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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Filter by language:

Language	Common/alternative name
English	hyssop
Afrikaans	hisop
Arabic	اشنان داوود
Arabic	إنفة
Arabic	حسل
Arabic	زوفا طبية
Arabic	سيف
Arabic	زوفا
Arabic	جسمي
Arabic	حشيشة القدس
Arabic	شاي جبلي
Azerbaijani	dərman çödükotu
Belarusian	Ісоп лекавы
Bulgarian	лечебен исоп
Catalan	hisop
Czech	yzop lékařský
Welsh	isop
Danish	Ægte isop
German	ysop
German	echter ysop
Greek	Ύσσωπος ο φαρμακευτικός
Esperanto	oficina hisopo
Estonian	harilik iisop
Basque	isipu-belar
Persian	زوفا
Finnish	rohtoiisoppi
Finnish	iisoppi
French	hysope
Irish	Íosóip
Irish	íosóip
Irish	íosóip íceach
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	hysop
Dutch	hyssop
Norwegian Nynorsk	isop
Polish	hyzop lekarski
Russian	иссоп лекарственный
Russian	Иссоп лекарственный
Slovak	yzop lekársky
Slovenian	navadni ožep
Slovenian	navadni ožepek
Serbian	Милодух
Swedish	isop
Thai	หุสบ
Turkish	züfa otu
Turkish	zufa 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

Suggest a correction or add new data!

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

Africa click to expand
- Northern Africa
  - Algeria
  - Morocco

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Siberia
  - Buryatiya
- Western Asia
  - Iran
  - Turkey

Europe click to expand
- 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 click to expand
- 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

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

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

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

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

Antioxidant Activity of Medicinal Herbs and Spices from Plants of the Lamiaceae, Apiaceae and Asteraceae Families: Chemometric Interpretation of the Data

Ulewicz-Magulska B, Wesolowski M

Antioxidants (Basel)

24-Nov-2023

PMCID:	PMC10740862
doi:	10.3390/antiox12122039
PMID:	38136159

Plant Extracts as Skin Care and Therapeutic Agents

Michalak M

Int J Mol Sci

22-Oct-2023

PMCID:	PMC10607442
doi:	10.3390/ijms242015444
PMID:	37895122

Therapeutic Potential of Myrtenal and Its Derivatives—A Review

Dragomanova S, Andonova V, Volcho K, Salakhutdinov N, Kalfin R, Tancheva L

Life (Basel)

20-Oct-2023

PMCID:	PMC10608190
doi:	10.3390/life13102086
PMID:	37895468

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

Inhibitory Mechanisms of trans-2-Hexenal on the Growth of Geotrichum citri-aurantii

Ouyang Q, Shi S, Liu Y, Yang Y, Zhang Y, Yuan X, Tao N, Li L

J Fungi (Basel)

15-Sep-2023

PMCID:	PMC10532542
doi:	10.3390/jof9090930
PMID:	37755038

Essential Oils and Their Combination with Lactic Acid Bacteria and Bacteriocins to Improve the Safety and Shelf Life of Foods: A Review

Bukvicki D, D’Alessandro M, Rossi S, Siroli L, Gottardi D, Braschi G, Patrignani F, Lanciotti R

Foods

01-Sep-2023

PMCID:	PMC10486891
doi:	10.3390/foods12173288
PMID:	37685221

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
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/FFJ.2730060109 https://doi.org/10.1021/JF00039A035 https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9
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/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-9 https://doi.org/10.1021/JF00039A035
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
(2S,3S,4S,5R,6S)-Methyl 3,4,5-trihydroxy-6-((5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl)oxy)tetrahydro-2H-pyran-2-carboxylate	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
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	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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