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Hyoscyamus pusillus

Hyoscyamus pusillus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644041229ff24389611899
Scientific name Hyoscyamus pusillus
Authority L.
First published in Sp. Pl. 1: 180. 1753.

Description Top

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Synonyms Top

Scientific name Authority First published in
Hyoscyamus micranthus Ledeb. ex G.Don Gen. Hist. 4: 472. 1837
Hyoscyamus pungens Griseb. Spic. Fl. Rumel. 2(4): 52. 1844

Common names Top

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Language Common/alternative name
Arabic بنج صغير
Arabic بنج صفاري
Azerbaijani kiçik batbat
Persian بذرالبنج کوتاه
Russian Белена крошечная
Chinese 中亚天仙子
Chinese 帕卡苯格哈兰特
Chinese 矮天仙子
Chinese 阿拉沙名多那

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

Area

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© OpenStreetMap
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Arabian Peninsula
      • Kuwait
      • Saudi Arabia
    • Caucasus
      • Transcaucasus
    • China
      • Tibet
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Western Asia
      • Afghanistan
      • Iran
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001021869
Tropicos 29604613
KEW urn:lsid:ipni.org:names:815947-1
The Plant List kew-2857458
Open Tree Of Life 434585
Observations.org 140474
NCBI Taxonomy 540805
IPNI 815947-1
GBIF 3802521
EPPO HSYPU
EOL 2894390
Elurikkus 417036
USDA GRIN 19533
CMAUP NPO10059

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
Cross-cultural ethnobotany of the Baltis and Shinas in the Kharmang district, Trans-Himalaya India-Pakistan border Hussain B, Abbas Z, Alam J, Harun N, Khan SM, Ahmad Z, Han H, Yoo S, Raposo A Heliyon 27-Mar-2024
PMCID:PMC10998220
doi:10.1016/j.heliyon.2024.e28613
PMID:38586350
Harmony in nature: understanding the cultural and ecological aspects of plant use in Ladakh Angmo K, Adhikari BS, Bussmann RW, Rawat GS J Ethnobiol Ethnomed 14-Mar-2024
PMCID:PMC10938689
doi:10.1186/s13002-024-00670-3
PMID:38486266
The evolution of ephemeral flora in Xinjiang, China: insights from plastid phylogenomic analyses of Brassicaceae Xiao TW, Song F, Vu DQ, Feng Y, Ge XJ BMC Plant Biol 15-Feb-2024
PMCID:PMC10868009
doi:10.1186/s12870-024-04796-0
PMID:38360561
Root Morphology and Biomass Allocation of 50 Annual Ephemeral Species in Relation to Two Soil Condition Wang T, Huang L, Zhang X, Wang M, Tan D Plants (Basel) 23-Sep-2022
PMCID:PMC9570868
doi:10.3390/plants11192495
PMID:36235362
Melatonin-Induced Inhibition of Shiraia Hypocrellin A Biosynthesis Is Mediated by Hydrogen Peroxide and Nitric Oxide Wang W, Huang Q, Wang Y, Li X, Wang J, Zheng L J Fungi (Basel) 10-Aug-2022
PMCID:PMC9410495
doi:10.3390/jof8080836
PMID:36012825
A Systematic Review of Traditionally Used Herbs and Animal-Derived Products as Potential Analgesics Rengasamy KR, Mahomoodally MF, Joaheer T, Zhang Y Curr Neuropharmacol 01-Apr-2021
PMCID:PMC8206464
doi:10.2174/1570159X18666200808151522
PMID:32781962
Preserving a Comprehensive Vegetation Knowledge Base – An Evaluation of Four Historical Soviet Vegetation Maps of the Western Pamirs (Tajikistan) Vanselow KA, Samimi C, Breckle SW PLoS One 16-Feb-2016
PMCID:PMC4755548
doi:10.1371/journal.pone.0148930
PMID:26881428
Comparative ethnobotany of the Wakhi agropastoralist and the Kyrgyz nomads of Afghanistan Soelberg J, Jäger AK J Ethnobiol Ethnomed 06-Jan-2016
PMCID:PMC4702329
doi:10.1186/s13002-015-0063-x
PMID:26739280
The Effects of Leaf Roughness, Surface Free Energy and Work of Adhesion on Leaf Water Drop Adhesion Wang H, Shi H, Li Y, Wang Y PLoS One 08-Sep-2014
PMCID:PMC4157819
doi:10.1371/journal.pone.0107062
PMID:25198355
A Checklist of the Flora of Shanjan Protected Area, East Azerbaijan Province, NW Iran Bibalani GH, Taheri E Afr J Tradit Complement Altern Med 03-Oct-2013
PMCID:PMC3847374
doi:10.4314/ajtcam.v10i6.1
PMID:24311859
Antibacterial and COX-1 Inhibitory Effect of Medicinal Plants from the Pamir Mountains, Afghanistan Jeppesen AS, Soelberg J, Jäger AK Plants (Basel) 24-Oct-2012
PMCID:PMC4844265
doi:10.3390/plants1020074
PMID:27137641
Alkaloids ofHyoscyamus pusillus S. F. Aripova Springer Science and Business Media LLC 30-Nov-2004
doi:10.1007/BF00714933

