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Isertia hypoleuca

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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 UUID643fdf7715681631034149
Scientific name Isertia hypoleuca
Authority Benth.
First published in J. Bot. (Hooker) 3: 220 (1841)

Description Top

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Synonyms Top

Scientific name Authority First published in
Isertia coccinea var. hypoleuca K.Schum. Fl. Bras. 6(6): 286 (1889)
Isertia hoehnei K.Krause Arch. Bot. São Paulo 1: 115 (1925)
Isertia scarlatina (K.Schum. & K.Krause) Standl. Publ. Field Columb. Mus., Bot. Ser. 8: 346 (1931)
Cassupa scarlatina K.Schum. & K.Krause Verh. Bot. Vereins Prov. Brandenburg 50: 98 (1908)

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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil West-central
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000217720
Tropicos 27901371
INPN 734779
KEW urn:lsid:ipni.org:names:753635-1
The Plant List kew-102798
Open Tree Of Life 243678
NCBI Taxonomy 60058
IUCN Red List 179314288
IPNI 753635-1
GBIF 2903528
EOL 1111489
USDA GRIN 461354

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
A highly contiguous, scaffold-level nuclear genome assembly for the fever tree (Cinchona pubescens Vahl) as a novel resource for Rubiaceae research Canales NA, Pérez-Escobar OA, Powell RF, Töpel M, Kidner C, Nesbitt M, Maldonado C, Barnes CJ, Rønsted N, Przelomska NA, Leitch IJ, Antonelli A GigaByte 06-Oct-2022
PMCID:PMC10027117
doi:10.46471/gigabyte.71
PMID:36950143
First typology of cacao (Theobroma cacao L.) systems in Colombian Amazonia, based on tree species richness, canopy structure and light availability Suárez Salazar JC, Ngo Bieng MA, Melgarejo LM, Di Rienzo JA, Casanoves F PLoS One 05-Feb-2018
PMCID:PMC5798779
doi:10.1371/journal.pone.0191003
PMID:29401499
Triterpenoids of Isertia hypoleuca leaves C.A. Lau-Cam Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(73)80051-2
Constituents of Isertia hypoleuca benth. (Rubiaceae)—I H. Bohrmann, C. Lau-Cam, J. Tashiro, H.W. Youngken Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)85415-1

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 / Triterpenoids
(3S,4aS,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 163022461 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(73)80051-2
(4aS,6aS,6bS,8aS,11R,12S,12aS,14aR,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydropicen-3-one 162908156 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(73)80051-2
4,4,6a,6b,8a,12,14b-Heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol 610148 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1016/0031-9422(73)80051-2
Taraxasterol 115250 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1016/0031-9422(73)80051-2
Urs-12-en-3-one 612828 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(73)80051-2
Urs-12-en-3beta-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(73)80051-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(73)80051-2
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/10.1016/0031-9422(73)80051-2
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
(+)-Epidihydroquinamine 177214 Click to see CCC1CN2CCC1CC2C34C(CCO3)(C5=CC=CC=C5N4)O 314.40 unknown https://doi.org/10.1016/S0031-9422(00)85415-1
(3aR,8bS)-3a-[(2R,4R,5R)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]-2,4-dihydro-1H-furo[2,3-b]indol-8b-ol 162942782 Click to see CCC1CN2CCC1CC2C34C(CCO3)(C5=CC=CC=C5N4)O 314.40 unknown https://doi.org/10.1016/S0031-9422(00)85415-1

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