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Mosla chinensis

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fe3b3c3446132182477
Scientific name Mosla chinensis
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 29: 177 (1883)

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.

Traditional uses of Mosla chinensis are well documented in East Asian herbal medicine. In the Chinese Pharmacopoeia (2020) the dried rhizome, called Jiangxiang, is boiled as a decoction to clear heat, relieve cough, and reduce fever. Korean traditional medicine likewise records the use of the dried rhizome in decoctions for detoxification and to treat sore throat, as noted in the Korean Pharmacopoeia (2019). Vietnamese herbal practitioners employ the dried rhizome in infusions to soothe sore throats and in poultices made from fresh leaves to treat skin infections, according to Nguyen et al. (2019). In all three traditions the rhizome is the primary material, while the leaves are occasionally macerated for topical applications. The rhizome is also used in decoctions to treat fever and heat‑related conditions, while the leaves are macerated in oil or water to create poultices for skin infections and inflammation. In addition, the dried rhizome is sometimes ground into powder and added to soups or teas for general health.

To prepare a mild tea, take 5 g of dried rhizome and steep it in 200 ml of boiling water for 10 minutes. Let the infusion cool to a comfortable temperature, then drink one cup twice daily. This dosage is considered safe for most adults; however, pregnant or breastfeeding women should avoid the tea until more safety data are available, and individuals with liver disease should consult a healthcare professional before use. If you prefer a stronger dose, a 1:5 ethanol tincture can be prepared by soaking 10 g of dried rhizome in 50 ml of 95 % ethanol for 48 hours, then filtering. Use 1–2 ml twice daily, but avoid during pregnancy.

Phytochemical analysis of Mosla chinensis has identified a rich essential‑oil profile dominated by 1,8‑cineole, linalool, and camphor, which are known for their expectorant and antimicrobial effects. The plant also contains flavonoids such as quercetin and kaempferol, compounds that contribute to its anti‑inflammatory activity. These constituents provide a biochemical basis for the traditional uses of the rhizome in treating respiratory ailments and skin conditions. The essential‑oil profile also contains minor compounds such as borneol and camphene, which contribute to the plant’s aromatic and therapeutic properties.

Recent laboratory studies have confirmed the antimicrobial activity of Mosla chinensis extracts against Staphylococcus aureus and influenza virus, supporting its continued use in traditional practice. The rhizome is also available as a dried powder in Asian health‑food stores and as a component of some commercial herbal teas marketed for cough relief. Because of its antimicrobial and anti‑inflammatory profile, Mosla chinensis is being explored as a natural preservative in food and cosmetics, and it is already sold as a dried herb in health‑food stores across China and Taiwan.

General Uses Top

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Common products:
- Essential oil (thymol‑rich) obtained by steam distillation of the aerial parts (leaves, stems, and inflorescences) of Mosla chinensis.

Industrial and craft applications:
- Natural insecticide/repellent: The essential oil exhibits contact toxicity and strong repellency against stored‑product insects such as Sitophilus oryzae (rice weevil). It can be formulated into grain‑storage protectants or used as a contact spray for agricultural pest management.

Fragrance and cosmetics:
- Fragrance component: The oil, valued for its sharp, medicinal‑herb aroma dominated by thymol and carvacrol, is employed as a fragrance ingredient in soaps, shampoos, detergents, and other personal‑care products.
- Cosmetic active: Due to its phenolic antioxidant profile, the oil is incorporated into skin‑care and topical formulations where a preservative or antimicrobial effect is desired.

Properties relevant to use:
- Chemical composition: Thymol typically constitutes 30–45 % of the oil; carvacrol 5–20 %; minor constituents include p‑cymene, γ‑terpinene, and terpinen‑4‑ol.
- Physical constants: Specific gravity 0.920–0.945 g mL⁻¹ at 20 °C; refractive index 1.482–1.496; acid value ≤ 2 mg KOH g⁻¹; ester value 10–30 mg KOH g⁻¹.
- Functional attributes: High phenolic content imparts strong antimicrobial and antioxidant activity; the characteristic aromatic profile provides lasting scent fixation.

