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Scaevola racemigera

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Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
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Genome
Scientific Literature
Phytochemical Profile
Biological Material
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Details Top

Internal ID UUID6440043554ee1427983416
Scientific name Scaevola racemigera
Authority Däniker
First published in Vierteljahrsschr. Naturf. Ges. Zürich 79(Beibl. 19): 78 (1933)

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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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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000497442
INPN 671988
KEW urn:lsid:ipni.org:names:384305-1
Open Tree Of Life 6060682
IPNI 384305-1
GBIF 5569501

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)!
Title Authors Publication Released IDs
ChemInform Abstract: PLANTS OF NEW CALEDONIA. 94. MONOTERPENE ALKALOIDS OF SCAEVOLA RACEMIGERA DAENIKER A.‐L. SKALTSOUNIS, S. MICHEL, F. TILLEQUIN, M. KOCH, J. PUSSET, G. CHAUVIERE Wiley 10-May-2016
doi:10.1002/CHIN.198550324
Four New Dimeric Monoterpene Alkaloids from Scaevola racemigera Däniker (Goodeniaceae) Michel Koch, Alexios-Leandros Skaltsounis, Fran腔is Tillequin, Jacques Pusset, Gerard Chauvi俊e The Japan Institute of Heterocyclic Chemistry 17-Feb-2009
doi:10.3987/R-1987-03-0599
Plantes de Nouvelle‐Calédonie. 94e Communication. Alcaloïdes monoterpéniques de <i>Scaevola racemigera</i> D<scp>ÄNIKER</scp> Alexios‐Léandros Skaltsounis, Sylvie Michel, François Tillequin, Michel Koch, Jacques Pusset, Gérard Chauvière Wiley 28-Dec-2004
doi:10.1002/HLCA.19850680622
Iridoids from Stilbe species H. Rimpler Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(72)80124-9

