Scientific name	Authority	First published in
Oligosporus monospermus	(Delile) Poljakov	Trudy Inst. Bot. Akad. Nauk Kazakhst. S.S.R. 11: 169 (1961)
Oligosporus monospermus	Decne. ex DC.	Prodr. 6: 95 (1838)
Artemisia monosperma var. libyca	Chiov.
Artemisia deliliana	Besser	Enum. Pl. , Suppl.: 89 (1822)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Arabic	الشيح وحيد البذرة
Hebrew	לענה חד-זרעית
Hebrew	לענה חד זרעית

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Egypt
  - Libya

Asia-temperate click to expand
- Arabian Peninsula
  - Gulf States
  - Kuwait
  - Oman
  - Saudi Arabia
- Western Asia
  - Lebanon-Syria
  - Palestine
  - Sinai

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000025868
Tropicos	50278810
KEW	urn:lsid:ipni.org:names:179828-1
The Plant List	gcc-124993
PaleoBotany	5480
Open Tree Of Life	536919
NCBI Taxonomy	72348
IPNI	179828-1
iNaturalist	868108
GBIF	3121634
EOL	6180344
USDA GRIN	417480
Wikipedia	Artemisia_monosperma

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

Composition and antimicrobial activity of Rosmarinus officinalis L. and Artemisia monosperma L. leaf essential oils and methanolic extracts from plants grown in normal and saline habitats in Egypt

Soliman MM, Elsaba YM, Soliman MS, Ahmed EZ

Sci Rep

28-Mar-2024

PMCID:	PMC10973528
doi:	10.1038/s41598-024-57301-w
PMID:	38538682

Chemotaxonomy, antibacterial and antioxidant activities of selected aromatic plants from Tabuk region-KSA

Elbalola AA, Abbas ZK

Heliyon

16-Dec-2023

PMCID:	PMC10772130
doi:	10.1016/j.heliyon.2023.e23641
PMID:	38192876

Abiotic Stress Tolerance in Crop and Medicinal Plants

Dobrikova AG

Plants (Basel)

15-Dec-2023

PMCID:	PMC10746992
doi:	10.3390/plants12244167
PMID:	38140494

The Bio-herbicidal potential of some wild plants with allelopathic effects from Tabuk Region on selected local weed species

Alanaz AR, Alatawi EA, Alotaibi RS, Alatawi EA, Albalawi AD, Alhumayri HA, Alatawi QS, Alharbi BM

Front Plant Sci

05-Dec-2023

PMCID:	PMC10739508
doi:	10.3389/fpls.2023.1286105
PMID:	38143576

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

Spatial Heterogeneity Effects on Meta-Community Stability of Annual Plants from a Coastal Dune Ecosystem

Bar (Kutiel) P, Katz O, Dorman M

Plants (Basel)

29-May-2023

PMCID:	PMC10255161
doi:	10.3390/plants12112151
PMID:	37299130

Saudi Arabian Plants: A Powerful Weapon against a Plethora of Diseases

El-Seedi HR, Kotb SM, Musharraf SG, Shehata AA, Guo Z, Alsharif SM, Saeed A, Hamdi OA, Tahir HE, Alnefaie R, Verpoorte R, Khalifa SA

Plants (Basel)

08-Dec-2022

PMCID:	PMC9783889
doi:	10.3390/plants11243436
PMID:	36559548

Differential activity of wheat antioxidant defense system and alterations in the accumulation of osmolytes at different developmental stages as influenced by marigold (Tagetes erecta L.) leachates

Mir RA, Argal S, Ahanger MA, Jatav KS, Agarwal RM

Front Plant Sci

01-Dec-2022

PMCID:	PMC9751799
doi:	10.3389/fpls.2022.1001394
PMID:	36531349

The Current State of Knowledge in Biological Properties of Cirsimaritin

Benali T, Jaouadi I, Ghchime R, El Omari N, Harboul K, Hammani K, Rebezov M, Shariati MA, Mubarak MS, Simal-Gandara J, Zengin G, Park MN, Kim B, Mahmud S, Lee LH, Bouyahya A

