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Archidendron jiringa

Archidendron jiringa - 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 UUID643fdc31a8b7f293051109
Scientific name Archidendron jiringa
Authority (Jack) I.C.Nielsen
First published in Adansonia, n.s., 19: 32 (1979)

Description Top

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Synonyms Top

Scientific name Authority First published in
Albizia jiringa (Jack) Kurz Prelim. Rep. Forest Pegu, App. A: 56 (1875)
Pithecellobium jiringa (Jack) Prain J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 66: 11. 267. 1897, in obs.; Merrill in Philipp. Journ. Sci. xiv. 243 (1919). [1898 publ. 1897]
Pithecellobium lobatum Benth. London J. Bot.3: 208 (1844)
Zygia jiringa (Jack) Kosterm. Bull. Organ. Natuurw. Onderz. Indonesië20: 27 (1954)
Inga jiringa (Jack) DC.
Mimosa jiringa Jack Malayan Misc.1(1): 14 (1820)
Feuilleea jiringa (Jack) Kuntze Revis. Gen. Pl.1: 185 (1891)
Mimosa kaeringa Roxb. Fl. Brit. India [J. D. Hooker] 2(5): 305, sphalm. 1878 [Jul 1878]
Inga kaeringa Voigt Hort. Suburb. Calcutt.: 258 (1845)
Mimosa koeringa Roxb. Fl. Ind. ed. 1832, 2: 543 (1832)
Zygia jiriuga (Jack) Kosterm. Bull. Organ. Natuurw. Onderz. Indonesië 20: 27 (1954)
Pithecellobium lateriflorum Blume ex Miq. Fl. Ned. Ind.1(1): 34 (1855)
Inga koeringa Kostel. Allg. Med.-Pharm. Fl.4: 1354 (1835)
Inga jiringa (Jack) Jack Malayan Misc.2(7): 78 (1822)
Pithecellobium jiringa (Jack) Prain J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist.66: 11 (1897)

Common names Top

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Language Common/alternative name
Japanese ジリンマメ
Malay jering
Chinese 胡豆
Chinese 缅尼猴耳环
Chinese 犬果

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
      • Bangladesh
    • Indo-China
      • Myanmar
      • Thailand
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000199807
Tropicos 13067394
KEW urn:lsid:ipni.org:names:475066-1
The Plant List ild-46285
Open Tree Of Life 3919243
NCBI Taxonomy 2934735
IPNI 475066-1
iNaturalist 347836
GBIF 2941605
Freebase /m/03ns4cg
EOL 654962
USDA GRIN 311920

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
Tree islands enhance biodiversity and functioning in oil palm landscapes Zemp DC, Guerrero-Ramirez N, Brambach F, Darras K, Grass I, Potapov A, Röll A, Arimond I, Ballauff J, Behling H, Berkelmann D, Biagioni S, Buchori D, Craven D, Daniel R, Gailing O, Ellsäßer F, Fardiansah R, Hennings N, Irawan B, Khokthong W, Krashevska V, Krause A, Kückes J, Li K, Lorenz H, Maraun M, Merk MS, Moura CC, Mulyani YA, Paterno GB, Pebrianti HD, Polle A, Prameswari DA, Sachsenmaier L, Scheu S, Schneider D, Setiajiati F, Setyaningsih CA, Sundawati L, Tscharntke T, Wollni M, Hölscher D, Kreft H Nature 24-May-2023
PMCID:PMC10247383
doi:10.1038/s41586-023-06086-5
PMID:37225981
Characterization and antimicrobial activity of lectins purified from three Egyptian leguminous seeds El-Araby MM, El-Shatoury EH, Soliman MM, Shaaban HF AMB Express 15-May-2020
PMCID:PMC7229064
doi:10.1186/s13568-020-01024-4
PMID:32415415
Structure-function and application of plant lectins in disease biology and immunity Mishra A, Behura A, Mawatwal S, Kumar A, Naik L, Mohanty SS, Manna D, Dokania P, Mishra A, Patra SK, Dhiman R Food Chem Toxicol 19-Sep-2019
PMCID:PMC7115788
doi:10.1016/j.fct.2019.110827
PMID:31542433
Two-Step Isolation, Purification, and Characterization of Lectin from Zihua Snap Bean (Phaseolus vulgaris) Seeds Jiang B, Wang X, Wang L, Lv X, Li D, Liu C, Feng Z Polymers (Basel) 02-May-2019
PMCID:PMC6571848
doi:10.3390/polym11050785
PMID:31052517
Traditional knowledge of wild edible plants with special emphasis on medicinal uses in Southern Shan State, Myanmar Shin T, Fujikawa K, Moe AZ, Uchiyama H J Ethnobiol Ethnomed 17-Jul-2018
PMCID:PMC6050729
doi:10.1186/s13002-018-0248-1
PMID:30016980
Antiulcer Agents: From Plant Extracts to Phytochemicals in Healing Promotion Sharifi-Rad M, Fokou PV, Sharopov F, Martorell M, Ademiluyi AO, Rajkovic J, Salehi B, Martins N, Iriti M, Sharifi-Rad J Molecules 17-Jul-2018
PMCID:PMC6100067
doi:10.3390/molecules23071751
PMID:30018251
Characterization of chickpea (Cicer arietinum L.) lectin for biological activity Gautam AK, Gupta N, Narvekar DT, Bhadkariya R, Bhagyawant SS Physiol Mol Biol Plants 20-Mar-2018
PMCID:PMC5911256
doi:10.1007/s12298-018-0508-5
PMID:29692547
Legume Lectins: Proteins with Diverse Applications Lagarda-Diaz I, Guzman-Partida AM, Vazquez-Moreno L Int J Mol Sci 12-Jun-2017
PMCID:PMC5486065
doi:10.3390/ijms18061242
PMID:28604616
Anti- and Pro-Lipase Activity of Selected Medicinal, Herbal and Aquatic Plants, and Structure Elucidation of an Anti-Lipase Compound Ado MA, Abas F, Mohammed AS, Ghazali HM Molecules 26-Nov-2013
PMCID:PMC6270111
doi:10.3390/molecules181214651
PMID:24287996
Flavan-3-ol gallates and proanthocyanidins from Pithecellobium lobatum Lee Min-Won, Satoshi Morimoto, Gen-Ichiro Nonaka, Itsuo Nishioka Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80375-O

