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Pamburus missionis

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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 UUID644042935fbaa869898932
Scientific name Pamburus missionis
Authority Swingle
First published in J. Washington Acad. Sci. 6: 338 (1916)

Description Top

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Synonyms Top

Scientific name Authority First published in
Paramignya missionis (Oliv.) Burkill Gard. Bull. Straits Settlem. 5: 213 (1931)
Atalantia missionis Oliv. J. Proc. Linn. Soc., Bot. 5(Suppl. 2): 25 (1861)
Chilocalyx elliptica Turcz. Bull. Soc. Imp. Naturalistes Moscou 36(I): 588 (1863)
Limonia missionis Wall. ex Wight Bot. Misc. 3: 291 (1833)

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-0001039039
Tropicos 100363319
KEW urn:lsid:ipni.org:names:774503-1
The Plant List tro-100363319
Open Tree Of Life 232704
NCBI Taxonomy 159062
IPNI 774503-1
GBIF 3835700
EPPO PBBMI
EOL 5624811
USDA GRIN 26370

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
Pest categorisation of Diaphorina citri Bragard C, Dehnen‐Schmutz K, Di Serio F, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Kertesz V, Streissl F, MacLeod A EFSA J 06-Jan-2021
PMCID:PMC7786542
doi:10.2903/j.efsa.2021.6357
PMID:33437319
Production of Plant-Associated Volatiles by Select Model and Industrially Important Streptomyces spp. Cheng Z, McCann S, Faraone N, Clarke JA, Hudson EA, Cloonan K, Hillier NK, Tahlan K Microorganisms 11-Nov-2020
PMCID:PMC7697265
doi:10.3390/microorganisms8111767
PMID:33187102
Polygonum minus essential oil modulates cisplatin-induced hepatotoxicity through inflammatory and apoptotic pathways Abd Rashid N, Hussan F, Hamid A, Adib Ridzuan NR, Halim SA, Abdul Jalil NA, Najib NH, Teoh SL, Budin SB EXCLI J 09-Sep-2020
PMCID:PMC7590832
doi:10.17179/excli2020-2355
PMID:33122975
Anti-Cancer Potential of Cannabinoids, Terpenes, and Flavonoids Present in Cannabis Tomko AM, Whynot EG, Ellis LD, Dupré DJ Cancers (Basel) 21-Jul-2020
PMCID:PMC7409346
doi:10.3390/cancers12071985
PMID:32708138
Medicinal Plants for the Treatment of Local Tissue Damage Induced by Snake Venoms: An Overview from Traditional Use to Pharmacological Evidence Félix-Silva J, Silva-Junior AA, Zucolotto SM, Fernandes-Pedrosa MD Evid Based Complement Alternat Med 21-Aug-2017
PMCID:PMC5585606
doi:10.1155/2017/5748256
PMID:28904556
DNA Barcode Authentication of Wood Samples of Threatened and Commercial Timber Trees within the Tropical Dry Evergreen Forest of India Nithaniyal S, Newmaster SG, Ragupathy S, Krishnamoorthy D, Vassou SL, Parani M PLoS One 26-Sep-2014
PMCID:PMC4178033
doi:10.1371/journal.pone.0107669
PMID:25259794
Molecular Cloning and Characterization of a Geranyl Diphosphate-Specific Aromatic Prenyltransferase from Lemon Munakata R, Inoue T, Koeduka T, Karamat F, Olry A, Sugiyama A, Takanashi K, Dugrand A, Froelicher Y, Tanaka R, Uto Y, Hori H, Azuma JI, Hehn A, Bourgaud F, Yazaki K Plant Physiol 30-Jul-2014
PMCID:PMC4149733
doi:10.1104/pp.114.246892
PMID:25077796
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
Coumarins and an indole alkaloid from Pamburus missionis Vijaya Kumar, Harshani N.K. Bulumulla, W.R. Wimalasiri, Johannes Reisch Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90455-2
Flavones and diterpenes of Pamburus missionis (rutaceae) David L. Dreyer, Kyong-Hwi Park Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(75)85361-1
Coumarins from Atalantia missionis A.K. Barua, S.K. Banerjee, A.B. Basak, S. Chakravarti, S. Ghosh, K. Sethi, P.K. Bose Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(74)85154-X

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 / Diterpenoids / Colensane and clerodane diterpenoids
Daniellic acid 6955052 Click to see CC12CCCC(C1CCC(=C)C2CCC3=COC=C3)(C)C(=O)O 316.40 unknown https://doi.org/10.1016/0031-9422(75)85361-1
Lambertianic acid 102582 Click to see CC12CCCC(C1CCC(=C)C2CCC3=COC=C3)(C)C(=O)O 316.40 unknown https://doi.org/10.1016/0031-9422(75)85361-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
6-(3,7-Dimethylocta-2,6-dienyl)-7-hydroxychromen-2-one 5357655 Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C)C 298.40 unknown https://doi.org/10.1016/S0031-9422(00)90455-2
8-(3,7-Dimethylocta-2,6-dienyl)-7-hydroxychromen-2-one 78151388 Click to see CC(=CCCC(=CCC1=C(C=CC2=C1OC(=O)C=C2)O)C)C 298.40 unknown https://doi.org/10.1016/S0031-9422(00)90455-2
8-Geranylumbelliferone 71694409 Click to see CC(=CCCC(=CCC1=C(C=CC2=C1OC(=O)C=C2)O)C)C 298.40 unknown https://doi.org/10.1016/S0031-9422(00)90455-2
Ostruthin 5281420 Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C)C 298.40 unknown https://doi.org/10.1016/S0031-9422(00)90455-2
https://doi.org/10.1016/0031-9422(74)85154-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/S0031-9422(00)90455-2
24-Ethylcholest-5-en-3beta-ol 22012 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/S0031-9422(00)90455-2
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
3-(3-Methyl-2-butenoyl)-1H-indole 11805712 Click to see CC(=CC(=O)C1=CNC2=CC=CC=C21)C 199.25 unknown https://doi.org/10.1016/S0031-9422(00)90455-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.1016/S0031-9422(00)90455-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1016/S0031-9422(00)90455-2
https://doi.org/10.1016/0031-9422(74)85154-X
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown https://doi.org/10.1016/S0031-9422(00)90455-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1016/S0031-9422(00)90455-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Dihydroluvangetin 11482357 Click to see CC1(CCC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)OC)C 260.28 unknown https://doi.org/10.1016/S0031-9422(00)90455-2
Luvangetin 343582 Click to see CC1(C=CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)OC)C 258.27 unknown https://doi.org/10.1016/S0031-9422(00)90455-2
Xanthyletin 65188 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 228.24 unknown https://doi.org/10.1016/S0031-9422(00)90455-2
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
Carpachromene 10449654 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C 336.30 unknown https://doi.org/10.1016/0031-9422(75)85361-1

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