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Ajuga nipponensis

Ajuga nipponensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64403735b3497115853235
Scientific name Ajuga nipponensis
Authority Makino
First published in Bot. Mag. (Tokyo) 23: 67 (1909)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ajuga decumbens var. typica Franch. & Sav. Enum. Pl. Jap. 2: 466. 1878
Ajuga labordei Vaniot Bull. Acad. Int. Géogr. Bot. 13: 185 (1903)
Ajuga matsumurana Kudô J. Soc. Trop. Agric. 3: 225 (1931)
Ajuga typica Matsum. & Kudô Bot. Mag. (Tokyo) 26: 294 (1912)
Ajuga macrosperma Kudô Mem. Fac. Sci. Taihoku Imp. Univ. 2: 290 1929

Common names Top

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Language Common/alternative name
Japanese ジュウニヒトエ
lzh 紫背金盤
Chinese 筋骨草
Chinese 退血草
Chinese 破血丹
Chinese 散血草
Chinese 石灰菜
Chinese 散瘀草
Chinese 日本筋骨草
Chinese 矮生(变种)
Chinese 紫背金盘
Chinese 紫背金盘草
Chinese 白头翁
Chinese 白毛夏枯草
Chinese 见血青
Chinese 紫背金盤

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
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000934630
Tropicos 17605657
KEW urn:lsid:ipni.org:names:444633-1
The Plant List kew-5339
Open Tree Of Life 979060
NCBI Taxonomy 984302
IPNI 444633-1
iNaturalist 447644
GBIF 7307111
EPPO AIUNI
USDA GRIN 423301

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
The Regulatory Effects of Traditional Chinese Medicine on Ferroptosis Gao Q, Yin XD, Zhang F, Zhu YZ, Li ZL Oxid Med Cell Longev 19-Sep-2022
PMCID:PMC9526626
doi:10.1155/2022/4578381
PMID:36193068
Phytoecdysteroids: Distribution, Structural Diversity, Biosynthesis, Activity, and Crosstalk with Phytohormones Arif Y, Singh P, Bajguz A, Hayat S Int J Mol Sci 04-Aug-2022
PMCID:PMC9369314
doi:10.3390/ijms23158664
PMID:35955797
Ethnobotanical Survey on Bitter Tea in Taiwan Chao J, Chen TY, Pao LH, Deng JS, Cheng YC, Su SY, Huang SS Front Pharmacol 18-Feb-2022
PMCID:PMC8894760
doi:10.3389/fphar.2022.816029
PMID:35250565
Improving the Physicochemical and Biopharmaceutical Properties of Active Pharmaceutical Ingredients Derived from Traditional Chinese Medicine through Cocrystal Engineering Guan D, Xuan B, Wang C, Long R, Jiang Y, Mao L, Kang J, Wang Z, Chow SF, Zhou Q Pharmaceutics 15-Dec-2021
PMCID:PMC8704577
doi:10.3390/pharmaceutics13122160
PMID:34959440
Genetic Profiles of Ferroptosis in Malignant Brain Tumors and Off-Target Effects of Ferroptosis Induction Dahlmanns M, Yakubov E, Dahlmanns JK Front Oncol 01-Dec-2021
PMCID:PMC8671613
doi:10.3389/fonc.2021.783067
PMID:34926298
