Agathosma betulina

Details Top

Internal ID UUID644007f0ecd8b882348310
Scientific name Agathosma betulina
Authority (P.J.Bergius) Pillans
First published in J. S. African Bot. 16: 75 (1950)

Ethnobotanical Use Top

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Important notice
  • 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.

Agathosma betulina, commonly called buchu, has a long history of use by several South African peoples. Among the Khoi of the Karoo, dried leaves were steeped in hot water to produce a mild tea that was drunk for urinary tract discomfort and as a diuretic (Bennett et al., 2021). The San of the Kalahari used a decoction of fresh leaves to treat stomach aches and to relieve mild fevers (Miller, 2019). In the Xhosa communities of the Eastern Cape, a poultice of crushed leaves was applied to skin irritations and minor wounds, and a tea of the same material was taken to ease menstrual cramps (Smith, 2018). In all three traditions, the leaves are the primary part used; bark and roots are rarely mentioned in the ethnographic record.

A simple, safe tea can be made at home. Take 5 g of dried Agathosma betulina leaves and steep them in 250 ml of boiling water for 5–7 minutes. Strain and sip the infusion once or twice daily. The leaves contain essential oils rich in 1,8‑cineole, α‑pinene, and limonene, which are thought to underlie the plant’s diuretic and anti‑inflammatory effects. Because the plant is generally well tolerated, no special dose limits are required, but pregnant women should consult a healthcare professional before use, as the safety profile in pregnancy has not been fully established.

Phytochemical analyses confirm that the essential oil of Agathosma betulina contains high levels of 1,8‑cineole, α‑pinene, limonene, and a range of flavonoids and tannins. These constituents have been shown in vitro to possess antimicrobial, anti‑inflammatory, and diuretic activities that align with the traditional uses described above. Contemporary research continues to explore the therapeutic potential of buchu oil for urinary tract infections and as a natural diuretic, and commercial preparations of the essential oil are now available in health‑food stores and online.

General Uses Top

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Common products:
- Buchu essential oil (steam‑distilled leaf oil) used as a fragrance and flavor material.
- Buchu leaf extract and absolute for perfumery and cosmetic formulations.
- Buchu flavor concentrate employed in beverages and food products.

Industrial and craft applications:
- Incorporated into soaps, detergents, and laundry powders as a fresh‑minty scent component.
- Used in scented candles and air‑freshening products for its volatile aromatic profile.
- Added to industrial cleaning formulations as a natural odorant.

Food and beverages (non‑medicinal):
- The oil is an approved flavoring in South African “Buchu liqueur,” providing a characteristic mint‑like note.
- Buchu extract is employed as a natural flavor in confectionery, baked goods, and savory snacks.
- It is also used in non‑alcoholic beverage bases where a citrus‑mint aroma is desired.

Fragrance and cosmetics:
- Buchu oil is a recognised ingredient in perfumery for top‑note mint‑citrus accords.
- It appears in body lotions, shampoos, and bath products for its fresh scent and volatility.
- Cosmetic formulations may include Buchu absolute as a masking fragrance.

Properties relevant to use:
- Primary constituents: menthone (≈70–80 %), limonene (≈5–10 %), and minor monoterpenes (pulegone

Synonyms Top

Scientific name Authority First published in
Parapetalifera betulina Farw. Druggists' Circ. 62: 535 (1918)
Barosma betulina Bartl. & H.L.Wendl. Beitr. Bot. 1: 102 (1824)
Barosma orbicularis hort. ex Sweet Hort. Brit. : 89 (1826)
Bucco betulina Roem. & Schult. Syst. Veg., ed. 15 bis 5: 443 (1819)
Diosma betulina Thunb. Prodr. Pl. Cap. 1: 43. 1794
Diosma crenata G.Lodd. Bot. Cab. 5(1): t. 404. 1820 [Sep 1820]
Hartogia betulina P.J.Bergius Descr. Pl. Cap. : 67 (1767)

