Halfordia kendack - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Halfordia kendack - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Internal ID UUID64401fa2a9f91391576012
Scientific name Halfordia kendack
Authority Guillaumin
First published in Notul. Syst. (Paris) 2: 98 (1911)

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Synonyms Top

Scientific name Authority First published in
Eriostemon kendack Montrouz. Mém. Acad. Imp. Sci. Lyon, Sect. Sci. , sér. 2, 10: 191 (1860)
Eriostemon leichhardtii F.Muell. Fragm. 5: 5 (1865)
Halfordia leichhardtii Baill. ex Guillaumin Notul. Syst. (Paris) 2: 98 (1911)
Halfordia papuana Lauterb. Bot. Jahrb. Syst. 55: 255 (1918)
Halfordia scleroxyla F.Muell. Fragm. 7: 142 (1871)

Common names Top

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Language Common/alternative name
English southern ghittoe

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000714659
Tropicos 28101731
INPN 674333
KEW urn:lsid:ipni.org:names:773848-1
Open Tree Of Life 800699
NCBI Taxonomy 354498
IUCN Red List 188875051
IPNI 773848-1
iNaturalist 185607
GBIF 3832180
USDA GRIN 455026
Wikipedia Halfordia_kendack

Genomes (via NCBI) Top

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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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Methoxyfuranocoumarins of Natural Origin–Updating Biological Activity Research and Searching for New Directions—A Review Bartnik M Curr Issues Mol Biol 19-Jan-2024
PMCID:PMC10813879
doi:10.3390/cimb46010055
PMID:38275669
Evaluation of the Antiseizure Activity of Endemic Plant Halfordia kendack Guillaumin and Its Main Constituent, Halfordin, on a Zebrafish Pentylenetetrazole (PTZ)-Induced Seizure Model Skiba A, Kozioł E, Luca SV, Budzyńska B, Podlasz P, Van Der Ent W, Shojaeinia E, Esguerra CV, Nour M, Marcourt L, Wolfender JL, Skalicka-Woźniak K Int J Mol Sci 30-Jan-2023
PMCID:PMC9916433
doi:10.3390/ijms24032598
PMID:36768918
Without management interventions, endemic wet‐sclerophyll forest is transitioning to rainforest in World Heritage listed K’gari (Fraser Island), Australia Krishnan V, Robinson N, Firn J, Applegate G, Herbohn J, Schmidt S Ecol Evol 15-Jan-2019
PMCID:PMC6374652
doi:10.1002/ece3.4853
PMID:30805167
Phylogenetic relationships of Vepris (Rutaceae) inferred from chloroplast, nuclear, and morphological data Morton CM PLoS One 08-Mar-2017
PMCID:PMC5342198
doi:10.1371/journal.pone.0172708
PMID:28273098
Major Clades of Australasian Rutoideae (Rutaceae) Based on rbcL and atpB Sequences Bayly MJ, Holmes GD, Forster PI, Cantrill DJ, Ladiges PY PLoS One 13-Aug-2013
PMCID:PMC3742607
doi:10.1371/journal.pone.0072493
PMID:23967311
Chilean Pitavia more closely related to Oceania and Old World Rutaceae than to Neotropical groups: evidence from two cpDNA non-coding regions, with a new subfamilial classification of the family Groppo M, Kallunki JA, Pirani JR, Antonelli A PhytoKeys 18-Dec-2012
PMCID:PMC3597001
doi:10.3897/phytokeys.19.3912
PMID:23717188
Alkaloids of the Australian Rutaceae: Halfordia scleroxyla. II. Isolation and structure of the alkaloids WD Crow, JH Hodgkin CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9640119
Alkaloids of the Australian Rutaceae: Halfordia scleroxyla and Halfordia kendack. IV. Co-occurrence of oxazole and quinoline alkaloids WD Crow, JH Hodgkin CSIRO Publishing 01-Sep-2010
doi:10.1071/CH9683075
The coumarins of Halfordia scleroxyla F. Muell MP Hegarty, FN Lahey CSIRO Publishing 01-Sep-2010
doi:10.1071/CH9560120
Frequency of Cyanogenesis in Tropical Rainforests of Far North Queensland, Australia MILLER RE, JENSEN R, WOODROW IE Ann Bot 01-Jun-2006
PMCID:PMC2803397
doi:10.1093/aob/mcl048
PMID:16520340
Synthesis of halfordamine, an alkaloid from Halfordia kendack R. Storer, D.W. Young Elsevier BV 25-Jul-2002
doi:10.1016/0040-4020(73)80104-8
3-Monoterpenyl-2,4-dioxygenated quinoline alkaloids from the aerial parts of Halfordia kendack. Sultana N, Waterman PG Phytochemistry 01-Sep-2001
doi:10.1016/S0031-9422(01)00196-0
PMID:11551559
3,5-Dimethoxy-3-(1,1-dimethylprop-2-enyl)-3,4-dihydropsoralen-4-one: an unusual furanocoumarin derivative from Halfordia kendack. Sultana N, Skelton BW, Waterman PG, White AH Phytochemistry 01-Nov-2000
doi:10.1016/S0031-9422(00)00152-7
PMID:11130679

