Hypecoum erectum - Unknown
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Internal ID UUID64404a16120af108537352
Scientific name Hypecoum erectum
Authority L.
First published in Sp. Pl. : 124 (1753)

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Synonyms Top

Scientific name Authority First published in
Chiazospermum erectum (L.) Bernh. Linnaea 12: 662 (1838)
Hypecoum millefolium H.Lév. & Vaniot Bull. Acad. Int. Géogr. Bot. 17(210-211): iii (1907)

Common names Top

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Language Common/alternative name
Azerbaijani dikduran dəlitərə
Chinese 黄花草
Chinese 麦黄草
Chinese 雪里青
Chinese 中亚天仙子
Chinese 角茴香
Chinese 咽喉草
Chinese 直立角茴香
Chinese 细叶角茴香

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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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Inner Mongolia
      • Manchuria
      • Xinjiang
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001090418
Tropicos 24000575
KEW urn:lsid:ipni.org:names:673235-1
The Plant List tro-24000575
Open Tree Of Life 5728017
Observations.org 124455
NCBI Taxonomy 1655241
IPNI 673235-1
iNaturalist 779063
GBIF 3601784
EPPO HCYER
Elurikkus 382513
Wikipedia Hypecoum_erectum

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
Traditional Tibetan medicine: therapeutic potential in lung diseases Li C, Li Y, Huang X, Li S, Sangji K, Gu R Front Pharmacol 18-Mar-2024
PMCID:PMC10986185
doi:10.3389/fphar.2024.1365911
PMID:38567353
Extreme Reconfiguration of Plastid Genomes in Papaveraceae: Rearrangements, Gene Loss, Pseudogenization, IR Expansion, and Repeats Cao J, Wang H, Cao Y, Kan S, Li J, Liu Y Int J Mol Sci 14-Feb-2024
PMCID:PMC10888665
doi:10.3390/ijms25042278
PMID:38396955
Effect of moderate livestock grazing on soil and vegetation characteristics in zokor mounds of different ages Zhang Q, Lu Y, Zhang C, Yao B, Su J Sci Rep 01-Aug-2023
PMCID:PMC10393963
doi:10.1038/s41598-023-39530-7
PMID:37528212
Traditional Tibetan medicine to fight against COVID-19: Basic theory and therapeutic drugs Zhang K, Wang L, Peng J, Sangji K, Luo Y, Zeng Y, Zeweng Y, Fan G Front Pharmacol 16-Feb-2023
PMCID:PMC9978713
doi:10.3389/fphar.2023.1098253
PMID:36874035
Exploring the Anti-inflammatory Effects of Protopine Total Alkaloids of Macleaya Cordata (Willd.) R. Br. Dong Z, Wang YH, Tang ZS, Li CH, Jiang T, Yang ZH, Zeng JG Front Vet Sci 05-Jul-2022
PMCID:PMC9294607
doi:10.3389/fvets.2022.935201
PMID:35865876
Progress in ICP-MS Analysis of Minerals and Heavy Metals in Traditional Medicine Chen W, Yang Y, Fu K, Zhang D, Wang Z Front Pharmacol 28-Jun-2022
PMCID:PMC9274010
doi:10.3389/fphar.2022.891273
PMID:35837276
Hypeisoxazole A, a Racemic Pair of Tetrahydroisoxazole-Fused Benzylisoquinoline Alkaloids from Hypecoum erectum and Structural Revision of Hypecoleptopine Sun PT, Cao YG, Xue GM, Li M, Zhang CL, Zhao F, Cao ZY, Wang D, Gustafson KR, Zheng XK, Feng WS, Chen H Org Lett 11-Feb-2022
PMCID:PMC10430687
doi:10.1021/acs.orglett.2c00096
PMID:35147434
Ligiamycins A and B, Decalin-Amino-Maleimides from the Co-Culture of Streptomyces sp. and Achromobacter sp. Isolated from the Marine Wharf Roach, Ligia exotica Lim HJ, An JS, Bae ES, Cho E, Hwang S, Nam SJ, Oh KB, Lee SK, Oh DC Mar Drugs 18-Jan-2022
PMCID:PMC8878407
doi:10.3390/md20020083
PMID:35200613
Identification and Quantification, Metabolism and Pharmacokinetics, Pharmacological Activities, and Botanical Preparations of Protopine: A Review Huang W, Kong L, Cao Y, Yan L Molecules 30-Dec-2021
PMCID:PMC8746401
doi:10.3390/molecules27010215
PMID:35011447
The Treatment of Cholecystitis and Cholelithiasis by Tibetan Medicine Pan L, Gao J, Han Y, Shi Y, Tang X, Pu L, Lai X, Dongzhu R, Zhang J, Xiangmao Q, Pengcuo J Evid Based Complement Alternat Med 30-Sep-2021
PMCID:PMC8497101
doi:10.1155/2021/9502609
PMID:34630620
Nigritanine as a New Potential Antimicrobial Alkaloid for the Treatment of Staphylococcus aureus-Induced Infections Casciaro B, Calcaterra A, Cappiello F, Mori M, Loffredo MR, Ghirga F, Mangoni ML, Botta B, Quaglio D Toxins (Basel) 01-Sep-2019
PMCID:PMC6783983
doi:10.3390/toxins11090511
PMID:31480508
Elaborated pollen packaging and dispensing mechanism induced by petal architecture from a Papaveraceae species Yang S, Chu G, Shi X, Wang S PeerJ 11-Jun-2019
PMCID:PMC6568250
doi:10.7717/peerj.7066
PMID:31218126
Natural Medicines Used in the Traditional Tibetan Medical System for the Treatment of Liver Diseases Li Q, Li HJ, Xu T, Du H, Huan Gang CL, Fan G, Zhang Y Front Pharmacol 30-Jan-2018
PMCID:PMC5797630
doi:10.3389/fphar.2018.00029
PMID:29441019
Secondary Metabolites from the Leaves of the Medicinal Plant Goldenseal (Hydrastis canadensis) Leyte-Lugo M, Britton ER, Foil DH, Brown AR, Todd DA, Rivera-Chávez J, Oberlies NH, Cech NB Phytochem Lett 15-Apr-2017
PMCID:PMC5516942
doi:10.1016/j.phytol.2017.03.012
PMID:28736584
Traditional use and management of NTFPs in Kangchenjunga Landscape: implications for conservation and livelihoods Uprety Y, Poudel RC, Gurung J, Chettri N, Chaudhary RP J Ethnobiol Ethnomed 03-May-2016
PMCID:PMC4855762
doi:10.1186/s13002-016-0089-8
PMID:27142597

