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Uvaria littoralis

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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 UUID643ffa27787e5491510167
Scientific name Uvaria littoralis
Authority Blume
First published in Fl. Javae 21-22: 26 (1830)

Description Top

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Synonyms Top

Scientific name Authority First published in
Magnolia fasciculata P.Parm. Bull. Sci. France Belgique 27: 265 (1895 publ. 1896)
Uva synsepala Kuntze Revis. Gen. Pl. 1: 7 (1891)
Uva microcarpa Kuntze Revis. Gen. Pl. 1: 7 (1891)
Uva cordata Kuntze Revis. Gen. Pl. 1: 7 (1891)
Uvaria cordata (Dunal) Wall. Numer. List [Wallich] n. 6486. 1832
Uvaria acrantha Miq. Fl. Ned. Ind., Eerste Bijv. : 368 (1861)
Unona camphorata Blanco Fl. Filip. : 468 (1837)
Unona littoralis Blume Bijdr. Fl. Ned. Ind. : 16 (1825)
Uvaria rufescens A.DC. Mém. Soc. Phys. Genève 5: 202 (1832)
Uvaria sorzogonensis C.Presl Reliq. Haenk. 2: 76 (1835)
Uvaria gamopetala Zoll. Linnaea 29(3): 310. 1858 [Sep 1858]
Uvaria ovalifolia Blume Fl. Javae 21-22: 27 (1830)
Uvaria macrophylla Roxb. Pl. Asiat. Rar. 2: 22 (1830)
Guatteria cordata Dunal Monogr. Anonac. : 129 (1817)
Uvaria ovalifolia var. acrantha (Miq.) Miq. Ann. Mus. Bot. Lugduno-Batavi 2: 7 1865
Uvaria macrophylla var. glabrior Miq. Fl. Ned. Ind., Eerste Bijv. 368 1861
Uvaria ovalifolia var. borneensis Miq. Ann. Mus. Bot. Lugduno-Batavi 2: 7 1865
Uvaria ovalifolia var. normalis Miq. Ann. Mus. Bot. Lugduno-Batavi 2: 7 1865
Uvaria ovalifolia var. racemiflora Miq. Ann. Mus. Bot. Lugduno-Batavi 2: 7 1865
Uvaria synsepala Miq. J. Bot. Néerl. 1: 128 (1861)
Uvaria macclurei Diels Notizbl. Bot. Gart. Berlin-Dahlem 11: 73 (1931)
Uvaria microcarpa Champ. ex Benth. Hooker's J. Bot. Kew Gard. Misc. 3: 257 (1851)
Uvaria dolichoclada Hayata Icon. Pl. Formosan. 3: 10 (1913)
Uvaria badiiflora Hance Ann. Bot. Syst. 2: 19 (1851)
Uvaria obovatifolia Hayata Icon. Pl. Formosan. 3: 11 (1913)
Uvaria macrophylla var. microcarpa (Champ. ex Benth.) Finet & Gagnep. Bull. Soc. Bot. France 53, Mem. 4: 67 1906

Common names Top

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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-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea
      • Solomon Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000416343
Tropicos 1600950
KEW urn:lsid:ipni.org:names:75784-1
The Plant List kew-2448176
NCBI Taxonomy 2993478
IPNI 75784-1
GBIF 3154314
EOL 304904
CMAUP NPO8443

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
Two New Flavones from Uvaria macrophylla Roxb. var. microcarpa and Their Cytotoxic Activities Qiong-ming Xu, Xue-Run Liu, Yan-Li Liu, Zhong Chen, Shi-lin Yang The Japan Institute of Heterocyclic Chemistry 24-Oct-2011
doi:10.3987/COM-11-12354
Amides from Uvaria microcarpa Xiang-Nan Yang, Yong-Sheng Jin, Ping Zhu, Hai-Sheng Chen Springer Science and Business Media LLC 19-May-2010
doi:10.1007/S10600-010-9605-6
Uvamalols D-G: novel polyoxygenated seco-cyclohexenes from the roots of Uvaria macrophylla. Wang S, Chen RY, Yu SS, Yu DQ J Asian Nat Prod Res 01-Mar-2003
doi:10.1080/1028602031000080414
PMID:12608634

