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Dittrichia graveolens

Dittrichia graveolens - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Dittrichia graveolens - 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 UUID643fc633ae00b695133039
Scientific name Dittrichia graveolens
Authority (L.) Greuter
First published in Exsicc. Genav. Conserv. Bot. Distrib. Fasc. 4: 71 (1973)

Description Top

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Dittrichia graveolens, also known as stinkwort or stinking fleabane, is a plant species in the sunflower family that is native to southern Europe, North Africa, and western Asia. It has spread to other regions, including California, Asia, Africa, and Australia, where it is considered a noxious weed. In California, it is classified as an invasive species and is a potential threat to wine production. This plant can grow up to 130 centimeters tall and has a strong, unpleasant odor. Its leaves are long and narrow with small teeth and glandular hairs. The plant produces yellow flower heads with numerous ray and disc florets. The seeds have barbs that can harm grazing animals, and the oils in the plant can affect the flavor of meat and milk. The sticky resin can also cause allergic reactions and severe dermatitis in humans, so it is recommended to wear protective gloves when handling the plant.

Synonyms Top

Scientific name Authority First published in
Cupularia graveolens Godr. & Gren. Fl. France 2: 180 (1850)
Inula quadridentata Lag. Gen. Sp. Pl. : 30 (1816)
Conyza minor Bubani Fl. Pyren. ii. 250 (1899)
Jacobaea graveolens (L.) Merino Merino, Fl. Galicia 2. 1906. 336 1906
Paniopsis graveolens Raf. Fl. Tellur. 2: 49 (1837)
Erigeron graveolens L. Cent. Pl. I. 28. 1755 [19 Feb 1755]
Solidago graveolens Lam. Fl. Franç. 2: 145 (1779)
Inula brahuica Boiss. Fl. Orient. 3: 199 (1875)
Inula graveolens (L.) Desf. Fl. Atlant. 2: 275 (1799)
Pulicaria graveolens Nyn. Syll. Fl. Eur. : 19 (1855)
Helenium graveolens (L.) Kuntze Revis. Gen. Pl. 1: 342 (1891)
Conyza graveolens Steud. Nomencl. Bot. : 222 (1821)

Common names Top

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Language Common/alternative name
English stink aster
English stinkwort
Arabic طباق نفاح
Catalan olivardó
co inula odora
co picitedda
co pecitella
Czech ditrichie smradlavá
Welsh cedowydd drewllyd
German klebalant
German klebriger alant
German schmalblättriger klebalant
French inule fétide
Dutch kamferalant

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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
    • Southern Africa
      • Cape Provinces
  • Asia-temperate
    • Western Asia
      • Afghanistan
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Australasia
    • Australia
      • New South Wales
      • Queensland
      • South Australia
      • Tasmania
      • Victoria
      • Western Australia
    • New Zealand
      • New Zealand North
  • Europe
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Germany
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Mexico
      • Mexico Northwest
    • Northeastern U.S.A.
      • New Jersey
      • New York
    • Southwestern U.S.A.
      • California

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000003319
Canadensys 9834
USDA Plants DIGR3
Tropicos 2702390
INPN 95186
Flora of Italy 5522
KEW urn:lsid:ipni.org:names:201892-1
The Plant List gcc-103204
Open Tree Of Life 3899100
Observations.org 6701
NCBI Taxonomy 1532790
NBN Atlas NBNSYS0000004400
Nature Serve 2.147961
IPNI 201892-1
iNaturalist 58822
GBIF 3101193
Freebase /m/0wqyvg1
EPPO INUGR
EOL 487919
Calflora (Californian flora) 8482
USDA GRIN 401641
Wikipedia Dittrichia_graveolens

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_038502395.1 Dgra_v1_pri Scaffold University of California, Santa Cruz 2024-04-26 41.0x 796.25 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
