Commiphora kua - Unknown
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Internal ID UUID644013003e9f4966789974
Scientific name Commiphora kua
Authority (R.Br. ex Royle) Vollesen
First published in Nordic J. Bot. 4: 37 (1984)

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Synonyms Top

Scientific name Authority First published in
Amyris kafal Forssk. Fl. Aegypt.-Arab. : 80 (1775)
Balsamea abyssinica Engl. Bot. Jahrb. Syst. 1: 41 (1880)
Balsamodendrum abyssinicum Engl. Bot. Jahrb. Syst. 1: 41 (1880)
Balsamodendrum habessinica O.Berg Bot. Zeitung (Berlin) 20: 161 (1862)
Balsamodendrum kua Brown ex Royle Man. Mat. Med. 341 (1847)
Balsamus kafal Stackh. Extr. Bruce' s Travels : 12 (1815)
Commiphora abyssinica Engl. Monogr. Phan. 4: 10 (1883)
Commiphora assaortensis Chiov. Fl. Somala 2: 64 (1932)
Commiphora atramentaria Chiov. Fl. Somala 2: 76 (1932)
Commiphora bruceae Chiov. Bull. Misc. Inform. Kew 1941: 133 (1941)
Commiphora candidula Sprague Hooker's Icon. Pl. 32: t. 3106 (1927)
Commiphora crenulata Chiov. Ann. Bot. (Rome) 13: 404. 1915
Commiphora dancaliensis Chiov. Ann. Bot. (Rome) 13: 403 (1915)
Commiphora ellenbeckii Engl. Bot. Jahrb. Syst. 34: 303 (1904)
Commiphora flaviflora Engl. Bot. Jahrb. Syst. 34: 304 (1904)
Commiphora gowlello Sprague Hooker's Icon. Pl. 32: t. 3109 (1927)
Commiphora gracilispina J.B.Gillett Fl. Trop. E. Africa , Burserac.: 18 (1991)
Commiphora habessinica (O.Berg) Engl. Monogr. Phan. 4: 10 (1883)
Commiphora habessinica var. crenulata A.Terracc. Annuario Reale Ist. Bot. Roma 5: 111 1893
Commiphora incisa Chiov. Res. Sci. Somalia Ital. 1: 45 (1916)
Commiphora kua var. gowlello (Sprague) J.B.Gillett Fl. Trop. E. Africa , Burserac.: 19 (1991)
Commiphora lindensis Engl. Bot. Jahrb. Syst. 34: 303 (1904)
Commiphora salubris Engl. Bot. Jahrb. Syst. 54: 294 (1917)
Commiphora subsessilifolia Engl. Bot. Jahrb. Syst. 34: 303 (1904)
Balsamodendrum kafal (Forssk.) Kunth ex DC. Prodr. 2: 76 (1825)
Balsamodendrum habessinicum O.Berg Bot. Zeitung (Berlin) 20: 161 (1862)
Commiphora habessinica subsp. tanganyikensis J.B.Gillett Fl. Trop. E. Africa , Burserac.: 26 (1991)

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Djibouti
      • Eritrea
      • Ethiopia
      • Socotra
      • Somalia
      • Sudan
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zambia
    • West-central Tropical Africa
      • Burundi
      • Rwanda
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000617330
Tropicos 4700456
KEW urn:lsid:ipni.org:names:913830-1
The Plant List kew-2733548
Open Tree Of Life 493265
NCBI Taxonomy 246356
IPNI 913830-1
iNaturalist 1066418
GBIF 7286744
CMAUP NPO21923

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
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Effects of prosopis juliflora on plant diversity on rangeland in Shilabo District, Somali Regional State, Ethiopia Bezaredie D, Tadesse Z, Tadesse Z Heliyon 26-Feb-2023
PMCID:PMC10011196
doi:10.1016/j.heliyon.2023.e14049
PMID:36925521
Commiphora myrrh: a phytochemical and pharmacological update Batiha GE, Wasef L, Teibo JO, Shaheen HM, Zakariya AM, Akinfe OA, Teibo TK, Al-kuraishy HM, Al-Garbee AI, Alexiou A, Papadakis M Naunyn Schmiedebergs Arch Pharmacol 18-Nov-2022
PMCID:PMC9672555
doi:10.1007/s00210-022-02325-0
PMID:36399185
Review of Ethnobotanical and Ethnopharmacological Evidence of Some Ethiopian Medicinal Plants Traditionally Used for Peptic Ulcer Disease Treatment Tadesse TY, Zeleke MM, Dagnew SB Clin Exp Gastroenterol 24-Sep-2022
PMCID:PMC9517940
doi:10.2147/CEG.S384395
PMID:36186925