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Tropane alkaloids
(S)-((1R,3r,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl) 3-hydroxy-2-phenylpropanoate 6931560 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1007/BF00714933
8-Methyl-8-azabicyclo[3.2.1]octan-3-ol 8424 Click to see CN1C2CCC1CC(C2)O 141.21 unknown https://doi.org/10.1007/BF00714933
https://doi.org/10.1007/BF00714933
Apoatropine 64695 Click to see CN1C2CCC1CC(C2)OC(=O)C(=C)C3=CC=CC=C3 271.35 unknown https://doi.org/10.1007/BF00714933
L-Hyoscyamine 3661 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1007/BF00714933
L-Hyoscyamine 64692 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1007/BF00714933
> Benzenoids / Benzene and substituted derivatives / Styrenes
(9-Methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl) 2-phenylprop-2-enoate 4486617 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(=C)C4=CC=CC=C4 285.34 unknown https://doi.org/10.1007/BF00714933
[(1S,2R,4R,5R)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl] 2-phenylprop-2-enoate 98104494 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(=C)C4=CC=CC=C4 285.34 unknown https://doi.org/10.1007/BF00714933
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
2-[[3-Hydroxy-5-(10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxolan-3-yl]methoxy]-6-methyloxane-3,4,5-triol 75034135 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(CO7)(COC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)OC1 855.00 unknown https://doi.org/10.1007/BF00714933
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(-)-Scopolamine 5184 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown https://doi.org/10.1007/BF00714933
[(2R,4S)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl] (2R)-3-hydroxy-2-phenylpropanoate 134767951 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown https://doi.org/10.1007/BF00714933
Tropic acid ester with scopine 153311 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown https://doi.org/10.1007/BF00714933
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
Nigericin 34230 Click to see CC1CCC(OC1C(C)C(=O)O)CC2CC(C(C3(O2)C(CC(O3)(C)C4CCC(O4)(C)C5C(CC(O5)C6C(CC(C(O6)(CO)O)C)C)C)C)C)OC 725.00 unknown https://doi.org/10.1007/BF00714933
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3-[4-[(R)-2,3-Dihydroxy-3-methylbutyloxy]phenyl]-2-propene-1-ol 23642603 Click to see CC(C)(C(COC1=CC=C(C=C1)C=CCO)O)O 252.31 unknown https://doi.org/10.1007/BF00714933
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-5-hydroxy-2-(2-hydroxy-4-methoxyphenyl)-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 101326868 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=C(C=C(C=C4)OC)O)O)C 436.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
ent-Gallocatechin 4'-methyl ether 10087345 Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(C=C(C=C3O2)O)O)O)O 320.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
3,5,7-trihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 101713180 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 508.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
2'-Hydroxygenistein 5282074 Click to see C1=CC(=C(C=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)O 286.24 unknown via CMAUP database
6-(1,1-Dimethylallyl)genistein 44257285 Click to see CC(C)(C=C)C1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O 338.40 unknown via CMAUP database
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Daidzin 107971 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown via CMAUP database
Genistin 5281377 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-[7-Hydroxy-5-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-3-phenylprop-2-en-1-one 5256732 Click to see CC(=CCCC1(C=CC2=C(C=C(C(=C2O1)C(=O)C=CC3=CC=CC=C3)O)OC)C)C 404.50 unknown https://doi.org/10.1007/BF00714933

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