Miliusa velutina - Unknown
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Internal ID UUID643ff5812361e424603511
Scientific name Miliusa velutina
Authority Hook.f. & Thomson
First published in Fl. Ind. 1: 151 (1855)

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Synonyms Top

Scientific name Authority First published in
Guatteria velutina A.DC. Mém. Soc. Phys. Genève 5: 218 (1832)
Guatteria villosa G.Don Gen. Hist. 1: 100. 1831 [early Aug 1831]
Uvaria velutina Dunal Monogr. Anonac. : 91 (1817)
Uvaria villosa Roxb. Fl. Ind. ed. 1832 , 2: 664 (1832)

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Language Common/alternative name
Malayalam വില്ലൂന്നി
Chinese 大叶野独活

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Varieties (abbr. var.) Top

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Name Authority First published in
Miliusa velutina var. deviyarina S.M.Rajendran, S.C.Agarwal & H.N.Verma Indian J. Forest. 26: 220 (2003)

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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-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Nepal
      • West Himalaya
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000372950
Tropicos 1600902
KEW urn:lsid:ipni.org:names:73961-1
The Plant List kew-2365302
Open Tree Of Life 740669
Observations.org 273395
NCBI Taxonomy 235758
IPNI 73961-1
GBIF 3156618
EOL 1054106
Elurikkus 367375
CMAUP NPO9752

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
Ethnobotany and phytochemistry of plants used to treat musculoskeletal disorders among Skaw Karen, Thailand Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A Pharm Biol 22-Dec-2023
PMCID:PMC10763916
doi:10.1080/13880209.2023.2292261
PMID:38131672
Seasonal Variations in Fungal Communities on the Surfaces of Lan Na Sandstone Sculptures and Their Biodeterioration Capacities Nonthijun P, Mills N, Mills N, Yongsawas R, Sansupa C, Suwannarach N, Jaikang C, Motanated K, Chayapakdee P, Jongjitngam S, Noirungsee N, Disayathanoowat T J Fungi (Basel) 08-Aug-2023
PMCID:PMC10455195
doi:10.3390/jof9080833
PMID:37623604
Medicinal Plants for Treating Musculoskeletal Disorders among Karen in Thailand Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A Plants (Basel) 28-Jun-2020
PMCID:PMC7412036
doi:10.3390/plants9070811
PMID:32605228
Cercosporoid fungi (Mycosphaerellaceae) 5. Species on dicots (Anacardiaceae to Annonaceae) Braun U, Crous PW, Nakashima C IMA Fungus 16-Jun-2016
PMCID:PMC4941684
doi:10.5598/imafungus.2016.07.01.10
PMID:27433446
High-resolution densitometry and elemental analysis of tropical wood Hietz P, Horsky M, Prohaska T, Lang I, Grabner M Trees (Berl West) 27-Nov-2014
PMCID:PMC4480964
doi:10.1007/s00468-014-1126-7
PMID:26146458
(+)-Isocorydine α-<i>N</i>−Oxide: A New Aporphine Alkaloid from<i>Miliusa velutina</i> Choudhury M. Hasan, Syeda Jumana, Mohammad A. Rashid Informa UK Limited 07-Jul-2007
doi:10.1080/10575630008043773
Alakaloids from the stem bark of Miliusa velutina. Jumana S, Hasan CM, Rashid MA Biochem Syst Ecol 01-Jun-2000
doi:10.1016/S0305-1978(99)00083-6
PMID:10725604

