Laurus nobilis - Unknown
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Details Top

Internal ID UUID643ff48fdc715387897579
Scientific name Laurus nobilis
Authority L.
First published in Sp. Pl. : 369 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Laurus tenuifolia Mill. Gard. Dict. ed. 8 : n.º 3 (1768)
Laurus undulata Mill. Gard. Dict. ed. 8 : n.º 2 (1768)
Laurus angusta Raf. Sylva Tellur. : 136 (1838)
Laurus nobilis f. lanceolata Meisn. A.P.de Candolle, Prodr. 15(1): 233 (1864)
Laurus nobilis f. latifolia (Risso) Maire Fl. Afrique N. 11: 263 (1964)
Laurus nobilis var. rotundifolia Emb. & Maire Mém. Soc. Sci. Nat. Maroc 21-22: 47 (1930)
Laurus nobilis var. undulata Meisn. A.P.de Candolle, Prodr. 15(1): 233 (1864)
Laurus nobilis var. floribunda Meisn. A.P.de Candolle, Prodr. 15(1): 233 (1864)
Laurus nobilis var. longifolia Risso Hist. Nat. Prod. Eur. Mérid. 2: 49 (1826)
Laurus nobilis var. angustifolia Nees Syst. Laur.: 580 (1836)
Laurus nobilis var. latifolia Risso Hist. Nat. Prod. Eur. Mérid. 2: 49 (1826)
Laurus nobilis subsp. lanceolata Meisn. A.P.de Candolle, Prodr. 15(1): 233 (1864)

Common names Top

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Language Common/alternative name
English sweet bay
English bay laurel
English laurel
Spanish laurel
Spanish los laureles
Spanish arbol de apolo
Spanish Árbol de apolo
Spanish choriu
Spanish lauredo
Spanish laurel comun
Spanish laurel común
Spanish laurel de apolo
Spanish laurel de cocina
Spanish laurel del mediterraneo
Spanish laurel del mediterráneo
Spanish laurel europeo
Spanish laurel hembra
Spanish laurel macho
Spanish laurel noble
Spanish laurelal
Spanish llaurer
Spanish llorea
Spanish llorel
Spanish lloreo
Spanish lloreolo
Spanish loreda
Spanish lorel
ab Адаҧа
Afrikaans lourierboom
Arabic الغار
Arabic ورق الغار
Arabic غار
Arabic رند
Arabic غار النصر
Arabic غارنبيل
Azerbaijani dəfnə
Azerbaijani nəcib dəfnə ağacı
Belarusian Лаўр высакародны
Bulgarian Лаврово дърво
Bulgarian лавър
Bosnian lovor
Catalan llor
Catalan llorer
co alloru
co addoru
Czech bobek
Czech vavřín ušlechtilý
Czech vavřín vznešený
Welsh llawrwydden
Danish lauerbær
Danish laurbær
Danish Ægte laurbær
German edler lorbeer
German fructus lauri
German lorbeer
German lorbeerbaum
German lorbeerblatt
German echter lorbeer
Greek Βαγιά
Greek Βάγια
Greek Δαφνολιά
Greek Φυλλάδα
Greek Δάφνη
Esperanto nobla laŭro
Estonian harilik loorberipuu
Basque erramu
Basque ereinotz
Persian برگ بو
Finnish välimerenlaakeripuu
Finnish laakeripuu
French laurier d'apollon
French laurier noble
French laurier sauce
French laurier-sauce
frr loorbeer
frr echt loorbeer
Irish labhras milis
Irish labhras
Galician loureiro
Manx billey buigh
Manx billey bwee
Manx billey millish
Manx laurys
Hebrew דפנה
Hebrew עלי דפנה
Hebrew ער אציל
Croatian lovor
Upper Sorbian prawy ławrjenc
Hungarian nemes babér
Indonesian dafnah
Igbo laurel
Igbo nwa laurel
Italian alloro
Japanese ローレル
Japanese ゲッケイジツ
Japanese ゲッケイジュ属
Japanese ゲッケイヨウ
Japanese 月桂実
Japanese 月桂樹
Japanese 月桂葉
Japanese ゲッケイジュ
jv laurel
Kabyle tarselt
Korean 월계꽃
Korean 월계수
lb lorber
lb lolber
li lawweleer
li loreer
li laurier
lij auföggio
Lithuanian kilnusis lauras
Lithuanian lauro lapai
Lithuanian lauro lapas
Lithuanian laurų lapai
Lithuanian kilnusis lauramedis
Latvian dižciltīgais lauru koks
Latvian dižciltīgais laurs
Malagasy laorely
Macedonian Ловор
Malay dafnah
mt siġra tar-rand
Norwegian Bokmål ekte laurbær
Norwegian Bokmål laurbærblad
Norwegian Bokmål laurbær
Dutch laurierboom
Dutch laurier
Norwegian Nynorsk l. nobilis
Norwegian Nynorsk laurbærbusk
Norwegian Nynorsk laurbær
nrm louori
nrm louothi
oc laurèir
oc laurèr
oc laurier
oc laurièr
os Уæздан лавр
Polish liść bobkowy
Polish liście bobkowe
Polish liście laurowe
Polish wawrzyn szlachetny
Portuguese loureiro
Romanian laur
Romanian dafin
Russian Благородный лавр
Russian Лавровое дерево
Russian лавр благородный
sc laru
Samogitian babka
Serbo-Croatian lovor
Slovak bobkový list
Slovak vavrín pravý
Slovenian lovor
Slovenian navadni lovor
Albanian dafina
Serbian ловор
Swedish lagerblad
Swedish lagerträd
Swedish lagrar
Swedish lager
Turkish akdeniz defnesi
Ukrainian Лавр благородний
Uzbek dafna (daraxt)
vec lavranèr
vec doraro
Vietnamese nguyệt quế hy lạp
Vietnamese nguyệt quế
wo lóriye
Chinese 月桂
Chinese 月桂叶
Chinese 月桂子
Chinese 月桂樱子
Chinese 月桂树

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
    • Macaronesia
      • Azores
    • Northern Africa
      • Algeria
      • Libya
      • Morocco
      • Tunisia
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Eastern Asia
      • Korea
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Europe
    • Eastern Europe
      • Krym
    • Northern Europe
      • Great Britain
      • Ireland
    • Southeastern Europe
      • Albania
      • Greece
      • Italy
      • Kriti
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000364153
UNII 3VA21I795E
USDA Plants LANO80
Tropicos 17804359
INPN 105295
Flora of Italy 1258
KEW urn:lsid:ipni.org:names:465049-1
The Plant List kew-2349094
Missouri Botanical Garden 281677
PaleoBotany 79079
Open Tree Of Life 571537
Observations.org 135856
NCBI Taxonomy 85223
NBN Atlas NBNSYS0000004619
Nature Serve 2.153656
IUCN Red List 203351
IPNI 465049-1
iNaturalist 54759
GBIF 3034015
Freebase /m/027f8z
EPPO LURNO
EOL 486835
Elurikkus 5410
Calflora (Californian flora) 8627
US Library of Congress sh88022873