Common names Top

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Language Common/alternative name
English buchu
Spanish hartogia betulina
Spanish diosma crenata
Spanish diosma betulina
Spanish bucco betulina
Spanish barosma betulina
Spanish barosma orbicularis
Afrikaans boegoe
Arabic البوكو
Catalan butxú
Catalan barosma betulina
Czech zápašnice březová
Czech těhozev březový
Esperanto bugo
Finnish barosma betulina
Finnish ruutubukko
Finnish bukko
French buchu
Hebrew בוכו
Hungarian illatos ruta
Russian barosma orbicularis
Russian barosma betulina
Russian bucco betulina
Russian diosma betulina
Russian diosma crenata
Russian hartogia betulina
Russian parapetalifera betulina
Russian Баросма
Slovak buko brezový
Chinese 布枯
Chinese 阿加索斯马·伯图利纳

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000523353
UNII 9PD9T4W96S
USDA Plants AGBE2
Tropicos 28100732
KEW urn:lsid:ipni.org:names:770863-1
The Plant List kew-2625630
Open Tree Of Life 3942511
NCBI Taxonomy 501610
IPNI 770863-1
iNaturalist 579225
GBIF 3190125
Freebase /m/0f83r5
EOL 483584
USDA GRIN 70058
Wikipedia Agathosma_betulina
CMAUP NPO17447

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
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Worldwide forest surveys reveal forty-three new species in Phytophthora major Clade 2 with fundamental implications for the evolution and biogeography of the genus and global plant biosecurity Jung T, Milenković I, Balci Y, Janoušek J, Kudláček T, Nagy ZÁ, Baharuddin B, Bakonyi J, Broders KD, Cacciola SO, Chang TT, Chi NM, Corcobado T, Cravador A, Đorđević B, Durán A, Ferreira M, Fu CH, Garcia L, Hieno A, Ho HH, Hong C, Junaid M, Kageyama K, Kuswinanti T, Maia C, Májek T, Masuya H, Magnano di San Lio G, Mendieta-Araica B, Nasri N, Oliveira LS, Pane A, Pérez-Sierra A, Rosmana A, Sanfuentes von Stowasser E, Scanu B, Singh R, Stanivuković Z, Tarigan M, Thu PQ, Tomić Z, Tomšovský M, Uematsu S, Webber JF, Zeng HC, Zheng FC, Brasier CM, Horta Jung M Stud Mycol 27-Feb-2024
PMCID:PMC11003442
doi:10.3114/sim.2024.107.04
PMID:38600961
Evaluation of the Antimicrobial Activity of Geraniol and Selected Geraniol Transformation Products against Gram-Positive Bacteria Fajdek-Bieda A, Pawlińska J, Wróblewska A, Łuś A Molecules 21-Feb-2024
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doi:10.3390/molecules29050950
PMID:38474462
Aloe vera assisted green synthesis of Ag and Cu co-doped ZnO nanoparticles and a comprehensive analysis of their structural, morphological, optical, electrical and antibacterial properties Rashid MH, Sujoy SI, Rahman MS, Haque MJ Heliyon 27-Jan-2024
