Euclea natalensis - Unknown
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Details Top

Internal ID UUID64401bb727d80738911823
Scientific name Euclea natalensis
Authority A.DC.
First published in Prodr. 8: 218 (1844)

Description Top

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Synonyms Top

Scientific name Authority First published in
Royena macrophylla E.Mey. ex A.DC. Prodr. 8: 218 (1844)

Common names Top

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Language Common/alternative name
Afrikaans harige ghwarrie
ts nhlangulane
Chinese 南非海柿

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Euclea natalensis subsp. acutifolia F.White Bull. Jard. Bot. Natl. Belg. 50: 397 (1980)
Euclea natalensis subsp. angolensis F.White Bull. Jard. Bot. Natl. Belg. 50: 397 (1980)
Euclea natalensis subsp. angustifolia F.White Bull. Jard. Bot. Natl. Belg. 50: 397 (1980)
Euclea natalensis subsp. capensis F.White Bull. Jard. Bot. Natl. Belg. 50: 397 (1980)
Euclea natalensis subsp. magutensis F.White Bull. Jard. Bot. Natl. Belg. 50: 398 (1980)
Euclea natalensis subsp. natalensis Unknown
Euclea natalensis subsp. obovata F.White Bull. Jard. Bot. Natl. Belg. 50: 398 (1980)
Euclea natalensis subsp. rotundifolia F.White Bull. Jard. Bot. Natl. Belg. 50: 398 (1980)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
    • Northeast Tropical Africa
      • Somalia
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland
    • West-central Tropical Africa
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000681111
Tropicos 11500031
KEW urn:lsid:ipni.org:names:323328-1
The Plant List kew-2802685
Open Tree Of Life 520661
NCBI Taxonomy 85202
IUCN Red List 173487
IPNI 323328-1
iNaturalist 430991
GBIF 6056978
Freebase /m/012bd6vh
EPPO EULNA
Wikipedia Euclea_natalensis
CMAUP NPO11261

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
A Review of the Potential of Poly-(lactide-co-glycolide) Nanoparticles as a Delivery System for an Active Antimycobacterial Compound, 7-Methyljuglone Diedericks B, Kok AM, Mandiwana V, Lall N Pharmaceutics 01-Feb-2024
PMCID:PMC10893214
doi:10.3390/pharmaceutics16020216
PMID:38399270
The Genus Diospyros: A Review of Novel Insights into the Biological Activity and Species of Mozambican Flora Ribeiro A, Serrano R, da Silva IB, Gomes ET, Pinto JF, Silva O Plants (Basel) 31-Jul-2023
PMCID:PMC10421099
doi:10.3390/plants12152833
PMID:37570987
Ethnobotanical uses, phytochemistry and biological activity of the genus Euclea: A review Taye AD, Bizuneh GK, Kasahun AE Front Pharmacol 19-Apr-2023
PMCID:PMC10154578
doi:10.3389/fphar.2023.1170145
PMID:37153774
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
The molecular interplay of known phytochemicals as Culex pipiens and Rift Valley fever virus inhibitors through molecular docking Abutaha N, AL-Mekhlafi FA, Wadaan MA, Moustafa Rady A, Baabbad AA, Al-Khalifa MS Saudi J Biol Sci 01-Mar-2023
PMCID:PMC10036733
doi:10.1016/j.sjbs.2023.103611
PMID:36970253
Diospyros villosa Root Monographic Quality Studies Ribeiro A, Serrano R, da Silva IB, Gomes ET, Pinto JF, Silva O Plants (Basel) 14-Dec-2022
PMCID:PMC9781556
doi:10.3390/plants11243506
PMID:36559618
