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Sophora pachycarpa

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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 UUID643fd9a2ac5f3524948635
Scientific name Sophora pachycarpa
Authority Schrenk ex C.A.Mey.
First published in Index Seminum (LE, Petropolitanus)9: 89 (1843)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vexibia pachycarpa (Schrenk ex C.A.Mey.) W.A.Weber Phytologia62: 438 (1987)
Goebelia pachycarpa (Schrenk ex C.A.Mey.) Bunge ex Boiss. Fl. Orient.2: 629 (1872)
Ammothamnus intermedius Kuntze Trudy Imp. S.-Peterburgsk. Bot. Sada10: 181 (1887)
Sophora intermedia Kuntze Nomencl. Bot. [Steudel], ed. 2. 2: 612 (Quid ?). 1841

Common names Top

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Language Common/alternative name
Arabic صفيراء غليظة الثمار
Azerbaijani gombulmeyvə sofora
Russian Софора толстоплодная
Uzbek achchiqmiya
Chinese 厚果槐
Chinese 甘肃槐树

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
  • Asia-temperate
    • China
      • China North-central
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Iran

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000186530
Tropicos 13033001
KEW urn:lsid:ipni.org:names:518906-1
The Plant List ild-33001
Open Tree Of Life 57102
NCBI Taxonomy 149668
IPNI 518906-1
GBIF 2959051
EPPO SOBPA
EOL 644013
USDA GRIN 315616

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
Supremacy of nanoparticles in the therapy of chronic myelogenous leukemia Janani G, Girigoswami A, Girigoswami K ADMET DMPK 26-Sep-2023
PMCID:PMC10626512
doi:10.5599/admet.2013
PMID:37937247
A Review of Effect of Saponins on Ruminal Fermentation, Health and Performance of Ruminants Kholif AE Vet Sci 10-Jul-2023
PMCID:PMC10385484
doi:10.3390/vetsci10070450
PMID:37505855
Treatment Effects of Natural Products on Inflammatory Bowel Disease In Vivo and Their Mechanisms: Based on Animal Experiments Zhou Y, Wang D, Yan W Nutrients 18-Feb-2023
PMCID:PMC9967064
doi:10.3390/nu15041031
PMID:36839389
Exercise Training and Verbena officinalis L. Affect Pre-Clinical and Histological Parameters Rodrigues Oliveira SM, Dias E, Girol AP, Silva H, Pereira MD Plants (Basel) 15-Nov-2022
PMCID:PMC9699298
doi:10.3390/plants11223115
PMID:36432843
A new strategy for osteoarthritis therapy: Inhibition of glycolysis Tan C, Li L, Han J, Xu K, Liu X Front Pharmacol 10-Nov-2022
PMCID:PMC9685317
doi:10.3389/fphar.2022.1057229
PMID:36438808
Plant–plant interactions determine natural restoration of plant biodiversity over time, in a degraded mined land Bashirzadeh M, Shefferson RP, Farzam M Ecol Evol 30-Apr-2022
PMCID:PMC9055295
doi:10.1002/ece3.8878
PMID:35509615
Protective effect of Sophora pachycarpa seed extract on carbon tetrachloride-induced toxicity in rats Aramjoo H, Mohammadparast-Tabas P, Farkhondeh T, Zardast M, Makhdoumi M, Samarghandian S, Kiani Z BMC Complement Med Ther 17-Mar-2022
PMCID:PMC8932233
doi:10.1186/s12906-022-03554-9
PMID:35300676
Do Uncommon Plant Phenolic Compounds Have Uncommon Properties? A Mini Review on Novel Flavonoids Carrillo JT, Borthakur D 12-Sep-2021
PMCID:PMC8445810
doi:10.1016/j.jobab.2021.09.001
Ethnobotany of the medicinal plants used by the ethnic communities of Kerman province, Southeast Iran Hosseini SH, Bibak H, Ghara AR, Sahebkar A, Shakeri A J Ethnobiol Ethnomed 28-Apr-2021
PMCID:PMC8082778
doi:10.1186/s13002-021-00438-z
PMID:33910616
Histone Deacetylase Inhibitory and Cytotoxic Activities of the Constituents from the Roots of Sophora Pachycarpa Soltani S, Boozari M, Nejad Ebrahimi S, Amin GR, Iranshahi M Iran J Pharm Res 01-Sep-2020
PMCID:PMC8019873
doi:10.22037/ijpr.2020.112442.13760
PMID:33841520
The osteogenesis of bacterial cellulose scaffold loaded with fisetin Vadaye Kheiry E, Parivar K, Baharara J, Fazly Bazzaz BS, Iranbakhsh A Iran J Basic Med Sci 01-Sep-2018
PMCID:PMC6272066
doi:10.22038/IJBMS.2018.25465.6296
PMID:30524698
Identification of Phlogacantholide C as a Novel ADAM10 Enhancer from Traditional Chinese Medicinal Plants Meineck M, Schuck F, Abdelfatah S, Efferth T, Endres K Medicines (Basel) 05-Dec-2016
PMCID:PMC5456242
doi:10.3390/medicines3040030
PMID:28930140
In-vitro Evaluation of Cytotoxic and Apoptogenic Properties of Sophora Pachycarpa Mousavi SH, Motaez M, Zamiri-Akhlaghi A, Emami SA, Tayarani-Najaran Z Iran J Pharm Res 01-Mar-2014
PMCID:PMC4157043
PMID:25237363
Annual Meeting Abstracts N/A J Med Toxicol 26-May-2012
PMCID:PMC3550232
doi:10.1007/s13181-012-0237-z
Enantiomeric Natural Products: Occurrence and Biogenesis Finefield JM, Sherman DH, Kreitman M, Williams RM Angew Chem Int Ed Engl 03-May-2012
PMCID:PMC3498912
doi:10.1002/anie.201107204
PMID:22555867

