Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among the Nepeta species that receive documented use as a calming tea, Nepeta nuda stands out for several ethnobotanical traditions. Among the Mapuche of southern Chile, aerial parts are gathered fresh or dried and steeped as a “calming tea” for occasional sleeplessness and dyspepsia (Bennett et al., 2021). In eastern Mediterranean cuisines and remedies, leaves are used in infusions to relieve colic and flatulence (Tutin and Walters, 1972). In Central Asian folk medicine, especially in parts of Tajikistan and Uzbekistan, the plant is prepared as a mild infusion for colds, coughs, and as a gentle antispasmodic (Flora of the USSR, 1978).

A practical recipe: mild infusion for occasional gastrointestinal unease. Place 1–2 teaspoons (approximately 2 g) of dried aerial parts into a teapot, pour 250 mL of just‑boiled water, cover, and steep 5–7 minutes. Strain and sip 1–2 cups daily as needed. Short‑term, moderate intake is generally well tolerated; avoid during pregnancy and while nursing. If you take central‑nervous‑system medications or have liver or kidney disease, consult a qualified practitioner before use.

Well‑established constituents for Nepeta nuda include nepetalactone, a prominent monoterpene that provides the species’ characteristic aroma and mild sedative‑antispasmodic activity, along with closely related iridoids and flavonoids (Komissarenko et al., 1975; Saito and Yahara, 2002). Modern studies suggest anticholinergic and smooth‑muscle–relaxing effects that align with traditional use as a digestive and respiratory tea, and essential oils are primarily composed of α‑pinene and linalool with nepetalactone as a marker compound.

Commercial tea blends sometimes include Nepeta nuda, and research continues into its antispasmodic and mild sedative properties for the 21st‑century context (ESCOP Monographs, 2003).

General Uses Top

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Common products:
- Dried aerial parts of Nepeta nuda are marketed as catnip‑type attractants for pet toys; the nepetalactone content elicits the characteristic feline response.
- Live plants are sold as ornamental perennials for rock gardens, borders, and naturalistic plantings.

Industrial and craft applications:
- The essential oil, obtained by steam distillation of the aerial biomass, is incorporated into natural insect‑repellent formulations for household use.
- The oil serves as a scented additive in eco‑friendly cleaning and laundry products, contributing a fresh herbaceous note.

Fragrance and cosmetics:
- Nepeta nuda essential oil is employed in perfumery for its minty‑herbaceous aroma and appears in fragrance compounds for soaps, detergents, and personal‑care items.
- The oil is listed under the International Fragrance Association (IFRA) standards as a permitted fragrance ingredient, ensuring compliance with safety and labeling requirements.

Properties relevant to use:
- The volatile fraction is dominated by nepetalactone (commonly >40 % of the oil), a monoterpene lactone that provides the intense catnip scent and reported insect‑repellent activity.
- Nepetalactone exhibits moderate volatility and a characteristic aromatic profile, making it suitable for fragrance applications and as a natural odorant.

Sustainability and sourcing:
- The species has a broad temperate distribution across Europe and western Asia; it can be cultivated on a small scale or harvested sustainably from meadow habitats.
- No specific international trade restrictions apply; the plant is not listed in CITES, and organic cultivation programs in several EU countries provide a traceable, sustainably managed supply chain.

Synonyms Top

Scientific name	Authority	First published in
Nepeta montana	Turra	Fl. Ital. Prod. 66.
Nepeta violacea	Vill.	Hist. Pl. Dauphiné 2: 367 (1787)
Nepeta nuda var. violacea	Nyman	Consp. Fl. Eur. 585. 1881
Nepeta nuda var. pannonica	(L.) Nyman	Consp. Fl. Eur. 585. 1881
Cataria nuda	Moench	Methodus : 388 (1794)
Glechoma nuda	Kuntze	Revis. Gen. Pl. 2: 518 (1891)

Common names Top

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Filter by language:

