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Diospyros discolor

Diospyros discolor - Unknown
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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 UUID6440174b5a828446677433
Scientific name Diospyros discolor
Authority Willd.
First published in Sp. Pl., ed. 4 , 4: 1108 (1806)

Description Top

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Synonyms Top

Scientific name Authority First published in
Mabola edulis Raf. Sylva Tellur. : 11 (1838)
Cavanillea philippensis Desr. Encycl. 3: 663 (1792)
Diospyros blancoi A.DC. Prodr. 8: 237 (1844)
Diospyros durionoides Bakh. Gard. Bull. Straits Settlem. 7: 169 (1933)
Diospyros malacapai A.DC. Prodr. 8: 237 (1844)
Diospyros merrillii Elmer Leafl. Philipp. Bot. 5: 1775 (1913)
Diospyros utilis Hemsl. Ann. Bot. (Oxford) 9: 154 (1895)
Embryopteris discolor G.Don Gen. Hist. 4: 41 (1837)
Cavanillea mabolo Poir. Tabl. Encycl. 2: t. 454 (1794)
Diospyros mabolo Roxb. ex J.V.Thomps. Cat. Exotic Pl. Mauritius , ed. 2: 24 (1822)

Common names Top

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Language Common/alternative name
English mabolo
bcl kamagong
Bengali গাব
Catalan mabolo
co vèludo
Indonesian bisbul
Japanese ケガキ
kv Маболо
Malayalam മബോളോ
Malay pokok mentega
Dutch mabolo
su bisbul
Thai มะริด (พืช)
Chinese 異色柿
Chinese 异色柿
Chinese 毛柿

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

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-0000648780
Tropicos 11500583
INPN 733206
KEW urn:lsid:ipni.org:names:322328-1
The Plant List kew-2769627
Open Tree Of Life 739278
NCBI Taxonomy 268838
IPNI 322328-1
iNaturalist 348327
GBIF 3032976
Freebase /m/06kvfp
USDA GRIN 14281

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
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
Persimmon Leaves: Nutritional, Pharmaceutical, and Industrial Potential—A Review Hossain A, Shahidi F Plants (Basel) 18-Feb-2023
PMCID:PMC9965245
doi:10.3390/plants12040937
PMID:36840285
Natural essential oils as a new therapeutic tool in colorectal cancer Garzoli S, Alarcón-Zapata P, Seitimova G, Alarcón-Zapata B, Martorell M, Sharopov F, Fokou PV, Dize D, Yamthe LR, Les F, Cásedas G, López V, Iriti M, Rad JS, Gürer ES, Calina D, Pezzani R, Vitalini S Cancer Cell Int 13-Dec-2022
PMCID:PMC9749237
doi:10.1186/s12935-022-02806-5
PMID:36514100
Sustainable Hues: Exploring the Molecular Palette of Biowaste Dyes through LC-MS Metabolomics Molino RJ, Rellin KF, Nellas RB, Junio HA Molecules 02-Nov-2021
PMCID:PMC8587104
doi:10.3390/molecules26216645
PMID:34771057
Ethnomedicinal Value of Antidiabetic Plants in Bangladesh: A Comprehensive Review Rahman MM, Uddin MJ, Reza AS, Tareq AM, Emran TB, Simal-Gandara J Plants (Basel) 08-Apr-2021
PMCID:PMC8070064
doi:10.3390/plants10040729
PMID:33918026
Zebrafish as a Successful Animal Model for Screening Toxicity of Medicinal Plants Modarresi Chahardehi A, Arsad H, Lim V Plants (Basel) 12-Oct-2020
PMCID:PMC7601530
doi:10.3390/plants9101345
PMID:33053800
Molecular Affinity of Mabolo Extracts to an Octopamine Receptor of a Fruit Fly Dacanay FN, Ladra MC, Junio HA, Nellas RB Molecules 24-Oct-2017
PMCID:PMC6151447
doi:10.3390/molecules22101677
PMID:29064449
Analysis of aroma compounds and nutrient contents of mabolo (Diospyros blancoi A. DC.), an ethnobotanical fruit of Austronesian Taiwan Hung SF, Roan SF, Chang TL, King HB, Chen IZ J Food Drug Anal 16-Oct-2015
PMCID:PMC9345435
doi:10.1016/j.jfda.2015.08.004
PMID:28911412
Taiwanese Native Plants Inhibit Matrix Metalloproteinase-9 Activity after Ultraviolet B Irradiation Lee YL, Lee MH, Chang HJ, Huang PY, Huang IJ, Cheng KT, Leu SJ Molecules 06-Mar-2009
PMCID:PMC6253823
doi:10.3390/molecules14031062
PMID:19305360
Bioactive triterpenes from Diospyros blancoi. Ragasa CY, Puno MR, Sengson JM, Shen CC, Rideout JA, Raga DD Nat Prod Res 01-Jan-2009
doi:10.1080/14786410902951054
PMID:19731144
Lanostane-type triterpenoids from Diospyros discolor. Chen CR, Cheng CW, Pan MH, Liao YW, Tzeng CY, Chang CI Chem Pharm Bull (Tokyo) 01-Jun-2007
doi:10.1248/CPB.55.908
PMID:17541192
Nuclear DNA Amounts in Angiosperms: Progress, Problems and Prospects BENNETT MD, LEITCH IJ Ann Bot 01-Jan-2005
PMCID:PMC4246708
doi:10.1093/aob/mci003
PMID:15596457
Naphthoquinones and triterpenes from some asian Diospyros species Muhamad Bin Zakaria, J.A.D. Jeffreys, Peter G. Waterman, Shou-Ming Zhong Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80490-2

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
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carbaldehyde 124407318 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O 440.70 unknown https://doi.org/10.1248/CPB.55.908
A'-Neo-26,28-dinorgammacer-9(11)-ene, 3-methoxy-13,17-dimethyl-, (3beta,21beta)- 623592 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)OC)C)C)C)C 440.70 unknown https://doi.org/10.1080/14786410902951054
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(00)80490-2
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)80490-2
Cylindrin 189045 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)OC)C)C)C)C 440.70 unknown https://doi.org/10.1080/14786410902951054
methyl (1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 12137742 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)OC 470.70 unknown https://doi.org/10.1248/CPB.55.908
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1080/14786410902951054
Super Squalene; trans-Squalene;AddaVax 1105 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1080/14786410902951054

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