Phytochemical Composition of Commiphora Oleogum Resins and Their Cytotoxicity against Skin Cancer Cells Ulrich J, Stiltz S, St-Gelais A, El Gaafary M, Simmet T, Syrovets T, Schmiech M Molecules 17-Jun-2022
PMCID:PMC9229828
doi:10.3390/molecules27123903
PMID:35745024
Therapeutic Potential of Phytoconstituents in Management of Alzheimer's Disease Singh AK, Rai SN, Maurya A, Mishra G, Awasthi R, Shakya A, Chellappan DK, Dua K, Vamanu E, Chaudhary SK, Singh MP Evid Based Complement Alternat Med 08-Jun-2021
PMCID:PMC8208882
doi:10.1155/2021/5578574
PMID:34211570
The inventory of camel feed resource and the evaluation of its chemical composition in south‐east rangelands of Ethiopia Habte M, Eshetu M, Andualem D, Maryo M, Legesse A Vet Med Sci 22-Mar-2021
PMCID:PMC8294363
doi:10.1002/vms3.471
PMID:33750028
Natural plant species inventory of hotspot areas in Arabian Peninsula: Southwest Al-Baha region, Saudi Arabia Al-Namazi AA, Al-Khulaidi AW, Algarni S, Al-Sagheer NA Saudi J Biol Sci 04-Mar-2021
PMCID:PMC8176062
doi:10.1016/j.sjbs.2021.02.076
PMID:34121869
Soil and plant phytoliths from the Acacia-Commiphora mosaics at Oldupai Gorge (Tanzania) Mercader J, Clarke S, Bundala M, Favreau J, Inwood J, Itambu M, Larter F, Lee P, Lewiski-McQuaid G, Mollel N, Mwambwiga A, Patalano R, Soto M, Tucker L, Walde D PeerJ 11-Dec-2019
PMCID:PMC6911344
doi:10.7717/peerj.8211
PMID:31844589
Seeing the Unseen of the Combination of Two Natural Resins, Frankincense and Myrrh: Changes in Chemical Constituents and Pharmacological Activities Cao B, Wei XC, Xu XR, Zhang HZ, Luo CH, Feng B, Xu RC, Zhao SY, Du XJ, Han L, Zhang DK Molecules 24-Aug-2019
PMCID:PMC6749531
doi:10.3390/molecules24173076
PMID:31450584
Species-specific molecular signature of Commiphora species of Saudi Arabia inferred from internal transcribed spacer sequences of nuclear ribosomal DNA Ali MA Saudi J Biol Sci 30-Jun-2018
PMCID:PMC6252017
doi:10.1016/j.sjbs.2018.06.010
PMID:30505173
Main vegetation types and plant species diversity along an altitudinal gradient of Al Baha region, Saudi Arabia Al-Aklabi A, Al-Khulaidi AW, Hussain A, Al-Sagheer N Saudi J Biol Sci 03-Mar-2016
PMCID:PMC5109499
doi:10.1016/j.sjbs.2016.02.007
PMID:27872563
A Survey of Chemical Compositions and Biological Activities of Yemeni Aromatic Medicinal Plants Chhetri BK, Awadh Ali NA, Setzer WN Medicines (Basel) 28-May-2015
PMCID:PMC5533162
doi:10.3390/medicines2020067
PMID:28930202
To move or to evolve: contrasting patterns of intercontinental connectivity and climatic niche evolution in “Terebinthaceae” (Anacardiaceae and Burseraceae) Weeks A, Zapata F, Pell SK, Daly DC, Mitchell JD, Fine PV Front Genet 28-Nov-2014
PMCID:PMC4247111
doi:10.3389/fgene.2014.00409
PMID:25506354
Picropolygamain: a New Lignan from<i>Commiphora incisa</i>Resin<sup>1,2</sup> Gordon Provan, Peter Waterman Georg Thieme Verlag KG 06-Mar-2007
doi:10.1055/S-2007-969479

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lignans, neolignans and related compounds / Lignan lactones
(5R,5aR,8aR)-5-(1,3-benzodioxol-5-yl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one 156202 Click to see C1C2COC(=O)C2C(C3=CC4=C(C=C31)OCO4)C5=CC6=C(C=C5)OCO6 352.30 unknown https://doi.org/10.1055/S-2007-969479
(5R,5aS,8aR)-5-(1,3-benzodioxol-5-yl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one 10338061 Click to see C1C2COC(=O)C2C(C3=CC4=C(C=C31)OCO4)C5=CC6=C(C=C5)OCO6 352.30 unknown https://doi.org/10.1055/S-2007-969479
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Carbocyclic fatty acids
3-(2-Hydroperoxy-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,4,5,5a,7,8,9-octahydrocyclopenta[a]naphthalen-6-yl)propanoic acid 162975300 Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CCC3=CC(CC32C)OO)C 362.50 unknown https://doi.org/10.1016/0031-9422(92)80364-K