Medicinal plants used for the management of respiratory diseases in Zimbabwe: Review and perspectives potential management of COVID-19 Nyagumbo E, Pote W, Shopo B, Nyirenda T, Chagonda I, Mapaya RJ, Maunganidze F, Mavengere WN, Mawere C, Mutasa I, Kademeteme E, Maroyi A, Taderera T, Bhebhe M Phys Chem Earth (2002) 21-Sep-2022
PMCID:PMC9489988
doi:10.1016/j.pce.2022.103232
PMID:36161239
Zirconia-based nanomaterials: recent developments in synthesis and applications Kumari N, Sareen S, Verma M, Sharma S, Sharma A, Sohal HS, Mehta SK, Park J, Mutreja V Nanoscale Adv 23-Aug-2022
PMCID:PMC9552756
doi:10.1039/d2na00367h
PMID:36321156
Nutritional composition and sensory Properties of wheat muffins enriched with Gonimbrasia zambesina, walker caterpillar flour Ouma FO, Muriithi AN, Anyango JO Int J Trop Insect Sci 03-Aug-2022
PMCID:PMC9362011
doi:10.1007/s42690-022-00848-w
PMID:35968495
Topical Agents for Nonrestorative Management of Dental Erosion: A Narrative Review Chawhuaveang DD, Yu OY, Yin IX, Lam WY, Chu CH Healthcare (Basel) 28-Jul-2022
PMCID:PMC9408325
doi:10.3390/healthcare10081413
PMID:36011070
Ethnopharmacological Study of Medicinal Plants Used for the Treatment of Cardiovascular Diseases and Their Associated Risk Factors in sub-Saharan Africa Odukoya JO, Odukoya JO, Mmutlane EM, Ndinteh DT Plants (Basel) 23-May-2022
PMCID:PMC9143319
doi:10.3390/plants11101387
PMID:35631812
A Review on Current Designation of Metallic Nanocomposite Hydrogel in Biomedical Applications Dzulkharnien NS, Rohani R Nanomaterials (Basel) 10-May-2022
PMCID:PMC9146518
doi:10.3390/nano12101629
PMID:35630851
Quorum sensing modulation and inhibition in biofilm forming foot ulcer pathogens by selected medicinal plants Mashamba TG, Adeosun IJ, Baloyi IT, Tshikalange ET, Cosa S Heliyon 27-Apr-2022
PMCID:PMC9062679
doi:10.1016/j.heliyon.2022.e09303
PMID:35520625
Antidiabetic Phytochemicals From Medicinal Plants: Prospective Candidates for New Drug Discovery and Development Alam S, Sarker MM, Sultana TN, Chowdhury MN, Rashid MA, Chaity NI, Zhao C, Xiao J, Hafez EE, Khan SA, Mohamed IN Front Endocrinol (Lausanne) 24-Feb-2022
PMCID:PMC8907382
doi:10.3389/fendo.2022.800714
PMID:35282429
Metabolomic profile of medicinal plants with anti-RVFV activity More GK, Vervoort J, Steenkamp PA, Prinsloo G Heliyon 12-Feb-2022
PMCID:PMC8857432
doi:10.1016/j.heliyon.2022.e08936
PMID:35243061

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Acylaminobenzoic acid and derivatives
4-[(2-amino-4-oxo-1H-pteridin-6-yl)methyl-formylamino]benzoic acid 97575 Click to see C1=CC(=CC=C1C(=O)O)N(CC2=CN=C3C(=N2)C(=O)N=C(N3)N)C=O 340.29 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
(1S,12R)-8,12,17-trihydroxy-6,15-dimethylpentacyclo[10.7.1.02,11.04,9.013,18]icosa-2(11),4(9),5,7,13(18),14,16-heptaene-3,10,19-trione 101821189 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C4CC3(C5=C(C4=O)C(=CC(=C5)C)O)O 376.40 unknown https://doi.org/10.1039/C39760000241
https://doi.org/10.1016/0031-9422(77)83026-4
5-Hydroxy-7-methyl-tetralin-1,4-dione 16072923 Click to see CC1=CC2=C(C(=O)CCC2=O)C(=C1)O 190.19 unknown https://doi.org/10.1016/J.SAJB.2005.09.009
https://doi.org/10.1021/NP030465D
https://doi.org/10.1248/BPB.31.1429
7-Methyljuglone 26905 Click to see CC1=CC2=C(C(=O)C=CC2=O)C(=C1)O 188.18 unknown https://doi.org/10.1248/BPB.31.1429
https://doi.org/10.1016/J.SAJB.2005.09.009
