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Plagiocarpus axillaris

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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 UUID643fda229e2b6013814511
Scientific name Plagiocarpus axillaris
Authority Benth.
First published in Hooker's Icon. Pl.12: t. 1162 (1873)

Description Top

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Synonyms Top

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Common names Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000188653
Tropicos 13054083
KEW urn:lsid:ipni.org:names:515171-1
The Plant List ild-35180
Open Tree Of Life 46803
NCBI Taxonomy 142531
IPNI 515171-1
GBIF 2974557
EOL 645080

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
Complete plastid genome sequence of the chickpea (Cicer arietinum) and the phylogenetic distribution of rps12 and clpP intron losses among legumes (Leguminosae) Jansen RK, Wojciechowski MF, Sanniyasi E, Lee SB, Daniell H Mol Phylogenet Evol 27-Jun-2008
PMCID:PMC2586962
doi:10.1016/j.ympev.2008.06.013
PMID:18638561
The alkaloid pattern of Plagiocarpus axillaris (Fabaceae: Brongniartieae) Roland Greinwald, James H. Ross, Ludger Witte, F.-C. Czygan Elsevier BV 12-May-2003
doi:10.1016/0305-1978(95)00059-3

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 / Lupin alkaloids / Anagyrine-type alkaloids
(1S,9S,10R,12S)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 131676079 Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown https://doi.org/10.1016/0305-1978(95)00059-3
Anagyrin 71056954 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/0305-1978(95)00059-3
Epibaptifoline 91747695 Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown https://doi.org/10.1016/0305-1978(95)00059-3
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 1747617 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1016/0305-1978(95)00059-3
1,5-Methano-8H-pyrido[1,2-a][1,5]diazocin-8-one, 3-(3-butenyl)-1,2,3,4,5,6-hexahydro-, (1R)- 547355 Click to see C=CCCN1CC2CC(C1)C3=CC=CC(=O)N3C2 244.33 unknown https://doi.org/10.1016/0305-1978(95)00059-3
Cytisine, N-formyl- 589870 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O 218.25 unknown https://doi.org/10.1016/0305-1978(95)00059-3
N-acetylcytisine 3716901 Click to see CC(=O)N1CC2CC(C1)C3=CC=CC(=O)N3C2 232.28 unknown https://doi.org/10.1016/0305-1978(95)00059-3
Pharmakon1600-01504027 6708720 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/0305-1978(95)00059-3
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
1-Epilupinine 92767 Click to see C1CCN2CCCC(C2C1)CO 169.26 unknown https://doi.org/10.1016/0305-1978(95)00059-3
Lupinine 91461 Click to see C1CCN2CCCC(C2C1)CO 169.26 unknown https://doi.org/10.1016/0305-1978(95)00059-3
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(1R,2R,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 92143189 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/0305-1978(95)00059-3
(2S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-8-one 139031726 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3CCCC4 248.36 unknown https://doi.org/10.1016/0305-1978(95)00059-3
14-Hydroxysparteine 523576 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4O 250.38 unknown https://doi.org/10.1016/0305-1978(95)00059-3
6-Phosphogluconic acid tri(cyclohexylammonium) salt, Grade V 16212687 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/0305-1978(95)00059-3
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/0305-1978(95)00059-3
alpha-ISOSPARTEINE 92759 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/0305-1978(95)00059-3
Sparteine 644020 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/0305-1978(95)00059-3
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
Ammodendrine 442625 Click to see CC(=O)N1CCCC(=C1)C2CCCCN2 208.30 unknown https://doi.org/10.1016/0305-1978(95)00059-3
> Organoheterocyclic compounds / Quinolizidines
Dehydrosparteine 6427218 Click to see C1CCN2CC3CC(C2C1)CN4C3CCC=C4 232.36 unknown https://doi.org/10.1016/0305-1978(95)00059-3
> Organoheterocyclic compounds / Quinolizines
Lusitanine 6452371 Click to see CC(=O)NC=C1CCCN2C1CCCC2 208.30 unknown https://doi.org/10.1016/0305-1978(95)00059-3

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