PlantaeDB Logo
Login Sign-up

Cladogynos orientalis

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

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 UUID6440304aede93430625898
Scientific name Cladogynos orientalis
Authority Zipp.
First published in Linnaea 15: 349 (1841)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Baprea bicolor Pierre ex Pax & K.Hoffm. Pflanzenr. , IV, 147, VII: 265 (1914)
Adenochlaena siamensis Ridl. J. Straits Branch Roy. Asiat. Soc. 59: 180 (1911)
Adenogynum odontophyllum Miq. Fl. Ned. Ind. 1(2): 400 (1859)
Rottlera albicans Hassk. Cat. Hort. Bot. Bogor. Alt. : 238 (1844)
Cephalocroton albicans var. virens Müll.Arg. Linnaea 34: 155. 1865
Cephalocroton discolor Müll.Arg. Prodr. 15(2): 761 (1866)
Cephalocroton orientalis Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 120 (1869)
Cladogynos orientalis var. grossedentata Pax & K.Hoffm. Pflanzenr. IV, 147 VII: 266. 1914
Cladogynos orientalis var. virens (Müll.Arg.) Pax & K.Hoffm. Pflanzenr. IV, 147 VII: 266 1914
Conceveiba tomentosa Span. Linnaea 15: 349 (1841)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Thai เจตพังคี
Chinese 白大凤

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
  • Asia-tropical
    • Indo-China
      • Cambodia
      • Laos
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000869122
Tropicos 50076247
KEW urn:lsid:ipni.org:names:341028-1
The Plant List kew-41385
Open Tree Of Life 3914748
NCBI Taxonomy 2068634
IPNI 341028-1
GBIF 3057416
EOL 1148081

