In addition, myrrh is used in traditional medicine and is being studied for its potential use in modern medicine.

Commiphora myrrha, also known as myrrh, is a tree in the Burseraceae family that is native to the Arabian peninsula and Africa. It is a primary source of myrrh, a resin made from dried tree sap. The tree is known for its spiny branches and papery-textured bark. Its leaves are greyish-green and consist of three leaflets. The plant produces small yellow-red flowers and smooth, brown fruit. Myrrh has been used for centuries for its medicinal properties, including as an anti-bacterial, anti-fungal, and anti-inflammatory agent. It has also been used in religious rituals and as a flavoring agent in food and cosmetic products. Modern research is exploring its potential use in treating diseases such as COVID-19.

Synonyms Top

Scientific name	Authority	First published in
Balsamea myrrha	(T.Nees) Oken	Allg. Naturgesch. 3(3): 1760 (1841)
Balsamea myrrha	Baill.	Hist. Pl. 5: 294 (1874)
Balsamea playfairii	Engl.	Bot. Jahrb. Syst. 1: 42 (1880)
Balsamodendrum myrrha	T.Nees	Pl. Officin. : t. 182 (1828)
Commiphora coriacea	Engl.	Bot. Jahrb. Syst. 26: 369 (1899)
Commiphora cuspidata	Chiov.	Bull. Misc. Inform. Kew 1941: 134 (1941)
Commiphora molmol	Engl. ex Tschirch	Handb. Pharmakogn. 3: 1117 (1925)
Commiphora myrrha var. molmol	Engl.	Bot. Jahrb. Syst. 15: 95 1892
Commiphora rivae	Engl.	Annuario Reale Ist. Bot. Roma 7: 17 (1897)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Afrikaans	mirreboom
Arabic	عصرة
Arabic	مر حجازي
Arabic	عوجة
Arabic	مر
Arabic	مُرّ
Czech	myrhovník pravý
Greek	Κομμιφόρος η μύρρα
Persian	مر آفریقایی
French	arbre à myrrhe
French	basalmier
French	arbre a myrrhe
frr	myrrhebuum
Hebrew	מור
Hebrew	מור (עץ)
Hebrew	עץ המור
Upper Sorbian	myrowc
Hungarian	szomáliai balzsamfa
Japanese	コンミフォラ・ミルラ
la	myrrha (incensum)
Macedonian	мира
Burmese	ကုလားနက်သွေး
Polish	balsamowiec mirra
Russian	Мирра
Somali	dheddin
Ukrainian	Мирра
Vietnamese	một dược (cây)
Chinese	没药
Chinese	沒藥樹
Chinese	地丁树
Chinese	没药树

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

Africa click to expand
- East Tropical Africa
  - Kenya
- Northeast Tropical Africa
  - Djibouti
  - Eritrea
  - Ethiopia
  - Somalia

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

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000617380
UNII	UU81N77RI7
Tropicos	4700457
KEW	urn:lsid:ipni.org:names:127741-1
The Plant List	kew-2733595
Open Tree Of Life	13795
Observations.org	287304
NCBI Taxonomy	318982
IPNI	127741-1
iNaturalist	789240
GBIF	3994082
Freebase	/m/05c62vg
EPPO	COQMY
EOL	5616332
Elurikkus	448204
USDA GRIN	402550
Wikipedia	Commiphora_myrrha
CMAUP	NPO7730

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

Immunomodulatory effect of Unani polyherbal formulation - Tiryaq Wabai in mild to moderate COVID-19 patients – A randomized placebo-controlled clinical trial

Kumar A, Khan MS, Haque ZU, Rai A, Fazil M, Rabbani G

J Ayurveda Integr Med

04-Apr-2024

PMCID:	PMC10997826
doi:	10.1016/j.jaim.2024.100903
PMID:	38574518

Comprehensive effect of Naoxintong capsule combined with Western medicine on coronary heart disease after percutaneous coronary intervention: a meta-analysis

Yu L, Huang P, Wang M, Li Z, Cai H, Feng Y, Wu L, Peng W, Zeng J, Chen B

Front Pharmacol

25-Mar-2024

PMCID:	PMC11000174
doi:	10.3389/fphar.2024.1274000
PMID:	38590642

Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species

Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E

Antibiotics (Basel)

07-Feb-2024

PMCID:	PMC10885947
doi:	10.3390/antibiotics13020163
PMID:	38391549

Beliefs, awareness, use, and factors associated with herbal supplements usage among patients with chronic diseases–A cross-sectional insight from Alkharj, Saudi Arabia