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
methyl (1R,4aS,6S,7R,7aS)-6-[(2S,3R,4S)-3-ethenyl-4-(2-oxoethyl)-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carbonyl]oxy-1-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 101967018 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)O)OC(=O)C3=COC(C(C3CC=O)C=C)OC4C(C(C(C(O4)CO)O)O)O 584.60 unknown https://doi.org/10.1016/0031-9422(72)80124-9
methyl (4S,4aS,6S,7R,7aS)-6-[(2S,3R,4S)-3-ethenyl-4-(2-oxoethyl)-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carbonyl]oxy-7-methyl-1-oxo-4,4a,5,6,7,7a-hexahydro-3H-cyclopenta[c]pyran-4-carboxylate 101425397 Click to see CC1C(CC2C1C(=O)OCC2C(=O)OC)OC(=O)C3=COC(C(C3CC=O)C=C)OC4C(C(C(C(O4)CO)O)O)O 584.60 unknown https://doi.org/10.1016/0031-9422(72)80124-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Loganic acid 89640 Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown https://doi.org/10.1016/0031-9422(72)80124-9
Loganin 87691 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/0031-9422(72)80124-9
methyl 6-[3-ethenyl-4-(2-oxoethyl)-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carbonyl]oxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 12302405 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C4=COC(C(C4CC=O)C=C)OC5C(C(C(C(O5)CO)O)O)O 746.70 unknown https://doi.org/10.1016/0031-9422(72)80124-9
> Organic acids and derivatives / Carboximidic acids and derivatives / Carboximidic acids / Cyclic carboximidic acids
methyl (4aS,6S,7R,7aS)-6-hydroxy-7-methyl-1-oxo-2,4a,5,6,7,7a-hexahydrocyclopenta[c]pyridine-4-carboxylate 14482794 Click to see CC1C(CC2C1C(=O)NC=C2C(=O)OC)O 225.24 unknown https://doi.org/10.1002/HLCA.19850680622
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(6S,7R)-6-hydroxy-7-methyl-2,3,4,5,6,7-hexahydro-1H-cyclopenta[c]pyridine-4-carboxylic acid 101415891 Click to see CC1C(CC2=C1CNCC2C(=O)O)O 197.23 unknown https://doi.org/10.1002/CHIN.198550324
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines / Naphthyridine carboxylic acids and derivatives
(4-Methoxycarbonyl-7-methyl-1-oxo-2,4a,5,6,7,7a-hexahydrocyclopenta[c]pyridin-6-yl) 1-methyl-2,7-naphthyridine-4-carboxylate 13857106 Click to see CC1C(CC2C1C(=O)NC=C2C(=O)OC)OC(=O)C3=CN=C(C4=C3C=CN=C4)C 395.40 unknown https://doi.org/10.3987/R-1987-03-0599
(4-methoxycarbonyl-7-methyl-2,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyridin-6-yl) 1-methyl-1,2-dihydro-2,7-naphthyridine-4-carboxylate 13857100 Click to see CC1C(CC2C1CNC=C2C(=O)OC)OC(=O)C3=CNC(C4=C3C=CN=C4)C 383.40 unknown https://doi.org/10.3987/R-1987-03-0599
(4-methoxycarbonyl-7-methyl-2,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyridin-6-yl) 1-methyl-2,7-naphthyridine-4-carboxylate 13857102 Click to see CC1C(CC2C1CNC=C2C(=O)OC)OC(=O)C3=CN=C(C4=C3C=CN=C4)C 381.40 unknown https://doi.org/10.3987/R-1987-03-0599
(4-methoxycarbonyl-7-methyl-6,7-dihydro-5H-cyclopenta[c]pyridin-6-yl) 1-methyl-1,2-dihydro-2,7-naphthyridine-4-carboxylate 13857104 Click to see CC1C(CC2=C(C=NC=C12)C(=O)OC)OC(=O)C3=CNC(C4=C3C=CN=C4)C 379.40 unknown https://doi.org/10.3987/R-1987-03-0599
[(4aS,6S,7R,7aS)-4-methoxycarbonyl-7-methyl-1-oxo-2,4a,5,6,7,7a-hexahydrocyclopenta[c]pyridin-6-yl] 1-methyl-2,7-naphthyridine-4-carboxylate 13857107 Click to see CC1C(CC2C1C(=O)NC=C2C(=O)OC)OC(=O)C3=CN=C(C4=C3C=CN=C4)C 395.40 unknown https://doi.org/10.3987/R-1987-03-0599
[(4aS,6S,7R,7aS)-4-methoxycarbonyl-7-methyl-2,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyridin-6-yl] (1S)-1-methyl-1,2-dihydro-2,7-naphthyridine-4-carboxylate 162978265 Click to see CC1C(CC2C1CNC=C2C(=O)OC)OC(=O)C3=CNC(C4=C3C=CN=C4)C 383.40 unknown https://doi.org/10.3987/R-1987-03-0599
[(4aS,6S,7R,7aS)-4-methoxycarbonyl-7-methyl-2,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyridin-6-yl] 1-methyl-2,7-naphthyridine-4-carboxylate 23242623 Click to see CC1C(CC2C1CNC=C2C(=O)OC)OC(=O)C3=CN=C(C4=C3C=CN=C4)C 381.40 unknown https://doi.org/10.3987/R-1987-03-0599