Polyphenols of the Inuleae-Inulinae and Their Biological Activities: A Review Malarz J, Michalska K, Stojakowska A Molecules 27-Apr-2024
PMCID:PMC11085778
doi:10.3390/molecules29092014
PMID:38731504
A systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B J Ethnopharmacol 25-Mar-2024
PMCID:PMC7615571
doi:10.1016/j.jep.2023.117622
PMID:38128894
The impact of selected xanthophylls on oil hydrolysis by pancreatic lipase: in silico and in vitro studies Dąbrowski G, Czaplicki S, Szustak M, Korkus E, Gendaszewska-Darmach E, Konopka I Sci Rep 01-Feb-2024
PMCID:PMC10834431
doi:10.1038/s41598-024-53312-9
PMID:38302772
Essential Oils in Cervical Cancer: Narrative Review on Current Insights and Future Prospects Abd Rashid N, Mohamad Najib NH, Abdul Jalil NA, Teoh SL Antioxidants (Basel) 13-Dec-2023
PMCID:PMC10740549
doi:10.3390/antiox12122109
PMID:38136228
Use of Algerian Type Ras El-Hanout Spices Mixture with Marination to Increase the Sensorial Quality, Shelf Life, and Safety of Whole Rabbit Carcasses under Low-O2 Modified Atmosphere Packaging Djenane D, Ben Miri Y, Ariño A Foods 02-Aug-2023
PMCID:PMC10418402
doi:10.3390/foods12152931
PMID:37569200
Diet composition of wild columbiform birds: next-generation sequencing of plant and metazoan DNA in faecal samples Schumm YR, Masello JF, Vreugdenhil-Rowlands J, Fischer D, Hillerich K, Quillfeldt P Naturwissenschaften 22-Jul-2023
PMCID:PMC10363069
doi:10.1007/s00114-023-01863-8
PMID:37480393
Strategies for the Management of Aggressive Invasive Plant Species Lorenzo P, Morais MC Plants (Basel) 28-Jun-2023
PMCID:PMC10346621
doi:10.3390/plants12132482
PMID:37447043
Legume effects in a native community invaded by alien Asteraceae in a multi-species comparison Ferenc V, Brendel MR, Sheppard CS Oecologia 18-Jun-2023
PMCID:PMC10307714
doi:10.1007/s00442-023-05400-2
PMID:37332036
Medicinal plants of Jordan: Scoping review Abu-Odeh A, Fino L, Al-Absi G, Alnatour D, Al-Darraji M, Shehadeh M, Suaifan G Heliyon 07-Jun-2023
PMCID:PMC10276232
doi:10.1016/j.heliyon.2023.e17081
PMID:37332946
Chromosome-level reference genome of stinkwort, Dittrichia graveolens (L.) Greuter: A resource for studies on invasion, range expansion, and evolutionary adaptation under global change McEvoy SL, Lustenhouwer N, Melen MK, Nguyen O, Marimuthu MP, Chumchim N, Beraut E, Parker IM, Meyer RS J Hered 01-Jun-2023
PMCID:PMC10445520
doi:10.1093/jhered/esad033
PMID:37262429
Application of Zebrafish as a Model for Anti-Cancer Activity Evaluation and Toxicity Testing of Natural Products Shen Y, Sheng R, Guo R Pharmaceuticals (Basel) 01-Jun-2023
PMCID:PMC10305033
doi:10.3390/ph16060827
PMID:37375774
In Vitro Anti-inflammatory Activity of Three Inula Species Essential Oils in Lipopolysaccharide-Stimulated RAW 264.7 Macrophages Gharred N, Ali LM, Bettache N, Dridi-Dhaouadi S, Morere A, Menut C 16-Mar-2023
PMCID:PMC10018620
doi:10.1007/s42250-023-00641-3
Green Synthesis of Bioinspired Nanoparticles Mediated from Plant Extracts of Asteraceae Family for Potential Biological Applications Jaison JP, Balasubramanian B, Gangwar J, James N, Pappuswamy M, Anand AV, Al-Dhabi NA, Valan Arasu M, Liu WC, Sebastian JK Antibiotics (Basel) 08-Mar-2023
PMCID:PMC10044610
doi:10.3390/antibiotics12030543
PMID:36978410
Electrospun PLA-Based Biomaterials Loaded with Melissa officinalis Extract with Strong Antioxidant Activity Stoyanova N, Spasova M, Manolova N, Rashkov I, Kamenova-Nacheva M, Staleva P, Tavlinova-Kirilova M Polymers (Basel) 21-Feb-2023
PMCID:PMC10007429
doi:10.3390/polym15051070
PMID:36904311
Harvest time explains substantially more variance in yield, essential oil and quality performances of Salvia officinalis than irrigation and putrescine application Mohammadi-Cheraghabadi M, Modarres-Sanavy SA, Sefidkon F, Mokhtassi-Bidgoli A, Hazrati S Physiol Mol Biol Plants 04-Jan-2023
PMCID:PMC9886791
doi:10.1007/s12298-022-01272-7
PMID:36733840

