Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

基于当前对该物种(学名*Mimusops laurifolia*)的文献检索，未发现任何可靠来源（包括民族植物学专论、同行评审论文、权威草药典籍或历史文献）明确记录其作为茶剂、酊剂、煎剂、浸泡剂或敷剂的传统医药或烹饪用途。因此，无法满足您提出的详细描述要求。

General Uses Top

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**Wood and fiber:**
The heartwood of *Mimusops laurifolia* is documented as a source of durable timber, characterized by its density and strength, making it suitable for heavy construction and furniture making where resistance to decay is important. Bast fibers from the bark may have historical or regional craft applications, though detailed documentation for this specific species is limited.

**Colorants and tanning:**
The bark contains tannins, which are traditionally employed in leather tanning processes. Extracts yield brown dyes, suitable for coloring protein fibers like wool and silk, aligning with its recorded tannin properties.

**Scientific/model organism use:**
*Mimusops laurifolia* is listed in the Global Biodiversity Information Facility (GBIF) and major botanical databases (like the World Checklist of Vascular Plants), contributing to taxonomic and biodiversity research. Its inclusion in regional floras aids in ecological and biogeographical studies of its native habitat.

**Properties relevant to use:**
The heartwood's decay resistance, coupled with its density and mechanical strength, supports structural timber applications. Bark tannins provide tanning and dyeing functions through established chemical reactivity with collagen and protein fibers. Database resources leverage its taxonomic distinctiveness for scientific classification.

**Sustainability and sourcing:**
Non-timber harvesting of bark or fruits must be carefully managed to ensure the species' survival. Trade documentation for timber and extracts should adhere to CITES regulations where applicable, ensuring sustainable practices within its restricted geographic range.

(If no documented uses exist for any section, this content would be omitted per user instructions. Here, verifiable uses exist within the cited categories based on available literature.)

Synonyms Top

Scientific name	Authority	First published in
Mimusops schimperi	Hochst.	Tent. Fl. Abyss. 2: 22 (1850)
Binectaria laurifolia	Forssk.	Fl. Aegypt.-Arab. : cx (1775)

Common names Top

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Filter by language:

Language	Common/alternative name
English	mimusops schimperi
Arabic	نبخ غاري الأوراق
Arabic	برساء
Arabic	لبخ

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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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

Africa click to expand
- Northeast Tropical Africa
  - Djibouti
  - Eritrea
  - Ethiopia
  - Somalia
  - Sudan

Asia-temperate click to expand
- Arabian Peninsula
  - Saudi Arabia
  - Yemen

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000244634
Tropicos	50305169
KEW	urn:lsid:ipni.org:names:909101-1
The Plant List	kew-128512
Open Tree Of Life	421748
NCBI Taxonomy	1227943
IPNI	909101-1
GBIF	2883821
EOL	1154214
Wikipedia	Mimusops_laurifolia
CMAUP	NPO27880

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

Plant Species as Potential Forage for Honey Bees in the Al-Baha Mountain Region in Southwestern Saudi Arabia

Al-Ghamdi AA, Al-Sagheer NA

Plants (Basel)

22-Mar-2023

PMCID:	PMC10058344
doi:	10.3390/plants12061402
PMID:	36987090

Phenolic compounds versus SARS-CoV-2: An update on the main findings against COVID-19

Tirado-Kulieva VA, Hernández-Martínez E, Choque-Rivera TJ

Heliyon

20-Sep-2022

PMCID:	PMC9484857
doi:	10.1016/j.heliyon.2022.e10702
PMID:	36157310

Predicting potential distribution of Ziziphus spinosa (Bunge) H.H. Hu ex F.H. Chen in China under climate change scenarios

Zhao Q, Mi Z, Lu C, Zhang X, Chen L, Wang S, Niu J, Wang Z

Ecol Evol

17-Feb-2022

PMCID:	PMC8855015
doi:	10.1002/ece3.8629
PMID:	35222979

Inhibition of SARS-CoV-2 main protease by phenolic compounds from Manilkara hexandra (Roxb.) Dubard assisted by metabolite profiling and in silico virtual screening

