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Eucalyptus camaldulensis

Eucalyptus camaldulensis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644039f0972e7586718575
Scientific name Eucalyptus camaldulensis
Authority Dehnh.
First published in Cat. Pl. Horti Camald. , ed. 2: 20 (1832)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eucalyptus camaldulensis var. camaldulensis Dehnh. -

Common names Top

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Language Common/alternative name
English murray red gum
English river red gum
English river redgum
Spanish eucalipto colorado
Afrikaans rooibloekom
Amharic ቀይ ባሕር ዛፍ
Arabic سرول
Arabic كينا
Arabic أوكالبتوس كمالدولي
Arabic الكافور
Arabic شجر صيدله
Arabic يوكالبتوس
Azerbaijani dimdikvari evkalipt
Czech blahovičník pobřežní
German roter eukalyptus
Esperanto rivera eŭkalipto
Persian اکالیپتوس کامالدول
Finnish punaeukalyptus
French gommier rouge
Galician eucalipto vermello
Hebrew אקליפטוס המקור
Upper Sorbian Čerwjeny eukalyptowc
Japanese カマダルユーカリ
Japanese ユーカリ・カマルドレンシス
Japanese セキザイユーカリ
Japanese ロストラタユーカリ
Japanese リバーレッドガム
Japanese リバー・レッドガム
Japanese ユーカリプタス・カマルドゥレンシス
Macedonian камалдулски евкалипт
Polish eukaliptus kamaldulski
Quechua china kalistu
Quechua chhina kalistu
Quechua chinakalistu
Quechua puka kalistu
Russian Эвкалипт камальдульский
Russian Речная красная камедь
Ukrainian Евкаліпт камальдульський
Vietnamese bạch đàn trắng
wo xott-biteel
Chinese 赤桉
Chinese 短喙赤桉
Chinese 渐尖赤桉
Chinese 洋草果

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Eucalyptus camaldulensis subsp. acuta Brooker & M.W.McDonald Austral. Syst. Bot. 22: 270 (2009)
Eucalyptus camaldulensis subsp. arida Brooker & M.W.McDonald Austral. Syst. Bot. 22: 273 (2009)
Eucalyptus camaldulensis subsp. camaldulensis Unknown
Eucalyptus camaldulensis subsp. minima Brooker & M.W.McDonald Austral. Syst. Bot. 22: 275 (2009)
Eucalyptus camaldulensis subsp. obtusa (Blakely) Brooker & M.W.McDonald Austral. Syst. Bot. 22: 277 (2009)
Eucalyptus camaldulensis subsp. refulgens Brooker & M.W.McDonald Austral. Syst. Bot. 22: 279 (2009)

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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
      • Uganda
    • Macaronesia
      • Canary Islands
    • Middle Atlantic Ocean
      • Ascension
    • Northeast Tropical Africa
      • Chad
      • Eritrea
      • Ethiopia
    • Northern Africa
      • Algeria
      • Libya
      • Morocco
      • Tunisia
    • South Tropical Africa
      • Angola
      • Malawi
      • Zambia
    • Southern Africa
      • Cape Provinces
      • Free State
      • Lesotho
    • West Tropical Africa
      • Benin
      • Gambia
    • West-central Tropical Africa
      • Rwanda
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
    • Caucasus
      • Transcaucasus
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Taiwan
    • Western Asia
      • East Aegean Islands
      • Palestine
      • Turkey
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
      • Pakistan
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Nicobar Nicobar
  • Australasia
    • Australia
      • New South Wales
      • Northern Territory
      • Queensland
      • South Australia
      • Victoria
      • Western Australia
  • Europe
    • Southeastern Europe
      • Albania
      • Greece
      • Italy
      • Sicilia
    • Southwestern Europe
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Mexico
      • Mexico Southeast
      • Mexico Southwest
    • Southwestern U.S.A.
      • Arizona
      • California
  • Pacific
    • North-central Pacific
      • Hawaii
    • South-central Pacific
      • Easter Island
    • Southwestern Pacific
      • New Caledonia
  • Southern America
    • Caribbean
      • Leeward Islands
      • Puerto Rico
    • Central America
      • Costa Rica
      • El Salvador
      • Nicaragua
      • Panamá
    • Southern South America
      • Argentina Northeast
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000954597
UNII T68A06JLOF
USDA Plants EUCA2
Tropicos 22101716
INPN 97398
KEW urn:lsid:ipni.org:names:592777-1
The Plant List kew-72616
Open Tree Of Life 505234
Observations.org 117679
NCBI Taxonomy 34316
Nature Serve 2.143883
IUCN Red List 61909812
IPNI 592777-1
iNaturalist 64128
GBIF 3176197
Freebase /m/05lqxj
EPPO EUCCM
EOL 301398
Calflora (Californian flora) 3531
USDA GRIN 15867
Wikipedia Eucalyptus_camaldulensis
CMAUP NPO10849
PaleoBotany 5429

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_019915185.1 ASM1991518v1 Contig BCL, KAUST 2021-09-09 51.0x 503.76 Mb

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
Study of medicinal plants used in ethnoveterinary medical system in riverine areas of Punjab, Pakistan Umair M, Altaf M, Ahsan T, Bussmann RW, Abbasi AM, Gatasheh MK, Elrobh M J Ethnobiol Ethnomed 07-May-2024
PMCID:PMC11077875
doi:10.1186/s13002-024-00686-9
PMID:38715115
Detailed analysis of agro-industrial byproducts/wastes to enable efficient sorting for various agro-industrial applications Priyanka G, Singiri JR, Adler-Agmon Z, Sannidhi S, Daida S, Novoplansky N, Grafi G Bioresour Bioprocess 04-May-2024
PMCID:PMC11069496
doi:10.1186/s40643-024-00763-7
PMID:38703254
Multilocus Gene Analyses Indicate Tamarix aphylla as Reservoir Host of Diverse Phytoplasmas Associated with Witches’ Broom and Yellowing Symptomatology Esmaeilzadeh-Hosseini SA, Babaei G, Pacini F, Bertaccini A Plants (Basel) 30-Apr-2024
