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Kopsia larutensis

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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
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Details Top

Internal ID UUID643fe021698f3648847759
Scientific name Kopsia larutensis
Authority King & Gamble
First published in J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 74: 432 (1908)

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-0000221372
Tropicos 100211685
KEW urn:lsid:ipni.org:names:60436658-2
The Plant List kew-106337
Open Tree Of Life 6068079
Observations.org 276366
IUCN Red List 37980
IPNI 60436658-2
iNaturalist 439430
GBIF 5535992
Freebase /m/02xb578
Elurikkus 539981
Wikipedia Kopsia_larutensis

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
Alkaloids from leaves of Kopsia larutensis Toh-Seok Kam, Poh-Suan Tan, Cheng-Hock Chuah Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83674-N
Eburnaminol and larutensine, alkaloids from Kopsia larutensis K. Awang, M. Païs, T. Sévenet, H. Schaller, A.M. Nasir, A.Hamid A. Hadi Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98283-9
Absolute configuration of C-16 of eburnane alkaloids from Kopsia larutensis Kam Toh-Seok, Tan Poh-Suan, Wei Chen Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85305-B

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 / Aspidofractine alkaloids
Kopsinine 7069830 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4 338.40 unknown https://doi.org/10.1016/S0031-9422(00)98283-9
Methyl (9R,18R,21S)-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-18-carboxylate 21123851 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4 338.40 unknown https://doi.org/10.1016/0031-9422(93)85305-B
https://doi.org/10.1016/S0031-9422(00)98283-9
Methyl aspidofractinine-3-carboxylate 573380 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4 338.40 unknown https://doi.org/10.1016/S0031-9422(00)98283-9
> Alkaloids and derivatives / Eburnan-type alkaloids
(+)-Isoeburnamine 118701077 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 296.40 unknown https://doi.org/10.1016/0031-9422(92)83674-N
(15R,17R,19R)-17-ethoxy-15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraene 163020495 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)OCC 324.50 unknown https://doi.org/10.1016/0031-9422(93)85305-B
(15S,17S,19R)-15-(2-hydroxyethyl)-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraen-17-ol 162987794 Click to see C1CC2(CC(N3C4=CC=CC=C4C5=C3C2N(C1)CC5)O)CCO 312.40 unknown https://doi.org/10.1016/S0031-9422(00)98283-9
15-(2-Hydroxyethyl)-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraen-17-ol 73006730 Click to see C1CC2(CC(N3C4=CC=CC=C4C5=C3C2N(C1)CC5)O)CCO 312.40 unknown https://doi.org/10.1016/S0031-9422(00)98283-9
17-Ethoxy-15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraene 163020493 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)OCC 324.50 unknown https://doi.org/10.1016/0031-9422(93)85305-B
1H-Indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine, 13a-ethyl-2,3,5,6,13a,13b-hexahydro- 610470 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C=C2 278.40 unknown https://doi.org/10.1016/0031-9422(93)85305-B
CID 163190001 163190001 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O.CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 592.80 unknown https://doi.org/10.1016/S0031-9422(00)98283-9
https://doi.org/10.1016/0031-9422(93)85305-B
Eburnamenin-14-ol, 14,15-dihydro-, (14alpha)- 442066 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 296.40 unknown https://doi.org/10.1016/0031-9422(93)85305-B
https://doi.org/10.1016/S0031-9422(00)98283-9
https://doi.org/10.1016/0031-9422(92)83674-N
Eburnamenin-14-ol, 14,15-dihydro-, (14beta)- 619344 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 296.40 unknown https://doi.org/10.1016/0031-9422(93)85305-B
https://doi.org/10.1016/S0031-9422(00)98283-9
https://doi.org/10.1016/0031-9422(92)83674-N
Eburnamenin-14(15H)-one 92112 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(=O)C2 294.40 unknown https://doi.org/10.1016/0031-9422(93)85305-B
https://doi.org/10.1016/S0031-9422(00)98283-9
https://doi.org/10.1016/0031-9422(92)83674-N
Eburnamenine 6857502 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C=C2 278.40 unknown https://doi.org/10.1016/0031-9422(93)85305-B
Eburnamine 101699 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 296.40 unknown https://doi.org/10.1016/0031-9422(92)83674-N
https://doi.org/10.1016/S0031-9422(00)98283-9
https://doi.org/10.1016/0031-9422(93)85305-B
Eburnamonine 3195 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(=O)C2 294.40 unknown https://doi.org/10.1016/0031-9422(92)83674-N
https://doi.org/10.1016/0031-9422(93)85305-B
https://doi.org/10.1016/S0031-9422(00)98283-9
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
18-Oxa-1,11-diazahexacyclo[9.8.2.115,19.02,7.08,20.015,21]docosa-2,4,6,8(20)-tetraene 78200886 Click to see C1CC23CCOC(C2)N4C5=CC=CC=C5C6=C4C3N(C1)CC6 294.40 unknown https://doi.org/10.1016/S0031-9422(00)98283-9

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