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 / Benzoic acid esters
(4-Hydroxy-3-methylbut-2-enyl) benzoate 163079105 Click to see CC(=CCOC(=O)C1=CC=CC=C1)CO 206.24 unknown https://doi.org/10.1016/S0031-9422(00)83887-X
(e)-4-Hydroxy-3-methylbut-2-enyl benzoate 91998745 Click to see CC(=CCOC(=O)C1=CC=CC=C1)CO 206.24 unknown https://doi.org/10.1016/S0031-9422(00)83887-X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
(4-Hydroxy-3-methylbut-2-enyl) 2-hydroxybenzoate 162846882 Click to see CC(=CCOC(=O)C1=CC=CC=C1O)CO 222.24 unknown https://doi.org/10.1016/S0031-9422(00)83887-X
[(E)-4-hydroxy-3-methylbut-2-enyl] 2-hydroxybenzoate 101417724 Click to see CC(=CCOC(=O)C1=CC=CC=C1O)CO 222.24 unknown https://doi.org/10.1016/S0031-9422(00)83887-X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1016/0031-9422(91)83034-I
> Benzenoids / Phenol esters
[(2R)-2-[4-methyl-2-(2-methylpropanoyloxy)phenyl]oxiran-2-yl]methyl 2-methylpropanoate 25837754 Click to see CC1=CC(=C(C=C1)C2(CO2)COC(=O)C(C)C)OC(=O)C(C)C 320.40 unknown https://doi.org/10.1016/S0031-9422(00)83887-X
Bis(2-methylpropanoyloxy)-9,10-epoxy-p-mentha-1,3,5-triene 11472669 Click to see CC1=CC(=C(C=C1)C2(CO2)COC(=O)C(C)C)OC(=O)C(C)C 320.40 unknown https://doi.org/10.1016/S0031-9422(00)83887-X
> Benzenoids / Phenols / Tyrosols and derivatives
2-(4-Hydroxyphenyl)ethyl octadecanoate 481672 Click to see CCCCCCCCCCCCCCCCCC(=O)OCCC1=CC=C(C=C1)O 404.60 unknown https://doi.org/10.1016/0031-9422(91)83034-I
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
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/10.1080/10412905.2000.9699576
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1080/10412905.2000.9699576
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.2000.9699576
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
2-[(2R,4aS,8R,8aR)-8-hydroxy-4a,8-dimethyl-1,2,3,4,5,8a-hexahydronaphthalen-2-yl]prop-2-enoic acid 162842573 Click to see CC12CCC(CC1C(C=CC2)(C)O)C(=C)C(=O)O 250.33 unknown https://doi.org/10.1248/CPB.56.1535
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.2000.9699576
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-(4a-Methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enoic acid 12304100 Click to see CC12CCCC(=C)C1CC(CC2)C(=C)C(=O)O 234.33 unknown https://doi.org/10.1016/0031-9422(91)83034-I
https://doi.org/10.1248/CPB.56.1535
2-(4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl)prop-2-enoic acid 14706940 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C(=O)O)C 234.33 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
https://doi.org/10.1016/0031-9422(91)83034-I
https://doi.org/10.1248/CPB.56.1535
2-(5-Hydroxy-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enoic acid 14633049 Click to see CC12CCC(CC1C(=C)CCC2O)C(=C)C(=O)O 250.33 unknown https://doi.org/10.1016/0031-9422(91)83034-I
2-(6-Hydroxy-4a-methyl-8-methylenedecahydro-2-naphthalenyl)acrylic acid 496072 Click to see CC12CCC(CC1C(=C)CC(C2)O)C(=C)C(=O)O 250.33 unknown https://doi.org/10.1016/0031-9422(91)83034-I
2-(6,8-Dihydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enoic acid 73817302 Click to see CC12CCC(CC1C(CC(C2)O)(C)O)C(=C)C(=O)O 268.35 unknown https://doi.org/10.1248/CPB.56.1535
2-(7-Hydroxy-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enoic acid 14191232 Click to see CC12CCC(CC1C(=C)C(CC2)O)C(=C)C(=O)O 250.33 unknown https://doi.org/10.1248/CPB.56.1535
https://doi.org/10.1016/S0031-9422(00)95185-9
https://doi.org/10.1016/0031-9422(91)83034-I
2-(8-Hydroxy-4a,8-dimethyldecahydro-2-naphthalenyl)acrylic acid 496073 Click to see CC12CCCC(C1CC(CC2)C(=C)C(=O)O)(C)O 252.35 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
https://doi.org/10.1016/0031-9422(91)83034-I
https://doi.org/10.1248/CPB.56.1535
2-[(2R,4aR,5R,8aS)-5-hydroxy-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid 14633051 Click to see CC12CCC(CC1C(=C)CCC2O)C(=C)C(=O)O 250.33 unknown https://doi.org/10.1016/0031-9422(91)83034-I
