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Archidendron ellipticum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fdc3115e9a938838081
Scientific name Archidendron ellipticum
Authority (Blume) I.C.Nielsen
First published in Adansonia, n.s., 19: 21 (1979)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Albizia elliptica (Blume) E.Fourn. Ann. Sci. Nat., Bot., sér. 4, 14: 374 (1860)
Abarema elliptica (Blume) Kosterm. Bull. Organ. Natuurw. Onderz. Indonesië20: 53 (1954)
Pithecellobium ellipticum (Blume) Hassk. Retzia1: 225 (1855)
Inga elliptica Blume Catalogus: 88 (1823)
Feuilleea elliptica (E.Fourn.) Kuntze Revis. Gen. Pl.1: 187 (1891)

Common names Top

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Language Common/alternative name
Chinese 椭圆叶猴耳环

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Archidendron ellipticum subsp. cordifoliolatum I.C.Nielsen Opera Bot.76: 68 (1984 publ. 1985)
Archidendron ellipticum subsp. ellipticum (Blume) I.C.Nielsen Unknown

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
      • East Himalaya
    • Indo-China
      • Nicobar Nicobar
      • Thailand
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Philippines
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000199797
Tropicos 13067390
KEW urn:lsid:ipni.org:names:475051-1
The Plant List ild-46276
Open Tree Of Life 700610
NCBI Taxonomy 392766
IUCN Red List 19891663
IPNI 475051-1
iNaturalist 139718
GBIF 2941613
EOL 654960
USDA GRIN 435648
CMAUP NPO25687

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 Kunitz chymotrypsin inhibitor from Erythrina velutina seeds displays activity against HeLa cells through arrest in cell cycle Lucena SV, Rufino FP, de Dantas Moura GE, Rabêlo LM, Monteiro NK, Ferreira AT, Perales JE, Uchôa AF, Justo GZ, de Oliveira CF, Migliolo L, Nader HB, Santos EA, Oliveira AS 3 Biotech 15-Dec-2021
PMCID:PMC8674401
doi:10.1007/s13205-021-03084-0
PMID:34926123
Multimeric Association of Purified Novel Bowman-Birk Inhibitor From the Medicinal Forage Legume Mucuna pruriens (L.) DC. Lone JK, Lekha MA, Bharadwaj RP, Ali F, Pillai MA, Wani SH, Yasin JK, Chandrashekharaiah KS Front Plant Sci 25-Nov-2021
PMCID:PMC8655843
doi:10.3389/fpls.2021.772046
PMID:34899797
Status and consolidated list of threatened medicinal plants of India Gowthami R, Sharma N, Pandey R, Agrawal A Genet Resour Crop Evol 25-May-2021
PMCID:PMC8148398
doi:10.1007/s10722-021-01199-0
PMID:34054223
Physico-Chemical and Antifungal Properties of a Trypsin Inhibitor from the Roots of Pseudostellaria heterophylla Cai X, Xie X, Fu N, Wang S Molecules 18-Sep-2018
PMCID:PMC6225307
doi:10.3390/molecules23092388
PMID:30231516
Crude Ethanol Extract of Pithecellobium ellipticum as a Potential Lipid-Lowering Treatment for Hypercholesterolaemia Wong JP, Wijaya S, Ting KN, Wiart C, Mustafa K, Shipton F, Khoo TJ Evid Based Complement Alternat Med 15-Apr-2014
PMCID:PMC4009285
doi:10.1155/2014/492703
PMID:24839451
JcTI-I: a novel trypsin inhibitor from Jatropha curcas seed cake with potential for bacterial infection treatment Costa HP, Oliveira JT, Sousa DO, Morais JK, Moreno FB, Monteiro-Moreira AC, Viegas RA, Vasconcelos IM Front Microbiol 30-Jan-2014
PMCID:PMC3906595
doi:10.3389/fmicb.2014.00005
PMID:24523715
Characterization and Pharmacological Properties of a Novel Multifunctional Kunitz Inhibitor from Erythrina velutina Seeds Machado RJ, Monteiro NK, Migliolo L, Silva ON, Pinto MF, Oliveira AS, Franco OL, Kiyota S, Bemquerer MP, Uchoa AF, Morais AH, Santos EA PLoS One 28-May-2013
PMCID:PMC3666885
doi:10.1371/journal.pone.0063571
PMID:23737945
High Correlation of 2,2-diphenyl-1-picrylhydrazyl (DPPH) Radical Scavenging, Ferric Reducing Activity Potential and Total Phenolics Content Indicates Redundancy in Use of All Three Assays to Screen for Antioxidant Activity of Extracts of Plants from the Malaysian Rainforest Clarke G, Ting KN, Wiart C, Fry J Antioxidants (Basel) 04-Jan-2013
PMCID:PMC4665400
doi:10.3390/antiox2010001
PMID:26787618
Reliability of Inhibition Models to Correctly Identify Type of Inhibition Kolhatkar V, Polli JE Pharm Res 14-Aug-2010
PMCID:PMC2962774
doi:10.1007/s11095-010-0236-1
PMID:20711748
Ethnomedical survey of plants used by the Orang Asli in Kampung Bawong, Perak, West Malaysia Samuel AJ, Kalusalingam A, Chellappan DK, Gopinath R, Radhamani S, Husain HA, Muruganandham V, Promwichit P J Ethnobiol Ethnomed 07-Feb-2010
PMCID:PMC2843656
doi:10.1186/1746-4269-6-5
PMID:20137098
Overexpression of a Weed (Solanum americanum) Proteinase Inhibitor in Transgenic Tobacco Results in Increased Glandular Trichome Density and Enhanced Resistance to Helicoverpa armigera and Spodoptera litura Luo M, Wang Z, Li H, Xia KF, Cai Y, Xu ZF Int J Mol Sci 23-Apr-2009
PMCID:PMC2680653
doi:10.3390/ijms10041896
PMID:19468345
Separation of High Molecular Weight Saponins of <i>Archidendron Ellipticum</i> by Hydrophilic Interaction Chromatography J. A. Beutler Informa UK Limited 07-Jul-2007
doi:10.1080/10826079708002712
Cytotoxic Triterpenoid Saponins of Albizia gummifera from the Madagascar Rain Forest Cao S, Norris A, Miller JS, Ratovoson F, Razafitsalama J, Andriantsiferana R, Rasamison VE, Kingston DG J Nat Prod 31-Jan-2007
PMCID:PMC2442826
doi:10.1021/np060506g
PMID:17263578
Avicins: Triterpenoid saponins from Acacia victoriae (Bentham) induce apoptosis by mitochondrial perturbation Haridas V, Higuchi M, Jayatilake GS, Bailey D, Mujoo K, Blake ME, Arntzen CJ, Gutterman JU Proc Natl Acad Sci U S A 08-May-2001
PMCID:PMC33297
doi:10.1073/pnas.101619098
PMID:11344312
Isolation and characterization of novel cytotoxic saponins from Archidendron ellipticum. Beutler JA, Kashman Y, Pannell LK, Cardellina JH 2nd, Alexander MR, Balaschak MS, Prather TR, Shoemaker RH, Boyd MR Bioorg Med Chem 01-Aug-1997
doi:10.1016/S0968-0896(97)00098-9
PMID:9313857