3-[(2S,5aR,6S,7S,9aR,9bR)-2-hydroperoxy-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,4,5,5a,7,8,9-octahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 162975301 Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CCC3=CC(CC32C)OO)C 362.50 unknown https://doi.org/10.1016/0031-9422(92)80364-K
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(3R)-3-(beta-D-Glucopyranosyloxy)-5-phenylpentanoic acid 11792570 Click to see C1=CC=C(C=C1)CCC(CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 356.40 unknown via CMAUP database
(3R)-3-(beta-D-Glucopyranosyloxy)-5-phenylpentanoic acid butyl ester 10693008 Click to see CCCCOC(=O)CC(CCC1=CC=CC=C1)OC2C(C(C(C(O2)CO)O)O)O 412.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4S,4aS,8aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 12302227 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(01)00413-7
2-Methyl-5-(6-methylhept-5-en-2-yl)phenol 520468 Click to see CC1=C(C=C(C=C1)C(C)CCC=C(C)C)O 218.33 unknown https://doi.org/10.1055/S-2006-957815
3-(6-Hydroxy-6-methylhept-4-en-2-yl)-6-methylbenzene-1,2-diol 85369727 Click to see CC1=C(C(=C(C=C1)C(C)CC=CC(C)(C)O)O)O 250.33 unknown https://doi.org/10.1248/CPB.51.479
3-(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 163037637 Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CCC3C2(CC=C3)C)C 330.50 unknown https://doi.org/10.1016/0031-9422(86)80027-9
3-[(3aR,5aR,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 101630480 Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CCC3C2(CC=C3)C)C 330.50 unknown https://doi.org/10.1016/0031-9422(86)80027-9
3-[(E,2R)-6-hydroxy-6-methylhept-4-en-2-yl]-6-methylbenzene-1,2-diol 11021311 Click to see CC1=C(C(=C(C=C1)C(C)CC=CC(C)(C)O)O)O 250.33 unknown https://doi.org/10.1248/CPB.51.479
4-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydro-1-naphthalenol 519662 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(01)00413-7
5-(6-Hydroxy-6-methylhept-4-en-2-yl)-2-methylphenol 163023193 Click to see CC1=C(C=C(C=C1)C(C)CC=CC(C)(C)O)O 234.33 unknown https://doi.org/10.1055/S-2006-957815
5-[(E,2R)-6-hydroxy-6-methylhept-4-en-2-yl]-2-methylphenol 76285515 Click to see CC1=C(C=C(C=C1)C(C)CC=CC(C)(C)O)O 234.33 unknown https://doi.org/10.1055/S-2006-957815
Cedrelanol 160799 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(01)00413-7
methyl 3-[(3aR,5aR,6S,7S,9aR,9bR)-9a,9b-dimethyl-7-prop-1-en-2-yl-3a,4,5,5a,6,7,8,9-octahydro-1H-cyclopenta[a]naphthalen-6-yl]propanoate 128211 Click to see CC(=C)C1CCC2(C(C1CCC(=O)OC)CCC3C2(CC=C3)C)C 330.50 unknown https://doi.org/10.1055/S-2006-959594
Xanthorrhizol 93135 Click to see CC1=C(C=C(C=C1)C(C)CCC=C(C)C)O 218.33 unknown https://doi.org/10.1055/S-2006-957815
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,5R,8R,9R,10R,13R,14R,16S,17R)-17-[(2R)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,16-diol 9981724 Click to see CC(=CCCC(C)(C1C2CCC3C4(CCC(C(C4CCC3(C2(CC1O)C)C)(C)C)O)C)O)C 460.70 unknown https://doi.org/10.1248/CPB.51.479
(3S,5R,8R,9R,10R,13R,14R,16S,17R)-17-[(E,2S)-2,6-dihydroxy-6-methylhept-4-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,16-diol 11826896 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CC(C4C(C)(CC=CC(C)(C)O)O)O)C)C)C 476.70 unknown https://doi.org/10.1248/CPB.51.479
(5R,8R,9R,10R,13R,14R,16S,17R)-16-hydroxy-17-[(2R)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 10027199 Click to see CC(=CCCC(C)(C1C2CCC3C4(CCC(=O)C(C4CCC3(C2(CC1O)C)C)(C)C)C)O)C 458.70 unknown https://doi.org/10.1016/S0031-9422(01)00413-7
https://doi.org/10.1016/0031-9422(86)80027-9
