Physostigma venenosum - Unknown
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Internal ID UUID6440458188274524840691
Scientific name Physostigma venenosum
Authority Balf.
First published in Trans. Roy. Soc. Edinburgh22: 310 (1861)

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Synonyms Top

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Common names Top

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Language Common/alternative name
English calabar bean
Spanish frijol de calabar
Arabic لوبيا كالابار
Arabic شجرة لوبية كالبار
Azerbaijani zəhərli fizostiqma
azb زهرلی فیزوستیقما
Bulgarian отровна физостигма
Catalan fava de calabar
German calabar-bohne
German calabarbohne
German gottesurteilbohne
German kalabarbohne
Finnish kalabarpapu
French fève de calabar
French feve de calabar
French éseré
Italian fava del calabar
Japanese カラバル豆
Japanese カラバルマメ
Polish bobotrutka kalabarska
Polish fasola kalabarska
Polish bobotrutka trująca
Russian Физостигма ядовитая
Russian Калабарские бобы
Uzbek fizostigma zaharli
Chinese 泡豆
Chinese 加刺拔豆
Chinese 毒扁豆

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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
  • Africa
    • West Tropical Africa
      • Ghana
      • Ivory Coast
      • Liberia
      • Mali
      • Nigeria
      • Sierra Leone
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001058100
UNII QYU9ZKY99Q
USDA Plants PHVE11
Tropicos 13054104
KEW urn:lsid:ipni.org:names:514320-1
The Plant List ild-2939
Open Tree Of Life 193139
NCBI Taxonomy 271807
IPNI 514320-1
GBIF 2946860
Freebase /m/08bq48
EPPO PGSVE
EOL 645358
USDA GRIN 28242
Wikipedia Physostigma_venenosum
CMAUP NPO228

