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Agathosma betulina

Agathosma betulina - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644007f0ecd8b882348310
Scientific name Agathosma betulina
Authority (P.J.Bergius) Pillans
First published in J. S. African Bot. 16: 75 (1950)

Description Top

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Agathosma betulina, also known as round leaf buchu, is a flowering plant native to western South Africa. It is an evergreen shrub with glossy, fragrant leaves and white or pale pink flowers. The plant has been traditionally used by indigenous people for various ailments and is still used today in the form of essential oils and extracts for teas, candy, and a liquor called buchu brandy. The plant is also being cultivated due to concerns about overharvesting in the wild. Its chemical composition is distinct from a similar plant, Agathosma crenulata, which is known as oval leaf buchu. The extract of A. betulina is said to have a blackcurrant flavor and has been used as a folk remedy for urinary tract infections. Dutch settlers also used the plant to make a brandy tincture.

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

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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No forms added yet.

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

Suggest others/fix!
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
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
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
PMCID:PMC10744145
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
Composition and Biological Activity of the Essential Oils from Wild Horsemint, Yarrow, and Yampah from Subalpine Meadows in Southwestern Montana: Immunomodulatory Activity of Dillapiole Schepetkin IA, Özek G, Özek T, Kirpotina LN, Klein RA, Khlebnikov AI, Quinn MT Plants (Basel) 14-Jul-2023
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
Propagation of Medicinal Plants for Sustainable Livelihoods, Economic Development, and Biodiversity Conservation in South Africa Fajinmi OO, Olarewaju OO, Van Staden J Plants (Basel) 03-Mar-2023
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
Exploring Physical Characterization and Different Bio-Applications of Elaeagnus angustifolia Orchestrated Nickel Oxide Nanoparticles Abbasi BA, Iqbal J, Yaseen T, Zahra SA, Ali S, Uddin S, Mahmood T, Kanwal S, El-Serehy HA, Chalgham W Molecules 09-Jan-2023
PMCID:PMC9864018
doi:10.3390/molecules28020654
PMID:36677716
Risk Assessment of Combined Exposure to Multiple Chemicals at the European Food Safety Authority: Principles, Guidance Documents, Applications and Future Challenges Cattaneo I, Kalian AD, Di Nicola MR, Dujardin B, Levorato S, Mohimont L, Nathanail AV, Carnessechi E, Astuto MC, Tarazona JV, Kass GE, Liem AK, Robinson T, Manini P, Hogstrand C, Price PS, Dorne JL Toxins (Basel) 04-Jan-2023
PMCID:PMC9861867
doi:10.3390/toxins15010040
PMID:36668860
Different Tactics of Synthesized Zinc Oxide Nanoparticles, Homeostasis Ions, and Phytohormones as Regulators and Adaptatively Parameters to Alleviate the Adverse Effects of Salinity Stress on Plants Ahmed M, Decsi K, Tóth Z Life (Basel) 27-Dec-2022
PMCID:PMC9867113
doi:10.3390/life13010073
PMID:36676021
Green synthesis and characterization of zinc oxide nanoparticles using bush tea ( Athrixia phylicoides DC) natural extract: assessment of the synthesis process. Kaningini GA, Azizi S, Nyoni H, Mudau FN, Mohale KC, Maaza M F1000Res 23-Aug-2022
PMCID:PMC9520229
doi:10.12688/f1000research.73272.1
PMID:36212902
BIOFILM: FORMATION AND NATURAL PRODUCTS’ APPROACH TO CONTROL – A REVIEW Oluwole OM Afr J Infect Dis 17-Aug-2022
PMCID:PMC9480886
doi:10.21010/Ajid.v16i2S.7
PMID:36124328

