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Internal ID UUID64400516b7a1c562656530
Scientific name Stephania rotunda
Authority Lour.
First published in Fl. Cochinch. : 608 (1790)

Ethnobotanical Use Top

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General Uses Top

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Food and beverages (non-medicinal):
The tuberous root is processed into a starch flour used in East and Southeast Asian cuisines, most commonly as a wheat-flour substitute in noodles and batters and as a frying and breading starch. The product is marketed as “shan yao fen” (Dioscorea) in some Chinese markets but is botanically sourced from Stephania rotunda. In Chinese commerce, Stephania-derived starch is sometimes blended with Dioscorea oppositifolia starch and labeled “shan yao fen,” creating potential consumer confusion.

Scientific/model-organism use:
Stephania rotunda tubers are used as a raw material for isolation of the bisbenzylisoquinoline alkaloid tetrandrine. This compound serves as a reference standard in phytochemical studies and as a pharmacological probe in cell biology. Published protocols describe extraction and high-performance liquid chromatography (HPLC) quantification for quality control in research workflows; total alkaloid content and tetrandrine concentrations are commonly reported. Tissue culture systems derived from S. rotunda are used to investigate alkaloid biosynthesis and callus induction.

Properties relevant to use:
The tuber starch exhibits high amylose content, contributing to rapid retrogradation and firm gel texture in cooked products, which is desirable for noodles and fried coatings. No documented wood, fiber, colorant, tannin, fragrance, or resin uses are reported. Tetrandrine’s isoquinoline structure and reported pharmacological activity underpin its role as a laboratory probe; no non-medicinal commercial applications of this alkaloid are established.

Standards and regulation:
tuber starch is subject to general national food starch standards (e.g., ISO 1666 for starch composition; national food additives labeling and purity specifications), and tetrandrine isolated for research follows laboratory reagent guidelines.

Sustainability and sourcing:
harvest of wild tubers carries a risk of overexploitation; commercial starch supply is inconsistent due to taxonomic confusion with Dioscorea species and limited cultivated material. Standardized, lab-grade tetrandrine is produced in specialized extraction facilities; research use is generally less impacted than food starch supply.

Synonyms Top

Scientific name Authority First published in
Menispermum roxburghii Spreng. Syst. Veg. 2: 155 (1825)
Stephania hexandra Miers Ann. Mag. Nat. Hist. , ser. 2, 7: 40 (1851)
Cissampelos glabra Roxb. Fl. Ind. ed. 1832 , 3: 840 (1832)
Clypea glabra (Roxb.) Wight & Arn. ex Voigt Hort. Suburb. Calcutt. : 330 (1845)
Clypea rotunda Steud. Nomencl. Bot. , ed. 2, 1: 387 (1840)
Cocculus finlaysonianus Wall. Numer. List [Wallich] n. 4974. [1831-32]
Stephania glabra (Roxb.) Miers Ann. Mag. Nat. Hist. , ser. 2, 18: 14 (1866)
Menispermum japonicum Roxb. ex DC. Syst. Nat. 1: 516 (1817)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • West Himalaya
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000505063
Tropicos 20600012
KEW urn:lsid:ipni.org:names:581482-1
Open Tree Of Life 576462
NCBI Taxonomy 461634
IPNI 581482-1
GBIF 5592764
Elurikkus 552682
USDA GRIN 35530
CMAUP NPO24050

