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Ochrosia elliptica

Ochrosia elliptica - 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 UUID643fe4bc1bbde405498545
Scientific name Ochrosia elliptica
Authority Labill.
First published in Sert. Austro-Caledon. : 25 (1824)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lactaria calocarpa Hassk. Ned. Kruidk. Arch. 4: 9 (1856)
Lactaria elliptica Kuntze Revis. Gen. Pl. 2: 415 (1891)
Lactaria parviflora Kuntze Revis. Gen. Pl. 2: 415 (1891)
Ochrosia calocarpa Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 139 (1869)
Ochrosia elliptica f. syncarpa Boiteau Adansonia , n.s., 15: 151 (1975)
Ochrosia noumeensis Baill. ex Guillaumin Bull. Soc. Bot. France 88: 34. 1941 (1941)
Ochrosia parviflora G.Don Gen. Hist. 4: 99 (1837)
Bleekeria calocarpa Hassk. Retzia 1: 40 (1855)
Bleekeria elliptica Koidz. Bot. Mag. (Tokyo) 37: 52 (1923)
Bleekeria kalocarpa Hassk. Retzia 1: 40 (1855)
Excavatia elliptica (Labill.) Markgr. Bull. Bernice P. Bishop Mus. 141: 128 (1936)

Common names Top

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Language Common/alternative name
English elliptic yellowwood
Persian چوبزرد خاگی
Chinese 古城玫瑰树

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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No forms added yet.

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
  • Pacific
    • Southwestern Pacific
      • Gilbert Islands
      • Nauru
      • New Caledonia
      • Vanuatu

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000253112
Florida Plant Atlas 288
USDA Plants OCEL
Tropicos 1803134
INPN 672039
KEW urn:lsid:ipni.org:names:80500-1
The Plant List kew-136707
Open Tree Of Life 773977
NCBI Taxonomy 141591
Nature Serve 2.132522
IUCN Red List 170446721
IPNI 80500-1
iNaturalist 165766
GBIF 3169645
Freebase /m/0h953gq
EOL 487444
USDA GRIN 25475
Wikipedia Ochrosia_elliptica

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
Understanding Cancer’s Defense against Topoisomerase-Active Drugs: A Comprehensive Review Sharma NK, Bahot A, Sekar G, Bansode M, Khunteta K, Sonar PV, Hebale A, Salokhe V, Sinha BK Cancers (Basel) 06-Feb-2024
PMCID:PMC10886629
doi:10.3390/cancers16040680
PMID:38398072
IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors Zhang J, Zhang R, Li W, Ma XC, Qiu F, Sun CP Int J Biol Sci 06-Aug-2023
PMCID:PMC10496512
doi:10.7150/ijbs.85158
PMID:37705738
Natural products modulate cell apoptosis: a promising way for treating endometrial cancer Zhou X, Zeng Y, Zheng R, Wang Y, Li T, Song S, Zhang S, Huang J, Ren Y Front Pharmacol 08-Jun-2023
PMCID:PMC10285317
doi:10.3389/fphar.2023.1209412
PMID:37361222
Phytochemicals: potential alternative strategy to fight Salmonella enterica serovar Typhimurium Almuzaini AM Front Vet Sci 16-May-2023
PMCID:PMC10228746
doi:10.3389/fvets.2023.1188752
PMID:37261108
9-Methoxyellipticine: Antibacterial Bioactive Compound Isolated from Ochrosia elliptica Labill. Roots Elshimy R, Khawagi WY, Naguib IA, Bukhari SI, El-Shiekh RA Metabolites 09-May-2023
PMCID:PMC10222304
doi:10.3390/metabo13050643
PMID:37233684
Women’s contribution in understanding how topoisomerases, supercoiling, and transcription control genome organization Martin L, Neguembor MV, Cosma MP Front Mol Biosci 27-Mar-2023
PMCID:PMC10083264
doi:10.3389/fmolb.2023.1155825
PMID:37051322
A Mini Review of Novel Topoisomerase II Inhibitors as Future Anticancer Agents Okoro CO, Fatoki TH Int J Mol Sci 28-Jan-2023
PMCID:PMC9916523
doi:10.3390/ijms24032532
PMID:36768852
Molecular Aspects and Therapeutic Implications of Herbal Compounds Targeting Different Types of Cancer Sharma A, Sharma L, Nandy SK, Payal N, Yadav S, Vargas-De-La-Cruz C, Anwer MK, Khan H, Behl T, Bungau SG Molecules 11-Jan-2023
PMCID:PMC9867434
doi:10.3390/molecules28020750
PMID:36677808
Exploration of aminoacyl-tRNA synthetases from eukaryotic parasites for drug development Gill J, Sharma A J Biol Chem 31-Dec-2022
PMCID:PMC9978631
doi:10.1016/j.jbc.2022.102860
PMID:36596362
Nucleolar Stress Response via Ribosomal Protein L11 Regulates Topoisomerase Inhibitor Sensitivity of P53-Intact Cancers Ishihara Y, Nakamura K, Nakagawa S, Okamoto Y, Yamamoto M, Furukawa T, Kawahara K Int J Mol Sci 15-Dec-2022
PMCID:PMC9784028
doi:10.3390/ijms232415986
PMID:36555627
Natural Products as Anticancer Agents: Current Status and Future Perspectives Naeem A, Hu P, Yang M, Zhang J, Liu Y, Zhu W, Zheng Q Molecules 30-Nov-2022
PMCID:PMC9737905
doi:10.3390/molecules27238367
PMID:36500466
Lead/Drug Discovery from Natural Resources Xu Z, Eichler B, Klausner EA, Duffy-Matzner J, Zheng W Molecules 28-Nov-2022
PMCID:PMC9736696
doi:10.3390/molecules27238280
PMID:36500375
Indigenous Uses, Phytochemical Analysis, and Anti-Inflammatory Properties of Australian Tropical Medicinal Plants Yeshi K, Turpin G, Jamtsho T, Wangchuk P Molecules 15-Jun-2022
PMCID:PMC9231311
doi:10.3390/molecules27123849
PMID:35744969
Small molecule SMU-CX24 targeting toll-like receptor 3 counteracts inflammation: A novel approach to atherosclerosis therapy Cen X, Wang B, Liang Y, Chen Y, Xiao Y, Du S, Nandakumar KS, Yin H, Liu S, Cheng K Acta Pharm Sin B 09-Jun-2022
PMCID:PMC9513496
doi:10.1016/j.apsb.2022.06.001
PMID:36176917
A Review on Mechanistic Insight of Plant Derived Anticancer Bioactive Phytocompounds and Their Structure Activity Relationship Mazumder K, Aktar A, Roy P, Biswas B, Hossain ME, Sarkar KK, Bachar SC, Ahmed F, Monjur-Al-Hossain AS, Fukase K Molecules 09-May-2022
PMCID:PMC9102595
doi:10.3390/molecules27093036
PMID:35566385