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)!
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Title Authors Publication Released IDs
The Meaning of Plants' Names: A New Discovering Approach to Its Medicinal and/or Toxic Properties dos Santos Dantas Lima L, Felipe Domingues Passero L, Indriunas A, de Souza Santos I, Francisco Uchôa Coqueiro L, Alexandre Souza da Cruz K, Batista de Almeida A, Carlos Fernandes Galduróz J, Rodrigues E Evid Based Complement Alternat Med 19-Feb-2024
PMCID:PMC10896657
doi:10.1155/2024/6678557
PMID:38410808
Role of apigenin in targeting metabolic syndrome: A systematic review Javadi B, Sobhani Z Iran J Basic Med Sci 01-Jan-2024
PMCID:PMC11017844
doi:10.22038/IJBMS.2024.71539.15558
PMID:38629096
Therapeutic Role of Alkaloids and Alkaloid Derivatives in Cancer Management Olofinsan K, Abrahamse H, George BP Molecules 22-Jul-2023
PMCID:PMC10386240
doi:10.3390/molecules28145578
PMID:37513450
Genetic influences on motor learning and superperformance mutants revealed by random mutational survey of mouse locomotion Jakkamsetti V, Ma Q, Angulo G, Scudder W, Beutler B, Pascual JM bioRxiv 29-Jun-2023
PMCID:PMC10327015
doi:10.1101/2023.06.28.546756
PMID:37425744
Evaluation of the Wound Healing Potential of Cynara humilis Extracts in the Treatment of Skin Burns Salhi N, El Guourrami O, Rouas L, Moussaid S, Moutawalli A, Benkhouili FZ, Ameggouz M, Alshahrani MM, Al Awadh AA, Bouyahya A, Faouzi ME, Cherrah Y Evid Based Complement Alternat Med 18-Apr-2023
PMCID:PMC10129424
doi:10.1155/2023/5855948
PMID:37114146
Phytochemicals: A Promising Alternative for the Prevention of Alzheimer’s Disease Koul B, Farooq U, Yadav D, Song M Life (Basel) 12-Apr-2023
PMCID:PMC10144079
doi:10.3390/life13040999
PMID:37109528
Neuro-Nutraceutical Polyphenols: How Far Are We? Gentile MT, Camerino I, Ciarmiello L, Woodrow P, Muscariello L, De Chiara I, Pacifico S Antioxidants (Basel) 21-Feb-2023
PMCID:PMC10044769
doi:10.3390/antiox12030539
PMID:36978787
Evaluation of Mollugo oppositifolia Linn. as cholinesterase and β-secretase enzymes inhibitor Das B, Bhardwaj PK, Sharma N, Sarkar A, Haldar PK, Mukherjee PK Front Pharmacol 04-Jan-2023
PMCID:PMC9846241
doi:10.3389/fphar.2022.990926
PMID:36686717
Metabolomics and Network Pharmacology in the Exploration of the Multi-Targeted Therapeutic Approach of Traditional Medicinal Plants Sharma B, Yadav DK Plants (Basel) 25-Nov-2022
PMCID:PMC9737206
doi:10.3390/plants11233243
PMID:36501282
Engineering medicinal plant-derived CYPs: a promising strategy for production of high-valued secondary metabolites Sethi A, Bhandawat A, Pati PK Planta 15-Nov-2022
PMCID:PMC9664027
doi:10.1007/s00425-022-04024-9
PMID:36378350
Indian traditional medicinal plants in ophthalmic diseases Nafees S, Akhtar J, Kaur J Avicenna J Phytomed 01-Nov-2022
PMCID:PMC9768859
doi:10.22038/AJP.2022.20345
PMID:36583172
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
Neurohormetic phytochemicals in the pathogenesis of neurodegenerative diseases Sahebnasagh A, Eghbali S, Saghafi F, Sureda A, Avan R Immun Ageing 11-Aug-2022
PMCID:PMC9367062
doi:10.1186/s12979-022-00292-x
PMID:35953850
Carbamate Pesticides: Shedding Light on Their Impact on the Male Reproductive System Moreira S, Silva R, Carrageta DF, Alves MG, Seco-Rovira V, Oliveira PF, de Lourdes Pereira M Int J Mol Sci 26-Jul-2022
PMCID:PMC9332211
doi:10.3390/ijms23158206
PMID:35897782
Exploring the Phytochemicals and Anti-Cancer Potential of the Members of Fabaceae Family: A Comprehensive Review Usman M, Khan WR, Yousaf N, Akram S, Murtaza G, Kudus KA, Ditta A, Rosli Z, Rajpar MN, Nazre M Molecules 16-Jun-2022
PMCID:PMC9230627
doi:10.3390/molecules27123863
PMID:35744986