Antioxidants (Basel)

19-Sep-2022

PMCID:	PMC9495358
doi:	10.3390/antiox11091842
PMID:	36139916

Artemisia spp.: An Update on Its Chemical Composition, Pharmacological and Toxicological Profiles

Sharifi-Rad J, Herrera-Bravo J, Semwal P, Painuli S, Badoni H, Ezzat SM, Farid MM, Merghany RM, Aborehab NM, Salem MA, Sen S, Acharya K, Lapava N, Martorell M, Tynybekov B, Calina D, Cho WC

Oxid Med Cell Longev

05-Sep-2022

PMCID:	PMC9467740
doi:	10.1155/2022/5628601
PMID:	36105486

Antispasmodic Potential of Medicinal Plants: A Comprehensive Review

Rauf A, Akram M, Semwal P, Mujawah AA, Muhammad N, Riaz Z, Munir N, Piotrovsky D, Vdovina I, Bouyahya A, Adetunji CO, Shariati MA, Almarhoon ZM, Mabkhot YN, Khan H

Oxid Med Cell Longev

11-Nov-2021

PMCID:	PMC8601825
doi:	10.1155/2021/4889719
PMID:	34804367

Screening of potential cytotoxic activities of some medicinal plants of Saudi Arabia

Khan M, Khan M, Adil SF, Alkhathlan HZ

Saudi J Biol Sci

25-Oct-2021

PMCID:	PMC8913393
doi:	10.1016/j.sjbs.2021.10.045
PMID:	35280530

Plant-Derived Pesticides as an Alternative to Pest Management and Sustainable Agricultural Production: Prospects, Applications and Challenges

Souto AL, Sylvestre M, Tölke ED, Tavares JF, Barbosa-Filho JM, Cebrián-Torrejón G

Molecules

10-Aug-2021

PMCID:	PMC8400533
doi:	10.3390/molecules26164835
PMID:	34443421

Structural and Chemical Adaptations of Artemisia monosperma Delile and Limbarda crithmoides (L.) Dumort. in Response to Arid Coastal Environments along the Mediterranean Coast of Egypt

El-Sherbeny GA, Dakhil MA, Eid EM, Abdelaal M

Plants (Basel)

04-Mar-2021

PMCID:	PMC7999453
doi:	10.3390/plants10030481
PMID:	33806408

Natural Compounds for Wood Protection against Fungi—A Review

Broda M

Molecules

02-Aug-2020

PMCID:	PMC7435604
doi:	10.3390/molecules25153538
PMID:	32748877

Phytochemical Profile Top

Add a new one!

