, Fotso GW, Andrae-Marobela K, Bezabih M, Ndom JC, Ngadjui BT, Ogundaini AO, Abegaz BM, Meva’a LM PLoS One 05-Mar-2014
PMCID:PMC3944075
doi:10.1371/journal.pone.0090655
PMID:24599120
Ethnopharmacological Survey of Plants Used in the Traditional Treatment of Gastrointestinal Pain, Inflammation and Diarrhea in Africa: Future Perspectives for Integration into Modern Medicine Stark TD, Mtui DJ, Balemba OB Animals (Basel) 04-Mar-2013
PMCID:PMC4495512
doi:10.3390/ani3010158
PMID:26487315
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
Nuclear DNA Amounts in Angiosperms: Progress, Problems and Prospects BENNETT MD, LEITCH IJ Ann Bot 01-Jan-2005
PMCID:PMC4246708
doi:10.1093/aob/mci003
PMID:15596457
Homoisoflavanones and stilbenoids from Scilla nervosa Vuyisile Bangani, Neil R. Crouch, Dulcie A. Mulholland Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00155-7
Homoisoflavonoids and stilbenes from the bulbs of Scilla nervosa subsp. rigidifolia Alfonse Silayo, Bonaventure T Ngadjui, Berhanu M Abegaz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00267-8

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Phenylpropanoids and polyketides / Homoisoflavonoids
(3E)-5,7-dihydroxy-6-methoxy-3-[(4-methoxyphenyl)methylidene]chromen-4-one 15484392 Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C(=C(C(=C3)O)OC)O 328.30 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
3-(4-Hydroxybenzylidene)-5,7-dihydroxy-6-methoxychroman-4-on e 5472706 Click to see COC1=C(C2=C(C=C1O)OCC(=CC3=CC=C(C=C3)O)C2=O)O 314.29 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
4'-Demethyleucomin 15484393 Click to see C1C(=CC2=CC=C(C=C2)O)C(=O)C3=C(C=C(C=C3O1)O)O 284.26 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
https://doi.org/10.1016/S0031-9422(99)00267-8
5-Hydroxy-3-[(4-hydroxyphenyl)methylidene]-7-methoxychromen-4-one 53438928 Click to see COC1=CC(=C2C(=C1)OCC(=CC3=CC=C(C=C3)O)C2=O)O 298.29 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
5-Hydroxy-7-methoxy-3-(4-hydroxybenzylidene)chroman-4-one 15484394 Click to see COC1=CC(=C2C(=C1)OCC(=CC3=CC=C(C=C3)O)C2=O)O 298.29 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
5,7-Dihydroxy-3-[(4-hydroxyphenyl)methylidene]-6-methoxychromen-4-one 404574 Click to see COC1=C(C2=C(C=C1O)OCC(=CC3=CC=C(C=C3)O)C2=O)O 314.29 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
5,7-Dihydroxy-6-methoxy-3-[(4-methoxyphenyl)methylidene]chromen-4-one 129716434 Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C(=C(C(=C3)O)OC)O 328.30 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
Demethyleucomine 73196193 Click to see C1C(=CC2=CC=C(C=C2)O)C(=O)C3=C(C=C(C=C3O1)O)O 284.26 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
https://doi.org/10.1016/S0031-9422(99)00155-7
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3R)-3-[(4-hydroxyphenyl)methyl]-5,7-dimethoxy-2,3-dihydrochromen-4-one 162976217 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(CO2)CC3=CC=C(C=C3)O 314.30 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
(3R)-5,7-dimethoxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 102210986 Click to see COC1=CC=C(C=C1)CC2COC3=C(C2=O)C(=CC(=C3)OC)OC 328.40 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
(3S)-3-[(3,4-dimethoxyphenyl)methyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 163004768 Click to see COC1=C(C=C(C=C1)CC2COC3=CC(=CC(=C3C2=O)O)O)OC 330.30 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
(3S)-3-[(4-hydroxyphenyl)methyl]-5,6,7-trimethoxy-2,3-dihydrochromen-4-one 162855132 Click to see COC1=C(C(=C2C(=C1)OCC(C2=O)CC3=CC=C(C=C3)O)OC)OC 344.40 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
(3S)-3-[(4-hydroxyphenyl)methyl]-5,7-dimethoxy-2,3-dihydrochromen-4-one 162976216 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(CO2)CC3=CC=C(C=C3)O 314.30 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
(3S)-5-hydroxy-3-[(3-hydroxy-4-methoxyphenyl)methyl]-7-methoxy-2,3-dihydrochromen-4-one 162975290 Click to see COC1=C(C=C(C=C1)CC2COC3=CC(=CC(=C3C2=O)O)OC)O 330.30 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
(3S)-5-hydroxy-3-[(4-hydroxy-3-methoxyphenyl)methyl]-6,7-dimethoxy-2,3-dihydrochromen-4-one 163007678 Click to see COC1=C(C=CC(=C1)CC2COC3=CC(=C(C(=C3C2=O)O)OC)OC)O 360.40 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
(3S)-5-hydroxy-3-[(4-hydroxy-3-methoxyphenyl)methyl]-7-methoxy-2,3-dihydrochromen-4-one 162967056 Click to see COC1=CC(=C2C(=C1)OCC(C2=O)CC3=CC(=C(C=C3)O)OC)O 330.30 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
(3S)-5-hydroxy-3-[(4-hydroxyphenyl)methyl]-7-methoxy-2,3-dihydrochromen-4-one 132989027 Click to see COC1=CC(=C2C(=C1)OCC(C2=O)CC3=CC=C(C=C3)O)O 300.30 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
(3S)-5,7-dihydroxy-3-[(3-hydroxy-4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 92155497 Click to see COC1=C(C=C(C=C1)CC2COC3=CC(=CC(=C3C2=O)O)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