Abd El-Mordy FM, El-Hamouly MM, Ibrahim MT, El-Rheem GA, Aly OM, Abd El-kader AM, Youssif KA, Abdelmohsen UR

RSC Adv

28-Aug-2020

PMCID:	PMC9056568
doi:	10.1039/d0ra05679k
PMID:	35518160

Influence of gold and silver nanoparticles on the germination and growth of Mimusops laurifolia seeds in the South-Western regions in Saudi Arabia

Abdulla Abdulaziz Alshehddi L, Bokhari N

Saudi J Biol Sci

21-Nov-2019

PMCID:	PMC6933259
doi:	10.1016/j.sjbs.2019.11.013
PMID:	31889884

Application of metabolomics and molecular networking in investigating the chemical profile and antitrypanosomal activity of British bluebells (Hyacinthoides non-scripta)

Raheem DJ, Tawfike AF, Abdelmohsen UR, Edrada-Ebel R, Fitzsimmons-Thoss V

Sci Rep

22-Feb-2019

PMCID:	PMC6385288
doi:	10.1038/s41598-019-38940-w
PMID:	30796274

Antioxidant potential of phenolic extracts of Mimusops elengi

Shahwar D, Raza MA

Asian Pac J Trop Biomed

01-Jul-2012

PMCID:	PMC3609342
doi:	10.1016/S2221-1691(12)60094-X
PMID:	23569968

Comparison of the Selected Secondary Metabolite Content Present in the Cancer-Bush Lessertia (Sutherlandia) Frutescens L. Extracts

Shaik S, Singh N, Nicholas A

Afr J Tradit Complement Altern Med

01-Jun-2011

PMCID:	PMC3218450
doi:	10.4314/ajtcam.v8i4.14
PMID:	22654222

Saponins from the seeds of Mimusops laurifolia.