[(3S,5R,8R,9R,10R,13R,14R,16S,17R)-17-[(E,2S)-2,6-dihydroxy-6-methylhept-4-en-2-yl]-16-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 11060372 Click to see CC(=O)OC1CCC2(C3CCC4C(C(CC4(C3(CCC2C1(C)C)C)C)O)C(C)(CC=CC(C)(C)O)O)C 518.80 unknown https://doi.org/10.1248/CPB.51.479
[17-(2,6-dihydroxy-6-methylhept-4-en-2-yl)-16-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 85384245 Click to see CC(=O)OC1CCC2(C3CCC4C(C(CC4(C3(CCC2C1(C)C)C)C)O)C(C)(CC=CC(C)(C)O)O)C 518.80 unknown https://doi.org/10.1248/CPB.51.479
16-Hydroxy-17-(2-hydroxy-6-methylhept-5-en-2-yl)-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 85096507 Click to see CC(=CCCC(C)(C1C2CCC3C4(CCC(=O)C(C4CCC3(C2(CC1O)C)C)(C)C)C)O)C 458.70 unknown https://doi.org/10.1016/0031-9422(86)80027-9
https://doi.org/10.1016/S0031-9422(01)00413-7
17-(2-hydroxy-6-methylhept-5-en-2-yl)-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,16-diol 85082126 Click to see CC(=CCCC(C)(C1C2CCC3C4(CCC(C(C4CCC3(C2(CC1O)C)C)(C)C)O)C)O)C 460.70 unknown https://doi.org/10.1248/CPB.51.479
17-(2,6-dihydroxy-6-methylhept-4-en-2-yl)-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,16-diol 73119259 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CC(C4C(C)(CC=CC(C)(C)O)O)O)C)C)C 476.70 unknown https://doi.org/10.1248/CPB.51.479
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/10.1002/CHIN.200342183
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(1R,2S,3R,4S,5R,10S,13R,14R,17R)-4,10,13,14-tetramethyl-17-[(2S)-6-methylhept-5-en-2-yl]-1,2,3,4,5,6,7,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthrene-1,2,3-triol 162843570 Click to see CC1C2CCC3=C(C2(C(C(C1O)O)O)C)CCC4(C3(CCC4C(C)CCC=C(C)C)C)C 444.70 unknown https://doi.org/10.1016/0031-9422(88)83028-0
29-Norlanosta-8,24-diene-1alpha,2alpha,3beta-triol 14191334 Click to see CC1C2CCC3=C(C2(C(C(C1O)O)O)C)CCC4(C3(CCC4C(C)CCC=C(C)C)C)C 444.70 unknown https://doi.org/10.1016/0031-9422(88)83028-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
[(1S,3S,4S,6S,8S,11R,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]-4-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 162950425 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C)O)OC(=O)C)C)C 484.80 unknown https://doi.org/10.1016/0031-9422(88)83028-0
[6-Hydroxy-7,7,12,16-tetramethyl-15-(6-methylhept-5-en-2-yl)-4-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 14191330 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C)O)OC(=O)C)C)C 484.80 unknown https://doi.org/10.1016/0031-9422(88)83028-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids
(3S,5S,8R,9R,10R,13R,14R)-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15-decahydro-1H-cyclopenta[a]phenanthren-3-ol 162962279 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CC=C4)C)C)C 316.50 unknown https://doi.org/10.1016/S0031-9422(01)00413-7
16-hydroperoxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-ol 163011085 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4=CC(CC43C)OO)C)C 348.50 unknown https://doi.org/10.1016/0031-9422(92)80364-K
4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15-decahydro-1H-cyclopenta[a]phenanthren-3-ol 85086993 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CC=C4)C)C)C 316.50 unknown https://doi.org/10.1016/0031-9422(86)80027-9
https://doi.org/10.1016/S0031-9422(01)00413-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-beta-hydroxysteroids
(3S,5R,8R,9R,10R,13R,14R)-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15-decahydro-1H-cyclopenta[a]phenanthren-3-ol 12071383 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CC=C4)C)C)C 316.50 unknown https://doi.org/10.1016/0031-9422(86)80027-9