PMCID:PMC11085372
doi:10.3390/plants13091248
PMID:38732463
The Analgesic Potential of Litsea Species: A Systematic Review Goh MP, Samsul RN, Mohaimin AW, Goh HP, Zaini NH, Kifli N, Ahmad N Molecules 30-Apr-2024
PMCID:PMC11085224
doi:10.3390/molecules29092079
PMID:38731572
Medicinal ethnoveterinary plants used for treating livestock ailments in the omo-gibe and rift valley basins of Ethiopia Wendimu A, Bojago E, Abrham Y BMC Vet Res 30-Apr-2024
PMCID:PMC11059770
doi:10.1186/s12917-024-04019-6
PMID:38689300
Ethnobotanical survey on herbal remedies for the management of type 2 diabetes in the Casablanca-Settat region, Morocco Arraji M, Al Wachami N, Boumendil K, Chebabe M, Mochhoury L, Laamiri FZ, Barkaoui M, Chahboune M BMC Complement Med Ther 15-Apr-2024
PMCID:PMC11017650
doi:10.1186/s12906-024-04468-4
PMID:38622669
Integration of local knowledge in the secondary school chemistry curriculum - A few examples of ethno-chemistry from Zambia Chibuye B, Singh IS Heliyon 08-Apr-2024
PMCID:PMC11021971
doi:10.1016/j.heliyon.2024.e29174
PMID:38633622
Antimicrobial and Cytotoxic Effect of Positively Charged Nanosilver-Coated Silk Sutures Monroy Caltzonci DA, Rasu Chettiar AD, Ibarra VC, Marasamy L, Loredo-Tovías M, Acosta-Torres LS, Manisekaran R ACS Omega 08-Apr-2024
PMCID:PMC11025086
doi:10.1021/acsomega.4c01257
PMID:38645349
Epidemiology and management of Fusarium wilt of Eucalyptus camaldulensis through systemic acquired resistance Ahmad I, Mazhar K, Atiq M, Khalaf AK, Rashid MH, Asif M, Ahmed S, Adil Z, Fayyaz A, Al-Sadoon MK, Al-Otaibi HS PeerJ 29-Mar-2024
PMCID:PMC10984168
doi:10.7717/peerj.17022
PMID:38563017
Genome-Wide Identification, Expression Analysis under Abiotic Stress and Co-Expression Analysis of MATE Gene Family in Torreya grandis Shen H, Hou Y, Wang X, Li Y, Wu J, Lou H Int J Mol Sci 29-Mar-2024
PMCID:PMC11012001
doi:10.3390/ijms25073859
PMID:38612669
Plasticity of repetitive sequences demonstrated by the complete mitochondrial genome of Eucalyptus camaldulensis Fukasawa Y, Driguez P, Bougouffa S, Carty K, Putra A, Cheung MS, Ermini L Front Plant Sci 27-Mar-2024
PMCID:PMC11005031
doi:10.3389/fpls.2024.1339594
PMID:38601302
Chitosan nanoparticle and its effect on Neoscytalidium novaehollandiae, the causal agent of mulberry canker in Tehran Mohammadi N, Safaie N, Nikkhah M, Moradi S Heliyon 26-Mar-2024
PMCID:PMC10999993
doi:10.1016/j.heliyon.2024.e28666
PMID:38590881
Identification of MATE Family and Characterization of GmMATE13 and GmMATE75 in Soybean’s Response to Aluminum Stress Gao P, Han R, Xu H, Wei Y, Yu Y Int J Mol Sci 26-Mar-2024
PMCID:PMC11011378
doi:10.3390/ijms25073711
PMID:38612522
Potential of Thuja occidentalis L. Essential Oil and Water Extracts against Field Crop Pests Gospodarek J, Krajewska A, Paśmionka IB, Bruździńska J, Tamiru G Molecules 24-Mar-2024
PMCID:PMC11013141
doi:10.3390/molecules29071457
PMID:38611736
Synthesis of eco-friendly layered double hydroxide and nanoemulsion for jasmine and peppermint oils and their larvicidal activities against Culex pipiens Linnaeus Radwan IT, Khater HF, Mohammed SH, Khalil A, Farghali MA, Mahmoud MG, Selim A, Manaa EA, Bagato N, Baz MM Sci Rep 22-Mar-2024
PMCID:PMC10959945
doi:10.1038/s41598-024-56802-y
PMID:38519561

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
(3R)-5,8-dihydroxy-3-methyl-3,4-dihydroisochromen-1-one 10442609 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)O 194.18 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1002/HLCA.201000164
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1016/0031-9422(93)85553-4
https://doi.org/10.1016/0031-9422(93)85448-Z
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
6-Methylsalicylic Acid 11279 Click to see CC1=C(C(=CC=C1)O)C(=O)O 152.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzophenones
2,4,6,3',5'-Pentahydroxybenzophenone 19910294 Click to see C1=C(C=C(C=C1O)O)C(=O)C2=C(C=C(C=C2O)O)O 262.21 unknown via CMAUP database
3,4,5,3'-Tetrahydroxybenzophenone 52948815 Click to see C1=CC(=CC(=C1)O)C(=O)C2=CC(=C(C(=C2)O)O)O 246.21 unknown via CMAUP database
3',6-Dihydroxy-2,4,4'-trimethoxybenzophenone 101763992 Click to see COC1=C(C=C(C=C1)C(=O)C2=C(C=C(C=C2OC)OC)O)O 304.29 unknown via CMAUP database
Maclurin 68213 Click to see C1=CC(=C(C=C1C(=O)C2=C(C=C(C=C2O)O)O)O)O 262.21 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Decane 15600 Click to see CCCCCCCCCC 142.28 unknown https://doi.org/10.4314/BCSE.V11I1.21012
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1992.9698059
https://doi.org/10.1080/10412905.2000.9699530
https://doi.org/10.1080/10412905.2000.9712194
https://doi.org/10.4314/BCSE.V11I1.21012
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides
1-(beta-D-Glucopyranosyl)-3-ethyl-4-methyl-1H-pyrrole-2,5-dione 100933901 Click to see CCC1=C(C(=O)N(C1=O)C2C(C(C(C(O2)CO)O)O)O)C 301.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citronellal 7794 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1080/10412905.1991.9697921
Citronellic acid 10402 Click to see CC(CCC=C(C)C)CC(=O)O 170.25 unknown https://doi.org/10.1080/10412905.1991.9697921
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.4314/BCSE.V11I1.21012
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown https://doi.org/10.1021/JF00035A065
https://doi.org/10.4314/BCSE.V11I1.21012
