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Clausena heptaphylla

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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 UUID6440119fc0609850233112
Scientific name Clausena heptaphylla
Authority Wight & Arn.
First published in Prodr. Fl. Ind. Orient. : 95 (1834)

Description Top

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Synonyms Top

Scientific name Authority First published in
Amyris anisata Roxb. ex Steud. Nomencl. Bot. , ed. 2, 1: 81 (1840)
Amyris heptaphylla Roxb. ex DC. Prodr. 2: 82 (1825)
Clausena heptaphylla var. engleri (Tanaka) Swingle J. Wash. Acad. Sci. 32: 26 1942
Clausena macrophylla Hook.f. Fl. Brit. India 1: 504 (1875)

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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Nepal
    • Indo-China
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000608663
Tropicos 28100020
KEW urn:lsid:ipni.org:names:772136-1
The Plant List kew-2724804
Open Tree Of Life 5762742
NCBI Taxonomy 1392232
IUCN Red List 215235491
IPNI 772136-1
GBIF 3836901
EOL 2877899
USDA GRIN 10809
CMAUP NPO28407

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
Sanitizing Hatching Eggs with Essential Oils: Avian and Microbiological Safety Oliveira GD, McManus C, de Araújo MV, de Sousa DE, de Macêdo IL, de Castro MB, dos Santos VM Microorganisms 26-Jul-2023
PMCID:PMC10456749
doi:10.3390/microorganisms11081890
PMID:37630450
Chemo-enzymatic synthesis and biological activity evaluation of propenylbenzene derivatives Hernik D, Szczepańska E, Ghezzi MC, Brenna E, Włoch A, Pruchnik H, Mularczyk M, Marycz K, Olejniczak T, Boratyński F Front Microbiol 26-Jun-2023
PMCID:PMC10330721
doi:10.3389/fmicb.2023.1223123
PMID:37434714
Use of stability statistics in the selection of Clausena heptaphylla (Roxb.) Wight & Arn for novel anethole rich strain (Jor Lab CH-2) Lal M, Munda S, Gogoi A, Begum T, Baruah J, Chanda SK, Lekhak H Front Plant Sci 14-Dec-2022
PMCID:PMC9794615
doi:10.3389/fpls.2022.1060492
PMID:36589129
3-Methoxy Carbazole Impedes the Growth of Human Breast Cancer Cells by Suppressing NF-κB Signaling Pathway Alanazi J, Unnisa A, Alanazi M, Alharby TN, Moin A, Rizvi SM, Hussain T, Awadelkareem AM, Elkhalifa AO, Faiyaz SS, Khalid M, Gowda DV Pharmaceuticals (Basel) 14-Nov-2022
PMCID:PMC9699412
doi:10.3390/ph15111410
PMID:36422540
Anethole rich Clausena heptaphylla (Roxb.) Wight & Arn., essential oil pharmacology and genotoxic efficiencies Lal M, Begum T, Gogoi R, Sarma N, Munda S, Pandey SK, Baruah J, Tamang R, Saikia S Sci Rep 15-Jun-2022
PMCID:PMC9200763
doi:10.1038/s41598-022-13511-8