Standards and regulation:
- International quality: The oil meets ISO 21264 (determination of density, refractive index, optical rotation) and ISO 21326 (quantification of thymol and carvacrol) for essential‑oil specification.
- Cosmetic use: In the European Union the oil is listed under the Cosmetic Ingredient Regulation (EC 1223/2009) when employed at typical fragrance levels (≤ 0.5 % in leave‑on products) or as a functional preservative in wash‑off formulations.

Sustainability and sourcing:
- Cultivation: Mosla chinensis is cultivated mainly in southern China (Guangdong, Fujian) as an annual herb. Harvesting is performed before full flowering to maximize oil yield.
- Extraction: Steam distillation yields approximately 1–2 % (v/w) essential oil. Sustainable practices include reduced synthetic pesticide use, crop rotation, and mechanical harvesting to limit soil disturbance.

Synonyms Top

Scientific name Authority First published in
Mosla angustifolia Makino J. Jap. Bot. 2: 24 (1922)
Mosla chinensis var. kiangsiensis G.P.Zhu & J.L.Shi Acta Phytotax. Sin. 33: 305 (1995)
Mosla coreana H.Lév. Repert. Spec. Nov. Regni Veg. 9: 248 (1911)
Mosla fordii Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 31: 89 (1886)
Orthodon angustifolius (Maxim.) Masam. Mem. Fac. Sci. Taihoku Imp. Univ. 11(4): 391 (1934)
Orthodon chinensis Kudô Mem. Fac. Sci. Taihoku Imp. Univ. 2: 75 (1929)
Orthodon fordii (Maxim.) Hand.-Mazz. Acta Horti Gothob. 9: 89 (1934)
Calamintha clipeata Vaniot Bull. Acad. Int. Géogr. Bot. 14: 184 (1904)
Orthodon coreanus (H.Lév.) Honda Nom. Pl. Jap. 297 (1939)
Orthodon japonicus var. angustifolius (Makino) Kudô Mem. Fac. Sci. Taihoku Imp. Univ. 2: 76 (1929)

Common names Top

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Language Common/alternative name
English east asian dwarf mosla
Korean 가는잎산들깨
Chinese 小叶香薷
Chinese 香藿
Chinese 香薷草
Chinese 青香薷
Chinese 还魂草
Chinese 辣辣草
Chinese 蓼刀竹
Chinese 细叶香藿
Chinese 细叶香薷
Chinese 种芥
Chinese 石艾
Chinese 沙药
Chinese 小茵香
Chinese 香草
Chinese 土香草
Chinese 凉芥
Chinese 七星剑
Chinese 乾汗草
Chinese 土香薷
Chinese 小香薷
Chinese 野香薷
Chinese 细叶七星剑
Chinese 石香薷
Chinese 土荆芥
Chinese 满山香
Chinese 土黄连
Chinese 香茹草
Chinese 香薷

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000246343
UNII 7H68PNG813
Tropicos 17603551
KEW urn:lsid:ipni.org:names:452191-1
The Plant List kew-130177
Open Tree Of Life 579927
NCBI Taxonomy 516065
IPNI 452191-1
iNaturalist 736751
GBIF 7309491
EOL 2893988
USDA GRIN 423671
CMAUP NPO18046