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
> Organoheterocyclic compounds / Azoles / Oxazoles / Phenyl-1,3-oxazoles
(2R)-3-methyl-1-[4-(2-pyridin-3-yl-1,3-oxazol-5-yl)phenoxy]butane-2,3-diol 162939511 Click to see CC(C)(C(COC1=CC=C(C=C1)C2=CN=C(O2)C3=CN=CC=C3)O)O 340.40 unknown https://doi.org/10.1071/CH9640119
https://doi.org/10.1071/CH9683075
3-Methyl-1-[4-(2-pyridin-3-yl-1,3-oxazol-5-yl)phenoxy]butan-2-one 163000587 Click to see CC(C)C(=O)COC1=CC=C(C=C1)C2=CN=C(O2)C3=CN=CC=C3 322.40 unknown https://doi.org/10.1071/CH9683075
https://doi.org/10.1071/CH9640119
3-Methyl-1-[4-(2-pyridin-3-yl-1,3-oxazol-5-yl)phenoxy]butane-2,3-diol 15559612 Click to see CC(C)(C(COC1=CC=C(C=C1)C2=CN=C(O2)C3=CN=CC=C3)O)O 340.40 unknown https://doi.org/10.1071/CH9640119
https://doi.org/10.1071/CH9683075
Halfordinol 442858 Click to see C1=CC(=CN=C1)C2=NC=C(O2)C3=CC=C(C=C3)O 238.24 unknown https://doi.org/10.1071/CH9640119
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown https://doi.org/10.1071/CH9683075
Kokusaginine 10227 Click to see COC1=C(C=C2C(=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1071/CH9683075
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4,6,8-trimethoxy-1H-quinolin-2-one 15559611 Click to see COC1=CC2=C(C(=C1)OC)NC(=O)C=C2OC 235.24 unknown https://doi.org/10.1016/0040-4020(73)80104-8
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroxyquinolones
4-Hydroxy-6,8-dimethoxy-1-methylquinolin-2-one 121015249 Click to see CN1C(=O)C=C(C2=C1C(=CC(=C2)OC)OC)O 235.24 unknown https://doi.org/10.1071/CH9683075
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
(2S,3S,5R,8S)-5,9,9,18-tetramethyl-4,10-dioxa-18-azapentacyclo[9.8.0.02,8.03,5.012,17]nonadeca-1(11),12,14,16-tetraen-19-one 162880102 Click to see CC1(C2CCC3(C(C2C4=C(O1)C5=CC=CC=C5N(C4=O)C)O3)C)C 325.40 unknown https://doi.org/10.1016/S0031-9422(01)00196-0
(5,9,9-Trimethyl-19-oxo-4,10-dioxa-18-azapentacyclo[9.8.0.02,8.03,5.012,17]nonadeca-1(11),12,14,16-tetraen-18-yl)methyl acetate 73880640 Click to see CC(=O)OCN1C2=CC=CC=C2C3=C(C1=O)C4C(CCC5(C4O5)C)C(O3)(C)C 383.40 unknown https://doi.org/10.1016/S0031-9422(01)00196-0
(6aR,9R,10S,10aR)-9,10-dihydroxy-6,6,9,12-tetramethyl-7,8,10,10a-tetrahydro-6aH-isochromeno[4,3-c]quinolin-11-one 162907656 Click to see CC1(C2CCC(C(C2C3=C(O1)C4=CC=CC=C4N(C3=O)C)O)(C)O)C 343.40 unknown https://doi.org/10.1016/S0031-9422(01)00196-0