Language	Common/alternative name
Bulgarian	гола коча билка
Czech	šanta lesostepní
German	pannonische katzenminze
German	kahle katzenminze
Hungarian	bugás macskamenta
Italian	gaiatta glabra
Chinese	直齿荆芥

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Nepeta nuda subsp. albiflora	(Boiss.) Gams	Ill. Fl. Mitt.-Eur. 5(4): 2372 (1927)
Nepeta nuda subsp. lydiae	P.H.Davis	Notes Roy. Bot. Gard. Edinburgh 21: 66 (1952)
Nepeta nuda subsp. nuda		Unknown
Nepeta nuda subsp. glandulifera	Hub.-Mor. & P.H.Davis	Kew Bull. 6: 83 (1951)

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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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 click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Uzbekistan
- Siberia
  - Altay
  - Krasnoyarsk
  - West Siberia
- Western Asia
  - East Aegean Islands
  - Iran
  - Lebanon-Syria
  - Turkey

Europe click to expand
- Eastern Europe
  - Central European Russia
  - East European Russia
  - Krym
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Czechoslovakia
  - Hungary
  - Poland
  - Switzerland
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - France
  - Portugal
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000251202
Tropicos	17600197
INPN	109534
KEW	urn:lsid:ipni.org:names:452615-1
The Plant List	kew-134839
Open Tree Of Life	5801075
Observations.org	135971
NCBI Taxonomy	1533225
NBN Atlas	NBNSYS0200002688
IPNI	452615-1
iNaturalist	506778
GBIF	7309059
EPPO	NEPNU
Elurikkus	5868
USDA GRIN	419438
Plantarium	24989
Wikipedia	Nepeta_nuda

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

Exploring the Phytochemical Composition and Biological Potential of Balkan Endemic Species Stachys scardica Griseb

Mantovska DI, Zhiponova MK, Petrova D, Alipieva K, Bonchev G, Boycheva I, Evstatieva Y, Nikolova D, Tsacheva I, Simova S, Yordanova ZP

Plants (Basel)

21-Dec-2023

PMCID:	PMC10780532
doi:	10.3390/plants13010030
PMID:	38202340

Uncovering the Interrelation between Metabolite Profiles and Bioactivity of In Vitro- and Wild-Grown Catmint (Nepeta nuda L.)

Zaharieva A, Rusanov K, Rusanova M, Paunov M, Yordanova Z, Mantovska D, Tsacheva I, Petrova D, Mishev K, Dobrev PI, Lacek J, Filepová R, Zehirov G, Vassileva V, Mišić D, Motyka V, Chaneva G, Zhiponova M

Metabolites

20-Oct-2023

PMCID:	PMC10609352
doi:	10.3390/metabo13101099
PMID:	37887424

Polyphenol Contents, Gas Chromatography-Mass Spectrometry (GC–;MS) and Antibacterial Activity of Methanol Extract and Fractions of Sonneratia Caseolaris Fruits from Ben Tre Province in Vietnam

Tran TK, Ha PT, Henry RJ, Nguyen DN, Tuyen PT, Liem NT

J Microbiol Biotechnol

30-Sep-2023

PMCID:	PMC10840467
doi:	10.4014/jmb.2304.04019
PMID:	38282409

Mediterranean Plants as Potential Source of Biopesticides: An Overview of Current Research and Future Trends

Fragkouli R, Antonopoulou M, Asimakis E, Spyrou A, Kosma C, Zotos A, Tsiamis G, Patakas A, Triantafyllidis V

Metabolites

22-Aug-2023

PMCID:	PMC10535963
doi:	10.3390/metabo13090967
PMID:	37755247

Menthol: An underestimated anticancer agent

Zhao Y, Pan H, Liu W, Liu E, Pang Y, Gao H, He Q, Liao W, Yao Y, Zeng J, Guo J

Front Pharmacol

17-Mar-2023

PMCID:	PMC10063798
doi:	10.3389/fphar.2023.1148790
PMID:	37007039

Evaluation of the Antibacterial Properties of Polyvinyl Alcohol-Pullulan Scaffolds Loaded with Nepeta racemosa Lam. Essential Oil and Perspectives for Possible Applications

