Diospyros lotus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Diospyros lotus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID644017616da47013488865
Scientific name Diospyros lotus
Authority L.
First published in Sp. Pl. : 1057 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Dactylus trapezuntinus Forssk. Fl. Aegypt.-Arab. : xxxvi (1775)
Diospyros lotus f. ellipsoidea Makino Bot. Mag. (Tokyo) 26: 397 1912
Diospyros lotus f. globosa Makino Bot. Mag. (Tokyo) 26: 396 1912
Diospyros lotus f. longifolia Z.Ying Zhang Fl. Tsinling. 1(4): 395 (1983)
Diospyros lotus f. ovoidea Makino Bot. Mag. (Tokyo) 26: 397 1912
Diospyros mediterranea Oken Allg. Naturgesch. 3(2): 935 (1841)
Diospyros umlovok Griff. Itin. Pl. Khasyah Mts. : 355 (1848)
Diospyros lotus var. mollissima C.Y.Wu Fl. Rep. Trop. Subtrop. Yunnan 1: 21 (1965)
Diospyros lotus var. laevis H.Ohba & S.Akiyama J. Jap. Bot. 91(Suppl.): 309 (2016)

Common names Top

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Language Common/alternative name
English date plum
ab Абнахәырма
Arabic خرمندي
Azerbaijani qafqaz xurması
Azerbaijani adi xurma
azb عادی خورما
Czech tomel obecný
German lotuspflaume
Esperanto lotusdiospiro
Persian دیت-پلام
Finnish taateliluumu
Irish dátphluma
Armenian խուրմա սովորական
hyw Ոսկեպտղի, Ժորի (Խարմա)
Japanese マメガキ
Georgian ჩვეულებრივი ხურმა
Korean 고욤나무
lzh 君遷子
Norwegian Bokmål daddelplomme
Dutch lotusboom
Polish hurma kaukaska
Russian хурма кавказская
Serbian Драгун
Turkish küçük trabzon hurması
Uzbek kavkaz xurmosi
Vietnamese thị sen
Chinese 君遷子
Chinese 黑枣
Chinese 软枣
Chinese 牛奶柿
Chinese 君迁子

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Manchuria
      • Tibet
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Tadzhikistan
    • Western Asia
      • Afghanistan
      • Iran
      • Turkey
  • Asia-tropical
    • Indian Subcontinent
      • Nepal
      • Pakistan
      • West Himalaya
  • Europe
    • Middle Europe
      • Switzerland
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • France
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000649239
USDA Plants DILO8
INPN 95048
Flora of Italy 3967
KEW urn:lsid:ipni.org:names:322629-1
The Plant List kew-2770056
Open Tree Of Life 918839
Observations.org 132547
NCBI Taxonomy 55363
IUCN Red List 63524
IPNI 322629-1
iNaturalist 83445
GBIF 3032980
Freebase /m/0b6l5s3
EPPO DOSLO
EOL 482113
Elurikkus 353333
Calflora (Californian flora) 12437
USDA GRIN 14296
Wikipedia Date-plum

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCF_014633365.1 ASM1463336v1 Chromosome BEIJING ACADEMY OF FORESTRY AND POMOLOGY SCIENCES 2020-09-21 167.0x 600.91 Mb