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
(3-Methylpenta-1,4-diyn-3-yl)benzene	71330150	Click to see CC(C#C)(C#C)C1=CC=CC=C1	154.21	unknown	https://doi.org/10.1016/0305-1978(85)90037-7 https://doi.org/10.1016/S0031-9422(00)84082-0
4,6-Dimethylhept-5-en-2-ylbenzene	86138847	Click to see CC(CC(C)C1=CC=CC=C1)C=C(C)C	202.33	unknown	https://doi.org/10.1016/0305-1978(85)90037-7
Bicyclo[3.3.1]non-2-en-9-ol, 1-phenyl-, syn-	607204	Click to see C1CC2CC=CC(C1)(C2O)C3=CC=CC=C3	214.30	unknown	https://doi.org/10.3109/13880209009082827
Norcapillene	10983572	Click to see CC#CC#CC1=CC=CC=C1	140.18	unknown	https://doi.org/10.1016/0305-1978(85)90037-7
> Benzenoids / Benzene and substituted derivatives / Acetophenones
1-[(2R)-2-[(2S)-1-hydroxypropan-2-yl]-2,3-dihydro-1-benzofuran-5-yl]ethanone	162905682	Click to see CC(CO)C1CC2=C(O1)C=CC(=C2)C(=O)C	220.26	unknown	https://doi.org/10.1002/CHIN.200847212
1-[(2S)-2-[(2R)-1-hydroxypropan-2-yl]-2,3-dihydro-1-benzofuran-5-yl]ethanone	14730831	Click to see CC(CO)C1CC2=C(O1)C=CC(=C2)C(=O)C	220.26	unknown	https://doi.org/10.1002/JLAC.198319830819 https://doi.org/10.1016/0031-9422(90)85231-4
1-[(2S)-2-[(2S)-1-hydroxypropan-2-yl]-2,3-dihydro-1-benzofuran-5-yl]ethanone	14730832	Click to see CC(CO)C1CC2=C(O1)C=CC(=C2)C(=O)C	220.26	unknown	https://doi.org/10.1002/JLAC.198319830819 https://doi.org/10.1016/0031-9422(90)85231-4
1-[(2S)-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-yl]ethanone	12414274	Click to see CC(=C)C1CC2=C(O1)C=CC(=C2)C(=O)C	202.25	unknown	https://doi.org/10.1016/0031-9422(90)85231-4
1-[2-(1-Hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethanone	14730830	Click to see CC(CO)C1CC2=C(O1)C=CC(=C2)C(=O)C	220.26	unknown	https://doi.org/10.1002/CHIN.200847212 https://doi.org/10.1002/JLAC.198319830819
> Benzenoids / Benzene and substituted derivatives / Aniline and substituted anilines
Diphenylamine	11487	Click to see C1=CC=C(C=C1)NC2=CC=CC=C2	169.22	unknown	https://doi.org/10.3109/13880209009082827
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Ethyl benzoate	7165	Click to see CCOC(=O)C1=CC=CC=C1	150.17	unknown	https://doi.org/10.3109/13880209009082827
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Capillin	10321	Click to see CC#CC#CC(=O)C1=CC=CC=C1	168.19	unknown	https://doi.org/10.1016/0031-9422(90)85231-4
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
Biphenyl	7095	Click to see C1=CC=C(C=C1)C2=CC=CC=C2	154.21	unknown	https://doi.org/10.3109/13880209009082827
> Hydrocarbons / Saturated hydrocarbons / Cycloalkanes
Isopropylcyclohexane	12763	Click to see CC(C)C1CCCCC1	126.24	unknown	https://doi.org/10.3109/13880209009082827
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
alpha-Myrcene	519324	Click to see CC(=C)CCCC(=C)C=C	136.23	unknown	https://doi.org/10.1016/0305-1978(85)90037-7
Artemisiatriene	5320377	Click to see CC(=C)C=CC(C)(C)C=C	136.23	unknown	https://doi.org/10.1016/0305-1978(85)90037-7
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid	10467	Click to see CCCCCCCCCCCCCCCCCCCC(=O)O	312.50	unknown	https://doi.org/10.1016/S0031-9422(00)88402-2
Myristic Acid	11005	Click to see CCCCCCCCCCCCCC(=O)O	228.37	unknown	https://doi.org/10.1016/S0031-9422(00)88402-2
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	https://doi.org/10.1016/S0031-9422(00)88402-2
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	https://doi.org/10.1016/S0031-9422(00)88402-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid	3893	Click to see CCCCCCCCCCCC(=O)O	200.32	unknown	https://doi.org/10.1016/S0031-9422(00)88402-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Dotriacontanoic acid	19255	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O	480.80	unknown	https://doi.org/10.1055/S-0028-1099670
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(3S,8S)-3,8-dihydroxydec-9-en-4,6-diynoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162982172	Click to see C=CC(C#CC#CC(CCOC1C(C(C(C(O1)CO)O)O)O)O)O	342.34	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.11.010
