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Urceola rosea

Urceola rosea - 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 UUID643ff030be2f9143827700
Scientific name Urceola rosea
Authority (Hook. & Arn.) D.J.Middleton
First published in Novon 4: 151 (1994)

Description Top

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Synonyms Top

Scientific name Authority First published in
Antirhea esquirolii H.Lév. Fl. Kouy-Tchéou : 364 (1915)
Parameria pedunculosa (Miq.) Radlk. Sitzungsber. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. München 14: 506, 517 (1884)
Ecdysanthera pedunculosa Miq. Fl. Ned. Ind., Eerste Bijv. : 557 (1861)
Ecdysanthera rosea Hook. & Arn. Bot. Beechey Voy. : 198 (1837)

Common names Top

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Language Common/alternative name
Vietnamese răng bừa hồng
Chinese 黑风藤
Chinese 酸藤
Chinese 红背酸藤
Chinese 酸叶胶藤
Chinese 酸野胶藤
Chinese 斑鸪藤
Chinese 酸叶藤

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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No forms added yet.

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
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
    • Indo-China
      • Cambodia
      • Laos
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Malaya
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000330504
Tropicos 1806200
KEW urn:lsid:ipni.org:names:977799-1
The Plant List kew-210965
Open Tree Of Life 67466
NCBI Taxonomy 141623
IPNI 977799-1
iNaturalist 556427
GBIF 5535797
EOL 2899730

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
Merging total synthesis and NMR technology for deciphering the realistic structure of natural 2,6-dideoxyglycosides Zhang Z, Wu R, Cao S, Li J, Huang G, Wang H, Yang T, Tang W, Xu P, Yu B Sci Adv 12-Apr-2024
PMCID:PMC11014444
doi:10.1126/sciadv.adn1305
PMID:38608021
Therapeutic potential of Thai herbal formula for cognitive impairment: A metabolomics approach for Comprehensive Insights Akarasereenont P, Pattanapholkornsakul S, Limsuvan S, Mamaethong D, Booranasubkajorn S, Pakaprot N, Tripatara P, Pilakasiri K Heliyon 16-Mar-2024
PMCID:PMC10981045
doi:10.1016/j.heliyon.2024.e28027
PMID:38560220
Ethnobotanical study on edible flowers in Xishuangbanna, China Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C J Ethnobiol Ethnomed 30-Sep-2023
PMCID:PMC10542681
doi:10.1186/s13002-023-00608-1
PMID:37777741
Water stress and exogenous carnitine on growth and essential oil profile of Eryngium foetidum L. dos Santos SK, da Silva Gomes D, de Oliveira AF, Silva AM, de Moura VS, Gusmão MH, de Matos EM, Viccini LF, Grazul RM, Henschel JM, Batista DS 3 Biotech 02-Sep-2023
PMCID:PMC10475002
doi:10.1007/s13205-023-03757-y
PMID:37667775
Bioactive Steroids Bearing Oxirane Ring Dembitsky VM Biomedicines 09-Aug-2023
PMCID:PMC10452232
doi:10.3390/biomedicines11082237
PMID:37626733
Analytical determination, antioxidant and anti-inflammatory activities of Bhamrung-Lohit a traditional Thai medicine Panchakul C, Thongdeeying P, Itharat A, Pipatrattanaseree W, Kongkwamcharoen C, Davies NM Res Pharm Sci 01-Jun-2023
PMCID:PMC10443669
doi:10.4103/1735-5362.378091
PMID:37614616
Progress and prediction of multicomponent quantification in complex systems with practical LC-UV methods Chen X, Yang Z, Xu Y, Liu Z, Liu Y, Dai Y, Chen S J Pharm Anal 05-Dec-2022
PMCID:PMC9999300
doi:10.1016/j.jpha.2022.11.011
PMID:36908853
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
Anti-Inflammatory Effects of Mitrephora sirikitiae Leaf Extract and Isolated Lignans in RAW 264.7 Cells Mangmool S, Limpichai C, Han KK, Reutrakul V, Anantachoke N Molecules 21-May-2022
PMCID:PMC9147141
doi:10.3390/molecules27103313
PMID:35630789
Recent Applications of Capillary Electrophoresis in the Determination of Active Compounds in Medicinal Plants and Pharmaceutical Formulations Gackowski M, Przybylska A, Kruszewski S, Koba M, Mądra-Gackowska K, Bogacz A Molecules 07-Jul-2021
PMCID:PMC8307982
doi:10.3390/molecules26144141
PMID:34299418
Ethnobotanical study on wild edible plants used by three trans-boundary ethnic groups in Jiangcheng County, Pu’er, Southwest China Cao Y, Li R, Zhou S, Song L, Quan R, Hu H J Ethnobiol Ethnomed 27-Oct-2020
PMCID:PMC7590688
doi:10.1186/s13002-020-00420-1
PMID:33109239
Pharmacological Targets of Kaempferol Within Inflammatory Pathways—A Hint Towards the Central Role of Tryptophan Metabolism Hofer S, Geisler S, Lisandrelli R, Nguyen Ngoc H, Ganzera M, Schennach H, Fuchs D, Fuchs JE, M. Gostner J, Kurz K Antioxidants (Basel) 21-Feb-2020
PMCID:PMC7070836
doi:10.3390/antiox9020180
PMID:32098277
Hydroquinone; A Novel Bioactive Compound from Plant-Derived Smoke Can Cue Seed Germination of Lettuce Kamran M, Khan AL, Ali L, Hussain J, Waqas M, Al-Harrasi A, Imran QM, Kim YH, Kang SM, Yun BW, Lee IJ Front Chem 12-May-2017
PMCID:PMC5427145
doi:10.3389/fchem.2017.00030
PMID:28553632
Synopsis of Phyllosticta in China Zhang K, Shivas RG, Cai L Mycology 17-Apr-2015
PMCID:PMC4409051
doi:10.1080/21501203.2015.1027507
PMID:26000199
Chemical Constituents from the Stems of Ecdysanthera rosea. Song CW, Lunga PK, Qin XJ, Cheng GG, Liu YP, Luo XD Nat Prod Bioprospect 01-Dec-2014
PMCID:PMC4250565
doi:10.1007/S13659-014-0041-3
PMID:25362577

Phytochemical Profile Top

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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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4250565/
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4250565/
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4250565/
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4250565/
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
butyl (1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylate 6481825 Click to see CCCCOC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 410.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4250565/
Butyl chlorogenate 12135130 Click to see CCCCOC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 410.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4250565/
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4250565/
Methyl chlorogenate 6476139 Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 368.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4250565/
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4250565/

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