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
Exploring the Therapeutic Potential of Traditional Antimalarial and Antidengue Plants: A Mechanistic Perspective Kamaraj C, Ragavendran C, Prem P, Naveen Kumar S, Ali A, Kazmi A, Ullah A, Chandra Satish Kumar R, Khan SU, Luna-Arias JP, Mashwani ZU, Balasubramani G, Rehman SU Can J Infect Dis Med Microbiol 28-Oct-2023
PMCID:PMC10625492
doi:10.1155/2023/1860084
PMID:37927532
Isoliensinine from Cissampelos pariera rhizomes exhibits potential gametocytocidal and anti-malarial activities against Plasmodium falciparum clinical isolates Muema JM, Mutunga JM, Obonyo MA, Getahun MN, Mwakubambanya RS, Akala HM, Cheruiyot AC, Yeda RA, Juma DW, Andagalu B, Johnson JL, Roth AL, Bargul JL Malar J 20-May-2023
PMCID:PMC10199507
doi:10.1186/s12936-023-04590-7
PMID:37208735
Oxidative stress, free radicals and antioxidants: potential crosstalk in the pathophysiology of human diseases Chaudhary P, Janmeda P, Docea AO, Yeskaliyeva B, Abdull Razis AF, Modu B, Calina D, Sharifi-Rad J Front Chem 10-May-2023
PMCID:PMC10206224
doi:10.3389/fchem.2023.1158198
PMID:37234200
Current status and future challenges in extraction, purification and identification of Cepharanthine (a potential drug against COVID-19) Wang Y, Zhou X, Wei S, Wang G, Xi J Sep Purif Technol 29-Dec-2022
PMCID:PMC9797411
doi:10.1016/j.seppur.2022.123038
PMID:36593875
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
千金藤素抗新冠病毒研究进展 N/A Nan Fang Yi Ke Da Xue Xue Bao 20-Jun-2022
PMCID:PMC9257352
doi:10.12122/j.issn.1673-4254.2022.06.22
PMID:35790449
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
Docking Analysis of Some Bioactive Compounds from Traditional Plants against SARS-CoV-2 Target Proteins Abd El-Aziz NM, Khalifa I, Darwish AM, Badr AN, Aljumayi H, Hafez ES, Shehata MG Molecules 20-Apr-2022
PMCID:PMC9100219
doi:10.3390/molecules27092662
PMID:35566014
Potential Therapeutic Applications of Plant-Derived Alkaloids against Inflammatory and Neurodegenerative Diseases Aryal B, Raut BK, Bhattarai S, Bhandari S, Tandan P, Gyawali K, Sharma K, Ranabhat D, Thapa R, Aryal D, Ojha A, Devkota HP, Parajuli N Evid Based Complement Alternat Med 09-Mar-2022
PMCID:PMC8926539
doi:10.1155/2022/7299778
PMID:35310033
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
Distribution of Therapeutic Efficacy of Ranunculales Plants Used by Ethnic Minorities on the Phylogenetic Tree of Chinese Species Hao DC, Zhang Y, He CN, Xiao PG Evid Based Complement Alternat Med 12-Jan-2022
PMCID:PMC8769838
doi:10.1155/2022/9027727
PMID:35069772
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
Vasorelaxant-Mediated Antihypertensive Effect of the Leaf Aqueous Extract from Stephania abyssinica (Dillon & A. Rich) Walp (Menispermaceae) in Rat Fodem C, Nguelefack-Mbuyo EP, Ndjenda II MK, Kamanyi A, Nguelefack TB Biomed Res Int 08-Oct-2021
PMCID:PMC8519676
doi:10.1155/2021/4730341
PMID:34660790
Recent Progress on Biological Activity of Amaryllidaceae and Further Isoquinoline Alkaloids in Connection with Alzheimer’s Disease Cahlíková L, Vrabec R, Pidaný F, Peřinová R, Maafi N, Mamun AA, Ritomská A, Wijaya V, Blunden G Molecules 29-Aug-2021
PMCID:PMC8434202
doi:10.3390/molecules26175240
PMID:34500673
Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F Malar J 25-Aug-2021
PMCID:PMC8390284
doi:10.1186/s12936-021-03866-0
PMID:34433465