2-(3,8-Dihydroxydec-9-en-4,6-diynoxy)-6-(hydroxymethyl)oxane-3,4,5-triol	85432326	Click to see C=CC(C#CC#CC(CCOC1C(C(C(C(O1)CO)O)O)O)O)O	342.34	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.11.010
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl propionate	8834	Click to see CCC(=O)OCCC(C)CCC=C(C)C	212.33	unknown	https://doi.org/10.1016/0305-1978(85)90037-7
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Ethylhexan-1-ol	7720	Click to see CCCCC(CC)CO	130.23	unknown	https://doi.org/10.3109/13880209009082827
9-Decene-4,6-diyne-1,3,8-triol, (3R,8R)-	10261702	Click to see C=CC(C#CC#CC(CCO)O)O	180.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.11.010
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(3R,8R,9Z)-heptadeca-1,9,16-trien-4,6-diyne-3,8-diol	11161235	Click to see C=CCCCCCC=CC(C#CC#CC(C=C)O)O	258.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.11.010
Heptadeca-1,9,16-trien-4,6-diyne-3,8-diol	1446	Click to see C=CCCCCCC=CC(C#CC#CC(C=C)O)O	258.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.11.010
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
[(1R,2R,6S,10R,11R,13S,14R,15R)-13-acetyloxy-8-formyl-1-hydroxy-4,12,12,15-tetramethyl-5-oxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] 2-(methylamino)benzoate	162901456	Click to see CC1C(C2(C(C2(C)C)C3C1(C4C=C(C(=O)C4CC(=C3)C=O)C)O)OC(=O)C)OC(=O)C5=CC=CC=C5NC	521.60	unknown	https://doi.org/10.1016/S0031-9422(00)88402-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(2E,4E)-3,7-dimethyl-2,4,6-octatrienal	11126441	Click to see CC(=CC=CC(=CC=O)C)C	150.22	unknown	https://doi.org/10.3109/13880209009082827
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.3109/13880209009082827
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1016/0305-1978(85)90037-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(E,Z)-farnesol	1549109	Click to see CC(=CCCC(=CCCC(=CCO)C)C)C	222.37	unknown	https://doi.org/10.3109/13880209009082827
Farnesol	3327	Click to see CC(=CCCC(=CCCC(=CCO)C)C)C	222.37	unknown	https://doi.org/10.3109/13880209009082827
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1016/0305-1978(85)90037-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4aR,7S,7aS,7bR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	13854258	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.11.010
(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/J.PHYTOCHEM.2004.11.010
1,1,7-Trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	522266	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.11.010
Spathulenol	92231	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.11.010
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,3R,5R,6S,8aR)-4,8a-dimethyl-6-propan-2-yl-2,3,5,6,7,8-hexahydro-1H-naphthalene-1,3,5-triol	10244059	Click to see CC1=C2C(C(CCC2(C(CC1O)O)C)C(C)C)O	254.36	unknown	https://doi.org/10.1021/NP030558V
(1S,3S,5S,6R,8aS)-4,8a-dimethyl-6-propan-2-yl-2,3,5,6,7,8-hexahydro-1H-naphthalene-1,3,5-triol	162882321	Click to see CC1=C2C(C(CCC2(C(CC1O)O)C)C(C)C)O	254.36	unknown	https://doi.org/10.1021/NP030558V
4,8a-dimethyl-6-propan-2-yl-2,3,5,6,7,8-hexahydro-1H-naphthalene-1,3,5-triol	162882320	Click to see CC1=C2C(C(CCC2(C(CC1O)O)C)C(C)C)O	254.36	unknown	https://doi.org/10.1021/NP030558V
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
Santonin	221071	Click to see CC1C2CCC3(C=CC(=O)C(=C3C2OC1=O)C)C	246.30	unknown	https://doi.org/10.1055/S-0028-1099670
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(6aR,6bR,8aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol	145706026	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)88402-2
[(4aR,6aS,6aR,6bR,8aR,12aS,14aS,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-yl] acetate	137704689	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C	468.80	unknown	https://doi.org/10.1016/S0031-9422(00)88402-2
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)88402-2
Taraxasterol, acetate	344468	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C	468.80	unknown	https://doi.org/10.1016/S0031-9422(00)88402-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	134766514	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/S0031-9422(00)88402-2
