Thymus transcaucasicus

We don't have an image yet. Upload an image!

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	UUID643fef59791ae004314568
Scientific name	Thymus transcaucasicus
Authority	Ronniger
First published in	Repert. Spec. Nov. Regni Veg. 31: 140 (1932)

Description Top

Suggest a correction or write a new one!

No description added yet. Help us by writing one.

Synonyms Top

Scientific name	Authority	First published in
Thymus fominii	Klokov & Des.-Shost.	Trudy Bot. Inst. (Baku) 2: 305 (1936)
Thymus superbus	Ronniger	Repert. Spec. Nov. Regni Veg. 31: 141 (1932)
Thymus ziaratinus	Klokov & Des.-Shost.	Trudy Bot. Inst. (Baku) 2: 303 (1936)
Thymus bakurianicus	Klokov	Rasoobrazov. Thymus Sov. Soyuza : 72 (1973)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Azerbaijani	zaqafqaziya
Persian	آویشن تفلیسی

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

Asia-temperate click to expand
- Caucasus
  - Transcaucasus
- Western Asia
  - Iran
  - Turkey

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000324911
Tropicos	100268129
KEW	urn:lsid:ipni.org:names:461731-1
The Plant List	kew-205608
Open Tree Of Life	6084067
Observations.org	148130
NCBI Taxonomy	2019959
IPNI	461731-1
iNaturalist	1120551
GBIF	5605119
Elurikkus	555367
USDA GRIN	446819
CMAUP	NPO1000

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

Impact of Temperature on Phenolic and Osmolyte Contents in In Vitro Cultures and Micropropagated Plants of Two Mediterranean Plant Species, Lavandula viridis and Thymus lotocephalus

Mansinhos I, Gonçalves S, Rodríguez-Solana R, Ordóñez-Díaz JL, Moreno-Rojas JM, Romano A

Plants (Basel)

14-Dec-2022

PMCID:	PMC9787929
doi:	10.3390/plants11243516
PMID:	36559631

Unity in diversity—food plants and fungi of Sakartvelo (Republic of Georgia), Caucasus

Bussmann RW, Paniagua Zambrana NY, Ur Rahman I, Kikvidze Z, Sikharulidze S, Kikodze D, Tchelidze D, Khutsishvili M, Batsatsashvili K

J Ethnobiol Ethnomed

31-Dec-2021

PMCID:	PMC8719402
doi:	10.1186/s13002-021-00490-9
PMID:	34972527

Metabolomics Analysis Reveals Drought Responses of Trifoliate Orange by Arbuscular Mycorrhizal Fungi With a Focus on Terpenoid Profile

Liang SM, Zhang F, Zou YN, Kuča K, Wu QS

Front Plant Sci

06-Oct-2021

PMCID:	PMC8528288
doi:	10.3389/fpls.2021.740524
PMID:	34691116

Potential anti-influenza effective plants used in Turkish folk medicine: A review

Sargin SA

J Ethnopharmacol

31-Aug-2020

PMCID:	PMC7458060
doi:	10.1016/j.jep.2020.113319
PMID:	32882361

Decoding Biosynthetic Pathways in Plants by Pulse-Chase Strategies Using 13CO2 as a Universal Tracer

