Strychnos cathayensis

Details Top

Internal ID UUID644047a66f860657093419
Scientific name Strychnos cathayensis
Authority Merr.
First published in Lingnan Sci. J. 13: 44 (1934)

Ethnobotanical Use Top

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General Uses Top

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Common products:
The species is a documented source of strychnine-type alkaloids, primarily found in the seeds and other plant parts. These compounds have established applications in biological research as neurotoxins for studying synaptic transmission and receptor mechanisms.

Industrial and craft applications:
There are no documented industrial or craft applications beyond research use.

Food and beverages (non-medicinal):
No documented food or beverage applications are reported for this species.

Colorants and tanning:
No documented use for dyes, inks, or tanning is reported.

Wood and fiber:
No documented timber or fiber applications are reported for this species.

Fragrance and cosmetics:
No documented fragrance or cosmetic applications are reported.

Properties relevant to use:
The seeds contain strychnine and related indole alkaloids (including brucine) that function as potent competitive antagonists of glycine receptors. These compounds exhibit high water solubility and are stable under standard laboratory conditions, enabling their use in precise neurobiological research applications.

Standards and regulation:
Strychnine is subject to strict regulatory controls in most jurisdictions due to its extreme toxicity. International conventions on chemical weapons and drug control treat strychnine as a regulated substance, and research applications require appropriate licensing and containment protocols.

Sustainability and sourcing:
The species occurs naturally in certain regions of Asia, but there is insufficient data on population status, harvesting practices, or sustainable cultivation protocols to assess sourcing sustainability. Research applications typically rely on small quantities obtained from specialized suppliers rather than wild harvest.

Synonyms Top

Scientific name Authority First published in
Strychnos henryi Merr. & Yamam. J. Soc. Trop. Agric. 7: 145 (1935)

Common names Top

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Language Common/alternative name
Chinese 华马钱
Chinese 牛目椒
Chinese 臺灣馬錢
Chinese 華馬錢
Chinese 三脉马钱
Chinese 牛耳椒
Chinese 登欧梅罗
Chinese 百节藤
Chinese 台湾马钱

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Strychnos cathayensis var. cathayensis Unknown
Strychnos cathayensis var. spinata P.T.Li S. China Agric. Sci. 1: 126 (1980)

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
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001074222
Tropicos 19001085
KEW urn:lsid:ipni.org:names:547102-1
The Plant List tro-19001085
Open Tree Of Life 5745791
NCBI Taxonomy 1603838
IPNI 547102-1
iNaturalist 570197
GBIF 5645598
EOL 2899649
USDA GRIN 411886
CMAUP NPO5287

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
Climbing strategies of Taiwan climbers Chen PH, Chung AC, Lin HC, Yang SZ Bot Stud 22-Sep-2023
PMCID:PMC10516820
doi:10.1186/s40529-023-00399-4
PMID:37736799
Crystal Engineering of a Chiral Crystalline Sponge That Enables Absolute Structure Determination and Enantiomeric Separation Deng C, Song BQ, Lusi M, Bezrukov AA, Haskins MM, Gao MY, Peng YL, Ma JG, Cheng P, Mukherjee S, Zaworotko MJ Cryst Growth Des 16-May-2023
PMCID:PMC10326857
doi:10.1021/acs.cgd.3c00446
PMID:37426545
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
Chemical Constituents from <i>Strychnos Cathayensis</i> Ming‐Jen Cheng, Ian‐Lih Tsai, Ih‐Sheng Chen Wiley 01-May-2015
doi:10.1002/JCCS.200100038

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Butylparaben 7184 Click to see CCCCOC(=O)C1=CC=C(C=C1)O 194.23 unknown https://doi.org/10.1002/JCCS.200100038
> Benzenoids / Phenols / Methoxyphenols
o-Vanillin 8991 Click to see 152.15 unknown https://doi.org/10.1002/JCCS.200100038
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R,5R)-2,3,5-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 11027254 Click to see 480.60 unknown via CMAUP database
20-Hydroxyecdysone 5459840 Click to see 480.60 unknown via CMAUP database
25S-Inokosterone 12358616 Click to see 480.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
Ponasterone A 115127 Click to see 464.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
22,23-Dihydrobrassicasterol 5283637 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
[(2R,3S,4S,5R,6R)-6-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl hexadecanoate 13051627 Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(C)C(C)C)C)C)O)O)O 801.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Sitoindoside I 9832350 Click to see 815.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
p-Aminopropiophenone 6270 Click to see 149.19 unknown https://doi.org/10.1002/JCCS.200100038
> Organoheterocyclic compounds / Azolidines / Oxazolidines / Oxazolidinones
(S)-(-)-4-tert-Butyl-2-oxazolidinone 6950844 Click to see CC(C)(C)C1COC(=O)N1 143.18 unknown https://doi.org/10.1002/JCCS.200100038
4-Tert-butyl-1,3-oxazolidin-2-one 3474206 Click to see 143.18 unknown https://doi.org/10.1002/JCCS.200100038
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
Indole-2-carboxylic acid 72899 Click to see 161.16 unknown https://doi.org/10.1002/JCCS.200100038
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
3-Acetylindole 12802 Click to see 159.18 unknown https://doi.org/10.1002/JCCS.200100038
Indoxyl acetate 11841 Click to see 175.18 unknown https://doi.org/10.1002/JCCS.200100038
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(4R,4aS)-4-ethenyl-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 21593837 Click to see C=CC1COC=C2C1CCOC2=O 180.20 unknown https://doi.org/10.1002/JCCS.200100038
4-ethenyl-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 73810073 Click to see C=CC1COC=C2C1CCOC2=O 180.20 unknown https://doi.org/10.1002/JCCS.200100038
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3R)-4-[(E)-2-carboxyethenyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carboxylic acid 10316325 Click to see C1=CC(=C(C=C1C2C(C3=C(C=CC(=C3O2)O)C=CC(=O)O)C(=O)O)O)O 358.30 unknown via CMAUP database
(3R,4R,5R)-5-[(2S,3R)-4-[(E)-2-carboxyethenyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carbonyl]oxy-3,4-dihydroxycyclohexene-1-carboxylic acid 10436502 Click to see 514.40 unknown via CMAUP database
Przewalskinic acid A 9975641 Click to see 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Woodorien 192694 Click to see 330.29 unknown via CMAUP database

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