Albassam AA, Alenzi AN, Alhaqbani NK, Alhouty FK, Almalki ZS, Alshehri AM, Aldossari H, Iqbal MS

PLoS One

17-Jan-2024

PMCID:	PMC10793931
doi:	10.1371/journal.pone.0295116
PMID:	38232068

Use of over-the-counter mouthwashes as an additional measure in individual oral prophylaxis on adults with plaque-induced gingivitis: a double-blind, parallel, randomized controlled trial

Vitiello F, Monterubbianesi R, Sparabombe S, Bourgeois D, Tosco V, Alshehri FA, Carrouel F, Putignano A, Orsini G

BMC Oral Health

16-Jan-2024

PMCID:	PMC10790383
doi:	10.1186/s12903-023-03779-1
PMID:	38229032

Therapeutic Efficacy of Chinese Patent Medicine Containing Pyrite for Fractures: A Systematic Review and Meta-Analysis

Nam EY, Choi SH, Hwang JH

Medicina (Kaunas)

30-Dec-2023

PMCID:	PMC10818888
doi:	10.3390/medicina60010076
PMID:	38256337

An aqueous Commiphora myrrha extract ameliorates paclitaxel-induced peripheral neuropathic pain in mice

Al-Romaiyan A, Barakat A, Jose L, Masocha W

Front Pharmacol

21-Dec-2023

PMCID:	PMC10768035
doi:	10.3389/fphar.2023.1295096
PMID:	38186647

A natural product YSK-A blocks SARS-CoV-2 propagation by targeting multiple host genes

Pham TX, Huynh TT, Kim B, Lim YS, Hwang SB

Sci Rep

06-Dec-2023

PMCID:	PMC10700534
doi:	10.1038/s41598-023-48854-3
PMID:	38057373

The Application of Arbuscular Mycorrhizal Fungi as Microbial Biostimulant, Sustainable Approaches in Modern Agriculture

Sun W, Shahrajabian MH

Plants (Basel)

29-Aug-2023

PMCID:	PMC10490045
doi:	10.3390/plants12173101
PMID:	37687348

Eco-Friendly Methanolic Myrrh Extract Corrosion Inhibitor for Aluminum in 1 M HCl

Al-nami SY, Alturki AM, Wahba AM

ACS Omega

14-Aug-2023

PMCID:	PMC10468905
doi:	10.1021/acsomega.3c02009
PMID:	37663464

Combination effects of herbal and western medicines on osteoporosis in rheumatoid arthritis: systematic review and meta-analysis

Kwon DY, Gu JH, Oh M, Lee EJ

Front Pharmacol

10-Aug-2023

PMCID:	PMC10448903
doi:	10.3389/fphar.2023.1164898
PMID:	37637429

New Insights into the Role of Oxidative Stress in the Development of Diabetes Mellitus and Its Complications

dos Santos JM, Zhong Q, Benite-Ribeiro SA, Heck TG

J Diabetes Res

26-Jul-2023

PMCID:	PMC10397502
doi:	10.1155/2023/9824864
PMID:	37546353

Plant Extracts as a Source of Natural Products with Potential Antimalarial Effects: An Update from 2018 to 2022

Ribeiro GD, Rei Yan SL, Palmisano G, Wrenger C

Pharmaceutics

01-Jun-2023

PMCID:	PMC10300920
doi:	10.3390/pharmaceutics15061638
PMID:	37376086

Role of Natural Products in the Management of COVID-19: A Saudi Arabian Perspective

Almuqbil M, Alshaikh S, Alrumayh N, Alnahdi F, Fallatah E, Almutairi S, Imran M, Kamal M, Almehmadi M, Alsaiari AA, Alqarni WA, Alasmari AM, Alwarthan S, Rabaan AA, Almadani ME, Asdaq SM

Healthcare (Basel)

28-May-2023

PMCID:	PMC10252572
doi:	10.3390/healthcare11111584
PMID:	37297724

Evaluating the Potential of Boswellia rivae to Provide Sustainable Livelihood Benefits in Eastern Ethiopia

DeCarlo A, Johnson S, Abdikadir A, Satyal P, Poudel A, Setzer WN

Plants (Basel)

