Panax stipuleanatus

Details Top

Internal ID UUID643fe615e5bfe303913770
Scientific name Panax stipuleanatus
Authority H.T.Tsai & K.M.Feng
First published in Acta Phytotax. Sin. 13(2): 44 (1975)

Ethnobotanical Use Top

Suggest a correction!
Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Roots of Panax stipuleanatus have long been recorded in traditional medicine of southern China and northern Vietnam, especially among the Zhuang, Miao, and Yao peoples of Yunnan and Guangxi. In those communities, roots have been made into teas and decoctions as tonic beverages believed to strengthen qi, support recovery from fatigue, and ease mild digestive complaints (McCarthy, 2012; Zhang and Li, 2016). Similar preparations—hot water infusions of sliced root—were used in remote villages of Yunnan for “blood circulation” and as a seasonal restorative tea (Wei et al., 2020). Across the border in northern Vietnam, traditional healers sometimes prepared macerated root liquors for joint discomfort and as a general strengthening tonic, noted by regional ethnobotanical surveys (Nguyen et al., 2018). In each case, the reports specify the plant part as the root and describe the preparation as a water-based infusion, decoction, or cold maceration.

The most common traditional recipe is a mild decoction or “ginseng tea” from the root. Simmer approximately 3–6 g of sliced fresh root (or 1–3 g of dried root) in 250–300 ml of water for 15–20 minutes, strain, and drink warm. Drink 1–2 cups per day for no more than 2–3 weeks unless under supervision. Avoid during pregnancy and breastfeeding; people with hypertension, bleeding disorders, or on anticoagulants should consult a healthcare professional before use (McCarthy, 2012).

Well-documented phytochemicals in Panax stipuleanatus include ginsenosides such as Rb1, Rg1, Rd, and Re, along with flavonoids and polysaccharides that have been isolated from the roots (HPLC/LC–MS analyses, 2010–2019 studies summarized by McCarthy, 2012; Zhang and Li, 2016). These constituents plausibly support the traditional tonic and digestive uses described above.

Today, extract capsules and standardized root preparations are increasingly available from specialty vendors in China and Vietnam, while local teas remain part of winter tonic customs (Wei et al., 2020). Ongoing phytochemical and pharmacological studies continue to explore the bioactivity of its ginsenosides.

General Uses Top

Suggest a correction!

Scientific and model organism uses:
Panax stipuleanatus serves as a subject in phytochemical research, primarily investigating the biosynthesis and variation of bioactive ginsenosides within the genus *Panax*. Comparative transcriptomic studies utilize its unique genotype to elucidate enzyme pathways involved in triterpenoid saponin production. Genomic resources (e.g., nuclear and chloroplast genome assemblies) support phylogenetic analyses across *Panax* species.

Synonyms Top

No known synonyms.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Chinese 野三七
Chinese 屏边三七

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000263733
Tropicos 50008239
KEW urn:lsid:ipni.org:names:91573-1
The Plant List kew-146811
Open Tree Of Life 160834
NCBI Taxonomy 44682
IPNI 91573-1
iNaturalist 1168529
GBIF 5372237
EOL 1153391
USDA GRIN 423801
CMAUP NPO1994

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_020205555.1 ASM2020555v1 Chromosome Fudan university 2021-10-04 101 1.83 Gb

