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Hyssopus seravschanicus

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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 UUID643fdf71374f8270038461
Scientific name Hyssopus seravschanicus
Authority (Dub.) Pazij
First published in Index Seminum (Hort. Bot. Univ. As. Med.) 1945: 4 (1945)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hyssopus ferganensis Boriss. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 12: 262 (1950)
Hyssopus officinalis var. seravschanicus Dubj. Consp. Fl. Turkest. 5: 131. 1913
Hyssopus tianschanicus Boriss. Index Seminum (Hort. Bot. Univ. As. Med.) 1945: 4 (1945)

Common names Top

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Language Common/alternative name
Chinese 硬尖海索草

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
  • Asia-temperate
    • Middle Asia
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan
    • Western Asia
      • Afghanistan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000217230
Tropicos 17600093
KEW urn:lsid:ipni.org:names:448523-1
The Plant List kew-102298
Open Tree Of Life 304966
Observations.org 144126
NCBI Taxonomy 260601
IPNI 448523-1
iNaturalist 919885
GBIF 5609159
EOL 5375009
Elurikkus 556313

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
Hyssopus Essential Oil: An Update of Its Phytochemistry, Biological Activities, and Safety Profile Sharifi-Rad J, Quispe C, Kumar M, Akram M, Amin M, Iqbal M, Koirala N, Sytar O, Kregiel D, Nicola S, Ertani A, Victoriano M, Khosravi-Dehaghi N, Martorell M, Alshehri MM, Butnariu M, Pentea M, Rotariu LS, Calina D, Cruz-Martins N, Cho WC Oxid Med Cell Longev 13-Jan-2022
PMCID:PMC8776447
doi:10.1155/2022/8442734
PMID:35069979
Aromatic Medicinal Plants of the Lamiaceae Family from Uzbekistan: Ethnopharmacology, Essential Oils Composition, and Biological Activities Mamadalieva NZ, Akramov DK, Ovidi E, Tiezzi A, Nahar L, Azimova SS, Sarker SD Medicines (Basel) 10-Feb-2017
PMCID:PMC5597069
doi:10.3390/medicines4010008
PMID:28930224
Essential Oils’ Chemical Characterization and Investigation of Some Biological Activities: A Critical Review Dhifi W, Bellili S, Jazi S, Bahloul N, Mnif W Medicines (Basel) 22-Sep-2016
PMCID:PMC5456241
doi:10.3390/medicines3040025
PMID:28930135
Antimicrobial, Antioxidant, and Anti-Inflammatory Activities of Essential Oils of Selected Aromatic Plants from Tajikistan Sharopov F, Braun MS, Gulmurodov I, Khalifaev D, Isupov S, Wink M Foods 02-Nov-2015
PMCID:PMC5224554
doi:10.3390/foods4040645
PMID:28231227
Aromatic Medicinal Plants from Tajikistan (Central Asia) Sharopov FS, Zhang H, Wink M, Setzer WN Medicines (Basel) 17-Feb-2015
PMCID:PMC5532974
doi:10.3390/medicines2010028
PMID:28933380
Triterpenoids and steroids of Hyssopus seravshanicus and H. ferganensis E. P. Zotov, R. L. Khazanovich Springer Science and Business Media LLC 09-Jul-2008
doi:10.1007/BF00570696
Investigation of the essential oil of Hyssopus zeravshanicus E. P. Zotov, M. I. Goryaev, F. S. Sharipova, R. L. Khazanovich, V. I. Vandysheva Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00568256

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1007/BF00568256
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1007/BF00568256
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1007/BF00568256
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1007/BF00568256
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1007/BF00568256
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Isopinocampheol 10524983 Click to see CC1C2CC(C2(C)C)CC1O 154.25 unknown https://doi.org/10.1007/BF00568256
(-)-Pinocampheol 7271803 Click to see CC1C2CC(C2(C)C)CC1O 154.25 unknown https://doi.org/10.1007/BF00568256
(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/10.1007/BF00568256
(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one 6973628 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1007/BF00568256
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1007/BF00568256
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1007/BF00568256
Fenchone 14525 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown https://doi.org/10.1007/BF00568256
Pinocamphone 6427105 Click to see CC1C2CC(C2(C)C)CC1=O 152.23 unknown https://doi.org/10.1007/BF00568256
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1007/BF00568256
Verbenone 29025 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1007/BF00568256
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Menthone 443159 Click to see CC1CCC(C(=O)C1)C(C)C 154.25 unknown https://doi.org/10.1007/BF00568256
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1007/BF00568256
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1007/BF00568256
p-Menthan-3-one 6986 Click to see CC1CCC(C(=O)C1)C(C)C 154.25 unknown https://doi.org/10.1007/BF00568256
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1007/BF00568256
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1007/BF00570696
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1007/BF00570696
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1007/BF00570696
> 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/10.1007/BF00570696
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/10.1007/BF00570696

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