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Clausena wallichii

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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 UUID644011a14136a390336490
Scientific name Clausena wallichii
Authority Oliv.
First published in J. Proc. Linn. Soc., Bot. 5(Suppl. 2): 35 (1861)

Description Top

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Synonyms Top

Scientific name Authority First published in
Bergera wallichii A.DC. ex Oliv. J. Proc. Linn. Soc., Bot. 5(Suppl. 2): 85 (1861)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Clausena wallichii var. guillauminii (Tanaka) Molino Bull. Mus. Natl. Hist. Nat., B, Adansonia 16: 137 (1994)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000608717
Tropicos 100312313
KEW urn:lsid:ipni.org:names:772175-1
The Plant List kew-2724853
Open Tree Of Life 907402
NCBI Taxonomy 159038
IUCN Red List 215235299
IPNI 772175-1
GBIF 7269430

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
Therapeutic Role of Alkaloids and Alkaloid Derivatives in Cancer Management Olofinsan K, Abrahamse H, George BP Molecules 22-Jul-2023
PMCID:PMC10386240
doi:10.3390/molecules28145578
PMID:37513450
Antimicrobial potentials of natural products against multidrug resistance pathogens: a comprehensive review Elmaidomy AH, Shady NH, Abdeljawad KM, Elzamkan MB, Helmy HH, Tarshan EA, Adly AN, Hussien YH, Sayed NG, Zayed A, Abdelmohsen UR RSC Adv 13-Oct-2022
PMCID:PMC9558262
doi:10.1039/d2ra04884a
PMID:36320761
Natural Enantiomers: Occurrence, Biogenesis and Biological Properties Yu JH, Yu ZP, Capon RJ, Zhang H Molecules 14-Feb-2022
PMCID:PMC8880303
doi:10.3390/molecules27041279
PMID:35209066
Naturally-Occurring Alkaloids of Plant Origin as Potential Antimicrobials against Antibiotic-Resistant Infections Casciaro B, Mangiardi L, Cappiello F, Romeo I, Loffredo MR, Iazzetti A, Calcaterra A, Goggiamani A, Ghirga F, Mangoni ML, Botta B, Quaglio D Molecules 09-Aug-2020
PMCID:PMC7466045
doi:10.3390/molecules25163619
PMID:32784887
Carbazole scaffolds in cancer therapy: a review from 2012 to 2018 Issa S, Prandina A, Bedel N, Rongved P, Yous S, Le Borgne M, Bouaziz Z J Enzyme Inhib Med Chem 22-Jul-2019
PMCID:PMC6691762
doi:10.1080/14756366.2019.1640692
PMID:31328585
Clausenawallines A and B, two new dimeric carbazole alkaloids from the roots of Clausena wallichii Wisanu Maneerat, Thunwadee Ritthiwigrom, Sarot Cheenpracha, Uma Prawat, Surat Laphookhieo Elsevier BV 25-Apr-2011
doi:10.1016/J.TETLET.2011.04.064
2-Hy­droxy-7-meth­oxy-9H-carbazole-3-carbaldehyde Fun HK, Maneerat W, Laphookhieo S, Chantrapromma S Acta Crystallogr Sect E Struct Rep Online 28-Aug-2010
PMCID:PMC3007870
doi:10.1107/S1600536810033805
PMID:21588744
Inhibitory effect of oxycoumarins isolated from the Thai medicinal plant Clausena guillauminii on the inflammation mediators, iNOS, TNF-alpha, and COX-2 expression in mouse macrophage RAW 264.7. Nakamura T, Kodama N, Arai Y, Kumamoto T, Higuchi Y, Chaichantipyuth C, Ishikawa T, Ueno K, Yano S J Nat Med 01-Jan-2009
doi:10.1007/S11418-008-0277-5
PMID:18636311

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 / Indoles and derivatives / Carbazoles
7-(9-hydroxy-3,3,10-trimethyl-7H-pyrano[3,2-g]carbazol-8-yl)-3,3,9-trimethyl-11H-pyrano[3,2-a]carbazol-8-ol 162960163 Click to see CC1=CC2=C(C(=C1O)C3=C(C(=CC4=C3C5=C(N4)C6=C(C=C5)OC(C=C6)(C)C)C)O)NC7=C2C8=C(C=C7)OC(C=C8)(C)C 556.60 unknown https://doi.org/10.1016/J.TETLET.2011.04.064
7-Methoxyheptaphylline 189688 Click to see CC(=CCC1=C(C(=CC2=C1NC3=C2C=CC(=C3)OC)C=O)O)C 309.40 unknown https://doi.org/10.1007/S11418-008-0277-5
Clausenawalline B 60165158 Click to see CC(=CCC1=C(C(=CC2=C1NC3=CC(=C(C(=C32)C4=C(C=C5C(=C4)C6=CC=CC=C6N5)O)O)OC)C=O)O)C 506.50 unknown https://doi.org/10.1016/J.TETLET.2011.04.064
Heptaphylline 5318015 Click to see CC(=CCC1=C(C(=CC2=C1NC3=CC=CC=C32)C=O)O)C 279.30 unknown https://doi.org/10.1007/S11418-008-0277-5
> Phenylpropanoids and polyketides / Coumarins and derivatives
Osthol 10228 Click to see CC(=CCC1=C(C=CC2=C1OC(=O)C=C2)OC)C 244.28 unknown https://doi.org/10.1007/S11418-008-0277-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Dentatin 342801 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC(=O)C=C3)OC)C 326.40 unknown https://doi.org/10.1007/S11418-008-0277-5
Xanthoxyletin 66548 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C 258.27 unknown https://doi.org/10.1007/S11418-008-0277-5

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