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Commiphora mukul

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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 UUID644013033a309220388493
Scientific name Commiphora mukul
Authority Engl.
First published in Monogr. Phan. 4: 12 (1883)

Description Top

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Synonyms Top

Scientific name Authority First published in
Balsamea mukul Baill. Hist. Pl. 5: 295 (1874)
Balsamodendrum mukul Hook. ex Stocks Hooker's J. Bot. Kew Gard. Misc. 1: 259 (1849)
Balsamodendrum roxburghii Stocks J. Asiat. Soc. Bombay 2(11): 391. 1847 [Jul 1847]

Common names Top

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Language Common/alternative name
Arabic مقل اليهود

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000617375
Tropicos 100314904
KEW urn:lsid:ipni.org:names:127738-1
The Plant List kew-2733590
Open Tree Of Life 7058218
NCBI Taxonomy 2067815
IPNI 127738-1
GBIF 3994129
Freebase /m/026bt3y
USDA GRIN 402551
CMAUP NPO25991

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
Evaluation of the anti-arthritic activity of Rhuflex-F – A proprietary Ayurvedic herbomineral formulation in albino rats Gupta V, Panigrahi B, De S, Nariya MB Ayu 21-Feb-2024
PMCID:PMC10946666
doi:10.4103/ayu.ayu_327_21
PMID:38505109
Farnesoid X receptor promotes non-small cell lung cancer metastasis by activating Jak2/STAT3 signaling via transactivation of IL-6ST and IL-6 genes Jin X, Shang B, Wang J, Sun J, Li J, Liang B, Wang X, Su L, You W, Jiang S Cell Death Dis 15-Feb-2024
PMCID:PMC10869786
doi:10.1038/s41419-024-06495-y
PMID:38360812
From immune checkpoints to therapies: understanding immune checkpoint regulation and the influence of natural products and traditional medicine on immune checkpoint and immunotherapy in lung cancer Zhou Y, Wang F, Li G, Xu J, Zhang J, Gullen E, Yang J, Wang J Front Immunol 15-Feb-2024
PMCID:PMC10902058
doi:10.3389/fimmu.2024.1340307
PMID:38426097
Role of Alternate Therapies to Improve the Quality of Life in Menopausal Women: A Systematic Review Aarshageetha P, Janci PR, Tharani ND J Midlife Health 30-Dec-2023
PMCID:PMC10836436
doi:10.4103/jmh.jmh_222_22
PMID:38312763
Consideration of SHP-1 as a Molecular Target for Tumor Therapy Lim S, Lee KW, Kim JY, Kim KD Int J Mol Sci 26-Dec-2023
PMCID:PMC10779157
doi:10.3390/ijms25010331
PMID:38203502