USDA GRIN 21664
Wikipedia Laurus_nobilis
CMAUP NPO29515

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
Underrated aspects of a true Mediterranean diet: understanding traditional features for worldwide application of a “Planeterranean” diet Godos J, Scazzina F, Paternò Castello C, Giampieri F, Quiles JL, Briones Urbano M, Battino M, Galvano F, Iacoviello L, de Gaetano G, Bonaccio M, Grosso G J Transl Med 21-Mar-2024
PMCID:PMC10956348
doi:10.1186/s12967-024-05095-w
PMID:38515140
Coriander (Coriandrum sativum L.) from Alentejo (South Portugal)—Ethnobotany and Potential Industrial Use Póvoa O, Farinha N, Lopes V, Machado AM, Figueiredo AC Foods 19-Mar-2024
PMCID:PMC10969941
doi:10.3390/foods13060929
PMID:38540919
Ultrasonic-assisted extraction to enhance the recovery of bioactive phenolic compounds from Commiphora gileadensis leaves Bin Mokaizh AA, Nour AH, Kerboua K Ultrason Sonochem 18-Mar-2024
PMCID:PMC10979263
doi:10.1016/j.ultsonch.2024.106852
PMID:38518410
Nuclear Magnetic Resonance Fingerprints and Mini DNA Markers for the Authentication of Cinnamon Species Ingredients Used in Food and Natural Health Products Ragupathy S, Thirugnanasambandam A, Vinayagam V, Newmaster SG Plants (Basel) 14-Mar-2024
PMCID:PMC10975438
doi:10.3390/plants13060841
PMID:38592863
Advances in the Applications of Clinoptilolite-Rich Tuffs Pavlović J, Hrenović J, Povrenović D, Rajić N Materials (Basel) 12-Mar-2024
PMCID:PMC10972338
doi:10.3390/ma17061306
PMID:38541460
Comparison of autoclaving and γ-radiation impact on four spices aroma profiles and microbial load using HS-SPME GC–MS and chemometric tools Baky MH, Elkenawy NM, El-Nashar HA, Abib B, Farag MA Sci Rep 08-Mar-2024
PMCID:PMC10923872
doi:10.1038/s41598-024-56422-6
PMID:38459176
Selected Australian Terminalia Species Extracts Inhibit β-Lactam Drug-Resistant Bacteria Growth and Potentiate the Activity of Conventional Antibiotics: Bioactivities and Phytochemistry Zai MJ, Cheesman MJ, Cock IE Microorganisms 29-Feb-2024
PMCID:PMC10972150
doi:10.3390/microorganisms12030498
PMID:38543548
Quantitative NMR Spectrometry of Phenylpropanoids, including Isoeugenol in Herbs, Spices, and Essential Oils Fabry P, Weber S, Teipel J, Richling E, Walch SG, Lachenmeier DW Foods 27-Feb-2024
PMCID:PMC10930604
doi:10.3390/foods13050720
PMID:38472833
Adulticidal synergy of two plant essential oils and their major constituents against the housefly Musca domestica and bioassay on non-target species Soonwera M, Moungthipmalai T, Puwanard C, Sittichok S, Sinthusiri J, Passara H Heliyon 27-Feb-2024
PMCID:PMC10920383
doi:10.1016/j.heliyon.2024.e26910
PMID:38463861
Comparative Analysis of Chloroplast Genomes of “Tiantai Wu-Yao” (Lindera aggregata) and Taxa of the Same Genus and Different Genera Shi Y, Chen Z, Jiang J, Li X, Zeng W Genes (Basel) 20-Feb-2024
PMCID:PMC10970223
doi:10.3390/genes15030263
PMID:38540322
Magnetic iron oxide-based nanozymes: from synthesis to application Ghazzy A, Nsairat H, Said R, Sibai OA, AbuRuman A, Shraim AS, Al hunaiti A Nanoscale Adv 19-Feb-2024
PMCID:PMC10929596
doi:10.1039/d3na00903c
PMID:38482039
Performance Evaluation of a Commercial Real-Time PCR Method for the Detection of Lupin Traces in Food Tramuta C, Decastelli L, Ingravalle F, Barcucci E, Fragassi S, Bianchi DM Foods 17-Feb-2024
PMCID:PMC10888417
doi:10.3390/foods13040609
PMID:38397586
Poisoning by Nerium oleander L. in Franconia Geese Pugliese N, Tinelli A, Crescenzo G, Nieddu M, Baralla E, Schiavone A, Zizzo N, Samarelli R, Dessì F, Circella E, Zizzadoro C, Saleh MS, Camarda A Animals (Basel) 14-Feb-2024
PMCID:PMC10885877
doi:10.3390/ani14040612
PMID:38396580
The effects of herbal plant extract on the growth performance, blood parameters, nutrient digestibility and carcase quality of rabbits: A meta-analysis Adli DN, Sugiharto S, Irawan A, Tribudi YA, Wibowo S, Azmi AF, Sjofjan O, Jayanegara A, Tistiana H, Wahyono T, Aditya S, Sholikin MM, Sadarman S Heliyon 10-Feb-2024
PMCID:PMC10877253
doi:10.1016/j.heliyon.2024.e25724
PMID:38380018
Characterisation of Dry-Salted Violino and Bresaola from Grass-Fed Bergamasca Sheep Lopez A, Mainardi E, Beretta E, Ratti S, Bellagamba F, Corino C, Moretti VM, Rossi R Animals (Basel) 01-Feb-2024
PMCID:PMC10854579
doi:10.3390/ani14030488
PMID:38338130

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
> Alkaloids and derivatives / Aporphines
(+)-Launobine 5318956 Click to see COC1=C(C2=C(CC3C4=C2C5=C(C=C4CCN3)OCO5)C=C1)O 311.30 unknown https://doi.org/10.1021/NP50023A008
(S)-Nandigerine 422682 Click to see COC1=C(C=CC2=C1C3=C4C(C2)NCCC4=CC5=C3OCO5)O 311.30 unknown https://doi.org/10.1021/NP50023A008
(S)-Neolitsine 12313196 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC6=C(C=C54)OCO6)OCO3 323.30 unknown https://doi.org/10.1021/NP50023A008
Actinodaphnine 160502 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C5=C(C=C4CCN3)OCO5)O 311.30 unknown https://doi.org/10.1021/NP50023A008
Boldine 10154 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O 327.40 unknown https://doi.org/10.1021/NP50023A008
Cassythicine 4440434 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)O)OCO3 325.40 unknown https://doi.org/10.1021/NP50023A008
Cryptodorine 11438278 Click to see C1CNC2CC3=CC4=C(C=C3C5=C2C1=CC6=C5OCO6)OCO4 309.30 unknown https://doi.org/10.1021/NP50023A008
Hernangerine 497804 Click to see COC1=C(C=CC2=C1C3=C4C(C2)NCCC4=CC5=C3OCO5)O 311.30 unknown https://doi.org/10.1021/NP50023A008