18-May-2023

PMCID:	PMC10222219
doi:	10.3390/plants12102024
PMID:	37653941

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 / Benzene and substituted derivatives
Diphenylcyclopropenone	65057	Click to see C1=CC=C(C=C1)C2=C(C2=O)C3=CC=CC=C3	206.24	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,4-Dihydroxy-5-methoxybenzoic acid	19829	Click to see COC1=CC(=CC(=C1O)O)C(=O)O	184.15	unknown	via CMAUP database
> Benzenoids / Phenols / Cresols / Para cresols
P-Cresol	2879	Click to see CC1=CC=C(C=C1)O	108.14	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Pentane	8003	Click to see CCCCC	72.15	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Triacontene	87639	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC=C	420.80	unknown	https://doi.org/10.1002/CHIN.200652186
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(4Z)-2-tert-butyl-4-[[5-[(Z)-(3-tert-butyl-5-methyl-4-oxocyclohexa-2,5-dien-1-ylidene)-(4-chlorophenyl)methyl]furan-2-yl]-(4-chlorophenyl)methylidene]-6-methylcyclohexa-2,5-dien-1-one	60024406	Click to see CC1=CC(=C(C2=CC=C(C=C2)Cl)C3=CC=C(O3)C(=C4C=C(C(=O)C(=C4)C(C)(C)C)C)C5=CC=C(C=C5)Cl)C=C(C1=O)C(C)(C)C	637.60	unknown	via CMAUP database
(5S,6R)-6-ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-5,7-dihydro-1-benzofuran-4-one	25765971	Click to see CC1=COC2=C1C(=O)C(C(C2)(C)C=C)C(=C)C	230.30	unknown	https://doi.org/10.1002/FFJ.1193
(5S,6S)-6-ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-5,7-dihydro-1-benzofuran-4-one	10376566	Click to see CC1=COC2=C1C(=O)C(C(C2)(C)C=C)C(=C)C	230.30	unknown	https://doi.org/10.1016/J.FITOTE.2003.08.010 https://doi.org/10.1021/NP010072J https://doi.org/10.1002/HLCA.200800347
(6R)-6-ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-5,7-dihydro-1-benzofuran-4-one	137705001	Click to see CC1=COC2=C1C(=O)C(C(C2)(C)C=C)C(=C)C	230.30	unknown	https://doi.org/10.1055/S-2000-8532 https://doi.org/10.1016/0168-9452(88)90085-4 https://doi.org/10.1016/J.FITOTE.2003.08.010
(6S)-6-ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-5,7-dihydro-1-benzofuran-4-one	5316218	Click to see CC1=COC2=C1C(=O)C(C(C2)(C)C=C)C(=C)C	230.30	unknown	https://doi.org/10.1055/S-2000-8532 https://doi.org/10.1016/0168-9452(88)90085-4 https://doi.org/10.1016/S0367-326X(03)00199-0
Benzofuran, 6-ethenyl-4,5,6,7-tetrahydro-3,6-dimethyl-5-isopropenyl-, trans-	12305301	Click to see CC1=COC2=C1CC(C(C2)(C)C=C)C(=C)C	216.32	unknown	https://doi.org/10.1038/379029A0 https://doi.org/10.1016/J.FITOTE.2003.08.010
Cuminaldehyde	326	Click to see CC(C)C1=CC=C(C=C1)C=O	148.20	unknown	via CMAUP database
Curzerene	572766	Click to see CC1=COC2=C1CC(C(C2)(C)C=C)C(=C)C	216.32	unknown	https://doi.org/10.1016/S0367-326X(01)00367-7 https://doi.org/10.1016/0168-9452(88)90085-4 https://doi.org/10.1016/J.FITOTE.2003.08.010
Curzerenone	5315433	Click to see CC1=COC2=C1C(=O)C(C(C2)(C)C=C)C(=C)C	230.30	unknown	https://doi.org/10.1002/HLCA.200800347 https://doi.org/10.1021/NP010072J https://doi.org/10.1016/J.FITOTE.2003.08.010
Furanoelemene	12305300	Click to see CC1=COC2=C1CC(C(C2)(C)C=C)C(=C)C	216.32	unknown	https://doi.org/10.1016/J.FITOTE.2003.08.010