Phytochemical Profile Top

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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
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 CC#CC#CC(=O)C1=CC=CC=C1 168.19 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol 14529 Click to see CC1=CC=C(C=C1)C(C)(C)O 150.22 unknown https://doi.org/10.1021/JF60201A021
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown https://doi.org/10.1021/JF60201A021
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1021/JF60201A021
Guaiacol 460 Click to see COC1=CC=CC=C1O 124.14 unknown https://doi.org/10.1021/JF60201A021
Phenol, 2-ethenyl-6-methoxy- 183539 Click to see COC1=CC=CC(=C1O)C=C 150.17 unknown https://doi.org/10.1021/JF60201A021
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1021/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 CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1021/JF60201A021
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-CITRONELLOL, (+/-)- 8842 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1021/JF60201A021
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1021/JF60201A021
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1021/JF60201A021
Linalool, (+)- 67179 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1021/JF60201A021
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1021/JF60201A021
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 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 CC1CCC2=C(C1)OC=C2C 150.22 unknown https://doi.org/10.1021/JF60201A021
3-Isopropyl-6-methylpyrocatechol 95873 Click to see CC1=C(C(=C(C=C1)C(C)C)O)O 166.22 unknown https://doi.org/10.1021/JF60201A021
Menthofuran 329983 Click to see CC1CCC2=C(C1)OC=C2C 150.22 unknown https://doi.org/10.1021/JF60201A021
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 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 CC(=O)OCC1=CCC2CC1C2(C)C 194.27 unknown https://doi.org/10.1021/JF60201A021
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/JF60201A021
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1021/JF60201A021
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1021/JF60201A021
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 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
Myrtenol 10582 Click to see CC1(C2CC=C(C1C2)CO)C 152.23 unknown https://doi.org/10.1021/JF60201A021
Myrtenyl acetate 61262 Click to see CC(=O)OCC1=CCC2CC1C2(C)C 194.27 unknown https://doi.org/10.1021/JF60201A021
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1021/JF60201A021
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 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
(+)-Menthone 443159 Click to see CC1CCC(C(=O)C1)C(C)C 154.25 unknown https://doi.org/10.1021/JF60201A021
(+)-Neomenthol 439263 Click to see CC1CCC(C(C1)O)C(C)C 156.26 unknown https://doi.org/10.1021/JF60201A021
(1S,2R,5S)-2-isopropyl-5-methylcyclohexyl acetate 62335 Click to see CC1CCC(C(C1)OC(=O)C)C(C)C 198.30 unknown https://doi.org/10.1021/JF60201A021
[4-(Prop-1-en-2-yl)cyclohexyl]methanol 519954 Click to see CC(=C)C1CCC(CC1)CO 154.25 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 CC1CC(=O)C(CC1O)C(C)C 170.25 unknown https://doi.org/10.1021/JF60201A021
8-Hydroxymenthone 13614904 Click to see CC1CCC(C(=O)C1)C(C)(C)O 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 CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1021/JF60201A021
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1021/JF60201A021
alpha,alpha-Dimethyl-4-methylenecyclohexanemethanol 81722 Click to see CC(C)(C1CCC(=C)CC1)O 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 CC(=C)C1CCC(CC1)(C)O 154.25 unknown https://doi.org/10.1021/JF60201A021
Carveol 7438 Click to see CC1=CCC(CC1O)C(=C)C 152.23 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
Carvone, (+/-)- 7439 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 CC1=CCC(CC1OC(=O)C)C(=C)C 194.27 unknown https://doi.org/10.1021/JF60201A021
Dihydrocarvone 24473 Click to see CC1CCC(CC1=O)C(=C)C 152.23 unknown https://doi.org/10.1021/JF60201A021
Isomenthone, (+/-)- 6432469 Click to see CC1CCC(C(=O)C1)C(C)C 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
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/JF60201A021
Menthol 1254 Click to see CC1CCC(C(C1)O)C(C)C 156.26 unknown https://doi.org/10.1021/JF60201A021
Menthyl acetate 27867 Click to see CC1CCC(C(C1)OC(=O)C)C(C)C 198.30 unknown https://doi.org/10.1021/JF60201A021
Neoisomenthol 19244 Click to see CC1CCC(C(C1)O)C(C)C 156.26 unknown https://doi.org/10.1021/JF60201A021
P-Menth-1-en-9-al 520440 Click to see CC1=CCC(CC1)C(C)C=O 152.23 unknown https://doi.org/10.1021/JF60201A021
p-Menth-1-en-9-ol 86753 Click to see CC1=CCC(CC1)C(C)CO 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 CC1=CC(=O)C(=C(C)C)CC1 150.22 unknown https://doi.org/10.1021/JF60201A021
Piperitone 6987 Click to see CC1=CC(=O)C(CC1)C(C)C 152.23 unknown https://doi.org/10.1021/JF60201A021
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 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,5R,9S)-4,5-Epoxy-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undecane 9991037 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