8-Hydroxy-2-(8-hydroxy-6-methyl-1,4-dioxonaphthalen-2-yl)-6-methylnaphthalene-1,4-dione 167673 Click to see CC1=CC2=C(C(=C1)O)C(=O)C(=CC2=O)C3=CC(=O)C4=C(C3=O)C(=CC(=C4)C)O 374.30 unknown https://doi.org/10.1016/J.SAJB.2005.09.009
8-Hydroxy-7-(4-hydroxy-2-methyl-5,8-dioxonaphthalen-1-yl)-2-(8-hydroxy-6-methyl-1,4-dioxonaphthalen-2-yl)-6-methylnaphthalene-1,4-dione 635975 Click to see CC1=CC2=C(C(=C1)O)C(=O)C(=CC2=O)C3=CC(=O)C4=C(C3=O)C(=C(C(=C4)C)C5=C6C(=O)C=CC(=O)C6=C(C=C5C)O)O 560.50 unknown https://doi.org/10.1016/0031-9422(77)83026-4
8,12,17-Trihydroxy-6,15-dimethylpentacyclo[10.7.1.02,11.04,9.013,18]icosa-2(11),4(9),5,7,13(18),14,16-heptaene-3,10,19-trione 85867621 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C4CC3(C5=C(C4=O)C(=CC(=C5)C)O)O 376.40 unknown https://doi.org/10.1039/C39760000241
https://doi.org/10.1016/0031-9422(77)83026-4
Diospyrin 308140 Click to see CC1=CC2=C(C(=C1)O)C(=O)C=C(C2=O)C3=C(C4=C(C=C3C)C(=O)C=CC4=O)O 374.30 unknown https://doi.org/10.1248/BPB.31.1429
https://doi.org/10.1016/J.SAJB.2005.09.009
Isodiospyrin 99298 Click to see CC1=CC2=C(C(=O)C=CC2=O)C(=C1C3=C4C(=O)C=CC(=O)C4=C(C=C3C)O)O 374.30 unknown https://doi.org/10.1016/J.SAJB.2005.09.009
Juglone 3806 Click to see C1=CC2=C(C(=O)C=CC2=O)C(=C1)O 174.15 unknown https://doi.org/10.1248/BPB.31.1429
Neodiospyrin 16072922 Click to see CC1=CC2=C(C(=C1)O)C(=O)C(=CC2=O)C3=C4C(=O)C=CC(=O)C4=C(C=C3C)O 374.30 unknown https://doi.org/10.1016/J.SAJB.2005.09.009
https://doi.org/10.1248/BPB.31.1429
> Benzenoids / Tetralins
(4R)-4,8-dihydroxy-6-methyl-tetralin-1-one 5273357 Click to see CC1=CC2=C(C(=O)CCC2O)C(=C1)O 192.21 unknown https://doi.org/10.1021/NP030465D
https://doi.org/10.1016/J.SAJB.2005.09.009
https://doi.org/10.1248/BPB.31.1429
(R)-Shinanolone 12315505 Click to see CC1=CC2=C(C(=O)CCC2O)C(=C1)O 192.21 unknown https://doi.org/10.1248/BPB.31.1429
https://doi.org/10.1021/NP030465D
> Lignans, neolignans and related compounds
(4R)-7-[(1R,2R)-1,8-dihydroxy-6-methyl-4-oxo-2,3-dihydro-1H-naphthalen-2-yl]-4,8-dihydroxy-6-methyl-3,4-dihydro-2H-naphthalen-1-one 162957333 Click to see CC1=CC2=C(C(C(CC2=O)C3=C(C4=C(C=C3C)C(CCC4=O)O)O)O)C(=C1)O 382.40 unknown https://doi.org/10.1021/NP030465D
(4S)-7-[(1S,2R)-1,8-dihydroxy-6-methyl-4-oxo-2,3-dihydro-1H-naphthalen-2-yl]-4,8-dihydroxy-6-methyl-3,4-dihydro-2H-naphthalen-1-one 162957334 Click to see CC1=CC2=C(C(C(CC2=O)C3=C(C4=C(C=C3C)C(CCC4=O)O)O)O)C(=C1)O 382.40 unknown https://doi.org/10.1021/NP030465D
Octahydroeuclein 5273355 Click to see CC1=CC2=C(C(C(CC2=O)C3=C(C4=C(C=C3C)C(CCC4=O)O)O)O)C(=C1)O 382.40 unknown https://doi.org/10.1021/NP030465D
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
Abscisic acid 5280896 Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C 264.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,5R,8S)-8-hydroxy-5-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]-2-oxabicyclo[3.3.1]nonane-3,6-dione 101683232 Click to see CC(=CCCC(=CCCC(=CCC12CC(C(CC1=O)O)OC(=O)C2)C)C)C 374.50 unknown https://doi.org/10.1016/0031-9422(77)83026-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,4S,5R,8S,10S,13S,14R,17S,18R,19S,20S)-10-hydroxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-23-one 162881016 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)O)(C)C)C)C 454.70 unknown https://doi.org/10.1016/0031-9422(75)85138-7