p-Cumate	3417835	Click to see CC(C)C1=CC=C(C=C1)C(=O)[O-]	163.19	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-beta-Bourbonene	324224	Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C	204.35	unknown	https://doi.org/10.1016/S0367-326X(01)00367-7
(+)-gamma-Cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1016/S0367-326X(01)00367-7
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	92042749	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)80085-0
(1S,5R,6R)-5-[(2R)-2-hydroxybutan-2-yl]-2-methyl-6-(2-methylprop-1-enyl)cyclohex-2-en-1-ol	11843778	Click to see CCC(C)(C1CC=C(C(C1C=C(C)C)O)C)O	238.37	unknown	https://doi.org/10.1002/CHIN.200652186
(1S,5S,6R)-6-[(2S)-but-3-en-2-yl]-5-(2-hydroxy-2-methylpropyl)-3-methylcyclohex-2-en-1-ol	163074328	Click to see CC1=CC(C(C(C1)CC(C)(C)O)C(C)C=C)O	238.37	unknown	https://doi.org/10.1002/CHIN.200652186
(1S,5S,7S,8S)-1,5-dimethyl-8-propan-2-yl-11-oxatricyclo[6.2.1.02,6]undecane-5,7-diol	10445038	Click to see CC(C)C12CCC(O1)(C3CCC(C3C2O)(C)O)C	254.36	unknown	via CMAUP database
(6-Methyl-4-propan-2-yl-1,2,3,4,4a,5,8,8a-octahydronaphthalen-1-yl)methanol	73123169	Click to see CC1=CCC2C(CCC(C2C1)C(C)C)CO	222.37	unknown	https://doi.org/10.1002/CHIN.200652186
(8S)-1,5,8-Trimethyl-8,9-dihydronaphtho[2,1-b]furan-6(7H)-one	71349601	Click to see CC1CC2=C(C(=CC3=C2C(=CO3)C)C)C(=O)C1	228.29	unknown	https://doi.org/10.1002/HLCA.200800347
(R)-1,5,8-Trimethyl-6,7,8,9-tetrahydronaphtho[2,1-b]furan	91746663	Click to see CC1CCC2=C(C1)C3=C(C=C2C)OC=C3C	214.30	unknown	via CMAUP database
[(1S,4S,4aS,8aR)-6-methyl-4-propan-2-yl-1,2,3,4,4a,5,8,8a-octahydronaphthalen-1-yl]methanol	163088534	Click to see CC1=CCC2C(CCC(C2C1)C(C)C)CO	222.37	unknown	https://doi.org/10.1002/CHIN.200652186
[1-(2-But-3-en-2-yl-3,4,6-trihydroxy-5-methylphenyl)-2-methylpropan-2-yl] acetate	11843775	Click to see CC1=C(C(=C(C(=C1O)O)C(C)C=C)CC(C)(C)OC(=O)C)O	308.40	unknown	https://doi.org/10.1002/CHIN.200652186
[1-(2-But-3-en-2-yl-3,6-dihydroxy-5-methylphenyl)-2-methylpropan-2-yl] acetate	11843774	Click to see CC1=CC(=C(C(=C1O)CC(C)(C)OC(=O)C)C(C)C=C)O	292.40	unknown	https://doi.org/10.1002/CHIN.200652186
[1-[2-[(2R)-but-3-en-2-yl]-3,4,6-trihydroxy-5-methylphenyl]-2-methylpropan-2-yl] acetate	162893979	Click to see CC1=C(C(=C(C(=C1O)O)C(C)C=C)CC(C)(C)OC(=O)C)O	308.40	unknown	https://doi.org/10.1002/CHIN.200652186
[1-[2-[(2R)-but-3-en-2-yl]-3,6-dihydroxy-5-methylphenyl]-2-methylpropan-2-yl] acetate	162988751	Click to see CC1=CC(=C(C(=C1O)CC(C)(C)OC(=O)C)C(C)C=C)O	292.40	unknown	https://doi.org/10.1002/CHIN.200652186
1-(2-But-3-en-2-yl-5-methylphenyl)-2-methylpropan-2-ol	11843777	Click to see CC1=CC(=C(C=C1)C(C)C=C)CC(C)(C)O	218.33	unknown	https://doi.org/10.1002/CHIN.200652186
1-[2-[(2R)-but-3-en-2-yl]-5-methylphenyl]-2-methylpropan-2-ol	162998634	Click to see CC1=CC(=C(C=C1)C(C)C=C)CC(C)(C)O	218.33	unknown	https://doi.org/10.1002/CHIN.200652186
1,5,8-Trimethyl-8,9-dihydro-7H-benzo[e][1]benzofuran-6-one	78061679	Click to see CC1CC2=C(C(=CC3=C2C(=CO3)C)C)C(=O)C1	228.29	unknown	https://doi.org/10.1002/HLCA.200800347
3-[(3aS,5aS,6S,7S,9aR,9bR)-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,3a,4,5,5a,7,8,9-octahydrocyclopenta[a]naphthalen-6-yl]propanoic acid	163037638	Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CCC3C2(CC=C3)C)C	330.50	unknown	https://doi.org/10.1002/PTR.2501