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
Exploring the Therapeutic Potential of Traditional Antimalarial and Antidengue Plants: A Mechanistic Perspective Kamaraj C, Ragavendran C, Prem P, Naveen Kumar S, Ali A, Kazmi A, Ullah A, Chandra Satish Kumar R, Khan SU, Luna-Arias JP, Mashwani ZU, Balasubramani G, Rehman SU Can J Infect Dis Med Microbiol 28-Oct-2023
PMCID:PMC10625492
doi:10.1155/2023/1860084
PMID:37927532
Enhancement of cell migration and wound healing by nano-herb ointment formulated with biosurfactant, silver nanoparticles and Tridax procumbens Muthukumar B, Nandini MS, Elumalai P, Balakrishnan M, Satheeshkumar A, AlSalhi MS, Devanesan S, Parthipan P, Rajasekar A, Malik T Front Microbiol 02-Aug-2023
PMCID:PMC10434256
doi:10.3389/fmicb.2023.1225769
PMID:37601383
A Review with Updated Perspectives on the Antiviral Potentials of Traditional Medicinal Plants and Their Prospects in Antiviral Therapy Saifulazmi NF, Rohani ER, Harun S, Bunawan H, Hamezah HS, Nor Muhammad NA, Azizan KA, Ahmed QU, Fakurazi S, Mediani A, Sarian MN Life (Basel) 22-Aug-2022
PMCID:PMC9410304
doi:10.3390/life12081287
PMID:36013466
Umbu Fruit Peel as Source of Antioxidant, Antimicrobial and α-Amylase Inhibitor Compounds Ribeiro LD, de Freitas BP, Lorentino CM, Frota HF, dos Santos AL, Moreira DD, do Amaral BS, Jung EP, Kunigami CN Molecules 09-Jan-2022
PMCID:PMC8781721
doi:10.3390/molecules27020410
PMID:35056726
Production, Transmission, Pathogenesis, and Control of Dengue Virus: A Literature-Based Undivided Perspective Islam MT, Quispe C, Herrera-Bravo J, Sarkar C, Sharma R, Garg N, Fredes LI, Martorell M, Alshehri MM, Sharifi-Rad J, Daştan SD, Calina D, Alsafi R, Alghamdi S, Batiha GE, Cruz-Martins N Biomed Res Int 15-Dec-2021
PMCID:PMC8694986
doi:10.1155/2021/4224816
PMID:34957305
Anti-dengue activity of super critical extract and isolated oleanolic acid of Leucas cephalotes using in vitro and in silico approach Kaushik S, Dar L, Kaushik S, Yadav JP BMC Complement Med Ther 08-Sep-2021
PMCID:PMC8425015
doi:10.1186/s12906-021-03402-2
PMID:34496833
Dengue Fever: Therapeutic Potential of Carica papaya L. Leaves Sarker MM, Khan F, Mohamed IN Front Pharmacol 26-Apr-2021
PMCID:PMC8109180
doi:10.3389/fphar.2021.610912
PMID:33981215
Potential Medicinal Plants for the Treatment of Dengue Fever and Severe Acute Respiratory Syndrome-Coronavirus Saleh MS, Kamisah Y Biomolecules 30-Dec-2020
PMCID:PMC7824034
doi:10.3390/biom11010042
PMID:33396926
Traditional Asian Herbs in Skin Whitening: The Current Development and Limitations Hu Y, Zeng H, Huang J, Jiang L, Chen J, Zeng Q Front Pharmacol 07-Jul-2020
PMCID:PMC7358643
doi:10.3389/fphar.2020.00982
PMID:32733239
Selection of Thai Medicinal Plants with Anti-Obesogenic Potential via In Vitro Methods Ruangaram W, Kato E Pharmaceuticals (Basel) 29-Mar-2020
PMCID:PMC7243097
doi:10.3390/ph13040056
PMID:32235329
The Methylene-Cycloalkylacetate (MCA) Scaffold in Terpenyl Compounds with Potential Pharmacological Activities Tobal IE, Roncero AM, Moro RF, Díez D, Marcos IS Molecules 05-Jun-2019
PMCID:PMC6600407
doi:10.3390/molecules24112120
PMID:31195609
Effects of the Ayurved Siriraj Wattana recipe on functional and phenotypic characterization of cytokine-induced killer cells and dendritic cells in vitro Wongkajornsilp A, Numchaisermsuk N, Sa-ngiamsuntorn K, Akarasereenont P, Wamanuttajinda V, Kasetsinsombat K, Duangsa-ard S, Laohapan T, Maneechotesuwan K BMC Complement Altern Med 29-Nov-2016
PMCID:PMC5129228
doi:10.1186/s12906-016-1480-7
PMID:27899095
Antioxidant Activity and Antibacterial Effects on Clinical Isolated Streptococcus suis and Staphylococcus intermedius of Extracts from Several Parts of Cladogynos orientalis and Their Phytochemical Screenings Sithisarn P, Rojsanga P, Sithisarn P, Kongkiatpaiboon S Evid Based Complement Alternat Med 11-Aug-2015
PMCID:PMC4548143
doi:10.1155/2015/908242
PMID:26347795
Protective effect of AVS073, a polyherbal formula, against UVA-induced melanogenesis through a redox mechanism involving glutathione-related antioxidant defense Panich U, Pluemsamran T, Tangsupa-a-nan V, Wattanarangsan J, Phadungrakwittaya R, Akarasereenont P, Laohapand T BMC Complement Altern Med 05-Jul-2013
PMCID:PMC3706233
doi:10.1186/1472-6882-13-159
PMID:23826868
Potential anti-dengue medicinal plants: a review Abd Kadir SL, Yaakob H, Mohamed Zulkifli R J Nat Med 17-Apr-2013
PMCID:PMC3765846
doi:10.1007/s11418-013-0767-y
PMID:23591999