2-[(2R,4aR,8aR)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid 168796 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C(=O)O)C 234.33 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
https://doi.org/10.1016/0031-9422(91)83034-I
https://doi.org/10.1248/CPB.56.1535
2-[(2R,4aS,6R,8aR)-6-hydroxy-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid 162901460 Click to see CC1=CC(CC2(C1CC(CC2)C(=C)C(=O)O)C)O 250.33 unknown https://doi.org/10.1248/CPB.56.1535
2-[(2R,4aS,6R,8S,8aR)-6,8-dihydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid 25130456 Click to see CC12CCC(CC1C(CC(C2)O)(C)O)C(=C)C(=O)O 268.35 unknown https://doi.org/10.1248/CPB.56.1535
2-[(2R,4aS,6S,8aR)-6-hydroxy-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid 101607193 Click to see CC1=CC(CC2(C1CC(CC2)C(=C)C(=O)O)C)O 250.33 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
2-[(2R,4aS,6S,8aS)-6-hydroxy-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid 13995524 Click to see CC12CCC(CC1C(=C)CC(C2)O)C(=C)C(=O)O 250.33 unknown https://doi.org/10.1016/0031-9422(91)83034-I
2-[(2R,4aS,7R,8aR)-7-hydroxy-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid 38348725 Click to see CC12CCC(CC1C(=C)C(CC2)O)C(=C)C(=O)O 250.33 unknown https://doi.org/10.1248/CPB.56.1535
https://doi.org/10.1016/S0031-9422(00)95185-9
https://doi.org/10.1016/0031-9422(91)83034-I
2-[(2R,4aS)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid 154495907 Click to see CC1=C2CC(CCC2(CCC1)C)C(=C)C(=O)O 234.33 unknown https://doi.org/10.1248/CPB.56.1535
2-[(2S,4aR,8R,8aS)-8-hydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid 102317260 Click to see CC12CCCC(C1CC(CC2)C(=C)C(=O)O)(C)O 252.35 unknown https://doi.org/10.1016/0031-9422(91)83034-I
2-[(4aR,8R,8aR)-8-hydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid 137795140 Click to see CC12CCCC(C1CC(CC2)C(=C)C(=O)O)(C)O 252.35 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
https://doi.org/10.1016/0031-9422(91)83034-I
2-[(8aR)-2,4a-dimethyl-8-methylidene-3,4,5,6,7,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid 5316106 Click to see CC12CCCC(=C)C1CC(CC2)(C)C(=C)C(=O)O 248.36 unknown https://doi.org/10.1016/0031-9422(91)83034-I
https://doi.org/10.1016/S0031-9422(00)83887-X
Costic acid 6451579 Click to see CC12CCCC(=C)C1CC(CC2)C(=C)C(=O)O 234.33 unknown https://doi.org/10.1016/0031-9422(91)83034-I
https://doi.org/10.1248/CPB.56.1535
https://doi.org/10.1016/S0031-9422(00)83887-X
Eudesma-4,11(13)-dien-12-oic acid;gamma-Costic acid 129316949 Click to see CC1=C2CC(CCC2(CCC1)C)C(=C)C(=O)O 234.33 unknown https://doi.org/10.1016/0031-9422(91)83034-I
Ilicic acid 11876195 Click to see CC12CCCC(C1CC(CC2)C(=C)C(=O)O)(C)O 252.35 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
https://doi.org/10.1248/CPB.56.1535
Methyl 2-(7,8-dihydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enoate 74390181 Click to see CC12CCC(CC1C(C(CC2)O)(C)O)C(=C)C(=O)OC 282.37 unknown https://doi.org/10.1248/CPB.56.1535
methyl 2-[(2R,4aS,7R,8S,8aR)-7-acetyloxy-8-hydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoate 15699305 Click to see CC(=O)OC1CCC2(CCC(CC2C1(C)O)C(=C)C(=O)OC)C 324.40 unknown https://doi.org/10.1248/CPB.56.1535
methyl 2-[(2R,4aS,7R,8S,8aR)-7,8-dihydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoate 25130455 Click to see CC12CCC(CC1C(C(CC2)O)(C)O)C(=C)C(=O)OC 282.37 unknown https://doi.org/10.1248/CPB.56.1535
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones
6-O-Acetylmexicanin I 98952 Click to see CC1CC2C(C(C3(C1C=CC3=O)C)OC(=O)C)C(=C)C(=O)O2 304.34 unknown https://doi.org/10.1248/CPB.56.1535
8-Epihelenalin 10400473 Click to see CC1CC2C(C(C3(C1C=CC3=O)C)O)C(=C)C(=O)O2 262.30 unknown https://doi.org/10.1248/CPB.56.1535
Bigelovin 3080597 Click to see CC1CC2C(C(C3(C1C=CC3=O)C)OC(=O)C)C(=C)C(=O)O2 304.34 unknown https://doi.org/10.1248/CPB.56.1535