https://doi.org/10.1007/S002170050405
Cuminaldehyde 326 Click to see CC(C)C1=CC=C(C=C1)C=O 148.20 unknown https://doi.org/10.4324/9780203219430_CHAPTER_13
https://doi.org/10.4314/BCSE.V11I1.21012
https://doi.org/10.1080/10412905.1992.9698059
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.4314/BCSE.V11I1.21012
https://doi.org/10.1080/10412905.2000.9712194
https://doi.org/10.1007/S002170050405
https://doi.org/10.1080/10412905.2000.9699530
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1007/S002170050405
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,2R,5R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hexan-2-ol 439727 Click to see CC(C)C12CCC(C1C2)(C)O 154.25 unknown https://doi.org/10.4314/BCSE.V11I1.21012
(1S,3R,5S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol 12314318 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1080/10412905.2000.9712194
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1991.9697921
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698428
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.4314/BCSE.V11I1.21012
Pinocarveol 102667 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1080/10412905.2000.9712194
https://doi.org/10.1080/10412905.1994.9698428
Sabinene hydrate 62367 Click to see CC(C)C12CCC(C1C2)(C)O 154.25 unknown https://doi.org/10.4314/BCSE.V11I1.21012
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(3R)-3alpha-Hydroxy-4beta-isopropylcyclohexene-1-carbaldehyde 91884957 Click to see CC(C)C1CCC(=CC1O)C=O 168.23 unknown https://doi.org/10.1021/JF00035A065
(3S,4S)-3-hydroxy-4-propan-2-ylcyclohexene-1-carbaldehyde 9989621 Click to see CC(C)C1CCC(=CC1O)C=O 168.23 unknown https://doi.org/10.1021/JF00035A065
1-Cyclohexene-1-carboxaldehyde, 3-hydroxy-4-(1-methylethyl)-, cis- 192578 Click to see CC(C)C1CCC(=CC1O)C=O 168.23 unknown https://doi.org/10.1021/JF00035A065
2-Cyclohexen-1-ol, 3-methyl-6-(1-methylethyl)-, (1R,6S)-rel- 85567 Click to see CC1=CC(C(CC1)C(C)C)O 154.25 unknown https://doi.org/10.4314/BCSE.V11I1.21012
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1994.9698428
https://doi.org/10.1080/10412905.1991.9697921
https://doi.org/10.1080/10412905.2000.9699530
https://doi.org/10.4314/BCSE.V11I1.21012
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.4314/BCSE.V11I1.21012
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1080/10412905.2000.9712194
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1007/S002170050405
https://doi.org/10.4314/BCSE.V11I1.21012
Eucamalol 12426239 Click to see CC(C)C1CCC(=CC1O)C=O 168.23 unknown https://doi.org/10.1021/JF00035A065
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.4314/BCSE.V11I1.21012
https://doi.org/10.1080/10412905.2000.9712194
https://doi.org/10.1080/10412905.1991.9697921
Phellandral 89488 Click to see CC(C)C1CCC(=CC1)C=O 152.23 unknown https://doi.org/10.4314/BCSE.V11I1.21012
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.4314/BCSE.V11I1.21012
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.4314/BCSE.V11I1.21012
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1992.9698059
https://doi.org/10.1080/10412905.2000.9699530
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1007/S002170050405
https://doi.org/10.4314/BCSE.V11I1.21012
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1080/10412905.1992.9698059
https://doi.org/10.1007/S002170050405
https://doi.org/10.4314/BCSE.V11I1.21012
Globulol 101716 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.2000.9699530
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4aS,6aR,6aS,6bR,8aR,10S,12aS,13R,14bS)-10-hydroxy-2-(hydroxymethyl)-13-methoxy-1,6a,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 10791592 Click to see CC1C(CCC2(C1C3=CC(C4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)OC)C(=O)O)CO 502.70 unknown https://doi.org/10.1021/NP960535Z
(1R,2R,4aS,6aR,6aS,6bR,8aR,10S,12aS,13S,14bS)-10-hydroxy-2-(hydroxymethyl)-13-methoxy-1,6a,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 154496294 Click to see CC1C(CCC2(C1C3=CC(C4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)OC)C(=O)O)CO 502.70 unknown https://doi.org/10.1021/NP960535Z
(1R,2S,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-2-acetyloxy-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 10577750 Click to see CC1C2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1(C)OC(=O)C)C(=O)O)C)C)(C)C)O)C 514.70 unknown https://doi.org/10.1021/NP960535Z
(1R,3aS,5aR,5bR,7aR,9R,10R,11aR,11bR,13aR,13bR)-10-hydroxy-9-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 102065962 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)OC)O)C)C)C(=O)O 648.90 unknown https://doi.org/10.1055/S-2006-957602
(1R,3aS,5aR,5bR,7aR,9R,10R,11aR,11bR,13aS,13bS)-10-hydroxy-9-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 163185636 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)OC)O)C)C)C(=O)O 648.90 unknown https://doi.org/10.1055/S-2006-957602
(1R,3aS,5aR,5bR,7aR,9R,10R,11aR,11bR,13aS,13bS)-10-hydroxy-9-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 163194777 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C(=O)O 618.80 unknown https://doi.org/10.1055/S-2006-957602
(1R,3aS,5aR,5bR,7aR,9R,10R,11aR,11bR,13aS,13bS)-10-hydroxy-9-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 163189624 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C(=O)O 618.80 unknown https://doi.org/10.1055/S-2006-957602