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/S0031-9422(00)88402-2
> 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/10.1016/S0031-9422(00)88402-2
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/10.1016/S0031-9422(00)88402-2
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)88402-2
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
3,3,6-Trimethylhepta-1,5-dien-4-ol	100197	Click to see CC(=CC(C(C)(C)C=C)O)C	154.25	unknown	https://doi.org/10.1016/0305-1978(85)90037-7
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
4-Cyclohexylcyclohexanol	75518	Click to see C1CCC(CC1)C2CCC(CC2)O	182.30	unknown	https://doi.org/10.3109/13880209009082827
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
methyl beta-D-fructofuranoside	128889	Click to see COC1(C(C(C(O1)CO)O)O)CO	194.18	unknown	https://doi.org/10.1002/CHIN.200847212
Methylbeta-D-fructofuranoside	14055124	Click to see COC1(C(C(C(O1)CO)O)O)CO	194.18	unknown	https://doi.org/10.1002/CHIN.200847212
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
3,3,6-Trimethylhepta-1,5-dien-4-one	68346	Click to see CC(=CC(=O)C(C)(C)C=C)C	152.23	unknown	https://doi.org/10.3109/13880209009082827
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
2-(But-2-en-1-yl)cyclohexan-1-one	54275877	Click to see CC=CCC1CCCCC1=O	152.23	unknown	https://doi.org/10.3109/13880209009082827
2-[(2E)-2-butenyl]cyclohexanone	11159422	Click to see CC=CCC1CCCCC1=O	152.23	unknown	https://doi.org/10.3109/13880209009082827
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(E)-4-(5-acetyl-2-hydroxyphenyl)-2-methylbut-2-enal	14730829	Click to see CC(=CCC1=C(C=CC(=C1)C(=O)C)O)C=O	218.25	unknown	https://doi.org/10.1016/S0031-9422(00)88807-X https://doi.org/10.1016/0031-9422(90)85231-4
1-[4-hydroxy-3-[(E)-4-hydroxy-3-methylbut-2-enyl]phenyl]ethanone	14290630	Click to see CC(=CCC1=C(C=CC(=C1)C(=O)C)O)CO	220.26	unknown	https://doi.org/10.1016/0031-9422(90)85231-4
3-[4-Hydroxyisopent-2(Z)-enyl]-4-hydroxyacetophenone	5375069	Click to see CC(=CCC1=C(C=CC(=C1)C(=O)C)O)CO	220.26	unknown	https://doi.org/10.1016/0031-9422(90)85231-4
4-(5-Acetyl-2-hydroxyphenyl)-2-methylbut-2-enal	85918218	Click to see CC(=CCC1=C(C=CC(=C1)C(=O)C)O)C=O	218.25	unknown	https://doi.org/10.1016/S0031-9422(00)88807-X
4-Hydroxy-3-(3-methyl-2-butenyl)acetophenone	442916	Click to see CC(=CCC1=C(C=CC(=C1)C(=O)C)O)C	204.26	unknown	https://doi.org/10.1016/0031-9422(90)85231-4
> Organic oxygen compounds / Organooxygen compounds / Ynols
Tetradecyn-1-ol	57508015	Click to see CCCCCCCCCCCCC#CO	210.36	unknown	https://doi.org/10.1016/0305-1978(85)90037-7
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
Dibenzofuran	568	Click to see C1=CC=C2C(=C1)C3=CC=CC=C3O2	168.19	unknown	https://doi.org/10.3109/13880209009082827
> Organoheterocyclic compounds / Coumarans
methyl (E)-3-[(2R)-2-[(2R)-1-hydroxypropan-2-yl]-2,3-dihydro-1-benzofuran-5-yl]prop-2-enoate	102502403	Click to see CC(CO)C1CC2=C(O1)C=CC(=C2)C=CC(=O)OC	262.30	unknown	https://doi.org/10.1016/0031-9422(90)85231-4
methyl (E)-3-[(2S)-2-[(2R)-1-hydroxypropan-2-yl]-2,3-dihydro-1-benzofuran-5-yl]prop-2-enoate	14730822	Click to see CC(CO)C1CC2=C(O1)C=CC(=C2)C=CC(=O)OC	262.30	unknown	https://doi.org/10.1016/0031-9422(90)85231-4
methyl (E)-3-[(2S)-2-[(2S)-1-hydroxypropan-2-yl]-2,3-dihydro-1-benzofuran-5-yl]prop-2-enoate	14730823	Click to see CC(CO)C1CC2=C(O1)C=CC(=C2)C=CC(=O)OC	262.30	unknown	https://doi.org/10.1016/0031-9422(90)85231-4
Methyl 3-[2-(1-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]prop-2-enoate	162881264	Click to see CC(CO)C1CC2=C(O1)C=CC(=C2)C=CC(=O)OC	262.30	unknown	https://doi.org/10.1016/0031-9422(90)85231-4
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3S,3aS,9bS)-3,6,9-trimethyl-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2,7-dione	16760094	Click to see CC1C2CCC(=C3C(C2OC1=O)C(=CC3=O)C)C	246.30	unknown	https://doi.org/10.1016/S0031-9422(00)84593-8
> Organoheterocyclic compounds / Tetrahydrofurans
(+)-nigrosporione A	146684210	Click to see CC12COC(C1C(=CC2=O)OC)O	184.19	unknown	https://doi.org/10.1016/0031-9422(90)85231-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
