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Cyclea sutchuenensis

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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 UUID644014d05be7d699175428
Scientific name Cyclea sutchuenensis
Authority Gagnep.
First published in Bull. Soc. Bot. France 55: 37 (1908)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cyclea sutchuenensis var. sessilis Y.C.Wu Bot. Jahrb. Syst. 71: 175 1940
Paracyclea sutchuenensis (Gagnep.) Yamam. J. Soc. Trop. Agric. 12: 247 (1940)
Paracyclea sutchuenensis var. sessilis (Y.C.Wu) Yamam. Taiwania 1: 38 1948

Common names Top

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Language Common/alternative name
Chinese 良藤
Chinese 四川轮环藤
Chinese 四川輪環藤

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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No germination or propagation data was added yet.

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-0000632086
Tropicos 50009327
KEW urn:lsid:ipni.org:names:580715-1
The Plant List kew-2750045
Open Tree Of Life 6129964
IPNI 580715-1
GBIF 3829698
EOL 5517421

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
Three cissampareine-type bisbenzylisoquinoline alkaloids from Cyclea species Wang Xian-Kai, Zhao Tong-Fang, Lai Sheng, Yoshikazu Shizuri, Shosuke Yamamura Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85059-Z
Head-to-tail bisbenzylisoquinoline alkaloids from Cyclea sutchuenensis Wang Xian-Kai, Zhao Tong-Fang, Lai Sheng, Yoshikazu Shizuri, Shosuke Yamamura Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85060-5

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 / Ethers / Diarylethers
(1R,16R)-10,26-dimethoxy-15,31-dimethyl-7,24,34-trioxa-15,31-diazaoctacyclo[19.10.3.23,6.18,12.118,22.025,33.028,32.016,36]octatriaconta-3(38),4,6(37),8(36),9,11,18(35),19,21,25,27,32-dodecaen-9-ol 10054414 Click to see CN1CCC2=CC(=C3C4=C2C1CC5=CC=C(C=C5)OC6=C7C(CC8=CC(=C(O4)C=C8)CO3)N(CCC7=CC(=C6O)OC)C)OC 606.70 unknown https://doi.org/10.1016/0031-9422(93)85060-5
(1R,16R)-9,10,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.218,21.18,12.027,31.016,35]heptatriaconta-3(37),4,6(36),8(35),9,11,18,20,24,26,31,33-dodecaen-32-ol 154495894 Click to see CN1CCC2=CC(=C3C(=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC=C(CO3)C=C7)N(CCC6=CC(=C5OC)OC)C)O)OC 622.70 unknown https://doi.org/10.1016/0031-9422(93)85059-Z
(1R,16S)-9,10,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.218,21.18,12.027,31.016,35]heptatriaconta-3(37),4,6(36),8(35),9,11,18,20,24,26,31,33-dodecaen-32-ol 162914405 Click to see CN1CCC2=CC(=C3C(=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC=C(CO3)C=C7)N(CCC6=CC(=C5OC)OC)C)O)OC 622.70 unknown https://doi.org/10.1016/0031-9422(93)85059-Z
(1S,16S)-9,10,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.218,21.18,12.027,31.016,35]heptatriaconta-3(37),4,6(36),8(35),9,11,18,20,24,26,31,33-dodecaen-32-ol 102153370 Click to see CN1CCC2=CC(=C3C(=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC=C(CO3)C=C7)N(CCC6=CC(=C5OC)OC)C)O)OC 622.70 unknown https://doi.org/10.1016/0031-9422(93)85059-Z
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/10.1016/0031-9422(93)85060-5
Isochondrodendrine 197726 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC=C(O3)C=C7)N(CCC6=CC(=C5O)OC)C)O)OC 594.70 unknown https://doi.org/10.1016/0031-9422(93)85060-5
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1R)-1-[[2-hydroxy-4-[[(1R)-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-yl]oxy]phenyl]methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-ol 162871283 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC4=CC(=C(C=C4)CC5C6=CC(=C(C=C6CCN5C)OC)O)O)OC 596.70 unknown https://doi.org/10.1016/0031-9422(93)85060-5
(1R)-1-[[3-hydroxy-4-[[(1R)-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-yl]oxy]phenyl]methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-ol 162913230 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC4=C(C=C(C=C4)CC5C6=CC(=C(C=C6CCN5C)OC)O)O)OC 596.70 unknown https://doi.org/10.1016/0031-9422(93)85060-5
(1R)-7-[4-[[(1R)-7-hydroxy-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-8-ol 102145804 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=C5CCN(C(C5=C4O)CC6=CC=C(C=C6)O)C)OC)O)OC 596.70 unknown https://doi.org/10.1016/0031-9422(93)85060-5
1-[[2-hydroxy-4-[[1-[(4-hydroxyphenyl)methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-yl]oxy]phenyl]methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-ol 102145803 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC4=CC(=C(C=C4)CC5C6=CC(=C(C=C6CCN5C)OC)O)O)OC 596.70 unknown https://doi.org/10.1016/0031-9422(93)85060-5
1-[[3-hydroxy-4-[[1-[(4-hydroxyphenyl)methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-yl]oxy]phenyl]methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-ol 102145797 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC4=C(C=C(C=C4)CC5C6=CC(=C(C=C6CCN5C)OC)O)O)OC 596.70 unknown https://doi.org/10.1016/0031-9422(93)85060-5
7-[4-[(7-hydroxy-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-8-ol 162916063 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=C5CCN(C(C5=C4O)CC6=CC=C(C=C6)O)C)OC)O)OC 596.70 unknown https://doi.org/10.1016/0031-9422(93)85060-5

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