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Stephania yunnanensis

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID6440551c8f215512443841
Scientific name Stephania yunnanensis
Authority H.S.Lo
First published in Bull. Bot. Res., Harbin 2(1): 45 (1982)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 粉防己
Chinese 地不容
Chinese 云南地不容

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Stephania yunnanensis var. trichocalyx H.S.Lo & M.Yang Guihaia 8: 313 (1988)
Stephania yunnanensis var. yunnanensis Unknown

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001238650
Tropicos 50098943
KEW urn:lsid:ipni.org:names:901056-1
The Plant List tro-50098943
Open Tree Of Life 867899
NCBI Taxonomy 152371
IPNI 901056-1
GBIF 7268735
EOL 5125420

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_039657365.1 ASM3965736v1 Chromosome Chengdu University of Traditional Chinese Medicine 2024-05-17 150 774.57 Mb

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
Cepharanthine analogs mining and genomes of Stephania accelerate anti-coronavirus drug discovery Leng L, Xu Z, Hong B, Zhao B, Tian Y, Wang C, Yang L, Zou Z, Li L, Liu K, Peng W, Liu J, An Z, Wang Y, Duan B, Hu Z, Zheng C, Zhang S, Li X, Li M, Liu Z, Bi Z, He T, Liu B, Fan H, Song C, Tong Y, Chen S Nat Commun 20-Feb-2024
PMCID:PMC10879537
doi:10.1038/s41467-024-45690-5
PMID:38378731
Recent Applications of Protoberberines as Privileged Starting Materials for the Development of Novel Broad-Spectrum Antiviral Agents: A Concise Review (2017–2023) Valipour M, Zakeri Khatir Z, Abdollahi E, Ayati A ACS Pharmacol Transl Sci 28-Dec-2023
PMCID:PMC10789142
doi:10.1021/acsptsci.3c00292
PMID:38230282
Anti-cancer effect of palmatine through inhibition of the PI3K/AKT pathway in canine mammary gland tumor CMT-U27 cells Yoo MJ, Choi J, Jang YJ, Park SY, Seol JW BMC Vet Res 25-Oct-2023
PMCID:PMC10601335
doi:10.1186/s12917-023-03782-2
PMID:37880653
Alkaloid variations within the genus Stephania (Menispermaceae) in China Qi B, Li L, Huang R Heliyon 16-May-2023
PMCID:PMC10256896
doi:10.1016/j.heliyon.2023.e16344
PMID:37305452
The anti-inflammatory and analgesic activities of 2Br-Crebanine and Stephanine from Stephania yunnanenses H. S.Lo Cui L, Peng C, Li J, Cheng X, Fan X, Li J, Yang Z, Zhao Y, Ma Y Front Pharmacol 04-Jan-2023
PMCID:PMC9845599
doi:10.3389/fphar.2022.1092583
PMID:36686697
Cepharanthine: A Promising Old Drug against SARS‐CoV‐2 Fan H, He S, Han P, Hong B, Liu K, Li M, Wang S, Tong Y Adv Biol (Weinh) 01-Jul-2022
PMCID:PMC9350037
doi:10.1002/adbi.202200148
PMID:35775953
A Comprehensive Review on the Chemical Properties, Plant Sources, Pharmacological Activities, Pharmacokinetic and Toxicological Characteristics of Tetrahydropalmatine Du Q, Meng X, Wang S Front Pharmacol 26-Apr-2022
PMCID:PMC9086320
doi:10.3389/fphar.2022.890078
PMID:35559252
Palmatine Attenuates Metastatic Lung Colonization of Triple Negative Breast Cancer Cells Ativui S, Danquah CA, Ossei PP, Ofori M Front Pharmacol 13-Apr-2022
PMCID:PMC9043321
doi:10.3389/fphar.2022.853230
PMID:35496301
Jatrorrhizine: A Review of Sources, Pharmacology, Pharmacokinetics and Toxicity Zhong F, Chen Y, Chen J, Liao H, Li Y, Ma Y Front Pharmacol 13-Jan-2022
PMCID:PMC8793695
doi:10.3389/fphar.2021.783127
PMID:35095493
The Analgesic Properties of Corydalis yanhusuo Alhassen L, Dabbous T, Ha A, Dang LH, Civelli O Molecules 10-Dec-2021
PMCID:PMC8704877
doi:10.3390/molecules26247498
PMID:34946576
Sinoacutine inhibits inflammatory responses to attenuates acute lung injury by regulating NF-κB and JNK signaling pathways Zhao Y, Cui L, Yang XX, Sun X, Liu Y, Yang Z, Zhu L, Peng C, Li D, Cai J, Ma Y BMC Complement Med Ther 20-Nov-2021
PMCID:PMC8605577
doi:10.1186/s12906-021-03458-0
PMID:34801005
Study of Nutraceuticals and Phytochemicals for the Management of Alzheimer's Disease: A Review Ahmad SS, Khalid M, Kamal MA, Younis K Curr Neuropharmacol 15-Nov-2021
PMCID:PMC9185787
doi:10.2174/1570159X19666210215122333
PMID:33588732
Palmatine, a Bioactive Protoberberine Alkaloid Isolated from Berberis cretica, Inhibits the Growth of Human Estrogen Receptor-Positive Breast Cancer Cells and Acts Synergistically and Additively with Doxorubicin Grabarska A, Wróblewska-Łuczka P, Kukula-Koch W, Łuszczki JJ, Kalpoutzakis E, Adamczuk G, Skaltsounis AL, Stepulak A Molecules 15-Oct-2021
PMCID:PMC8538708
doi:10.3390/molecules26206253
PMID:34684834
Interpol review of controlled substances 2016–2019 Jones NS, Comparin JH Forensic Sci Int Synerg 24-May-2020
PMCID:PMC7770462
doi:10.1016/j.fsisyn.2020.01.019
PMID:33385148
Countercurrent Separation of Natural Products: An Update Friesen JB, McAlpine JB, Chen SN, Pauli GF J Nat Prod 15-Jul-2015
PMCID:PMC4517501
doi:10.1021/np501065h
PMID:26177360

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 / Aporphines
(R)-Roemerine 235224 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown https://doi.org/10.1016/S0031-9422(00)80650-0
> Alkaloids and derivatives / Proaporphines
5',6'-Dimethoxy-2',3',8',8a'-tetrahydro-1'h,4h-spiro[cyclohexa-2,5-diene-1,7'-cyclopenta[ij]isoquinolin]-4-one 98455 Click to see 297.30 unknown https://doi.org/10.1080/14786410903125393
Stepharine 193686 Click to see 297.30 unknown https://doi.org/10.1016/S0031-9422(00)80650-0
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(-)-Corydalmine 161665 Click to see 341.40 unknown https://doi.org/10.1016/S0031-9422(00)80650-0
Dehydrocorydalmine 3083983 Click to see COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC(=C(C4=C3)OC)O)OC 338.40 unknown https://doi.org/10.1016/S0031-9422(00)80650-0
Palmatine 19009 Click to see 352.40 unknown https://doi.org/10.1016/S0031-9422(00)80650-0
Stepharanine 10358881 Click to see 324.30 unknown https://doi.org/10.1016/S0031-9422(00)80650-0
Stepholidine 6917970 Click to see 327.40 unknown https://doi.org/10.1016/S0031-9422(00)80650-0
> Benzenoids / Phenanthrenes and derivatives
Salutaridine 5408233 Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=C3C(=C(C=C4)OC)O)OC 327.40 unknown https://doi.org/10.1016/S0031-9422(00)80650-0

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