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
> Alkaloids and derivatives / Aporphines
(6R,6aS)-1,2,10-trimethoxy-6-methyl-6-oxido-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-11-ol 76960010 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC)[O-] 357.40 unknown https://doi.org/10.1080/10575630008043773
Isocorydine 10143 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown https://doi.org/10.1080/10575630008043773
https://doi.org/10.1016/S0305-1978(99)00083-6
Isocorydine N-oxide 71587071 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC)[O-] 357.40 unknown https://doi.org/10.1080/10575630008043773
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown https://doi.org/10.1016/S0305-1978(99)00083-6
Norcorydine 179491 Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)O)C=C1)OC 327.40 unknown https://doi.org/10.1016/S0305-1978(99)00083-6
https://doi.org/10.1080/10575630008043773
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Rhein 10168 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)C(=O)O 284.22 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
Anthraquinone 6780 Click to see C1=CC=C2C(=C1)C(=O)C3=CC=CC=C3C2=O 208.21 unknown via CMAUP database
Chrysophanic acid 10208 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 254.24 unknown via CMAUP database
Fallacinol 3083633 Click to see COC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)CO 300.26 unknown via CMAUP database
Physcion 8-glucoside 5319323 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)OC 446.40 unknown via CMAUP database
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown via CMAUP database
Rheochrysin 168938 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)OC 446.40 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Citreorosein 361512 Click to see C1=C(C=C(C2=C1C(=O)C3=C(C2=O)C(=CC(=C3)O)O)O)CO 286.24 unknown via CMAUP database
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown via CMAUP database
Emodin 1-O-beta-D-glucoside 5319333 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)O 432.40 unknown via CMAUP database
Emodin-8-glucoside 99649 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database
Questin 160717 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC)O 284.26 unknown via CMAUP database
Questinol 147621 Click to see COC1=CC(=CC2=C1C(=O)C3=C(C2=O)C=C(C=C3O)CO)O 300.26 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2,6-Dihydroxybenzoic acid 9338 Click to see C1=CC(=C(C(=C1)O)C(=O)O)O 154.12 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
2-Methoxystypandrone 158739 Click to see CC1=CC2=C(C(=O)C=C(C2=O)OC)C(=C1C(=O)C)O 260.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(2S)-2-Hydroxybutanedioic acid 222656 Click to see C(C(C(=O)O)O)C(=O)O 134.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-[3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-phenyl]ethanone 71593490 Click to see CC(=O)C1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)O)O 330.29 unknown via CMAUP database
Tachioside 11962143 Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)CO)O)O)O)O 302.28 unknown via CMAUP database
Torachrysone 8-O-Glucoside 11972479 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)OC 408.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
L-Tartaric acid 444305 Click to see C(C(C(=O)O)O)(C(=O)O)O 150.09 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
7-Hydroxy-2,5-dimethyl-4H-1-benzopyran-4-one 5316891 Click to see CC1=CC(=CC2=C1C(=O)C=C(O2)C)O 190.19 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-azaniumyl-3-(1H-indol-3-yl)propanoate 6923516 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)[O-])[NH3+] 204.22 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Reticulin 10233 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1016/S0305-1978(99)00083-6
Reticuline 439653 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1016/S0305-1978(99)00083-6
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-4-methoxy-5-methylchromen-2-one 5318268 Click to see CC1=CC(=CC2=C1C(=CC(=O)O2)OC)O 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
[(1S,8S,9R,11S,17R,18R,19S)-17-(3,4-dihydroxyphenyl)-3,11-dihydroxy-9-(4-hydroxyphenyl)-13-oxo-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-10,16-dioxapentacyclo[9.7.1.02,7.08,19.015,19]nonadeca-2(7),3,5,14-tetraen-18-yl] 3,4,5-trihydroxybenzoate 72195698 Click to see C1C(=O)C=C2C34C1(OC(C3C5=C(C4C(C(O2)C6=CC(=C(C=C6)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O)C(=CC(=C5)OC8C(C(C(C(O8)CO)O)O)O)O)C9=CC=C(C=C9)O)O 846.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(+)-Catechin 5-O-beta-D-glucopyranoside 6324898 Click to see C1C(C(OC2=C1C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Guaijaverin 5481224 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Quercetin 3-O-beta-D-xylopyranoside 5320861 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
Quercetin-3-o-rutinose 46936193 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(Z)-resveratrol 1548910 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown via CMAUP database
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2R,3S,4R,5R,6S)-2-[4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 71528811 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 390.40 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[3-hydroxy-5-[(1R,2S)-1-hydroxy-2-[4-hydroxy-2-[(E)-2-(4-hydroxyphenyl)ethenyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2-(4-hydroxyphenyl)ethyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 21586804 Click to see C1=CC(=CC=C1C=CC2=C(C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C(C4=CC=C(C=C4)O)C(C5=CC(=CC(=C5)OC6C(C(C(C(O6)CO)O)O)O)O)O)O 796.80 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[3-hydroxy-5-[2-(4-hydroxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73642 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown via CMAUP database
(E)-Resveratrol 3-(6''-galloyl)-O-beta-D-glucopyranoside 11330189 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O)O 542.50 unknown via CMAUP database
2,3,5,4'-tetrahydroxystilbene-2-O-beta-D-glucoside 5321884 Click to see C1=CC(=CC=C1C=CC2=C(C(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O 406.40 unknown via CMAUP database
5,5'-[(1S)-3beta,4alpha-Bis(4-hydroxyphenyl)cyclobutane-1alpha,2beta-diyl]bis[3-(beta-D-glucopyranosyloxy)phenol] 10327899 Click to see C1=CC(=CC=C1C2C(C(C2C3=CC(=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC(=CC(=C5)OC6C(C(C(C(O6)CO)O)O)O)O)C7=CC=C(C=C7)O)O 780.80 unknown via CMAUP database
cis-Piceid 10178463 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown via CMAUP database
Piceatannol 3'-O-glucoside 11968990 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O 406.40 unknown via CMAUP database
Piceid 5281718 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown via CMAUP database
Resveratroloside 5322089 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 390.40 unknown via CMAUP database

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