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
Antiviral and anti-inflammatory activities of chemical constituents from twigs of Mosla chinensis Maxim Feng SY, Jiang N, Yang JY, Yang LY, Du JC, Chen XQ, Liu D, Li RT, Zhong JD Nat Prod Bioprospect 01-May-2024
PMCID:PMC11063020
doi:10.1007/s13659-024-00448-w
PMID:38691189
Moslae Herba: Botany, Traditional Uses, Phytochemistry, and Pharmacology Duan ZY, Sun YP, Wang ZB, Kuang HX Molecules 10-Apr-2024
PMCID:PMC11051901
doi:10.3390/molecules29081716
PMID:38675535
Exploration of the in vitro Antiviral Effects and the Active Components of Changyanning Tablets Against Enterovirus 71 Ge Q, Zhang Z, Cao Z, Wu D, Xu C, Yao J, Gao J, Feng Y Drug Des Devel Ther 02-Mar-2024
PMCID:PMC10916518
doi:10.2147/DDDT.S444625
PMID:38450095
New insights into the influence of encapsulation materials on the feasibility of ultrasonic-assisted encapsulation of Mosla chinensis essential oil Wu H, Jiang X, Dong Z, Fan Q, Huang J, Liu H, Chen L, Li Z, Ming L Ultrason Sonochem 30-Jan-2024
PMCID:PMC10862064
doi:10.1016/j.ultsonch.2024.106787
PMID:38310739
TCM and related active compounds in the treatment of gout: the regulation of signaling pathway and urate transporter Sun X, Yang L, Sun H, Sun Y, Wei S, Han Y, Wang W, Kong L, Wang X Front Pharmacol 29-Nov-2023
PMCID:PMC10716793
doi:10.3389/fphar.2023.1275974
PMID:38094893
HPLC–DAD Analysis, SFE-CO2 Extraction, and Antibacterial Activity on Bioactive Compounds from Mosla chinensis Maxim Gao R, Han B, Zeng Y, Shen L, Liu X, Wang Q, Liao M, Li J Molecules 23-Nov-2023
PMCID:PMC10707893
doi:10.3390/molecules28237724
PMID:38067455
Ethnobotanical, Phytochemical, and Pharmacological Properties of the Subfamily Nepetoideae (Lamiaceae) in Inflammatory Diseases Ortiz-Mendoza N, Martínez-Gordillo MJ, Martínez-Ambriz E, Basurto-Peña FA, González-Trujano ME, Aguirre-Hernández E Plants (Basel) 02-Nov-2023
PMCID:PMC10648697
doi:10.3390/plants12213752
PMID:37960108
Edible Coatings and Future Trends in Active Food Packaging–Fruits’ and Traditional Sausages’ Shelf Life Increasing Nunes C, Silva M, Farinha D, Sales H, Pontes R, Nunes J Foods 02-Sep-2023
PMCID:PMC10486622
doi:10.3390/foods12173308
PMID:37685240
Research progress on the effect of traditional Chinese medicine on the activation of PRRs-mediated NF-κB signaling pathway to inhibit influenza pneumonia Zhang L, Ye X, Liu Y, Zhang Z, Xia X, Dong S Front Pharmacol 07-Apr-2023
PMCID:PMC10119400
doi:10.3389/fphar.2023.1132388
PMID:37089926
Specialized metabolites from plants as a source of new multi-target antiviral drugs: a systematic review Ponticelli M, Bellone ML, Parisi V, Iannuzzi A, Braca A, de Tommasi N, Russo D, Sileo A, Quaranta P, Freer G, Pistello M, Milella L Phytochem Rev 12-Mar-2023
PMCID:PMC10008214
doi:10.1007/s11101-023-09855-2
PMID:37359711
Inhibitory Effects and Related Molecular Mechanisms of Huanglian-Ganjiang Combination Against H1N1 Influenza Virus Sun Y, Yu CL, Yan YL, Zhang FL, Chen J, Hu ZY, He J, Meng XY, Wu QF Rev Bras Farmacogn 08-Mar-2023
PMCID:PMC9994783
doi:10.1007/s43450-023-00372-z
PMID:37151218
Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK Int J Mol Sci 01-Jan-2023
PMCID:PMC9821772
doi:10.3390/ijms24010739
PMID:36614181
Chamomile: A Review of Its Traditional Uses, Chemical Constituents, Pharmacological Activities and Quality Control Studies Dai YL, Li Y, Wang Q, Niu FJ, Li KW, Wang YY, Wang J, Zhou CZ, Gao LN Molecules 23-Dec-2022
PMCID:PMC9822300
doi:10.3390/molecules28010133
PMID:36615326
‘Food and medicine continuum’ in the East and West: Old tradition and current regulation Yao R, He C, Xiao P Chin Herb Med 17-Dec-2022
PMCID:PMC9975626
doi:10.1016/j.chmed.2022.12.002
PMID:36875443
Exploring the active ingredients and pharmacological mechanisms of the oral intake formula Huoxiang Suling Shuanghua Decoction on influenza virus type A based on network pharmacology and experimental exploration Tang R, Wang L, Zhang J, Li X, Tan L, He W, Han H, Liu Y, Wang K, Wang M Front Microbiol 01-Nov-2022
PMCID:PMC9663660
doi:10.3389/fmicb.2022.1040056
PMID:36386710

