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Cinnamodendron axillare

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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 UUID6440112825b77199848083
Scientific name Cinnamodendron axillare
Authority Endl. ex Walp.
First published in Repert. Bot. Syst. 1: 398 (1842)

Description Top

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Synonyms Top

Scientific name Authority First published in
Canella axillaris Nees & Mart. Flora 4: 298 (1821)

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-0000604841
Tropicos 50249579
KEW urn:lsid:ipni.org:names:146017-1
The Plant List kew-2721077
Open Tree Of Life 1016783
NCBI Taxonomy 549613
IUCN Red List 177818776
IPNI 146017-1
iNaturalist 184193
GBIF 3877817
Freebase /m/0125y9b_
EOL 5035517
Wikipedia Cinnamodendron_axillare

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
Access to 3,3-disubstituted oxindoles via microwave-assisted Cannizzaro and aldol reactions of formaldehyde with isatins and their imines Huang X, Wang H, Cao Q, Li Y, Zhang J RSC Adv 11-May-2021
PMCID:PMC9033177
doi:10.1039/d1ra02150h
PMID:35479673
Paratunamides A-D, oxindole alkaloids from Cinnamodendron axillare. Kagata T, Saito S, Shigemori H, Ohsaki A, Ishiyama H, Kubota T, Kobayashi J J Nat Prod 01-Oct-2006
doi:10.1021/NP0602968
PMID:17067176

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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3S,4S,4aS,6R)-4-ethenyl-6-hydroxy-7-[2-[(3S)-3-hydroxy-2-oxo-1H-indol-3-yl]ethyl]-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyridin-8-one 162875930 Click to see C=CC1C2CC(N(C(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O)CCC4(C5=CC=CC=C5NC4=O)O)O 548.50 unknown https://doi.org/10.1021/NP0602968
(3S,4S,4aS,6R)-4-ethenyl-7-[2-[(3S)-3-hydroxy-2-oxo-1H-indol-3-yl]ethyl]-6-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyridin-8-one 162861350 Click to see COC1CC2C(C(OC=C2C(=O)N1CCC3(C4=CC=CC=C4NC3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C=C 562.60 unknown https://doi.org/10.1021/NP0602968
(3S,4S,4aS)-4-ethenyl-7-[2-[(3R)-3-hydroxy-2-oxo-1H-indol-3-yl]ethyl]-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,4a,5-tetrahydropyrano[3,4-c]pyridine-6,8-dione 162972444 Click to see C=CC1C2CC(=O)N(C(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O)CCC4(C5=CC=CC=C5NC4=O)O 546.50 unknown https://doi.org/10.1021/NP0602968
(3S,4S,4aS)-4-ethenyl-7-[2-[(3S)-3-hydroxy-2-oxo-1H-indol-3-yl]ethyl]-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,4a,5-tetrahydropyrano[3,4-c]pyridine-6,8-dione 162972445 Click to see C=CC1C2CC(=O)N(C(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O)CCC4(C5=CC=CC=C5NC4=O)O 546.50 unknown https://doi.org/10.1021/NP0602968
19-Ethenyl-18-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-oxa-3,13-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosa-2(11),4,6,8,15-pentaene-10,14-dione 14440700 Click to see C=CC1C2CC3C4=C(CN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C(=O)C6=CC=CC=C6N4 512.50 unknown https://doi.org/10.1021/NP0602968
4-ethenyl-7-[2-(3-hydroxy-2-oxo-1H-indol-3-yl)ethyl]-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,4a,5-tetrahydropyrano[3,4-c]pyridine-6,8-dione 73240855 Click to see C=CC1C2CC(=O)N(C(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O)CCC4(C5=CC=CC=C5NC4=O)O 546.50 unknown https://doi.org/10.1021/NP0602968
4-ethenyl-7-[2-(3-hydroxy-2-oxo-1H-indol-3-yl)ethyl]-6-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyridin-8-one 73240854 Click to see COC1CC2C(C(OC=C2C(=O)N1CCC3(C4=CC=CC=C4NC3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C=C 562.60 unknown https://doi.org/10.1021/NP0602968
Paratunamide A 16091680 Click to see COC1CC2C(C(OC=C2C(=O)N1CCC3(C4=CC=CC=C4NC3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C=C 562.60 unknown https://doi.org/10.1021/NP0602968
paratunamide B 16091681 Click to see C=CC1C2CC(=O)N(C(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O)CCC4(C5=CC=CC=C5NC4=O)O 546.50 unknown https://doi.org/10.1021/NP0602968
paratunamide C 16091683 Click to see C=CC1C2CC(=O)N(C(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O)CCC4(C5=CC=CC=C5NC4=O)O 546.50 unknown https://doi.org/10.1021/NP0602968
paratunamide D 16091682 Click to see C=CC1C2CC(N(C(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O)CCC4(C5=CC=CC=C5NC4=O)O)O 548.50 unknown https://doi.org/10.1021/NP0602968
Paratunamide D (not validated) 73240856 Click to see C=CC1C2CC(N(C(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O)CCC4(C5=CC=CC=C5NC4=O)O)O 548.50 unknown https://doi.org/10.1021/NP0602968
Pumiloside 10346314 Click to see C=CC1C2CC3C4=C(CN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C(=O)C6=CC=CC=C6N4 512.50 unknown https://doi.org/10.1021/NP0602968
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
3-epi-Vincosamide; Isovincoside lactam; Strictosidine lactam 5015264 Click to see C=CC1C2CC3C4=C(CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C6=CC=CC=C6N4 498.50 unknown https://doi.org/10.1021/NP0602968
Strictosamide 10345799 Click to see C=CC1C2CC3C4=C(CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C6=CC=CC=C6N4 498.50 unknown https://doi.org/10.1021/NP0602968

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