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds
7R,8S-Guaiacylglycerol-8-O-4'-(Coniferyl Alcohol)Ether 14274760 Click to see 376.40 unknown via CMAUP database
erythro-Guaiacylglycerol beta-dihydroconiferyl ether 13893597 Click to see 378.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Azelaic Acid 2266 Click to see C(CCCC(=O)O)CCCC(=O)O 188.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Tocopherol quinone 2734086 Click to see 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S)-4alpha-Ethenyl-2alpha-hydroxy-3beta-[1-(hydroxymethyl)ethenyl]-6alpha-[[2-(hydroxymethyl)-1-oxo-2-propenyl]oxy 13891365 Click to see CC1(CC(C(C(C1C(=C)CO)O)C(=C)C(=O)OC)OC(=O)C(=C)CO)C=C 380.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Avicin D 44566777 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CC(C7(C6CC(C(C7)OC(=O)C(=CCCC(C)(C=C)OC8C(C(C(C(O8)C)OC(=O)C(=CCCC(C)(C=C)O)CO)O)O)CO)(C)C)C(=O)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)C)OC1C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)C)C)C)NC(=O)C)O)O)OC1C(C(C(CO1)O)O)O)O)O 2083.30 unknown https://doi.org/10.1080/10826079708002712
https://doi.org/10.1016/S0968-0896(97)00098-9
Elliptoside A 5352078 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CC(C7(C6CC(C(C7)OC(=O)C(=CCCC(C)(C=C)OC8C(C(C(C(O8)C)OC(=O)C(=CCCC(C)(C=C)O)C)O)O)CO)(C)C)C(=O)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)C)OC1C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)C)C)C)NC(=O)C)O)O)OC1C(C(C(CO1)O)O)O)O)O 2067.30 unknown https://doi.org/10.1080/10826079708002712
https://doi.org/10.1016/S0968-0896(97)00098-9
Elliptoside B 5352079 Click to see 2026.20 unknown https://doi.org/10.1016/S0968-0896(97)00098-9
https://doi.org/10.1080/10826079708002712
Elliptoside G 5352080 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CC(C7(C6CC(C(C7)OC(=O)C(=CCCC(C)(C=C)OC8C(C(C(C(O8)C)OC(=O)C(=CCCC(C)(C=C)O)CO)O)O)CO)(C)C)C(=O)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)C)OC1C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)C)C)C)NC(=O)C)O)O)OC1C(C(C(CO1)O)O)O)O)O 2083.30 unknown https://doi.org/10.1080/10826079708002712
https://doi.org/10.1016/S0968-0896(97)00098-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones
Hemistepsin 10043230 Click to see 346.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aS,4S,5E,9Z,11aR)-6-formyl-10-methyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 53494931 Click to see 346.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3S,3aR,4S,6aR,8S,9aR,9bR)-4,8-dihydroxy-3-methyl-6,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 12047617 Click to see 264.32 unknown via CMAUP database
[(3S,3aR,4S,6aR,8S,9aR,9bR)-8-hydroxy-3-methyl-6,9-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 71503391 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)OC(=O)C(=C)CO 348.40 unknown via CMAUP database
Cynaropicrin 119093 Click to see 346.40 unknown via CMAUP database
Desacylcynaropicrin 13943205 Click to see 262.30 unknown via CMAUP database
Isolipidiol 14589530 Click to see CC1C(CC2C1C3C(C(C(=O)O3)C)C(CC2=C)O)O 266.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Taraxasterol 115250 Click to see 426.70 unknown via CMAUP database
Taraxasterol Acetate 13889352 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde 8768 Click to see 138.12 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
Indole-3-carboxylic acid 69867 Click to see C1=CC=C2C(=C1)C(=CN2)C(=O)O 161.16 unknown via CMAUP database
Methyl indole-3-carboxylate 589098 Click to see 175.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3,4-Dihydroxycinnamic acid methyl ester 92202 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database

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