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Stephania suberosa

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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 UUID644005166c204264603162
Scientific name Stephania suberosa
Authority Forman
First published in Kew Bull. 34: 563 (1980)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Thai บอระเพ็ดพุงช้าง

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000505056
KEW urn:lsid:ipni.org:names:581489-1
The Plant List kew-2601342
Open Tree Of Life 6130074
NCBI Taxonomy 1924985
IPNI 581489-1
GBIF 5592748
Elurikkus 552676
Wikipedia Stephania_suberosa

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
Activity of Cinnamic Acid Derivatives with 4-Chloro-2-mercaptobenzenesulfonamide Moiety against Clinical HLAR and VRE Enterococcus spp. Hałasa R, Bułakowska A, Sławiński J, Smoktunowicz M, Rapacka-Zdończyk A, Mizerska U Antibiotics (Basel) 02-Dec-2023
PMCID:PMC10741072
doi:10.3390/antibiotics12121691
PMID:38136725
Stephania suberosa Forman extract synergistically inhibits ampicillin- and vancomycin-resistant Enterococcus faecium Teethaisong Y, Chueakwon P, Poolpol K, Ayamuang IO, Suknasang S, Apinundecha C, Eumkeb G Saudi J Biol Sci 16-Jan-2023
PMCID:PMC9876979
doi:10.1016/j.sjbs.2023.103557
PMID:36712182
Characterization and Potentiating Effects of the Ethanolic Extracts of the Red Seaweed Gracillaria sp. on the Activity of Carbenicillin against Vibrios Lu WJ, Tsui YC, Chang CJ, Hsu PH, Huang MY, Lai M, Lian YW, Chen CL, Lin HT ACS Omega 09-Dec-2022
PMCID:PMC9773811
doi:10.1021/acsomega.2c05288
PMID:36570316
Genome analysis of secondary metabolite‑biosynthetic gene clusters of Photorhabdus akhurstii subsp. akhurstii and its antibacterial activity against antibiotic-resistant bacteria Muangpat P, Meesil W, Ngoenkam J, Teethaisong Y, Thummeepak R, Sitthisak S, Tandhavanant S, Chantratita N, Bode HB, Vitta A, Thanwisai A PLoS One 21-Sep-2022
PMCID:PMC9491552
doi:10.1371/journal.pone.0274956
PMID:36129957
Effects of Traditional Chinese Medicine and its Active Ingredients on Drug-Resistant Bacteria Li J, Feng S, Liu X, Jia X, Qiao F, Guo J, Deng S Front Pharmacol 02-Jun-2022
PMCID:PMC9204478
doi:10.3389/fphar.2022.837907
PMID:35721131
Computational study and in vitro alpha-glucosidase inhibitory effects of medicinal plants from a Thai folk remedy Eawsakul K, Panichayupakaranant P, Ongtanasup T, Warinhomhoun S, Noonong K, Bunluepuech K Heliyon 29-Sep-2021
PMCID:PMC8488491
doi:10.1016/j.heliyon.2021.e08078
PMID:34632145
Antibacterial activity of Xenorhabdus and Photorhabdus isolated from entomopathogenic nematodes against antibiotic-resistant bacteria Muangpat P, Suwannaroj M, Yimthin T, Fukruksa C, Sitthisak S, Chantratita N, Vitta A, Thanwisai A PLoS One 05-Jun-2020
PMCID:PMC7274414
doi:10.1371/journal.pone.0234129
PMID:32502188
Celery (Apium graveolens) as a potential antibacterial agent and its effect on cytokeratin-17 and other healing promoters in skin wounds infected with methicillin-resistant Staphylococcus aureus Prakoso YA, Rini CS, Rahayu A, Sigit M, Widhowati D Vet World 09-May-2020
PMCID:PMC7311862
doi:10.14202/vetworld.2020.865-871
PMID:32636580
Transport of Phage in Melon Plants and Inhibition of Progression of Bacterial Fruit Blotch Rahimi-Midani A, Choi TJ Viruses 23-Apr-2020
PMCID:PMC7232510
doi:10.3390/v12040477
PMID:32340158
In Vitro Antibacterial Activity and Mechanism of Vanillic Acid against Carbapenem-Resistant Enterobacter cloacae Qian W, Fu Y, Liu M, Wang T, Zhang J, Yang M, Sun Z, Li X, Li Y Antibiotics (Basel) 13-Nov-2019
PMCID:PMC6963763
doi:10.3390/antibiotics8040220
PMID:31766130
Anti-inflammatory, anti-cholinergic and cytotoxic effects of Sida rhombifolia Mah SH, Teh SS, Ee GC Pharm Biol 02-Feb-2017
PMCID:PMC6130616
doi:10.1080/13880209.2017.1285322
PMID:28152649
In Vitro Anti-AChE, Anti-BuChE, and Antioxidant Activity of 12 Extracts of Eleutherococcus Species Załuski D, Kuźniewski R Oxid Med Cell Longev 10-Oct-2016
PMCID:PMC5075622
doi:10.1155/2016/4135135
PMID:27803761
Antibacterial Activity of Alkaloid Fractions from Berberis microphylla G. Forst and Study of Synergism with Ampicillin and Cephalothin Manosalva L, Mutis A, Urzúa A, Fajardo V, Quiroz A Molecules 11-Jan-2016
PMCID:PMC6272980
doi:10.3390/molecules21010076
PMID:26760994
Synergistic activity and mechanism of action of Stephania suberosa Forman extract and ampicillin combination against ampicillin-resistant Staphylococcus aureus Teethaisong Y, Autarkool N, Sirichaiwetchakoon K, Krubphachaya P, Kupittayanant S, Eumkeb G J Biomed Sci 11-Sep-2014
PMCID:PMC4428530
doi:10.1186/s12929-014-0090-2
PMID:25208614
UPLC-QTOF/MS Analysis of Alkaloids in Traditional Processed Coptis chinensis Franch. Jiang X, Huang LF, Wu LB, Wang ZH, Chen SL Evid Based Complement Alternat Med 13-Dec-2012
PMCID:PMC3532920
doi:10.1155/2012/942384
PMID:23304228