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 / Aristolactams
14-Hydroxy-6,15-dimethoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1,3,5,7,9(16),12,14-heptaen-11-one 10913436 Click to see COC1=CC=CC2=C3C4=C(C=C21)NC(=O)C4=CC(=C3OC)O 295.29 unknown https://doi.org/10.1007/S10600-010-9605-6
6,14,15-Trimethoxy-10-azatetracyclo[7.6.1.02,7.012,16]hexadeca-1,3,5,7,9(16),12,14-heptaen-11-one 10859838 Click to see COC1=CC=CC2=C3C4=C(C=C21)NC(=O)C4=CC(=C3OC)OC 309.30 unknown https://doi.org/10.1007/S10600-010-9605-6
Aristolactam AIa 86129027 Click to see COC1=C(C=C2C3=C(C=C4C(=C31)C=CC=C4O)NC2=O)O 281.26 unknown https://doi.org/10.1007/S10600-010-9605-6
Aristolactam AII 148657 Click to see COC1=C(C=C2C3=C1C4=CC=CC=C4C=C3NC2=O)O 265.26 unknown https://doi.org/10.1007/S10600-010-9605-6
Aristolactam BII 162739 Click to see COC1=C(C2=C3C(=C1)C(=O)NC3=CC4=CC=CC=C42)OC 279.29 unknown https://doi.org/10.1007/S10600-010-9605-6
Aristolactam BIII 14526428 Click to see COC1=CC2=C3C4=C(C=C2C=C1)NC(=O)C4=CC(=C3OC)OC 309.30 unknown https://doi.org/10.1007/S10600-010-9605-6
Goniopedaline 183523 Click to see COC1=C(C(=C2C3=C1C4=CC=CC=C4C=C3NC2=O)OC)O 295.29 unknown https://doi.org/10.1007/S10600-010-9605-6
Griffithinam 5317823 Click to see COC1=CC=CC2=C3C4=C(C=C21)NC(=O)C4=CC(=C3O)OC 295.29 unknown https://doi.org/10.1007/S10600-010-9605-6
Velutinam 9994639 Click to see COC1=C(C2=C3C=CC=C(C3=CC4=C2C(=C1)C(=O)N4)O)OC 295.29 unknown https://doi.org/10.1007/S10600-010-9605-6
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
N-(4-benzamidobutyl)benzamide 226276 Click to see C1=CC=C(C=C1)C(=O)NCCCCNC(=O)C2=CC=CC=C2 296.40 unknown https://doi.org/10.1007/S10600-010-9605-6
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
[(Z)-5-(benzoyloxymethyl)-4,5,6-trihydroxyhex-2-enyl] benzoate 11143529 Click to see C1=CC=C(C=C1)C(=O)OCC=CC(C(CO)(COC(=O)C2=CC=CC=C2)O)O 386.40 unknown https://doi.org/10.1080/1028602031000080414
Uvamalol D 10873992 Click to see CC(=O)OCC(COC(=O)C1=CC=CC=C1)(C(C=CCOC(=O)C2=CC=CC=C2)Cl)O 446.90 unknown https://doi.org/10.1080/1028602031000080414
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(+)-Nortrachelogenin 479756 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O 374.40 unknown via CMAUP database
3-Hydroxy-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 321311 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O 374.40 unknown via CMAUP database
Nortrachelogenin 394846 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O 374.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,5,6,9,10,10a-octahydrophenanthrene-1-carboxylic acid 92166187 Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C(=O)O)C 302.50 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
Dextropimarinal 12304198 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C=O)C)C=C 286.50 unknown via CMAUP database
Isopimara-7,15-dienal 12311183 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C=O)C)C1)C=C 286.50 unknown via CMAUP database
Isopimaric Acid 442048 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C 302.50 unknown via CMAUP database
Levopimaric acid 221062 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Neoabietic acid 221118 Click to see CC(=C1CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C 302.50 unknown via CMAUP database
Palustric acid 443613 Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C(=O)O)C 302.50 unknown via CMAUP database
Pimaric acid 220338 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown via CMAUP database
Retene 10222 Click to see CC1=C2C=CC3=C(C2=CC=C1)C=CC(=C3)C(C)C 234.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-Fenchol 439711 Click to see CC1(C2CCC(C2)(C1O)C)C 154.25 unknown via CMAUP database
Borneol 6552009 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
Limonene, (-)- 439250 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene 1796220 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2S)-5-hydroxy-6-[(2-hydroxy-5-methoxyphenyl)methyl]-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one 101966360 Click to see COC1=CC(=C(C=C1)O)CC2=C(C=C3C(=C2O)C(=O)CC(O3)C4=CC=CC=C4)OC 406.40 unknown https://doi.org/10.3987/COM-11-12354
(2S)-5-hydroxy-8-[(2-hydroxy-5-methoxyphenyl)methyl]-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one 101966361 Click to see COC1=CC(=C(C=C1)O)CC2=C(C=C(C3=C2OC(CC3=O)C4=CC=CC=C4)O)OC 406.40 unknown https://doi.org/10.3987/COM-11-12354
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4S)-4-benzylsulfanyl-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 10372558 Click to see C1=CC=C(C=C1)CSC2C(C(OC3=C(C(=CC(=C23)O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)C7=CC(=C(C=C7)O)O)O 700.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(4S)-Epicatechin benzylthioether 10645351 Click to see C1=CC=C(C=C1)CSC2C(C(OC3=CC(=CC(=C23)O)O)C4=CC(=C(C=C4)O)O)O 412.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Pinobanksin 73202 Click to see C1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown https://doi.org/10.3987/COM-11-12354
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.3987/COM-11-12354
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.3987/COM-11-12354
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 https://doi.org/10.3987/COM-11-12354
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxy-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162817332 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=C(C4=O)O)C5=CC(=C(C=C5)O)OC)O)OC)O)O)O)O)O)O 654.60 unknown https://doi.org/10.1080/1028602031000080414
> Phenylpropanoids and polyketides / Stilbenes
3,5-Dimethoxystilbene 5316874 Click to see COC1=CC(=CC(=C1)C=CC2=CC=CC=C2)OC 240.30 unknown via CMAUP database
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database

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