(1R,5S,9S)-4,8-Dimethylene-11,11-dimethylbicyclo[7.2.0]undecan-5-ol 14524924 Click to see CC1(CC2C1CCC(=C)C(CCC2=C)O)C 220.35 unknown via CMAUP database
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene 101708 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 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
beta-Ionone 638014 Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C 192.30 unknown https://doi.org/10.1021/JF60201A021
Calamenene 6429077 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1021/JF60201A021
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Fgpdtarjoxrwjd-rrfjbimhsa- 11435962 Click to see CC(C)C1=CCC2(C(CCC(=C)C2C1)O)C 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
Oplopanone 10466745 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 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 CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 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 CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1021/JF60201A021
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1021/JF60201A021
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S)-3alpha-Vinyl-3-methyl-2beta-(1-methylvinyl)-6beta-isopropylcyclohexane-1alpha-ol 102012174 Click to see CC(C)C1CCC(C(C1O)C(=C)C)(C)C=C 222.37 unknown via CMAUP database
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 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 CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown via CMAUP database
Pygmol 14167388 Click to see CC12CCCC(C1C(C(CC2)C(C)(C)O)O)(C)O 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,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 CC1=CCCC2(C(O2)C(C(CC1)C(C)C)O)C 238.37 unknown via CMAUP database
(1R,2R,3S,7R,10S)-6-Methylene-10-methyl-3-isopropyl-11-oxabicyclo[8.1.0]undecane-2,7-diol 10610977 Click to see CC(C)C1CCC(=C)C(CCC2(C(C1O)O2)C)O 254.36 unknown via CMAUP database
(1R,2S,6E,10S)-3-Methylene-7-methyl-10-isopropyl-6-cyclodecene-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
(1R,4E,6R,7R)-4-Methyl-7-(1-hydroxy-1-methylethyl)-10-methylene-4-cyclodecene-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,4S,5E,7S)-4-methyl-10-methylidene-7-propan-2-ylcyclodec-5-ene-1,4-diol 9991811 Click to see CC(C)C1CCC(=C)C(CCC(C=C1)(C)O)O 238.37 unknown via CMAUP database
(1S,4E,6R,7R)-4-Methyl-7-(1-hydroxy-1-methylethyl)-10-methylene-4-cyclodecene-1,6-diol 15479892 Click to see CC1=CC(C(CCC(=C)C(CC1)O)C(C)(C)O)O 254.36 unknown via CMAUP database
(1S,4E,6R,7S)-4-Methyl-7-isopropyl-10-methylene-4-cyclodecene-1,6-diol 100982187 Click to see CC1=CC(C(CCC(=C)C(CC1)O)C(C)C)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 CC1=CC2C(CCC(=C)C(=O)CC1)C(OC(O2)(C)C)(C)C 292.40 unknown via CMAUP database
(4E,6R,7R)-4-Methyl-6-hydroxy-7-(1-hydroxy-1-methylethyl)-10-methylene-4-cyclodecene-1-one 10729506 Click to see CC1=CC(C(CCC(=C)C(=O)CC1)C(C)(C)O)O 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 CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CC(C2(CCC1=C)C)O)C)C)(C)C)O)C 442.70 unknown via CMAUP database
Calenduladiol 461835 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C 442.70 unknown via CMAUP database
CID 14137680 14137680 Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C)C 468.80 unknown via CMAUP database
Dammaradienol 13893946 Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)C 426.70 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 CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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 CC(CC(C)(C)O)O 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 CC1CCCC(=O)C1 112.17 unknown https://doi.org/10.1021/JF60201A021
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(5R)-2-[(E)-2,4-Hexadiyne-1-ylidene]-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
(5R)-2-[(Z)-2,4-Hexadiyne-1-ylidene]-1,6-dioxaspiro[4.4]nona-3,7-diene 44575223 Click to see CC#CC#CC=C1C=CC2(O1)CC=CO2 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 CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 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 CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 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 CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 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 CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 256.25 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
Pinol 101153 Click to see CC1=CCC2CC1OC2(C)C 152.23 unknown https://doi.org/10.1021/JF60201A021
> Phenylpropanoids and polyketides / Coumarins and derivatives
7,8-Methylenedioxy-6-methoxycoumarin 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 COC1=C(C=C2C=CC(=O)OC2=C1)O 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 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)O 610.60 unknown https://doi.org/10.1016/S0731-7085(01)00476-9
Diosmin 5281613 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)O 608.50 unknown https://doi.org/10.1016/S0731-7085(01)00476-9
Hesperidin 10621 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)O 610.60 unknown https://doi.org/10.1016/S0731-7085(01)00476-9

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