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 / Hasubanan alkaloids
(1S,10S)-4,5,11,12-tetramethoxy-17-azatetracyclo[8.4.3.01,10.02,7]heptadeca-2,4,6,11-tetraen-13-one 163078338 Click to see COC1=C(C=C2C(=C1)CCC34C2(CCN3)CC(=O)C(=C4OC)OC)OC 359.40 unknown https://doi.org/10.1016/S0031-9422(00)84726-3
(1S,13S)-14,15-dimethoxy-20-methyl-5,7-dioxa-20-azapentacyclo[11.4.3.01,13.02,10.04,8]icosa-2,4(8),9,14-tetraen-16-one 44584410 Click to see CN1CCC23C1(CCC4=CC5=C(C=C42)OCO5)C(=C(C(=O)C3)OC)OC 357.40 unknown https://doi.org/10.1016/S0031-9422(00)84726-3
(1S,13S)-14,15-dimethoxy-5,7-dioxa-20-azapentacyclo[11.4.3.01,13.02,10.04,8]icosa-2,4(8),9,14-tetraen-16-one 162987925 Click to see COC1=C(C23CCC4=CC5=C(C=C4C2(CCN3)CC1=O)OCO5)OC 343.40 unknown https://doi.org/10.1016/S0031-9422(00)84726-3
14,15-Dimethoxy-5,7-dioxa-20-azapentacyclo[11.4.3.01,13.02,10.04,8]icosa-2,4(8),9,14-tetraen-16-one 13855909 Click to see COC1=C(C23CCC4=CC5=C(C=C4C2(CCN3)CC1=O)OCO5)OC 343.40 unknown https://doi.org/10.1016/S0031-9422(00)84726-3
4,5,11,12-Tetramethoxy-17-azatetracyclo[8.4.3.01,10.02,7]heptadeca-2,4,6,11-tetraen-13-one 13855918 Click to see COC1=C(C=C2C(=C1)CCC34C2(CCN3)CC(=O)C(=C4OC)OC)OC 359.40 unknown https://doi.org/10.1016/S0031-9422(00)84726-3
4,5,11,12-Tetramethoxy-17-methyl-17-azatetracyclo[8.4.3.01,10.02,7]heptadeca-2,4,6,11-tetraen-13-one 73669785 Click to see CN1CCC23C1(CCC4=CC(=C(C=C42)OC)OC)C(=C(C(=O)C3)OC)OC 373.40 unknown https://doi.org/10.1016/S0031-9422(00)84726-3
Hasubanan-7-one,6-didehyydro-4,6-dimethoxy-17-methyl-2,3-[methylene bis(oxy)]- 360850 Click to see CN1CCC23C1(CCC4=CC5=C(C=C42)OCO5)C(=C(C(=O)C3)OC)OC 357.40 unknown https://doi.org/10.1016/S0031-9422(00)84726-3
Runanine 119026174 Click to see CN1CCC23C1(CCC4=CC(=C(C=C42)OC)OC)C(=C(C(=O)C3)OC)OC 373.40 unknown https://doi.org/10.1016/S0031-9422(00)84726-3
> Alkaloids and derivatives / Morphinans
(1R,9S,10S)-4,5,12,13-tetramethoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6,12-tetraen-11-one 13855903 Click to see CN1CCC23CC(=C(C(=O)C2C1CC4=CC(=C(C=C34)OC)OC)OC)OC 373.40 unknown https://doi.org/10.1016/S0031-9422(00)84726-3
4,5,12,13-Tetramethoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6,12-tetraen-11-one 13855901 Click to see CN1CCC23CC(=C(C(=O)C2C1CC4=CC(=C(C=C34)OC)OC)OC)OC 373.40 unknown https://doi.org/10.1016/S0031-9422(00)84726-3
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(-)-Coreximine 601259 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)O)O 327.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
(-)-Tetrahydrostephabine 44584402 Click to see COC1=C(C(=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)OC)O)OC 371.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
(-)-trans-Xylopinine N-oxide 163184420 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4C[N+]3(CCC2=C1)[O-])OC)OC)OC 371.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
(13aS)-2,3,10-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-1,11-diol 162984723 Click to see COC1=C(C(=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)O)O)OC 357.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
(13aS)-2,3,9-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-1,10-diol 14263918 Click to see COC1=C(C(=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)OC)O)OC 357.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
(7R,13aR)-2,3,10,11-tetramethoxy-7-oxido-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium 163193778 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4C[N+]3(CCC2=C1)[O-])OC)OC)OC 371.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
(7S,13aR)-2,3,10,11-tetramethoxy-7-oxido-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium 163185676 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4C[N+]3(CCC2=C1)[O-])OC)OC)OC 371.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
2,3,10-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-1,11-diol 162984722 Click to see COC1=C(C(=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)O)O)OC 357.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
2,3,10,11-tetramethoxy-6,8-dihydro-5H-isoquinolino[2,1-b]isoquinoline 15699333 Click to see COC1=C(C=C2C(=C1)CCN3C2=CC4=CC(=C(C=C4C3)OC)OC)OC 353.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
