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Kopsia hainanensis

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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 UUID643fe0211e386495831129
Scientific name Kopsia hainanensis
Authority Tsiang
First published in Sunyatsenia 2: 111 (1934)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 海南蕊木

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-0000221365
Tropicos 1805966
KEW urn:lsid:ipni.org:names:79500-1
The Plant List kew-106330
Open Tree Of Life 6068075
IPNI 79500-1
GBIF 5536013
CMAUP NPO22720

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
Indole alkaloids from Kopsia jasminiflora Mariko Kitajima, Minako Anbe, Noriyuki Kogure, Sumphan Wongseripipatana, Hiromitsu Takayama Elsevier BV 18-Oct-2014
doi:10.1016/J.TET.2014.10.002
Kopsihainanines A and B, two unusual alkaloids from Kopsia hainanensis. Chen J, Chen JJ, Yao X, Gao K Org Biomol Chem 07-Aug-2011
doi:10.1039/C1OB05724C
PMID:21677983
Grandilodines A-C, biologically active indole alkaloids from Kopsia grandifolia. Yap WS, Gan CY, Low YY, Choo YM, Etoh T, Hayashi M, Komiyama K, Kam TS J Nat Prod 27-May-2011
doi:10.1021/NP200008G
PMID:21428274
Indole Alkaloids from<i>Kopsia hainanensis</i> Jiping Zhu, Armin Guggisberg, Manfred Hesse Georg Thieme Verlag KG 07-Mar-2007
doi:10.1055/S-2007-969073

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
(-)-Kopsanone 101289843 Click to see C1CC23CCC45C(C2)C(=O)C6C4(C3N(C1)C6)C7=CC=CC=C7N5 306.40 unknown https://doi.org/10.1055/S-2007-969073
(1R,9R,16R,18S,21S)-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-18-carboxylic acid 162924422 Click to see C1CC23CCC4(C(C2)C(=O)O)C5(C3N(C1)CC5)C6=CC=CC=C6N4 324.40 unknown https://doi.org/10.1055/S-2007-969073
Kopsanone 433961 Click to see C1CC23CCC45C(C2)C(=O)C6C4(C3N(C1)C6)C7=CC=CC=C7N5 306.40 unknown https://doi.org/10.1016/J.TET.2014.10.002
Kopsihainanine B 54590592 Click to see C1CC23CCC4(C5(C2N(C1)CC5C(=O)C3)C6=CC=CC=C6N4)C(=O)O 338.40 unknown https://doi.org/10.1039/C1OB05724C
Kopsinine 7069830 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4 338.40 unknown https://doi.org/10.1055/S-2007-969073
Kopsininic acid 102597247 Click to see C1CC23CCC4(C(C2)C(=O)O)C5(C3N(C1)CC5)C6=CC=CC=C6N4 324.40 unknown https://doi.org/10.1016/J.TET.2014.10.002
Kopsinoline 139291937 Click to see COC(=O)C1CC23CCC[N+]4(C2C5(C1(CC3)NC6=CC=CC=C65)CC4)[O-] 354.40 unknown https://doi.org/10.1016/J.TET.2014.10.002
Kopsoffine 158148 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)C6=CC7=C(C=C6)NC89C71CCN2C1C(CCC2)(CC8)CC9C(=O)OC 616.80 unknown https://doi.org/10.1016/J.TET.2014.10.002
methyl (1R,9R,16R,18R,21S)-11-oxo-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-18-carboxylate 21607614 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4=O 352.40 unknown https://doi.org/10.1016/J.TET.2014.10.002
methyl (1R,9R,16R,18R,21S)-6-[(15S,17R,19S)-15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraen-17-yl]-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6-triene-18-carboxylate 102150443 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)C6=CC7=C(C=C6)NC89C71CCN2C1C(CCC2)(CC8)CC9C(=O)OC 616.80 unknown https://doi.org/10.1055/S-2007-969073
methyl (1S,9R,16S,18R,21S)-11-oxo-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-18-carboxylate 51412688 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4=O 352.40 unknown https://doi.org/10.1055/S-2007-969073
methyl (1S,9S,12S,16S,18S,21R)-12-oxido-2-aza-12-azoniahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-18-carboxylate 163188228 Click to see COC(=O)C1CC23CCC[N+]4(C2C5(C1(CC3)NC6=CC=CC=C65)CC4)[O-] 354.40 unknown https://doi.org/10.1055/S-2007-969073
methyl (1S,9S,16S,18S,21R)-12-oxido-2-aza-12-azoniahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-18-carboxylate 163188227 Click to see COC(=O)C1CC23CCC[N+]4(C2C5(C1(CC3)NC6=CC=CC=C65)CC4)[O-] 354.40 unknown https://doi.org/10.1055/S-2007-969073
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/J.TET.2014.10.002
Methyl aspidofractinine-3-carboxylate 573380 Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4 338.40 unknown https://doi.org/10.1021/NP200008G
> 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/J.TET.2014.10.002
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/J.TET.2014.10.002
Eburnamenine 6857502 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C=C2 278.40 unknown https://doi.org/10.1055/S-2007-969073
https://doi.org/10.1016/J.TET.2014.10.002
Eburnamine 101699 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 296.40 unknown https://doi.org/10.1016/J.TET.2014.10.002
> Alkaloids and derivatives / Strychnos alkaloids
Dihydrocondylocarpine 100004 Click to see CCC1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC 324.40 unknown https://doi.org/10.1016/J.TET.2014.10.002
Tubotaiwin 78358510 Click to see CCC1C2CCN3C1C4(CC3)C5=CC=CC=C5NC4=C2C(=O)OC 324.40 unknown https://doi.org/10.1016/J.TET.2014.10.002
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(1R,13S,16R)-16-hydroxy-5,14-diazapentacyclo[12.3.3.01,13.04,12.06,11]icosa-4(12),6,8,10-tetraen-15-one 54590501 Click to see C1CC23CCC4=C(C2N(C1)C(=O)C(C3)O)C5=CC=CC=C5N4 296.40 unknown https://doi.org/10.1039/C1OB05724C
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Capparin B 24813533 Click to see COC1=CC2=C(C=C1)C(=C(N2)SC)C=O 221.28 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
6-Methoxyindoline-2,3-dione 10374972 Click to see COC1=CC2=C(C=C1)C(=O)C(=O)N2 177.16 unknown via CMAUP database
Capparin A 101457836 Click to see COC1=CC2=C(C=C1)C3(CN=C(S3)SC)C(=O)N2 280.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Oroxylin A 5320315 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Wogonin 5281703 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)O 284.26 unknown via CMAUP database

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