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Flacourtia inermis

Flacourtia inermis - 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 UUID644036089f814999368078
Scientific name Flacourtia inermis
Authority Roxb.
First published in Pl. Coromandel 3(1): 16. 1811 [1819 publ. Jul 1811]

Description Top

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Synonyms Top

Scientific name Authority First published in
Flacourtia quintuplinervis Turcz. Bull. Soc. Imp. Naturalistes Moscou 36(I): 553 (1863)

Common names Top

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Language Common/alternative name
English batoko plum
Arabic فلاكورة عزلاء
Persian آلوی باتوکو
Indonesian lobi-lobi
Tamil சீமைக்கொட்டைக்களா
Chinese 罗比梅
Chinese 羅比梅

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Flacourtia inermis var. rindjanica (Slooten) Sleumer in Fl. Males. 5: 71 1954

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

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000925657
USDA Plants FLIN3
Tropicos 50225573
INPN 839806
KEW urn:lsid:ipni.org:names:111655-1
The Plant List kew-4813256
Open Tree Of Life 3915225
NCBI Taxonomy 1857402
IPNI 1009131-1
iNaturalist 344840
GBIF 5331166
EPPO FLCIE
EOL 487583
USDA GRIN 17119
Wikipedia Flacourtia_inermis

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
Anti-diabetic and anti-inflammatory bioactive hits from Coriaria intermedia Matsum. stem and Dracontomelon dao (Blanco) Merr. & Rolfe bark through bioassay-guided fractionation and liquid chromatography-tandem mass spectrometry Fabian MC, Astorga RM, Atis AA, Pilapil LA, Hernandez CC Front Pharmacol 08-Mar-2024
PMCID:PMC10957545
doi:10.3389/fphar.2024.1349725
PMID:38523640
Standardization of Euphorbia tithymaloides (L.) Poit. (Root) by Conventional and DNA Barcoding Methods Patil S, Imran M, Jaquline RS, Aeri V ACS Omega 04-Aug-2023
PMCID:PMC10433337
doi:10.1021/acsomega.3c02543
PMID:37599932
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
Secondary metabolites from the Endophytic fungi Fusarium decemcellulare F25 and their antifungal activities Song Z, Sun YJ, Xu S, Li G, Yuan C, Zhou K Front Microbiol 01-Feb-2023
PMCID:PMC9929939
doi:10.3389/fmicb.2023.1127971
PMID:36819056
Pest categorisation of Nipaecoccus viridis Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 18-Jan-2023
PMCID:PMC9846308
doi:10.2903/j.efsa.2023.7770
PMID:36698490
Siwalik plant megafossil diversity in the Eastern Himalayas: A review Khan MA, Mahato S, Spicer RA, Spicer TE, Ali A, Hazra T, Bera S Plant Divers 17-Dec-2022
PMCID:PMC10311196
doi:10.1016/j.pld.2022.12.003
PMID:37397603
Molecular diversity of exotic durian (Durio spp.) germplasm: a case study of Kalimantan, Indonesia Mursyidin DH, Makruf MI, Badruzsaufari, Noor A J Genet Eng Biotechnol 01-Mar-2022
PMCID:PMC8888783
doi:10.1186/s43141-022-00321-8
PMID:35230532
Frequent ploidy changes in Salicaceae indicates widespread sharing of the salicoid whole genome duplication by the relatives of Populus L. and Salix L. Zhang ZS, Zeng QY, Liu YJ BMC Plant Biol 13-Nov-2021
PMCID:PMC8590345
doi:10.1186/s12870-021-03313-x
PMID:34773988
Plant-Derived and Dietary Hydroxybenzoic Acids—A Comprehensive Study of Structural, Anti-/Pro-Oxidant, Lipophilic, Antimicrobial, and Cytotoxic Activity in MDA-MB-231 and MCF-7 Cell Lines Kalinowska M, Gołębiewska E, Świderski G, Męczyńska-Wielgosz S, Lewandowska H, Pietryczuk A, Cudowski A, Astel A, Świsłocka R, Samsonowicz M, Złowodzka AB, Priebe W, Lewandowski W Nutrients 04-Sep-2021
PMCID:PMC8466373
doi:10.3390/nu13093107
PMID:34578985
A Narrative Review on Therapeutic Potentials of Watercress in Human Disorders Panahi Kokhdan E, Khodabandehloo H, Ghahremani H, Doustimotlagh AH Evid Based Complement Alternat Med 07-May-2021
PMCID:PMC8123986
doi:10.1155/2021/5516450
PMID:34055006
A Comparative Investigation on Phenolic Composition, Characterization and Antioxidant Potentials of Five Different Australian Grown Pear Varieties Wang Z, Barrow CJ, Dunshea FR, Suleria HA Antioxidants (Basel) 20-Jan-2021
PMCID:PMC7909527
doi:10.3390/antiox10020151
PMID:33498549
Total Vitamin C, Ascorbic Acid, Dehydroascorbic Acid, Antioxidant Properties, and Iron Content of Underutilized and Commonly Consumed Fruits in Sri Lanka Abeysuriya HI, Bulugahapitiya VP, Loku Pulukkuttige J Int J Food Sci 20-Aug-2020
PMCID:PMC7474787
doi:10.1155/2020/4783029
PMID:32908860
Phytopharmacological Strategies in the Management of Type 2 Diabetes Mellitus Duarte AM, Guarino MP, Barroso S, Gil MM Foods 02-Mar-2020
PMCID:PMC7143818
doi:10.3390/foods9030271
PMID:32131470
Intergeneric Relationships within the Family Salicaceae s.l. Based on Plastid Phylogenomics Li MM, Wang DY, Zhang L, Kang MH, Lu ZQ, Zhu RB, Mao XX, Xi ZX, Ma T Int J Mol Sci 02-Aug-2019
PMCID:PMC6696080
doi:10.3390/ijms20153788
PMID:31382526
Internal transcribed spacer 2 (ITS2) molecular morphometric analysis based species delimitation of foliar endophytic fungi from Aglaia elaeagnoidea, Flacourtia inermis and Premna serratifolia Sundaresan N, Jagan EG, Kathamuthu G, Pandi M PLoS One 09-Apr-2019
PMCID:PMC6456209
doi:10.1371/journal.pone.0215024
PMID:30964914