(6aR,9S,10S,10aR)-9,10-dihydroxy-6,6,9,12-tetramethyl-7,8,10,10a-tetrahydro-6aH-isochromeno[4,3-c]quinolin-11-one 162907655 Click to see CC1(C2CCC(C(C2C3=C(O1)C4=CC=CC=C4N(C3=O)C)O)(C)O)C 343.40 unknown https://doi.org/10.1016/S0031-9422(01)00196-0
(9,10-dihydroxy-6,6,9-trimethyl-11-oxo-7,8,10,10a-tetrahydro-6aH-isochromeno[4,3-c]quinolin-12-yl)methyl acetate 162864843 Click to see CC(=O)OCN1C2=CC=CC=C2C3=C(C1=O)C4C(CCC(C4O)(C)O)C(O3)(C)C 401.50 unknown https://doi.org/10.1016/S0031-9422(01)00196-0
[(6aR,9R,10S,10aR)-9,10-dihydroxy-6,6,9-trimethyl-11-oxo-7,8,10,10a-tetrahydro-6aH-isochromeno[4,3-c]quinolin-12-yl]methyl acetate 162864844 Click to see CC(=O)OCN1C2=CC=CC=C2C3=C(C1=O)C4C(CCC(C4O)(C)O)C(O3)(C)C 401.50 unknown https://doi.org/10.1016/S0031-9422(01)00196-0
5,9,9,18-Tetramethyl-4,10-dioxa-18-azapentacyclo[9.8.0.02,8.03,5.012,17]nonadeca-1(11),12,14,16-tetraen-19-one 162880101 Click to see CC1(C2CCC3(C(C2C4=C(O1)C5=CC=CC=C5N(C4=O)C)O3)C)C 325.40 unknown https://doi.org/10.1016/S0031-9422(01)00196-0
9,10-dihydroxy-6,6,9,12-tetramethyl-7,8,10,10a-tetrahydro-6aH-isochromeno[4,3-c]quinolin-11-one 162907654 Click to see CC1(C2CCC(C(C2C3=C(O1)C4=CC=CC=C4N(C3=O)C)O)(C)O)C 343.40 unknown https://doi.org/10.1016/S0031-9422(01)00196-0
trans-Erioaustralasine 636897 Click to see CC(=O)OCN1C2=CC=CC=C2C3=C(C1=O)C4C(CCC5(C4O5)C)C(O3)(C)C 383.40 unknown https://doi.org/10.1016/S0031-9422(01)00196-0
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Linear furanocoumarins
(6S)-4,6-dimethoxy-6-(2-methylbut-3-en-2-yl)furo[3,2-g]chromene-5,7-dione 637215 Click to see CC(C)(C=C)C1(C(=O)C2=C(C=C3C(=C2OC)C=CO3)OC1=O)OC 330.30 unknown https://doi.org/10.1016/S0031-9422(00)00152-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
7H-Furo[3,2-g][1]benzopyran-7-one, 4,5,6-trimethoxy- 623929 Click to see COC1=C2C=COC2=CC3=C1C(=C(C(=O)O3)OC)OC 276.24 unknown https://doi.org/10.1071/CH9560120
https://doi.org/10.1016/S0031-9422(00)00152-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
5,6,9-Trimethoxyfuro[3,2-g]chromen-7-one 623933 Click to see COC1=C(C(=O)OC2=C1C=C3C=COC3=C2OC)OC 276.24 unknown https://doi.org/10.1071/CH9560120
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthoxyletin 66548 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C 258.27 unknown https://doi.org/10.1071/CH9560120

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