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Bouchardatia neurococca

Bouchardatia neurococca - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64400d9f2aec0823235497
Scientific name Bouchardatia neurococca
Authority Baill.
First published in Adansonia 9: 110 (1868)

Description Top

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Synonyms Top

Scientific name Authority First published in
Melicope neurococca Benth. Fl. Austral. 1: 360 (1863)
Bouchardatia australis Baill. Adansonia 7: 351 (1867)

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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No germination or propagation data was added yet.

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-0000569860
Tropicos 100299719
KEW urn:lsid:ipni.org:names:771732-1
The Plant List kew-2680725
Open Tree Of Life 5233172
NCBI Taxonomy 1226055
IPNI 771732-1
iNaturalist 538010
GBIF 3831416
EOL 5623428
Wikipedia Bouchardatia_neurococca

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
The multifaceted roles of natural products in mitochondrial dysfunction Chen Q, Ruan D, Shi J, Du D, Bian C Front Pharmacol 13-Feb-2023
PMCID:PMC9968749
doi:10.3389/fphar.2023.1093038
PMID:36860298
Recent advances and prospects in the organocatalytic synthesis of quinazolinones Borah B, Swain S, Patat M, Chowhan LR Front Chem 14-Sep-2022
PMCID:PMC9515322
doi:10.3389/fchem.2022.991026
PMID:36186594
Sunflower-Assisted Bio-Derived ZnO-NPs as an Efficient Nanocatalyst for the Synthesis of Novel Quinazolines with Highly Antioxidant Activities S. M, Narasaiah BP, B. H, G. L. B, Pradeepkiran JA, Padhy H Antioxidants (Basel) 31-Mar-2022
PMCID:PMC9025409
doi:10.3390/antiox11040688
PMID:35453373
The Effects of Antioxidants from Natural Products on Obesity, Dyslipidemia, Diabetes and Their Molecular Signaling Mechanism Khutami C, Sumiwi SA, Khairul Ikram NK, Muchtaridi M Int J Mol Sci 12-Feb-2022
PMCID:PMC8875143
doi:10.3390/ijms23042056
PMID:35216172
LKB1 deficiency-induced metabolic reprogramming in tumorigenesis and non-neoplastic diseases Zhang Y, Meng Q, Sun Q, Xu ZX, Zhou H, Wang Y Mol Metab 03-Dec-2020
PMCID:PMC7753952
doi:10.1016/j.molmet.2020.101131
PMID:33278637
Bouchardatine analogue alleviates non‐alcoholic hepatic fatty liver disease/non‐alcoholic steatohepatitis in high‐fat fed mice by inhibiting ATP synthase activity Rao Y, Lu Y, Li C, Song Q, Xu Y, Xu Z, Hu Y, Yu H, Gao L, Gu L, Ye J, Huang Z Br J Pharmacol 04-Jul-2019
PMCID:PMC6637044
doi:10.1111/bph.14713
PMID:31113010
Natural alkaloid bouchardatine ameliorates metabolic disorders in high‐fat diet‐fed mice by stimulating the sirtuin 1/liver kinase B‐1/AMPK axis Rao Y, Yu H, Gao L, Lu Y, Xu Z, Liu H, Gu L, Ye J, Huang Z Br J Pharmacol 21-Jun-2017
PMCID:PMC5513868
doi:10.1111/bph.13855
PMID:28493443
Essential Oil of<i>Bouchardatia neurococca</i>(Rutaceae) Leaves Joseph J. Brophy, Robert J. Goldsack, Paul I. Forster Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1994.9698435
Progress in the Studies on Rutaecarpine Lee SH, Son JK, Jeong BS, Jeong TC, Chang HW, Lee ES, Jahng Y Molecules 06-Feb-2008
PMCID:PMC6245441
doi:10.3390/molecules13020272
PMID:18305418
Alkaloids and Limonoids from Bouchardatia neurococca: Systematic Significance. C. Wattanapiromsakul, P. I. Forster, P. G. Waterman Wiley 28-Jul-2005
doi:10.1002/CHIN.200402199
Alkaloids and limonoids from Bouchardatia neurococca: systematic significance. Wattanapiromsakul C, Forster PI, Waterman PG Phytochemistry 01-Sep-2003
doi:10.1016/S0031-9422(03)00205-X
PMID:12943784