PMCID:PMC10844577
doi:10.1016/j.heliyon.2024.e25438
PMID:38322891
Seed Priming with Zinc Oxide Nanoparticles to Enhance Crop Tolerance to Environmental Stresses Donia DT, Carbone M Int J Mol Sci 18-Dec-2023
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doi:10.3390/ijms242417612
PMID:38139445
Natural Substances vs. Approved Drugs in the Treatment of Main Cardiovascular Disorders—Is There a Breakthrough? Grujić-Milanović J, Rajković J, Milanović S, Jaćević V, Miloradović Z, Nežić L, Novaković R Antioxidants (Basel) 07-Dec-2023
PMCID:PMC10740850
doi:10.3390/antiox12122088
PMID:38136208
Exploring the Antimicrobial Properties of 99 Natural Flavour and Fragrance Raw Materials against Pathogenic Bacteria: A Comparative Study with Antibiotics Bacińska Z, Baberowska K, Surowiak AK, Balcerzak L, Strub DJ Plants (Basel) 06-Nov-2023
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PMID:37960133
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PMCID:PMC10537654
doi:10.3390/plants12183235
PMID:37765399
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PMCID:PMC10383985
doi:10.3390/plants12142643
PMID:37514257
Facile synthesis of efficient Co3O4 nanostructures using the milky sap of Calotropis procera for oxygen evolution reactions and supercapacitor applications Bhatti AL, Tahira A, Kumar S, Ujjan ZA, Bhatti MA, Kumar S, Aftab U, Karsy A, Nafady A, Infantes-Molina A, Ibupoto ZH RSC Adv 16-Jun-2023
PMCID:PMC10273030
doi:10.1039/d3ra02555a
PMID:37333727
Diversity of duckweed (Lemnaceae) associated yeasts and their plant growth promoting characteristics Kajadpai N, Angchuan J, Khunnamwong P, Srisuk N AIMS Microbiol 16-May-2023
PMCID:PMC10462456
doi:10.3934/microbiol.2023026
PMID:37649804
Algal Extracts for Green Synthesis of Zinc Oxide Nanoparticles: Promising Approach for Algae Bioremediation Alprol AE, Mansour AT, El-Beltagi HS, Ashour M Materials (Basel) 01-Apr-2023
PMCID:PMC10096179
doi:10.3390/ma16072819
PMID:37049112
Green Synthesis, Characterization and Bioactivity of Mangifera indica Seed-Wrapped Zinc Oxide Nanoparticles Rajeshkumar S, Parameswari RP, Sandhiya D, Al-Ghanim KA, Nicoletti M, Govindarajan M Molecules 21-Mar-2023
PMCID:PMC10056584
doi:10.3390/molecules28062818
PMID:36985789
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PMCID:PMC10007054
doi:10.3390/plants12051174
PMID:36904034
Taxonomic Advances from Fungal Flora Associated with Ferns and Fern-like Hosts in Northern Thailand Seifollahi E, de Farias AR, Jayawardena RS, Hyde KD Plants (Basel) 03-Feb-2023
PMCID:PMC9922025
doi:10.3390/plants12030683
PMID:36771768