(4,5,9,9,13,19,20-Heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl) acetate 73800256 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)OC(=O)C)(C)C)C)C 496.70 unknown https://doi.org/10.1016/0031-9422(75)85138-7
[(1R,3aR,5aR,5bR,7aR,9S,11aS,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] (E)-3-(4-methoxy-3-methylphenyl)prop-2-enoate 163027608 Click to see CC1=C(C=CC(=C1)C=CC(=O)OC2CCC3(C4CCC5C6C(CCC6(CCC5(C4(CCC3C2(C)C)C)C)C)C(=C)C)C)OC 600.90 unknown https://doi.org/10.1021/NP030465D
[(1S,4S,5R,8R,10S,13S,14R,17S,18R,19S,20S)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl] acetate 162938227 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)OC(=O)C)(C)C)C)C 496.70 unknown https://doi.org/10.1016/0031-9422(75)85138-7
2-Propenoic acid, 3-(3-hydroxy-4-methoxyphenyl)-, (3beta,19epsilon)-lup-20(29)-en-3-yl ester, (2E)- 162801021 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC(=C(C=C6)OC)O)C)C 602.90 unknown https://doi.org/10.1021/NP030465D
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1021/NP030465D
CID 4450096 4450096 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)O)(C)C)C)C 454.70 unknown https://doi.org/10.1016/0031-9422(75)85138-7
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/10.1021/NP030465D
https://doi.org/10.1248/BPB.31.1429
Lup-20(29)-ene-3beta,28-diol 221023 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1021/NP030465D
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/10.1248/BPB.31.1429
https://doi.org/10.1021/NP030465D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids
(5S,6S,8S,9S,10S,11R,13S,14S)-6,11-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one 92835934 Click to see CC12CCCCC1C(CC3C2C(CC4(C3CCC4=O)C)O)O 306.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
(3beta,5alpha,7alpha)-3,7-Dihydroxyandrostan-17-one 9815044 Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O 306.40 unknown via CMAUP database
(3R,5R,7S,8R,9S,10S,13S,14S)-3,7-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one 57386710 Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O 306.40 unknown via CMAUP database
(3R,5R,8R,9S,10S,13S,14S,17S)-3,17-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one 69924431 Click to see CC12CCC3C(C1CCC2O)C(=O)CC4C3(CCC(C4)O)C 306.40 unknown via CMAUP database
(3R,5R,8R,9S,10S,13S,14S)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthrene-7,17-dione 57386713 Click to see CC12CCC(CC1CC(=O)C3C2CCC4(C3CCC4=O)C)O 304.40 unknown via CMAUP database
(3R,5S,6S,8R,9S,10R,13S,14S)-3,6-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one 69766330 Click to see CC12CCC(CC1C(CC3C2CCC4(C3CCC4=O)C)O)O 306.40 unknown via CMAUP database
(3S,5R,7R,8S,9S,10S,13R,14S,16S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,7,16-triol 99574281 Click to see CC12CCC3C(C1CC(C2)O)C(CC4C3(CCC(C4)O)C)O 308.50 unknown via CMAUP database
(3S,5R,7S,8S,9S,10S,13S,14S,16S)-3,7,16-trihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one 99572894 Click to see CC12CCC(CC1CC(C3C2C(=O)CC4(C3CC(C4)O)C)O)O 322.40 unknown via CMAUP database
(3S,5R,8S,9S,10S,13R,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one 99573267 Click to see CC12CCC3C(C1CC(C2)O)C(=O)CC4C3(CCC(C4)O)C 306.40 unknown via CMAUP database