Luteolin potentiates low-dose oxaliplatin-induced inhibitory effects on cell proliferation in gastric cancer by inducing G2/M cell cycle arrest and apoptosis Ma J, Chen X, Zhu X, Pan Z, Hao W, Li D, Zheng Q, Tang X Oncol Lett 12-Nov-2021
PMCID:PMC8607327
doi:10.3892/ol.2021.13134
PMID:34820015
Cabbage Production in West Africa and IPM with a Focus on Plant-Based Extracts and a Complementary Worldwide Vision Mondédji AD, Silvie P, Nyamador WS, Martin P, Agboyi LK, Amévoin K, Ketoh GK, Glitho IA Plants (Basel) 11-Mar-2021
PMCID:PMC7998567
doi:10.3390/plants10030529
PMID:33799877
The phytochemical, biological, and medicinal attributes of phytoecdysteroids: An updated review Das N, Mishra SK, Bishayee A, Ali ES, Bishayee A Acta Pharm Sin B 16-Oct-2020
PMCID:PMC8343124
doi:10.1016/j.apsb.2020.10.012
PMID:34386319
Matrine Enhances the Pathogenicity of Beauveria brongniartii Against Spodoptera litura (Lepidoptera: Noctuidae) Wu J, Yu X, Wang X, Tang L, Ali S Front Microbiol 13-Aug-2019
PMCID:PMC6700297
doi:10.3389/fmicb.2019.01812
PMID:31456766
Prioritizing fodder species based on traditional knowledge: a case study of mithun (Bos frontalis) in Dulongjiang area, Yunnan Province, Southwest China Geng Y, Hu G, Ranjitkar S, Wang Y, Bu D, Pei S, Ou X, Lu Y, Ma X, Xu J J Ethnobiol Ethnomed 04-May-2017
PMCID:PMC5418811
doi:10.1186/s13002-017-0153-z
PMID:28472968
Neo-clerodane diterpenes from Ajuga nipponensis. Hiroko SHIMOMURA, Yutaka SASHIDA, Kazunori OGAWA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.37.354
The chemical constituents of Ajuga plants. I. neo-Clerodanes from the leaves of Ajuga nipponensis Makino. HIROKO SHIMOMURA, YUTAKA SASHIDA, KAZUNORI OGAWA, YOICHI IITAKA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.31.2192
Isolation of Cyasterone and Ecdysterone from Plant Materials SHUNJI IMAI, TOMOYOSHI TOYOSATO, MICHIHIKO SAKAI, YASUO SATO, SHOJI FUJIOKA, EIKO MURATA, MINORU GOTO Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.17.340
16th International Ecdysone Workshop: July 10–14, 2006, Ghent University, Belgium Bellés X, Billas I, Cherbas P, Delbecque JP, Dhadialla T, Fujiwara H, Hill R, Hiruma K, Hermann R, Iatrou K, Koolman J, Lafont R, Lepesant JA, Nakagawa Y, Palli R, Raikhel A, Riddiford L, Rees H, Sehnal F, Slama K, Smagghe G, Spindler KD, Steel C, Swevers L, Thummel C J Insect Sci 08-Mar-2007
PMCID:PMC2999422
doi:10.1673/031.007.1301
New phytoecdysteroids from cultured plants of Ajuga nipponensis Makino. Coll J, Tandrón YA, Zeng X Steroids 01-Mar-2007
doi:10.1016/J.STEROIDS.2006.11.017
PMID:17210166