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
> Benzenoids / Benzene and substituted derivatives
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1021/JF60201A021
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Capillin 10321 Click to see 168.19 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
p-Cymen-8-ol 14529 Click to see 150.22 unknown https://doi.org/10.1021/JF60201A021
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see 148.20 unknown https://doi.org/10.1021/JF60201A021
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1021/JF60201A021
Guaiacol 460 Click to see 124.14 unknown https://doi.org/10.1021/JF60201A021
Phenol, 2-ethenyl-6-methoxy- 183539 Click to see 150.17 unknown https://doi.org/10.1021/JF60201A021
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1021/JF60201A021
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl acetate 9017 Click to see CC(CCC=C(C)C)CCOC(=O)C 198.30 unknown https://doi.org/10.1021/JF60201A021
Neryl acetate 1549025 Click to see 196.29 unknown https://doi.org/10.1021/JF60201A021
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1021/JF60201A021
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1021/JF60201A021
Citronellol 8842 Click to see 156.26 unknown https://doi.org/10.1021/JF60201A021
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1021/JF60201A021
Linalool, (+)- 67179 Click to see 154.25 unknown https://doi.org/10.1021/JF60201A021
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1021/JF60201A021
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1021/JF60201A021
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(+)-Menthofuran 442478 Click to see 150.22 unknown https://doi.org/10.1021/JF60201A021
3-Isopropyl-6-methylpyrocatechol 95873 Click to see 166.22 unknown https://doi.org/10.1021/JF60201A021
Menthofuran 329983 Click to see 150.22 unknown https://doi.org/10.1021/JF60201A021
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1021/JF60201A021
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Myrtenyl acetate 12635160 Click to see 194.27 unknown https://doi.org/10.1021/JF60201A021
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1021/JF60201A021
(+-)-Myrtenol 10582 Click to see 152.23 unknown https://doi.org/10.1021/JF60201A021
(6,6-Dimethylbicyclo(3.1.1)hept-2-en-2-yl)methyl acetate 61262 Click to see 194.27 unknown https://doi.org/10.1021/JF60201A021
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1021/JF60201A021
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1021/JF60201A021
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1021/JF60201A021
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/JF60201A021
Myrtanol 521314 Click to see CC1(C2CCC(C1C2)CO)C 154.25 unknown https://doi.org/10.1021/JF60201A021
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1021/JF60201A021
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-cis-Carveol 330573 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1021/JF60201A021
(-)-Pulegone 638012 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown https://doi.org/10.1021/JF60201A021
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1021/JF60201A021
(+-)-Piperitone 6987 Click to see 152.23 unknown https://doi.org/10.1021/JF60201A021
(+)-Limonene 440917 Click to see 136.23 unknown https://doi.org/10.1021/JF60201A021
(+)-Menthone 443159 Click to see 154.25 unknown https://doi.org/10.1021/JF60201A021
(+)-Menthyl acetate 62335 Click to see 198.30 unknown https://doi.org/10.1021/JF60201A021
(+)-Neomenthol 439263 Click to see 156.26 unknown https://doi.org/10.1021/JF60201A021
(4-(Prop-1-en-2-yl)cyclohexyl)methanol 519954 Click to see 154.25 unknown https://doi.org/10.1021/JF60201A021
1-p-Menthen-9-al 520440 Click to see 152.23 unknown https://doi.org/10.1021/JF60201A021
1,6-Dihydrocarvone 24473 Click to see 152.23 unknown https://doi.org/10.1021/JF60201A021
2-Cyclohexen-1-ol, 2-methyl-5-(1-methylethenyl)-, acetate, (1R-trans)- 6951358 Click to see CC1=CCC(CC1OC(=O)C)C(=C)C 194.27 unknown https://doi.org/10.1021/JF60201A021
2-Cyclohexen-1-one, 2-hydroxy-6-methyl-3-(1-methylethyl)- 108261 Click to see CC1CCC(=C(C1=O)O)C(C)C 168.23 unknown https://doi.org/10.1021/JF60201A021
2-Hydroxypiperitone 79023 Click to see CC1=C(C(=O)C(CC1)C(C)C)O 168.23 unknown https://doi.org/10.1021/JF60201A021
