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Hyssopus officinalis

Hyssopus officinalis - 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 UUID643fdf70c9c23133898903
Scientific name Hyssopus officinalis
Authority L.
First published in Sp. Pl. : 569 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Hyssopus officinalis var. angustifolius (M.Bieb.) Benth. Prodr. [A. P. de Candolle] 12: 252. 1848
Hyssopus officinalis subsp. borealis Domin Preslia 13-15: 197. 1935 (1935)
Hyssopus officinalis var. latifolius Fisch. ex Benth. Prodr. [A. P. de Candolle] 12: 252. 1848
Hyssopus schleicheri G.Don ex Loudon Hort. Brit. [Loudon] 233. 1830
Thymus hyssopus E.H.L.Krause Deutschl. Fl. Abbild. , ed. 2, 11: 172 (1903)
Hyssopus officinalis var. decussata Pers. Syn. Pl. 2: 114. 1806
Hyssopus officinalis var. decumbens (Jord. & Fourr.) Briq. Lab. Alp. Mar. 385 1893

Common names Top

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Language Common/alternative name
English hyssop
Afrikaans hisop
Arabic زوفا
Arabic سيف
Arabic حسل
Arabic زوفا طبية
Arabic إنفة
Arabic اشنان داوود
Arabic جسمي
Arabic حشيشة القدس
Arabic شاي جبلي
Azerbaijani dərman çödükotu
Belarusian крузбень
Belarusian Ісоп лекавы
Belarusian красвяк
Belarusian красвень
Belarusian ізоп
Bulgarian лечебен исоп
Catalan hisop
Czech yzop lékařský
Welsh isop
Danish Ægte isop
German echter ysop
German ysop
Greek Ύσσωπος ο φαρμακευτικός
Esperanto oficina hisopo
Estonian harilik iisop
Basque isipu-belar
Persian زوفا
Finnish rohtoiisoppi
Finnish iisoppi
French hysope
Irish íosóip íceach
Irish íosóip
Irish Íosóip
Croatian izop
Upper Sorbian jězop
Hungarian kerti izsóp
Italian issopo officinale
Italian issopo
Japanese ヤナギハッカ
lb ysop
Lithuanian vaistinis isopas
Macedonian милодух
Macedonian изоп
Norwegian Bokmål isop
Dutch hyssop
Dutch hysop
Norwegian Nynorsk isop
os Хосгæнæн цъæх цæвæгхос
Polish hyzop lekarski
Russian синий зверобой
Russian Пчелиная трава
Russian иссопова трава
Russian Иссоп обыкновенный
Russian Душница
Russian иссоп лекарственный
Russian Иссоп лекарственный
Slovak yzop lekársky
Slovenian navadni ožep
Slovenian navadni ožepek
Serbian Милодух
Swedish isop
Thai หุสบ
Turkish zufa otu
Turkish züfa otu
Ukrainian Гісоп лікарський
Urdu زوفا
Chinese 牛膝草
Chinese 海索草
Chinese 柳薄荷
Chinese 神香草
Chinese 宽唇神香草

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Hyssopus officinalis subsp. aristatus (Godr.) Nyman Consp. Fl. Eur. : 587 (1881)
Hyssopus officinalis subsp. canescens (DC.) Nyman Consp. Fl. Eur. : 587 (1881)
Hyssopus officinalis subsp. montanus (Jord. & Fourr.) Briq. Lab. Alp. Mar. : 386 (1893)
Hyssopus officinalis subsp. officinalis Unknown

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Darkness: These seeds need to be covered with soil or otherwise kept in the dark to germinate properly. Light inhibits their germination process.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Siberia
      • Buryatiya
    • Western Asia
      • Iran
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Hungary
      • Poland
      • Switzerland
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Yugoslavia
    • Southwestern Europe
      • France
      • Spain
  • Northern America
    • North-central U.S.A.
      • Wisconsin
    • Northeastern U.S.A.
      • New York
      • Vermont

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000217205
UNII 0IQW001KPE
Canadensys 6380
USDA Plants HYOF
Tropicos 17600092
INPN 103406
Flora of Italy 4607
KEW urn:lsid:ipni.org:names:127231-2
The Plant List kew-102273
Missouri Botanical Garden 281391
PFAF Hyssopus officinalis
Open Tree Of Life 880695
Observations.org 6891
NCBI Taxonomy 39324
NBN Atlas NBNSYS0000004211
Nature Serve 2.151307
IPNI 127231-2
iNaturalist 164026
GBIF 5341387
Freebase /m/04ydkfd
WisFlora 8283
EPPO HYSOF
EOL 579591
Elurikkus 5221
USDA GRIN 19644
Wikipedia Hyssopus_officinalis
Plantarium 20560