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
Genomics insights into flowering and floral pattern formation: regional duplication and seasonal pattern of gene expression in Camellia Hu Z, Fan Z, Li S, Wang M, Huang M, Ma X, Liu W, Wang Y, Yu Y, Li Y, Sun Y, Li X, Li J, Yin H BMC Biol 27-Feb-2024
PMCID:PMC10900828
doi:10.1186/s12915-024-01851-y
PMID:38414012
Exploring the benefits of wild plants in dietary nutrition: investigating perspectives, choices, health impacts and sustainable practices Anwar T, Qureshi H, Shahzadi S, Siddiqi EH, Ali HM, Abdelhamid MM, Nazim M BMC Complement Med Ther 14-Feb-2024
PMCID:PMC10865668
doi:10.1186/s12906-024-04379-4
PMID:38355544
Anti-Inflammatory Herbal Extracts and Their Drug Discovery Perspective in Atopic Dermatitis Lee JW, Kim EN, Jeong GS Biomol Ther (Seoul) 01-Jan-2024
PMCID:PMC10762282
doi:10.4062/biomolther.2023.102
PMID:38148551
Chromosome-level genome assembly and demographic history of Euryodendron excelsum in monotypic genus endemic to China Wang ZF, Fu L, Yu EP, Zhu WG, Zeng SJ, Cao HL DNA Res 26-Dec-2023
PMCID:PMC10781514
doi:10.1093/dnares/dsad028
PMID:38147541
Wild Edible Fruits as a Source of Food and Medicine: A Study among Tribal Communities of Southern Khyber Pakhtunkhwa Ul Abidin SZ, Khan R, Ahmad M, Cuerrier A, Zafar M, Ullah A, Khan J, Saeed A, Al-Qahtani WH, Kazi M Plants (Basel) 21-Dec-2023
PMCID:PMC10780817
doi:10.3390/plants13010039
PMID:38202347
Kiwifruit Monodehydroascorbate Reductase 3 Gene Negatively Regulates the Accumulation of Ascorbic Acid in Fruit of Transgenic Tomato Plants Jia D, Gao H, He Y, Liao G, Lin L, Huang C, Xu X Int J Mol Sci 06-Dec-2023
PMCID:PMC10742914
doi:10.3390/ijms242417182
PMID:38139009
Botanical memory: five centuries of floristic changes revealed by a Renaissance herbarium (Ulisse Aldrovandi, 1551–1586) Buldrini F, Alessandrini A, Mossetti U, Muzzi E, Pezzi G, Soldano A, Nascimbene J R Soc Open Sci 08-Nov-2023
PMCID:PMC10645095
doi:10.1098/rsos.230866
PMID:38026021
Mulberry MnGolS2 Mediates Resistance to Botrytis cinerea on Transgenic Plants Wang D, Liu Z, Qin Y, Zhang S, Yang L, Shang Q, Ji X, Xin Y, Li X Genes (Basel) 06-Oct-2023
PMCID:PMC10606925
doi:10.3390/genes14101912
PMID:37895261
Transcriptomic and Hormone Analyses Provide Insight into the Regulation of Axillary Bud Outgrowth of Eucommia ulmoides Oliver Zhang Y, Du D, Wei H, Xie S, Tian X, Yang J, Xiao S, Tang Z, Li D, Liu Y Curr Issues Mol Biol 07-Sep-2023
PMCID:PMC10528246
doi:10.3390/cimb45090462
PMID:37754246
Ethnobotany for food security and ecological transition: wild food plant gathering and consumption among four cultural groups in Kurram District, NW Pakistan Hussain ST, Muhammad S, Khan S, Hussain W, Pieroni A J Ethnobiol Ethnomed 01-Sep-2023
PMCID:PMC10472554
doi:10.1186/s13002-023-00607-2
PMID:37658453
Transcriptome Analyses Reveal the Aroma Terpeniods Biosynthesis Pathways of Primula forbesii Franch. and the Functional Characterization of the PfDXS2 Gene Jia Y, Yin X, Yang H, Xiang Y, Ding K, Pan Y, Jiang B, Yong X Int J Mol Sci 12-Aug-2023
PMCID:PMC10454305
doi:10.3390/ijms241612730
PMID:37628910
Development of sex-linked markers for gender identification of Actinidia arguta Guo D, Wang R, Fang J, Zhong Y, Qi X Sci Rep 07-Aug-2023
PMCID:PMC10406875
doi:10.1038/s41598-023-39561-0
PMID:37550389
Ongoing Rapid Evolution of a Post-Y Region Revealed by Chromosome-Scale Genome Assembly of a Hexaploid Monoecious Persimmon (Diospyros kaki) Horiuchi A, Masuda K, Shirasawa K, Onoue N, Fujita N, Ushijima K, Akagi T Mol Biol Evol 07-Jul-2023
PMCID:PMC10350624
doi:10.1093/molbev/msad151
PMID:37414545
Comparative transcriptomic analysis of male and females in the dioecious weeds Amaranthus palmeri and Amaranthus tuberculatus Bobadilla LK, Baek Y, Tranel PJ BMC Plant Biol 26-Jun-2023
PMCID:PMC10291800
doi:10.1186/s12870-023-04286-9
PMID:37365527
Population Genetic Analysis in Persimmons (Diospyros kaki Thunb.) Based on Genome-Wide Single-Nucleotide Polymorphisms Park S, Park YO, Park Y Plants (Basel) 24-May-2023
PMCID:PMC10255057
doi:10.3390/plants12112097
PMID:37299077