(1R,3aS,5aR,5bR,7aR,9R,10R,11aR,11bR,13aS,13bS)-9,10-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 162914129 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C(=O)O 472.70 unknown https://doi.org/10.1055/S-2006-957602
(1R,3aS,5aS,5bR,9R,10R,11aR)-9,10-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13b-tetradecahydrocyclopenta[a]chrysene-3a-carboxylic acid 470606 Click to see CC(=C)C1CCC2(C1C3=CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C(=O)O 470.70 unknown https://doi.org/10.1055/S-2006-957602
(1S,2R,4aS,6aR,6aR,6bR,7S,8aR,10R,11R,12aS,13R,14bS)-7,10,11-trihydroxy-13-methoxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 15552098 Click to see CC1CCC2(CCC3(C(=CC(C4C3(C(CC5C4(CC(C(C5(C)C)O)O)C)O)C)OC)C2C1C)C)C(=O)O 518.70 unknown https://doi.org/10.1016/S0031-9422(00)00058-3
(1S,2R,4aS,6aS,6aR,6bR,7S,8aS,10R,11R,12aS,13R,14bS)-7,10,11-trihydroxy-13-methoxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 162951396 Click to see CC1CCC2(CCC3(C(=CC(C4C3(C(CC5C4(CC(C(C5(C)C)O)O)C)O)C)OC)C2C1C)C)C(=O)O 518.70 unknown https://doi.org/10.1016/S0031-9422(00)00058-3
(1S,4R,5S,6S,10R,11R,14S,16R,19R,20S)-4,5,11,15,15,19,20-heptamethyl-24-oxahexacyclo[12.8.2.01,6.07,20.010,19.011,16]tetracos-7-en-23-one 163031367 Click to see CC1CCC23CCC4(C(=CCC5C4(CCC6C5(CCC(C6(C)C)OC2=O)C)C)C3C1C)C 438.70 unknown https://doi.org/10.1055/S-2006-957602
(1S,4S,5R,8R,9R,10R,11R,13S,14R,17S,18R,19S,20R)-10,11-dihydroxy-9-(hydroxymethyl)-4,5,9,13,19,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-23-one 25181529 Click to see CC1CCC23CCC4(C5(CCC6C(C5C=CC4(C2C1C)OC3=O)(CC(C(C6(C)CO)O)O)C)C)C 486.70 unknown https://doi.org/10.1002/HLCA.200890226
(2alpha,3beta)-2,3-Dihydroxyoleana-11,13(18)-dien-28-oic acid 77595191 Click to see CC1(CCC2(CCC3(C(=C2C1)C=CC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C)C(=O)O)C 470.70 unknown https://doi.org/10.1021/NP960535Z
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 345510 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.002
(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/J.PHYTOL.2011.05.002
(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) formate 85116432 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)OC=O)(C)C)C)C 482.70 unknown https://doi.org/10.1021/NP9902340
https://doi.org/10.1016/S0031-9422(00)00058-3
(4,5,9,9,13,19,20-Heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-10-yl) acetate 73819422 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5CCC4(C2C1C)OC3=O)C)OC(=O)C)(C)C)C)C 498.70 unknown https://doi.org/10.1021/NP9902340
(4aS,6aR,6bS,8aR,10S,12aS,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,14b-dodecahydropicene-4a-carboxylic acid 637092 Click to see CC1(CCC2(CCC3(C(=CC=C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 454.70 unknown https://doi.org/10.1021/NP020127X
(4aS,6aR,6bS,8aR,10S,12aS,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,14b-dodecahydropicene-4a-carboxylic acid 12967160 Click to see CC1(CCC2(CCC3(C(=CC=C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 454.70 unknown https://doi.org/10.1021/NP020127X
(4aS,6bR,10S,12aR,14bS)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 5315977 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1021/NP020127X
10-hydroxy-2-(hydroxymethyl)-13-methoxy-1,6a,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 85136190 Click to see CC1C(CCC2(C1C3=CC(C4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)OC)C(=O)O)CO 502.70 unknown https://doi.org/10.1021/NP960535Z
10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,14b-dodecahydropicene-4a-carboxylic acid 22297573 Click to see CC1(CCC2(CCC3(C(=CC=C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 454.70 unknown https://doi.org/10.1021/NP020127X
10-Hydroxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-23-one 73819421 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5CCC4(C2C1C)OC3=O)C)O)(C)C)C)C 456.70 unknown https://doi.org/10.1021/NP9902340
10-Hydroxy-9-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 162990901 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)OC)O)C)C)C(=O)O 648.90 unknown https://doi.org/10.1055/S-2006-957602
10-Hydroxy-9-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 73088393 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C(=O)O 618.80 unknown https://doi.org/10.1055/S-2006-957602
11-Hydroxy-10-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 137796426 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)OC)O)C)C)C2C1)C)C(=O)O)C 648.90 unknown https://doi.org/10.1055/S-2006-957602
11-Hydroxy-10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 75110902 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1)C)C(=O)O)C 618.80 unknown https://doi.org/10.1055/S-2006-957602
2-Acetyloxy-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 85192213 Click to see CC1C2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1(C)OC(=O)C)C(=O)O)C)C)(C)C)O)C 514.70 unknown https://doi.org/10.1021/NP960535Z
3-Acetoxy-11-ursen-28,13-olide 21606662 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/J.PHYTOL.2011.05.002
3-beta-O-(trans-p-Coumaroyl)maslinic acid 14335962 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1)C)C(=O)O)C 618.80 unknown https://doi.org/10.1055/S-2006-957602
3-Hydroxy-11-ursen-28,13-olide 21606663 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/S0031-9422(00)00058-3