Isodomesticine 69523059 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC5=C(C=C43)OCO5)OC)O 325.40 unknown https://doi.org/10.1021/NP50023A008
Neolitsine 10064778 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC6=C(C=C54)OCO6)OCO3 323.30 unknown via CMAUP database
R-(-)-actinodaphnine 11957301 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C5=C(C=C4CCN3)OCO5)O 311.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Methyl Salicylate 4133 Click to see COC(=O)C1=CC=CC=C1O 152.15 unknown https://doi.org/10.1080/10412905.2001.9699624
> 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/10.1021/JF051513Y
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
1,2-Dimethoxy-4-(prop-1-en-2-yl)benzene 13022452 Click to see CC(=C)C1=CC(=C(C=C1)OC)OC 178.23 unknown https://doi.org/10.1007/BF00600858
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1080/10412905.1989.9697798
https://doi.org/10.1080/10412905.2001.9699624
https://doi.org/10.1080/10412905.1989.9697781
https://doi.org/10.1021/JF049033E
> Benzenoids / Phenol esters
Eugenol acetate 7136 Click to see CC(=O)OC1=C(C=C(C=C1)CC=C)OC 206.24 unknown https://doi.org/10.1080/10412905.1989.9697798
> Benzenoids / Phenol ethers / Anisoles
Anethole 637563 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown https://doi.org/10.1021/JF051513Y
Elemicin 10248 Click to see COC1=CC(=CC(=C1OC)OC)CC=C 208.25 unknown https://doi.org/10.1080/10412905.2001.9699624
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown https://doi.org/10.1021/JF051513Y
Methoxy-4-propenylbenzene 7703 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown https://doi.org/10.1021/JF051513Y
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1080/10412905.1989.9697798
https://doi.org/10.1080/10412905.2001.9699624
https://doi.org/10.1080/10412905.1989.9697781
o-Methoxy-o-methyl-p-allylphenol 45266909 Click to see CC1=CC(=CC(=C1O)OC)CC=C 178.23 unknown https://doi.org/10.1021/JF049033E
Phenol, 2-methoxy-4-(1-methylethenyl)- 2723653 Click to see CC(=C)C1=CC(=C(C=C1)O)OC 164.20 unknown https://doi.org/10.1007/BF00600858
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1007/BF00600858
https://doi.org/10.1080/10412905.1989.9697798
https://doi.org/10.1080/10412905.1989.9697781
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5R)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 14521039 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O 552.60 unknown https://doi.org/10.1021/JF048782T
Lyoniside 14521038 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O 552.60 unknown https://doi.org/10.1021/JF048782T
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Docosyl tetradecanoate 45934025 Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC 537.00 unknown https://doi.org/10.1021/NP50087A023
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
12-Deuteriododecanoic acid 11252659 Click to see CCCCCCCCCCCC(=O)O 201.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(4R,5S)-4-hydroxy-5-(hydroxymethyl)-3,3-dimethyl-4-[(E,3S)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohexan-1-one 11486522 Click to see CC(C=CC1(C(CC(=O)CC1(C)C)CO)O)OC2C(C(C(C(O2)CO)O)O)O 404.50 unknown https://doi.org/10.1021/JF048782T
2-[4-(1,4-Dihydroxy-2,2,6-trimethylcyclohexyl)but-3-en-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73319510 Click to see CC1CC(CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C)O 390.50 unknown https://doi.org/10.1021/JF048782T
3-(Hydroxymethyl)-5,5-dimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one 73821784 Click to see CC(C=CC1C(=CC(=O)CC1(C)C)CO)OC2C(C(C(C(O2)CO)O)O)O 386.40 unknown https://doi.org/10.1021/JF048782T
4-Hydroxy-3,3,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohexan-1-one 72777210 Click to see CC1CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 388.50 unknown https://doi.org/10.1021/JF048782T
4-Hydroxy-5-(hydroxymethyl)-3,3-dimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohexan-1-one 72757780 Click to see CC(C=CC1(C(CC(=O)CC1(C)C)CO)O)OC2C(C(C(C(O2)CO)O)O)O 404.50 unknown https://doi.org/10.1021/JF048782T
https://doi.org/10.1021/NP100688G
alangionoside A 21630900 Click to see CC1CC(CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C)O 390.50 unknown https://doi.org/10.1021/JF048782T
Ampelopsisionoside 11269249 Click to see CC1CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 388.50 unknown https://doi.org/10.1021/JF048782T
Lauroside A 101367899 Click to see CC1CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 388.50 unknown https://doi.org/10.1021/JF048782T
Lauroside B 11223421 Click to see CC(C=CC1(C(CC(=O)CC1(C)C)CO)O)OC2C(C(C(C(O2)CO)O)O)O 404.50 unknown https://doi.org/10.1021/JF048782T
https://doi.org/10.1021/NP100688G
Macarangioside D 101412231 Click to see CC(C=CC1C(=CC(=O)CC1(C)C)CO)OC2C(C(C(C(O2)CO)O)O)O 386.40 unknown https://doi.org/10.1021/JF048782T
Turpinionoside B 101165165 Click to see CC1CC(CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C)O 390.50 unknown https://doi.org/10.1021/JF048782T
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1989.9697798
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
5-Hydroxy-1-(4-hydroxy-3-methoxycyclohexyl)decan-3-one 42675 Click to see CCCCCC(CC(=O)CCC1CCC(C(C1)OC)O)O 300.40 unknown https://doi.org/10.1021/JF051513Y