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 / Lupin alkaloids / Cytisine and derivatives
(+)-Cytisine 683511 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/S0031-9422(00)80699-8
(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 1747617 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1007/BF00574779
Pharmakon1600-01504027 6708720 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1007/BF00574779
https://doi.org/10.1007/BF00565838
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(+)-Matrine 285698 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown https://doi.org/10.1002/CBER.19340670119
5-(6-Oxo-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-5-yl)-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 3830379 Click to see C1CC2CN3C(CCC(C3=O)C4=CCC5C6CCCN7C6C(CCC7)CN5C4=O)C8C2N(C1)CCC8 492.70 unknown https://doi.org/10.1007/BF00574779
https://doi.org/10.2307/4117899
7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 618867 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4 246.35 unknown https://doi.org/10.1002/CBER.19340670119
Ammothamnine 114850 Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-] 264.36 unknown https://doi.org/10.1007/BF00565838
https://doi.org/10.1007/BF00574779
Matrine 91466 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown https://doi.org/10.1007/BF00565838
https://doi.org/10.1007/BF00574779
https://doi.org/10.1002/CBER.19340670119
Sophocarpine 115269 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4 246.35 unknown https://doi.org/10.1016/S0031-9422(00)80699-8
https://doi.org/10.1007/BF00574779
https://doi.org/10.1002/CBER.19340670119
https://doi.org/10.1007/BF00565838
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Sparteine 7014 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1007/BF00565838
https://doi.org/10.1007/BF00574779
(1S,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 5320360 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1007/BF00565838
https://doi.org/10.1007/BF00574779
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1007/BF00575192
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1007/BF00575192
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1007/BF00575192
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
(1R,9R,17S)-5-benzyl-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadeca-2,4-dien-6-one 21627980 Click to see C1CC2CN3C(=CC=C(C3=O)CC4=CC=CC=C4)C5C2N(C1)CCC5 334.50 unknown https://doi.org/10.1007/BF00574779
https://doi.org/10.1007/BF00565838
Neosophoramine 618327 Click to see C1CC2CN3C(=O)C=CC=C3C4C2N(C1)CCC4 244.33 unknown https://doi.org/10.1007/BF00574779
Sophoramine 169014 Click to see C1CC2CN3C(=O)C=CC=C3C4C2N(C1)CCC4 244.33 unknown https://doi.org/10.1007/BF00574779
https://doi.org/10.1007/BF00565838
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1007/BF00575192
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1007/BF00575192
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1007/BF00575192
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
Marini 73198 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown https://doi.org/10.1007/S10600-006-0050-5
Sophoraflavanone G 72936 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown https://doi.org/10.1007/S10600-006-0050-5
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF00575192
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1007/BF00575192
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1007/BF00575192

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