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Paulownin 3084131 Click to see C1C2C(OCC2(C(O1)C3=CC4=C(C=C3)OCO4)O)C5=CC6=C(C=C5)OCO6 370.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hentriacontanol 68345 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 452.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17R)-17-[(E,2R,5R)-5-ethyl-6-methylhept-3-en-2-yl]-3,10,13-trimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene 50930798 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)C)C)C)C(C)C 410.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Inositol phosphates
Phytic acid 890 Click to see C1(C(C(C(C(C1OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O 660.04 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(4R,5R)-4,5-Dihydroxy-4-[2-(beta-D-glucopyranosyloxy)ethyl]-2-cyclohexen-1-one 101999360 Click to see C1C(C(C=CC1=O)(CCOC2C(C(C(C(O2)CO)O)O)O)O)O 334.32 unknown via CMAUP database
(4S,5S)-4,5-Dihydroxy-4-[2-(beta-D-glucopyranosyloxy)ethyl]-2-cyclohexen-1-one 101999361 Click to see C1C(C(C=CC1=O)(CCOC2C(C(C(C(O2)CO)O)O)O)O)O 334.32 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-ethyl-O-beta-D-glucopyranoside 5316821 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)O)O)O)O 316.30 unknown via CMAUP database
2-Phenylethyl D-rutinoside 11166301 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=CC=C3)O)O)O)O)O)O 430.40 unknown via CMAUP database
4beta-Hydroxy-4-[2-(beta-D-glucopyranosyloxy)ethyl]-2-cyclohexen-1-one 101921144 Click to see C1CC(C=CC1=O)(CCOC2C(C(C(C(O2)CO)O)O)O)O 318.32 unknown via CMAUP database
CID 11809239 11809239 Click to see C1=CC(C=CC1=O)(CCOC2C(C(C(C(O2)CO)O)O)O)O 316.30 unknown via CMAUP database
Rengyoside B 11045420 Click to see C1CC(CCC1=O)(CCOC2C(C(C(C(O2)CO)O)O)O)O 320.34 unknown via CMAUP database
Salidroside 159278 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
beta-D-Glucosylisoeugenol 14189874 Click to see CC=CC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC 326.34 unknown via CMAUP database
p-Coumaryl alcohol 4-O-glucoside 5280847 Click to see C1=CC(=CC=C1C=CCO)OC2C(C(C(C(O2)CO)O)O)O 312.31 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
(+)-Rengyolone 10725564 Click to see C1COC2C1(C=CC(=O)C2)O 154.16 unknown via CMAUP database
(3aR,6S,7aS)-3,4,5,6,7,7a-hexahydro-2H-1-benzofuran-3a,6-diol 11084146 Click to see C1CC2(CCOC2CC1O)O 158.19 unknown via CMAUP database
2,3,3a,6,7,7abeta-Hexahydrobenzofuran-3abeta,6alpha-diol 101921142 Click to see C1COC2C1(C=CC(C2)O)O 156.18 unknown via CMAUP database
Cleroindicin C 10975728 Click to see C1CC2(CCOC2CC1=O)O 156.18 unknown via CMAUP database
Cleroindicin E 11744892 Click to see C1CC2(CCOC2CC1O)O 158.19 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives
1,2-Oxazino[6,5-b]indol-6-ol, 2,3,4,4a,9,9a-hexahydro-2,4a,9-trimethyl-, methylcarbamate, (4aS-cis)- 520214 Click to see CC12CCN(OC1N(C3=C2C=C(C=C3)OC(=O)NC)C)C 291.35 unknown via CMAUP database
3a,8-Dimethyl-3,3a,8,8a-tetrahydro-2H-furo[2,3-b]indol-5-yl methylcarbamate 110765 Click to see CC12CCOC1N(C3=C2C=C(C=C3)OC(=O)NC)C 262.30 unknown https://doi.org/10.1039/JR9640001503
Physovenine 442113 Click to see CC12CCOC1N(C3=C2C=C(C=C3)OC(=O)NC)C 262.30 unknown https://doi.org/10.2307/4117899
https://doi.org/10.1039/JR9640001503
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
[(8bS)-4,8b-dimethyl-3-(methylcarbamoyl)-2,3a-dihydro-1H-pyrrolo[2,3-b]indol-7-yl] N-methylcarbamate 3083935 Click to see CC12CCN(C1N(C3=C2C=C(C=C3)OC(=O)NC)C)C(=O)NC 318.37 unknown via CMAUP database
1,3a,8-Trimethyl-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indol-5-yl methylcarbamate 4811 Click to see CC12CCN(C1N(C3=C2C=C(C=C3)OC(=O)NC)C)C 275.35 unknown https://doi.org/10.1039/JR9640001503
Eseramine 442077 Click to see CC12CCN(C1N(C3=C2C=C(C=C3)OC(=O)NC)C)C(=O)NC 318.37 unknown https://doi.org/10.1039/JR9640001503
https://doi.org/10.2307/4117899
Physostigmine 5983 Click to see CC12CCN(C1N(C3=C2C=C(C=C3)OC(=O)NC)C)C 275.35 unknown https://doi.org/10.2307/4117899
https://doi.org/10.1039/JR9640001503
Pyemnabyodprpp-uhfffaoysa- 621491 Click to see CC12CCN(C1N(C3=C2C=C(C=C3)OC(=O)NC)C)C(=O)NC 318.37 unknown https://doi.org/10.1039/JR9640001503
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Scutellarein 5281697 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Apigenin 7-glucuronide 5319484 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown via CMAUP database
Hispidulin 7-O-beta-D-methylglucuronopyranoside 15219280 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)C(=O)OC)O)O)O 490.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
6,7-dihydroxy-2-(4-hydroxyphenyl)-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5321202 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Homoplantaginin 5318083 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown via CMAUP database
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown via CMAUP database

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