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Internal ID UUID6440175a80906039757303
Scientific name Diospyros ismailii
Authority Ng
First published in Malaysian Forester 40: 222 (1977)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

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Database ID/link to page
World Flora Online wfo-0000649119
Tropicos 100324685
KEW urn:lsid:ipni.org:names:322538-1
The Plant List kew-2769943
Open Tree Of Life 6047073
IUCN Red List 31457
IPNI 322538-1
iNaturalist 191549
GBIF 4071444

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
Title Authors Publication Released IDs
ChemInform Abstract: HOMOLOGS OF JUGLONE WITH 4‐HYDROXY‐5‐METHYL‐2‐OXO‐2H‐CHROMEN‐3‐YL SUBSTITUENTS FROM DIOSPYROS SPECIES. A NEW CLASS OF NATURAL PRODUCT P. G. WATERMAN, S.‐M. ZHONG, J. A. D. JEFFREY, M. BIN ZAKARIA Wiley 09-May-2016
doi:10.1002/CHIN.198528357
4-Hydroxy-5-methylcoumarin from<i>Diospyros ismailii</i> Muhamad Zakaria Georg Thieme Verlag KG 02-Feb-2007
doi:10.1055/S-2006-961932
A new class of natural product: homologues of juglone bearing 4-hydroxy-5-methyl-coumarin-3-yl units from Diospyros species J.A.D. Jeffreys, Muhamad bin Zakaria, Peter G. Waterman, Shouming Zhong Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)81611-1
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
Pharmacology and chemotaxonomy of Diospyros. Mallavadhani UV, Panda AK, Rao YR Phytochemistry 01-Oct-1998
doi:10.1016/S0031-9422(97)01020-0
PMID:9788142

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 / Naphthalenes / Naphthoquinones
5-Hydroxy-2,3-bis(2-hydroxy-5-methyl-4-oxochromen-3-yl)-7-methylnaphthalene-1,4-dione 342160 Click to see CC1=C2C(=CC=C1)OC(=C(C2=O)C3=C(C(=O)C4=C(C3=O)C=C(C=C4O)C)C5=C(OC6=CC=CC(=C6C5=O)C)O)O 536.50 unknown https://doi.org/10.1016/S0040-4039(00)81611-1
https://doi.org/10.1016/S0031-9422(97)01020-0
7-Methyljuglone 26905 Click to see CC1=CC2=C(C(=O)C=CC2=O)C(=C1)O 188.18 unknown https://doi.org/10.1002/CHIN.198528357
8-Hydroxy-2-(5-hydroxy-7-methyl-1,4-dioxonaphthalen-2-yl)-6-methylnaphthalene-1,4-dione 12173109 Click to see CC1=CC2=C(C(=C1)O)C(=O)C(=CC2=O)C3=CC(=O)C4=C(C3=O)C=C(C=C4O)C 374.30 unknown https://doi.org/10.1016/S0031-9422(00)80490-2
https://doi.org/10.1002/CHIN.198528357
Neodiospyrin 16072922 Click to see CC1=CC2=C(C(=C1)O)C(=O)C(=CC2=O)C3=C4C(=O)C=CC(=O)C4=C(C=C3C)O 374.30 unknown https://doi.org/10.1002/CHIN.198528357
> Lignans, neolignans and related compounds
(2,2'-Binaphthalene)-5,5',8,8'-tetrone, 1,1'-dihydroxy-6,6'-dimethyl- 146680 Click to see CC1=CC(=O)C2=C(C1=O)C=CC(=C2O)C3=C(C4=C(C=C3)C(=O)C(=CC4=O)C)O 374.30 unknown https://doi.org/10.1016/S0031-9422(00)80490-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 293273 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(00)80490-2
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-carboxylic acid 2371 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/10.1002/CHIN.198528357
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/10.1002/CHIN.198528357
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/10.1002/CHIN.198528357
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1002/CHIN.198528357
Lup-20(29)-ene-3beta,28-diol 221023 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/10.1002/CHIN.198528357
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1002/CHIN.198528357
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 4-hydroxycoumarins
Ismailin 135454728 Click to see CC1=C2C(=CC=C1)OC(=O)C(=C2O)C3=C(C(=O)C4=C(C3=O)C=C(C=C4O)C)C5=C(C6=C(C=CC=C6OC5=O)C)O 536.50 unknown https://doi.org/10.1016/S0031-9422(97)01020-0
https://doi.org/10.1002/CHIN.198528357
https://doi.org/10.1016/S0040-4039(00)81611-1
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(1R,18S,19S,21S,22S)-6,7,8,11,12,13,22-heptahydroxy-21-(hydroxymethyl)-3,16-dioxo-2,17,20-trioxatetracyclo[16.3.1.04,9.010,15]docosa-4,6,8,10,12,14-hexaen-19-yl] 3,4,5-trihydroxybenzoate 159801914 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1055/S-2006-961932

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