(3S,5R,8S,9S,10S,13R,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one 99573266 Click to see CC12CCC3C(C1CC(C2)O)C(=O)CC4C3(CCC(C4)O)C 306.40 unknown via CMAUP database
(3S,5S,6S,8S,9S,10R,13R,14S,16R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,6,16-triol 99574278 Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(C4)O)C)O 308.50 unknown via CMAUP database
(3S,5S,8S,9S,10R,13R,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 99571962 Click to see CC12CCC3C(C1CC(C2)O)CC(=O)C4C3(CCC(C4)O)C 306.40 unknown via CMAUP database
(3S,5S,8S,9S,10R,13R,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 99571961 Click to see CC12CCC3C(C1CC(C2)O)CC(=O)C4C3(CCC(C4)O)C 306.40 unknown via CMAUP database
(3S,5S,8S,9S,10S,13S,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one 99601533 Click to see CC12CCC(CC1CCC3C2C(=O)CC4(C3CC(C4)O)C)O 306.40 unknown via CMAUP database
(3S,5S,8S,9S,10S,13S,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one 99575783 Click to see CC12CCC(CC1CCC3C2C(=O)CC4(C3CC(C4)O)C)O 306.40 unknown via CMAUP database
(5R,8S,9S,10S,13R,14S,16S)-16-hydroxy-10,13-dimethyl-2,4,5,6,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,7-dione 99571971 Click to see CC12CCC3C(C1CC(C2)O)C(=O)CC4C3(CCC(=O)C4)C 304.40 unknown via CMAUP database
(5S,6R,8S,9S,10R,13R,14S,16S)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one 99573707 Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(=O)C4)C)O 306.40 unknown via CMAUP database
(5S,6S,8S,9S,10R,13R,14S,16R)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one 99573706 Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(=O)C4)C)O 306.40 unknown via CMAUP database
(5S,6S,8S,9S,10R,13R,14S,16S)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one 99573705 Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(=O)C4)C)O 306.40 unknown via CMAUP database
(5S,6S,8S,9S,10S,11R,13S,14S)-6,11-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one 99574441 Click to see CC12CCCC1C3CC(C4CC(=O)CCC4(C3C(C2)O)C)O 306.40 unknown via CMAUP database
(5S,8S,9R,10S,13S,14S,16R)-9,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,11-dione 99571360 Click to see CC12CCC(=O)CC1CCC3C2(C(=O)CC4(C3CC(C4)O)C)O 320.40 unknown via CMAUP database
(5S,8S,9R,10S,13S,14S,16S)-9,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,11-dione 99571358 Click to see CC12CCC(=O)CC1CCC3C2(C(=O)CC4(C3CC(C4)O)C)O 320.40 unknown via CMAUP database
(5S,8S,9S,10S,13S,14S,16R)-16-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 99574177 Click to see CC12CCC(=O)CC1CCC3C2C(=O)CC4(C3CC(C4)O)C 304.40 unknown via CMAUP database
(5S,8S,9S,10S,13S,14S,16S)-16-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 99574175 Click to see CC12CCC(=O)CC1CCC3C2C(=O)CC4(C3CC(C4)O)C 304.40 unknown via CMAUP database
11-Hydroxyandrosterone 21139727 Click to see CC12CCC(CC1CCC3C2C(CC4(C3CCC4=O)C)O)O 306.40 unknown via CMAUP database
11alpha-Hydroxy-5alpha-androstane-3,17-dione 101709630 Click to see CC12CCC(=O)CC1CCC3C2C(CC4(C3CCC4=O)C)O 304.40 unknown via CMAUP database
11alpha,16alpha-Dihydroxy-5alpha-androstan-3-one 100922644 Click to see CC12CCC(=O)CC1CCC3C2C(CC4(C3CC(C4)O)C)O 306.40 unknown via CMAUP database