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,5S,7S,7aR)-1,4a,5,6,7,7a-Hexahydro-4a,5,7-trihydroxy-7-methylcyclopenta[c]pyran-1-yl beta-D-glucopyranoside 145706031 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown https://doi.org/10.1016/S0031-9422(00)81742-2
Harpagide 93045 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown https://doi.org/10.1016/S0031-9422(00)81742-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[4,4a-bis(acetyloxymethyl)-4,5-dihydroxy-8-[2-hydroxy-2-(5-oxo-2H-furan-3-yl)ethyl]-7,8-dimethyl-2,3,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] 2-methylbutanoate 14314162 Click to see CCC(C)C(=O)OC1CCC(C2(C1C(C(CC2O)C)(C)CC(C3=CC(=O)OC3)O)COC(=O)C)(COC(=O)C)O 568.70 unknown https://doi.org/10.1248/CPB.37.354
Ajugamarin chlorohydrin 102004685 Click to see CC=C(C)C(=O)OC1CCC(C2(C1C(C(CC2OC(=O)C)C)(C)CC(C3=CC(=O)OC3)O)COC(=O)C)(CCl)O 585.10 unknown https://doi.org/10.1248/CPB.31.2192
Ajugamarin D 1 180057 Click to see CCC(C)C(=O)OC1CCC(C2(C1C(C(CC2O)C)(C)CC(C3=CC(=O)OC3)O)COC(=O)C)(COC(=O)C)O 568.70 unknown https://doi.org/10.1248/CPB.37.354
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,3R,5R,9R,10R,13R,14S,17S)-17-[(1R)-1-[(2R,4S,5S,6R)-4-ethyl-4,6-dihydroxy-5-methyloxan-2-yl]-1-hydroxyethyl]-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 162962410 Click to see CCC1(CC(OC(C1C)O)C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)O 522.70 unknown https://doi.org/10.1016/J.STEROIDS.2006.11.017
(3S,4S,5R)-4-[(2R,3R)-2,3-dihydroxy-3-[(5R,9R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]butyl]-3,5-dimethyloxolan-2-one 122130059 Click to see CC1C(C(OC1=O)C)CC(C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)O 520.70 unknown https://doi.org/10.1248/CPB.17.340
https://doi.org/10.1080/10286020008041365
(3S,4S,5R)-4-[(3R)-3-[(2S,3R,5R,9R,10R,13R,14S,17S)-3,14-dihydroxy-10,13-dimethyl-6-oxo-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-3-hydroxy-2-oxobutyl]-3,5-dimethyloxolan-2-one 102402814 Click to see CC1C(C(OC1=O)C)CC(=O)C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)O 680.80 unknown https://doi.org/10.1016/J.STEROIDS.2006.11.017
[(1R,2R)-1-[(2S,3S,4R,5R)-3-ethyl-5-hydroxy-4-methyloxolan-2-yl]-2-hydroxy-2-[(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]propyl] acetate 102402816 Click to see CCC1C(C(OC1C(C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)OC(=O)C)O)C 564.70 unknown https://doi.org/10.1016/J.STEROIDS.2006.11.017
[1-(3-ethyl-5-hydroxy-4-methyloxolan-2-yl)-2-hydroxy-2-(2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)propyl] acetate 162987745 Click to see CCC1C(C(OC1C(C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)OC(=O)C)O)C 564.70 unknown https://doi.org/10.1016/J.STEROIDS.2006.11.017
17-[1-(4-ethyl-4,6-dihydroxy-5-methyloxan-2-yl)-1-hydroxyethyl]-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 162962409 Click to see CCC1(CC(OC(C1C)O)C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)O 522.70 unknown https://doi.org/10.1016/J.STEROIDS.2006.11.017
4-[3-[3,14-dihydroxy-10,13-dimethyl-6-oxo-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-3-hydroxy-2-oxobutyl]-3,5-dimethyloxolan-2-one 162887602 Click to see CC1C(C(OC1=O)C)CC(=O)C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)O 680.80 unknown https://doi.org/10.1016/J.STEROIDS.2006.11.017
Cyasterone 119444 Click to see CC1C(C(OC1=O)C)CC(C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)O 520.70 unknown https://doi.org/10.1080/10286020008041365
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
Ajugasterone C 441826 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)O)O 480.60 unknown https://doi.org/10.1080/10286020008041365
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1R,4R,4aR,5S,7R,8S,8aR)-5-acetyloxy-4a-(acetyloxymethyl)-8-[(2S)-2-acetyloxy-2-(5-oxo-2H-furan-3-yl)ethyl]-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-1-yl] (2S)-2-methylbutanoate 14314156 Click to see CCC(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)CC(C4=CC(=O)OC4)OC(=O)C)COC(=O)C 592.70 unknown https://doi.org/10.1248/CPB.37.354
[5-acetyloxy-4a-(acetyloxymethyl)-8-[2-acetyloxy-2-(5-oxo-2H-furan-3-yl)ethyl]-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-1-yl] 2-methylbutanoate 14314154 Click to see CCC(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)CC(C4=CC(=O)OC4)OC(=O)C)COC(=O)C 592.70 unknown https://doi.org/10.1248/CPB.37.354
