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Kopsia profunda

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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
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Details Top

Internal ID UUID643fe021ee5ad044473019
Scientific name Kopsia profunda
Authority Markgr.
First published in Blumea 20: 424 (1972 publ. 1973)

Description Top

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Synonyms Top

Scientific name Authority First published in
Kopsia terengganensis L.Allorge & Wiart Acta Bot. Gallica 142: 434 (1995 publ. 1996)

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-0000221387
Tropicos 50274597
KEW urn:lsid:ipni.org:names:79519-1
The Plant List kew-106350
Open Tree Of Life 6068082
Observations.org 276369
NCBI Taxonomy 1750997
IUCN Red List 31728
IPNI 79519-1
iNaturalist 439431
GBIF 5535926
Freebase /m/02xb57z
Elurikkus 539957
Wikipedia Kopsia_profunda
CMAUP NPO4663

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
Dehydropleiocarpine alkaloids from Kopsia profunda T Kam Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(94)00938-P
Terengganensines A and B, dihydroeburnane alkaloids from Kopsia terengganensis Shasya Uzir, Ali M. Mustapha, A.Hamid A. Hadi, Khalijah Awang, Christophe Wiart, Jean-François Gallard, Mary Païs Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(97)00152-4
Plumeran alkaloids from Kopsia profunda Toh-Seok Kam, Poh-Suan Tan Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)83060-E

