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Cyanotis arachnoidea

Cyanotis arachnoidea - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Cyanotis arachnoidea - 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 UUID643ff4da8af23503002060
Scientific name Cyanotis arachnoidea
Authority C.B.Clarke
First published in Monogr. Phan. 3: 250 (1881)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cyanotis arachnoidea var. obtusa Trimen J. Bot. 23: 266. 1885
Cyanotis bodinieri H.Lév. & Vaniot Mém. Soc. Sci. Nat. Cherbourg 35: 385 (1906)
Cyanotis labordei H.Lév. & Vaniot Mém. Soc. Sci. Nat. Cherbourg 35: 386 (1906)
Cyanotis nilagirica Hassk. Commelin. Ind. : 127 (1870)
Cyanotis obtusa Trimen Handb. Fl. Ceylon 4: 812 (1898)
Cyanotis pilosa Wight Icon. Pl. Ind. Orient. 6: t. 2083 (1853)
Tonningia arachnodea Kuntze Revis. Gen. Pl. 2: 722 (1891)
Tradescantia incana B.Heyne ex C.B.Clarke Monogr. Phan. 3: 250 (1881)
Tradescantia lanata B.Heyne ex C.B.Clarke Monogr. Phan. 3: 250 (1881)

Common names Top

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Language Common/alternative name
Chinese 露水草
Chinese 珍珠露水草
Chinese 蛛丝毛蓝耳草
Chinese 蛛絲毛藍耳草
Chinese 鴨舌疝
Chinese 鸡冠参

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
    • Northeast Tropical Africa
      • Sudan
    • South Tropical Africa
      • Zimbabwe
    • West Tropical Africa
      • Ghana
      • Ivory Coast
      • Liberia
      • Nigeria
      • Togo
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Equatorial Guinea
      • Gabon
      • Rwanda
      • Zaïre
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • India
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000366326
UNII FKI9P49M8M
Tropicos 8300763
INPN 986285
KEW urn:lsid:ipni.org:names:172445-1
The Plant List kew-235333
Open Tree Of Life 3945545
NCBI Taxonomy 1503182
IPNI 172445-1
iNaturalist 627503
GBIF 5303388
EOL 1122264