https://doi.org/10.1016/J.PHYTOL.2011.05.002
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)00058-3
https://doi.org/10.1016/J.PHYTOL.2011.05.002
https://doi.org/10.1002/HLCA.200890226
https://doi.org/10.1055/S-2006-957602
3-O-Acetyloleanolic acid 151202 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1021/NP020127X
3beta-Hydroxy-28,13-ursanolide 131752032 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5CCC4(C2C1C)OC3=O)C)O)(C)C)C)C 456.70 unknown https://doi.org/10.1055/S-2006-957602
https://doi.org/10.1016/S0031-9422(00)00058-3
4,5,11,15,15,19,20-Heptamethyl-24-oxahexacyclo[12.8.2.01,6.07,20.010,19.011,16]tetracos-7-en-23-one 77212461 Click to see CC1CCC23CCC4(C(=CCC5C4(CCC6C5(CCC(C6(C)C)OC2=O)C)C)C3C1C)C 438.70 unknown https://doi.org/10.1055/S-2006-957602
7,10,11-trihydroxy-13-methoxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 85136327 Click to see CC1CCC2(CCC3(C(=CC(C4C3(C(CC5C4(CC(C(C5(C)C)O)O)C)O)C)OC)C2C1C)C)C(=O)O 518.70 unknown https://doi.org/10.1016/S0031-9422(00)00058-3
9-Acetyloxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 289984 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C(=O)O 498.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.002
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1002/HLCA.200890226
https://doi.org/10.1021/NP9902340
https://doi.org/10.1055/S-2006-957602
https://doi.org/10.1021/NP020127X
https://doi.org/10.1016/S0031-9422(00)00058-3
9,10-Dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 12305767 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C(=O)O 472.70 unknown https://doi.org/10.1055/S-2006-957602
Acetobetulinic acid 10300534 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C(=O)O 498.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.002
Alphitolic acid 12305768 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C(=O)O 472.70 unknown https://doi.org/10.1055/S-2006-957602
beta-Amyrin acetate 92156 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/J.PHYTOL.2011.05.002
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)00058-3
https://doi.org/10.1016/J.PHYTOL.2011.05.002
https://doi.org/10.1002/HLCA.200890226
https://doi.org/10.1055/S-2006-957602
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1021/NP9902340
https://doi.org/10.1016/S0031-9422(00)00058-3
https://doi.org/10.1021/NP020127X
https://doi.org/10.1002/HLCA.200890226
https://doi.org/10.1055/S-2006-957602
Camaldulenic acid 10528366 Click to see CC1(CCC2(CCC3(C(=C2C1)C=CC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C)C(=O)O)C 470.70 unknown https://doi.org/10.1021/NP960535Z
Camaldulin 10767151 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)OC=O)(C)C)C)C 482.70 unknown https://doi.org/10.1021/NP9902340
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/S0031-9422(00)00058-3
https://doi.org/10.1016/J.PHYTOL.2011.05.002
Eucalyptolic acid 102004763 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)OC)O)C)C)C2C1)C)C(=O)O)C 648.90 unknown https://doi.org/10.1055/S-2006-957602
Methyl acetyl oleanolate 11124097 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC)C)C)C 512.80 unknown https://doi.org/10.1021/NP020127X
Methylacetyleucalyptanoate 10874898 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2=CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC)C)C)C 510.70 unknown https://doi.org/10.1021/NP020127X
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1002/HLCA.200890226
https://doi.org/10.1016/S0031-9422(00)00058-3
https://doi.org/10.1021/NP020127X
https://doi.org/10.1055/S-2006-957602
https://doi.org/10.1016/J.PHYTOL.2011.05.002
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1002/HLCA.200890226
https://doi.org/10.1016/S0031-9422(00)00058-3
https://doi.org/10.1055/S-2006-957602
https://doi.org/10.1016/J.PHYTOL.2011.05.002
Ursolic acid lactone 21669105 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5CCC4(C2C1C)OC3=O)C)O)(C)C)C)C 456.70 unknown https://doi.org/10.1021/NP9902340
Ursolic acid lactone acetate 21669106 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5CCC4(C2C1C)OC3=O)C)OC(=O)C)(C)C)C)C 498.70 unknown https://doi.org/10.1021/NP9902340
> Lipids and lipid-like molecules / Saccharolipids
[(2R,3S,4S,5R,6S)-6-[[(2S)-2,5-dihydroxy-2-methyl-4-oxo-3H-chromen-7-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (4R)-4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylate 163016567 Click to see CC1(CC(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)COC(=O)C4=CCC(CC4)C(C)(C)O)O)O)O)O)O 538.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.004
[3,4,5-Trihydroxy-6-(5-hydroxy-2-methyl-4-oxochromen-7-yl)oxyoxan-2-yl]methyl 6-hydroxy-2,6-dimethylocta-2,7-dienoate 75110918 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)COC(=O)C(=CCCC(C)(C=C)O)C)O)O)O)O 520.50 unknown https://doi.org/10.1002/HLCA.201000164
Cypellocarpa C 10625791 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)COC(=O)C4=CCC(CC4)C(C)(C)O)O)O)O)O 520.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.004
Eucamalduside A 95224159 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)COC(=O)C(=CCCC(C)(C=C)O)C)O)O)O)O 520.50 unknown https://doi.org/10.1002/HLCA.201000164
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