methyl (E)-3-[4-hydroxy-3-(3-methylbut-2-enoyl)phenyl]prop-2-enoate	100951833	Click to see CC(=CC(=O)C1=C(C=CC(=C1)C=CC(=O)OC)O)C	260.28	unknown	https://doi.org/10.1016/0031-9422(90)85231-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-[2,4-dihydroxy-3-[(E)-4-hydroxy-3-methylbut-2-enyl]-5-(3-methylbut-2-enyl)phenyl]prop-2-enoic acid	11267570	Click to see CC(=CCC1=CC(=C(C(=C1O)CC=C(C)CO)O)C=CC(=O)O)C	332.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.11.010
3-[2,4-Dihydroxy-3-(4-hydroxy-3-methylbut-2-enyl)-5-(3-methylbut-2-enyl)phenyl]prop-2-enoic acid	72776535	Click to see CC(=CCC1=CC(=C(C(=C1O)CC=C(C)CO)O)C=CC(=O)O)C	332.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.11.010
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
6-Hydroxy-7,8-dimethoxycoumarin	11345068	Click to see COC1=C(C=C2C=CC(=O)OC2=C1OC)O	222.19	unknown	https://doi.org/10.1002/CHIN.200847212
Fraxinol	3047739	Click to see COC1=C(C(=C2C=CC(=O)OC2=C1)OC)O	222.19	unknown	https://doi.org/10.1002/CHIN.200847212
Tomentin	14059525	Click to see COC1=C(C(=C2C=CC(=O)OC2=C1)O)OC	222.19	unknown	https://doi.org/10.1002/CHIN.200847212
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Flavone	10680	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=CC=CC=C3O2	222.24	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Patuletin	5281678	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O	332.26	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
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/S0031-9422(00)80845-6
Rhamnazin	5320945	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)OC)O	330.29	unknown	https://doi.org/10.1016/0031-9422(90)85231-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	163011126	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	162845817	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O	594.50	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	44257674	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O	594.50	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6 https://doi.org/10.1016/S0031-9422(00)84593-8
Lucenin 2	44257937	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
Lucenin-2	442615	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6 https://doi.org/10.1016/S0031-9422(00)84593-8
Luteolin 6-C-glucoside 8-C-arabinoside	3549960	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
Vicenin-2	3084407	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O	594.50	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	52946987	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	464.40	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
2-(3,4-Dihydroxyphenyl)-3,7-dihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	22635124	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	464.40	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
Isorhamnetin 5-glucoside	44259378	Click to see CCC1C(C(C(C(O1)OC2=CC(=CC3=C2C(=O)C(=C(O3)C4=CC(=C(C=C4)O)OC)O)O)O)O)O	476.40	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6 https://doi.org/10.1016/S0031-9422(00)84593-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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/S0031-9422(00)84593-8 https://doi.org/10.1016/S0031-9422(00)80845-6
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl]Oxy-Chromen-4-one	12304323	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/S0031-9422(00)80845-6
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/10.1016/S0031-9422(00)80845-6
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	162845680	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=C(C3=O)C(=C(C(=C4)O)OC)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	640.50	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	11968829	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O	494.40	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	14134315	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O	494.40	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6 https://doi.org/10.1016/S0031-9422(00)84593-8