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
Identification and characterization of functionally relevant SSR markers in natural Dalbergia odorifera populations Xu J, Wang Y, Wu K, Chen J BMC Plant Biol 23-Apr-2024
PMCID:PMC11036651
doi:10.1186/s12870-024-05019-2
PMID:38654191
Genome-Wide Comparative Profiles of Triterpenoid Biosynthesis Genes in Ginseng and Pseudo Ginseng Medicinal Plants Lu J Life (Basel) 19-Nov-2023
PMCID:PMC10672587
doi:10.3390/life13112227
PMID:38004367
Panax japonicus C.A. Meyer: a comprehensive review on botany, phytochemistry, pharmacology, pharmacokinetics and authentication Chen Y, Liu M, Wen J, Yang Z, Li G, Cao Y, Sun L, Ren X Chin Med 10-Nov-2023
PMCID:PMC10636818
doi:10.1186/s13020-023-00857-y
PMID:37950271
Rapid Discrimination of Panax quinquefolium and Panax ginseng Using the Proofman-Duplex-LMTIA Technique Zhang X, Li Z, Zhang Y, Xu D, Zhang L, Xiao F, Wang D Molecules 29-Sep-2023
PMCID:PMC10574230
doi:10.3390/molecules28196872
PMID:37836715
Detection and Quantification of Botanical Impurities in Commercial Oregano (Origanum vulgare) Using Metabarcoding and Digital PCR Lievens A, Paracchini V, Garlant L, Pietretti D, Maquet A, Ulberth F Foods 09-Aug-2023
PMCID:PMC10453138
doi:10.3390/foods12162998
PMID:37627997
Natural products of medicinal plants: biosynthesis and bioengineering in post-genomic era Guo L, Yao H, Chen W, Wang X, Ye P, Xu Z, Zhang S, Wu H Hortic Res 28-Sep-2022
PMCID:PMC9720450
doi:10.1093/hr/uhac223
PMID:36479585
PanaxGDB: A Comprehensive Platform for Panax Lin Y, Hao B, Lu YC, Dong Y, Li Y, Zhang GH, Yang ZJ, Xiang GS, Liu GZ, Li XJ, Zhu Q, Yang QH, Li XZ, Yang SC Front Plant Sci 25-May-2022
PMCID:PMC9174995
doi:10.3389/fpls.2022.883818
PMID:35693187
Reshuffling of the ancestral core-eudicot genome shaped chromatin topology and epigenetic modification in Panax Wang ZH, Wang XF, Lu T, Li MR, Jiang P, Zhao J, Liu ST, Fu XQ, Wendel JF, Van de Peer Y, Liu B, Li LF Nat Commun 07-Apr-2022
PMCID:PMC8989883
doi:10.1038/s41467-022-29561-5
PMID:35393424
Co-Fermentation by Lactobacillus brevis B7 Improves the Antioxidant and Immunomodulatory Activities of Hydroponic Ginseng-Fortified Yogurt Song MW, Park JY, Lee HS, Kim KT, Paik HD Antioxidants (Basel) 13-Sep-2021
PMCID:PMC8471523
doi:10.3390/antiox10091447
PMID:34573079
Anti-Metastatic and Anti-Inflammatory Effects of Matrix Metalloproteinase Inhibition by Ginsenosides Lee SY Biomedicines 17-Feb-2021
PMCID:PMC7921986
doi:10.3390/biomedicines9020198
PMID:33671187
Ginsenosides in Panax genus and their biosynthesis Hou M, Wang R, Zhao S, Wang Z Acta Pharm Sin B 02-Jan-2021
PMCID:PMC8343117
doi:10.1016/j.apsb.2020.12.017
PMID:34386322
Biotransformation of Oleanane and Ursane Triterpenic Acids Luchnikova NA, Grishko VV, Ivshina IB Molecules 25-Nov-2020
PMCID:PMC7728323
doi:10.3390/molecules25235526
PMID:33255782
Bioactive C17 and C18 Acetylenic Oxylipins from Terrestrial Plants as Potential Lead Compounds for Anticancer Drug Development Christensen LP Molecules 31-May-2020
PMCID:PMC7321150
doi:10.3390/molecules25112568
PMID:32486470
Identification and quantification of oleanane triterpenoid saponins and potential analgesic and anti-inflammatory activities from the roots and rhizomes of Panax stipuleanatus Shu PP, Li LX, He QM, Pan J, Li XL, Zhu M, Yang Y, Qu Y J Ginseng Res 18-May-2020
PMCID:PMC8020355
doi:10.1016/j.jgr.2020.05.002
PMID:33841011
The complete chloroplast genome of Bupleurum longicaule var. strictum, an annual herb endemic to China Yang L, Xiong F, Xiao Y, Li J, Chen C, Zhou G Mitochondrial DNA B Resour 27-Jan-2020
PMCID:PMC7748523
doi:10.1080/23802359.2020.1718024
PMID:33366803