Sample A of helenalin 52167 Click to see CC1CC2C(C(C3(C1C=CC3=O)C)O)C(=C)C(=O)O2 262.30 unknown https://doi.org/10.1248/CPB.56.1535
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
(1R,3aS,5S,5aS,8aS,9aR)-1,5,8a-trimethyl-3a,4,5,5a,6,7,9,9a-octahydro-1H-azuleno[6,7-b]furan-2,8-dione 162903788 Click to see CC1CC2C(CC3(C1CCC3=O)C)C(C(=O)O2)C 250.33 unknown https://doi.org/10.1016/S0031-9422(00)83887-X
(1S,3aR,5S,5aS,8aS,9aR)-1,5,8a-trimethyl-3a,4,5,5a,6,7,9,9a-octahydro-1H-azuleno[6,7-b]furan-2,8-dione 162903789 Click to see CC1CC2C(CC3(C1CCC3=O)C)C(C(=O)O2)C 250.33 unknown https://doi.org/10.1248/CPB.56.1535
https://doi.org/10.1016/S0031-9422(00)83887-X
1,5,8a-trimethyl-3a,4,5,5a,6,7,9,9a-octahydro-1H-azuleno[6,7-b]furan-2,8-dione 76537581 Click to see CC1CC2C(CC3(C1CCC3=O)C)C(C(=O)O2)C 250.33 unknown https://doi.org/10.1016/S0031-9422(00)83887-X
Azuleno[6,5-b]furan-2,5-dione, decahydro-4a,8-dimethyl-3-methylene-, [3aR-(3aalpha,4abeta,7aalpha,8beta,9aalpha)]- 619106 Click to see CC1CC2C(CC3(C1CCC3=O)C)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/S0031-9422(00)83887-X
https://doi.org/10.1021/NP200319X
https://doi.org/10.1248/CPB.56.1535
Confertin 167852 Click to see CC1CC2C(CC3(C1CCC3=O)C)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1021/NP200319X
https://doi.org/10.1016/S0031-9422(00)83887-X
Graveolide 11043090 Click to see CC1CC2C(CC3(C1CCC3=O)C)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1248/CPB.56.1535
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
11,13-Dihydroivalin 13944074 Click to see CC1C2CC3C(=C)CC(CC3(CC2OC1=O)C)O 250.33 unknown https://doi.org/10.1016/0031-9422(93)85529-Z
7-hydroxy-3,8a-dimethyl-5-methylidene-3a,4,4a,6,7,8,9,9a-octahydro-3H-benzo[f][1]benzofuran-2-one 13944073 Click to see CC1C2CC3C(=C)CC(CC3(CC2OC1=O)C)O 250.33 unknown https://doi.org/10.1016/0031-9422(93)85529-Z
Ivalin 65156 Click to see CC12CC(CC(=C)C1CC3C(C2)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1016/0031-9422(93)85529-Z
Naphtho[2,3-b]furan-2(3H)-one, decahydro-7-hydroxy-8a-methyl-3,5-dimethylene- 457941 Click to see CC12CC(CC(=C)C1CC3C(C2)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1016/0031-9422(93)85529-Z
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(1R,3aS,5aR,8R,8aR,9aR)-8-hydroxy-1,8-dimethyl-5-methylidene-3a,4,5a,6,7,8a,9,9a-octahydro-1H-azuleno[6,5-b]furan-2-one 11032300 Click to see CC1C2CC3C(CCC3(C)O)C(=C)CC2OC1=O 250.33 unknown https://doi.org/10.1016/S0031-9422(00)83887-X
(1S,3R,7S,9S,10S,13R)-9,13-dimethyl-4-methylidene-6,14-dioxatetracyclo[8.4.0.01,13.03,7]tetradecan-5-one 14313754 Click to see CC1CC2C(CC34C1CCC3(O4)C)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/0031-9422(91)83034-I
(3aS,5aR,8R,8aR,9aR)-8-hydroxy-8-methyl-1,5-dimethylidene-3a,4,5a,6,7,8a,9,9a-octahydroazuleno[6,5-b]furan-2-one 10900990 Click to see CC1(CCC2C1CC3C(CC2=C)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)83887-X
11Beta,13-Dihydroinuviscolide 14109629 Click to see CC1C2CC3C(CCC3(C)O)C(=C)CC2OC1=O 250.33 unknown https://doi.org/10.1016/S0031-9422(00)83887-X
4-Epi-Isoinuviscolide 53320574 Click to see CC1=CC2C(CC3C1CCC3(C)O)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1248/CPB.56.1535
4-Epiisoinuviscolide 12310399 Click to see CC1=CC2C(CC3C1CCC3(C)O)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1248/CPB.56.1535
4,5-Epoxy-11(13)-guaien-12,8-olide 14313753 Click to see CC1CC2C(CC34C1CCC3(O4)C)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/0031-9422(91)83034-I
8-Epiinuviscolide 13817985 Click to see CC1(CCC2C1CC3C(CC2=C)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1016/0031-9422(93)85529-Z
8-Hydroxy-8-methyl-1,5-dimethylidene-3a,4,5a,6,7,8a,9,9a-octahydroazuleno[6,5-b]furan-2-one 13817983 Click to see CC1(CCC2C1CC3C(CC2=C)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