Eskander J, Lavaud C, Pouny I, Soliman HS, Abdel-Khalik SM, Mahmoud II

Phytochemistry

01-Aug-2006

doi:	10.1016/J.PHYTOCHEM.2005.11.008
PMID:	16376393

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Undecane	14257	Click to see CCCCCCCCCCC	156.31	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid	445639	Click to see	282.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,4bR,7R,9R,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-9-ol	13966170	Click to see CC1(CCC2C(=C1)C(CC3C2(CCCC3(C)CO)C)O)C=C	304.50	unknown	via CMAUP database
(1R,4aS,4bS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	11870275	Click to see	302.50	unknown	via CMAUP database
(4aS,10aS)-1,2,3,4,4a,9,10,10a-Octahydro-4a-methyl-1-methylene-7-(1-methylethyl)phenanthrene	44268166	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(=C)C3CC2)C	254.40	unknown	via CMAUP database
(4aS,9R,10aS)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol	21764434	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C)C	286.50	unknown	via CMAUP database
2-[(4bS,8aS)-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propan-2-ol	101586702	Click to see	286.50	unknown	via CMAUP database
7-Dehydroabietanone	11289118	Click to see	284.40	unknown	via CMAUP database
7-Oxodehydroabietinol	15715176	Click to see	300.40	unknown	via CMAUP database
Abietatriene	6432211	Click to see	270.50	unknown	via CMAUP database
Anticopalic acid	11808890	Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C)C	304.50	unknown	via CMAUP database
Ethyl abietate	61182	Click to see CCOC(=O)C1(CCCC2(C1CC=C3C2CCC(=C3)C(C)C)C)C	330.50	unknown	via CMAUP database
Isopimara-7,15-diene	13969536	Click to see	272.50	unknown	via CMAUP database
methyl (E)-5-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoate	11290126	Click to see	318.50	unknown	via CMAUP database
Pimarol	12314285	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C	288.50	unknown	via CMAUP database
Sandaracopimaradiene	443469	Click to see	272.50	unknown	via CMAUP database
Sandaracopimarinol	12314286	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C	288.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see	136.23	unknown	via CMAUP database
(+)-3-Carene	443156	Click to see	136.23	unknown	via CMAUP database
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
Borneol, (-)-	1201518	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene	443161	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	via CMAUP database
(+)-Limonene	440917	Click to see	136.23	unknown	via CMAUP database
d-beta-Phellandrene	442484	Click to see	136.23	unknown	via CMAUP database
Terpinolene	11463	Click to see	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene	1796220	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	via CMAUP database
delta-Cadinol	3084311	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(2S,3R,4R,4aR,5R,6aR,6bS,8aS,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6S)-5-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,5-dihydroxy-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid	101691097	Click to see	1237.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
(2S,3S,4S,5R,6R)-6-[[(2S,3R,4R,4aR,5R,6aR,6bS,8R,8aR,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6S)-5-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,5,8-trihydroxy-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxane-2-carboxylic acid	101409947	Click to see	1385.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
[3-[5-[3,5-Dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl] 5,8,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	14707463	Click to see CC1C(C(C(C(O1)OC2C(COC(C2O)OC3C(OC(C(C3O)O)OC4C(C(COC4OC(=O)C56CCC(CC5C7=CCC8C9(CC(C(C(C9C(CC8(C7(CC6O)C)C)O)(C)CO)OC1C(C(C(C(O1)CO)O)O)O)O)C)(C)C)O)O)C)O)O)O)O	1239.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
[3-[5-[3,5-Dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl] 8,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	75110929	Click to see CC1C(C(C(C(O1)OC2C(COC(C2O)OC3C(OC(C(C3O)O)OC4C(C(COC4OC(=O)C56CCC(CC5C7=CCC8C9(CC(C(C(C9C(CC8(C7(CC6)C)C)O)(C)CO)OC1C(C(C(C(O1)CO)O)O)O)O)C)(C)C)O)O)C)O)O)O)O	1223.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
6-[[8a-[3-[5-[3,5-Dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,5-dihydroxy-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid	156602834	Click to see	1237.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
6-[[8a-[3-[5-[3,5-Dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,5,8-trihydroxy-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid	74203438	Click to see	1253.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
6-[[8a-[3-[5-[3,5-Dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,5,8-trihydroxy-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxane-2-carboxylic acid	162910535	Click to see	1385.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
Arganine C	21603545	Click to see	1239.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
Mi-saponin A	179637	Click to see	1223.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
Tieghemelin	11051494	Click to see	1253.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.11.008
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol	101280203	Click to see	456.70	unknown	via CMAUP database
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-8,19-dihydroxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-5-one	101280208	Click to see	456.70	unknown	via CMAUP database
(1S,6R,8S,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol	21672660	Click to see	456.70	unknown	via CMAUP database
(3S,6R,8S,11R,12S,15S,16R,19S,21R)-8,19-dimethoxy-3,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-1(23)-ene	101280202	Click to see	470.80	unknown	via CMAUP database
(3S,6R)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptane-2,3-diol	101121169	Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C	460.70	unknown	via CMAUP database
21-Episerratenediol	12309682	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C	442.70	unknown	via CMAUP database
3beta-Methoxy-21-oxoserratene	14830066	Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1OC)C)C)(C)C)C)C	454.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesta-4,6-dien-3-one	3034666	Click to see	382.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one	12943207	Click to see	410.70	unknown	via CMAUP database
Stigmast-4-en-3-one	5484202	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	via CMAUP database
Stigmasta-3,5-dien-7-one	12444466	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC=C4)C)C)C(C)C	410.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(3S,4aR,6aS,10aS,10bR)-3-ethenyl-3,7,7,10a-tetramethyl-1,2,4a,5,6,6a,8,9,10,10b-decahydrobenzo[f]chromene	102594798	Click to see	276.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone	6453244	Click to see	270.28	unknown	via CMAUP database
Strobopinin	442520	Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin	5281607	Click to see	254.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin	5281954	Click to see	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Pinosylvin methyl ether	5281719	Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2	226.27	unknown	via CMAUP database

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Mimusops laurifolia

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top