3beta-Hydroxy-27-norcycloarta-23-ene-25-one 21626061 Click to see CC(CC=CC(=O)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Ethinyl Estradiol 5991 Click to see CC12CCC3C(C1CCC2(C#C)O)CCC4=C3C=CC(=C4)O 296.40 unknown https://doi.org/10.1080/10412905.1991.9697921
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1021/NP020127X
https://doi.org/10.1002/HLCA.200890226
https://doi.org/10.1016/J.PHYTOL.2011.05.002
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP020127X
Beta-Sitosterol 222284 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/J.PHYTOL.2011.05.002
https://doi.org/10.1002/HLCA.200890226
https://doi.org/10.1021/NP020127X
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP9902340
https://doi.org/10.1002/HLCA.201000164
https://doi.org/10.1016/J.PHYTOL.2011.05.002
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1021/NP9902340
https://doi.org/10.1016/S0031-9422(00)00058-3
https://doi.org/10.1002/HLCA.201000164
https://doi.org/10.1016/J.PHYTOL.2011.05.002
> Organic nitrogen compounds / Organonitrogen compounds / Guanidines / Biguanides
Metformin 4091 Click to see CN(C)C(=N)N=C(N)N 129.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Garcimangosone D 11003703 Click to see C1=CC=C(C=C1)C(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O 392.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Botryosphaerinone 102161310 Click to see CCC=CCC1CC(=O)CC1CC(=O)O 210.27 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
4-Isopropyl-2-cyclohexenone 92780 Click to see CC(C)C1CCC(=O)C=C1 138.21 unknown https://doi.org/10.4314/BCSE.V11I1.21012
https://doi.org/10.4324/9780203219430_CHAPTER_13
https://doi.org/10.1007/S002170050405
Botryosphaeridione 44605081 Click to see CC1C(=O)C=CC2=CC(=O)C(=CC12C)O 204.22 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,7-Trihydroxy-2-methoxyxanthone 12133315 Click to see COC1=C(C2=C(C=C1O)OC3=C(C2=O)C=C(C=C3)O)O 274.22 unknown via CMAUP database
1,4,5,6-Tetrahydroxy-2-(2-methylbut-3-en-2-yl)xanthen-9-one 10426622 Click to see CC(C)(C=C)C1=CC(=C2C(=C1O)C(=O)C3=C(O2)C(=C(C=C3)O)O)O 328.30 unknown via CMAUP database
2-(1,1-Dimethyl-2-propenyl)-1,4,5-trihydroxy-9H-xanthen-9-one 364825 Click to see CC(C)(C=C)C1=CC(=C2C(=C1O)C(=O)C3=C(O2)C(=CC=C3)O)O 312.30 unknown via CMAUP database
BR-Xanthone B 14034125 Click to see COC1=C(C=C(C2=C1C(=O)C3=C(O2)C(=CC=C3)O)O)O 274.22 unknown via CMAUP database
Euxanthone 5281631 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 228.20 unknown via CMAUP database
Gentisein 5281635 Click to see C1=CC2=C(C=C1O)C(=O)C3=C(C=C(C=C3O2)O)O 244.20 unknown via CMAUP database
Norathyriol 5281656 Click to see C1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)O)O)O 260.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
1-Hydroxy-3,6,7-trimethoxy-2-(3-methyl-2-butenyl)-8-(3-hydroxy-3-methyl-1E-butenyl)-xanthone 5319715 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(C(=C(C=C3O2)OC)OC)C=CC(C)(C)O)OC)C 454.50 unknown via CMAUP database
1,3,7-Trihydroxy-2-prenylxanthone 5495920 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=C(C=C3)O)O)C 312.30 unknown via CMAUP database
1,5-Dihydroxy-3-methoxy-2-prenylxanthone 10449043 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C(=CC=C3)O)OC)C 326.30 unknown via CMAUP database
1,5,8-Trihydroxy-3-methoxy-2-(3-methylbut-2-en-1-yl)-9H-xanthen-9-one 14162674 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(C=CC(=C3O2)O)O)OC)C 342.30 unknown via CMAUP database
1,6-Dihydroxy-3-methoxy-2-prenylxanthone 14162675 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C=C3)O)OC)C 326.30 unknown via CMAUP database
1,6-Dihydroxy-3,7-dimethoxy-2-(3-methyl-2-butenyl)-8-(3-hydroxy-3-methyl-1E-butenyl)-xanthone 5319262 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C(=C3C=CC(C)(C)O)OC)O)OC)C 440.50 unknown via CMAUP database
1,7-Dihydroxy-3-methoxy-2-prenylxanthone 509269 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=CC(=C3)O)OC)C 326.30 unknown via CMAUP database
2-(3,7-Dimethylocta-2,6-dienyl)-1,3,5,8-tetrahydroxyxanthen-9-one 72988981 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C=CC(=C3C2=O)O)O)O)C)C 396.40 unknown via CMAUP database
Cowagarcinone B 5316764 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)O)OC)OC)C 356.40 unknown via CMAUP database
garcinone B 5495928 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C(=C3)O)OC(C=C4)(C)C)O)C 394.40 unknown via CMAUP database
Mangostenone D 11696901 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C(=C3)O)OC(CC4)(C)C)O)C 396.40 unknown via CMAUP database
Mangostinone 6478778 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)O)C)C 380.40 unknown via CMAUP database
Smeathxanthone A 11509473 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C=CC(=C3C2=O)O)O)O)C)C 396.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
1,3,8-trihydroxy-4-(3-hydroxy-3-methylbutanoyl)-2-(3-methylbut-2-enyl)xanthen-9-one 102234394 Click to see CC(=CCC1=C(C2=C(C(=C1O)C(=O)CC(C)(C)O)OC3=CC=CC(=C3C2=O)O)O)C 412.40 unknown via CMAUP database
1,5,8-Trihydroxy-3-methoxy-2,4-bis(3-methylbut-2-enyl)xanthen-9-one 11711264 Click to see CC(=CCC1=C(C2=C(C(=C1OC)CC=C(C)C)OC3=C(C=CC(=C3C2=O)O)O)O)C 410.50 unknown via CMAUP database
10,16-Dihydroxy-6,6,19,19-tetramethyl-15-(3-methylbut-2-enyl)-5,13,18-trioxapentacyclo[12.8.0.03,12.04,9.017,22]docosa-1(22),3(12),4(9),7,10,14,16,20-octaen-2-one 71437595 Click to see CC(=CCC1=C2C(=C3C=CC(OC3=C1O)(C)C)C(=O)C4=C(O2)C=C(C5=C4OC(C=C5)(C)C)O)C 460.50 unknown via CMAUP database