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 / Protoberberine alkaloids and derivatives
Coptisine 72322 Click to see C1C[N+]2=C(C=C3C=CC4=C(C3=C2)OCO4)C5=CC6=C(C=C51)OCO6 320.30 unknown https://doi.org/10.1007/BF00580105
> Alkaloids and derivatives / Protopine alkaloids
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown https://doi.org/10.1007/BF00580073
https://doi.org/10.1007/BF00580105
> Organoheterocyclic compounds / Isoquinolines and derivatives
Corydamine 5316094 Click to see CNCCC1=CC2=C(C=C1C3=NC=C4C(=C3)C=CC5=C4OCO5)OCO2 350.40 unknown https://doi.org/10.1007/BF00580105
> Organoheterocyclic compounds / Tetrahydroisoquinolines
6'-Methylspiro[6,9-dihydro-[1,3]dioxolo[4,5-h]isochromene-7,5'-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinoline] 21632927 Click to see CN1CCC2=CC3=C(C=C2C14CC5=C(CO4)C6=C(C=C5)OCO6)OCO3 353.40 unknown https://doi.org/10.1007/BF00580073
Hypecorinine 13997263 Click to see CN1CCC2=CC3=C(C=C2C14C(=O)C5=C(CO4)C6=C(C=C5)OCO6)OCO3 367.40 unknown https://doi.org/10.1007/BF00580073
Hyperectine 137796412 Click to see CN1CCC2=CC3=C(C=C2C14CC5=C(C4C6=C(C(=O)NC6=O)N)C7=C(C=C5)OCO7)OCO3 447.40 unknown https://doi.org/10.1007/BF00629644
https://doi.org/10.1007/BF00580073
Isohyperectine 15765611 Click to see CN1CCC2=CC3=C(C=C2C14CC5=C(C4C6=C(C(=O)NC6=O)N)C7=C(C=C5)OCO7)OCO3 447.40 unknown https://doi.org/10.1007/BF00629644

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