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-methoxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	74978462	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=C(C3=O)C(=C(C(=C4)O)OC)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	640.50	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
2-Phenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	22446905	Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=CC=CC=C3O2)OC4C(C(C(C(O4)CO)O)O)O	400.40	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
Flavonol 3-O-D-glucoside	11953828	Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=CC=CC=C3O2)OC4C(C(C(C(O4)CO)O)O)O	400.40	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
Patuletin-3-rutinoside	44259784	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=C(C3=O)C(=C(C(=C4)O)OC)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	640.50	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6 https://doi.org/10.1016/S0031-9422(00)84593-8
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0031-9422(00)84593-8 https://doi.org/10.1016/S0031-9422(00)80845-6
Vitamin P	5293655	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-phenyl-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	162971822	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C(=O)C=C(O4)C5=CC=CC=C5)O)O)O)O)O)O	546.50	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
2-Phenyl-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	162971821	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C(=O)C=C(O4)C5=CC=CC=C5)O)O)O)O)O)O	546.50	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
3,5-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	162951222	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	478.40	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
3,5-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	12302035	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	478.40	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
5-hydroxy-2-(4-methoxyphenyl)-7-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	22870817	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O	446.40	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6
7-(beta-D-Galactopyranosyloxy)-5-hydroxy-2-(4-Methoxyphenyl)-	5291487	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O	446.40	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6 https://doi.org/10.1016/S0031-9422(00)84593-8
Linarin	5317025	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O	592.50	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6 https://doi.org/10.1016/S0031-9422(00)84593-8
Tilianin	5321954	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O	446.40	unknown	https://doi.org/10.1016/S0031-9422(00)80845-6 https://doi.org/10.1016/S0031-9422(00)84593-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
Caryatin	5489501	Click to see COC1=CC(=CC2=C1C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O	330.29	unknown	https://doi.org/10.1016/0031-9422(90)85231-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupatilin	5273755	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC	344.30	unknown	https://doi.org/10.1076/PHBI.34.2.134.13191
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/S0031-9422(00)84593-8
Jaceosidin	5379096	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O	330.29	unknown	https://doi.org/10.1016/S0031-9422(00)84593-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3,7-Di-O-methylquercetin	5280417	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O	330.29	unknown	https://doi.org/10.1016/0031-9422(90)85231-4
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(90)85231-4
7-O-Methyleriodictyol	1268276	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)O)O	302.28	unknown	https://doi.org/10.1016/0031-9422(90)85231-4 https://doi.org/10.1016/J.PHYTOCHEM.2004.11.010
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(90)85231-4
Sternbin	4872981	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)O)O	302.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.11.010

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Artemisia monosperma

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top