(3S)-5,7-dihydroxy-3-[(4-hydroxyphenyl)methyl]-6-methoxy-2,3-dihydrochromen-4-one 92155498 Click to see COC1=C(C2=C(C=C1O)OCC(C2=O)CC3=CC=C(C=C3)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
(3S)-5,7-dimethoxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 50900355 Click to see COC1=CC=C(C=C1)CC2COC3=C(C2=O)C(=CC(=C3)OC)OC 328.40 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
https://doi.org/10.1016/S0031-9422(99)00267-8
(3S)-6-hydroxy-5,7-dimethoxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 163038466 Click to see COC1=CC=C(C=C1)CC2COC3=CC(=C(C(=C3C2=O)OC)O)OC 344.40 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
(3S)-8-hydroxy-5,7-dimethoxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 163040329 Click to see COC1=CC=C(C=C1)CC2COC3=C(C2=O)C(=CC(=C3O)OC)OC 344.40 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
3-(3-Hydroxy-4-methoxybenzyl)-5,7-dihydroxychroman-4-one 404571 Click to see COC1=C(C=C(C=C1)CC2COC3=CC(=CC(=C3C2=O)O)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
3-(4-Hydroxybenzyl)-5,7-dihydroxy-6-methoxychroman-4-one 404572 Click to see COC1=C(C2=C(C=C1O)OCC(C2=O)CC3=CC=C(C=C3)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
3-(4-Methoxybenzyl)-5,7-dimethoxychroman-4-one 404573 Click to see COC1=CC=C(C=C1)CC2COC3=C(C2=O)C(=CC(=C3)OC)OC 328.40 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
https://doi.org/10.1016/S0031-9422(99)00267-8
3-[(3,4-Dimethoxyphenyl)methyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 15484398 Click to see COC1=C(C=C(C=C1)CC2COC3=CC(=CC(=C3C2=O)O)O)OC 330.30 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
3-[(4-Hydroxyphenyl)methyl]-5,6,7-trimethoxy-2,3-dihydrochromen-4-one 15484400 Click to see COC1=C(C(=C2C(=C1)OCC(C2=O)CC3=CC=C(C=C3)O)OC)OC 344.40 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
3-[(4-Hydroxyphenyl)methyl]-5,7-dimethoxy-2,3-dihydrochromen-4-one 10686713 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(CO2)CC3=CC=C(C=C3)O 314.30 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
5-Hydroxy-3-(4-hydroxybenzyl)-7-methoxychroman-4-one 404855 Click to see COC1=CC(=C2C(=C1)OCC(C2=O)CC3=CC=C(C=C3)O)O 300.30 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
5-Hydroxy-3-[(3-hydroxy-4-methoxyphenyl)methyl]-7-methoxy-2,3-dihydrochromen-4-one 10640151 Click to see COC1=C(C=C(C=C1)CC2COC3=CC(=CC(=C3C2=O)O)OC)O 330.30 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
5-Hydroxy-3-[(4-hydroxy-3-methoxyphenyl)methyl]-6,7-dimethoxy-2,3-dihydrochromen-4-one 100998074 Click to see COC1=C(C=CC(=C1)CC2COC3=CC(=C(C(=C3C2=O)O)OC)OC)O 360.40 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
5-Hydroxy-3-[(4-hydroxy-3-methoxyphenyl)methyl]-7-methoxy-2,3-dihydrochromen-4-one 100998073 Click to see COC1=CC(=C2C(=C1)OCC(C2=O)CC3=CC(=C(C=C3)O)OC)O 330.30 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
5-Hydroxy-7-methoxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 11324481 Click to see COC1=CC=C(C=C1)CC2COC3=CC(=CC(=C3C2=O)O)OC 314.30 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
6-Hydroxy-5,7-dimethoxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 15484399 Click to see COC1=CC=C(C=C1)CC2COC3=CC(=C(C(=C3C2=O)OC)O)OC 344.40 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
8-Hydroxy-5,7-dimethoxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 15484401 Click to see COC1=CC=C(C=C1)CC2COC3=C(C2=O)C(=CC(=C3O)OC)OC 344.40 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
> Phenylpropanoids and polyketides / Stilbenes
1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]- 5056 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
3,4',5-Trihydroxy-3'-methoxystilbene 53395093 Click to see COC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)O)O)O 258.27 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
3',4-Dihydroxy-3,5'-dimethoxystilbene 85446349 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC(=C(C=C2)O)OC 272.29 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
4-[(E)-2-(3-hydroxy-5-methoxyphenyl)ethenyl]-2-methoxyphenol 15698947 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC(=C(C=C2)O)OC 272.29 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
5-[(E)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]benzene-1,3-diol 53394021 Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)O)O)O 258.27 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
https://doi.org/10.1016/S0031-9422(99)00267-8
Isorhapontigenin 5318650 Click to see COC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)O)O)O 258.27 unknown https://doi.org/10.1016/S0031-9422(99)00267-8
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
Rhapontigenin 5320954 Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)O)O)O 258.27 unknown https://doi.org/10.1016/S0031-9422(99)00155-7
https://doi.org/10.1016/S0031-9422(99)00267-8

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