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Crossyne flava

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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 UUID644016a85f787326645532
Scientific name Crossyne flava
Authority (W.F.Barker ex Snijman) D.Müll.-Doblies & U.Müll.-Doblies
First published in Feddes Repert. 105: 358 (1994)

Description Top

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Synonyms Top

Scientific name Authority First published in
Boophone flava W.F.Barker ex Snijman J. S. African Bot. 49: 243 (1983)

Common names Top

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Language Common/alternative name
Chinese 黄刺花盏

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000644233
Tropicos 100174245
KEW urn:lsid:ipni.org:names:979954-1
The Plant List kew-276490
Open Tree Of Life 192999
NCBI Taxonomy 527290
IPNI 979954-1
iNaturalist 583022
GBIF 2853222
EOL 991701

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
Alkaloids in Future Drug Discovery Ferreira MJ Molecules 16-Feb-2022
PMCID:PMC8875739
doi:10.3390/molecules27041347
PMID:35209135
Neuroprotective Activities of Crossyne flava Bulbs and Amaryllidaceae Alkaloids: Implications for Parkinson’s Disease Omoruyi SI, Ibrakaw AS, Ekpo OE, Boatwright JS, Cupido CN, Hussein AA Molecules 30-Jun-2021
PMCID:PMC8272225
doi:10.3390/molecules26133990
PMID:34208814
Alkaloids from Boophane flava Francesc Viladomat, Jaume Bastida, Carles Codina, William E. Campbell, Shaheed Mathee Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00191-9

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(+)-Crinamine 118701061 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/0031-9422(95)00191-9
11-Epicrinamine 5281172 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1016/0031-9422(95)00191-9
3-O-Acetylhamayne 443671 Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 329.30 unknown https://doi.org/10.1016/0031-9422(95)00191-9
9,15-Dimethoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-triene 271606 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C6C1O6 331.40 unknown https://doi.org/10.1016/0031-9422(95)00191-9
Augustine 157561 Click to see COC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C6C1O6 301.34 unknown https://doi.org/10.1016/0031-9422(95)00191-9
Buphanisin 12302149 Click to see COC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 285.34 unknown https://doi.org/10.1016/0031-9422(95)00191-9
Crinine 398937 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1016/0031-9422(95)00191-9
Hamayne 443670 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown https://doi.org/10.1016/0031-9422(95)00191-9
Undulatine 3083985 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C6C1O6 331.40 unknown https://doi.org/10.1016/0031-9422(95)00191-9
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Lycorine 72378 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown https://doi.org/10.1016/0031-9422(95)00191-9
> Benzenoids / Phenol ethers / Anisoles
2,3-Dimethoxy-6-methyl-5,6,7,8-tetrahydrodibenzo[c,e]azocine 10016689 Click to see CN1CCC2=CC=CC=C2C3=CC(=C(C=C3C1)OC)OC 283.40 unknown https://doi.org/10.1016/0031-9422(95)00191-9
4-Methoxy-9-methyl-9-azatricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaen-5-ol 10015908 Click to see CN1CCC2=CC=CC=C2C3=CC(=C(C=C3C1)O)OC 269.34 unknown https://doi.org/10.1016/0031-9422(95)00191-9
> Organoheterocyclic compounds / Benzazepines
(1R,13S,15R,16S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.013,18]nonadeca-2,4(8),9,17-tetraen-16-ol 102586382 Click to see COC1CC2C(=CC1O)C3CN2CC4=CC5=C(C=C34)OCO5 301.34 unknown https://doi.org/10.1016/0031-9422(95)00191-9

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