PMID:35705583
Phyto-Carbazole Alkaloids from the Rutaceae Family as Potential Protective Agents against Neurodegenerative Diseases Tan MA, Sharma N, An SS Antioxidants (Basel) 01-Mar-2022
PMCID:PMC8944741
doi:10.3390/antiox11030493
PMID:35326143
Synthesis of indole derivatives as prevalent moieties present in selected alkaloids Heravi MM, Amiri Z, Kafshdarzadeh K, Zadsirjan V RSC Adv 15-Oct-2021
PMCID:PMC9042329
doi:10.1039/d1ra05972f
PMID:35497516
Traditional Herbal Medicines Against CNS Disorders from Bangladesh Uddin MJ, Zidorn C Nat Prod Bioprospect 14-Oct-2020
PMCID:PMC7648845
doi:10.1007/s13659-020-00269-7
PMID:33057963
Design, Synthesis and In Vitro Characterization of Novel Antimicrobial Agents Based on 6-Chloro-9H-carbazol Derivatives and 1,3,4-Oxadiazole Scaffolds Bordei Telehoiu AT, Nuță DC, Căproiu MT, Dumitrascu F, Zarafu I, Ioniță P, Bădiceanu CD, Avram S, Chifiriuc MC, Bleotu C, Limban C Molecules 09-Jan-2020
PMCID:PMC7024163
doi:10.3390/molecules25020266
PMID:31936505
Clausmarin A, Potential Immunosuppressant Revealed by Yeast-Based Assay and Interleukin-2 Production Assay in Jurkat T Cells Suauam P, Yingyongnarongkul BE, Palaga T, Miyakawa T, Yompakdee C PLoS One 27-Aug-2015
PMCID:PMC4552291
doi:10.1371/journal.pone.0136804
PMID:26313553
In vitro and in vivo anti-angiogenic activity of girinimbine isolated from Murraya koenigii Iman V, Karimian H, Mohan S, Hobani YH, Noordin MI, Mustafa MR, Noor SM Drug Des Devel Ther 03-Mar-2015
PMCID:PMC4354401
doi:10.2147/DDDT.S71557
PMID:25767375
Simultaneous determination of nine analytes in Clausena harmandiana Pierre. by new developed high-performance liquid chromatography method and the influence of locations in Thailand on level of nordentatin and dentatin Wangboonskul J, Tunsirikongkon A, Sasithornwetchakun W Pharmacogn Mag 01-Jan-2015
PMCID:PMC4329607
doi:10.4103/0973-1296.149666
PMID:25709203
Antioxidant, antimicrobial, toxicity and analgesic properties of ethanol extract of Solena amplexicaulis root Kabir MG, Rahman MM, Ahmed NU, Fakruddin M, Islam S, Mazumdar RM Biol Res 19-Aug-2014
PMCID:PMC4193138
doi:10.1186/0717-6287-47-36
PMID:25287979
Antibacterial, antifungal and antioxidant activities of the ethanol extract of the stem bark of Clausena heptaphylla Fakruddin M, Mannan KS, Mazumdar RM, Afroz H BMC Complement Altern Med 27-Nov-2012
PMCID:PMC3533896
doi:10.1186/1472-6882-12-232
PMID:23181593
Major Components of the Leaf and Fruit Oil of<i>Clausena heptaphylla</i>W&amp;A Growing in Northeast India Subhan C. Nath, Dina N. Bordoloi Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1992.9698154