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1016/0031-9422(92)80375-O
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S)-2-(3,4,5-trihydroxyphenyl)-8-[(2R,3R,4S)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 101630509 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80375-O
Procyanidin B3 146798 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(92)80375-O
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(92)80375-O
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(92)80375-O
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown https://doi.org/10.1016/0031-9422(92)80375-O
(-)-Epicatechingallate 367141 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown https://doi.org/10.1016/0031-9422(92)80375-O
[(2S,3R)-2-[3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxyphenyl]-3,5-dihydroxy-3,4-dihydro-2H-chromen-7-yl] 3,4,5-trihydroxybenzoate 163195225 Click to see C1C(C(OC2=CC(=CC(=C21)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)C4=CC(=C(C(=C4)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80375-O
[(2S,3R)-2-[3,5-dihydroxy-4-(3,4,5-trihydroxybenzoyl)oxyphenyl]-3,5-dihydroxy-3,4-dihydro-2H-chromen-7-yl] 3,4,5-trihydroxybenzoate 163055242 Click to see C1C(C(OC2=CC(=CC(=C21)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)C4=CC(=C(C(=C4)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80375-O
[2-[3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxyphenyl]-3,5-dihydroxy-3,4-dihydro-2H-chromen-7-yl] 3,4,5-trihydroxybenzoate 74977181 Click to see C1C(C(OC2=CC(=CC(=C21)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)C4=CC(=C(C(=C4)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80375-O
[2-[3,5-dihydroxy-4-(3,4,5-trihydroxybenzoyl)oxyphenyl]-3,5-dihydroxy-3,4-dihydro-2H-chromen-7-yl] 3,4,5-trihydroxybenzoate 74977182 Click to see C1C(C(OC2=CC(=CC(=C21)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)C4=CC(=C(C(=C4)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80375-O
[2-hydroxy-4-(3,5,7-trihydroxy-3,4-dihydro-2H-chromen-2-yl)phenyl] 3,4,5-trihydroxybenzoate 74191796 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 442.40 unknown https://doi.org/10.1016/0031-9422(92)80375-O
[2-hydroxy-5-(3,5,7-trihydroxy-3,4-dihydro-2H-chromen-2-yl)phenyl] 3,4,5-trihydroxybenzoate 74977173 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O 442.40 unknown https://doi.org/10.1016/0031-9422(92)80375-O
[2,3-dihydroxy-5-(3,5,7-trihydroxy-3,4-dihydro-2H-chromen-2-yl)phenyl] 3,4,5-trihydroxybenzoate 74977179 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O 458.40 unknown https://doi.org/10.1016/0031-9422(92)80375-O
[2,6-dihydroxy-4-(3,5,7-trihydroxy-3,4-dihydro-2H-chromen-2-yl)phenyl] 3,4,5-trihydroxybenzoate 74155559 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 458.40 unknown https://doi.org/10.1016/0031-9422(92)80375-O
[2,6-dihydroxy-4-[(2S,3R)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-2-yl]phenyl] 3,4,5-trihydroxybenzoate 23928136 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 458.40 unknown https://doi.org/10.1016/0031-9422(92)80375-O
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate 1287 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.1016/0031-9422(92)80375-O
Catechin 3'-O-gallate 44257105 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O 442.40 unknown https://doi.org/10.1016/0031-9422(92)80375-O
Catechin 4'-O-gallate 44257106 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 442.40 unknown https://doi.org/10.1016/0031-9422(92)80375-O
Epigallocatechin Gallate 65064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.1016/0031-9422(92)80375-O
Gallocatechin 3'-O-gallate 44257114 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O 458.40 unknown https://doi.org/10.1016/0031-9422(92)80375-O
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Flavan-3,3',4',5,5',7-hexol 1249 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1016/0031-9422(92)80375-O
Gallocatechin 65084 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1016/0031-9422(92)80375-O

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