https://doi.org/10.1016/S0031-9422(01)00413-7
(3S,5R,8R,9R,10R,14R,16S)-16-hydroperoxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-ol 163011086 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4=CC(CC43C)OO)C)C 348.50 unknown https://doi.org/10.1016/0031-9422(92)80364-K
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(15-Hydroxy-4,8,10,14-tetramethyl-3-oxo-1,2,5,6,7,9,11,12,13,15-decahydrocyclopenta[a]phenanthren-4-yl)methyl acetate 22297209 Click to see CC(=O)OCC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(C(C=C4)O)C)C)C 388.50 unknown https://doi.org/10.1016/S0031-9422(01)00413-7
(5R,8R,9R,10R,13R,14R,15S)-15-hydroxy-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15-decahydrocyclopenta[a]phenanthren-3-one 5318259 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(C(C=C4)O)C)C)C 330.50 unknown https://doi.org/10.1016/S0031-9422(01)00413-7
(5R,8R,9R,10R,14R,16S)-16-hydroperoxy-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-3-one 162960353 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4=CC(CC43C)OO)C)C 346.50 unknown https://doi.org/10.1016/0031-9422(92)80364-K
(5R,8R,9R,10R,14R)-16-hydroperoxy-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-3-one 101630482 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4=CC(CC43C)OO)C)C 346.50 unknown https://doi.org/10.1016/0031-9422(92)80364-K
(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/10.1016/S0031-9422(01)00413-7
https://doi.org/10.1055/S-2006-959594
https://doi.org/10.1016/0031-9422(86)80027-9
(5S,8R,9R,10R,13R,14R)-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15-decahydrocyclopenta[a]phenanthren-3-one 162901806 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CC=C4)C)C)C 314.50 unknown https://doi.org/10.1016/S0031-9422(01)00413-7
15-Hydroxy-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15-decahydrocyclopenta[a]phenanthren-3-one 78385083 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(C(C=C4)O)C)C)C 330.50 unknown https://doi.org/10.1016/S0031-9422(01)00413-7
16-Hydroperoxy-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-3-one 162960352 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4=CC(CC43C)OO)C)C 346.50 unknown https://doi.org/10.1016/0031-9422(92)80364-K
28-Acetoxy-15alpha-hydroxymansumbinone 636531 Click to see CC(=O)OCC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(C(C=C4)O)C)C)C 388.50 unknown https://doi.org/10.1016/S0031-9422(01)00413-7
4,4,8,10,14-Pentamethyl-1,2,5,6,7,9,11,12,13,15-decahydrocyclopenta[a]phenanthren-3-one 53420917 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CC=C4)C)C)C 314.50 unknown https://doi.org/10.1016/0031-9422(86)80027-9
https://doi.org/10.1016/S0031-9422(01)00413-7
Mansumbinone 12071382 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4C3(CC=C4)C)C)C 314.50 unknown https://doi.org/10.1016/S0031-9422(01)00413-7
https://doi.org/10.1055/S-2006-959594
https://doi.org/10.1016/0031-9422(86)80027-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Querciturone 5274585 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
4'-[(6-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)oxy]-2'-hydroxy-3',6'-dimethoxy-alpha,beta-dihydrochalcone 10699171 Click to see COC1=CC(=C(C(=C1C(=O)CCC2=CC=CC=C2)O)OC)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O 626.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-chromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl] 3,4,5-trihydroxybenzoate 5480249 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 616.50 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database

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