Targeting Farnesoid X Receptor in Tumor and the Tumor Microenvironment: Implication for Therapy Nenkov M, Shi Y, Ma Y, Gaßler N, Chen Y Int J Mol Sci 19-Dec-2023
PMCID:PMC10778939
doi:10.3390/ijms25010006
PMID:38203175
Medicinal Herbs: Promising Immunomodulators for the Treatment of Infectious Diseases Alanazi HH, Elasbali AM, Alanazi MK, El Azab EF Molecules 12-Dec-2023
PMCID:PMC10745476
doi:10.3390/molecules28248045
PMID:38138535
Acute and sub-chronic toxicity of Liberin, an anti-diabetic polyherbal formulation in rats Suvarna R, Suryakanth VB, Bakthavatchalam P, Kalthur G, Nayak M D, Prabhu MM, Hadapad BS, Shenoy RP J Ayurveda Integr Med 15-Oct-2023
PMCID:PMC10585375
doi:10.1016/j.jaim.2023.100804
PMID:37847964
Effects of natural products on polycystic ovary syndrome: From traditional medicine to modern drug discovery Jung W, Choi H, Kim J, Kim J, Kim W, Nurkolis F, Kim B Heliyon 11-Oct-2023
PMCID:PMC10589870
doi:10.1016/j.heliyon.2023.e20889
PMID:37867816
Cardiocentrism in ancient medicines Zampieri F, Thiene G, Zanatta A Int J Cardiol Heart Vasc 25-Aug-2023
PMCID:PMC10471923
doi:10.1016/j.ijcha.2023.101261
PMID:37663613
Water extract of frankincense and myrrh inhibits liver cancer progression and epithelial‑mesenchymal transition through Wnt/β‑catenin signaling Lu X, Mao J, Wang Y, Huang Y, Gu M Mol Clin Oncol 18-Aug-2023
PMCID:PMC10502803
doi:10.3892/mco.2023.2673
PMID:37719039
Effective management of Colles fracture using Murivenna and Abha Guggulu – A case report Alias Benny G, Varghese T, Vijayakumar S, Robin DT J Ayurveda Integr Med 31-Jul-2023
PMCID:PMC10415758
doi:10.1016/j.jaim.2023.100786
PMID:37531707
The Anticancer Effect of Napabucasin (BBI608), a Natural Naphthoquinone Shao Z, Wang H, Ren H, Sun Y, Chen X Molecules 27-Jul-2023
PMCID:PMC10420168
doi:10.3390/molecules28155678
PMID:37570646
A Narrative Review of the Herbal Preparation of Ayurvedic, Traditional Chinese, and Kampō Medicines Applied as Radioprotectors Ibáñez B, Melero A, Montoro A, Merino-Torres JF, Soriano JM, San Onofre N Antioxidants (Basel) 17-Jul-2023
PMCID:PMC10376155
doi:10.3390/antiox12071437
PMID:37507975
In Silico and In Vitro Identification of P-Glycoprotein Inhibitors from a Library of 375 Phytochemicals Schäfer J, Klösgen VJ, Omer EA, Kadioglu O, Mbaveng AT, Kuete V, Hildebrandt A, Efferth T Int J Mol Sci 16-Jun-2023
PMCID:PMC10299530
doi:10.3390/ijms241210240
PMID:37373385

