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Cyclotrichium niveum

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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
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Details Top

Internal ID UUID644037298451c429212979
Scientific name Cyclotrichium niveum
Authority (Boiss.) Manden. & Scheng.
First published in Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 15: 337 (1953)

Description Top

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Synonyms Top

Scientific name Authority First published in
Satureja nivea Briq. Nat. Pflanzenfam. 4(3a): 299 (1896)
Calamintha nivea Boiss. Ann. Sci. Nat., Bot. , sér. 4, 2: 253 (1854)
Clinopodium niveum Kuntze Revis. Gen. Pl. 2: 515 (1891)

Common names Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000934157
Tropicos 100175347
KEW urn:lsid:ipni.org:names:446347-1
The Plant List kew-52942
Open Tree Of Life 352562
NCBI Taxonomy 751776
IPNI 446347-1
GBIF 5610842
EOL 5362220

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
Plant Essential Oils as Biopesticides: Applications, Mechanisms, Innovations, and Constraints Gupta I, Singh R, Muthusamy S, Sharma M, Grewal K, Singh HP, Batish DR Plants (Basel) 10-Aug-2023
PMCID:PMC10458566
doi:10.3390/plants12162916
PMID:37631128
Pulegone Prevents Hypertension through Activation of Muscarinic Receptors and Cyclooxygenase Pathway in L-NAME-Induced Hypertensive Rats Razzaq MA, Younis W, Malik MN, Alsahli TG, Alamgeer, Jahan S, Ehsan R, Gasparotto Junior A, Bashir A Cardiovasc Ther 09-May-2023
PMCID:PMC10195173
doi:10.1155/2023/8166840
PMID:37214130
Essential Oils for a Sustainable Control of Honeybee Varroosis Bava R, Castagna F, Palma E, Marrelli M, Conforti F, Musolino V, Carresi C, Lupia C, Ceniti C, Tilocca B, Roncada P, Britti D, Musella V Vet Sci 23-Apr-2023
PMCID:PMC10221473
doi:10.3390/vetsci10050308
PMID:37235392
Multidirectional Characterization of Phytochemical Profile and Health-Promoting Effects of Ziziphora bungeana Juz. Extracts Zhaparkulova K, Karaubayeva A, Sakipova Z, Biernasiuk A, Gaweł-Bęben K, Laskowski T, Kusniyeva A, Omargali A, Bekezhanova T, Ibragimova L, Ibadullayeva G, Jakiyanov A, Czech K, Tastambek K, Głowniak K, Malm A, Kukula-Koch W Molecules 16-Dec-2022
PMCID:PMC9788533
doi:10.3390/molecules27248994
PMID:36558125
In vitro cytotoxic potential of extracts from Aristolochia foetida Kunth against MCF-7 and bMECs cell lines Lerma-Herrera MA, Beiza-Granados L, Ochoa-Zarzosa A, López-Meza JE, Hernández-Hernández JD, Aviña-Verduzco J, García-Gutiérrez HA Saudi J Biol Sci 09-Aug-2021
PMCID:PMC8626259
doi:10.1016/j.sjbs.2021.08.007
PMID:34867010
An In Vitro Evaluation of the Molecular Mechanisms of Action of Medical Plants from the Lamiaceae Family as Effective Sources of Active Compounds against Human Cancer Cell Lines Sitarek P, Merecz-Sadowska A, Śliwiński T, Zajdel R, Kowalczyk T Cancers (Basel) 13-Oct-2020
PMCID:PMC7601952
doi:10.3390/cancers12102957
PMID:33066157
Molecular Targets for Components of Essential Oils in the Insect Nervous System—A Review Jankowska M, Rogalska J, Wyszkowska J, Stankiewicz M Molecules 23-Dec-2017
PMCID:PMC5943938
doi:10.3390/molecules23010034
PMID:29295521
Calamintha nepeta (L.) Savi and its Main Essential Oil Constituent Pulegone: Biological Activities and Chemistry Božović M, Ragno R Molecules 14-Feb-2017
PMCID:PMC6155702
doi:10.3390/molecules22020290
PMID:28216606
Natural AChE Inhibitors from Plants and their Contribution to Alzheimer’s Disease Therapy Murray AP, Faraoni MB, Castro MJ, Alza NP, Cavallaro V Curr Neuropharmacol 01-Jul-2013
PMCID:PMC3744903
doi:10.2174/1570159X11311040004
PMID:24381530
The Essential Oil of<i>Cyclotrichium niveum</i>(Boiss.) Manden. et Scheng. K. H.C. Baser, S. Sarikardasoglu, G. Tümen Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1994.9698316
Flavanones from Cyclotrichium niveum S. Doganca, A. Ulubelen, E. Tuzlaci Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80396-6