3beta-Hydroxy-5alpha-androstane-7,17-dione 11954160 Click to see CC12CCC(CC1CC(=O)C3C2CCC4(C3CCC4=O)C)O 304.40 unknown via CMAUP database
3beta,6alpha,17beta-Trihydroxy-5alpha-androstane 170796 Click to see CC12CCC3C(C1CCC2O)CC(C4C3(CCC(C4)O)C)O 308.50 unknown via CMAUP database
5,17beta-Dihydroxy-5alpha-androstane-3-one 10979706 Click to see CC12CCC3C(C1CCC2O)CCC4(C3(CCC(=O)C4)C)O 306.40 unknown via CMAUP database
5alpha-Androstan-11-one, 3alpha,17beta-dihydroxy- 10125601 Click to see CC12CCC(CC1CCC3C2C(=O)CC4(C3CCC4O)C)O 306.40 unknown via CMAUP database
5alpha-Androstan-3-one, 11alpha,17beta-dihydroxy- 22796602 Click to see CC12CCC(=O)CC1CCC3C2C(CC4(C3CCC4O)C)O 306.40 unknown via CMAUP database
5alpha-Androstan-3beta,17beta-diol-7-one 11868973 Click to see CC12CCC3C(C1CCC2O)C(=O)CC4C3(CCC(C4)O)C 306.40 unknown via CMAUP database
5alpha-Androstan-6-one, 3beta,17beta-dihydroxy- 11551286 Click to see CC12CCC3C(C1CCC2O)CC(=O)C4C3(CCC(C4)O)C 306.40 unknown via CMAUP database
5alpha-Androstane-3,7,17-trione 11266632 Click to see CC12CCC(=O)CC1CC(=O)C3C2CCC4(C3CCC4=O)C 302.40 unknown via CMAUP database
5alpha-Androstane-3beta,11alpha,16beta-triol 100922640 Click to see CC12CCC(CC1CCC3C2C(CC4(C3CC(C4)O)C)O)O 308.50 unknown via CMAUP database
5alpha-Androstane-3beta,11alpha,17beta-triol 57396177 Click to see CC12CCC(CC1CCC3C2C(CC4(C3CCC4O)C)O)O 308.50 unknown via CMAUP database
6alpha-Hydroxy-EPIA 15917986 Click to see CC12CCC(CC1C(CC3C2CCC4(C3CCC4=O)C)O)O 306.40 unknown via CMAUP database
7-beta-Hydroxyepiandrosterone 9836181 Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O 306.40 unknown via CMAUP database
Androstan-3-one, 6,17-dihydroxy-, (5alpha,6alpha,17beta)- 15838416 Click to see CC12CCC3C(C1CCC2O)CC(C4C3(CCC(=O)C4)C)O 306.40 unknown via CMAUP database
Androstan-6-one, 3,17-dihydroxy-, (3alpha,5alpha,17beta)- 15929496 Click to see CC12CCC3C(C1CCC2O)CC(=O)C4C3(CCC(C4)O)C 306.40 unknown via CMAUP database
Androstane-3,17-dione, 6-hydroxy-, (5alpha,6alpha)- 22296022 Click to see CC12CCC(=O)CC1C(CC3C2CCC4(C3CCC4=O)C)O 304.40 unknown via CMAUP database
Jgd4N79M5A 68995028 Click to see CC12CCC3C(C1CCC2O)C(CC4C3(CCC(C4)O)C)O 308.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
10-Hydroxy-3-oxoestr-4-en-17-yl acetate 91691749 Click to see CC(=O)OC1CCC2C1(CCC3C2CCC4=CC(=O)CCC34O)C 332.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-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 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(75)85138-7
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/10.1016/0031-9422(75)85138-7
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron 21883788 Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-] 116.07 unknown via CMAUP database
Butanedioate;hydron 21952380 Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-] 118.09 unknown via CMAUP database
Glutaric acid 743 Click to see C(CC(=O)O)CC(=O)O 132.11 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
2-Oxonioacetate 3698251 Click to see C(C(=O)[O-])[OH2+] 76.05 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinoline carboxylic acids
Quininic acid 345824 Click to see COC1=CC2=C(C=CN=C2C=C1)C(=O)O 203.19 unknown via CMAUP database

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