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Phthalate esters / m-Phthalate esters
8-Hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carboxylic acid 5242129 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C(=O)O 222.19 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(6R,9S)-3-Oxo-alpha-ionol glucoside 73815024 Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C 370.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027
(6R,9S)-Roseoside 11165077 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027
3Eec4Q65S4 21630888 Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C 370.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(1S,5S,6R)-5-[2-(furan-3-yl)ethyl]-1,5,6-trimethyl-2,3,4,6,7,8-hexahydronaphthalene-1-carboxylic acid 11404306 Click to see CC1CCC2=C(C1(C)CCC3=COC=C3)CCCC2(C)C(=O)O 316.40 unknown https://doi.org/10.1021/NP049877S
5-[2-(Furan-3-yl)ethyl]-1,5,6-trimethyl-2,3,4,6,7,8-hexahydronaphthalene-1-carboxylic acid 23928093 Click to see CC1CCC2=C(C1(C)CCC3=COC=C3)CCCC2(C)C(=O)O 316.40 unknown https://doi.org/10.1021/NP049877S
Chettaphanin II 11151979 Click to see CC1CCC2=C3C1(CC(=C3C(=O)CC2(C)C(=O)OC)C4=COC=C4)C 340.40 unknown https://doi.org/10.1021/NP049877S
methyl (1R,2S,7R,13R)-9-(furan-3-yl)-2,7,13-trimethyl-4-oxo-10-oxatricyclo[5.3.3.01,6]trideca-5,8-diene-2-carboxylate 11187407 Click to see CC1CCC23C(=CC(=O)CC2(C)C(=O)OC)C1(C=C(O3)C4=COC=C4)C 356.40 unknown https://doi.org/10.1021/NP049877S
methyl (1S,5S,6R,8aR)-5-[2-(furan-3-yl)-2-oxoethyl]-8a-hydroxy-1,5,6-trimethyl-3-oxo-2,6,7,8-tetrahydronaphthalene-1-carboxylate 102022433 Click to see CC1CCC2(C(=CC(=O)CC2(C)C(=O)OC)C1(C)CC(=O)C3=COC=C3)O 374.40 unknown https://doi.org/10.1021/NP049877S
methyl (1S,5S,6R,8aS)-5-[2-(furan-3-yl)-2-oxoethyl]-8a-hydroxy-1,5,6-trimethyl-3-oxo-2,6,7,8-tetrahydronaphthalene-1-carboxylate 11291777 Click to see CC1CCC2(C(=CC(=O)CC2(C)C(=O)OC)C1(C)CC(=O)C3=COC=C3)O 374.40 unknown https://doi.org/10.1021/NP049877S
methyl 2-(furan-3-yl)-5,8,8a-trimethyl-3-oxo-4,6,7,8-tetrahydro-1H-acenaphthylene-5-carboxylate 12302909 Click to see CC1CCC2=C3C1(CC(=C3C(=O)CC2(C)C(=O)OC)C4=COC=C4)C 340.40 unknown https://doi.org/10.1021/NP049877S
Methyl 5-[2-(furan-3-yl)-2-oxoethyl]-8a-hydroxy-1,5,6-trimethyl-3-oxo-2,6,7,8-tetrahydronaphthalene-1-carboxylate 398786 Click to see CC1CCC2(C(=CC(=O)CC2(C)C(=O)OC)C1(C)CC(=O)C3=COC=C3)O 374.40 unknown https://doi.org/10.1021/NP049877S
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4R,6S,7S)-1,4-dimethyl-7-prop-1-en-2-yl-1,2,3,4,5,6,7,8-octahydroazulen-6-ol 162937442 Click to see CC1CCC2=C1CC(C(CC2C)O)C(=C)C 220.35 unknown https://doi.org/10.1021/NP049877S
(1S,4S,6R,7R)-1,4-dimethyl-7-prop-1-en-2-yl-1,2,3,4,5,6,7,8-octahydroazulen-6-ol 11321984 Click to see CC1CCC2=C1CC(C(CC2C)O)C(=C)C 220.35 unknown https://doi.org/10.1021/NP049877S
1,4-Dimethyl-7-prop-1-en-2-yl-1,2,3,4,5,6,7,8-octahydroazulen-6-ol 72800862 Click to see CC1CCC2=C1CC(C(CC2C)O)C(=C)C 220.35 unknown https://doi.org/10.1021/NP049877S
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1021/NP049877S
beta-Spathulenol 522266 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1021/NP049877S
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1021/NP049877S
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Epitaraxerol 344467 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP049877S
methyl (4aS,6aR,6bR,8aR,10S,12aR,14aS,14bS)-10-acetyloxy-2,2,6b,9,9,12a,14a-heptamethyl-1,3,4,5,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydropicene-4a-carboxylate 14781553 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C(=O)OC)C)C)C 512.80 unknown https://doi.org/10.1021/NP049877S