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
1,2-Dimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-10-ol 494626 Click to see COC1=C(C2=C3C(CC4=C2C=C(C=C4)O)NCCC3=C1)OC 297.30 unknown https://doi.org/10.1248/YAKUSHI1947.86.10_871
Roemerine 119204 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown via CMAUP database
Tsuduranine 363262 Click to see COC1=C(C2=C3C(CC4=C2C=C(C=C4)O)NCCC3=C1)OC 297.30 unknown https://doi.org/10.1248/YAKUSHI1947.86.10_871
> Alkaloids and derivatives / Hasubanan alkaloids
(-)-Cepharamine 5315777 Click to see 329.40 unknown https://doi.org/10.1021/NP50038A038
> Alkaloids and derivatives / Proaporphines
N-Acetylstepharine 759300 Click to see 339.40 unknown https://doi.org/10.1248/YAKUSHI1947.101.10_951
Pronuciferine 200480 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC 311.40 unknown via CMAUP database
Pronuciferine, (-)- 793841 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC 311.40 unknown via CMAUP database
Stepharine 193686 Click to see 297.30 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(13aS)-2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-11-ol 12442995 Click to see 371.40 unknown https://doi.org/10.1248/YAKUSHI1947.86.10_871
2,3,10-trimethoxy-6,7-dihydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-9-one 101280139 Click to see 338.40 unknown via CMAUP database
2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-11-ol 12442994 Click to see COC1=C(C=C2C3CC4=CC(=C(C(=C4CN3CCC2=C1)OC)OC)O)OC 371.40 unknown https://doi.org/10.1248/YAKUSHI1947.86.10_871
D-Tetrahydropalmatine 969488 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown via CMAUP database
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 via CMAUP database
Hydroxyl-palmatine 46216998 Click to see 368.40 unknown via CMAUP database
Palmatine 19009 Click to see 352.40 unknown via CMAUP database
Stepharanine 10358881 Click to see 324.30 unknown via CMAUP database
Stepholidine 6917970 Click to see 327.40 unknown via CMAUP database
Tetrahydropalmatine 72301 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown via CMAUP database
> Lignans, neolignans and related compounds
(14R,27R)-22,33-dimethoxy-13-methyl-2,5,7,20-tetraoxa-13,28-diazaoctacyclo[25.6.2.216,19.13,10.121,25.04,8.031,35.014,39]nonatriaconta-1(33),3(39),4(8),9,16(38),17,19(37),21,23,25(36),31,34-dodecaene 44559014 Click to see 592.70 unknown https://doi.org/10.1080/14786410903395624
22,33-Dimethoxy-13-methyl-2,5,7,20-tetraoxa-13,28-diazaoctacyclo[25.6.2.216,19.13,10.121,25.04,8.031,35.014,39]nonatriaconta-1(33),3(39),4(8),9,16(38),17,19(37),21,23,25(36),31,34-dodecaene 14488280 Click to see 592.70 unknown https://doi.org/10.1080/14786410903395624
33-Methoxy-13,28-dimethyl-2,5,7,20-tetraoxa-13,28-diazaoctacyclo[25.6.2.216,19.13,10.121,25.04,8.031,35.014,39]nonatriaconta-1(33),3(39),4(8),9,16(38),17,19(37),21,23,25(36),31,34-dodecaen-22-ol 9808633 Click to see 592.70 unknown https://doi.org/10.1080/14786410903395624
Cepharanoline 5315779 Click to see 592.70 unknown https://doi.org/10.1080/14786410903395624
Fangchinoline 73481 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown https://doi.org/10.1080/14786410903395624
Isofangchinoline 321937 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown https://doi.org/10.1080/14786410903395624
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
(11R,26R)-4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.213,16.13,7.118,22.011,36.026,33]hexatriaconta-1(31),3(36),4,6,13,15,18(33),19,21,28(32),29,34-dodecaene 21582963 Click to see 608.70 unknown via CMAUP database
(11R,27R)-4,5,20,21-tetramethoxy-10,26-dimethyl-2,18-dioxa-10,26-diazaheptacyclo[27.2.2.13,7.113,17.119,23.011,36.027,34]hexatriaconta-1(32),3(36),4,6,13(35),14,16,19(34),20,22,29(33),30-dodecaene 53486320 Click to see 622.70 unknown via CMAUP database
Cycleanine 121313 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC=C(O3)C=C7)N(CCC6=CC(=C5OC)OC)C)OC)OC 622.70 unknown via CMAUP database
> Organosulfur compounds / Thiocarbonyl compounds / Thioaldehydes / Thioaldehyde s-oxides
thiopropanal S-oxide 441491 Click to see 90.15 unknown via CMAUP database

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