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols
Hispidin 54685921 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=O)O2)O)O)O 246.21 unknown via CMAUP database
Hypholomine B 54730031 Click to see C1=CC(=C(C=C1C=CC2=CC3=C(C(C(O3)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=O)O5)O)C(=O)O2)O)O 490.40 unknown via CMAUP database
interfungin A 54726789 Click to see CC(=O)C=C(C(=CC1=CC(=C(C=C1)O)O)C2=C(C=C(OC2=O)C=CC3=CC(=C(C=C3)O)O)O)O 464.40 unknown via CMAUP database
Phellinstatin 54728876 Click to see C1=CC(=C(C=C1C=CC2=CC(=C(C(=O)O2)C3=CC(=C(C=C3C=CC4=CC5=C(C(C(O5)C6=CC(=C(C=C6)O)O)C7=CC(=CC(=O)O7)O)C(=O)O4)O)O)O)O)O 734.60 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Methyldavallialactone 54726724 Click to see CC1=CC(=O)C(C(O1)C2=CC(=C(C=C2)O)O)C3=C(C=C(OC3=O)C=CC4=CC(=C(C=C4)O)OC)O 478.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Diayangambin 167452 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC 446.50 unknown https://doi.org/10.1248/CPB.52.1200
> Lignans, neolignans and related compounds / Lignan lactones
(5aR,8aR,9S)-4-hydroxy-9-(4-hydroxy-3,5-dimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one 11860863 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O 400.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Cembrane diterpenoids
(1E,3Z,6E,10E)-3,7,11-trimethyl-14-propan-2-ylcyclotetradeca-1,3,6,10-tetraene 6427092 Click to see CC1=CCCC(=CCC=C(C=CC(CC1)C(C)C)C)C 272.50 unknown https://doi.org/10.1021/NP8004453
Agn-PC-00G18Q 564745 Click to see CC1=CCCC(=CC(C(CCC(=CCC1)C)C(C)C)O)C 290.50 unknown https://doi.org/10.1002/ARDP.19723050703
Epimukulol 13255923 Click to see CC1=CCCC(=CC(C(CCC(=CCC1)C)C(C)C)O)C 290.50 unknown https://doi.org/10.1021/NP8004453
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
Lindestrene 12311270 Click to see CC1=COC2=C1CC3C(=C)CC=CC3(C2)C 214.30 unknown https://doi.org/10.1016/J.FITOTE.2003.12.003
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2E,6E,10E)-13-[(1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-6-oxo-1,3,4,4a,7,8-hexahydronaphthalen-1-yl]-2,6,10-trimethyltrideca-2,6,10-trienoic acid 102242792 Click to see CC(=CCCC1C2(CCC(=O)C(C2CCC1(C)O)(C)C)C)CCC=C(C)CCC=C(C)C(=O)O 472.70 unknown https://doi.org/10.1248/CPB.52.1200
(2S,6R)-1,1,4a,6-tetramethyl-5-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]decalin-2,6-diol 57401582 Click to see CC(=CCCC(=CCCC(=CCCC1C2(CCC(C(C2CCC1(C)O)(C)C)O)C)C)C)C 444.70 unknown via CMAUP database
(4aS,5R,6R,8aS)-6-hydroxy-5-[(3E,7E,11E)-13-hydroxy-4,8,12-trimethyltrideca-3,7,11-trienyl]-1,1,4a,6-tetramethyl-3,4,5,7,8,8a-hexahydronaphthalen-2-one 102242791 Click to see CC(=CCCC1C2(CCC(=O)C(C2CCC1(C)O)(C)C)C)CCC=C(C)CCC=C(C)CO 458.70 unknown https://doi.org/10.1248/CPB.52.1200
Myrrhanol A 42608309 Click to see CC(=CCCC1C2(CCC(C(C2CCC1(C)O)(C)C)O)C)CCC=C(C)CCC=C(C)CO 460.70 unknown https://doi.org/10.1016/S0960-894X(01)00111-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
E-Guggulsterone 6439929 Click to see CC=C1C(=O)CC2C1(CCC3C2CCC4=CC(=O)CCC34C)C 312.40 unknown https://doi.org/10.1093/JAOAC/84.1.24
https://doi.org/10.1021/NP8004453
https://doi.org/10.1016/S0378-4347(97)00626-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
17-(2-hydroxy-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,16-diol 85803537 Click to see CC(C)CCCC(C)(C1C(CC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)O)O 418.70 unknown https://doi.org/10.1515/ZNB-2005-1114
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
Ergosterol peroxide 5351516 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C 428.60 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
(2R,3S,4R,5R)-2-(hydroxymethyl)-5-[6-[hydroxy(methyl)amino]purin-9-yl]oxolane-3,4-diol 101518 Click to see CN(C1=NC=NC2=C1N=CN2C3C(C(C(O3)CO)O)O)O 297.27 unknown via CMAUP database
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Protocatechualdehyde 8768 Click to see C1=CC(=C(C=C1C=O)O)O 138.12 unknown via CMAUP database
> Organoheterocyclic compounds / Furopyrans
Phellifuropyranone A 24770409 Click to see C1=CC(=C(C=C1C=CC2=CC3=C(C=C(O3)C4=CC(=C(C=C4)O)O)C(=O)O2)O)O 378.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
Phelligridin C 10248188 Click to see C1=CC(=CC=C1C=CC2=CC3=C(C4=CC(=C(C=C4C(=O)O3)O)O)C(=O)O2)O 364.30 unknown via CMAUP database
phelligridin D 10339712 Click to see C1=CC(=C(C=C1C=CC2=CC3=C(C4=CC(=C(C=C4C(=O)O3)O)O)C(=O)O2)O)O 380.30 unknown via CMAUP database
> 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 via CMAUP database

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