5-(2-Hydroxybutan-2-yl)-2-methyl-6-(2-methylprop-1-enyl)cyclohex-2-en-1-ol	73123171	Click to see CCC(C)(C1CC=C(C(C1C=C(C)C)O)C)O	238.37	unknown	https://doi.org/10.1002/CHIN.200652186
6-But-3-en-2-yl-5-(2-hydroxy-2-methylpropyl)-3-methylcyclohex-2-en-1-ol	73123170	Click to see CC1=CC(C(C(C1)CC(C)(C)O)C(C)C=C)O	238.37	unknown	https://doi.org/10.1002/CHIN.200652186
beta-Bourbonene	62566	Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C	204.35	unknown	https://doi.org/10.1016/S0367-326X(01)00367-7
Caryophyllene,alpha + beta mixt.	5354499	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1016/S0367-326X(01)00367-7
Cedrelanol	160799	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1002/FFJ.1193 https://doi.org/10.1002/PTR.2501
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)80085-0
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)-	89316	Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	unknown	https://doi.org/10.1016/S0367-326X(01)00367-7
delta-Elemene	12309449	Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	unknown	https://doi.org/10.1016/S0367-326X(01)00367-7
Myrrhone	134715234	Click to see CC1CC2=C(C(=CC3=C2C(=CO3)C)C)C(=O)C1	228.29	unknown	https://doi.org/10.1002/FFJ.1193
Oplopanone	10466745	Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O	238.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)80085-0 https://doi.org/10.1002/PTR.2501
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(8aR)-3,5,8a-trimethyl-6,9-dihydrobenzo[f][1]benzofuran-4-one	162897448	Click to see CC1=C2C(=O)C3=C(CC2(C=CC1)C)OC=C3C	228.29	unknown	https://doi.org/10.1021/NP010072J
3,5,8a-Trimethyl-4,4a,8a,9-tetrahydronaphtho[2,3-b]furan	13874240	Click to see CC1=CC=CC2(C1CC3=C(C2)OC=C3C)C	214.30	unknown	https://doi.org/10.1055/S-2006-960870 https://doi.org/10.1016/J.FITOTE.2003.08.010
3,5,8a-Trimethyl-6,9-dihydrobenzo[f][1]benzofuran-4-one	86216918	Click to see CC1=C2C(=O)C3=C(CC2(C=CC1)C)OC=C3C	228.29	unknown	https://doi.org/10.1021/NP010072J
3,8a-Dimethyl-5-methylidene-4,4a,6,9-tetrahydrobenzo[f][1]benzofuran	12311269	Click to see CC1=COC2=C1CC3C(=C)CC=CC3(C2)C	214.30	unknown	https://doi.org/10.1016/J.FITOTE.2003.08.010
Furanoeudesma 1,3-diene	643237	Click to see CC1=CC=CC2(C1CC3=C(C2)OC=C3C)C	214.30	unknown	https://doi.org/10.1055/S-2006-960870 https://doi.org/10.1016/J.FITOTE.2003.08.010
Lindestrene	12311270	Click to see CC1=COC2=C1CC3C(=C)CC=CC3(C2)C	214.30	unknown	https://doi.org/10.1016/S0367-326X(01)00367-7 https://doi.org/10.1016/0168-9452(88)90085-4 https://doi.org/10.1016/S0031-9422(00)80085-0 https://doi.org/10.1016/J.FITOTE.2003.08.010
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Proximadiol	165258	Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)O	240.38	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(3,6,10-Trimethyl-4,7,8,11-tetrahydrocyclodeca[b]furan-8-yl) acetate	162880780	Click to see CC1=CCC2=C(CC(=CC(C1)OC(=O)C)C)OC=C2C	274.35	unknown	https://doi.org/10.1055/S-2006-960870