Octacosane-1,10-diol 163189740 Click to see CCCCCCCCCCCCCCCCCCC(CCCCCCCCCO)O 426.80 unknown https://doi.org/10.1021/NP50087A023
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(+)-11-Hydroxy-9-triacontanone 131750939 Click to see CCCCCCCCCCCCCCCCCCCC(CC(=O)CCCCCCCC)O 452.80 unknown https://doi.org/10.1021/NP50087A023
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
Ipsdienol 92301 Click to see CC(=CC(CC(=C)C=C)O)C 152.23 unknown https://doi.org/10.1080/10412905.2001.9699624
Linalool, (+)- 67179 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1007/BF00600858
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1021/JF00056A055
https://doi.org/10.1080/10412905.2001.9699624
https://doi.org/10.1007/BF00600858
https://doi.org/10.1080/10412905.1989.9697798
https://doi.org/10.1080/10412905.1989.9697781
Linalyl acetate 8294 Click to see CC(=CCCC(C)(C=C)OC(=O)C)C 196.29 unknown https://doi.org/10.1080/10412905.1989.9697798
https://doi.org/10.1080/10412905.1989.9697781
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1007/BF00600858
https://doi.org/10.1080/10412905.1989.9697798
https://doi.org/10.1080/10412905.1989.9697781
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
Pseudoionone 1757003 Click to see CC(=CCCC(=CC=CC(=O)C)C)C 192.30 unknown https://doi.org/10.1021/ACS.JAFC.5B02941
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1021/JF051513Y
https://doi.org/10.1021/JF00056A055
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1007/BF00600858
https://doi.org/10.1080/10412905.1989.9697798
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1021/JF049033E
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1007/BF00600858
(-)-Sabinene 11051711 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1021/JF049033E
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1007/BF00600858
(+)-beta-Pinene 10290825 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1021/JF049033E
(1S,5R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-3-en-2-ol 163189159 Click to see CC(C)C12CC1C(C=C2)(C)O 152.23 unknown https://doi.org/10.1016/S0031-9422(00)84909-2
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/10.1080/10412905.1989.9697798
https://doi.org/10.1080/10412905.1989.9697781
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1989.9697781
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1021/JF970110Y
https://doi.org/10.1080/10412905.2001.9699624
https://doi.org/10.1007/BF00600858
https://doi.org/10.1080/10412905.1989.9697798
https://doi.org/10.1080/10412905.1989.9697781
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1021/JF970110Y
https://doi.org/10.1080/10412905.2001.9699624
https://doi.org/10.1080/10412905.1989.9697798
https://doi.org/10.1080/10412905.1989.9697781
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1989.9697798
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1007/BF00600858
https://doi.org/10.1080/10412905.1989.9697798
https://doi.org/10.1080/10412905.1989.9697781
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1021/JF00056A055
cis-Sabinene hydrate 11744854 Click to see CC(C)C12CCC(C1C2)(C)O 154.25 unknown https://doi.org/10.1007/BF00600858
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1080/10412905.2001.9699624
https://doi.org/10.1080/10412905.1989.9697798
https://doi.org/10.1080/10412905.1989.9697781
Sabinene 10887971 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1021/JF049033E
Sabinene hydrate 62367 Click to see CC(C)C12CCC(C1C2)(C)O 154.25 unknown https://doi.org/10.1007/BF00600858
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1989.9697798
https://doi.org/10.1080/10412905.1989.9697781
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol 443162 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1007/BF00600858
(+)-beta-Phellandrene 442484 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1007/BF00600858
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1007/BF00600858
(1R,4S)-1-hydroperoxy-p-menth-2-en-8-ol acetate 10889657 Click to see CC(=O)OC(C)(C)C1CCC(C=C1)(C)OO 228.28 unknown https://doi.org/10.1248/CPB.50.1514
2-(4-Hydroperoxy-4-methylcyclohex-2-en-1-yl)propan-2-yl acetate 72974200 Click to see CC(=O)OC(C)(C)C1CCC(C=C1)(C)OO 228.28 unknown https://doi.org/10.1248/CPB.50.1514
2-[(1S)-4-methylcyclohex-3-en-1-yl]propan-2-yl acetate 93317 Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C 196.29 unknown https://doi.org/10.1007/BF00600858
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1007/BF00600858
https://doi.org/10.1080/10412905.2001.9699624
https://doi.org/10.1080/10412905.1989.9697798
https://doi.org/10.1021/JF970110Y
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1007/BF00600858
https://doi.org/10.1080/10412905.1989.9697781
alpha-PHELLANDRENE, (-)- 442482 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1007/BF00600858
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1021/JF049033E
https://doi.org/10.1080/10412905.1989.9697781
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1080/10412905.2001.9699624
https://doi.org/10.1021/JF049033E
https://doi.org/10.1007/BF00600858
https://doi.org/10.1080/10412905.1989.9697798
https://doi.org/10.1080/10412905.1989.9697781
alpha-Terpinyl acetate 111037 Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C 196.29 unknown https://doi.org/10.1007/BF00600858
https://doi.org/10.1021/JF049033E