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
Application of Common Culinary Herbs for the Development of Bioactive Materials Lupuliasa AI, Baroi AM, Avramescu SM, Vasile BS, Prisada RM, Fierascu RC, Fierascu I, Sărdărescu (Toma) DI, Ripszky Totan A, Voicu-Bălășea B, Pițuru SM, Popa L, Ghica MV, Dinu-Pîrvu CE Plants (Basel) 30-Mar-2024
PMCID:PMC11013859
doi:10.3390/plants13070997
PMID:38611526
Antimicrobial Action Mechanisms of Natural Compounds Isolated from Endophytic Microorganisms Eshboev F, Mamadalieva N, Nazarov PA, Hussain H, Katanaev V, Egamberdieva D, Azimova S Antibiotics (Basel) 18-Mar-2024
PMCID:PMC10967585
doi:10.3390/antibiotics13030271
PMID:38534706
Saving the local tradition: ethnobotanical survey on the use of plants in Bologna district (Italy) Chiocchio I, Marincich L, Mandrone M, Trincia S, Tarozzi C, Poli F J Ethnobiol Ethnomed 12-Mar-2024
PMCID:PMC10936038
doi:10.1186/s13002-024-00664-1
PMID:38475780
Identification of Flavonoids, Antioxidant and Antiproliferative Activity of Aqueous Infusions of Calendula officinalis L., Chelidonium majus L., Teucrium chamaedrys L. and Alchemilla vulgaris L. Bilušić T, Šola I, Čikeš Čulić V Food Technol Biotechnol 01-Mar-2024
PMCID:PMC11002451
doi:10.17113/ftb.62.01.24.8175
PMID:38601959
Traditional Use of Wild Edible Plants in Slovenia: A Field Study and an Ethnobotanical Literature Review Papež Kristanc A, Kreft S, Strgulc Krajšek S, Kristanc L Plants (Basel) 24-Feb-2024
PMCID:PMC10934440
doi:10.3390/plants13050621
PMID:38475472
Caffeic Acid O-Methyltransferase Gene Family in Mango (Mangifera indica L.) with Transcriptional Analysis under Biotic and Abiotic Stresses and the Role of MiCOMT1 in Salt Tolerance Wang H, Chen Z, Luo R, Lei C, Zhang M, Gao A, Pu J, Zhang H Int J Mol Sci 24-Feb-2024
PMCID:PMC10931984
doi:10.3390/ijms25052639
PMID:38473886
Exploring the benefits of wild plants in dietary nutrition: investigating perspectives, choices, health impacts and sustainable practices Anwar T, Qureshi H, Shahzadi S, Siddiqi EH, Ali HM, Abdelhamid MM, Nazim M BMC Complement Med Ther 14-Feb-2024
PMCID:PMC10865668
doi:10.1186/s12906-024-04379-4
PMID:38355544
Chemical profile and biological properties of the Piper corcovadense C.DC. essential oil Henrique Fontoura B, Cristina Perin E, Paula Buratto A, Francisco Schreiner J, Menezes Cavalcante K, Dias Teixeira S, Manica D, Antônio Narzetti R, Bruno da Silva G, Dulce Bagatini M, Luiza Cadorin Oldoni T, Teresinha Carpes S Saudi Pharm J 12-Feb-2024
PMCID:PMC10879029
doi:10.1016/j.jsps.2024.101993
PMID:38384478
Community based integrated wound care: Results of a pilot formative research conducted in Benin and Côte d’Ivoire, West Africa Wadagni AC, Yao TA, Diez G, Balle FH, Koffi AP, Aoulou P, Zahiri MH, Djossou P, Barogui YT, Assé H, Houezo JG, Sopoh GE, Nichter M, Johnson RC PLOS Glob Public Health 09-Feb-2024
PMCID:PMC10857723
doi:10.1371/journal.pgph.0002889
PMID:38335227
Exploring nature's hidden treasure: Unraveling the untapped phytochemical and pharmacological potentials of Clinopodium vulgare L. – A hidden gem in the Lamiaceae family Qureshi KA, Parvez A, Uzzaman Khan MM, Aspatwar A, Atiya A, Elhassan GO, Khan RA, Erattil Ahammed SY, Khan WU, Jaremko M Heliyon 20-Jan-2024
PMCID:PMC10834805
doi:10.1016/j.heliyon.2024.e24781
PMID:38312627
Ethnobotanical and ethnomedicinal research into medicinal plants in the Mt Stara Planina region (south-eastern Serbia, Western Balkans) Jarić S, Kostić O, Miletić Z, Marković M, Sekulić D, Mitrović M, Pavlović P J Ethnobiol Ethnomed 10-Jan-2024
PMCID:PMC10782642
doi:10.1186/s13002-024-00647-2
PMID:38200599
A review on mechanisms and impacts of cold plasma treatment as a non‐thermal technology on food pigments Ramezan Y, Kamkari A, Lashkari A, Moradi D, Tabrizi AN Food Sci Nutr 26-Dec-2023
PMCID:PMC10916563
doi:10.1002/fsn3.3897
PMID:38455202
Traditional Knowledge Evolution over Half of a Century: Local Herbal Resources and Their Changes in the Upper Susa Valley of Northwest Italy Sulaiman N, Zocchi DM, Borrello MT, Mattalia G, Antoniazzi L, Berlinghof SE, Bewick A, Häfliger I, Schembs M, Torri L, Pieroni A Plants (Basel) 22-Dec-2023
PMCID:PMC10780445
doi:10.3390/plants13010043
PMID:38202351
RNA-Seq-Based Transcriptomics and GC–MS Quantitative Analysis Reveal Antifungal Mechanisms of Essential Oil of Clausena lansium (Lour.) Skeels Seeds against Candida albicans Ma Y, Sui J, Wang Y, Sun W, Yi G, Wu J, Qiu S, Wang L, Zhang A, He X Molecules 12-Dec-2023
PMCID:PMC10745804
doi:10.3390/molecules28248052
PMID:38138542
Latin American Plants against Microorganisms Cuevas-Cianca SI, Romero-Castillo C, Gálvez-Romero JL, Sánchez-Arreola E, Juárez ZN, Hernández LR Plants (Basel) 28-Nov-2023
PMCID:PMC10708099
doi:10.3390/plants12233997
PMID:38068631