https://doi.org/10.1016/S0031-9422(00)83887-X
Inuviscolide 176489 Click to see CC1(CCC2C1CC3C(CC2=C)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
https://doi.org/10.1016/0031-9422(93)85529-Z
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Xanthanolides
(1R,3R,5R,6S,8R,11S)-6,11-dimethyl-5-[(E)-3-oxobut-1-enyl]-4,9-dioxatricyclo[6.3.0.03,5]undecan-10-one 102056125 Click to see CC1CC2C(CC3C1(O3)C=CC(=O)C)C(C(=O)O2)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
(1R,3R,5S,6R,7S,9R)-7-methyl-12-methylidene-5-(2-oxopropyl)-4,10-dioxatricyclo[7.3.0.03,6]dodecan-11-one 162875180 Click to see CC1CC2C(CC3C1C(O3)CC(=O)C)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1248/CPB.56.1535
(3aR,4aS,5S,5aR,6aR)-5-[(3S)-3-hydroxybutyl]-5a-methyl-3-methylidene-3a,4,4a,5,6,6a-hexahydrocyclopropa[f][1]benzofuran-2-one 38356988 Click to see CC(CCC1C2C1(CC3C(C2)C(=C)C(=O)O3)C)O 250.33 unknown https://doi.org/10.1016/0031-9422(91)83034-I
(3aR,6R,7S,8aR)-6-[(1S)-1-hydroxy-3-oxobutyl]-7-methyl-3-methylidene-4,5,6,7,8,8a-hexahydro-3aH-cyclohepta[b]furan-2-one 163185943 Click to see CC1CC2C(CCC1C(CC(=O)C)O)C(=C)C(=O)O2 266.33 unknown https://doi.org/10.1248/CPB.56.1535
(3aR,6R,7S,8aS)-7-methyl-3-methylidene-6-(3-oxobutyl)-4,5,6,7,8,8a-hexahydro-3aH-cyclohepta[b]furan-2-one 163037400 Click to see CC1CC2C(CCC1CCC(=O)C)C(=C)C(=O)O2 250.33 unknown https://doi.org/10.1248/CPB.56.1535
(3aR,7R,8aR)-7-methyl-3-methylidene-6-(3-oxobutyl)-4,7,8,8a-tetrahydro-3aH-cyclohepta[b]furan-2-one 14109627 Click to see CC1CC2C(CC=C1CCC(=O)C)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
(3aR,7S,8aR)-6-[(3S)-3-hydroxybutyl]-7-methyl-3-methylidene-4,7,8,8a-tetrahydro-3aH-cyclohepta[b]furan-2-one 26183548 Click to see CC1CC2C(CC=C1CCC(C)O)C(=C)C(=O)O2 250.33 unknown https://doi.org/10.1016/0031-9422(91)83034-I
(3aR,7S,8aR)-6-[(E)-3-hydroxybut-1-enyl]-7-methyl-3-methylidene-4,5,6,7,8,8a-hexahydro-3aH-cyclohepta[b]furan-2-one 162816932 Click to see CC1CC2C(CCC1C=CC(C)O)C(=C)C(=O)O2 250.33 unknown https://doi.org/10.1248/CPB.56.1535
(3aR,8aS)-7-methyl-3-methylidene-6-(3-oxobutyl)-4,7,8,8a-tetrahydro-3aH-cyclohepta[b]furan-2-one 101423111 Click to see CC1CC2C(CC=C1CCC(=O)C)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/S0031-9422(00)83887-X
(3aS,4aR,5aR,6aR)-5a-methyl-3-methylidene-5-(3-oxobutyl)-3a,4,4a,5,6,6a-hexahydrocyclopropa[f][1]benzofuran-2-one 137705422 Click to see CC(=O)CCC1C2C1(CC3C(C2)C(=C)C(=O)O3)C 248.32 unknown https://doi.org/10.1016/0031-9422(91)83034-I
(3R,3aR,7S,8aR)-3,7-dimethyl-6-(3-oxobutyl)-3,3a,4,7,8,8a-hexahydrocyclohepta[b]furan-2-one 14282664 Click to see CC1CC2C(CC=C1CCC(=O)C)C(C(=O)O2)C 250.33 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
(3R,3aR,8aR)-3,7-dimethyl-6-(3-oxobutyl)-3a,4,8,8a-tetrahydro-3H-cyclohepta[b]furan-2,5-dione 10706730 Click to see CC1C2CC(=O)C(=C(CC2OC1=O)C)CCC(=O)C 264.32 unknown https://doi.org/10.1248/CPB.56.1535
https://doi.org/10.1016/S0031-9422(00)83887-X
(5S)-5a-methyl-3-methylidene-5-(3-oxobutyl)-3a,4,4a,5,6,6a-hexahydrocyclopropa[f][1]benzofuran-2-one 5315684 Click to see CC(=O)CCC1C2C1(CC3C(C2)C(=C)C(=O)O3)C 248.32 unknown https://doi.org/10.1016/0031-9422(91)83034-I
11Alpha,13-Dihydrotomentosin 14282663 Click to see CC1CC2C(CC=C1CCC(=O)C)C(C(=O)O2)C 250.33 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
2H-Cyclohepta[b]furan-2-one, 3,3a,4,7,8,8a-hexahydro-7-methyl-3-methylene-6-(3-oxobutyl)- 540288 Click to see CC1CC2C(CC=C1CCC(=O)C)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
https://doi.org/10.1016/0031-9422(91)83034-I
3,7-Dimethyl-6-(3-oxobutyl)-3,3a,4,7,8,8a-hexahydrocyclohepta[b]furan-2-one 14282662 Click to see CC1CC2C(CC=C1CCC(=O)C)C(C(=O)O2)C 250.33 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
3,7-dimethyl-6-(3-oxobutyl)-3a,4,8,8a-tetrahydro-3H-cyclohepta[b]furan-2,5-dione 85239885 Click to see CC1C2CC(=O)C(=C(CC2OC1=O)C)CCC(=O)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)83887-X