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1007/BF00600858
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1007/BF00600858
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/JF00056A055
https://doi.org/10.1007/BF00600858
https://doi.org/10.1080/10412905.1989.9697798
https://doi.org/10.1080/10412905.1989.9697781
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1007/BF00600858
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4S,5R,9S)-4,5-Epoxy-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undecane 9991037 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0968-0896(00)00127-9
4-(3-Hydroxybutyl)-3,5,5-trimethylcyclohex-2-en-1-one 118284 Click to see CC1=CC(=O)CC(C1CCC(C)O)(C)C 210.31 unknown https://doi.org/10.1055/S-2005-864191
4-Hydroxy-4-(3-hydroxybut-1-en-1-yl)-3,3,5-trimethylcyclohexan-1-one 71344200 Click to see CC1CC(=O)CC(C1(C=CC(C)O)O)(C)C 226.31 unknown https://doi.org/10.1021/JF048782T
4,5-Dihydroblumenol A 21630916 Click to see CC1CC(=O)CC(C1(C=CC(C)O)O)(C)C 226.31 unknown https://doi.org/10.1021/JF048782T
7-Acetyl-2-hydroxy-2-methyl-5-isopropylbicyclo[4.3.0]nonane 539857 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 238.37 unknown https://doi.org/10.1016/S0024-3205(00)00542-7
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0968-0896(00)00127-9
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1S,4E,9R)- 26318 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1007/BF00600858
https://doi.org/10.1016/S0968-0896(00)00127-9
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1021/JF00056A055
https://doi.org/10.1007/BF00600858
https://doi.org/10.1080/10412905.1989.9697781
https://doi.org/10.1016/S0968-0896(00)00127-9
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0968-0896(00)00127-9
Oplopanone 10466745 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 238.37 unknown https://doi.org/10.1016/S0024-3205(00)00542-7
Ueejdiuocucvhn-pwsuyjocsa- 14135400 Click to see CC1=CC(=O)CC(C1CCC(C)O)(C)C 210.31 unknown https://doi.org/10.1055/S-2005-864191
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(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/10.1016/S0024-3205(00)00542-7
(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/10.1016/S0024-3205(00)00542-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1S,2R,4aR,8R,8aS)-2-[(2S)-1,2-dihydroxypropan-2-yl]-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,8-diol 102508874 Click to see CC12CCCC(C1C(C(CC2)C(C)(CO)O)O)(C)O 272.38 unknown https://doi.org/10.1055/S-2005-864191
2-(1,2-Dihydroxypropan-2-yl)-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,8-diol 74931872 Click to see CC12CCCC(C1C(C(CC2)C(C)(CO)O)O)(C)O 272.38 unknown https://doi.org/10.1055/S-2005-864191
2-(4a-Methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)propan-2-ol 521215 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1016/S0968-0896(00)00127-9
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0024-3205(00)00542-7
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1016/S0024-3205(00)00542-7
https://doi.org/10.1016/S0968-0896(00)00127-9
https://doi.org/10.1016/S0960-894X(99)00442-4
CID 23426951 23426951 Click to see CC1=CCC(C2(C1CC(CC2)C(=C)C)C)O 220.35 unknown https://doi.org/10.1016/S0024-3205(00)00542-7
gamma-EUDESMOL 6432005 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown https://doi.org/10.1016/S0024-3205(00)00542-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
[(2S)-2-hydroxy-2-[(1R,2E,4S,7E)-4-hydroxy-4,8-dimethylcyclodeca-2,7-dien-1-yl]propyl] acetate 162957375 Click to see CC1=CCCC(C=CC(CC1)C(C)(COC(=O)C)O)(C)O 296.40 unknown https://doi.org/10.1016/0031-9422(92)83320-X
[2-Hydroxy-2-(4-hydroxy-4,8-dimethylcyclodeca-2,7-dien-1-yl)propyl] acetate 162957374 Click to see CC1=CCCC(C=CC(CC1)C(C)(COC(=O)C)O)(C)O 296.40 unknown https://doi.org/10.1016/0031-9422(92)83320-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4S,5S,6R)-2-[(1S,4S,5R)-4-hydroxy-4-[(E,3R)-3-hydroxybut-1-enyl]-3,3,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 21630913 Click to see CC1CC(CC(C1(C=CC(C)O)O)(C)C)OC2C(C(C(C(O2)CO)O)O)O 390.50 unknown https://doi.org/10.1021/JF048782T
2-[4-Hydroxy-4-(3-hydroxybut-1-enyl)-3,3,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 73089503 Click to see CC1CC(CC(C1(C=CC(C)O)O)(C)C)OC2C(C(C(C(O2)CO)O)O)O 390.50 unknown https://doi.org/10.1021/JF048782T
CID 14312560 14312560 Click to see CC(=O)C=C=C1C(CC(CC1(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown https://doi.org/10.1021/JF048782T
CID 15628135 15628135 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C 386.40 unknown https://doi.org/10.1021/JF048782T
Icariside B1 15628136 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C 386.40 unknown https://doi.org/10.1021/JF048782T
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3aS,7R,10Z,11aR)-7-hydroperoxy-10-methyl-3,6-dimethylidene-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-2-one 101316838 Click to see CC1=CC2C(CCC(=C)C(CC1)OO)C(=C)C(=O)O2 264.32 unknown via CMAUP database
7-hydroxy-10-methyl-3,6-dimethylidene-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-2-one 99962 Click to see CC1=CC2C(CCC(=C)C(CC1)O)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1248/CPB.54.1187
Artemorin 5281428 Click to see CC1=CC2C(CCC(=C)C(CC1)O)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1248/CPB.54.1187
https://doi.org/10.1021/NP50010A016