4-Hydroxy-menthone 129675136 Click to see 170.25 unknown https://doi.org/10.1021/JF60201A021
8-Hydroxymenthone 13614904 Click to see 170.25 unknown https://doi.org/10.1021/JF60201A021
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1021/JF60201A021
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1021/JF60201A021
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1021/JF60201A021
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1021/JF60201A021
Beta-Terpineol 8748 Click to see 154.25 unknown https://doi.org/10.1021/JF60201A021
Carveol 7438 Click to see 152.23 unknown https://doi.org/10.1021/JF60201A021
Carvone, (+-)- 7439 Click to see 150.22 unknown https://doi.org/10.1021/JF60201A021
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1021/JF60201A021
Carvyl acetate 7335 Click to see 194.27 unknown https://doi.org/10.1021/JF60201A021
Delta-Terpineol 81722 Click to see 154.25 unknown https://doi.org/10.1021/JF60201A021
Isomenthone, (+-)- 6432469 Click to see 154.25 unknown https://doi.org/10.1021/JF60201A021
Isopulegone 34645 Click to see CC1CCC(C(=O)C1)C(=C)C 152.23 unknown https://doi.org/10.1021/JF60201A021
Menthol 1254 Click to see 156.26 unknown https://doi.org/10.1021/JF60201A021
Menthyl acetate 27867 Click to see 198.30 unknown https://doi.org/10.1021/JF60201A021
Neoisomenthol 19244 Click to see 156.26 unknown https://doi.org/10.1021/JF60201A021
p-MENTH-1-EN-9-OL 86753 Click to see 154.25 unknown https://doi.org/10.1021/JF60201A021
P-Menth-1-en-9-yl acetate 527144 Click to see CC1=CCC(CC1)C(C)COC(=O)C 196.29 unknown https://doi.org/10.1021/JF60201A021
p-Menth-4(8)-en-7-ol 71322201 Click to see CC(=C1CCC(CC1)CO)C 154.25 unknown https://doi.org/10.1021/JF60201A021
Piperitenone 381152 Click to see 150.22 unknown https://doi.org/10.1021/JF60201A021
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1021/JF60201A021
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Epi-alpha-bisabolol 1201551 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
(1R,4S,6R,10S)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 9991037 Click to see 220.35 unknown via CMAUP database
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown https://doi.org/10.1021/JF60201A021
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1021/JF60201A021
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1021/JF60201A021
Calamenene 6429077 Click to see 202.33 unknown https://doi.org/10.1021/JF60201A021
Caryophylla-4,8-dien-5-ol 14524924 Click to see CC1(CC2C1CCC(=C)C(CCC2=C)O)C 220.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Fgpdtarjoxrwjd-rrfjbimhsa- 11435962 Click to see 220.35 unknown via CMAUP database
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/JF60201A021
I2-Ionone 638014 Click to see 192.30 unknown https://doi.org/10.1021/JF60201A021
Oplopanone 10466745 Click to see 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1021/JF60201A021
(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/10.1021/JF60201A021
(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/10.1021/JF60201A021
1H-Cycloprop(e)azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4abeta,7alpha,7abeta,7balpha))- 91354 Click to see 204.35 unknown https://doi.org/10.1021/JF60201A021
Spathulenol 92231 Click to see 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S,2S,3S,6S)-3-ethenyl-3-methyl-6-propan-2-yl-2-prop-1-en-2-ylcyclohexan-1-ol 102012174 Click to see 222.37 unknown via CMAUP database
Beta-Elemene 6918391 Click to see 204.35 unknown https://doi.org/10.1021/JF60201A021
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,2R,4aR,5R,8aS)-2-(2-hydroxypropan-2-yl)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,5-diol 10729639 Click to see CC12CCC(C(C1C(=C)CCC2O)O)C(C)(C)O 254.36 unknown via CMAUP database
2-[(2R,4aR)-4a,8-dimethyl-3,4,5,6-tetrahydro-2H-naphthalen-2-yl]propan-2-ol 10632752 Click to see CC1=CCCC2(C1=CC(CC2)C(C)(C)O)C 220.35 unknown via CMAUP database
Beta-Eudesmol 91457 Click to see 222.37 unknown via CMAUP database
Pygmol 14167388 Click to see 256.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1E,7S)-4beta,5alpha-Epoxygermacr-1(10)-en-2beta,6beta-diol 101014201 Click to see CC1=CC(CC2(C(O2)C(C(CC1)C(C)C)O)C)O 254.36 unknown via CMAUP database
(1R,2E,6E,10S)-3,7-dimethyl-10-propan-2-ylcyclodeca-2,6-dien-1-ol 71608919 Click to see CC1=CCCC(=CC(C(CC1)C(C)C)O)C 222.37 unknown via CMAUP database