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
6-Methyl-2-(4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,12,15,16,17-octahydrocyclopenta[a]phenanthren-17-yl)hept-5-enoic acid 72967543 Click to see CC(=CCCC(C1CCC2(C1(CC=C3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C)C(=O)O)C 452.70 unknown https://doi.org/10.1080/14786419.2011.586638
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(2S)-2-Hydroxybutanedioic acid 222656 Click to see C(C(C(=O)O)O)C(=O)O 134.09 unknown https://doi.org/10.1080/14786419.2011.586638
Malic Acid 525 Click to see C(C(C(=O)O)O)C(=O)O 134.09 unknown https://doi.org/10.1080/14786419.2011.586638
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-Butyl 3-(((E)-3-(3,4-dihydroxyphenyl)acryloyl)oxy)-1,4,5-trihydroxycyclohexanecarboxylate 15523673 Click to see CCCCOC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 410.40 unknown https://doi.org/10.1080/14786419.2011.586638
1,3,4,5-Tetrahydroxycyclohexanecarboxylic acid 1064 Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O 192.17 unknown https://doi.org/10.1080/14786419.2011.586638
Butyl 3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxycyclohexane-1-carboxylate 78384630 Click to see CCCCOC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 410.40 unknown https://doi.org/10.1080/14786419.2011.586638
Butyl chlorogenate 12135130 Click to see CCCCOC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 410.40 unknown https://doi.org/10.1080/14786419.2011.586638
Methyl 3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxycyclohexane-1-carboxylate 73412063 Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 368.30 unknown https://doi.org/10.1080/14786419.2011.586638
Methyl 4-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,3,5-trihydroxycyclohexane-1-carboxylate 78158136 Click to see COC(=O)C1(CC(C(C(C1)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 368.30 unknown https://doi.org/10.1080/14786419.2011.586638
Methyl chlorogenate 6476139 Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 368.30 unknown https://doi.org/10.1080/14786419.2011.586638
Neochlorogenic acid methyl ester 46230348 Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 368.30 unknown https://doi.org/10.1080/14786419.2011.586638
Quinic acid 6508 Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O 192.17 unknown https://doi.org/10.1080/14786419.2011.586638

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