Verlotorin 13895607 Click to see CC1=CC2C(CCC(=C)C(CC1)OO)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1021/NP50010A016
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R)-3,4-Dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 2579 Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O 330.40 unknown https://doi.org/10.1021/JF051513Y
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,5aS,6S,9aR,9bR)-6-hydroxy-9-(hydroxymethyl)-5a-methyl-3-methylidene-4,5,6,7,9a,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one 163194661 Click to see CC12CCC3C(C1C(=CCC2O)CO)OC(=O)C3=C 264.32 unknown https://doi.org/10.1055/S-2005-864191
(3aS,5aR,6R)-6-hydroxy-5a,9-dimethyl-3-methylidene-4,5,6,7,8,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one 5319200 Click to see CC1=C2C3C(CCC2(C(CC1)O)C)C(=C)C(=O)O3 248.32 unknown https://doi.org/10.1016/S0024-3205(00)00542-7
(5a-Methyl-3,9-dimethylidene-2-oxo-3a,4,5,8,9a,9b-hexahydrobenzo[g][1]benzofuran-8-yl) acetate 14466113 Click to see CC(=O)OC1C=CC2(CCC3C(C2C1=C)OC(=O)C3=C)C 288.34 unknown https://doi.org/10.1016/S0968-0896(00)00127-9
[(3aS,5aS,8R,9aR,9bS)-5a-methyl-3,9-dimethylidene-2-oxo-3a,4,5,8,9a,9b-hexahydrobenzo[g][1]benzofuran-8-yl] acetate 10469367 Click to see CC(=O)OC1C=CC2(CCC3C(C2C1=C)OC(=O)C3=C)C 288.34 unknown https://doi.org/10.1016/S0968-0896(00)00127-9
3-Oxo-6betaH-eudesm-1,4,11-trien-6,13-olide 181840 Click to see CC1=C2C3C(CCC2(C=CC1=O)C)C(=C)C(=O)O3 244.28 unknown https://doi.org/10.1016/S0968-0896(00)00127-9
5a,9-Dimethyl-3-methylidene-3a,4,5,9b-tetrahydrobenzo[g][1]benzofuran-2,8-dione 3874468 Click to see CC1=C2C3C(CCC2(C=CC1=O)C)C(=C)C(=O)O3 244.28 unknown https://doi.org/10.1016/S0968-0896(00)00127-9
6-Hydroxy-5a-methyl-3,9-dimethylidenedecahydronaphtho[1,2-b]furan-2(3h)-one 98958 Click to see CC12CCC3C(C1C(=C)CCC2O)OC(=O)C3=C 248.32 unknown https://doi.org/10.1021/NP50010A016
https://doi.org/10.1016/S0968-0896(00)00127-9
https://doi.org/10.1055/S-2005-864191
6-hydroxy-9-(hydroxymethyl)-5a-methyl-3-methylidene-4,5,6,7,9a,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one 72983010 Click to see CC12CCC3C(C1C(=CCC2O)CO)OC(=O)C3=C 264.32 unknown https://doi.org/10.1055/S-2005-864191
Magnolialide 636954 Click to see CC1=C2C3C(CCC2(C(CC1)O)C)C(=C)C(=O)O3 248.32 unknown https://doi.org/10.1016/S0024-3205(00)00542-7
Reynosin 482788 Click to see CC12CCC3C(C1C(=C)CCC2O)OC(=O)C3=C 248.32 unknown https://doi.org/10.1021/NP50010A016
https://doi.org/10.1016/S0968-0896(00)00127-9
https://doi.org/10.1055/S-2005-864191
Santamarine 188297 Click to see CC1=CCC(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O 248.32 unknown https://doi.org/10.1021/NP50010A016
https://doi.org/10.1016/S0024-3205(00)00542-7
https://doi.org/10.1016/S0968-0896(00)00127-9
https://doi.org/10.1055/S-2005-864191
https://doi.org/10.1016/S0960-894X(99)00442-4
Sesquiterpene lactone CP-1 331391 Click to see CC1=CCC(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O 248.32 unknown https://doi.org/10.1016/S0968-0896(00)00127-9
https://doi.org/10.1055/S-2005-864191
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1R,5S,8S)-8,12-dimethyl-4-methylidene-2-oxatricyclo[6.5.0.01,5]tridec-12-en-3-one 16082053 Click to see CC1=CC23C(CCC2(CCC1)C)C(=C)C(=O)O3 232.32 unknown https://doi.org/10.1248/CPB.54.1187
(3,6,10-trimethyl-2-oxo-3a,4,7,8,11,11a-hexahydro-3H-cyclodeca[b]furan-4-yl) acetate 163027219 Click to see CC1C2C(CC(=CCCC(=CC2OC(=O)C)C)C)OC1=O 292.40 unknown https://doi.org/10.1248/CPB.24.667
(3aS,4R,5E,9E,11aS)-3a,4,7,8,11,11a-Hexahydro-4-hydroxy-6,10-dimethyl-3-methylenecyclodeca[b]furan-2(3H)-one 14191561 Click to see CC1=CC(C2C(CC(=CCC1)C)OC(=O)C2=C)O 248.32 unknown https://doi.org/10.1248/CPB.24.667
https://doi.org/10.1080/14786419.2010.502532
(3aS,6E,11aR)-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 133640194 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1016/S0960-894X(99)00442-4
https://doi.org/10.1016/S0968-0896(00)00127-9
https://doi.org/10.1021/NP50010A016
https://doi.org/10.1093/ALCALC/37.2.121
https://doi.org/10.1016/0031-9422(92)83320-X
https://doi.org/10.1016/S0024-3205(00)00542-7
(3R,3aS,4R,5E,9E,11aS)-4-hydroxy-3,6,10-trimethyl-3a,4,7,8,11,11a-hexahydro-3H-cyclodeca[b]furan-2-one 163097729 Click to see CC1C2C(CC(=CCCC(=CC2O)C)C)OC1=O 250.33 unknown https://doi.org/10.1248/CPB.24.667
(6,10-Dimethyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl) acetate 299917 Click to see CC1=CC(C2C(CC(=CCC1)C)OC(=O)C2=C)OC(=O)C 290.40 unknown https://doi.org/10.1248/CPB.24.667
[(3aR,4R,5Z,9Z,11aS)-6,10-dimethyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl] acetate 90471674 Click to see CC1=CC(C2C(CC(=CCC1)C)OC(=O)C2=C)OC(=O)C 290.40 unknown https://doi.org/10.1021/NP50010A016
[(3R,3aR,4R,5E,9E,11aS)-3,6,10-trimethyl-2-oxo-3a,4,7,8,11,11a-hexahydro-3H-cyclodeca[b]furan-4-yl] acetate 163027220 Click to see CC1C2C(CC(=CCCC(=CC2OC(=O)C)C)C)OC1=O 292.40 unknown https://doi.org/10.1248/CPB.24.667
[(4S,5E,9E)-6,10-dimethyl-3-methylidene-2-oxo-2,3,3a,4,7,8,11,11a-octahydrocyclodeca[b]furan-4-yl] acetate 44602428 Click to see CC1=CC(C2C(CC(=CCC1)C)OC(=O)C2=C)OC(=O)C 290.40 unknown via CMAUP database
[(5E,9E)-6,10-dimethyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl] acetate 5383546 Click to see CC1=CC(C2C(CC(=CCC1)C)OC(=O)C2=C)OC(=O)C 290.40 unknown via CMAUP database
