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Parkia javanica

Parkia javanica - 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 UUID643fd9c3b839f678831116
Scientific name Parkia javanica
Authority (Lam.) Merr.
First published in Sp. Blancoan.: 169 (1918)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Gleditsia javanica Lam. Encycl.2: 466 (1788)
Acacia javanica DC. Prodr.2: 471 (1825)
Gleditschia javanica Lam. Encycl. 2: 466 1788

Common names Top

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Language Common/alternative name
Bengali কুকিতেঁতই
Persian پارکیا جاوانیکا
Indonesian kedawung
Indonesian kedaung
jv kedawung
jv kêdawung
jv kedhawung
mad keḍhâbung
Malay pokok petai kerayong
Malay petai kerayung
Dutch kedaung
pam kupang
Chinese 爪哇派克豆
Chinese 爪哇球花豆

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000187192
Tropicos 13057749
INPN 447357
KEW urn:lsid:ipni.org:names:512208-1
The Plant List ild-33704
Open Tree Of Life 5148112
NCBI Taxonomy 1914267
IPNI 512208-1
iNaturalist 427329
GBIF 5348865
Freebase /m/0gkxx5p
EPPO PRKJA
EOL 644047
USDA GRIN 310530
Wikipedia Parkia_javanica
CMAUP NPO17793

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
Investigation of anti-proliferative and anti-angiogenic properties of Parkia javanica bark and fruit extracts in zebrafish Dhakal R, Kalladka K, Singha A, Pandyanda Nanjappa D, Ravindra J, Vittal R, Sil SK, Chakraborty A, Chakraborty G PLoS One 21-Jul-2023
PMCID:PMC10361473
doi:10.1371/journal.pone.0289117
PMID:37478119
Complete chloroplast genome data for Mimosa diplotricha and Mimosa diplotricha var. inermis from China Wang Q, Zhang CH, Wang CJ, Wan JZ Data Brief 09-Mar-2023
PMCID:PMC10060582
doi:10.1016/j.dib.2023.109045
PMID:37006391
The Molecular Architecture of Pseudomonas aeruginosa Quorum-Sensing Inhibitors Li Q, Mao S, Wang H, Ye X Mar Drugs 28-Jul-2022
PMCID:PMC9409833
doi:10.3390/md20080488
PMID:36005489
Wound Healing Properties and Antimicrobial Effects of Parkia clappertoniana Keay Fruit Husk Extract in a Rat Excisional Wound Model Kuma DN, Boye A, Kwakye-Nuako G, Boakye YD, Addo JK, Asiamah EA, Aboagye EA, Martey O, Essuman MA, Atsu Barku VY Biomed Res Int 23-Jul-2022
PMCID:PMC9338854
doi:10.1155/2022/9709365
PMID:35915797
Exploring the Phytochemicals and Anti-Cancer Potential of the Members of Fabaceae Family: A Comprehensive Review Usman M, Khan WR, Yousaf N, Akram S, Murtaza G, Kudus KA, Ditta A, Rosli Z, Rajpar MN, Nazre M Molecules 16-Jun-2022
PMCID:PMC9230627
doi:10.3390/molecules27123863
PMID:35744986
Seeds as Potential Sources of Phenolic Compounds and Minerals for the Indian Population Sahu PK, Cervera-Mata A, Chakradhari S, Singh Patel K, Towett EK, Quesada-Granados JJ, Martín-Ramos P, Rufián-Henares JA Molecules 17-May-2022
PMCID:PMC9144825
doi:10.3390/molecules27103184
PMID:35630662
Control of antibiotic resistance and superinfections as a strategy to manage COVID-19 deaths El-Ansary A, Balto H, Al-Hadlaq SM, Auda SH, Marraiki N Data Science for COVID-19 14-Jan-2022
PMCID:PMC8988903
doi:10.1016/B978-0-323-90769-9.00016-5
In Vitro Selective Antibacterial and Antiproliferative Effects of Ethanolic Extracts from Cambodian and Philippine Plants Used in Folk Medicine for Diarrhea Treatment Kudera T, Fiserova B, Korytakova M, Doskocil I, Salmonova H, Tulin EE, Nguon S, Bande MM, Kokoska L Front Pharmacol 26-Nov-2021
PMCID:PMC8661004
doi:10.3389/fphar.2021.746808
PMID:34899301
Interactions with Microbial Proteins Driving the Antibacterial Activity of Flavonoids Donadio G, Mensitieri F, Santoro V, Parisi V, Bellone ML, De Tommasi N, Izzo V, Dal Piaz F Pharmaceutics 05-May-2021
PMCID:PMC8147964
doi:10.3390/pharmaceutics13050660
PMID:34062983
Bioguided Fractionation of Local Plants against Matrix Metalloproteinase9 and Its Cytotoxicity against Breast Cancer Cell Models: In Silico and In Vitro Study Hariono M, Rollando R, Karamoy J, Hariyono P, Atmono M, Djohan M, Wiwy W, Nuwarda R, Kurniawan C, Salin N, Wahab H Molecules 14-Oct-2020
PMCID:PMC7587335
doi:10.3390/molecules25204691
PMID:33066411
Inhibitory studies of HepG2 and human immune cells using Solanum nigrum Kumar AG, Bupesh G, Sankarganesh P, Vasanth S, Nandagopal S, Joseph B Bioinformation 31-Jul-2020
PMCID:PMC7505242
doi:10.6026/97320630016525
PMID:32994677
Unraveling the Chloroplast Genomes of Two Prosopis Species to Identify Its Genomic Information, Comparative Analyses and Phylogenetic Relationship Asaf S, Khan AL, Khan A, Al-Harrasi A Int J Mol Sci 06-May-2020
PMCID:PMC7247323
doi:10.3390/ijms21093280
PMID:32384622
The complete chloroplast genome sequence of Afzelia xylocarpa Zhang J, Li Y, Heng S, Seab K, Wang Y Mitochondrial DNA B Resour 21-Jan-2020
PMCID:PMC7748567
doi:10.1080/23802359.2020.1715857
PMID:33366739
Antiviral Activity of Cananga odorata Against Hepatitis B Virus INDRASETIAWAN P, AOKI-UTSUBO C, HANAFI M, HARTATI S, WAHYUNI TS, KAMEOKA M, YANO Y, HOTTA H, HAYASHI Y Kobe J Med Sci 12-Nov-2019
PMCID:PMC7012192
PMID:31956259
The complete chloroplast genome of Stryphnodendron adstringens (Leguminosae - Caesalpinioideae): comparative analysis with related Mimosoid species Souza UJ, Nunes R, Targueta CP, Diniz-Filho JA, Telles MP Sci Rep 02-Oct-2019
PMCID:PMC6775074
doi:10.1038/s41598-019-50620-3
PMID:31578450

