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Ormosia macrocalyx

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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 UUID643fd634dfb42307347686
Scientific name Ormosia macrocalyx
Authority Ducke
First published in Arch. Jard. Bot. Rio de Janeiro3: 137 (1922)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ormosia apulensis Cortes
Ormosia chlorocalyx Ducke Bol. Técn. Inst. Agron. N.2: 23 (1944)
Ormosia toledoana Standl. Publ. Carnegie Inst. Wash.461: 64 (1935)

Common names Top

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Language Common/alternative name
Chinese 大萼红豆

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
    • Caribbean
      • Puerto Rico
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000168275
Tropicos 13011069
KEW urn:lsid:ipni.org:names:176377-2
The Plant List ild-14599
Open Tree Of Life 972683
NCBI Taxonomy 681472
IUCN Red List 176101048
IPNI 176377-2
iNaturalist 206776
GBIF 5355476
EOL 415953
USDA GRIN 436738

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
Silicon-based anti-herbivore defense in tropical tree seedlings Klotz M, Schaller J, Engelbrecht BM Front Plant Sci 12-Oct-2023
PMCID:PMC10602810
doi:10.3389/fpls.2023.1250868
PMID:37900768
Method for selecting ornamental species for different shading intensity in urban green spaces Francini A, Toscano S, Ferrante A, Romano D Front Plant Sci 04-Oct-2023
PMCID:PMC10582628
doi:10.3389/fpls.2023.1271341
PMID:37860234
CAM photosynthesis: the acid test Winter K, Smith JA New Phytol 05-Nov-2021
PMCID:PMC9298356
doi:10.1111/nph.17790
PMID:34637529
Evidence of within-species specialization by soil microbes and the implications for plant community diversity Eck JL, Stump SM, Delavaux CS, Mangan SA, Comita LS Proc Natl Acad Sci U S A 06-Mar-2019
PMCID:PMC6462086
doi:10.1073/pnas.1810767116
PMID:30842279
Determination of the water gap and the germination ecology of Adenanthera pavonina (Fabaceae, Mimosoideae); the adaptive role of physical dormancy in mimetic seeds Jaganathan GK, Yule KJ, Biddick M AoB Plants 23-Aug-2018
PMCID:PMC6146125
doi:10.1093/aobpla/ply048
PMID:30254728
Contributions of a global network of tree diversity experiments to sustainable forest plantations Verheyen K, Vanhellemont M, Auge H, Baeten L, Baraloto C, Barsoum N, Bilodeau-Gauthier S, Bruelheide H, Castagneyrol B, Godbold D, Haase J, Hector A, Jactel H, Koricheva J, Loreau M, Mereu S, Messier C, Muys B, Nolet P, Paquette A, Parker J, Perring M, Ponette Q, Potvin C, Reich P, Smith A, Weih M, Scherer-Lorenzen M Ambio 12-Aug-2015
PMCID:PMC4709352
doi:10.1007/s13280-015-0685-1
PMID:26264716
Growth response and acclimation of CO2 exchange characteristics to elevated temperatures in tropical tree seedlings Cheesman AW, Winter K J Exp Bot 19-Jul-2013
PMCID:PMC3745734
doi:10.1093/jxb/ert211
PMID:23873999
Leaf life span spectrum of tropical woody seedlings: effects of light and ontogeny and consequences for survival Kitajima K, Cordero RA, Wright SJ Ann Bot 26-Mar-2013
PMCID:PMC3736767
doi:10.1093/aob/mct036
PMID:23532047
Perception of silent and motionless prey on vegetation by echolocation in the gleaning bat Micronycteris microtis Geipel I, Jung K, Kalko EK Proc Biol Sci 07-Mar-2013
PMCID:PMC3574334
doi:10.1098/rspb.2012.2830
PMID:23325775
Responses of Legume Versus Nonlegume Tropical Tree Seedlings to Elevated CO2 Concentration Cernusak LA, Winter K, Martínez C, Correa E, Aranda J, Garcia M, Jaramillo C, Turner BL Plant Physiol 25-Jul-2011
PMCID:PMC3165885
doi:10.1104/pp.111.182436
PMID:21788363
Dormancy as exaptation to protect mimetic seeds against deterioration before dispersal Brancalion PH, Novembre AD, Rodrigues RR, Marcos Filho J Ann Bot 30-Mar-2010
PMCID:PMC2876011
doi:10.1093/aob/mcq068
PMID:20354070
Prediction of Desiccation Sensitivity in Seeds of Woody Species: A Probabilistic Model Based on Two Seed Traits and 104 Species DAWS MI, GARWOOD NC, PRITCHARD HW Ann Bot 01-Apr-2006
PMCID:PMC3291879
doi:10.1093/aob/mcl022
PMID:16464874
Alkaloid distribution in seeds of Ormosia, Pericopsis and Haplormosia A. Douglas Kinghorn, Raouf A. Hussain, Eugene F. Robbins, Manuel F. Balandrin, Charles H. Stirton, Stephen V. Evans Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)83116-9