5,8,9-Trihydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one 10046140 Click to see CC(=CCC1=C2C(=CC(=C1O)O)C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)C 394.40 unknown via CMAUP database
8-Deoxygartanin 392450 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C(=CC=C3)O)CC=C(C)C)O)C 380.40 unknown via CMAUP database
Cudraxanthone G 42645953 Click to see CC(=CCC1=C(C2=C(C(=C1OC)CC=C(C)C)OC3=C(C2=O)C=CC=C3O)O)C 394.50 unknown via CMAUP database
Garcinone A 70689919 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C=C(C=C3)O)CC=C(C)C)O)C 380.40 unknown via CMAUP database
Gartanin 5281633 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(C=CC(=C3O2)O)O)CC=C(C)C)O)C 396.40 unknown via CMAUP database
Mangostenone B 21672078 Click to see CC(=CCC1=C2C(=C3CCC(OC3=C1O)(C)C)C(=O)C4=C(C5=C(C=C4O2)OC(C=C5)(C)C)O)C 462.50 unknown via CMAUP database
Tovophyllin A 42645954 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C(=C4C(=C3C2=O)C=CC(O4)(C)C)O)CC=C(C)C)O)C 462.50 unknown via CMAUP database
Tovophyllin B 509268 Click to see CC(=CCC1=C2C(=C3C=CC(OC3=C1O)(C)C)C(=O)C4=C(C5=C(C=C4O2)OC(C=C5)(C)C)O)C 460.50 unknown via CMAUP database
Trapezifolixanthone 188341 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=CC=C4O)O)C=CC(O2)(C)C)C 378.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
(2S,3R)-3,4,8-trihydroxy-2-(2-hydroxypropan-2-yl)-7-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]xanthen-5-one 11546716 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4O)C(C)(C)O)O)O)OC)C 442.50 unknown via CMAUP database
(3S)-3,5,9-trihydroxy-8-methoxy-2,2-dimethyl-7-(3-methylbut-2-enyl)-3,4-dihydropyrano[3,2-b]xanthen-6-one 92448128 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C(C4)O)(C)C)O)O)OC)C 426.50 unknown via CMAUP database
1-(3,3-Dimethylbutyl)-3,6,8-trihydroxy-2-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one 89172625 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CCC(C)(C)C)O)C 426.50 unknown via CMAUP database
1-Isomangostin 5281641 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C4=C3OC(CC4)(C)C)O)O)OC)C 410.50 unknown via CMAUP database
1,3,6,7-Tetrahydroxy-8-prenylxanthone 15307924 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)O)C 328.30 unknown via CMAUP database
1,3,7-Trihydroxy-2-(3-methyl-2-butenyl)-8-(3-methyl-3-hydroxybutyl)-9H-xanthene-9-one 102234393 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C=C3)O)CCC(C)(C)O)O)C 398.40 unknown via CMAUP database
11Alpha-Mangostanin 46880204 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4)C(C)(C)O)O)O)OC)C 426.50 unknown via CMAUP database
3-Isomangostin 13873655 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(CC4)(C)C)O)O)OC)C 410.50 unknown via CMAUP database
3,5,9-Trihydroxy-8-methoxy-2,2-dimethyl-7-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one 68229267 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C(=C4)O)(C)C)O)O)OC)C 424.40 unknown via CMAUP database
3,6-Dimethylmangostin 231412 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(C(=C(C=C3O2)OC)OC)CC=C(C)C)OC)C 438.50 unknown via CMAUP database
4-Hydroxy-7,8-dimethoxy-6-(3-methylbut-2-enyl)furo[3,2-b]xanthen-5-one 101193830 Click to see CC(=CCC1=C2C(=CC(=C1OC)OC)OC3=C(C2=O)C(=C4C=COC4=C3)O)C 380.40 unknown via CMAUP database
6-Deoxy-gamma-mangostin 13873657 Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)C 380.40 unknown via CMAUP database
7-Methoxy-2-(3-methyl-2-butenyl)-8-(3-methyl-2-oxo-3-butenyl)-1,3,6-trihydroxyxanthone 69074110 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CC(=O)C(=C)C)O)C 424.40 unknown via CMAUP database
9-Hydroxycalabaxanthone 5495929 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)O)OC)C 408.40 unknown via CMAUP database
9-Hydroxycalabaxanthone hydrate 56840489 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C=C(C(=C4CCC(C)(C)O)OC)O)C 426.50 unknown via CMAUP database
Beta-Mangostin 5495925 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C(=C3CC=C(C)C)OC)O)OC)C 424.50 unknown via CMAUP database
Cratoxyxanthone 46879489 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4C5=C(C(=C(C6=C5OC7=C(C6=O)C(=C(C(=C7)O)OC)CC=C(C)C)O)CC=C(C)C)O)C(C)(C)O)O)O)OC)C 834.90 unknown via CMAUP database
Demethylcalabaxanthone 509270 Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)O)C 378.40 unknown via CMAUP database
Dulxanthone D 10405091 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)C 342.30 unknown via CMAUP database
gamma-Mangostin 5464078 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)O)CC=C(C)C)O)C 396.40 unknown via CMAUP database
Garcimangosone A 10874207 Click to see CC(=CCC1=C2C(=C(C3=C1C(=O)C4=C(C5=C(C=C4O3)OC(C=C5)(C)C)O)O)C=CC(O2)(C)C)C 460.50 unknown via CMAUP database
Garcinone C 44159808 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)O)CCC(C)(C)O)O)C 414.40 unknown via CMAUP database
Garcinone D 5495926 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CCC(C)(C)O)O)C 428.50 unknown via CMAUP database
Garcinone E 10298511 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C(=C(C(=C3C2=O)CC=C(C)C)O)O)CC=C(C)C)O)C 464.50 unknown via CMAUP database
Mangostenone A 509267 Click to see CC(=CCC1=C2C(=C3C=CC(OC3=C1O)(C)C)OC4=CC5=C(C=CC(O5)(C)C)C(=C4C2=O)O)C 460.50 unknown via CMAUP database
Mangostin 5281650 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CC=C(C)C)O)C 410.50 unknown via CMAUP database