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
1-Phenylethanol 7409 Click to see CC(C1=CC=CC=C1)O 122.16 unknown https://doi.org/10.1002/FFJ.2730060109
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1002/FFJ.2730060109
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see C1=CC=C(C=C1)CO 108.14 unknown https://doi.org/10.1002/FFJ.2730060109
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1021/JF00039A035
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown https://doi.org/10.1021/JF00039A035
> Benzenoids / Phenols / Methoxyphenols
2-Hydroxy-3-methoxybenzaldehyde 8991 Click to see COC1=CC=CC(=C1O)C=O 152.15 unknown https://doi.org/10.1002/FFJ.2730060109
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1002/FFJ.2730060109
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Eicosane 8222 Click to see CCCCCCCCCCCCCCCCCCCC 282.50 unknown https://doi.org/10.1021/JF00039A035
Tetradecane 12389 Click to see CCCCCCCCCCCCCC 198.39 unknown https://doi.org/10.1021/JF00039A035
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(2S,3S)-2,3-dihydroxy-3-(4-hydroxy-3,5-dimethoxyphenyl)propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 10092725 Click to see COC1=CC(=CC(=C1O)OC)C(C(COC2C(C(C(C(O2)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.10.009
[(2R,3S,4S,5R,6R)-6-[(2S,3S)-2,3-dihydroxy-3-(4-hydroxy-3,5-dimethoxyphenyl)propoxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-phenylprop-2-enoate 10369920 Click to see COC1=CC(=CC(=C1O)OC)C(C(COC2C(C(C(C(O2)COC(=O)C=CC3=CC=CC=C3)O)O)O)O)O 536.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.10.009
[6-[2,3-Dihydroxy-3-(4-hydroxy-3,5-dimethoxyphenyl)propoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-phenylprop-2-enoate 85123749 Click to see COC1=CC(=CC(=C1O)OC)C(C(COC2C(C(C(C(O2)COC(=O)C=CC3=CC=CC=C3)O)O)O)O)O 536.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.10.009
2-[2,3-Dihydroxy-3-(4-hydroxy-3,5-dimethoxyphenyl)propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162959542 Click to see COC1=CC(=CC(=C1O)OC)C(C(COC2C(C(C(C(O2)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.10.009
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
3-Octanol 11527 Click to see CCCCCC(CC)O 130.23 unknown https://doi.org/10.1002/FFJ.2730060109
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1021/JF00039A035
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
https://doi.org/10.1002/FFJ.2730060109
https://doi.org/10.1021/JF00039A035
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
https://doi.org/10.1021/JF00039A035
> 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/10.1007/978-1-4615-3012-1_17
(1R,2R,5S)-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one 10329459 Click to see CC1C2CC(C2(C)C)CC1=O 152.23 unknown https://doi.org/10.1002/FFJ.2730060109
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
3-Pinanone 11038 Click to see CC1C2CC(C2(C)C)CC1=O 152.23 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
https://doi.org/10.1021/JF00039A035
https://doi.org/10.1002/FFJ.2730060109
3-Thujanone 11027 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1021/JF00039A035
3,5,5-Trimethylbicyclo[2.2.1]heptan-2-one 86707 Click to see CC1C2CC(C1=O)CC2(C)C 152.23 unknown https://doi.org/10.1002/FFJ.2730060109
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1021/JF00039A035
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1002/FFJ.2730060109
https://doi.org/10.1021/JF00039A035
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1021/JF00039A035
Bicyclo[3.1.1]Heptan-3-One, 2,6,6-Trimethyl-, [1S-(1a,2ss,5a)]- 12311188 Click to see CC1C2CC(C2(C)C)CC1=O 152.23 unknown https://doi.org/10.1002/FFJ.2730060109
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1021/JF00039A035
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1002/FFJ.2730060109
Myrtenol 10582 Click to see CC1(C2CC=C(C1C2)CO)C 152.23 unknown https://doi.org/10.1021/JF00039A035
https://doi.org/10.1002/FFJ.2730060109
Pinocamphone 6427105 Click to see CC1C2CC(C2(C)C)CC1=O 152.23 unknown https://doi.org/10.1021/JF00039A035
Pinocarveol 102667 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1021/JF00039A035
Pinocarvone 121719 Click to see CC1(C2CC1C(=C)C(=O)C2)C 150.22 unknown https://doi.org/10.1021/JF00039A035
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
https://doi.org/10.1021/JF00039A035
Thujone 261491 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1021/JF00039A035
Verbenol 61126 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1002/FFJ.2730060109
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730060109
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1021/JF00039A035
https://doi.org/10.1002/FFJ.2730060109
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/JF00039A035
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-beta-Bourbonene 324224 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