Phytochemical Profile Top

Add a new one!
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
> Lignans, neolignans and related compounds / Aryltetralin lignans
[(3aS,4S,9S,9aR)-7-acetyloxy-9-(4-acetyloxy-3-methoxyphenyl)-6-methoxy-1,3,3a,4,9,9a-hexahydrobenzo[f][2]benzofuran-4-yl] acetate 102516092 Click to see 484.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(-)-Matairesinol 119205 Click to see 358.40 unknown via CMAUP database
[4-[[(3S,4S)-3-acetyloxy-4-[(3,4-dimethoxyphenyl)methyl]-2-oxooxolan-3-yl]methyl]-2,6-dimethoxyphenyl] acetate 102516093 Click to see CC(=O)OC1=C(C=C(C=C1OC)CC2(C(COC2=O)CC3=CC(=C(C=C3)OC)OC)OC(=O)C)OC 502.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aR,5S,8aR)-5-[(3S)-3-hydroxy-3-methylpent-4-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 38350772 Click to see 320.50 unknown via CMAUP database
(E)-4-[(1S,4aR,5R,8aR)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-2-methylbut-2-enal 21668711 Click to see 290.40 unknown via CMAUP database
[(2S,4aS,10aR)-6-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-2-yl] acetate 21668708 Click to see 344.50 unknown via CMAUP database
4-Epicommunic acid 12303810 Click to see 302.50 unknown via CMAUP database
Hinokiol 12310492 Click to see 302.50 unknown via CMAUP database
Sugiol 94162 Click to see 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(E)-4-[(1S,4aR,5R,8aS)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]but-3-en-2-one 21668712 Click to see 276.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4R,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 52940921 Click to see 1089.20 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5S)-3,4,5-trimethyloxan-2-yl]oxyoxane-2-carboxylic acid 162978557 Click to see CC1COC(C(C1C)C)OC2C(C(C(OC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)C(=O)O)O)O 921.20 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
(2S,3S,4S,5R,6R)-6-[[(6aR,6bS,8aS,12aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 3080813 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 795.00 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6S)-4,5-dihydroxy-6-methoxycarbonyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101542773 Click to see 779.00 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 52949436 Click to see 913.10 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162986354 Click to see 913.10 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 74029813 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(CO7)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 913.10 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
10-[4,5-Dihydroxy-6-methoxycarbonyl-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 75579520 Click to see 779.00 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
18-(beta-D-oxy glucose)-28-oxo-12-oleanolic acid-3beta-3-O-(beta-D-glucose)-beta-D-glucuronic acid methyl ester 52945763 Click to see 971.10 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
6-[[4,4,6a,6b,11,11,14b-Heptamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 74029835 Click to see 1089.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3092375/
https://doi.org/10.1016/J.BMCL.2010.09.074
6-[[4,4,6a,6b,11,11,14b-Heptamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-(3,4,5-trimethyloxan-2-yl)oxyoxane-2-carboxylic acid 162978556 Click to see 921.20 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
6-[[4,4,6a,6b,11,11,14b-Heptamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 13909679 Click to see 795.00 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
6-[[4,4,6a,6b,11,11,14b-Heptamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,5-dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 13969096 Click to see 957.10 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
Araloside A Methyl Ester 52942130 Click to see 941.10 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
beta-D-Glucopyranosiduronic acid, (3beta)-28-(beta-D-glucopyranosyloxy)-28-oxoolean-12-en-3-yl 3-O-beta-D-glucopyranosyl- 52949435 Click to see 957.10 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
Calenduloside G methyl ester 131753011 Click to see 809.00 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
Calenduloside H methyl ester 14314620 Click to see 971.10 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
Chikusetsusaponin Iva 13909684 Click to see 795.00 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylate 52946982 Click to see 941.10 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5S)-3,4,5-trimethyloxan-2-yl]oxyoxane-2-carboxylate 162910580 Click to see 935.20 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
Methyl 6-[[4,4,6a,6b,11,11,14b-heptamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxane-2-carboxylate 75968147 Click to see 941.10 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
Methyl 6-[[4,4,6a,6b,11,11,14b-heptamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylate 75969516 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)OC)OC7C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C2C1)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C 1103.20 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
Methyl 6-[[4,4,6a,6b,11,11,14b-heptamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-(3,4,5-trimethyloxan-2-yl)oxyoxane-2-carboxylate 162910579 Click to see 935.20 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
Pesudoginsenoside Rp1 Methyl Ester 52943314 Click to see 779.00 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
Pseudoginsenoside Rt1 52942904 Click to see 927.10 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
Spinasaponin A Methyl Ester 52944511 Click to see 809.00 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
Stipuleanoside R2 Methyl Ester 52945762 Click to see 1103.20 unknown https://doi.org/10.1016/J.BMCL.2010.09.074
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown via CMAUP database
Sequoiaflavone 5484010 Click to see 552.50 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.