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Adina rubella

Adina rubella - 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 UUID6440284a91fe4200539679
Scientific name Adina rubella
Authority Hance
First published in J. Bot. 6: 114 (1868)

Description Top

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Synonyms Top

Scientific name Authority First published in
Nauclea rubella (Hance) Nakai J. Jap. Bot. 18: 216 (1942)
Adina fauriei H.Lév. Repert. Spec. Nov. Regni Veg. 8: 283 (1930)

Common names Top

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Language Common/alternative name
Chinese 水杨梅
Chinese 水杨梅根
Chinese 细叶水团花
Chinese 细叶水团花（水杨梅）
Chinese 細葉水圑花

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 North-central
      • China Southeast
    • Eastern Asia
      • Korea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000788889
UNII 1S210XS3BZ
Tropicos 27913291
KEW urn:lsid:ipni.org:names:742932-1
The Plant List kew-3275
Missouri Botanical Garden 286741
Open Tree Of Life 240341
NCBI Taxonomy 170036
IPNI 742932-1
GBIF 2895028
EOL 1108821
USDA GRIN 1494
PFAF Adina rubella

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
Treatment of Chronic Gastritis with Traditional Chinese Medicine: Pharmacological Activities and Mechanisms Chen L, Wei S, He Y, Wang X, He T, Zhang A, Jing M, Li H, Wang R, Zhao Y Pharmaceuticals (Basel) 15-Sep-2023
PMCID:PMC10537303
doi:10.3390/ph16091308
PMID:37765116
The phytochemical properties, pharmacological effects and traditional uses of Actinidia eriantha Benth.: A review Wang S, Gao X, Sun Q, Zhu Y, Qin L, Zhu B Front Pharmacol 19-Aug-2022
PMCID:PMC9437332
doi:10.3389/fphar.2022.959900
PMID:36059997
Original karst tiankeng with underground virgin forest as an inaccessible refugia originated from a degraded surface flora in Yunnan, China Shui W, Chen Y, Jian X, Jiang C, Wang Q, Zeng Y, Zhu S, Guo P, Li H Sci Rep 07-Jun-2022
PMCID:PMC9174222
doi:10.1038/s41598-022-13678-0
PMID:35672447
Exploring potential targets of Actinidia chinensis Planch root against hepatocellular carcinoma based on network pharmacology and molecular docking and development and verification of immune-associated prognosis features for hepatocellular carcinoma Qu M, Han T, Chen X, Sun Q, Li Q, Zhao M J Gastrointest Oncol 01-Jun-2022
PMCID:PMC9274039
doi:10.21037/jgo-22-398
PMID:35837167
Terniopsisyongtaiensis (Podostemaceae), a new species from South East China based on morphological and genomic data Zhang M, Zhang XH, Ge CL, Chen BH PhytoKeys 18-Apr-2022
PMCID:PMC9038898
doi:10.3897/phytokeys.194.83080
PMID:35586323
Traditional Chinese Medicines as Effective Reversals of Epithelial-Mesenchymal Transition Induced-Metastasis of Colorectal Cancer: Molecular Targets and Mechanisms Ge H, Xu C, Chen H, Liu L, Zhang L, Wu C, Lu Y, Yao Q Front Pharmacol 04-Mar-2022
PMCID:PMC8931761
doi:10.3389/fphar.2022.842295
PMID:35308223
Chemical profiles of the active fraction from Prinsepia utilis Royle leaves and its anti-benign prostatic hyperplasia evaluation in animal models Peng Y, Peng C, Wu Y, Sun C, Li X BMC Complement Med Ther 29-Oct-2021
PMCID:PMC8555178
doi:10.1186/s12906-021-03446-4
PMID:34715848
Ethnobotanical study on medicinal plants used by Mulam people in Guangxi, China Hu R, Lin C, Xu W, Liu Y, Long C J Ethnobiol Ethnomed 02-Jul-2020
PMCID:PMC7333293
doi:10.1186/s13002-020-00387-z
PMID:32616044
Pharmacological Modulation of Steroid Activity in Hormone-Dependent Breast and Prostate Cancers: Effect of Some Plant Extract Derivatives Bayala B, Zoure AA, Baron S, de Joussineau C, Simpore J, Lobaccaro JM Int J Mol Sci 23-May-2020
PMCID:PMC7279356
doi:10.3390/ijms21103690
PMID:32456259
Anti-acne vulgaris effect including skin barrier improvement and 5α-reductase inhibition by tellimagrandin I from Carpinus tschonoskii Yin J, Hwang IH, Lee MW BMC Complement Altern Med 21-Nov-2019
PMCID:PMC6869165
doi:10.1186/s12906-019-2734-y
PMID:31752827
Inhibitory Activities of Phenolic Compounds Isolated from Adina rubella Leaves Against 5α-Reductase Associated with Benign Prostatic Hypertrophy Yin J, Heo JH, Hwang YJ, Le TT, Lee MW Molecules 07-Jul-2016
PMCID:PMC6273293
doi:10.3390/molecules21070887
PMID:27399661
Secondary Metabolites from Rubiaceae Species Martins D, Nunez CV Molecules 22-Jul-2015
PMCID:PMC6331836
doi:10.3390/molecules200713422
PMID:26205062
Extensive screening for herbal extracts with potent antioxidant properties Niwano Y, Saito K, Yoshizaki F, Kohno M, Ozawa T J Clin Biochem Nutr 28-Dec-2010
PMCID:PMC3022069
doi:10.3164/jcbn.11-013FR
PMID:21297917
27-nor-triterpenoid glycosides from Adina rubella Zhi-sheng He, Shi-Yue Fang, Ping Wang, Jing-Hai Gao Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(96)00075-1
Triterpenoid glycosides from Adina rubella. Fan GJ, He ZS Phytochemistry 01-Mar-1997
doi:10.1016/S0031-9422(96)00660-7
PMID:9101666

