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Urceola laevigata

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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 UUID644069594b849415540896
Scientific name Urceola laevigata
Authority (Juss.) D.J.Middleton & Livsh.
First published in Taxon 67(2): 356. 2018

Description Top

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Synonyms Top

Scientific name Authority First published in
Parameria angustior Boerl. Handl. Fl. Ned. Ind. 2: 399 (1899)
Parameria barbata K.Schum. Nat. Pflanzenfam. 4(2): 162 (1895)
Parameria glandulifera var. philippinensis (Radlk.) Stapf Trans. Linn. Soc. London, Bot. 4: 207. 1894
Parameria glandulifera (Wall. & G.Don) Benth. & Hook.f. ex Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 46: 255 (1877)
Parameria laevigata (Juss.) Moldenke Revista Sudamer. Bot. 6: 176 (1940)
Parameria philippinensis Radlk. Sitzungsber. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. München 14: 518 (1884)
Parameria pierrei Baill. Hist. Pl. 10: 167 (1888)
Parameria vulneraria Radlk. Sitzungsber. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. München 14: 519 (1884)
Parsonsia barbata Blume Bijdr. Fl. Ned. Ind. : 1042 (1826)
Parameria glandulifera var. pieirrei Pit. Fl. Indo-Chine 3: 1201 1933
Parameria glandulifera var. poilanei Pit. Fl. Indo-Chine 3: 1203. 1933
Parameria barbata var. pieirrei (Pit.) Kerr Fl. Siam. 2: 464 1939
Aegiphila laevigata Juss. Ann. Mus. Hist. Nat. 7: 76 (1806)
Chonemorpha densiflora G.Don Gen. Hist. 4: 76 (1837)
Ecdysanthera barbata Miq. Fl. Ned. Ind. 2: 451 (1857)
Ecdysanthera barbata var. angustior Miq. Fl. Ned. Ind. 2: 452. 1857
Ecdysanthera densiflora Miq. Fl. Ned. Ind. 2: 452 (1857)
Ecdysanthera glandulifera A.DC. Prodr. 8: 443 (1844)
Ecdysanthera griffithii Wight Icon. Pl. Ind. Orient. 4: t. 1307 (1848)
Echites barbatus D.Dietr. Syn. Pl. 1: 651 (1839)
Echites densiflorus Blume Bijdr. Fl. Ned. Ind. : 1040 (1826)
Echites glanduliferus Wall. & G.Don Gen. Hist. 4: 75 (1837)

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
      • Bangladesh
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001425303
KEW urn:lsid:ipni.org:names:77186120-1
IPNI 77186120-1
GBIF 9827170
CMAUP NPO10684

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)!
Title Authors Publication Released IDs
A-Type Proanthocyanidins from the Bark of Parameria laevigata Toshiko Satake, Kohei Kamiya, Akiko Ohno, Yukiko Horii, Hanani Endang, Mansur Umar The Japan Institute of Heterocyclic Chemistry 05-Mar-2009
doi:10.3987/COM-03-9793
Studies on the constituents of bark of Parameria laevigata Moldenke. Kamiya K, Watanabe C, Endang H, Umar M, Satake T Chem Pharm Bull (Tokyo) 01-May-2001
doi:10.1248/CPB.49.551
PMID:11383605

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 / Steroids and steroid derivatives / Stigmastanes and derivatives
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1R,5R,13R,17R,18R,19S,23R,31R,32R)-5,17,23-tris(3,4-dihydroxyphenyl)-19-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,6,16,22,24-pentaoxaoctacyclo[21.7.1.15,13.02,21.03,14.07,12.015,20.025,30]dotriaconta-2,7,9,11,14,20,25,27,29-nonaene-9,11,18,27,29,31,32-heptol 163040018 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C5C6C(C(OC7=CC(=CC(=C67)O)O)(OC5=C8C9C(C(OC1=CC(=CC(=C91)O)O)(OC8=C34)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1151.00 unknown https://doi.org/10.1248/CPB.49.551
(1R,5R,17R,18R,19S,23R,31R,32R)-5,17,23-tris(3,4-dihydroxyphenyl)-19-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,6,16,22,24-pentaoxaoctacyclo[21.7.1.15,13.02,21.03,14.07,12.015,20.025,30]dotriaconta-2,7,9,11,14,20,25,27,29-nonaene-9,11,18,27,29,31,32-heptol 163195609 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C5C6C(C(OC7=CC(=CC(=C67)O)O)(OC5=C8C9C(C(OC1=CC(=CC(=C91)O)O)(OC8=C34)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1151.00 unknown https://doi.org/10.1248/CPB.49.551
(1R,5R,6R,7R,13S,21R)-5,13-bis(3,4-dihydroxyphenyl)-7-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-10-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2,8,10,15,17,19-hexaene-6,9,17,19,21-pentol 163030952 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C5C6C(C(OC7=CC(=CC(=C67)O)O)(OC5=C(C(=C34)O)C8C(C(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown https://doi.org/10.3987/COM-03-9793
(1R,5S,6R,7R,13S,21R)-5,13-bis(3,4-dihydroxyphenyl)-7-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 100875781 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1248/CPB.49.551
Aescultitannin B 10010849 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown via CMAUP database
Cinnamtannin B2 16130973 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=C(C(=CC(=C67)O)O)C8C(C(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown https://doi.org/10.1248/CPB.49.551
Parameritannin A-1 16146159 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C5C6C(C(OC7=CC(=CC(=C67)O)O)(OC5=C(C(=C34)O)C8C(C(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown via CMAUP database
Pavetannin B2 13990886 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1248/CPB.49.551
Proanthocyanidin A-6 45359583 Click to see C1C(C(OC2=CC3=C(C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)C(=C21)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown https://doi.org/10.1248/CPB.49.551
Procyanidin A2 124025 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown https://doi.org/10.1248/CPB.49.551
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-5-hydroxy-2-(2-hydroxy-4-methoxyphenyl)-8,8-dimethyl-6-(3-methylbut-2-enyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 101326868 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=C(C=C(C=C4)OC)O)O)C 436.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
ent-Gallocatechin 4'-methyl ether 10087345 Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(C=C(C=C3O2)O)O)O)O 320.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
3,4',5,7-Tetrahydroxy-3',5'-dimethoxy-6-beta-D-glucopyranosylflavone 101713180 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 508.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
2'-Hydroxygenistein 5282074 Click to see C1=CC(=C(C=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)O 286.24 unknown via CMAUP database
6-(1,1-Dimethylallyl)genistein 44257285 Click to see CC(C)(C=C)C1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O 338.40 unknown via CMAUP database
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Daidzin 107971 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown via CMAUP database
Genistin 5281377 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database

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