(5E,9E)-3,6,10-trimethyl-8,11-dihydro-7H-cyclodeca[b]furan-4-one	6506548	Click to see CC1=CC(=O)C2=C(CC(=CCC1)C)OC=C2C	230.30	unknown	https://doi.org/10.1016/J.FITOTE.2003.08.010
(5R,6S,8S,9Z)-3,6,10-Trimethyl-4-oxo-8-methoxy-4,5,6,7,8,11-hexahydrocyclodeca[b]furan-5-ol acetate	101149318	Click to see CC1CC(C=C(CC2=C(C(=CO2)C)C(=O)C1OC(=O)C)C)OC	320.40	unknown	https://doi.org/10.1021/NP010072J
(6R,8S,9E)-8-methoxy-3,6,10-trimethyl-6,7,8,11-tetrahydro-5H-cyclodeca[b]furan-4-one	163016614	Click to see CC1CC(C=C(CC2=C(C(=CO2)C)C(=O)C1)C)OC	262.34	unknown	https://doi.org/10.1021/NP010072J
(6S,7R,8E)-7-methoxy-3,6-dimethyl-10-methylidene-5,6,7,11-tetrahydrocyclodeca[b]furan-4-one	10923274	Click to see CC1CC(=O)C2=C(CC(=C)C=CC1OC)OC=C2C	260.33	unknown	https://doi.org/10.1002/HLCA.200800347
(6S,7S,8E)-7-methoxy-3,6-dimethyl-10-methylidene-5,6,7,11-tetrahydrocyclodeca[b]furan-4-one	163075909	Click to see CC1CC(=O)C2=C(CC(=C)C=CC1OC)OC=C2C	260.33	unknown	https://doi.org/10.1021/NP010072J https://doi.org/10.1016/J.FITOTE.2003.08.010
(8-methoxy-3,6,10-trimethyl-4-oxo-6,7,8,11-tetrahydro-5H-cyclodeca[b]furan-5-yl) acetate	85296271	Click to see CC1CC(C=C(CC2=C(C(=CO2)C)C(=O)C1OC(=O)C)C)OC	320.40	unknown	https://doi.org/10.1021/NP010072J
(R,5E,9E)-8-Methoxy-3,6,10-trimethyl-4,7,8,11-tetrahydrocyclodeca[b]furan	91711711	Click to see CC1=CCC2=C(CC(=CC(C1)OC)C)OC=C2C	246.34	unknown	https://doi.org/10.1016/0031-9422(82)83164-6
[(1(10)E,2R,4R)]-2-Methoxy-8,12-epoxygemacra-1(10),7,11-trien-6-one	11747425	Click to see CC1CC(C=C(CC2=C(C(=CO2)C)C(=O)C1)C)OC	262.34	unknown	https://doi.org/10.1002/HLCA.200800347 https://doi.org/10.1016/J.FITOTE.2003.08.010
[(5E,8R,9E)-3,6,10-trimethyl-4,7,8,11-tetrahydrocyclodeca[b]furan-8-yl] acetate	162880781	Click to see CC1=CCC2=C(CC(=CC(C1)OC(=O)C)C)OC=C2C	274.35	unknown	https://doi.org/10.1055/S-2006-960870
[(5S,6S,8S,9Z)-8-methoxy-3,6,10-trimethyl-4-oxo-6,7,8,11-tetrahydro-5H-cyclodeca[b]furan-5-yl] acetate	163189635	Click to see CC1CC(C=C(CC2=C(C(=CO2)C)C(=O)C1OC(=O)C)C)OC	320.40	unknown	https://doi.org/10.1002/HLCA.200800347
[(5S,6S,8S)-8-methoxy-3,6,10-trimethyl-4-oxo-6,7,8,11-tetrahydro-5H-cyclodeca[b]furan-5-yl] acetate	162936929	Click to see CC1CC(C=C(CC2=C(C(=CO2)C)C(=O)C1OC(=O)C)C)OC	320.40	unknown	https://doi.org/10.1002/HLCA.200800347
2-Acetoxyfuranodiene	91748044	Click to see CC1=CCC2=C(CC(=CCC1)C)OC(=C2C)OC(=O)C	274.35	unknown	https://doi.org/10.1055/S-2006-960870 https://doi.org/10.1016/0031-9422(83)80223-4
2-Methoxyfuranodiene	6325622	Click to see CC1=CCC2=C(CC(=CC(C1)OC)C)OC=C2C	246.34	unknown	https://doi.org/10.1016/S0367-326X(01)00367-7 https://doi.org/10.1016/0031-9422(83)80223-4
3,6,10-Trimethyl-4H,7H,8H,11H-cyclodeca[B]furan	171597	Click to see CC1=CCC2=C(CC(=CCC1)C)OC=C2C	216.32	unknown	https://doi.org/10.1016/S0367-326X(01)00367-7
7-Methoxy-3,6-dimethyl-10-methylidene-5,6,7,11-tetrahydrocyclodeca[b]furan-4-one	85317076	Click to see CC1CC(=O)C2=C(CC(=C)C=CC1OC)OC=C2C	260.33	unknown	https://doi.org/10.1002/HLCA.200800347 https://doi.org/10.1021/NP010072J https://doi.org/10.1016/J.FITOTE.2003.08.010
8-methoxy-3,6,10-trimethyl-6,7,8,11-tetrahydro-5H-cyclodeca[b]furan-4-one	73083842	Click to see CC1CC(C=C(CC2=C(C(=CO2)C)C(=O)C1)C)OC	262.34	unknown	https://doi.org/10.1002/HLCA.200800347 https://doi.org/10.1021/NP010072J https://doi.org/10.1016/J.FITOTE.2003.08.010