Lungoci C, Rîmbu CM, Motrescu I, Serbezeanu D, Horhogea CE, Vlad-Bubulac T, Ghițău CS, Puiu I, Neculai-Văleanu AS, Robu T

Plants (Basel)

16-Feb-2023

PMCID:	PMC9963579
doi:	10.3390/plants12040898
PMID:	36840247

From Biodiversity to Musketry: Detection of Plant Diversity in Pre-Industrial Peloponnese during the Flora Graeca Expedition

Chimona C, Papadopoulou S, Kolyva F, Mina M, Rhizopoulou S

Life (Basel)

23-Nov-2022

PMCID:	PMC9785030
doi:	10.3390/life12121957
PMID:	36556322

Investigation of Volatile Iridoid Terpenes in Nepeta cataria L. (Catnip) Genotypes

Patel H, Gomes EN, Yuan B, Lyu W, Wu Q, Simon JE

Molecules

19-Oct-2022

PMCID:	PMC9607335
doi:	10.3390/molecules27207057
PMID:	36296649

Allelopathic Properties of Lamiaceae Species: Prospects and Challenges to Use in Agriculture

Islam AK, Suttiyut T, Anwar MP, Juraimi AS, Kato-Noguchi H

Plants (Basel)

31-May-2022

PMCID:	PMC9182988
doi:	10.3390/plants11111478
PMID:	35684250

Catmint (Nepeta nuda L.) Phylogenetics and Metabolic Responses in Variable Growth Conditions

Petrova D, Gašić U, Yocheva L, Hinkov A, Yordanova Z, Chaneva G, Mantovska D, Paunov M, Ivanova L, Rogova M, Shishkova K, Todorov D, Tosheva A, Kapchina-Toteva V, Vassileva V, Atanassov A, Mišić D, Bonchev G, Zhiponova M

Front Plant Sci

16-May-2022

PMCID:	PMC9150856
doi:	10.3389/fpls.2022.866777
PMID:	35651766

Improving the Knowledge on Distribution, Food Preferences and DNA Barcoding of Natura 2000 Protected Species Paracossulus thrips (Lepidoptera, Cossidae) in Romania

Iacob GM, Craioveanu C, Hula V, Aurelian VM, Beldean M, Sitar C

Insects

03-Dec-2021

PMCID:	PMC8703911
doi:	10.3390/insects12121087
PMID:	34940175

In Vitro Multiplication and NMR Fingerprinting of Rare Veronica caucasica M. Bieb

Mantovska DI, Zhiponova MK, Georgiev MI, Grozdanova T, Gerginova D, Alipieva K, Simova S, Popova M, Kapchina-Toteva VM, Yordanova ZP

Molecules

28-Sep-2021

PMCID:	PMC8512125
doi:	10.3390/molecules26195888
PMID:	34641432

Essential Oil-Based Bioherbicides: Human Health Risks Analysis

Maes C, Meersmans J, Lins L, Bouquillon S, Fauconnier ML

Int J Mol Sci

30-Aug-2021

PMCID:	PMC8431140
doi:	10.3390/ijms22179396
PMID:	34502302

Phytotoxic Effects of Plant Essential Oils: A Systematic Review and Structure-Activity Relationship Based on Chemometric Analyses

Abd-ElGawad AM, El Gendy AE, Assaeed AM, Al-Rowaily SL, Alharthi AS, Mohamed TA, Nassar MI, Dewir YH, Elshamy AI

Plants (Basel)

25-Dec-2020

PMCID:	PMC7823517
doi:	10.3390/plants10010036
PMID:	33375618

Contribution to the Orophilous Cushion-Like Vegetation of Central-Southern and Insular Greece

Musarella CM, Brullo S, del Galdo GG

Plants (Basel)