beta-Bourbonene 62566 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
https://doi.org/10.1021/JF00039A035
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
Cedrelanol 160799 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1021/JF00039A035
cis-Nerolidol 5320128 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1002/FFJ.2730060109
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1021/JF00039A035
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(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/10.1021/JF00039A035
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1021/JF00039A035
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1021/JF00039A035
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730060109
2-[(3Z,7Z)-4,8-dimethylcyclodeca-3,7-dien-1-yl]propan-2-ol 5365392 Click to see CC1=CCCC(=CCC(CC1)C(C)(C)O)C 222.37 unknown https://doi.org/10.1021/JF00039A035
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730060109
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Inositol 892 Click to see C1(C(C(C(C(C1O)O)O)O)O)O 180.16 unknown https://doi.org/10.1006/BBRC.1995.1639
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Rosmarinic acid 5281792 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1515/ZNC-1999-1-204
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate 101937123 Click to see COC1=C(C=C(C=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O 356.32 unknown https://doi.org/10.1055/S-2006-957401
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate 73009461 Click to see COC1=C(C=C(C=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O 356.32 unknown https://doi.org/10.1055/S-2006-957401
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Isoferulic acid 736186 Click to see COC1=C(C=C(C=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1055/S-2006-957401
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1080/10286020.2010.533120
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 5387370 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1080/10286020.2010.533120
Apigenin 7-glucuronide 5319484 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1080/10286020.2010.533120
Apigenin 7-O-methylglucuronide 13844658 Click to see COC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O 460.40 unknown https://doi.org/10.1080/10286020.2010.533120
Apigenin 7-O-methylglucuronide 5387369 Click to see COC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O 460.40 unknown https://doi.org/10.1080/10286020.2010.533120
butyl (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylate 5319489 Click to see CCCCOC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O 502.50 unknown https://doi.org/10.1080/10286020.2010.533120
Butyl 3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylate 73981660 Click to see CCCCOC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O 502.50 unknown https://doi.org/10.1080/10286020.2010.533120
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 5353588 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)O 608.50 unknown https://doi.org/10.1055/S-2006-957401
https://doi.org/10.1080/10286020.2010.533120
5-Hydroxy-2-(4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 5480901 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/10.1080/10286020.2010.533120
7-[(2S,3R,4S,5R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-3,5-dihydroxychromen-4-one 49845605 Click to see C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)OC5C(C(CO5)(CO)O)O)O)O 566.50 unknown https://doi.org/10.1080/10286020.2010.533120
7-[(2S,3R,4S,5R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-2-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 49845606 Click to see C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O)O)OC6C(C(CO6)(CO)O)O)O)O 728.60 unknown https://doi.org/10.1080/10286020.2010.533120
7-[3-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-3,5-dihydroxychromen-4-one 75303119 Click to see C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)OC5C(C(CO5)(CO)O)O)O)O 566.50 unknown https://doi.org/10.1080/10286020.2010.533120
7-[3-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-2-[4-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 75303120 Click to see C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O)O)OC6C(C(CO6)(CO)O)O)O)O 728.60 unknown https://doi.org/10.1080/10286020.2010.533120
Apigenin 7-O-glucoside 5385553 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1080/10286020.2010.533120
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1080/10286020.2010.533120
Diosmin 5281613 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)O 608.50 unknown https://doi.org/10.1080/10286020.2010.533120
https://doi.org/10.1055/S-2006-957401
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/10.1080/10286020.2010.533120

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