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
> Benzenoids / Anthracenes / Anthraquinones
2-Methylanthraquinone 6773 Click to see CC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O 222.24 unknown https://doi.org/10.1016/S0031-9422(00)88768-3
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
p-Anisaldehyde 31244 Click to see COC1=CC=C(C=C1)C=O 136.15 unknown https://doi.org/10.1002/RECL.19470660608
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
4-Methoxyphenylacetone 31231 Click to see CC(=O)CC1=CC=C(C=C1)OC 164.20 unknown https://doi.org/10.1002/RECL.19470660608
> Benzenoids / Phenol ethers / Anisoles
Anethole 637563 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown https://doi.org/10.1080/10412905.1992.9698154
https://doi.org/10.1002/RECL.19470660608
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown https://doi.org/10.1002/RECL.19470660608
https://doi.org/10.1080/10412905.1992.9698154
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Nerolic acid 5312583 Click to see CC(=CCCC(=CC(=O)O)C)C 168.23 unknown https://doi.org/10.1080/10575639908045434
https://doi.org/10.1016/S0367-326X(00)00320-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
Boydone B 73346125 Click to see CCC(C)C1=C(C(C(C1=O)(C)CC)O)OC 226.31 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Elemene 80048 Click to see CC(C)C1=CC(=C(C)C)CCC1(C)C=C 204.35 unknown https://doi.org/10.1002/RECL.19470660608
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Pseudacyclin A 46848855 Click to see CCC(C)C1C(=O)NC(C(=O)NCCCC(C(=O)NC(C(=O)N2CCCC2C(=O)N1)CC3=CC=CC=C3)NC(=O)C(C(C)CC)NC(=O)C)C(C)CC 739.90 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
D-Lactic acid 61503 Click to see CC(C(=O)O)O 90.08 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Ovalicin 10957430 Click to see CC(=CCC1C(O1)(C)C2(C(C(=O)CCC23CO3)OC)O)C 296.36 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
1-Methoxy-3-methyl-9H-carbazole 375150 Click to see CC1=CC2=C(C(=C1)OC)NC3=CC=CC=C32 211.26 unknown https://doi.org/10.1016/0031-9422(73)80423-6
10-hydroxy-3,3-dimethyl-2,11-dihydro-1H-pyrano[3,2-a]carbazole-5-carbaldehyde 14282355 Click to see CC1(CCC2=C(O1)C(=CC3=C2NC4=C3C=CC=C4O)C=O)C 295.30 unknown https://doi.org/10.1016/S0031-9422(00)80575-0
3-Methyl-9H-carbazole 20746 Click to see CC1=CC2=C(C=C1)NC3=CC=CC=C32 181.23 unknown https://doi.org/10.1016/S0031-9422(00)91444-4
Clausenal 10377645 Click to see COC1=CC=CC2=C1NC3=C2C=C(C=C3OC)C=O 255.27 unknown https://doi.org/10.1016/0031-9422(94)00666-H
Heptaphylline 5318015 Click to see CC(=CCC1=C(C(=CC2=C1NC3=CC=CC=C32)C=O)O)C 279.30 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Delta valerolactones
Mevalonolactone 6419891 Click to see CC1(CCOC(=O)C1)O 130.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
5-hydroxy-2,2-dimethyl-6-(2-methylbut-3-en-2-yl)-3H-pyrano[2,3-h]chromene-4,8-dione 10404227 Click to see CC1(CC(=O)C2=C(O1)C3=C(C(=C2O)C(C)(C)C=C)OC(=O)C=C3)C 328.40 unknown https://doi.org/10.1016/S0040-4039(01)89728-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
(3R,6R,8R)-6-(2-hydroxypropan-2-yl)-3-methyl-14-(2-methylbut-3-en-2-yl)-2,7,16-trioxatetracyclo[8.8.0.03,8.012,17]octadeca-1(10),11,13,17-tetraen-15-one 92272919 Click to see CC12CCC(OC1CC3=C(O2)C=C4C(=C3)C=C(C(=O)O4)C(C)(C)C=C)C(C)(C)O 398.50 unknown https://doi.org/10.1016/S0367-326X(00)00320-8
5-hydroxy-2,2-dimethyl-3H-pyrano[3,2-g]chromene-4,8-dione 5315948 Click to see CC1(CC(=O)C2=C(O1)C=C3C(=C2O)C=CC(=O)O3)C 260.24 unknown https://doi.org/10.1016/S0040-4039(01)89728-8
Clausmarin A 49940 Click to see CC12CCC(OC1CC3=C(O2)C=C4C(=C3)C=C(C(=O)O4)C(C)(C)C=C)C(C)(C)O 398.50 unknown https://doi.org/10.1016/S0305-1978(99)00035-6
https://doi.org/10.1016/S0367-326X(00)00320-8
> Phenylpropanoids and polyketides / Depsides and depsidones
Botryorhodine C 46916752 Click to see CC1=CC(=C(C2=C1C(=O)OC3=C(O2)C(=CC(=C3C)O)C)CO)O 316.30 unknown via CMAUP database

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