4-hydroxy-3,6,10-trimethyl-3a,4,7,8,11,11a-hexahydro-3H-cyclodeca[b]furan-2-one 163097728 Click to see CC1C2C(CC(=CCCC(=CC2O)C)C)OC1=O 250.33 unknown https://doi.org/10.1248/CPB.24.667
4-Hydroxy-6,10-dimethyl-3-methylidene-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-2-one 73718740 Click to see CC1=CC(C2C(CC(=CCC1)C)OC(=O)C2=C)O 248.32 unknown https://doi.org/10.1248/CPB.24.667
https://doi.org/10.1080/14786419.2010.502532
6,10-Dimethyl-3-methylene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 556919 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1093/ALCALC/37.2.121
8,12-Dimethyl-4-methylidene-2-oxatricyclo[6.5.0.01,5]tridec-12-en-3-one 73236253 Click to see CC1=CC23C(CCC2(CCC1)C)C(=C)C(=O)O3 232.32 unknown https://doi.org/10.1248/CPB.54.1187
Costunolid 6436243 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown via CMAUP database
Costunolide 5281437 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1016/S0960-894X(99)00442-4
https://doi.org/10.1016/S0968-0896(00)00127-9
https://doi.org/10.1021/NP50010A016
https://doi.org/10.1093/ALCALC/37.2.121
https://doi.org/10.1016/0031-9422(92)83320-X
https://doi.org/10.1016/S0024-3205(00)00542-7
Laurenobiolide 5281475 Click to see CC1=CC(C2C(CC(=CCC1)C)OC(=O)C2=C)OC(=O)C 290.40 unknown https://doi.org/10.1021/NP50010A016
https://doi.org/10.1248/CPB.24.667
Tulipinolide 5281504 Click to see CC1=CC2C(C(CC(=CCC1)C)OC(=O)C)C(=C)C(=O)O2 290.40 unknown https://doi.org/10.1021/NP50010A016
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3,6,9-Trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-8-yl) acetate 12445011 Click to see CC(=O)OC1CC2C(C1=C)C3C(CCC2=C)C(=C)C(=O)O3 288.34 unknown https://doi.org/10.1248/CPB.50.1514
https://doi.org/10.1016/S0968-0896(00)00127-9
3,6,9-Trimethyldecahydroazuleno[4,5-b]furan-2(9bh)-one 5316109 Click to see CC1CCC2C(C(=O)OC2C3C1CCC3C)C 236.35 unknown via CMAUP database
3beta-Chlorodehydrocostuslactone 10659317 Click to see C=C1CCC2C(C3C1CC(C3=C)Cl)OC(=O)C2=C 264.74 unknown https://doi.org/10.1248/CPB.54.1187
8-Chloro-3,6,9-trimethylidene-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 85222801 Click to see C=C1CCC2C(C3C1CC(C3=C)Cl)OC(=O)C2=C 264.74 unknown https://doi.org/10.1248/CPB.54.1187
Dehydrocostus lactone, (-)- 73174 Click to see C=C1CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1002/PCA.825
https://doi.org/10.1016/S0024-3205(00)00542-7
https://doi.org/10.1016/0031-9422(92)83320-X
https://doi.org/10.1248/CPB.54.1187
https://doi.org/10.1248/CPB.50.1514
https://doi.org/10.1016/S0968-0896(00)00127-9
https://doi.org/10.1016/S0960-894X(99)00442-4
Dehydrocostuslactone 4426320 Click to see C=C1CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1248/CPB.54.1187
https://doi.org/10.1016/S0968-0896(00)00127-9
https://doi.org/10.1002/PCA.825
https://doi.org/10.1016/0031-9422(92)83320-X
https://doi.org/10.1248/CPB.50.1514
Eremanthin 100572 Click to see CC1=CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1016/0031-9422(92)83320-X
https://doi.org/10.1016/S0024-3205(00)00542-7
Eremanthine 23928144 Click to see CC1=CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1016/S0024-3205(00)00542-7
Zaluzanin C 72646 Click to see C=C1CCC2C(C3C1CC(C3=C)O)OC(=O)C2=C 246.30 unknown https://doi.org/10.1016/S0024-3205(00)00542-7
Zaluzanin D 12445012 Click to see CC(=O)OC1CC2C(C1=C)C3C(CCC2=C)C(=C)C(=O)O3 288.34 unknown https://doi.org/10.1248/CPB.50.1514
https://doi.org/10.1016/S0968-0896(00)00127-9
https://doi.org/10.1016/0031-9422(92)83320-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Enol esters
3,7-Dimethyl-trans-2,6-octadien-1-yl acetate 24832062 Click to see CC(=CCCC(=COC(=O)C)C)C 182.26 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
cis-Aconitic acid 643757 Click to see C(C(=CC(=O)O)C(=O)O)C(=O)O 174.11 unknown via CMAUP database
trans-Aconitic acid 444212 Click to see C(C(=CC(=O)O)C(=O)O)C(=O)O 174.11 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
(2S,3R,4S,5S,6R)-2-[(1R)-1,2-dihydroxyethyl]-6-(hydroxymethyl)oxane-2,3,4,5-tetrol 162870234 Click to see C(C1C(C(C(C(O1)(C(CO)O)O)O)O)O)O 240.21 unknown https://doi.org/10.1271/BBB1961.53.2539
2-(1,2-Dihydroxyethyl)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol 162870232 Click to see C(C1C(C(C(C(O1)(C(CO)O)O)O)O)O)O 240.21 unknown https://doi.org/10.1271/BBB1961.53.2539
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(4-Hydroxy-3-methoxyphenyl)ethyl beta-D-glucopyranoside 11381926 Click to see COC1=C(C=CC(=C1)CCOC2C(C(C(C(O2)CO)O)O)O)O 330.33 unknown https://doi.org/10.1021/JF048782T
2-[2-(4-Hydroxy-3-methoxyphenyl)ethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 72825138 Click to see COC1=C(C=CC(=C1)CCOC2C(C(C(C(O2)CO)O)O)O)O 330.33 unknown https://doi.org/10.1021/JF048782T
Benzyl alcohol xylopyranosyl-(1-6)-glucopyranoside 14730864 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O 402.40 unknown https://doi.org/10.1021/JF048782T
Benzyl beta-primeveroside 131248 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O 402.40 unknown https://doi.org/10.1021/JF048782T
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Octoses
d-Gluco-l-glycero-3-octulose 129650461 Click to see C(C(C(C(C(C(=O)C(CO)O)O)O)O)O)O 240.21 unknown https://doi.org/10.1271/BBB1961.53.2539
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol 6251 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown https://doi.org/10.1021/NP50010A016