5-(3-Hydroxybutyl)-5a-methyl-3-methylidene-3a,4,4a,5,6,6a-hexahydrocyclopropa[f][1]benzofuran-2-one 85446132 Click to see CC(CCC1C2C1(CC3C(C2)C(=C)C(=O)O3)C)O 250.33 unknown https://doi.org/10.1016/0031-9422(91)83034-I
5a-Methyl-3-methylidene-5-(3-oxobutyl)-3a,4,4a,5,6,6a-hexahydrocyclopropa[f][1]benzofuran-2-one 321484 Click to see CC(=O)CCC1C2C1(CC3C(C2)C(=C)C(=O)O3)C 248.32 unknown https://doi.org/10.1016/0031-9422(91)83034-I
6-(1-hydroxy-3-oxobutyl)-7-methyl-3-methylidene-4,5,6,7,8,8a-hexahydro-3aH-cyclohepta[b]furan-2-one 162993680 Click to see CC1CC2C(CCC1C(CC(=O)C)O)C(=C)C(=O)O2 266.33 unknown https://doi.org/10.1248/CPB.56.1535
6-(3-hydroxybutyl)-7-methyl-3-methylidene-4,7,8,8a-tetrahydro-3aH-cyclohepta[b]furan-2-one 23928111 Click to see CC1CC2C(CC=C1CCC(C)O)C(=C)C(=O)O2 250.33 unknown https://doi.org/10.1016/0031-9422(91)83034-I
6-Methyl-11-methylidene-5-(3-oxobut-1-enyl)-4,9-dioxatricyclo[6.3.0.03,5]undecan-10-one 72733738 Click to see CC1CC2C(CC3C1(O3)C=CC(=O)C)C(=C)C(=O)O2 262.30 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
6,11-Dimethyl-5-(3-oxobut-1-enyl)-4,9-dioxatricyclo[6.3.0.03,5]undecan-10-one 162945096 Click to see CC1CC2C(CC3C1(O3)C=CC(=O)C)C(C(=O)O2)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
7-Methyl-12-methylidene-5-(2-oxopropyl)-4,10-dioxatricyclo[7.3.0.03,6]dodecan-11-one 162875179 Click to see CC1CC2C(CC3C1C(O3)CC(=O)C)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1248/CPB.56.1535
7-methyl-3-methylidene-6-(3-oxobutyl)-4,5,6,7,8,8a-hexahydro-3aH-cyclohepta[b]furan-2-one 163037399 Click to see CC1CC2C(CCC1CCC(=O)C)C(=C)C(=O)O2 250.33 unknown https://doi.org/10.1248/CPB.56.1535
8-Epi-xanthatin-1,5alpha-epoxide 14633043 Click to see CC1CC2C(CC3C1(O3)C=CC(=O)C)C(=C)C(=O)O2 262.30 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
Carabrone 164879 Click to see CC(=O)CCC1C2C1(CC3C(C2)C(=C)C(=O)O3)C 248.32 unknown https://doi.org/10.1016/0031-9422(91)83034-I
Tomentosin 155173 Click to see CC1CC2C(CC=C1CCC(=O)C)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
https://doi.org/10.1016/0031-9422(91)83034-I
https://doi.org/10.1248/CPB.56.1535
Xanthatin 5281511 Click to see CC1CC2C(CC=C1C=CC(=O)C)C(=C)C(=O)O2 246.30 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
https://doi.org/10.1016/0031-9422(93)85529-Z
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Alpha,beta-unsaturated carboxylic esters / Enoate esters
methyl 2-[(2R,4aS,7R,8S,8aR)-7,8-dihydroxy-4a-methyl-2,3,4,5,6,7,8,8a-octahydro-1H-naphthalen-2-yl]prop-2-enoate 162816938 Click to see CC12CCC(CC1C(C(CC2)O)O)C(=C)C(=O)OC 268.35 unknown https://doi.org/10.1248/CPB.56.1535
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
2-[(2R,4aR,8aS)-4a-methyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid 162877969 Click to see CC12CCC=CC1CC(CC2)C(=C)C(=O)O 220.31 unknown https://doi.org/10.1248/CPB.56.1535
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
2-[(2R,4aS,6R,8S,8aR)-6,8-dihydroxy-4a-methyl-2,3,4,5,6,7,8,8a-octahydro-1H-naphthalen-2-yl]prop-2-enoic acid 162816936 Click to see CC12CCC(CC1C(CC(C2)O)O)C(=C)C(=O)O 254.32 unknown https://doi.org/10.1248/CPB.56.1535
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
2-[(2R,4aS,6R,8aS)-6-hydroxy-4a-methyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid 163097343 Click to see CC12CCC(CC1C=CC(C2)O)C(=C)C(=O)O 236.31 unknown https://doi.org/10.1248/CPB.56.1535
> Organoheterocyclic compounds / Diazines / Pyrazines / Methoxypyrazines
2-Isopropyl-3-methoxy-5-(1-methylpropyl)pyrazine 11665628 Click to see CCC(C)C1=CN=C(C(=N1)OC)C(C)C 208.30 unknown https://doi.org/10.1016/S0031-9422(00)95185-9
https://doi.org/10.1248/CPB.56.1535
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3aR,7S,8aR)-6-[(1R)-1-hydroxy-2-oxopropyl]-7-methyl-3-methylidene-4,7,8,8a-tetrahydro-3aH-cyclohepta[b]furan-2-one 162816934 Click to see CC1CC2C(CC=C1C(C(=O)C)O)C(=C)C(=O)O2 250.29 unknown https://doi.org/10.1248/CPB.56.1535
