Aeginetia indica - Unknown
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Internal ID UUID6440078e0c0a3432707142
Scientific name Aeginetia indica
Authority L.
First published in Sp. Pl. : 632 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aeginetia aeginetia Huth Helios xi. 132 (1893).
Aeginetia boninensis Nakai Bot. Mag. (Tokyo) 45: 134 (1931)
Aeginetia indica var. gracilis Nakai Bot. Mag. (Tokyo) 45: 136 (1931)
Aeginetia japonica Siebold & Zucc. Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 141 (1846)
Aeginetia mairei H.Lév. Cat. Pl. Yun-Nan : 199 (1916)
Orobanche aeginetia L. Sp. Pl., ed. 2. 2: 883. 1763 [Aug 1763]

Common names Top

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Language Common/alternative name
English ye gu
Japanese ナンバンギセル
Malayalam ചെങ്കുമിൾ
mnw ကဴကလအ်တိ (ကဴလံင်တိ)
pam sampaga ning atbu
Thai ดอกดิน
Vietnamese tai đất Ấn
Vietnamese lệ dương
Chinese 野菰
Chinese 土灵芝草
Chinese 烟斗花
Chinese 马口含珠
Chinese 鸭脚板

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Ogasawara-Shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Philippines
    • Papuasia
      • New Guinea

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000521508
USDA Plants AEIN6
Tropicos 23600255
KEW urn:lsid:ipni.org:names:661840-1
The Plant List kew-2623431
Open Tree Of Life 714982
NCBI Taxonomy 290220
IUCN Red List 18783621
IPNI 661840-1
iNaturalist 84830
GBIF 3173321
Freebase /m/0_82vwc
EPPO AEIIN
EOL 590102
USDA GRIN 413728
Wikipedia Aeginetia_indica

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
Elucidating the multichromosomal structure within the Brasenia schreberi mitochondrial genome through assembly and analysis Shan Y, Li J, Duan X, Zhang X, Yu J BMC Genomics 29-Apr-2024
PMCID:PMC11059650
doi:10.1186/s12864-024-10331-0
PMID:38684976
Optimized Conditions for the Extraction of Phenolic Compounds from Aeginetia indica L. and Its Potential Biological Applications On-Nom N, Thangsiri S, Inthachat W, Temviriyanukul P, Sahasakul Y, Aursalung A, Chupeerach C, Suttisansanee U Molecules 28-Feb-2024
PMCID:PMC10935255
doi:10.3390/molecules29051050
PMID:38474563
Comprehensive Analysis of the Complete Mitochondrial Genome of Rehmannia chingii: An Autotrophic Species in the Orobanchaceae Family Han Y, Feng YL, Wang J, Zhu SS, Jin XJ, Wu ZQ, Zhang YH Genes (Basel) 15-Jan-2024
PMCID:PMC10815111
doi:10.3390/genes15010098
PMID:38254987
Ethnobotanical study of medicinal plants used by the indigenous community of the western region of Mizoram, India Ralte L, Sailo H, Singh YT J Ethnobiol Ethnomed 03-Jan-2024
PMCID:PMC10765666
doi:10.1186/s13002-023-00642-z
PMID:38172927
Fertilization benefits the facultative parasitic plant Rhamphicarpa fistulosa while gains by the infected host Oryza sativa are marginalized Rodenburg J, Dümmer R, Ho YH, Bastiaans L Ann Bot 13-Dec-2023
PMCID:PMC11005769
doi:10.1093/aob/mcad190
PMID:38092463
Effects of Ottonia anisum plant extract on local anesthetic, analgesic, anti-inflammatory and HCl‑induced acute lung injury activities: a study in animal models Liu M, Wang H, Yue Q, Liu J Bioresour Bioprocess 30-Nov-2023
PMCID:PMC10992343
doi:10.1186/s40643-023-00706-8
The Mitochondrial Genome of the Holoparasitic Plant Thonningia sanguinea Provides Insights into the Evolution of the Multichromosomal Structure Zhou S, Wei N, Jost M, Wanke S, Rees M, Liu Y, Zhou R Genome Biol Evol 21-Aug-2023
PMCID:PMC10476698
doi:10.1093/gbe/evad155
PMID:37603455
Invited Review Beyond parasitic convergence: unravelling the evolution of the organellar genomes in holoparasites Sanchez-Puerta MV, Ceriotti LF, Gatica-Soria LM, Roulet ME, Garcia LE, Sato HA Ann Bot 28-Jul-2023
PMCID:PMC10808021
doi:10.1093/aob/mcad108
PMID:37503831
Factors contributing to mitogenome size variation and a recurrent intracellular DNA transfer in Melastoma Zhou S, Zhi X, Yu R, Liu Y, Zhou R BMC Genomics 01-Jul-2023
PMCID:PMC10315049
doi:10.1186/s12864-023-09488-x
PMID:37393222
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Health Benefits and Pharmacological Properties of Stigmasterol Bakrim S, Benkhaira N, Bourais I, Benali T, Lee LH, El Omari N, Sheikh RA, Goh KW, Ming LC, Bouyahya A Antioxidants (Basel) 27-Sep-2022
PMCID:PMC9598710
doi:10.3390/antiox11101912
PMID:36290632
Highly active repeat-mediated recombination in the mitogenome of the holoparasitic plant Aeginetia indica Zhong Y, Yu R, Chen J, Liu Y, Zhou R Front Plant Sci 21-Sep-2022
PMCID:PMC9532969
doi:10.3389/fpls.2022.988368
PMID:36212306
Comparing complete organelle genomes of holoparasitic Christisonia kwangtungensis (Orabanchaceae) with its close relatives: how different are they? Zhang C, Lin Q, Zhang J, Huang Z, Nan P, Li L, Song Z, Zhang W, Yang J, Wang Y BMC Plant Biol 17-Sep-2022
PMCID:PMC9482287
doi:10.1186/s12870-022-03814-3
PMID:36114450
The complete mitochondrial genome of okra (Abelmoschus esculentus): using nanopore long reads to investigate gene transfer from chloroplast genomes and rearrangements of mitochondrial DNA molecules Li J, Li J, Ma Y, Kou L, Wei J, Wang W BMC Genomics 29-Jun-2022
PMCID:PMC9245263
doi:10.1186/s12864-022-08706-2
PMID:35768783
Unprecedented organelle genomic variations in morning glories reveal independent evolutionary scenarios of parasitic plants and the diversification of plant mitochondrial complexes Lin Y, Li P, Zhang Y, Akhter D, Pan R, Fu Z, Huang M, Li X, Feng Y BMC Biol 16-Feb-2022
PMCID:PMC8851834
doi:10.1186/s12915-022-01250-1
PMID:35172831