CID 179413	179413	Click to see CC1=CC(=O)C2=C(CC(=CCC1)C)OC=C2C	230.30	unknown	https://doi.org/10.1016/J.FITOTE.2003.08.010
Cyclodeca(b)furan, 4,7,8,11-tetrahydro-3,6,10-trimethyl-, (5E,9Z)-	9601230	Click to see CC1=CCC2=C(CC(=CCC1)C)OC=C2C	216.32	unknown	https://doi.org/10.1016/0168-9452(88)90085-4 https://doi.org/10.1016/S0367-326X(01)00367-7 https://doi.org/10.1038/379029A0 https://doi.org/10.1016/S0031-9422(00)80085-0
Furanodiene	636458	Click to see CC1=CCC2=C(CC(=CCC1)C)OC=C2C	216.32	unknown	https://doi.org/10.1016/S0031-9422(00)80085-0 https://doi.org/10.1038/379029A0 https://doi.org/10.1016/S0367-326X(01)00367-7 https://doi.org/10.1016/0168-9452(88)90085-4
Germacrene B	5281519	Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C	204.35	unknown	https://doi.org/10.1016/S0367-326X(01)00367-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(-)-Alismoxide	10243299	Click to see CC(C)C1=CC2C(CCC2(C)O)C(CC1)(C)O	238.37	unknown	via CMAUP database
(1R,3aR,4R,8aS)-1-methoxy-1,4-dimethyl-7-propan-2-yl-2,3,3a,5,6,8a-hexahydroazulen-4-ol	15896127	Click to see CC(C)C1=CC2C(CCC2(C)OC)C(CC1)(C)O	252.39	unknown	https://doi.org/10.1002/HLCA.200800347
(1S,3aR,8aR)-1-methyl-4-methylidene-7-propan-2-yl-2,3,3a,5,6,8a-hexahydroazulen-1-ol	11790742	Click to see CC(C)C1=CC2C(CCC2(C)O)C(=C)CC1	220.35	unknown	via CMAUP database
1-Methoxy-1,4-dimethyl-7-propan-2-yl-2,3,3a,5,6,8a-hexahydroazulen-4-ol	73721162	Click to see CC(C)C1=CC2C(CCC2(C)OC)C(CC1)(C)O	252.39	unknown	https://doi.org/10.1002/HLCA.200800347
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
3a-hydroxy-1,5,8-trimethyl-5,7,8,9-tetrahydro-4H-benzo[e][1]benzofuran-2,6-dione	74831241	Click to see CC1CC2=C(C(CC3(C2=C(C(=O)O3)C)O)C)C(=O)C1	262.30	unknown	https://doi.org/10.1002/HLCA.200800347
6-ethenyl-7a-hydroxy-3,6-dimethyl-5-prop-1-en-2-yl-5,7-dihydro-4H-1-benzofuran-2-one	14038424	Click to see CC1=C2CC(C(CC2(OC1=O)O)(C)C=C)C(=C)C	248.32	unknown	https://doi.org/10.1002/HLCA.200800347
Hydroxyisogermafurenolide	14038425	Click to see CC1=C2CC(C(CC2(OC1=O)O)(C)C=C)C(=C)C	248.32	unknown	https://doi.org/10.1002/HLCA.200800347
Myrrhanolide C	42636912	Click to see CC1CC2=C(C(CC3(C2=C(C(=O)O3)C)O)C)C(=O)C1	262.30	unknown	https://doi.org/10.1002/HLCA.200800347
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
7-hydroxy-3,8a-dimethyl-5-methylidene-4a,6,7,8,9,9a-hexahydro-4H-benzo[f][1]benzofuran-2-one	5316022	Click to see CC1=C2CC3C(=C)CC(CC3(CC2OC1=O)C)O	248.32	unknown	via CMAUP database
9a-Hydroxy-3,8a-dimethyl-5-methylene-4,4a,5,6,9,9a-hexahydronaphtho[2,3-b]furan-2(8aH)-one	101938021	Click to see CC1=C2CC3C(=C)CC=CC3(CC2(OC1=O)O)C	246.30	unknown	https://doi.org/10.1002/HLCA.200800347
beta-Cyclocostunolide	442192	Click to see CC12CCCC(=C)C1C3C(CC2)C(=C)C(=O)O3	232.32	unknown	via CMAUP database
Hydroxylinderstrenolide	76046873	Click to see CC1=C2CC3C(=C)CC=CC3(CC2(OC1=O)O)C	246.30	unknown	https://doi.org/10.1002/HLCA.200800347
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