Methyl 10-acetyloxy-2,2,6b,9,9,12a,14a-heptamethyl-1,3,4,5,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydropicene-4a-carboxylate 14781554 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C(=O)OC)C)C)C 512.80 unknown https://doi.org/10.1021/NP049877S
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP049877S
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1S,5R,6S,9S)-6-[2-(furan-3-yl)-2-oxoethyl]-1,5,6-trimethyl-10-oxatricyclo[7.2.1.02,7]dodec-2(7)-en-11-one 11461605 Click to see CC1CCC2=C(C1(C)CC(=O)C3=COC=C3)CC4CC2(C(=O)O4)C 328.40 unknown https://doi.org/10.1021/NP049877S
(1S,5R,6S,9S)-6-[2-(furan-3-yl)ethyl]-1,5,6-trimethyl-10-oxatricyclo[7.2.1.02,7]dodec-2(7)-en-11-one 21574257 Click to see CC1CCC2=C(C1(C)CCC3=COC=C3)CC4CC2(C(=O)O4)C 314.40 unknown https://doi.org/10.1021/NP049877S
6-[2-(Furan-3-yl)-2-oxoethyl]-1,5,6-trimethyl-10-oxatricyclo[7.2.1.02,7]dodec-2(7)-en-11-one 72970694 Click to see CC1CCC2=C(C1(C)CC(=O)C3=COC=C3)CC4CC2(C(=O)O4)C 328.40 unknown https://doi.org/10.1021/NP049877S
6-[2-(Furan-3-yl)ethyl]-1,5,6-trimethyl-10-oxatricyclo[7.2.1.02,7]dodec-2(7)-en-11-one 73797068 Click to see CC1CCC2=C(C1(C)CCC3=COC=C3)CC4CC2(C(=O)O4)C 314.40 unknown https://doi.org/10.1021/NP049877S
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
(1R,8R,11R)-11,12,12-trimethyltricyclo[6.3.1.01,5]dodec-4-ene-4-carboxylic acid 162955243 Click to see CC1CCC2CCC3=C(CCC13C2(C)C)C(=O)O 248.36 unknown https://doi.org/10.1021/NP049877S
11,12,12-Trimethyltricyclo[6.3.1.01,5]dodec-4-ene-4-carboxylic acid 162955242 Click to see CC1CCC2CCC3=C(CCC13C2(C)C)C(=O)O 248.36 unknown https://doi.org/10.1021/NP049877S
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-(3,4,5-trimethoxyphenoxy)oxane-3,4,5-triol 159732830 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)CO)O)O)O 346.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027
2-(Hydroxymethyl)-6-(3,4,5-trimethoxyphenoxy)oxane-3,4,5-triol 13922637 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)CO)O)O)O 346.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027
Koaburaside monomethyl ether 636454 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)CO)O)O)O 346.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027
methyl 2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxybenzoate 21770576 Click to see COC(=O)C1=CC=CC=C1OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027
Methyl 2-[(6-o-pentopyranosylhexopyranosyl)oxy]benzoate 10278 Click to see COC(=O)C1=CC=CC=C1OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
3,5-Dihydroxy-1,2-dimethoxy-9H-xanthen-9-one 154926285 Click to see COC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)OC 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-6-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 10929956 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 584.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 11813924 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 584.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Glucosyringic acid 10383888 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C(=O)O 360.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027
Syringic acid-4-beta-D-glucopyranoside 14132338 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C(=O)O 360.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.027

Biological Material Top ebay Auctions

Please wait .. loading items ..

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.