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
> Alkaloids and derivatives / Morphinans
(5alpha,6beta)-7,8-Didehydro-4,5-epoxy-17-methylmorphinan-3,6-diol 5324287 Click to see CN1CCC23C4C1CC5=C2C(=C(C=C5)O)OC3C(C=C4)O 285.34 unknown https://doi.org/10.1002/CJOC.201180379
> Benzenoids / Benzene and substituted derivatives
3-Butenylbenzene 13033 Click to see 132.20 unknown via CMAUP database
Benzaldehyde, oxime, (Z)- 5324470 Click to see C1=CC=C(C=C1)C=NO 121.14 unknown via CMAUP database
Benzylacetone 17355 Click to see CC(=O)CCC1=CC=CC=C1 148.20 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown https://doi.org/10.1248/CPB.17.124
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see 106.12 unknown https://doi.org/10.1002/CJOC.201180379
> Benzenoids / Benzene and substituted derivatives / Cumenes
m-Cymene 10812 Click to see CC1=CC(=CC=C1)C(C)C 134.22 unknown https://doi.org/10.1002/CJOC.201180379
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
4-tert-Pentylphenol 6643 Click to see 164.24 unknown via CMAUP database
> Benzenoids / Fluorenes
Fluorene 6853 Click to see 166.22 unknown via CMAUP database
> Benzenoids / Indenes and isoindenes
Indene 7219 Click to see 116.16 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
2,4-Dimethylanisole 81221 Click to see CC1=CC(=C(C=C1)OC)C 136.19 unknown via CMAUP database
Benzene, 2-methoxy-1,3,5-trimethyl- 77648 Click to see 150.22 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
3,4-Diethylphenol 522880 Click to see 150.22 unknown https://doi.org/10.1002/CJOC.201180379
> Benzenoids / Phenols / Methoxyphenols
6-Allylguaiacol 347577 Click to see 164.20 unknown https://doi.org/10.1002/CJOC.201180379
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1002/CJOC.201180379
> Hydrocarbons / Polycyclic hydrocarbons
beta-Patchoulene 101731 Click to see 204.35 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons
6-Methyltritriacontane 5319806 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC(C)CCCCC 478.90 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dodecane 8182 Click to see 170.33 unknown https://doi.org/10.1002/CJOC.201180379
Hexadecane 11006 Click to see CCCCCCCCCCCCCCCC 226.44 unknown https://doi.org/10.1002/CJOC.201180379
Pentadecane 12391 Click to see 212.41 unknown https://doi.org/10.1002/CJOC.201180379
Tetradecane 12389 Click to see 198.39 unknown https://doi.org/10.1002/CJOC.201180379
Tridecane 12388 Click to see 184.36 unknown https://doi.org/10.1002/CJOC.201180379
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown https://doi.org/10.1002/CJOC.201180379
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
2,3-Dimethylhexane 11447 Click to see 114.23 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(6S)-2-ethenylbicyclo[4.2.0]oct-1-ene 163077299 Click to see C=CC1=C2CCC2CCC1 134.22 unknown https://doi.org/10.1002/CJOC.201180379
2,3,3-Trimethyl-1,4-pentadiene 136569 Click to see 110.20 unknown via CMAUP database
Artemisiatriene 5320377 Click to see CC(=C)C=CC(C)(C)C=C 136.23 unknown via CMAUP database
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.4268/CJCMM20111319
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkadienes
1,4-Pentadiene 11587 Click to see C=CCC=C 68.12 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkatetraenes
2,6-Dimethyl-1,3,5,7-Octatetraene 562418 Click to see 134.22 unknown https://doi.org/10.1002/CJOC.201180379
Cosmene 5368451 Click to see CC(=C)C=CC=C(C)C=C 134.22 unknown https://doi.org/10.1002/CJOC.201180379
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Butyl butyrate 7983 Click to see 144.21 unknown https://doi.org/10.1002/CJOC.201180379
Ethyl heptadecanoate 26397 Click to see 298.50 unknown via CMAUP database
Isobutyl butyrate 10885 Click to see 144.21 unknown https://doi.org/10.1002/CJOC.201180379
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Decanoate 8050 Click to see 186.29 unknown via CMAUP database
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Glycidol esters
(Oxiran-2-yl)methyl decanoate 14833269 Click to see 228.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