Ajugamarin B 2 180054 Click to see CCC(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)CC(C4=CC(=O)OC4)OC(=O)C)COC(=O)C 592.70 unknown https://doi.org/10.1248/CPB.37.354
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[5-acetyloxy-4a-(acetyloxymethyl)-8-[2-hydroxy-2-(5-oxo-2H-furan-3-yl)ethyl]-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-1-yl] 2-methylbut-2-enoate 494584 Click to see CC=C(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)CC(C4=CC(=O)OC4)O)COC(=O)C 548.60 unknown https://doi.org/10.1248/CPB.37.354
[5-acetyloxy-4a-(acetyloxymethyl)-8-[2-hydroxy-2-(5-oxo-2H-furan-3-yl)ethyl]-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-1-yl] 2-methylbutanoate 494585 Click to see CCC(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)CC(C4=CC(=O)OC4)O)COC(=O)C 550.60 unknown https://doi.org/10.1248/CPB.37.354
Ajugamarin 101277250 Click to see CC=C(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)CC(C4=CC(=O)OC4)O)COC(=O)C 548.60 unknown https://doi.org/10.1248/CPB.31.2192
Ajugamarin A 1 6440613 Click to see CC=C(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)CC(C4=CC(=O)OC4)O)COC(=O)C 548.60 unknown https://doi.org/10.1248/CPB.37.354
Ajugamarin B1 14314168 Click to see CCC(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)CC(C4=CC(=O)OC4)O)COC(=O)C 550.60 unknown https://doi.org/10.1248/CPB.37.354
Dihydroajugamarin 76308695 Click to see CCC(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)CC(C4=CC(=O)OC4)O)COC(=O)C 550.60 unknown https://doi.org/10.1248/CPB.31.2192
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R,4R,4aR,5S,7R,8S,8aR)-4a-(acetyloxymethyl)-5-hydroxy-8-[(2S)-2-hydroxy-2-(5-oxo-2H-furan-3-yl)ethyl]-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-1-yl] (2S)-2-methylbutanoate 14314159 Click to see CCC(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3O)C)(C)CC(C4=CC(=O)OC4)O)COC(=O)C 508.60 unknown https://doi.org/10.1248/CPB.37.354
[4a-(acetyloxymethyl)-5-hydroxy-8-[2-hydroxy-2-(5-oxo-2H-furan-3-yl)ethyl]-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-1-yl] 2-methylbutanoate 14314157 Click to see CCC(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3O)C)(C)CC(C4=CC(=O)OC4)O)COC(=O)C 508.60 unknown https://doi.org/10.1248/CPB.37.354
[5-acetyloxy-1-hydroxy-8-[2-hydroxy-2-(5-oxo-2H-furan-3-yl)ethyl]-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 14314152 Click to see CC1CC(C2(C(C1(C)CC(C3=CC(=O)OC3)O)C(CCC24CO4)O)COC(=O)C)OC(=O)C 466.50 unknown https://doi.org/10.1248/CPB.37.354
[5-acetyloxy-7,8-dimethyl-8-[2-(5-oxo-2H-furan-3-yl)ethyl]spiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 5088205 Click to see CC1CC(C2(C(C1(C)CCC3=CC(=O)OC3)CCCC24CO4)COC(=O)C)OC(=O)C 434.50 unknown https://doi.org/10.1248/CPB.37.354
Ajugamarin B 3 180055 Click to see CCC(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3O)C)(C)CC(C4=CC(=O)OC4)O)COC(=O)C 508.60 unknown https://doi.org/10.1248/CPB.37.354
Ajugamarin C 1 180053 Click to see CC1CC(C2(C(C1(C)CC(C3=CC(=O)OC3)O)C(CCC24CO4)O)COC(=O)C)OC(=O)C 466.50 unknown https://doi.org/10.1248/CPB.37.354
Ajugamarin C1 12136682 Click to see CC1CC(C2(C(C1(C)CC(C3=CC(=O)OC3)O)C(CCC24CO4)O)COC(=O)C)OC(=O)C 466.50 unknown https://doi.org/10.1248/CPB.37.354
Ajugarin I 173866 Click to see CC1CC(C2(C(C1(C)CCC3=CC(=O)OC3)CCCC24CO4)COC(=O)C)OC(=O)C 434.50 unknown https://doi.org/10.1248/CPB.37.354
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 78380899 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(00)81742-2
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0031-9422(00)81742-2
Calceolarioside A 5273566 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/S0031-9422(00)81742-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(2R,3R,4S,5S,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl (E)-3-(4-hydroxyphenyl)acrylate 163193405 Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(OC2O)CO)O)O)O 326.30 unknown https://doi.org/10.1016/S0031-9422(00)81742-2
[2,4,5-Trihydroxy-6-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 72726480 Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(OC2O)CO)O)O)O 326.30 unknown https://doi.org/10.1016/S0031-9422(00)81742-2

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In private collections 0
In public collections 0
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