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Lupin alkaloids / Aloperine and related alkaloids / Ormosia-type alkaloids
(1R,11S,13R,14R)-7,19,23-triazahexacyclo[9.9.1.11,13.12,6.07,21.014,19]tricosane 118701607 Click to see C1CCN2CC34CC(C2C1)CC5C3N(CCC5)C6CCCC4N6 315.50 unknown https://doi.org/10.1016/0031-9422(88)83116-9
(1S,2S,7S,9R,10R)-1-[(2R)-piperidin-2-yl]-3,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 124708158 Click to see C1CCNC(C1)C23CC(CC4C2NCCC4)C5CCCCN5C3 317.50 unknown https://doi.org/10.1016/0031-9422(88)83116-9
(7R)-1-[(2S)-piperidin-2-yl]-3,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 5320310 Click to see C1CCNC(C1)C23CC(CC4C2NCCC4)C5CCCCN5C3 317.50 unknown https://doi.org/10.1016/0031-9422(88)83116-9
18-Epiormosanine 558826 Click to see C1CCNC(C1)C23CC(CC4C2NCCC4)C5CCCCN5C3 317.50 unknown https://doi.org/10.1016/0031-9422(88)83116-9
Homo-6-epipodopetaline 91746457 Click to see C1CCN2CC34CC(C2C1)C=C5C3N(CCC5)CN6C4CCCC6 327.50 unknown https://doi.org/10.1016/0031-9422(88)83116-9
Ormosanine 904194 Click to see C1CCNC(C1)C23CC(CC4C2NCCC4)C5CCCCN5C3 317.50 unknown https://doi.org/10.1016/0031-9422(88)83116-9
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 1747617 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1016/0031-9422(88)83116-9
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(-)-Sparteine 3966 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/0031-9422(88)83116-9
(1R,2R,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 92143189 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/0031-9422(88)83116-9
(1R,2S,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 1715130 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/0031-9422(88)83116-9
17-Oxolupanine 14139904 Click to see C1CCN2C(C1)C3CC(C2=O)C4CCCC(=O)N4C3 262.35 unknown https://doi.org/10.1016/0031-9422(88)83116-9
6-Phosphogluconic acid tri(cyclohexylammonium) salt, Grade V 16212687 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/0031-9422(88)83116-9
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/0031-9422(88)83116-9
Hydrorhombinine 7018997 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/0031-9422(88)83116-9
Sparteine 644020 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/0031-9422(88)83116-9
> Organoheterocyclic compounds / Quinolizidines / Quinolizidinones
(2R,10S)-10-prop-2-enyl-7,11-diazatricyclo[7.3.1.02,7]tridecan-6-one 102004777 Click to see C=CCC1C2CC(CN1)C3CCCC(=O)N3C2 234.34 unknown https://doi.org/10.1016/0031-9422(88)83116-9
Tetrahydrorhombifoline 15511175 Click to see C=CCCN1CC2CC(C1)C3CCCC(=O)N3C2 248.36 unknown https://doi.org/10.1016/0031-9422(88)83116-9

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