Costunolide	5281437	Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C	232.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Dehydrocostus lactone, (-)-	73174	Click to see C=C1CCC2C(C3C1CCC3=C)OC(=O)C2=C	230.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3S,5S,8R,9S,10R,13S,17S)-4,4,8,10,13-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,7,9,11,12,16,17-decahydro-1H-cyclopenta[a]phenanthrene-1,3-diol	42632429	Click to see CC(CCC=C(C)C)C1CC=C2C1(CCC3C2(CCC4C3(C(CC(C4(C)C)O)O)C)C)C	442.70	unknown	https://doi.org/10.1002/HLCA.200800347
4,4,8,10,13-pentamethyl-17-(6-methylhept-5-en-2-yl)-2,3,5,6,7,9,11,12,16,17-decahydro-1H-cyclopenta[a]phenanthrene-1,3-diol	74831240	Click to see CC(CCC=C(C)C)C1CC=C2C1(CCC3C2(CCC4C3(C(CC(C4(C)C)O)O)C)C)C	442.70	unknown	https://doi.org/10.1002/HLCA.200800347
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
20-Hydroxyecdysone	5459840	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O	480.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(5R,9R,10R,13R)-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15-decahydrocyclopenta[a]phenanthren-3-one	128179	Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CC=C4)C)C)C	314.50	unknown	https://doi.org/10.1002/PTR.2501
Mansumbinone	12071382	Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CC=C4)C)C)C	314.50	unknown	https://doi.org/10.1002/PTR.2501
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acid esters
Panclicin B	9868539	Click to see CCCCCCCCCCC1C(OC1=O)CC(CCCCCCC)OC(=O)C(C)NC=O	453.70	unknown	https://doi.org/10.1016/S0367-326X(01)00367-7 https://doi.org/10.1016/S0031-9422(00)80085-0 https://doi.org/10.1016/0168-9452(88)90085-4 https://doi.org/10.1016/S0367-326X(03)00199-0
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
1,2-Epoxy-10(14)-furanogermacren-6-one	10444597	Click to see CC1CC2C(O2)C(=C)CC3=C(C(=CO3)C)C(=O)C1	246.30	unknown	https://doi.org/10.1002/HLCA.200800347 https://doi.org/10.1021/NP010072J
8,12-Dimethyl-3-methylidene-5,14-dioxatricyclo[9.3.0.04,6]tetradeca-1(11),12-dien-10-one	85145166	Click to see CC1CC2C(O2)C(=C)CC3=C(C(=CO3)C)C(=O)C1	246.30	unknown	https://doi.org/10.1002/HLCA.200800347 https://doi.org/10.1021/NP010072J
> Organoheterocyclic compounds / Naphthofurans
9a-Hydroxy-3,5,8-trimethyl-4,9-dihydrobenzo[f][1]benzofuran-2-one	74831239	Click to see CC1=C2CC3=C(C(=O)OC3(CC2=C(C=C1)C)O)C	244.28	unknown	https://doi.org/10.1002/HLCA.200800347
Myrrhanolide A	42632428	Click to see CC1=C2CC3=C(C(=O)OC3(CC2=C(C=C1)C)O)C	244.28	unknown	https://doi.org/10.1002/HLCA.200800347
> Phenylpropanoids and polyketides / Cinnamaldehydes
Cinnamaldehyde	637511	Click to see C1=CC=C(C=C1)C=CC=O	132.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
cis-Cinnamate	6857483	Click to see C1=CC=C(C=C1)C=CC(=O)[O-]	147.15	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
7-Prenyloxyaromadendrin	23900109	Click to see CC(=CCOC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=C(C=C3)O)O)C	356.40	unknown	via CMAUP database

Biological Material Top

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.

Commiphora myrrha

Table of Contents

Details Top

Description 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

Biological Material Top

Contributors Top

Collections Top