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Hydnophytum formicarum

Hydnophytum formicarum - Unknown
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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 UUID643fdf4b0e92e109254433
Scientific name Hydnophytum formicarum
Authority Jack
First published in Trans. Linn. Soc. London 14: 124 (1823)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hydnophytum amboinense Becc. Malesia 2: 124 (1884)
Hydnophytum andamanense Becc. Malesia 2: 155 (1885)
Hydnophytum blumei Becc. Malesia 2: 125 (1884)
Hydnophytum borneense Becc. Malesia 2: 125 (1884)
Hydnophytum coriaceum Becc. Malesia 2: 156 (1885)
Hydnophytum gaudichaudii Becc. Malesia 2: 124 (1884)
Hydnophytum inerme (Gaudich.) Bremek. Blumea 5: 245 (1942)
Hydnophytum intermedium Elmer Leafl. Philipp. Bot. 3: 1039 (1911)
Hydnophytum leytense Merr. Philipp. J. Sci., C 8: 390 (1913)
Hydnophytum membranaceum Merr. Philipp. J. Sci., C 10: 143 (1915)
Hydnophytum mindorense Merr. Philipp. J. Sci., C 10: 143 (1915)
Hydnophytum montanum Blume Bijdr. Fl. Ned. Ind. : 956 (1826)
Hydnophytum nitidum Merr. Philipp. J. Sci., C 2: 307 (1907)
Hydnophytum orbiculatum Elmer Leafl. Philipp. Bot. 5: 1860 (1913)
Hydnophytum selebicum Becc. Malesia 2: 125 (1884)
Hydnophytum sumatranum Becc. Malesia 2: 124 (1884)
Lasiostoma formicarum Spreng. Syst. Veg. 1: 423 (1824)
Myrmecodia inermis Gaudich. Voy. Uranie : 472 (1830)
Hydnophytum formicarum var. latifolium (Miq.) Becc. Malesia 2: 160 1885
Hydnophytum montanum var. latifolia Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 257. 1869
Hydnophytum formicarum var. longifolium Becc. Malesia 2: 161. 1885
Hydnophytum formicarum var. minor Becc. Malesia 2: 161. 1885
Hydnophytum formicarum var. borneense (Becc.) Becc. Malesia 2: 162 1885
Hydnophytum formicarum var. buxifolium Becc. Malesia 2: 163. 1885
Hydnophytum formicarum var. cochincinense Becc. Malesia 2: 163. 1885
Hydnophytum formicarum var. lucidum Becc. Malesia 2: 164. 1885
Hydnophytum formicarum subsp. zollingeri (Becc.) Boerl. Handl. Fl. Ned. Ind. 2(1): 143. 1891 (1891)
Hydnophytum formicarum subsp. blumei Boerl. Handl. Fl. Ned. Ind. 2(1): 143. 1891 (1891)
Hydnophytum formicarum subsp. dubium (Becc.) Boerl. Handl. Fl. Ned. Ind. 2(1): 143. 1891 (1891)
Hydnophytum formicarum subsp. siamense (Becc.) Boerl. Handl. Fl. Ned. Ind. 2(1): 143. 1891 (1891)
Hydnophytum formicarum f. borneense (Becc.) Becc. Malesia 2: 162 1885
Hydnophytum formicarum f. latifolium (Miq.) Becc. Malesia 2: 160 1885

Common names Top

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Language Common/alternative name
Thai หัวร้อยรู
Chinese 南亚蚁茜
Chinese 安德曼蚁茜
Chinese 无刺蚁茜
Chinese 莱特蚁茜
Chinese 西里伯斯蚁茜

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-tropical
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000215798
Tropicos 100000487
KEW urn:lsid:ipni.org:names:753446-1
The Plant List kew-100941
Open Tree Of Life 233588
NCBI Taxonomy 29797
IPNI 753446-1
iNaturalist 425668
GBIF 2895700
EOL 1103651
USDA GRIN 413403
Wikipedia Hydnophytum_formicarum