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
> Alkaloids and derivatives / Pleiocarpaman alkaloids
methyl (13Z,14S,16S,18R)-13-ethylidene-1,11-diazapentacyclo[12.3.1.02,7.08,17.011,16]octadeca-2,4,6,8(17)-tetraene-18-carboxylate 163087785 Click to see CC=C1CN2CCC3=C4C2CC1C(N4C5=CC=CC=C35)C(=O)OC 322.40 unknown https://doi.org/10.1021/JA01517A031
Pleiocarpamine 5385014 Click to see CC=C1CN2CCC3=C4C2CC1C(N4C5=CC=CC=C35)C(=O)OC 322.40 unknown https://doi.org/10.1515/ZNC-1986-0402
> Alkaloids and derivatives / Strychnos alkaloids
Norfluorocurarine 5581319 Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=CC=CC=C45)C=O 292.40 unknown https://doi.org/10.1021/JA01517A031
> Alkaloids and derivatives / Vallesaman alkaloids
Apparicine 5281349 Click to see CC=C1CN2CCC1C(=C)C3=C(C2)C4=CC=CC=C4N3 264.40 unknown https://doi.org/10.1021/JA01517A031
CID 6912322 6912322 Click to see CC=C1CN2CCC1C(=C)C3=C(C2)C4=CC=CC=C4N3 264.40 unknown https://doi.org/10.1515/ZNC-1986-0402
> Alkaloids and derivatives / Yohimbine alkaloids
Cathenamine 443361 Click to see CC1C2=CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 350.40 unknown https://doi.org/10.1515/ZNC-1986-0402
Elliptamine 234846 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC(=C(C=C45)OC)OC 412.50 unknown https://doi.org/10.1021/JA01517A031
Isoreserpiline 161345 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC(=C(C=C45)OC)OC 412.50 unknown https://doi.org/10.1016/S0176-1617(85)80229-7
https://doi.org/10.1021/JA01517A031
https://doi.org/10.1021/NP50035A022
Reserpiline 67228 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC(=C(C=C45)OC)OC 412.50 unknown https://doi.org/10.1016/S0176-1617(85)80229-7
Tetrahydroalstonine 72340 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1021/JA01517A031
https://doi.org/10.1515/ZNC-1986-0402
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
5,11-dimethyl-6H-pyrido[4,3-b]carbazol-9-ol 91643 Click to see CC1=C2C=CN=CC2=C(C3=C1NC4=C3C=C(C=C4)O)C 262.30 unknown https://doi.org/10.1016/S0021-9673(01)86824-2
9-Methoxyellipticine 72512 Click to see CC1=C2C=CN=CC2=C(C3=C1NC4=C3C=C(C=C4)OC)C 276.30 unknown https://doi.org/10.1016/S0021-9673(01)86824-2
https://doi.org/10.1016/S0176-1617(85)80229-7
https://doi.org/10.1021/NP50035A022
Ellipticine 3213 Click to see CC1=C2C=CN=CC2=C(C3=C1NC4=CC=CC=C43)C 246.31 unknown https://doi.org/10.1021/NP50035A022
https://doi.org/10.1016/0040-4020(86)80002-3
https://doi.org/10.1016/S0176-1617(85)80229-7
https://doi.org/10.1016/S0021-9673(01)86824-2
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines
Elliptinine 15559115 Click to see CCC1C2CCN(C1O)C3C2=CC4=C(C3)C5=C(N4)C=C(C=C5)OC 324.40 unknown https://doi.org/10.1021/NP50035A022
https://doi.org/10.1016/S0176-1617(85)80229-7

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