Albertisia delagoensis - Unknown
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Internal ID UUID6440082a3c311744056903
Scientific name Albertisia delagoensis
Authority (N.E.Br.) Forman
First published in Kew Bull. 30: 83 (1975)

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Synonyms Top

Scientific name Authority First published in
Synclisia delagoensis N.E.Br. Bull. Misc. Inform. Kew 1892: 196 (1892)
Synclisia zambesiaca N.E.Br. Bull. Misc. Inform. Kew 1892: 496 (1892)
Synclisia junodii Schinz ex Diels Pflanzenr. , IV, 94: 93 (1910)
Anisocycla triplinervia Diels Pflanzenr. , IV, 94: 93 (1910)
Epinetrum delagoense Diels Pflanzenr. , IV, 94: 96 (1910)
Synclisia delagoense N.E.Br.

Common names Top

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Language Common/alternative name
ts cudodo
ts cumbato
Chinese 德拉瓜湾崖藤
Chinese 德拉瓜灣崖藤
Zulu umgandaganda

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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
  • Africa
    • South Tropical Africa
      • Mozambique
    • Southern Africa
      • Kwazulu-Natal

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000524951
Tropicos 20600221
KEW urn:lsid:ipni.org:names:580107-1
The Plant List kew-2627190
Open Tree Of Life 6129884
IPNI 580107-1
iNaturalist 499378
GBIF 5592693
EOL 5517125

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
Polar Compounds Isolated from the Leaves of Albertisia delagoensis (Menispermaceae) Hawkes GE, de Wet H, Li J Molecules 02-Nov-2011
PMCID:PMC6264132
doi:10.3390/molecules16119153
PMID:22048698
Antiplasmodial activity and cytotoxicity of Albertisia delagoensis. De Wet H, Van Heerden FR, Van Wyk BE, Van Zyl RL Fitoterapia 01-Sep-2007
doi:10.1016/J.FITOTE.2007.02.018
PMID:17570613

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 / Aporphines
(-)-Dicentrine 317843 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)OC)OCO3 339.40 unknown https://doi.org/10.1016/J.FITOTE.2007.02.018
(+/-)-Dicentrine 630859 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)OC)OCO3 339.40 unknown https://doi.org/10.1016/J.FITOTE.2007.02.018
Dicentrine 101300 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)OC)OCO3 339.40 unknown https://doi.org/10.1016/J.FITOTE.2007.02.018
> Lignans, neolignans and related compounds
(+)-Cocsoline 3085062 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7)O4)O)OC 548.60 unknown https://doi.org/10.1016/J.FITOTE.2007.02.018
(8R,21S)-27-methoxy-7,22-dimethyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaen-13-ol 14482093 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7C)O4)O)OC 562.70 unknown https://doi.org/10.1016/J.FITOTE.2007.02.018
(8S,21R)-13,27-dimethoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaene 3246541 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7)O4)OC)OC 562.70 unknown https://doi.org/10.1016/J.FITOTE.2007.02.018
(8S,21R)-27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaen-13-ol 163065545 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7)O4)O)OC 548.60 unknown https://doi.org/10.1016/J.FITOTE.2007.02.018
27-Methoxy-7,22-dimethyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaen-13-ol 10099394 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7C)O4)O)OC 562.70 unknown https://doi.org/10.1016/J.FITOTE.2007.02.018
Cocsoline 21579624 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7)O4)O)OC 548.60 unknown https://doi.org/10.1016/J.FITOTE.2007.02.018
Oxyacanthan-12'-ol, 6',7-epoxy-6-methoxy-2,2'-dimethyl-, (1'alpha)- 21579625 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7C)O4)O)OC 562.70 unknown https://doi.org/10.1016/J.FITOTE.2007.02.018
Trigilletine 301935 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(O3)C=C8CCN7)O4)OC)OC 562.70 unknown https://doi.org/10.1016/J.FITOTE.2007.02.018
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / N-carbamoyl-alpha amino acids and derivatives / N-carbamoyl-alpha amino acids
Allantoic acid 203 Click to see C(C(=O)O)(NC(=O)N)NC(=O)N 176.13 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264132/
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
1,2,3,4,5-Cyclohexanepentol 101715 Click to see C1C(C(C(C(C1O)O)O)O)O 164.16 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264132/
Quercitol 441437 Click to see C1C(C(C(C(C1O)O)O)O)O 164.16 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264132/
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
4,5,19,20-Tetramethoxy-10,25-dimethyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.213,16.13,7.118,22.011,36.026,33]hexatriaconta-1(30),3(36),4,6,13(35),14,16(34),18(33),19,21,28,31-dodecaene 357329 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC=C(O3)C=C7)N(CCC6=CC(=C5OC)OC)C)OC)OC 622.70 unknown https://doi.org/10.1016/J.FITOTE.2007.02.018
Cycleanine 121313 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC=C(O3)C=C7)N(CCC6=CC(=C5OC)OC)C)OC)OC 622.70 unknown https://doi.org/10.1016/J.FITOTE.2007.02.018

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