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Internal ID UUID64405cb39f5ae435023082
Scientific name Conchocarpus coeruleus
Authority (Nees & Mart.) Bruniera & Groppo
First published in PLoS ONE 10(5): e0125650, 17. 2015 [7 May 2015]

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Synonyms Top

Scientific name Authority First published in
Almeidea caerulea (Nees & Mart.) A.St.-Hil. Gen. Hist. 1: 798. 1831 [early Aug 1831] (as caerulea)
Aruba coerulea Nees & Mart. Nova Acta Phys.-Med. Acad. Caes. Leop.-Carol. Nat. Cur. 40: 174 (1823)

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Distribution (via POWO/KEW) Top

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- Doubtful data
- Extinct
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Database ID/link to page
World Flora Online wfo-0001317200
Tropicos 100435683
KEW urn:lsid:ipni.org:names:77200743-1
NCBI Taxonomy 1654679
IUCN Red List 176133095
IPNI 77200743-1
GBIF 10273074

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Almeidea A. St.-Hil. Belongs to Conchocarpus J.C. Mikan (Galipeinae, Rutaceae): Evidence from Morphological and Molecular Data, with a First Analysis of Subtribe Galipeinae Poleselli Bruniera C, Kallunki JA, Groppo M PLoS One 07-May-2015
PMCID:PMC4423776
doi:10.1371/journal.pone.0125650
PMID:25951371
Alkaloids and triterpene from Almeidea coerulea (Nees and Mart.) a. St.-Hil. and anti-leishmanial activity Lucia Elaine Ranieri Cortez, Izabel Cristina Piloto Ferreira, Valdrinez Campana Lonardoni, Antonio Gilberto Ferreira, Paulo Cesar Vieira, Maria Fátima das Graças Fernandes da Silva, João Batista Fernandes, Diógenes Aparicio Garcia Cortez FapUNIFESP (SciELO) 31-Mar-2011
doi:10.1590/S1516-89132011000100008
Cycloartane Triterpenoid and Alkaloids from Ameidea SPP Celcione S. Santos, Ana H. Januário, Paulo C. Vieira, João B. Fernandes, M. Fátima G.F. da Silva, José R. Pirani FapUNIFESP (SciELO) 20-Mar-2008
doi:10.1590/S0103-50531998000100007
Constituintes químicos de Almeidea coerulea (Nees & Mart.) A. St.-Hil. Rutaceae Lucia Elaine Ranieri Cortez, Diógenes Aparício Garcia Cortez, Antônio Gilberto Ferreira, Paulo Cezar Vieira, Maria Fátima das Garças Fernandes d Silva, João Batista Fernandes Springer Science and Business Media LLC 13-Feb-2008
doi:10.1590/S0102-695X2006000200006

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
(1R,3aR,5aR,5bR,9S,11aR)-1-(2-hydroxypropan-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 118403971 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C 444.70 unknown https://doi.org/10.1590/S1516-89132011000100008
Monoginol A 15560607 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5(C4C(CC5)C(C)(C)O)C)C)C)C 444.70 unknown https://doi.org/10.1590/S0102-695X2006000200006
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1590/S0103-50531998000100007
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1590/S0103-50531998000100007
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,12S,16R)-15-(5,6-dimethylheptan-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 163083704 Click to see CC(C)C(C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 442.80 unknown https://doi.org/10.1590/S0103-50531998000100007
[(1S,3R,6S,12S,16R)-15-(5,6-dimethylheptan-2-yl)-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] (E)-2-methylbut-2-enoate 162820295 Click to see CC=C(C)C(=O)OC1CCC23CC24CCC5(C(CCC5(C4CCC3C1(C)C)C)C(C)CCC(C)C(C)C)C 524.90 unknown https://doi.org/10.1590/S0103-50531998000100007
[(1S,3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylheptan-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] (E)-2-methylbut-2-enoate 162996354 Click to see CC=C(C)C(=O)OC1CCC23CC24CCC5(C(CCC5(C4CCC3C1(C)C)C)C(C)CCCC(C)C)C 510.80 unknown https://doi.org/10.1590/S0103-50531998000100007
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromenopyridines
Dutadrupine 622343 Click to see CC1(C=CC2=C(O1)C=CC3=C2N=C4C(=C3OC)C=CO4)C 281.30 unknown https://doi.org/10.1590/S0103-50531998000100007
> Organoheterocyclic compounds / Furopyridines
[(7R,8R)-4,8-dimethoxy-8-(3-methylbut-2-enyl)-6,7-dihydro-5H-furo[2,3-b]quinolin-7-yl] acetate 7274570 Click to see CC(=CCC1(C(CCC2=C1N=C3C(=C2OC)C=CO3)OC(=O)C)OC)C 359.40 unknown https://doi.org/10.1590/S0103-50531998000100007
Acetic acid 4,8-dimethoxy-8-(3-methyl-but-2-enyl)-5,6,7,8-tetrahydro-furo[2,3-b]quinolin-7-yl ester 3151987 Click to see CC(=CCC1(C(CCC2=C1N=C3C(=C2OC)C=CO3)OC(=O)C)OC)C 359.40 unknown https://doi.org/10.1590/S0103-50531998000100007
Haplophyllidine 442910 Click to see CC(=CCC1(C(CCC2=C1N=C3C(=C2OC)C=CO3)O)OC)C 317.40 unknown https://doi.org/10.1590/S0103-50531998000100007
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
6-Hydroxy-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4(9),5,7,15,17,19-octaen-14-one 136734737 Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C4=C1C5=C(N4)C=C(C=C5)O 303.30 unknown https://doi.org/10.1590/S1516-89132011000100008
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
4,7-Dimethoxy-8-(3-methylbut-2-enyl)furo[2,3-b]quinoline 162820497 Click to see CC(=CCC1=C(C=CC2=C1N=C3C(=C2OC)C=CO3)OC)C 297.30 unknown https://doi.org/10.1590/S0103-50531998000100007
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
11-Methoxy-4,4-dimethyl-3,15-dioxa-17-azatetracyclo[8.7.0.02,7.012,16]heptadeca-1(10),2(7),5,8,11,13,16-heptaene 162820600 Click to see CC1(C=CC2=C(O1)C3=C(C=C2)C(=C4C=COC4=N3)OC)C 281.30 unknown https://doi.org/10.1590/S0103-50531998000100007
4,4,17-Trimethyl-3,15-dioxa-17-azatetracyclo[8.7.0.02,7.012,16]heptadeca-1(10),2(7),5,8,12(16),13-hexaen-11-one 162846324 Click to see CC1(C=CC2=C(O1)C3=C(C=C2)C(=O)C4=C(N3C)OC=C4)C 281.30 unknown https://doi.org/10.1590/S0103-50531998000100007

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