2,3,10,11-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-1-ol 75051990 Click to see COC1=C(C(=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)OC)O)OC 371.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
2,3,9-trimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-1,10-diol 5315668 Click to see COC1=C(C(=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)OC)O)OC 357.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
beta-Norcoralydine 10653 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)OC)OC 355.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
Coreximine 7037179 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)O)O 327.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
Corydalmine 161665 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)OC)OC 341.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
Corytenchine 46919623 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)O)OC 341.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
D-Tetrahydropalmatine 969488 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
Discretine 821491 Click to see COC1=C(C=C2CN3CCC4=CC(=C(C=C4C3CC2=C1)OC)O)OC 341.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
l-Stepholidine 6917970 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)OC)O 327.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
Pseudopalmatine 644002 Click to see COC1=C(C=C2C(=C1)CC[N+]3=CC4=CC(=C(C=C4C=C23)OC)OC)OC 352.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
Tetrahydropalmatine 72301 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
Tetrahydropalmatrubine 11282465 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)O 341.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
Xylopinine 226520 Click to see COC1=C(C=C2C3CC4=CC(=C(C=C4CN3CCC2=C1)OC)OC)OC 355.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
> Benzenoids / Phenanthrenes and derivatives
(1S,13R)-3,16-dimethoxy-20-methyl-5,7-dioxa-20-azapentacyclo[11.4.3.01,13.02,10.04,8]icosa-2,4(8),9,16-tetraen-15-one 101306720 Click to see CN1CCC23C1(CCC4=CC5=C(C(=C42)OC)OCO5)CC(=O)C(=C3)OC 357.40 unknown https://doi.org/10.1016/S0031-9422(00)84726-3
> Lignans, neolignans and related compounds
(+)-2'-Norcepharanthine 181384 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(C=C8CCN7)OC)O4)OC)OCO3 592.70 unknown https://doi.org/10.1021/NP50045A006
(14aS,26aR)-2,3,13,14,14a,15,26,26a-Octahydro-22,30-dimethoxy-14-methyl-1H-4,6:16,19-dietheno-21,25-metheno-12H-[1,3]dioxolo[4,5-g]pyrido[2 inverted exclamation marka,3 inverted exclamation marka:17,18][1,10]dioxacycloeicosino[2,3,4-ij]isoquinoline 14488278 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=C(O3)C8=C(C=C7CCN6)OCO8)C=C5)OC 592.70 unknown https://doi.org/10.1021/NP50045A006
Cepharanthine 10206 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(C=C8CCN7C)OC)O4)OC)OCO3 606.70 unknown https://doi.org/10.1021/NP50045A006
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
6,6',12'-Trimethoxy-1,1',2,2',3,4-hexadehydrooxyacanthan-7-ol 190798 Click to see COC1=C2C=C(CC3=NCCC4=CC(=C(C=C43)OC5=C6C(=NC=CC6=CC(=C5O)OC)CC7=CC=C(O2)C=C7)OC)C=C1 574.60 unknown https://doi.org/10.1021/NP50045A006
6,6',12'-Trimethoxy-1,2,3,4-tetradehydrooxyacanthan-7-ol 184297 Click to see COC1=C2C=C(CC3C4=CC(=C(C=C4CCN3)OC)OC5=C6C(=NC=CC6=CC(=C5O)OC)CC7=CC=C(O2)C=C7)C=C1 576.60 unknown https://doi.org/10.1021/NP50045A006
Stephasubine 190799 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6=NC=CC7=CC(=C(C(=C67)O3)O)OC)C=C5)OC 590.70 unknown https://doi.org/10.1021/NP50045A006
> Organoheterocyclic compounds / Dihydroisoquinolines
2,3,10,11-Tetramethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-1-one 163192656 Click to see COC1=CC2=CC3=C4C(=CC(=C(C4=O)OC)OC)CCN3C=C2C=C1OC 367.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
2,3,10,11-Tetramethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-8-one 392605 Click to see COC1=C(C=C2C(=C1)CCN3C2=CC4=CC(=C(C=C4C3=O)OC)OC)OC 367.40 unknown https://doi.org/10.1016/S0031-9422(00)81451-X

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