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1080/10412905.1994.9698435
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1080/10412905.1994.9698435
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-beta-Bourbonene 324224 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
(+)-Eudesma-5,7(11)-diene 6428860 Click to see CC1CCCC2(C1=CC(=C(C)C)CC2)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315594 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698435
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698435
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698435
alpha-Cubebene 442359 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
beta-Bourbonene 62566 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1994.9698435
Boscialin 6442487 Click to see CC1CC(CC(C1(C=CC(=O)C)O)(C)C)O 226.31 unknown https://doi.org/10.1016/S0031-9422(03)00205-X
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1994.9698435
Cedrelanol 160799 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698435
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698435
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
T-Muurolol 3084331 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698435
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698435
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1080/10412905.1994.9698435
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1080/10412905.1994.9698435
Globulol 101716 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698435
Palustrol 110745 Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698435
Viridiflorene 10910653 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698435
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698435
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1R,2R,3R,6R)-3-ethenyl-3,7,7-trimethyl-2-prop-1-en-2-ylbicyclo[4.1.0]heptane 101973934 Click to see CC(=C)C1C2C(C2(C)C)CCC1(C)C=C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
7-epi-alpha-Selinene 10123 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
alpha-Selinene 10856614 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
beta-Selinene 442393 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698435
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
2-Descarboxy-2-(methoxycarbonyl)-19-deoxylimonoic acid 16,17-lactone 3646272 Click to see CC1(C2CC(=O)C3(C(C2(C(O1)CC(=O)OC)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 486.60 unknown https://doi.org/10.1016/S0031-9422(03)00205-X
methyl 2-[(1R,2R,4S,7R,8S,11R,12R,13R,16R)-7-(furan-3-yl)-1,8,12,15,15-pentamethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-13-yl]acetate 163069215 Click to see CC1(C2CC(=O)C3(C(C2(C(O1)CC(=O)OC)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 486.60 unknown https://doi.org/10.1016/S0031-9422(03)00205-X
methyl 2-[(1R,2R,4S,7R,8S,11R,12R,13R,16R)-7-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]-1,8,12,15,15-pentamethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-13-yl]acetate 162855891 Click to see CC1(C2CC(=O)C3(C(C2(C(O1)CC(=O)OC)C)CCC4(C35C(O5)C(=O)OC4C6=CC(=O)OC6O)C)C)C 518.60 unknown https://doi.org/10.1016/S0031-9422(03)00205-X
methyl 2-[(1R,2R,4S,7R,8S,11R,12R,13R,16R)-7-[(2R)-2-hydroxy-5-oxo-2H-furan-4-yl]-1,8,12,15,15-pentamethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-13-yl]acetate 162850175 Click to see CC1(C2CC(=O)C3(C(C2(C(O1)CC(=O)OC)C)CCC4(C35C(O5)C(=O)OC4C6=CC(OC6=O)O)C)C)C 518.60 unknown https://doi.org/10.1016/S0031-9422(03)00205-X
methyl 2-[(1R,2R,4S,7R,8S,11R,12R,13R,16R)-7-[(2S)-2-hydroxy-5-oxo-2H-furan-3-yl]-1,8,12,15,15-pentamethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-13-yl]acetate 162855890 Click to see CC1(C2CC(=O)C3(C(C2(C(O1)CC(=O)OC)C)CCC4(C35C(O5)C(=O)OC4C6=CC(=O)OC6O)C)C)C 518.60 unknown https://doi.org/10.1016/S0031-9422(03)00205-X
methyl 2-[(1R,2R,4S,7R,8S,11R,12R,13R,16R)-7-[(2S)-2-hydroxy-5-oxo-2H-furan-4-yl]-1,8,12,15,15-pentamethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-13-yl]acetate 162850176 Click to see CC1(C2CC(=O)C3(C(C2(C(O1)CC(=O)OC)C)CCC4(C35C(O5)C(=O)OC4C6=CC(OC6=O)O)C)C)C 518.60 unknown https://doi.org/10.1016/S0031-9422(03)00205-X
methyl 2-[(1R,2R,4S,7S,8S,11R,12R,13R,16R)-7-(furan-3-yl)-1,8,12,15,15-pentamethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-13-yl]acetate 21576498 Click to see CC1(C2CC(=O)C3(C(C2(C(O1)CC(=O)OC)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 486.60 unknown https://doi.org/10.1016/S0031-9422(03)00205-X
methyl 2-[7-(2-hydroxy-5-oxo-2H-furan-3-yl)-1,8,12,15,15-pentamethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-13-yl]acetate 73802630 Click to see CC1(C2CC(=O)C3(C(C2(C(O1)CC(=O)OC)C)CCC4(C35C(O5)C(=O)OC4C6=CC(=O)OC6O)C)C)C 518.60 unknown https://doi.org/10.1016/S0031-9422(03)00205-X
methyl 2-[7-(2-hydroxy-5-oxo-2H-furan-4-yl)-1,8,12,15,15-pentamethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-13-yl]acetate 73802631 Click to see CC1(C2CC(=O)C3(C(C2(C(O1)CC(=O)OC)C)CCC4(C35C(O5)C(=O)OC4C6=CC(OC6=O)O)C)C)C 518.60 unknown https://doi.org/10.1016/S0031-9422(03)00205-X
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
2-(4-oxo-1H-quinazolin-2-yl)-1H-indole-3-carbaldehyde 21576497 Click to see C1=CC=C2C(=C1)C(=C(N2)C3=NC(=O)C4=CC=CC=C4N3)C=O 289.29 unknown https://doi.org/10.1016/S0031-9422(03)00205-X
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
1-Hydroxyrutaecarpine 10447696 Click to see C1CN2C(=NC3=C(C2=O)C=CC=C3O)C4=C1C5=CC=CC=C5N4 303.30 unknown https://doi.org/10.1016/S0031-9422(03)00205-X
1,2-Dihydroxyrutaecarpine 23250595 Click to see C1CN2C(=NC3=C(C2=O)C=CC(=C3O)O)C4=C1C5=CC=CC=C5N4 319.30 unknown https://doi.org/10.1016/S0031-9422(03)00205-X
Rutaecarpine 65752 Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C4=C1C5=CC=CC=C5N4 287.30 unknown https://doi.org/10.1002/CHIN.200402199
https://doi.org/10.1016/S0031-9422(03)00205-X
Thorectandroic acid 10108152 Click to see C1=CC=C(C(=C1)C(=O)O)N2C=CC3=C4C=CC=CC4=NC3=C2 288.30 unknown https://doi.org/10.1016/S0031-9422(03)00205-X
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown https://doi.org/10.1002/CHIN.200402199
https://doi.org/10.1016/S0031-9422(03)00205-X

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