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Stephania excentrica

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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 UUID6440551d817e3707866697
Scientific name Stephania excentrica
Authority H.S.Lo
First published in Acta Phytotax. Sin. 16(1): 33 (1978)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 江南地不容

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-0001238664
Tropicos 50098966
KEW urn:lsid:ipni.org:names:581422-1
The Plant List tro-50098966
Open Tree Of Life 5503512
NCBI Taxonomy 1501462
IPNI 581422-1
GBIF 5592887
EOL 5125341

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
An Alkaloid with a Novel Skeleton from the Roots of<i>Stephania excentrica</i> Jing-Zhen Deng, Shou-Xun Zhao, Zhen-Chun Miao Informa UK Limited 07-Jul-2007
doi:10.1080/10575639308043823
2-<i>N</i>-Methylexcentricine, a New Alkaloid from Roots of <i>Stephania excentrica</i> Jing-Zhen Deng, Shou-Xun Zhao American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/NP960371M

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
(R)-Roemerine 235224 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown https://doi.org/10.1021/NP960371M
https://doi.org/10.1080/10575639308043823
12-methoxy-8H-benzo[g][1,3]benzodioxolo[6,5,4-de]quinolin-8-one 639590 Click to see COC1=CC=CC2=C1C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O 305.30 unknown https://doi.org/10.1080/10575639308043823
https://doi.org/10.1021/NP960371M
Isoboldine 133323 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown https://doi.org/10.1021/NP960371M
https://doi.org/10.1080/10575639308043823
Oxoanolobine 135985965 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=C3C=CC(=C5)O 291.26 unknown https://doi.org/10.1080/10575639308043823
https://doi.org/10.1021/NP960371M
Roemerine 119204 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown https://doi.org/10.1080/10575639308043823
https://doi.org/10.1021/NP960371M
> Benzenoids / Phenanthrenes and derivatives
Sinococuline 5489400 Click to see COC1=C(C2=C(CC3C4=C(C(C(CC42CCN3)O)O)OC)C=C1)O 333.40 unknown https://doi.org/10.1021/NP960371M
https://doi.org/10.1080/10575639308043823
> Lignans, neolignans and related compounds
Homoaromoline 99620 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)O)OC 608.70 unknown https://doi.org/10.1021/NP960371M
https://doi.org/10.1080/10575639308043823
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(R)-Coclaurine 440989 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1080/10575639308043823
https://doi.org/10.1021/NP960371M
(S)-N-Methylcoclaurine 440584 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC 299.40 unknown https://doi.org/10.1021/NP960371M
Coclaurine 160487 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1021/NP960371M
Machiline 281691 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1021/NP960371M
N-Methylcoclaurine 2752274 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC 299.40 unknown https://doi.org/10.1021/NP960371M
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(2Z,5R,7R,8S,9R)-15,16-dimethoxy-10-methyl-18-oxa-10-azatetracyclo[7.7.1.12,8.013,17]octadeca-1(17),2,13,15-tetraene-5,7-diol 10712664 Click to see CN1CCC2=CC(=C(C3=C2C1C4C(CC(CC=C3O4)O)O)OC)OC 347.40 unknown https://doi.org/10.1021/NP960371M
(2Z,5S,7R,8S,9R)-15,16-dimethoxy-10-methyl-18-oxa-10-azatetracyclo[7.7.1.12,8.013,17]octadeca-1(17),2,13,15-tetraene-5,7-diol 101700819 Click to see CN1CCC2=CC(=C(C3=C2C1C4C(CC(CC=C3O4)O)O)OC)OC 347.40 unknown https://doi.org/10.1021/NP960371M
(2Z,5S,7R,8S,9R)-15,16-dimethoxy-18-oxa-10-azatetracyclo[7.7.1.12,8.013,17]octadeca-1(17),2,13,15-tetraene-5,7-diol 101701407 Click to see COC1=C(C2=C3C(C4C(CC(CC=C2O4)O)O)NCCC3=C1)OC 333.40 unknown https://doi.org/10.1080/10575639308043823
https://doi.org/10.1021/NP960371M
(5R,7R,8S,9R)-15,16-dimethoxy-10-methyl-18-oxa-10-azatetracyclo[7.7.1.12,8.013,17]octadeca-1(17),2,13,15-tetraene-5,7-diol 162902567 Click to see CN1CCC2=CC(=C(C3=C2C1C4C(CC(CC=C3O4)O)O)OC)OC 347.40 unknown https://doi.org/10.1021/NP960371M
15,16-Dimethoxy-10-methyl-18-oxa-10-azatetracyclo[7.7.1.12,8.013,17]octadeca-1(17),2,13,15-tetraene-5,7-diol 85241732 Click to see CN1CCC2=CC(=C(C3=C2C1C4C(CC(CC=C3O4)O)O)OC)OC 347.40 unknown https://doi.org/10.1021/NP960371M
15,16-Dimethoxy-18-oxa-10-azatetracyclo[7.7.1.12,8.013,17]octadeca-1(17),2,13,15-tetraene-5,7-diol 73809152 Click to see COC1=C(C2=C3C(C4C(CC(CC=C2O4)O)O)NCCC3=C1)OC 333.40 unknown https://doi.org/10.1021/NP960371M

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