PlantaeDB Logo
Login Sign-up

Diospyros mollis

Diospyros mollis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID64401767c2295278382218
Scientific name Diospyros mollis
Authority Griff.
First published in J. Agric. Soc. India 3: 145 (1844)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

No known synonyms.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Thai มะเกลือ
Vietnamese mặc nưa
Chinese 软毛乌木

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000649357
Tropicos 50179996
KEW urn:lsid:ipni.org:names:322726-1
The Plant List kew-2770166
Open Tree Of Life 164680
NCBI Taxonomy 268842
IPNI 322726-1
GBIF 4070936
USDA GRIN 70232
Wikipedia Diospyros_mollis

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
Bio-mordants: a review Benli H Environ Sci Pollut Res Int 23-Feb-2024
PMCID:PMC10948525
doi:10.1007/s11356-024-32174-8
PMID:38396176
Convergent evolution of plant specialized 1,4-naphthoquinones: metabolism, trafficking, and resistance to their allelopathic effects Meyer GW, Bahamon Naranjo MA, Widhalm JR J Exp Bot 01-Dec-2020
PMCID:PMC7853596
doi:10.1093/jxb/eraa462
PMID:33258472
Anti-Infectious Plants of the Thai Karen: A Meta-Analysis Phumthum M, Balslev H Antibiotics (Basel) 02-Jun-2020
PMCID:PMC7345792
doi:10.3390/antibiotics9060298
PMID:32498413
In-vitro Studies of Anti-EGFR Tyrosine Kinase Activity of Thai nutraceutical Plants Semsri S, seatew C, Rattanabunyong S, Ruekit S, Horata N, Panya A, Yenchitsomanus PT, Sawatdichaikul O, Choowongkomon K Iran J Pharm Res 01-Mar-2020
PMCID:PMC7667552
doi:10.22037/ijpr.2017.2022
PMID:33224225
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986
Genistein: is the multifarious botanical a natural anthelmintic too? Tandon V, Das B J Parasit Dis 05-Mar-2018
PMCID:PMC5962493
doi:10.1007/s12639-018-0984-0
PMID:29844617
Identification of a new plant extract for androgenic alopecia treatment using a non-radioactive human hair dermal papilla cell-based assay Jain R, Monthakantirat O, Tengamnuay P, De-Eknamkul W BMC Complement Altern Med 21-Jan-2016
PMCID:PMC4721057
doi:10.1186/s12906-016-1004-5
PMID:26796631
Comparative study of double blind clinical trial in side-effects among Areca catechu l., Thai traditional herbal formula and mebendazole Samappito S, Srichaikul B, Viroj J, Bakker G Trop Parasitol 01-Jul-2012
PMCID:PMC3680873
doi:10.4103/2229-5070.105176
PMID:23767018
Evaluation of Effectiveness of Herbal Medication in Cancer Care: A Review Study Tavakoli J, Miar S, Majid Zadehzare M, Akbari H Iran J Cancer Prev 01-Jun-2012
PMCID:PMC4294537
PMID:25628834
Anticestodal activity of Houttuynia cordata leaf extract against Hymenolepis diminuta in experimentally infected rats Yadav AK, Temjenmongla J Parasit Dis 24-Jun-2011
PMCID:PMC3235387
doi:10.1007/s12639-011-0050-7
PMID:23024502
A new diospyrol glycoside from Diospyros mollis Griff. Somboun Paphassarang, Michel Becchi, Jean Raynaud Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)99927-1
A new diglucoside from the anthelmintic berries of diospyros mollis Laddawun Borsub, Yodhathai Thebtaranonth, Somsak Ruchirawat, Chiravat Sadavongvivad Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)93032-6
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
[Components of fruits of Diospyros mollis]. Sturm G, Zilliken F Planta Med 01-May-1972
doi:10.1055/S-0028-1099558
PMID:5047484
[Ingredients of Diospyros mollis fruits]. Sturm G, Zilliken F Planta Med 01-Feb-1972
doi:10.1055/S-0028-1099523
PMID:5012070

Phytochemical Profile Top

Add a new one!
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
> Benzenoids / Naphthalenes / Naphthols and derivatives
1,8-Dihydroxy-3-methylnaphthalene 443778 Click to see CC1=CC2=C(C(=CC=C2)O)C(=C1)O 174.20 unknown https://doi.org/10.1016/S0040-4039(00)93032-6
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown https://doi.org/10.1055/S-0028-1099523
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1055/S-0028-1099523
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
9-Octadecenoic acid, methyl ester 8202 Click to see CCCCCCCCC=CCCCCCCCC(=O)OC 296.50 unknown https://doi.org/10.1055/S-0028-1099558
Methyl heptadecanoate 15609 Click to see CCCCCCCCCCCCCCCCC(=O)OC 284.50 unknown https://doi.org/10.1055/S-0028-1099558
Methyl oleate 5364509 Click to see CCCCCCCCC=CCCCCCCCC(=O)OC 296.50 unknown https://doi.org/10.1055/S-0028-1099558
Methyl palmitate 8181 Click to see CCCCCCCCCCCCCCCC(=O)OC 270.50 unknown https://doi.org/10.1055/S-0028-1099558
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown https://doi.org/10.1055/S-0028-1099558
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 7092730 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(97)01020-0
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1055/S-0028-1099558
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1099523
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/10.1055/S-0028-1099558
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1099523
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/10.1055/S-0028-1099558
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/10.1055/S-0028-1099523
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(97)01020-0
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/10.1055/S-0028-1099523
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1055/S-0028-1099558
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 162965363 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1099523
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1099523
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[7-[8-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-1-hydroxy-6-methylnaphthalen-2-yl]-8-hydroxy-3-methylnaphthalen-1-yl]oxyoxane-3,4,5-triol 21673194 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)C(=C(C=C2)C5=C(C6=C(C=C5)C=C(C=C6OC7C(C(C(C(O7)COC8C(C(CO8)(CO)O)O)O)O)O)C)O)O 934.90 unknown https://doi.org/10.1016/S0040-4039(00)99927-1
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[7-[8-[6-[[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-1-hydroxy-6-methylnaphthalen-2-yl]-8-hydroxy-3-methylnaphthalen-1-yl]oxyoxane-3,4,5-triol 73821373 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)C(=C(C=C2)C5=C(C6=C(C=C5)C=C(C=C6OC7C(C(C(C(O7)COC8C(C(CO8)(CO)O)O)O)O)O)C)O)O 934.90 unknown https://doi.org/10.1016/S0040-4039(00)99927-1

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.