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 / Diterpene glycosides
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aR,6bR,8aR,10S,12aR,14bS)-2,2,6b,9,9,12a-hexamethyl-10-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydro-1H-picene-4a-carboxylate 101995320 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5=C(C4(CCC3C2(C)C)C)CCC6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O)C)O)O)O 913.10 unknown https://doi.org/10.1016/0031-9422(96)00075-1
[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] 2,2,6b,9,9,12a-hexamethyl-10-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydro-1H-picene-4a-carboxylate 85408197 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5=C(C4(CCC3C2(C)C)C)CCC6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O)C)O)O)O 913.10 unknown https://doi.org/10.1016/0031-9422(96)00075-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bR)-10-[(2R,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 124870393 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)OC7C(C(C(C(O7)CO)O)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O 795.00 unknown https://doi.org/10.1016/0031-9422(95)00119-R
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bR)-10-[(2R,3R,4S,5S,6R)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 162955478 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O 795.00 unknown https://doi.org/10.1016/0031-9422(95)00119-R
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-4a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 102066408 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)OC7C(C(C(C(O7)CO)O)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)OC8C(C(C(C(O8)CO)O)O)O 957.10 unknown https://doi.org/10.1016/S0031-9422(96)00660-7
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-4a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 102066409 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)OC7C(C(C(C(O7)CO)O)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)OC8C(C(C(C(O8)CO)O)O)O 957.10 unknown https://doi.org/10.1016/S0031-9422(96)00660-7
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-4a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 102066410 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1C)C(=O)O)C(=O)OC8C(C(C(C(O8)CO)O)O)O 973.10 unknown https://doi.org/10.1016/S0031-9422(96)00660-7
(4aS,6aS,6aR,6bR,8aS,12aR,14bR)-10-[3,4-dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 129317017 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)OC7C(C(C(C(O7)CO)O)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O 795.00 unknown https://doi.org/10.1016/0031-9422(95)00119-R
10-[3,4-dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 74095099 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)OC7C(C(C(C(O7)CO)O)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O 795.00 unknown https://doi.org/10.1016/S0031-9422(96)00660-7
https://doi.org/10.1016/0031-9422(95)00119-R
10-[3,4-dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-4a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 75061280 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)OC7C(C(C(C(O7)CO)O)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)OC8C(C(C(C(O8)CO)O)O)O 957.10 unknown https://doi.org/10.1016/S0031-9422(96)00660-7
10-[3,5-dihydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 14060283 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O 795.00 unknown https://doi.org/10.1016/0031-9422(95)00119-R
10-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-4a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 162890430 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1C)C(=O)O)C(=O)OC8C(C(C(C(O8)CO)O)O)O 973.10 unknown https://doi.org/10.1016/S0031-9422(96)00660-7
Rubelloside B 91895455 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)OC7C(C(C(C(O7)CO)O)O)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O 795.00 unknown https://doi.org/10.1016/S0031-9422(96)00660-7
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(4aS,6aR,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6b,9,9,12a-hexamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 101995319 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5=C(C4(CCC3C2(C)C)C)CCC6(C5CC(CC6)(C)C)C(=O)O)C)OC7C(C(C(C(O7)CO)O)O)O)O)O 751.00 unknown https://doi.org/10.1016/0031-9422(96)00075-1
10-[4,5-dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6b,9,9,12a-hexamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 162879718 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5=C(C4(CCC3C2(C)C)C)CCC6(C5CC(CC6)(C)C)C(=O)O)C)OC7C(C(C(C(O7)CO)O)O)O)O)O 751.00 unknown https://doi.org/10.1016/0031-9422(96)00075-1

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