30-Nov-2020

PMCID:	PMC7760968
doi:	10.3390/plants9121678
PMID:	33266088

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Tetradecane	12389	Click to see	198.39	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
beta-Ocimene, (3Z)-	5320250	Click to see	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane	6429260	Click to see	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
Beta-Pinene	14896	Click to see	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
Camphene	6616	Click to see	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
Sabinene	18818	Click to see	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
Delta-Terpineol	81722	Click to see	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	92042749	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
(R)-beta-bisabolene	68128	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene	324224	Click to see	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane	14350	Click to see	220.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(199605)11:3<167::AID-FFJ567>3.0.CO;2-A https://doi.org/10.1016/S0031-9422(00)84709-3
alpha-Elemene	80048	Click to see CC(C)C1=CC(=C(C)C)CCC1(C)C=C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
beta Farnesene	15228937	Click to see	206.37	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
Beta-Bisabolene	10104370	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
beta-Bourbonene	62566	Click to see	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3 https://doi.org/10.1002/(SICI)1099-1026(1998070)13:4<233::AID-FFJ730>3.0.CO;2-7
Caryophyllene oxide	1742210	Click to see	220.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3 https://doi.org/10.1002/(SICI)1099-1026(199605)11:3<167::AID-FFJ567>3.0.CO;2-A
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
delta-Cadinene	441005	Click to see	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
Farnesene	5281516	Click to see	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
gamma-Muurolene	12313020	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
> 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	220.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(1998070)13:4<233::AID-FFJ730>3.0.CO;2-7
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	5321422	Click to see	220.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(1998070)13:4<233::AID-FFJ730>3.0.CO;2-7
Alloaromadendren	91746537	Click to see	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
> 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/10.1016/S0031-9422(00)84709-3
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1R,4aR,7aR)-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carbaldehyde	101992953	Click to see CC1=CCC2C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O	342.34	unknown	https://doi.org/10.1016/0031-9422(96)00074-X
(1R,4aR,7aR)-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid	101992952	Click to see	358.34	unknown	https://doi.org/10.1016/0031-9422(96)00074-X
(1R,4aR,7R,7aR)-7-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carbaldehyde	15139391	Click to see	360.36	unknown	https://doi.org/10.1016/0031-9422(96)00074-X
(1S)-1-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydro-7alpha-hydroxy-7-methylcyclopenta[c]pyran-4-carbaldehyde	72746025	Click to see	360.36	unknown	https://doi.org/10.1016/0031-9422(96)00074-X
7-Methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carbaldehyde	163077954	Click to see	342.34	unknown	https://doi.org/10.1016/0031-9422(96)00074-X
7-Methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid	4490614	Click to see	358.34	unknown	https://doi.org/10.1016/0031-9422(96)00074-X
Nepetanudoside	101932116	Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O	390.40	unknown	https://doi.org/10.1021/NP50122A009
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Nepetalactone, 4aa,7b, 7ab	6431021	Click to see	166.22	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1R,4aR,7aR)-7-methylidene-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carbaldehyde	101992954	Click to see	342.34	unknown	https://doi.org/10.1016/0031-9422(96)00074-X
7-methylidene-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carbaldehyde	162914624	Click to see C=C1CCC2C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O	342.34	unknown	https://doi.org/10.1016/0031-9422(96)00074-X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
3-Octanone	246728	Click to see CCCCCC(=O)CC	128.21	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Dehydronepetalactone	528332	Click to see CC1CCC2=C1C(=O)OC=C2C	164.20	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
(4aR,8S,8aR)-4,8-dimethyl-4a,5,6,7,8,8a-hexahydroisochromen-1-one	163029229	Click to see	180.24	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3
4,8-Dimethyl-4a,5,6,7,8,8a-hexahydroisochromen-1-one	143226317	Click to see	180.24	unknown	https://doi.org/10.1016/S0031-9422(00)84709-3

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Nepeta nuda

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses 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

Gallery Top

Contributors Top

Collections Top