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
Butein Ameliorates Oxidative Stress in H9c2 Cardiomyoblasts through Activation of the NRF2 Signaling Pathway Tungalag T, Park KW, Yang DK Antioxidants (Basel) 23-Jul-2022
PMCID:PMC9331242
doi:10.3390/antiox11081430
PMID:35892632
Cellular Growth in Aerial Roots Differs From That in Typical Substrate Roots Eskov AK, Viktorova VA, Abakumov E, Zotz G Front Plant Sci 26-May-2022
PMCID:PMC9199517
doi:10.3389/fpls.2022.894647
PMID:35720525
Mangrove floristic composition dataset of the Setiu Lagoon, Terengganu Malaysia Muhammad Nor SM, Sahari MS, Razali NA, Salam MR, Wan Mustaffa WF, Stephen ER, Yusof RM, Jamaludin PN, Jamaludin PN, Mokhetar N Data Brief 04-Mar-2022
PMCID:PMC8960900
doi:10.1016/j.dib.2022.108020
PMID:35360048
Antioxidant Effects of Protocatechuic Acid and Protocatechuic Aldehyde: Old Wine in a New Bottle Zhang S, Gai Z, Gui T, Chen J, Chen Q, Li Y Evid Based Complement Alternat Med 08-Nov-2021
PMCID:PMC8592717
doi:10.1155/2021/6139308
PMID:34790246
Mechanisms and Neuroprotective Activities of Stigmasterol Against Oxidative Stress-Induced Neuronal Cell Death via Sirtuin Family Pratiwi R, Nantasenamat C, Ruankham W, Suwanjang W, Prachayasittikul V, Prachayasittikul S, Phopin K Front Nutr 12-May-2021
PMCID:PMC8149742
doi:10.3389/fnut.2021.648995
PMID:34055852
Potential anti-Acanthamoeba and anti-adhesion activities of Annona muricata and Combretum trifoliatum extracts and their synergistic effects in combination with chlorhexidine against Acanthamoeba triangularis trophozoites and cysts Mitsuwan W, Sin C, Keo S, Sangkanu S, de Lourdes Pereira M, Jimoh TO, Salibay CC, Nawaz M, Norouzi R, Siyadatpanah A, Wiart C, Wilairatana P, Mutombo PN, Nissapatorn V Heliyon 10-May-2021
PMCID:PMC8131895
doi:10.1016/j.heliyon.2021.e06976
PMID:34027178
Butein, isoliquiritigenin, and scopoletin attenuate neurodegeneration via antioxidant enzymes and SIRT1/ADAM10 signaling pathway Gay NH, Suwanjang W, Ruankham W, Songtawee N, Wongchitrat P, Prachayasittikul V, Prachayasittikul S, Phopin K RSC Adv 27-Apr-2020
PMCID:PMC9053097
doi:10.1039/c9ra06056a
PMID:35498835
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
Assessing the Identity of Commercial Herbs From a Cambodian Market Using DNA Barcoding Cui X, Li W, Wei J, Qi Y, Li R, Yang Y, Shi Y, Meng X, Mi Y, Huot T, Sun W, Zheng X Front Pharmacol 24-Mar-2020
PMCID:PMC7105672
doi:10.3389/fphar.2020.00244
PMID:32265692
Vascular Epiphytic Medicinal Plants as Sources of Therapeutic Agents: Their Ethnopharmacological Uses, Chemical Composition, and Biological Activities Nugraha AS, Triatmoko B, Wangchuk P, Keller PA Biomolecules 24-Jan-2020
PMCID:PMC7072150
doi:10.3390/biom10020181
PMID:31991657
HPTLC – Bioautographic methods for selective detection of the antioxidant and α-amylase inhibitory activity in plant extracts Agatonovic-Kustrin S, Morton DW MethodsX 20-Jul-2018
PMCID:PMC6082773
doi:10.1016/j.mex.2018.07.013
PMID:30101083
Targeting Histone Deacetylases with Natural and Synthetic Agents: An Emerging Anticancer Strategy Singh AK, Bishayee A, Pandey AK Nutrients 06-Jun-2018
PMCID:PMC6024317
doi:10.3390/nu10060731
PMID:29882797
Hypoglycaemic activity of Mathurameha, a Thai traditional herbal formula aqueous extract, and its effect on biochemical profiles of streptozotocin-nicotinamide-induced diabetic rats Chayarop K, Peungvicha P, Temsiririrkkul R, Wongkrajang Y, Chuakul W, Rojsanga P BMC Complement Altern Med 29-Jun-2017
PMCID:PMC5492915
doi:10.1186/s12906-017-1851-8
PMID:28662699
Anticancer Natural Compounds as Epigenetic Modulators of Gene Expression Ratovitski EA Curr Genomics 01-Apr-2017
PMCID:PMC5345332
doi:10.2174/1389202917666160803165229
PMID:28367075
GC-MS Based Metabolite Profiling, Antioxidant and Antimicrobial Properties of Different Solvent Extracts of Malaysian Plectranthus amboinicus Leaves Swamy MK, Arumugam G, Kaur R, Ghasemzadeh A, Yusoff MM, Sinniah UR Evid Based Complement Alternat Med 23-Mar-2017
PMCID:PMC5382359
doi:10.1155/2017/1517683
PMID:28424737

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
(3S,8S,9S,10R,13R,14S,17R)-17-[(Z,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11761435 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245381/
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245381/
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Protocatechualdehyde 8768 Click to see C1=CC(=C(C=C1C=O)O)O 138.12 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245381/
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
3',4',7-Trihydroxyflavanone 3496769 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O 272.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245381/
Butin 92775 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O 272.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245381/
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2',3,4,4'-tetrahydroxy Chalcone 2483 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O)O 272.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245381/
Butein 5281222 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O)O 272.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245381/
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245381/
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245381/

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