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
> 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/10.1080/10412905.1994.9698316
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.1994.9698316
> 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/10.1080/10412905.1994.9698316
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1080/10412905.1994.9698316
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1080/10412905.1994.9698316
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698316
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698316
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1080/10412905.1994.9698316
Thujone 261491 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698316
> 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/10.1080/10412905.1994.9698316
1-Methylene-4-(1-methylvinyl)cyclohexane 68140 Click to see CC(=C)C1CCC(=C)CC1 136.23 unknown https://doi.org/10.1080/10412905.1994.9698316
Isomenthone, (+/-)- 6432469 Click to see CC1CCC(C(=O)C1)C(C)C 154.25 unknown https://doi.org/10.1080/10412905.1994.9698316
Isopiperitenone 79036 Click to see CC1=CC(=O)C(CC1)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.1994.9698316
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698316
p-Menthan-3-one 6986 Click to see CC1CCC(C(=O)C1)C(C)C 154.25 unknown https://doi.org/10.1080/10412905.1994.9698316
Piperitenone 381152 Click to see CC1=CC(=O)C(=C(C)C)CC1 150.22 unknown https://doi.org/10.1080/10412905.1994.9698316
Piperitone 6987 Click to see CC1=CC(=O)C(CC1)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698316
Pulegone 442495 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown https://doi.org/10.1080/10412905.1994.9698316
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1080/10412905.1994.9698316
> 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/10.1080/10412905.1994.9698316
1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane 5317024 Click to see CC(=C1CCC(C(C1)(C)C(=C)C)(C)C=C)C 218.38 unknown https://doi.org/10.1080/10412905.1994.9698316
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane 6432312 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698316
beta-Bourbonene 62566 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698316
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1080/10412905.1994.9698316
(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/10.1080/10412905.1994.9698316
> 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/10.1080/10412905.1994.9698316
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698316
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aS,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol 40469639 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(89)80396-6
(4aS,6aR,6aS,6bR,8aR,10R,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 7061300 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/10.1016/0031-9422(89)80396-6
3-Hydroxyolean-12-en-28-oic acid 619166 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/10.1016/0031-9422(89)80396-6
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(89)80396-6
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(89)80396-6
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/10.1016/0031-9422(89)80396-6
Virgatic acid 14489125 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 470.70 unknown https://doi.org/10.1016/0031-9422(89)80396-6
> 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/10.1016/0031-9422(89)80396-6
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/10.1016/0031-9422(89)80396-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4a-Hydroxy-4-(oxiran-2-yl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,5,6-tetrahydropyrano[3,4-c]pyran-8-one 14543432 Click to see C1COC(=O)C2=COC(C(C21O)C3CO3)OC4C(C(C(C(O4)CO)O)O)O 390.34 unknown https://doi.org/10.1016/0031-9422(89)80396-6
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Hexanal 6184 Click to see CCCCCC=O 100.16 unknown https://doi.org/10.1080/10412905.1994.9698316
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown https://doi.org/10.1080/10412905.1994.9698316
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
3-Methylcyclohexanone 11567 Click to see CC1CCCC(=O)C1 112.17 unknown https://doi.org/10.1080/10412905.1994.9698316
> 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/10.1016/0031-9422(89)80396-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13093776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(89)80396-6
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 133612283 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown https://doi.org/10.1016/0031-9422(89)80396-6
5-hydroxy-2-(4-methoxyphenyl)-7-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 162906359 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)OC)O)O)O)O 430.40 unknown https://doi.org/10.1016/0031-9422(89)80396-6
Didymin 16760075 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O 594.60 unknown https://doi.org/10.1016/0031-9422(89)80396-6
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/10.1016/0031-9422(89)80396-6
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(89)80396-6
Neopoucirin 85705 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O 594.60 unknown https://doi.org/10.1016/0031-9422(89)80396-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Isosakuranetin 160481 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(89)80396-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1016/0031-9422(89)80396-6

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