[(6S,7R)-4-methoxycarbonyl-7-methyl-6,7-dihydro-5H-cyclopenta[c]pyridin-6-yl] (1R)-1-methyl-1,2-dihydro-2,7-naphthyridine-4-carboxylate 162880802 Click to see CC1C(CC2=C(C=NC=C12)C(=O)OC)OC(=O)C3=CNC(C4=C3C=CN=C4)C 379.40 unknown https://doi.org/10.3987/R-1987-03-0599
> Organoheterocyclic compounds / Pyranopyridines
methyl (2S,4R)-2-methyl-3-oxa-9-azatricyclo[4.4.0.02,4]deca-1(6),7,9-triene-7-carboxylate 162917042 Click to see CC12C(O1)CC3=C2C=NC=C3C(=O)OC 205.21 unknown https://doi.org/10.1002/HLCA.19850680622
Methyl 2-methyl-3-oxa-9-azatricyclo[4.4.0.02,4]deca-1(6),7,9-triene-7-carboxylate 23258399 Click to see CC12C(O1)CC3=C2C=NC=C3C(=O)OC 205.21 unknown https://doi.org/10.1002/HLCA.19850680622
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
methyl (4aS,6S,7R,7aS)-6-hydroxy-7-methyl-2,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyridine-4-carboxylate 21606099 Click to see CC1C(CC2C1CNC=C2C(=O)OC)O 211.26 unknown https://doi.org/10.1002/HLCA.19850680622
Methyl 6-hydroxy-7-methyl-1-oxo-2,4a,5,6,7,7a-hexahydrocyclopenta[c]pyridine-4-carboxylate 14482793 Click to see CC1C(CC2C1C(=O)NC=C2C(=O)OC)O 225.24 unknown https://doi.org/10.1002/HLCA.19850680622
methyl 6-hydroxy-7-methyl-2,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyridine-4-carboxylate 73800010 Click to see CC1C(CC2C1CNC=C2C(=O)OC)O 211.26 unknown https://doi.org/10.1002/HLCA.19850680622
Strychnovoline 178920 Click to see CC1C(CC2C1C(=O)NC=C2C(=O)OC)O 225.24 unknown https://doi.org/10.1002/CHIN.198550324
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Cantleyine 442515 Click to see CC1C(CC2=C(C=NC=C12)C(=O)OC)O 207.23 unknown https://doi.org/10.1002/HLCA.19850680622
https://doi.org/10.1002/CHIN.198550324
CID 3530570 3530570 Click to see CC1C(CC2=C(C=NC=C12)C(=O)OC)O 207.23 unknown https://doi.org/10.1002/HLCA.19850680622
methyl (4aS,6S,7R,7aS)-6-(5-ethenylpyridine-3-carbonyl)oxy-7-methyl-2,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyridine-4-carboxylate 23258396 Click to see CC1C(CC2C1CNC=C2C(=O)OC)OC(=O)C3=CN=CC(=C3)C=C 342.40 unknown https://doi.org/10.1002/HLCA.19850680622
methyl (4aS,6S,7R,7aS)-7-methyl-1-oxo-6-(pyridine-3-carbonyloxy)-2,4a,5,6,7,7a-hexahydrocyclopenta[c]pyridine-4-carboxylate 23258397 Click to see CC1C(CC2C1C(=O)NC=C2C(=O)OC)OC(=O)C3=CN=CC=C3 330.33 unknown https://doi.org/10.1002/HLCA.19850680622
methyl (4aS,6S,7R,7aS)-7-methyl-6-(pyridine-3-carbonyloxy)-2,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyridine-4-carboxylate 21606100 Click to see CC1C(CC2C1CNC=C2C(=O)OC)OC(=O)C3=CN=CC=C3 316.35 unknown https://doi.org/10.1002/HLCA.19850680622
methyl (7R)-7-hydroxy-7-methylcyclopenta[c]pyridine-4-carboxylate 163084991 Click to see CC1(C=CC2=C1C=NC=C2C(=O)OC)O 205.21 unknown https://doi.org/10.1002/HLCA.19850680622
methyl 6-(5-ethenylpyridine-3-carbonyl)oxy-7-methyl-2,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyridine-4-carboxylate 74036688 Click to see CC1C(CC2C1CNC=C2C(=O)OC)OC(=O)C3=CN=CC(=C3)C=C 342.40 unknown https://doi.org/10.1002/HLCA.19850680622
Methyl 7-hydroxy-7-methylcyclopenta[c]pyridine-4-carboxylate 14378644 Click to see CC1(C=CC2=C1C=NC=C2C(=O)OC)O 205.21 unknown https://doi.org/10.1002/HLCA.19850680622
https://doi.org/10.1002/CHIN.198550324
Methyl 7-methyl-1-oxo-6-(pyridine-3-carbonyloxy)-2,4a,5,6,7,7a-hexahydrocyclopenta[c]pyridine-4-carboxylate 74036689 Click to see CC1C(CC2C1C(=O)NC=C2C(=O)OC)OC(=O)C3=CN=CC=C3 330.33 unknown https://doi.org/10.1002/HLCA.19850680622
methyl 7-methyl-5H-cyclopenta[c]pyridine-4-carboxylate 23258398 Click to see CC1=CCC2=C(C=NC=C12)C(=O)OC 189.21 unknown https://doi.org/10.1002/HLCA.19850680622
https://doi.org/10.1002/CHIN.198550324
methyl 7-methyl-6-(pyridine-3-carbonyloxy)-2,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyridine-4-carboxylate 73800011 Click to see CC1C(CC2C1CNC=C2C(=O)OC)OC(=O)C3=CN=CC=C3 316.35 unknown https://doi.org/10.1002/HLCA.19850680622

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