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Griselinia scandens

Griselinia scandens - 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 UUID64403d507f786721832829
Scientific name Griselinia scandens
Authority Taub.
First published in Bot. Jahrb. Syst. 16(3): 398. 1892 [23 Dec 1892]

Description Top

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Synonyms Top

Scientific name Authority First published in
Decostea scandens Ruiz & Pav. Syst. Veg. Fl. Peruv. Chil. 1: 259. 1798 [late Dec 1798]
Griselinia alata Ball J. Linn. Soc., Bot. 22: 161 (1886)

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000975575
Tropicos 8700038
KEW urn:lsid:ipni.org:names:113663-2
The Plant List kew-92693
Open Tree Of Life 898317
NCBI Taxonomy 218624
IPNI 271811-1
iNaturalist 776930
GBIF 5581556
USDA GRIN 18037
CMAUP NPO28500

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)!
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Title Authors Publication Released IDs
Triterpenoid constituents ofGriselinia scandens M. Silva, M. Balocchi, P.G. Sammes Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)86334-7

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 / Triterpenoids
(4aS,6aR,6aR,6bS,8aR,10S,12aS,14bR)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163013837 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/S0031-9422(00)86334-7
10-Acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 619165 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/S0031-9422(00)86334-7
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
2-Hydroxy-7-methoxy-9H-carbazole-3-carbaldehyde 189687 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=C(C(=C3)C=O)O 241.24 unknown via CMAUP database
2-methoxy-9H-carbazol-3-ol 15182256 Click to see COC1=C(C=C2C3=CC=CC=C3NC2=C1)O 213.23 unknown via CMAUP database
2-methoxy-9H-carbazole-3-carbaldehyde 6483032 Click to see COC1=CC2=C(C=C1C=O)C3=CC=CC=C3N2 225.24 unknown via CMAUP database
3-Formyl-2-hydroxy-6-methoxycarbazole 101508363 Click to see C1=CC2=C(C=C1O)C3=C(N2)C=C(C(=C3)C=O)O 227.21 unknown via CMAUP database
3,3-dimethyl-7H-pyrano[2,3-c]carbazole-10-carbaldehyde 71623858 Click to see CC1(C=CC2=C(O1)C=CC3=C2C4=C(N3)C=CC(=C4)C=O)C 277.30 unknown via CMAUP database
7-Hydroxyheptaphylline 15767846 Click to see CC(=CCC1=C(C(=CC2=C1NC3=C2C=CC(=C3)O)C=O)O)C 295.30 unknown via CMAUP database
7-Methoxyheptaphylline 189688 Click to see CC(=CCC1=C(C(=CC2=C1NC3=C2C=CC(=C3)OC)C=O)O)C 309.40 unknown via CMAUP database
9H-Carbazole-3-carbaldehyde 504067 Click to see C1=CC=C2C(=C1)C3=C(N2)C=CC(=C3)C=O 195.22 unknown via CMAUP database
9H-Carbazole-3-carboxaldehyde, 2,7-dimethoxy- 5317755 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=C(C(=C3)C=O)OC 255.27 unknown via CMAUP database
Clauraila D 51039828 Click to see CC1(C=CC2=C(O1)C=CC3=C2C4=C(N3)C=C(C(=C4)C=O)O)C 293.30 unknown via CMAUP database
Clausenawalline H 71623801 Click to see CC(=CCC1=C(C=CC2=C1C3=C(N2)C=C(C(=C3)C=O)O)O)C 295.30 unknown via CMAUP database
Clausenawalline K 71623860 Click to see CC1(C(C(C2=C(O1)C=CC3=C2C4=C(N3)C=C(C(=C4)C=O)O)O)O)C 327.30 unknown via CMAUP database
Clausine H 5315952 Click to see COC1=CC2=C(C=C1)C3=CC(=C(C=C3N2)OC)C(=O)OC 285.29 unknown via CMAUP database
Clausine K 504070 Click to see COC1=CC2=C(C=C1)C3=CC(=C(C=C3N2)OC)C(=O)O 271.27 unknown via CMAUP database
Clauszoline K 10537169 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=CC(=C3)C=O 225.24 unknown via CMAUP database
Girinimbine 96943 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=CC=CC=C42 263.30 unknown via CMAUP database
Heptaphylline 5318015 Click to see CC(=CCC1=C(C(=CC2=C1NC3=CC=CC=C32)C=O)O)C 279.30 unknown via CMAUP database
Lansine 5278451 Click to see COC1=CC2=C(C=C1)NC3=C2C=C(C(=C3)O)C=O 241.24 unknown via CMAUP database
methyl 1,6-dihydroxy-5-(3-methylbut-2-enyl)-9H-carbazole-3-carboxylate 71623800 Click to see CC(=CCC1=C(C=CC2=C1C3=C(N2)C(=CC(=C3)C(=O)OC)O)O)C 325.40 unknown via CMAUP database
Methyl 3-carbazolecarboxylate 504069 Click to see COC(=O)C1=CC2=C(C=C1)NC3=CC=CC=C32 225.24 unknown via CMAUP database
methyl 8-hydroxy-3,3-dimethyl-7H-pyrano[2,3-c]carbazole-10-carboxylate 71623859 Click to see CC1(C=CC2=C(O1)C=CC3=C2C4=C(N3)C(=CC(=C4)C(=O)OC)O)C 323.30 unknown via CMAUP database
Mukonal 504068 Click to see C1=CC=C2C(=C1)C3=C(N2)C=C(C(=C3)C=O)O 211.22 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown via CMAUP database
Gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown via CMAUP database

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