Rubraxanthone 9953366 Click to see CC(=CCCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)C)C 410.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
10,22-Dihydroxy-7,7,18,18-tetramethyl-8,13,17-trioxapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(22),3(12),4(9),10,14,16(21),19-heptaen-2-one 56840488 Click to see CC1(CCC2=C(O1)C(=CC3=C2C(=O)C4=C(C5=C(C=C4O3)OC(C=C5)(C)C)O)O)C 394.40 unknown via CMAUP database
Br-Xanthone A 13964005 Click to see CC1(CCC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C=C(C5=C4CCC(O5)(C)C)O)C 396.40 unknown via CMAUP database
Brasilixanthone B 5324261 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C=C(C5=C4C=CC(O5)(C)C)O)C 392.40 unknown via CMAUP database
Garcimangosone B 11143989 Click to see CC1(CCC2=C3C(=CC(=C2O1)OC)OC4=CC5=C(C=CC(O5)(C)C)C(=C4C3=O)O)C 408.40 unknown via CMAUP database
Macluraxanthone 5281646 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC4=C(C3=O)C=CC(=C4O)O)O)C 394.40 unknown via CMAUP database
O-Demethylforbexanthone 45269778 Click to see CC1(C=CC2=CC3=C(C(=C2O1)O)OC4=CC(=CC(=C4C3=O)O)O)C 326.30 unknown via CMAUP database
Thwaitesixanthone 392169 Click to see CC1(C=CC2=C(O1)C=CC3=C2C(=O)C4=C(C5=C(C=C4O3)OC(C=C5)(C)C)O)C 376.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(3R)-8-Hydroxy-3-methyl-3,4-dihydro-1H-2-benzopyran-1-one 114679 Click to see CC1CC2=C(C(=CC=C2)O)C(=O)O1 178.18 unknown via CMAUP database
cis-4-Hydroxymellein 10420140 Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O 194.18 unknown via CMAUP database
trans-4-Hydroxymellein 10262028 Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O 194.18 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,3-dioxanes
Botryosphaerihydrofuran 44605288 Click to see CC1COC23C1(O2)CC4(C(C=CC4=C3)C)C 218.29 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3S,4S)-4-acetyl-3-methyloxolan-2-one 118708002 Click to see CC1C(COC1=O)C(=O)C 142.15 unknown via CMAUP database
Botryosphaerilactone A 102161309 Click to see CC1C(C(OC1OCC2C(C(=O)OC2C)C)C)CO 272.34 unknown via CMAUP database
Botryosphaerilactone B 44605080 Click to see CC1C(COC1OCC2C(C(=O)OC2C)C)C(=O)C 270.32 unknown via CMAUP database
Botryosphaerilactone C 102161308 Click to see CC1C(C(OC1OCC2C(C(=O)OC2C)C)C)CO 272.34 unknown via CMAUP database
Dihydro-4-(hydroxymethyl)-3,5-dimethyl-2 102125217 Click to see CC1C(C(OC1=O)C)CO 144.17 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
Lasiolactone 89352705 Click to see CCCC1CC=CC(=O)O1 140.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Egonol 485186 Click to see COC1=CC(=CC2=C1OC(=C2)C3=CC4=C(C=C3)OCO4)CCCO 326.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
5-Hydroxy-8-[5-hydroxy-7-methoxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]-7-methoxy-2-(4-methoxyphenyl)chromen-4-one 11103936 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)OC)O)OC 594.60 unknown via CMAUP database
Proanthocyanidin A1 9872976 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown via CMAUP database
Procyanidin A2 124025 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown via CMAUP database
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B5 124017 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-2-(3,4-dihydroxyphenyl)-5-hydroxy-8-[(Z)-4-hydroxy-3-methylbut-2-enyl]-7-methoxy-2,3-dihydrochromen-4-one 163193739 Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC(=C(C=C3)O)O)O)OC)CO 386.40 unknown https://doi.org/10.1002/HLCA.200890226
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/0031-9422(93)85448-Z
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1016/0031-9422(93)85448-Z
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/0031-9422(93)85448-Z
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Spiraeoside 5320844 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(93)85448-Z
https://doi.org/10.1016/0031-9422(93)85553-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(2,3-Dihydroxyphenyl)-5,7-dihydroxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 53399169 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=C(C(=CC=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 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 https://doi.org/10.1016/0031-9422(93)85448-Z
Astilbin 119258 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 450.40 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 https://doi.org/10.1016/0031-9422(93)85448-Z
> Phenylpropanoids and polyketides / Macrolides and analogues
(5R) 5-hydroxylasiodiplodin 10638525 Click to see CC1CC(CCCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1)O 308.40 unknown via CMAUP database
(5S) 5-hydroxylasiodiplodin 10733600 Click to see CC1CC(CCCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1)O 308.40 unknown via CMAUP database
Lasiodiplodin 14562696 Click to see CC1CCCCCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1 292.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
CID 442690 442690 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1016/0031-9422(93)85448-Z
Cypellocarpin A 10696653 Click to see CC(C)(C1CCC(=CC1)C(=O)OCC2C(C(C(C(O2)OC3=CC(=CC(=C3O)O)C(=O)O)O)O)O)O 498.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.004
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 https://doi.org/10.1016/0031-9422(93)85553-4

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