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1002/JCCS.200400160
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown https://doi.org/10.1002/JCCS.200400160
4-Hydroxy-3-methoxycinnamaldehyde 5280536 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown https://doi.org/10.1002/JCCS.200400160
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
[(1aS,4aR,5R,6R,7S,7aR,7bS)-6,7-dihydroxy-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[e]azulen-5-yl] acetate 101997925 Click to see CC(=O)OC1C2C(C3C(C3(C)C)CCC2=C)C(C1O)(C)O 294.40 unknown https://doi.org/10.1002/JCCS.200300183
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
2-[2-Hydroxy-2-(5-hydroxy-3-methylpenta-1,3-dienyl)-1,3,3-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162870026 Click to see CC(=CCO)C=CC1(C(CCCC1(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C)O 416.50 unknown https://doi.org/10.1248/CPB.27.2807
> 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/10.1016/0378-8741(85)90026-1
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/10.1016/0378-8741(85)90026-1
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown https://doi.org/10.1002/JCCS.200400160
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+/-)-Balanophonin 72729357 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O 356.40 unknown https://doi.org/10.1002/JCCS.200300183
(2R,3R,4S,5S,6R)-2-[(Z)-3-[(2R,3S)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163193707 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCOC4C(C(C(C(O4)CO)O)O)O 520.50 unknown https://doi.org/10.1002/JCCS.200300183
2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-carbaldehyde 14274766 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=O 330.30 unknown https://doi.org/10.1002/JCCS.200300183
Balanophonin 21582569 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O 356.40 unknown https://doi.org/10.1002/JCCS.200300183
Ficusal 10496641 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=O 330.30 unknown https://doi.org/10.1002/JCCS.200300183
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4S,5R,6R)-5-acetyloxy-4-[(2S,3R,4R,5S,6S)-4-acetyloxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 163186736 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)O)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)OC(=O)C)O 708.70 unknown https://doi.org/10.1002/JCCS.200400160
[5-Acetyloxy-4-(4-acetyloxy-3,5-dihydroxy-6-methyloxan-2-yl)oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 163025129 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)O)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)OC(=O)C)O 708.70 unknown https://doi.org/10.1002/JCCS.200400160
[5-Hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 73157771 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O 638.60 unknown https://doi.org/10.1002/JCCS.200400160
2-Acetylacteoside 21629996 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)O)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O 666.60 unknown https://doi.org/10.1002/JCCS.200400160
2'-Acetylacteoside 73814627 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)O)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O 666.60 unknown https://doi.org/10.1002/JCCS.200400160
Acteoside;Kusaginin;TJC160 354009 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1002/JCCS.200400160
Jionoside D 9895632 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O 638.60 unknown https://doi.org/10.1002/JCCS.200400160
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1002/JCCS.200400160
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
[3,5-Dihydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 162968681 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)O)O)O)O 488.40 unknown https://doi.org/10.1002/JCCS.200400160
Rha(a1-3)Glc(b)-O-coumaroyl(3-OH) 163189008 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)O)O)O)O 488.40 unknown https://doi.org/10.1002/JCCS.200400160
> 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/10.1016/0378-8741(85)90026-1

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