Bacher A, Chen F, Eisenreich W

Metabolites

14-Jul-2016

PMCID:	PMC5041120
doi:	10.3390/metabo6030021
PMID:	27429012

Components ofThymus transcaucasicus

F. Yu. Kasumov, T. G. Gadzhieva

Springer Science and Business Media LLC

20-Nov-2004

doi:	10.1007/BF00575075

Triterpene acids of some representatives of the genus Thymus

A. V. Simonyan, A. L. Shinkarenko

Springer Science and Business Media LLC

20-Nov-2004

doi:	10.1007/BF00563472

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 / Biphenols
Euphorbetin	5317297	Click to see C1=CC(=O)OC2=C1C(=C(C(=C2)O)O)C3=C(C(=CC4=C3C=CC(=O)O4)O)O	354.30	unknown	via CMAUP database
Isoeuphorbetin	71438018	Click to see C1=CC(=O)OC2=C(C(=C(C=C21)O)O)C3=C(C(=CC4=C3C=CC(=O)O4)O)O	354.30	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane	12410	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	436.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[(1'R,2R,3'E,5'R,7'S,11'R,12'R,13'S,14'S)-1',11'-diacetyloxy-3',6',6',14'-tetramethyl-2'-oxospiro[oxirane-2,10'-tricyclo[10.3.0.05,7]pentadec-3-ene]-13'-yl] 2-phenylacetate	10626539	Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C	552.70	unknown	via CMAUP database
[(1'R,2R,3'E,5'S,7'S,11'R,12'R,13'S,14'S)-1',11'-diacetyloxy-3',6',6',14'-tetramethyl-2'-oxospiro[oxirane-2,10'-tricyclo[10.3.0.05,7]pentadec-3-ene]-13'-yl] 2-phenylacetate	100933326	Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C	552.70	unknown	via CMAUP database
[(1R,3E,5R,7S,10E,12S,13S,14S)-1-acetyloxy-10-(acetyloxymethyl)-3,6,6,14-tetramethyl-2-oxo-13-tricyclo[10.3.0.05,7]pentadeca-3,10-dienyl] (E)-3-phenylprop-2-enoate	44241674	Click to see CC1CC2(C(C1OC(=O)C=CC3=CC=CC=C3)C=C(CCC4C(C4(C)C)C=C(C2=O)C)COC(=O)C)OC(=O)C	548.70	unknown	via CMAUP database
[(1R,3E,5R,7S,10Z,12S,13S,14S)-1-acetyloxy-10-(hydroxymethyl)-3,6,6,14-tetramethyl-2-oxo-13-tricyclo[10.3.0.05,7]pentadeca-3,10-dienyl] hexanoate	11754671	Click to see CCCCCC(=O)OC1C(CC2(C1C=C(CCC3C(C3(C)C)C=C(C2=O)C)CO)OC(=O)C)C	474.60	unknown	via CMAUP database
[(1R,3E,5R,7S,9E,11R,12R,13S,14S)-1,11-diacetyloxy-10-(acetyloxymethyl)-3,6,6,14-tetramethyl-2-oxo-13-tricyclo[10.3.0.05,7]pentadeca-3,9-dienyl] benzoate	44241675	Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=CCC4C(C4(C)C)C=C(C2=O)C)COC(=O)C)OC(=O)C)OC(=O)C	580.70	unknown	via CMAUP database
[(1R,3E,5R,7S,9S,11R,12R,13S,14S)-1,11-diacetyloxy-13-benzoyloxy-3,6,6,14-tetramethyl-10-methylidene-2-oxo-9-tricyclo[10.3.0.05,7]pentadec-3-enyl] benzoate	45270942	Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=C)C(CC4C(C4(C)C)C=C(C2=O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C	642.70	unknown	via CMAUP database
[(1R,3E,5S,7S,11R,12R,13S,14S)-1,11-diacetyloxy-3,6,6,14-tetramethyl-10-methylidene-2-oxo-13-tricyclo[10.3.0.05,7]pentadec-3-enyl] pyridine-3-carboxylate	100933329	Click to see CC1CC2(C(C1OC(=O)C3=CN=CC=C3)C(C(=C)CCC4C(C4(C)C)C=C(C2=O)C)OC(=O)C)OC(=O)C	523.60	unknown	via CMAUP database
[(1R,5R,7S,11R,12R,13S,14S)-1,11-diacetyloxy-3,6,6,14-tetramethyl-10-methylidene-2-oxo-13-tricyclo[10.3.0.05,7]pentadec-3-enyl] benzoate	85364164	Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=C)CCC4C(C4(C)C)C=C(C2=O)C)OC(=O)C)OC(=O)C	522.60	unknown	via CMAUP database
CID 5281376	5281376	Click to see CC1CC2(C(C1O)C(C(=C)CCC3C(C3(C)C)C=C(C2=O)C)O)O	334.40	unknown	via CMAUP database
Diacetyl benzoyl lathyrol	10577938	Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=C)CCC4C(C4(C)C)C=C(C2=O)C)OC(=O)C)OC(=O)C	522.60	unknown	via CMAUP database
Euphorbia factor L1	11238221	Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C	552.70	unknown	via CMAUP database
Euphorbia factor L8	10697375	Click to see CC1CC2(C(C1OC(=O)C3=CN=CC=C3)C(C(=C)CCC4C(C4(C)C)C=C(C2=O)C)OC(=O)C)OC(=O)C	523.60	unknown	via CMAUP database
Euphorbiasteroid	15940183	Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C	552.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
Ingenol	442042	Click to see CC1CC2C(C2(C)C)C3C=C(C(C4(C1(C3=O)C=C(C4O)C)O)O)CO	348.40	unknown	via CMAUP database
Ingenol 3-palmitate	56841025	Click to see CCCCCCCCCCCCCCCC(=O)OC1C(=CC23C1(C(C(=CC(C2=O)C4C(C4(C)C)CC3C)CO)O)O)C	586.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(3S,4aR,6aR,6aS,8aR,12aR,14aS,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol	11876268	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,4aS,6aR,6aS,6bS,8aS,10S,12aR,14bR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	162948465	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/BF00563472
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol	11870460	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	via CMAUP database
beta-Ursolic acid	220774	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/BF00563472
