Paramignya monophylla - Unknown
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Internal ID UUID6440008098174284127042
Scientific name Paramignya monophylla
Authority Wight
First published in Ill. Ind. Bot. 1: 109 (1838)

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Synonyms Top

Scientific name Authority First published in
Micromelum monophyllum Wight Ill. Ind. Bot. 1: t. 42 (1838)
Atalantia correae Guillaumin Notul. Syst. (Paris) 1: 179 (1910)

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Paramignya monophylla var. obtusa B.C.Stone Revis. Handb. Fl. Ceylon 5: 469 (1985)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Sri Lanka
    • Indo-China
      • Myanmar
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000470440
Tropicos 28100031
KEW urn:lsid:ipni.org:names:774527-1
Open Tree Of Life 232708
NCBI Taxonomy 159064
IPNI 774527-1
iNaturalist 985108
GBIF 7269299
USDA GRIN 26751

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 CentralĀ®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Multi-Gene Phylogeny and Morphology Reveal Haplohelminthosporium gen. nov. and Helminthosporiella gen. nov. Associated with Palms in Thailand and A Checklist for Helminthosporium Reported Worldwide Konta S, Hyde KD, Karunarathna SC, Mapook A, Senwanna C, Dauner LA, Nanayakkara CM, Xu J, Tibpromma S, Lumyong S Life (Basel) 19-May-2021
PMCID:PMC8161214
doi:10.3390/life11050454
PMID:34069619
Efficacy of traditional treatment regimen on Kati Shoola with special reference to lumbar spondylolisthesis Ediriweera ER, Gunathilka HD, Weerasinghe KD, Kalawana OT Ayu 01-Jan-2013
PMCID:PMC3764887
doi:10.4103/0974-8520.115435
PMID:24049411
Anti-Viral Activity of Indian Plants Dhawan BN Proc Natl Acad Sci India Sect B Biol Sci 18-Jan-2012
PMCID:PMC7099914
doi:10.1007/s40011-011-0016-7
PMID:32226204
Coumarins from stem bark of Paramignya monophylla Vijaya Kumar, N.M.Mohamed Niyaz, D.B.Mahinda Wickramaratne Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(94)00485-C
Coumarins from Paramignya monophylla root bark Vijaya Kumar, N.M.Mohamed Niyaz, Shanthini Saminathan, D.B.Mahinda Wickramaratne Elsevier BV 26-Jul-2002
doi:10.1016/S0031-9422(97)00760-7
Tirucallane derivatives from Paramignya monophylla fruits Vijaya Kumar, N.M.Mohammed Niyaz, D.B.Mahinda Wickramaratne, Sinnathamby Balasubramaniam Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)95207-5

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
10-(3,7-Dimethylocta-1,6-dien-3-yl)-5-hydroxy-2,2-dimethylpyrano[3,2-g]chromen-8-one 15228828 Click to see CC(=CCCC(C)(C=C)C1=C2C(=C(C3=C1OC(C=C3)(C)C)O)C=CC(=O)O2)C 380.50 unknown https://doi.org/10.1016/0031-9422(94)00485-C
10-(3,7-Dimethylocta-1,6-dien-3-yl)-5-methoxy-2,2-dimethylpyrano[3,2-g]chromen-8-one 15228829 Click to see CC(=CCCC(C)(C=C)C1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CC(O2)(C)C)C 394.50 unknown https://doi.org/10.1016/0031-9422(94)00485-C
10-[(3R)-3,7-dimethylocta-1,6-dien-3-yl]-5-hydroxy-2,2-dimethylpyrano[3,2-g]chromen-8-one 163038614 Click to see CC(=CCCC(C)(C=C)C1=C2C(=C(C3=C1OC(C=C3)(C)C)O)C=CC(=O)O2)C 380.50 unknown https://doi.org/10.1016/0031-9422(94)00485-C
10-[(3S)-3,7-dimethylocta-1,6-dien-3-yl]-5-methoxy-2,2-dimethylpyrano[3,2-g]chromen-8-one 163021502 Click to see CC(=CCCC(C)(C=C)C1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CC(O2)(C)C)C 394.50 unknown https://doi.org/10.1016/0031-9422(94)00485-C
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2R,4R)-2-[(3S,5R,9S,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylhept-5-ene-1,4-diol 162982656 Click to see CC(=CC(CC(CO)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C)O)C 458.70 unknown https://doi.org/10.1016/S0031-9422(00)95207-5
(3S,5R,9S,10R,13S,14S,17S)-17-[(2S,4R)-4-hydroxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 163092654 Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)95207-5
(5R,9R,10R,13S,14S,17S)-17-[(2R,3S,5R)-2-hydroxy-5-(2-methylpropyl)oxolan-3-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 101606411 Click to see CC(C)CC1CC(C(O1)O)C2CCC3(C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)95207-5
(5R,9R,10R,13S,14S,17S)-17-[(2S,4R)-4-hydroxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 50994391 Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(00)95207-5
(5S,9R,10R,13S,14S,17S)-17-[(2R,4R)-1,4-dihydroxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 162896301 Click to see CC(=CC(CC(CO)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)95207-5
17-(1,4-Dihydroxy-6-methylhept-5-en-2-yl)-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 14830827 Click to see CC(=CC(CC(CO)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)95207-5
17-(4-Hydroxy-6-methylhept-5-en-2-yl)-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 14830823 Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(00)95207-5
2-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-methylhept-5-ene-1,4-diol 14830834 Click to see CC(=CC(CC(CO)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C)O)C 458.70 unknown https://doi.org/10.1016/S0031-9422(00)95207-5
Deoxyflindissone 70698213 Click to see CC(=CC1CC(CO1)C2CCC3(C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C)C)C 438.70 unknown https://doi.org/10.1016/S0031-9422(00)95207-5
> 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/S0031-9422(97)00760-7
https://doi.org/10.1016/0031-9422(94)00485-C
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/10.1016/S0031-9422(97)00760-7
https://doi.org/10.1016/0031-9422(94)00485-C
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
6,7,8-Trihydroxy-2H-1-benzopyran-2-one 11819936 Click to see C1=CC(=O)OC2=C(C(=C(C=C21)O)O)O 194.14 unknown https://doi.org/10.1016/S0031-9422(00)95207-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Nordentatin 5320206 Click to see CC1(C=CC2=C(O1)C3=C(C(=C2O)C(C)(C)C=C)OC(=O)C=C3)C 312.40 unknown https://doi.org/10.1016/0031-9422(94)00485-C
https://doi.org/10.1016/S0031-9422(97)00760-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Dentatin 342801 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC(=O)C=C3)OC)C 326.40 unknown https://doi.org/10.1016/S0031-9422(97)00760-7
https://doi.org/10.1016/0031-9422(94)00485-C
nor-Dentatin 5495613 Click to see CC1(C=CC2=C(O1)C(=C3C(=C2O)C=CC(=O)O3)C(C)(C)C=C)C 312.40 unknown https://doi.org/10.1016/S0031-9422(97)00760-7
https://doi.org/10.1016/0031-9422(94)00485-C
Xanthyletin 65188 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 228.24 unknown https://doi.org/10.1016/S0031-9422(97)00760-7

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