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Reticuline 439653 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1021/NP50023A008
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3aS,5aS,10aS,10bS)-5a,10-dimethyl-3-methylene-3a,4,5,5a,10a,10b-hexahydrooxepino[4,5-g]benzofuran-2(3H)-one 14757922 Click to see CC1=COC=CC2(C1C3C(CC2)C(=C)C(=O)O3)C 246.30 unknown https://doi.org/10.1016/S0024-3205(00)00542-7
alpha-Methylene-gamma-butyrolactone 68352 Click to see C=C1CCOC1=O 98.10 unknown https://doi.org/10.1016/S0968-0896(00)00127-9
https://doi.org/10.1016/S0960-894X(99)00442-4
> Organoheterocyclic compounds / Pyridines and derivatives / Pyrrolidinylpyridines
Nicotine 89594 Click to see CN1CCCC1C2=CN=CC=C2 162.23 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
(1S,4R,5R)-4,7,7-trimethyl-6-oxabicyclo[3.2.1]oct-2-ene 162867472 Click to see CC1C=CC2CC1OC2(C)C 152.23 unknown https://doi.org/10.1016/S0031-9422(00)91156-7
> Organosulfur compounds / Sulfonyls / Sulfones
Dimethyl sulfone 6213 Click to see CS(=O)(=O)C 94.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1021/JF051513Y
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1021/JF051513Y
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3R)-2-(3,4-dihydroxyphenyl)-6-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 13990894 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 https://doi.org/10.1016/S0031-9422(97)00563-3
(2R,3S)-2-(3,4-dihydroxyphenyl)-6-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 102266638 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 https://doi.org/10.1016/S0031-9422(97)00563-3
(2S,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 154497278 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 https://doi.org/10.1016/S0031-9422(97)00563-3
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 https://doi.org/10.1016/S0031-9422(97)00563-3
> 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 https://doi.org/10.1016/S0031-9422(97)00563-3
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/S0031-9422(97)00563-3
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin 65084 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1016/S0031-9422(97)00563-3
> 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/10.1021/JF051513Y
https://doi.org/10.1016/S0031-9422(97)00563-3
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/10.1021/JF051513Y
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4R,5S,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4-hydroxy-5-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-2-methyloxan-3-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate 163038913 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown https://doi.org/10.1016/S0031-9422(97)00563-3
[2-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 74978080 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(97)00563-3
https://doi.org/10.1021/JF048782T
[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-5-hydroxy-4-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-2-methyloxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 156602915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown https://doi.org/10.1016/S0031-9422(97)00563-3
https://doi.org/10.1021/JF048782T
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(97)00563-3
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 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/10.1248/BPB.25.102
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 26339717 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(97)00563-3
2''-O-E-p-Coumaroylafzelin 49836074 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(97)00563-3
https://doi.org/10.1021/JF048782T
2'',4''-Di-O-(E-p-Coumaroyl)afzelin 11765457 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown https://doi.org/10.1016/S0031-9422(97)00563-3
2'',4''-Di-O-(Z-p-coumaroyl)afzelin 49822436 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown https://doi.org/10.1016/S0031-9422(97)00563-3
2",4"-Di-O-(Z-p-coumaroyl)afzelin 73066482 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown https://doi.org/10.1016/S0031-9422(97)00563-3
3'',4''-Di-O-p-coumaroylafzelin 51136469 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O 724.70 unknown https://doi.org/10.1016/S0031-9422(97)00563-3
https://doi.org/10.1021/JF048782T
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 https://doi.org/10.1248/BPB.25.102
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Kaempferol-7-rhamnoside 25079965 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolactams
Hitachimycin 5384563 Click to see CC1=CC2CC(C(=C2C(=O)CC(CCC=CCC(NC(=O)C=CC=C1)C3=CC=CC=C3)O)O)OC 477.60 unknown https://doi.org/10.1021/NP50023A008
Palustrine 442867 Click to see CCC(C1CC=CC2N1CCCNCCCCNC(=O)C2)O 309.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues / Pectenotoxins and derivatives
14-(2,3-Dihydroxy-4-methyloxan-2-yl)-28-hydroxy-5,7,9,19,29-pentamethyl-18,31-dioxo-13,17,38,39,40,41,42,43-octaoxaoctacyclo[31.4.1.11,35.12,5.120,24.124,27.129,32.012,16]tritetraconta-8,10-diene-35-carbaldehyde 74051868 Click to see CC1CCOC(C1O)(C2CC3C(O2)C=CC(=CC(CC4(CCC(O4)C56CCC(O5)(CC(O6)C7C(=O)CC(O7)(C(C8CCC9(O8)CCCC(O9)C(C(=O)O3)C)O)C)C=O)C)C)C)O 873.00 unknown https://doi.org/10.1021/JF048782T

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