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Vinca alkaloids
methyl (1R,9R,10S,11R,12R,19R)-11-acetyloxy-12-ethyl-4-[(13S,15S,17S)-17-ethyl-17-hydroxy-13-methoxycarbonyl-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-4(12),5,7,9-tetraen-13-yl]-10-hydroxy-5-methoxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,13-tetraene-10-carboxylate 241903 Click to see CCC1(CC2CC(C3=C(CCN(C2)C1)C4=CC=CC=C4N3)(C5=C(C=C6C(=C5)C78CCN9C7C(C=CC9)(C(C(C8N6C)(C(=O)OC)O)OC(=O)C)CC)OC)C(=O)OC)O 811.00 unknown https://doi.org/10.1007/S11130-009-0133-0
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see C1=CC(=C(C=C1O)C(=O)O)O 154.12 unknown https://doi.org/10.1021/JF960741C
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1021/JF960741C
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1021/JF960741C
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown https://doi.org/10.1021/JF960741C
> 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/10.1021/JF960741C
https://doi.org/10.1007/S11130-009-0133-0
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown https://doi.org/10.1007/S11130-009-0133-0
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1021/JF960741C
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see C1=CC=C(C(=C1)C(=O)O)O 138.12 unknown https://doi.org/10.1021/JF960741C
> Benzenoids / Naphthalenes / Naphthoquinones
5-Hydroxy-2-[5-hydroxy-6-(4-hydroxy-2-methyl-5,8-dioxonaphthalen-1-yl)-7-methyl-1,4-dioxonaphthalen-2-yl]-6-(4-hydroxy-2-methyl-5,8-dioxonaphthalen-1-yl)-7-methylnaphthalene-1,4-dione 157288178 Click to see CC1=CC2=C(C(=O)C=C(C2=O)C3=CC(=O)C4=C(C3=O)C=C(C(=C4O)C5=C6C(=O)C=CC(=O)C6=C(C=C5C)O)C)C(=C1C7=C8C(=O)C=CC(=O)C8=C(C=C7C)O)O 746.70 unknown 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/10.1016/S0031-9422(00)80490-2
https://doi.org/10.1016/S0021-9673(01)87659-7
https://doi.org/10.1016/0165-1218(83)90182-9
8-Hydroxy-2-(8-hydroxy-6-methyl-1,4-dioxonaphthalen-2-yl)-6-methylnaphthalene-1,4-dione 167673 Click to see CC1=CC2=C(C(=C1)O)C(=O)C(=CC2=O)C3=CC(=O)C4=C(C3=O)C(=CC(=C4)C)O 374.30 unknown https://doi.org/10.1016/0165-1218(83)90182-9
Isodiospyrin 99298 Click to see CC1=CC2=C(C(=O)C=CC2=O)C(=C1C3=C4C(=O)C=CC(=O)C4=C(C=C3C)O)O 374.30 unknown https://doi.org/10.1016/0165-1218(83)90182-9
https://doi.org/10.1016/S0021-9673(01)87659-7
> Benzenoids / Tetralins
Isoshinanolone 443777 Click to see CC1CC(=O)C2=C(C1O)C=CC=C2O 192.21 unknown https://doi.org/10.1016/S0031-9422(00)80490-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hentriacontanol 68345 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 452.80 unknown https://doi.org/10.1016/S0031-9422(00)97297-2
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(4aR,6aR,6aS,8aR,12aS,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-2,4a,5,6,8,9,10,12,12a,13,14,14a-dodecahydro-1H-picen-3-one 392170 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1007/BF00567057
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1007/BF00567057
Taraxerol acetate 94225 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC4(C3=CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)80490-2
Taraxerone 92785 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1007/BF00567057
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aR,6aS,6bR,10S,12aR,14bS)-10-acetyloxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 15917992 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1007/BF00567057
(3S,4aR,6aR,6aR,8aR,12aS,14aR,14bR)-4,4,6a,8a,11,11,14b-heptamethyl-2,3,4a,5,6,6a,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picen-3-ol 162879940 Click to see CC1(CCC2(CC=C3C(C2C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80490-2
(4aR,6aR,6aR,8aR,12aS,14aR,14bR)-4,4,6a,8a,11,11,14b-heptamethyl-1,2,4a,5,6,6a,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-one 102035711 Click to see CC1(CCC2(CC=C3C(C2C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(00)80490-2
10-Acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 619165 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/S0031-9422(00)80490-2
28-Oxoallobetulin 12305934 Click to see CC1(CCC23CCC4(C(C2C1OC3=O)CCC5C4(CCC6C5(CCC(C6(C)C)O)C)C)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(97)01020-0
4,4,6a,8a,11,11,14b-Heptamethyl-1,2,4a,5,6,6a,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-one 162993022 Click to see CC1(CCC2(CC=C3C(C2C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(00)80490-2
4,4,6a,8a,11,11,14b-heptamethyl-2,3,4a,5,6,6a,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picen-3-ol 162879938 Click to see CC1(CCC2(CC=C3C(C2C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)80490-2
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1007/BF00567057
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 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/10.1007/BF00567057
Urs-12-ene-3,28-diol, (3beta)- 3266408 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
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)80490-2
Ursolic acid acetate 6475119 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1007/BF00567057
Uvaol 92802 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
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1021/JF960741C
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/S11130-009-0133-0
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1007/S11130-009-0133-0
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1007/S11130-009-0133-0
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown https://doi.org/10.1007/S11130-009-0133-0

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