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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	11870456	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alanine and derivatives
Alanine	5950	Click to see CC(C(=O)O)N	89.09	unknown	https://doi.org/10.1007/BF00575075
D-alanine	71080	Click to see CC(C(=O)O)N	89.09	unknown	https://doi.org/10.1007/BF00575075
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
2-Aminobutyric acid	6657	Click to see CCC(C(=O)O)N	103.12	unknown	https://doi.org/10.1007/BF00575075
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
Arginine	6322	Click to see C(CC(C(=O)O)N)CN=C(N)N	174.20	unknown	https://doi.org/10.1007/BF00575075
Glutamine	5961	Click to see C(CC(=O)N)C(C(=O)O)N	146.14	unknown	https://doi.org/10.1007/BF00575075
Threonine	6288	Click to see CC(C(C(=O)O)N)O	119.12	unknown	https://doi.org/10.1007/BF00575075
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Asparagine and derivatives
Asparagine	6267	Click to see C(C(C(=O)O)N)C(=O)N	132.12	unknown	https://doi.org/10.1007/BF00575075
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
Aspartic Acid	5960	Click to see C(C(C(=O)O)N)C(=O)O	133.10	unknown	https://doi.org/10.1007/BF00575075
D-Aspartic acid	83887	Click to see C(C(C(=O)O)N)C(=O)O	133.10	unknown	https://doi.org/10.1007/BF00575075
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
DL-Glutamic acid	611	Click to see C(CC(=O)O)C(C(=O)O)N	147.13	unknown	https://doi.org/10.1007/BF00575075
Glutamic Acid	33032	Click to see C(CC(=O)O)C(C(=O)O)N	147.13	unknown	https://doi.org/10.1007/BF00575075
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
Histidine	6274	Click to see C1=C(NC=N1)CC(C(=O)O)N	155.15	unknown	https://doi.org/10.1007/BF00575075
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
Leucine	6106	Click to see CC(C)CC(C(=O)O)N	131.17	unknown	https://doi.org/10.1007/BF00575075
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
Levodopa	6047	Click to see C1=CC(=C(C=C1CC(C(=O)O)N)O)O	197.19	unknown	via CMAUP database
Tyrosine	6057	Click to see C1=CC(=CC=C1CC(C(=O)O)N)O	181.19	unknown	https://doi.org/10.1007/BF00575075
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
Valine	6287	Click to see CC(C)C(C(=O)O)N	117.15	unknown	https://doi.org/10.1007/BF00575075
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Cysteine and derivatives
D-Cystine	6857538	Click to see C(C(C(=O)O)N)SSCC(C(=O)O)N	240.30	unknown	https://doi.org/10.1007/BF00575075
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Cysteine and derivatives / L-cysteine-S-conjugates
Cystine	67678	Click to see C(C(C(=O)O)N)SSCC(C(=O)O)N	240.30	unknown	https://doi.org/10.1007/BF00575075
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Fumaric Acid	444972	Click to see C(=CC(=O)O)C(=O)O	116.07	unknown	https://doi.org/10.1007/BF00575075
Oxalic Acid	971	Click to see C(=O)(C(=O)O)O	90.03	unknown	https://doi.org/10.1007/BF00575075
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
Malic Acid	525	Click to see C(C(C(=O)O)O)C(=O)O	134.09	unknown	https://doi.org/10.1007/BF00575075
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal	107526	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	https://doi.org/10.1007/BF00575075
(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal	3037556	Click to see C(C(C(C(C(C=O)O)O)O)O)O	180.16	unknown	https://doi.org/10.1007/BF00575075
D-Galactose	6036	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	https://doi.org/10.1007/BF00575075
D-Glucose	5793	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	https://doi.org/10.1007/BF00575075
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
(2S,3R,4R)-2,3,4,5-tetrahydroxypentanal	66308	Click to see C(C(C(C(C=O)O)O)O)O	150.13	unknown	https://doi.org/10.1007/BF00575075
L-Arabinose	439195	Click to see C1C(C(C(C(O1)O)O)O)O	150.13	unknown	https://doi.org/10.1007/BF00575075
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
DL-Tartaric acid	875	Click to see C(C(C(=O)O)O)(C(=O)O)O	150.09	unknown	https://doi.org/10.1007/BF00575075
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin	5281417	Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O	340.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin	5281416	Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O	178.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Daphnetin	5280569	Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)O	178.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Kaempferol 3-glucuronide	5318759	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O	462.40	unknown	via CMAUP database

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.

Thymus transcaucasicus

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