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aspidofractine alkaloids
dimethyl (1S,12R,19R,24S)-5,7-dioxa-2,15-diazaheptacyclo[17.2.2.112,15.01,12.03,11.04,8.019,24]tetracosa-3(11),4(8),9,20-tetraene-2,21-dicarboxylate 102056165 Click to see COC(=O)C1=CC23CCCN4C2C5(C1(CC3)N(C6=C5C=CC7=C6OCO7)C(=O)OC)CC4 438.50 unknown https://doi.org/10.1016/0031-9422(94)00938-P
https://doi.org/10.1016/0031-9422(90)83060-E
dimethyl (1S,9R,16R,21S)-4-hydroxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6,17-tetraene-2,18-dicarboxylate 162993784 Click to see COC(=O)C1=CC23CCCN4C2C5(C1(CC3)N(C6=C5C=CC=C6O)C(=O)OC)CC4 410.50 unknown https://doi.org/10.1016/0031-9422(94)00938-P
dimethyl (1S,9R,16R,21S)-4-methoxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6,17-tetraene-2,18-dicarboxylate 102056166 Click to see COC1=CC=CC2=C1N(C34C25CCN6C5C(CCC6)(CC3)C=C4C(=O)OC)C(=O)OC 424.50 unknown https://doi.org/10.1016/0031-9422(94)00938-P
https://doi.org/10.1016/0031-9422(90)83060-E
Dimethyl 4-hydroxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6,17-tetraene-2,18-dicarboxylate 162993783 Click to see COC(=O)C1=CC23CCCN4C2C5(C1(CC3)N(C6=C5C=CC=C6O)C(=O)OC)CC4 410.50 unknown https://doi.org/10.1016/0031-9422(94)00938-P
Dimethyl 4-methoxy-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3(8),4,6,17-tetraene-2,18-dicarboxylate 14655117 Click to see COC1=CC=CC2=C1N(C34C25CCN6C5C(CCC6)(CC3)C=C4C(=O)OC)C(=O)OC 424.50 unknown https://doi.org/10.1016/0031-9422(94)00938-P
https://doi.org/10.1016/0031-9422(90)83060-E
Dimethyl 5,7-dioxa-2,15-diazaheptacyclo[17.2.2.112,15.01,12.03,11.04,8.019,24]tetracosa-3(11),4(8),9,20-tetraene-2,21-dicarboxylate 14655115 Click to see COC(=O)C1=CC23CCCN4C2C5(C1(CC3)N(C6=C5C=CC7=C6OCO7)C(=O)OC)CC4 438.50 unknown https://doi.org/10.1016/0031-9422(90)83060-E
https://doi.org/10.1016/0031-9422(94)00938-P
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(94)00938-P
> Alkaloids and derivatives / Eburnan-type alkaloids
(15S,17R,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 15287568 Click to see C1CC2(CC(N3C4=CC=CC=C4C5=C3C2N(C1)CC5)O)CCO 312.40 unknown https://doi.org/10.1016/S0040-4039(97)00152-4
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/S0040-4039(97)00152-4
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/S0040-4039(97)00152-4
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/S0040-4039(97)00152-4
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/S0040-4039(97)00152-4
Eburnamine 101699 Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O 296.40 unknown https://doi.org/10.1016/S0040-4039(97)00152-4
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
(1R,11R,15R,16R)-17-oxa-4,14-diazahexacyclo[12.5.3.01,15.04,16.05,10.011,16]docosa-2,5,7,9-tetraen-11-ol 102064796 Click to see C1CC23CCOC45C2N(C1)CCC4(C6=CC=CC=C6N5C=C3)O 310.40 unknown https://doi.org/10.1016/S0040-4039(97)00152-4
(1S,11R,15R,16R)-17-oxa-4,14-diazahexacyclo[12.5.3.01,15.04,16.05,10.011,16]docosa-2,5,7,9-tetraen-11-ol 15287567 Click to see C1CC23CCOC45C2N(C1)CCC4(C6=CC=CC=C6N5C=C3)O 310.40 unknown https://doi.org/10.1016/S0040-4039(97)00152-4
17-Oxa-4,14-diazahexacyclo[12.5.3.01,15.04,16.05,10.011,16]docosa-2,5,7,9-tetraen-11-ol 163001392 Click to see C1CC23CCOC45C2N(C1)CCC4(C6=CC=CC=C6N5C=C3)O 310.40 unknown https://doi.org/10.1016/S0040-4039(97)00152-4
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/S0040-4039(97)00152-4
> Alkaloids and derivatives / Quebrachamine alkaloids
(15S)-15-ethyl-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-4(12),5,7,9-tetraene 10446525 Click to see CCC12CCCN(C1)CCC3=C(CC2)NC4=CC=CC=C34 282.40 unknown https://doi.org/10.1016/S0040-4039(97)00152-4
Kamassine 624708 Click to see CCC12CCCN(C1)CCC3=C(CC2)NC4=CC=CC=C34 282.40 unknown https://doi.org/10.1016/S0040-4039(97)00152-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides
(1R,9R,16R,18R,20R,22R)-19,21-dioxa-2,12-diazaheptacyclo[10.9.1.116,20.01,9.02,18.03,8.016,22]tricosa-3,5,7-trien-9-ol 163067048 Click to see C1CC23CC4N5C6=CC=CC=C6C7(C5(C2N(C1)CC7)OC(C3)O4)O 326.40 unknown https://doi.org/10.1016/S0040-4039(97)00152-4
(1R,9R,16R,22R)-19,21-dioxa-2,12-diazaheptacyclo[10.9.1.116,20.01,9.02,18.03,8.016,22]tricosa-3,5,7-trien-9-ol 102064795 Click to see C1CC23CC4N5C6=CC=CC=C6C7(C5(C2N(C1)CC7)OC(C3)O4)O 326.40 unknown https://doi.org/10.1016/S0040-4039(97)00152-4
19,21-Dioxa-2,12-diazaheptacyclo[10.9.1.116,20.01,9.02,18.03,8.016,22]tricosa-3,5,7-trien-9-ol 163067047 Click to see C1CC23CC4N5C6=CC=CC=C6C7(C5(C2N(C1)CC7)OC(C3)O4)O 326.40 unknown https://doi.org/10.1016/S0040-4039(97)00152-4
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
4-Methoxy-9-[[(Z)-3-(hydroxymethyl)-2-butenyl]oxy]-7H-furo[3,2-g][1]benzopyran-7-one 102465417 Click to see CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)CO 316.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl]Oxy-Chromen-4-one 12304323 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
2-(3,4-Dimethoxyphenyl)-5,6-dimethoxy-4H-1-benzopyran-4-one 14055876 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=CC(=C3OC)OC)OC 342.30 unknown via CMAUP database
5,6,2',3',4'-Pentamethoxyflavone 14055877 Click to see COC1=C(C(=C(C=C1)C2=CC(=O)C3=C(O2)C=CC(=C3OC)OC)OC)OC 372.40 unknown via CMAUP database
5,6,2',3',5',6'-Hexamethoxyflavone 21580515 Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=C(C(=CC(=C3OC)OC)OC)OC)OC 402.40 unknown via CMAUP database
5,6,2',3',6'-Pentamethoxyflavone 21580516 Click to see COC1=C(C(=C(C=C1)OC)OC)C2=CC(=O)C3=C(O2)C=CC(=C3OC)OC 372.40 unknown via CMAUP database
Cerosilin B 44257603 Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=CC(=C(C(=C3)OC)OC)OC)OC 372.40 unknown via CMAUP database
Cerrosillin 44257600 Click to see COC1=C(C2=C(C=C1)OC(=CC2=O)C3=CC(=CC(=C3)OC)OC)OC 342.30 unknown via CMAUP database

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