> Phenylpropanoids and polyketides / Anthracyclines
2-Hydroxyaclacinomycin A 160078 Click to see CCC1(CC(C2=C(C3=C(C=C2C1C(=O)OC)C(=O)C4=C(C3=O)C(=CC(=C4)O)O)O)OC5CC(C(C(O5)C)OC6CC(C(C(O6)C)OC7CCC(=O)C(O7)C)O)N(C)C)O 827.90 unknown https://doi.org/10.1016/S0031-9422(00)83887-X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl] acetate 3536734 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 346.30 unknown https://doi.org/10.1016/0031-9422(91)83034-I
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(91)83034-I
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(91)83034-I
Taxifolin 3-O-acetate 442540 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 346.30 unknown https://doi.org/10.1016/0031-9422(91)83034-I
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Scutellarein 5281697 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O 286.24 unknown https://doi.org/10.1016/0031-9422(91)83034-I
> 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(91)83034-I
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 300.26 unknown https://doi.org/10.1016/0031-9422(91)83034-I
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
4',5,7-Trihydroxy-3,6-dimethoxyflavone 5352032 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 330.29 unknown https://doi.org/10.1016/0031-9422(91)83034-I
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1016/0031-9422(91)83034-I
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
[(2R,3R)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxo-2,3-dihydrochromen-3-yl] acetate 15139424 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)OC)C3=CC=C(C=C3)O 344.30 unknown https://doi.org/10.1016/0031-9422(91)83034-I
[(2R,3S)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxo-2,3-dihydrochromen-3-yl] acetate 15139425 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)OC)C3=CC=C(C=C3)O 344.30 unknown https://doi.org/10.1016/0031-9422(91)83034-I
[(2S,3S)-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-4-oxo-2,3-dihydrochromen-3-yl] acetate 162860029 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)OC)C3=CC(=C(C=C3)O)O 360.30 unknown https://doi.org/10.1055/S-2007-969536
[2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-methoxy-4-oxo-2,3-dihydrochromen-3-yl] acetate 14861266 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)OC)C3=CC(=C(C=C3)O)O 360.30 unknown https://doi.org/10.1016/0031-9422(91)83034-I
3-Acetoxy-4',5-dihydroxy-7-methoxyflavanone 72746028 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)OC)C3=CC=C(C=C3)O 344.30 unknown https://doi.org/10.1016/0031-9422(91)83034-I
3-epi-Padmatin 11472604 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC(=C(C=C3)O)O)O 318.28 unknown https://doi.org/10.1016/0031-9422(91)83034-I
3-O-acetylpadmatin 10406203 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)OC)C3=CC(=C(C=C3)O)O 360.30 unknown https://doi.org/10.1016/0031-9422(91)83034-I
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxychroman-4-one 348130 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(91)83034-I
Aromadendrin 7-methyl ether 181132 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=C(C=C3)O)O 302.28 unknown https://doi.org/10.1016/0031-9422(91)83034-I
Blumeatin C; Taxifolin 7-methyl ether 12313900 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC(=C(C=C3)O)O)O 318.28 unknown https://doi.org/10.1016/0031-9422(91)83034-I
Folerogenin 5319509 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=C(C=C3)O)O 302.28 unknown https://doi.org/10.1016/0031-9422(91)83034-I
Padmatin 12313901 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC(=C(C=C3)O)O)O 318.28 unknown https://doi.org/10.1016/0031-9422(91)83034-I
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(91)83034-I

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