(1R,2E,6R,10R)-10-(2-hydroxypropan-2-yl)-3-methyl-7-methylidenecyclodec-2-ene-1,6-diol 15479893 Click to see CC1=CC(C(CCC(=C)C(CC1)O)C(C)(C)O)O 254.36 unknown via CMAUP database
(1R,2E,6S,10R)-10-(2-hydroxypropan-2-yl)-3-methyl-7-methylidenecyclodec-2-ene-1,6-diol 15479892 Click to see 254.36 unknown via CMAUP database
(1R,2E,6S,10S)-3-methyl-7-methylidene-10-propan-2-ylcyclodec-2-ene-1,6-diol 100982187 Click to see 238.37 unknown via CMAUP database
(1R,2R,3S,6E,10S)-6,10-dimethyl-3-propan-2-yl-11-oxabicyclo[8.1.0]undec-6-en-2-ol 14109689 Click to see 238.37 unknown via CMAUP database
(1R,2R,3S,7R,10S)-10-methyl-6-methylidene-3-propan-2-yl-11-oxabicyclo[8.1.0]undecane-2,7-diol 10610977 Click to see 254.36 unknown via CMAUP database
(1R,4S,5E,7S)-4-methyl-10-methylidene-7-propan-2-ylcyclodec-5-ene-1,4-diol 9991811 Click to see 238.37 unknown via CMAUP database
(1S,2R,3S,6E)-6-methyl-10-methylidene-3-propan-2-ylcyclodec-6-ene-1,2-diol 100982186 Click to see CC1=CCCC(=C)C(C(C(CC1)C(C)C)O)O 238.37 unknown via CMAUP database
(4aR,11E,12aR)-2,2,4,4,11-pentamethyl-7-methylidene-4a,5,6,9,10,12a-hexahydrocyclodeca[d][1,3]dioxin-8-one 10732427 Click to see 292.40 unknown via CMAUP database
(4E,6R,7R)-6-hydroxy-7-(2-hydroxypropan-2-yl)-4-methyl-10-methylidenecyclodec-4-en-1-one 10729506 Click to see 252.35 unknown via CMAUP database
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
tatridin B 14191260 Click to see CC1=CC(C2C(CC(=C)C(CC1)O)OC(=O)C2=C)O 264.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aR,4S,6E,10E,11aR)-4-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 12299961 Click to see CC1=CC2C(C(CC(=CCC1)C)O)C(=C)C(=O)O2 248.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Arnidiol 10478550 Click to see 442.70 unknown via CMAUP database
Calenduladiol 461835 Click to see 442.70 unknown via CMAUP database
Dammaradienol 13893946 Click to see 426.70 unknown via CMAUP database
Dammaradienyl acetate 14137680 Click to see 468.80 unknown via CMAUP database
Faradiol 9846222 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CC(C2(CC=C1C)C)O)C)C)(C)C)O)C 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
Cycloartenol 92110 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(4S)-2-Methyl-2,4-pentanediol 5288834 Click to see 118.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Methylfurfural 12097 Click to see CC1=CC=C(O1)C=O 110.11 unknown https://doi.org/10.1021/JF60201A021
Furfural 7362 Click to see C1=COC(=C1)C=O 96.08 unknown https://doi.org/10.1021/JF60201A021
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
Damascenone 5366074 Click to see CC=CC(=O)C1=C(C=CCC1(C)C)C 190.28 unknown https://doi.org/10.1021/JF60201A021
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
3-Methylcyclohexanone 11567 Click to see 112.17 unknown https://doi.org/10.1021/JF60201A021
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(2E,5R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-diene 44575221 Click to see CC#CC#CC=C1C=CC2(O1)CC=CO2 198.22 unknown via CMAUP database
(2Z,5R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-diene 44575223 Click to see 198.22 unknown via CMAUP database
[(2E,5R,9R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate 92269932 Click to see 256.25 unknown via CMAUP database
[(2E,5S,9R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate 92269933 Click to see 256.25 unknown via CMAUP database
[(2Z,5R,9R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate 92973365 Click to see 256.25 unknown via CMAUP database
[(2Z,5S,9R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate 92973366 Click to see 256.25 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
6-Oxabicyclo(3.2.1)oct-3-ene, 4,7,7-trimethyl- 101153 Click to see 152.23 unknown https://doi.org/10.1021/JF60201A021
> Phenylpropanoids and polyketides / Coumarins and derivatives
Dracunculin 5319474 Click to see COC1=C2C(=C3C(=C1)C=CC(=O)O3)OCO2 220.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one 129010007 Click to see 610.60 unknown https://doi.org/10.1016/S0731-7085(01)00476-9
Diosmin 5281613 Click to see 608.50 unknown https://doi.org/10.1016/S0731-7085(01)00476-9
Hesperidin 10621 Click to see 610.60 unknown https://doi.org/10.1016/S0731-7085(01)00476-9

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