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(17alpha,23E)-5alpha-Dammara-20,23-diene-3beta,25-diol 9955042 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C(=C)CC=CC(C)(C)O)C)C)C 442.70 unknown via CMAUP database
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
Yamogenin 441900 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(25R)-3beta-[4-O-[4-O-(alpha-L-Rhamnopyranosyl)-alpha-L-rhamnopyranosyl]-beta-D-glucopyranosyloxy]spirosta-5-ene 21603983 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 21603986 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1 1015.20 unknown via CMAUP database
Borassoside A 16204068 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
Borassoside B 102155844 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O 901.00 unknown via CMAUP database
Borassoside C 102155845 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O 901.00 unknown via CMAUP database
Borassoside D 16204180 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
Borassoside E 16204181 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
Borassoside F 16204183 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1 1015.20 unknown via CMAUP database
Collettinside III 10653210 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
Dioscin 119245 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
Disogluside 11827970 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)OC1 576.80 unknown via CMAUP database
Methylprotodioscin 11263254 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC 1063.20 unknown via CMAUP database
Progenin II 44429638 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
Prosapogenin A 11061578 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
Protodioscin 441891 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown via CMAUP database
Pseudoprotodioscin 21637110 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC8C7C(=C(O8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O 1031.20 unknown via CMAUP database
Trigonelloside C 441899 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown via CMAUP database
Yamogenin 3-O-neohesperidoside 441901 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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 / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-O-beta-D-mannopyranosyl-alpha-D-mannopyranose 5288769 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Gal(a1-6)a-Man 11724912 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
beta-D-Manp-(1->4)-beta-D-Manp-(1->4)-beta-D-Manp 5287808 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O 504.40 unknown via CMAUP database

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