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
Ecdysterone and Turkesterone—Compounds with Prominent Potential in Sport and Healthy Nutrition Todorova V, Ivanova S, Chakarov D, Kraev K, Ivanov K Nutrients 02-May-2024
PMCID:PMC11085066
doi:10.3390/nu16091382
PMID:38732627
17-Oxime ethers of oxidized ecdysteroid derivatives modulate oxidative stress in human brain endothelial cells and dose-dependently might protect or damage the blood-brain barrier Vágvölgyi M, Laczkó D, Santa-Maria AR, Vigh JP, Walter FR, Berkecz R, Deli MA, Tóth G, Hunyadi A PLoS One 22-Feb-2024
PMCID:PMC10883584
doi:10.1371/journal.pone.0290526
PMID:38386637
Efficacy of oral 20-hydroxyecdysone (BIO101), a MAS receptor activator, in adults with severe COVID-19 (COVA): a randomized, placebo-controlled, phase 2/3 trial Lobo SM, Plantefève G, Nair G, Joaquim Cavalcante A, Franzin de Moraes N, Nunes E, Barnum O, Berdun Stadnik CM, Lima MP, Lins M, Hajjar LA, Lipinski C, Islam S, Ramos F, Simon T, Martinot JB, Guimard T, Desclaux A, Lioger B, Neuenschwander FC, DeSouza Paolino B, Amin A, Acosta SA, Dilling DF, Cartagena E, Snyder B, Devaud E, Barreto Berselli Marinho AK, Tanni S, Milhomem Beato PM, De Wit S, Selvan V, Gray J, Fernandez R, Pourcher V, Maddox L, Kay R, Azbekyan A, Chabane M, Tourette C, Esmeraldino LE, Dilda PJ, Lafont R, Mariani J, Camelo S, Rabut S, Agus S, Veillet S, Dioh W, van Maanen R, Morelot-Panzini C eClinicalMedicine 03-Jan-2024
PMCID:PMC10965409
doi:10.1016/j.eclinm.2023.102383
PMID:38545090
Correction to “Highly Oxidized Ecdysteroids from a Commercial Cyanotis arachnoidea Root Extract as Potent Blood–Brain Barrier Protective Agents” Tóth G, Santa-Maria AR, Herke I, Gáti T, Galvis-Montes D, Walter FR, Deli MA, Hunyadi A J Nat Prod 23-Nov-2023
PMCID:PMC10749464
doi:10.1021/acs.jnatprod.3c00927
PMID:37994035
Identification of quality markers for Cyanotis arachnoidea and analysis of its physiological mechanism based on chemical pattern recognition, network pharmacology, and experimental validation Hu J, Feng Y, Li B, Wang F, Qian Q, Tian W, Niu L, Wang X PeerJ 11-Sep-2023
PMCID:PMC10501370
doi:10.7717/peerj.15948
PMID:37719108
Cyclodextrins for the Delivery of Bioactive Compounds from Natural Sources: Medicinal, Food and Cosmetics Applications Christaki S, Spanidi E, Panagiotidou E, Athanasopoulou S, Kyriakoudi A, Mourtzinos I, Gardikis K Pharmaceuticals (Basel) 08-Sep-2023
PMCID:PMC10535610
doi:10.3390/ph16091274
PMID:37765082
Ethnobotanical study on medicinal plants used by Bulang people in Yunnan, China Zhou H, Zhang J, Kirbis BS, Mula Z, Zhang W, Kuang Y, Huang Q, Yin L J Ethnobiol Ethnomed 07-Sep-2023
PMCID:PMC10486041
doi:10.1186/s13002-023-00609-0
PMID:37679773
3-Hydroxy-3-methylglutaryl coenzyme A reductase genes from Glycine max regulate plant growth and isoprenoid biosynthesis Wang S, Feng Y, Lou Y, Niu J, Yin C, Zhao J, Du W, Yue A Sci Rep 08-Mar-2023
PMCID:PMC9995466
doi:10.1038/s41598-023-30797-4
PMID:36890158
Highly Oxidized Ecdysteroids from a Commercial Cyanotis arachnoidea Root Extract as Potent Blood–Brain Barrier Protective Agents Tóth G, Santa-Maria AR, Herke I, Gáti T, Galvis-Montes D, Walter FR, Deli MA, Hunyadi A J Nat Prod 24-Feb-2023
PMCID:PMC10152481
doi:10.1021/acs.jnatprod.2c00948
PMID:36825873
The Distribution of Phytoecdysteroids among Terrestrial Vascular Plants: A Comparison of Two Databases and Discussion of the Implications for Plant/Insect Interactions and Plant Protection Dinan L, Lafont F, Lafont R Plants (Basel) 09-Feb-2023
PMCID:PMC9967490
doi:10.3390/plants12040776
PMID:36840124
Autophagy: An important target for natural products in the treatment of bone metabolic diseases Li Z, Li D, Su H, Xue H, Tan G, Xu Z Front Pharmacol 18-Nov-2022
PMCID:PMC9716086
doi:10.3389/fphar.2022.999017
PMID:36467069
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
Market survey on the traditional medicine of the Lijiang area in Yunnan Province, China Zhang M, Li H, Wang J, Tang M, Zhang X, Yang S, Liu J, Li Y, Huang X, Li Z, Huang L J Ethnobiol Ethnomed 23-May-2022
PMCID:PMC9125852
doi:10.1186/s13002-022-00532-w
PMID:35606860
Transcriptome and Metabolome Analysis of the Synthesis Pathways of Allelochemicals in Eupatorium adenophorum Cheng W, Jia G, Zhang J, Lin L, Cui M, Zhang D, Jiao M, Zhao X, Wang S, Dong J, Xing Z ACS Omega 04-May-2022
PMCID:PMC9118424
doi:10.1021/acsomega.2c01816
PMID:35601343
Diversity-Oriented Synthesis Catalyzed by Diethylaminosulfur-Trifluoride—Preparation of New Antitumor Ecdysteroid Derivatives Vágvölgyi M, Kocsis E, Nové M, Szemerédi N, Spengler G, Kele Z, Berkecz R, Gáti T, Tóth G, Hunyadi A Int J Mol Sci 22-Mar-2022
PMCID:PMC8998355
doi:10.3390/ijms23073447
PMID:35408806

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 / Androstane steroids / Androgens and derivatives
2,3,14-Trihydroxy-10,13-dimethyl-1,2,3,4,5,9,11,12,15,16-decahydrocyclopenta[a]phenanthrene-6,17-dione 536348 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2=O)O 334.40 unknown https://doi.org/10.1080/1028602031000105830
5beta-Androst-7-en-6-one, 2beta,3beta,14,17beta-tetrahydroxy- 22213160 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2O)O 336.40 unknown https://doi.org/10.1080/1028602031000105830
Rubrosterone 12315102 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2=O)O 334.40 unknown https://doi.org/10.1080/1028602031000105830
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
20-Hydroxyecdysone 5459840 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown https://doi.org/10.1080/10286020290019631
20,26-Dihydroxyecdysone 21123946 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(CO)O)O)O)O 496.60 unknown https://doi.org/10.1080/10286020290019631
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/10.1080/10286020290019631
Turkesterone 14376672 Click to see CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O)O 496.60 unknown https://doi.org/10.1080/10286020290019631
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
Poststerone 441835 Click to see CC(=O)C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O 362.50 unknown https://doi.org/10.1080/1028602031000105830
> 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://doi.org/10.1080/1028602031000105830
https://doi.org/10.1080/10286020290019631
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://doi.org/10.1080/10286020290019631
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://doi.org/10.1080/1028602031000105830

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