2-Methylbutanoic Acid 8314 Click to see 102.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Hydroxy fatty acids
(2E)-4-hydroxy-2-methylbut-2-enoic acid 13855819 Click to see 116.11 unknown via CMAUP database
2-Pentenoic acid, 4-hydroxy-4-methyl-, (E)- 12734618 Click to see 130.14 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Hexanoic Acid 8892 Click to see 116.16 unknown via CMAUP database
Lauric Acid 3893 Click to see 200.32 unknown via CMAUP database
Octanoic Acid 379 Click to see CCCCCCCC(=O)O 144.21 unknown via CMAUP database
Undecanoic Acid 8180 Click to see CCCCCCCCCCC(=O)O 186.29 unknown via CMAUP database
> 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 via CMAUP database
Citronellyl formate 7778 Click to see 184.27 unknown via CMAUP database
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown via CMAUP database
Neryl acetate 1549025 Click to see 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(+)-3-Octanol 6999002 Click to see 130.23 unknown via CMAUP database
(2E,5E)-1,7-dihydroxy-3,7-dimethylocta-2,5-dien-4-one 13855812 Click to see 184.23 unknown via CMAUP database
(2E,5E)-7-hydroperoxy-1-hydroxy-3,7-dimethylocta-2,5-dien-4-one 13855814 Click to see 200.23 unknown via CMAUP database
(R)-oct-1-en-3-ol 6992244 Click to see 128.21 unknown https://doi.org/10.1002/CJOC.201180379
(S)-1-Octen-3-ol 2724898 Click to see CCCCCC(C=C)O 128.21 unknown via CMAUP database
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1002/CJOC.201180379
1-Undecanol 8184 Click to see 172.31 unknown via CMAUP database
3-Octanol 11527 Click to see 130.23 unknown via CMAUP database
Npc194396 5363138 Click to see 168.28 unknown via CMAUP database
Octan-3R-ol 445789 Click to see 130.23 unknown via CMAUP database
trans-3-Hexen-1-ol 5284503 Click to see 100.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Stearyl Alcohol 8221 Click to see 270.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
Hexadecanal 984 Click to see CCCCCCCCCCCCCCCC=O 240.42 unknown via CMAUP database
Tetradecanal 31291 Click to see 212.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives / Jasmonic acids
(-)-Methyl jasmonate 5281929 Click to see 224.30 unknown via CMAUP database
a Methyl jasmonate 5319693 Click to see 224.30 unknown via CMAUP database
Cyclopentaneacetic acid, 3-oxo-2-(2-pentenyl)-, methyl ester 62388 Click to see CCC=CCC1C(CCC1=O)CC(=O)OC 224.30 unknown via CMAUP database
Cyclopentaneacetic acid, 3-oxo-trans-2-(cis-2-pentenyl), methyl ester 6432008 Click to see CCC=CCC1C(CCC1=O)CC(=O)OC 224.30 unknown via CMAUP database
Methyl 2-(3-Oxo-2-((E)-Pent-2-Enyl)Cyclopentyl)Acetate 5367719 Click to see 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Phytane 12523 Click to see CCC(C)CCCC(C)CCCC(C)CCCC(C)C 282.50 unknown via CMAUP database
Pristane 15979 Click to see 268.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
(S)-(-)-Citronellal 443157 Click to see 154.25 unknown via CMAUP database
3,7-Dimethyl-2,6-octadienol 4458 Click to see 154.25 unknown https://doi.org/10.1002/CJOC.201180379
5,9-Dimethyldec-8-enoate 21612892 Click to see CC(CCCC(=O)[O-])CCC=C(C)C 197.29 unknown via CMAUP database
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1002/CJOC.201180379
https://doi.org/10.1002/CJOC.201180379
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1002/CJOC.201180379
Citral 638011 Click to see 152.23 unknown via CMAUP database
Citronellal 7794 Click to see 154.25 unknown via CMAUP database
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1002/CJOC.201180379
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1002/CJOC.201180379
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Linalool, (+)- 67179 Click to see 154.25 unknown https://doi.org/10.1002/CJOC.201180379
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.4268/CJCMM20111319
https://doi.org/10.1002/CJOC.201180379
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
> 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/10.1002/CJOC.201180379
https://doi.org/10.4268/CJCMM20111319
Carvacryl acetate 80792 Click to see 192.25 unknown via CMAUP database
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.4268/CJCMM20111319
https://doi.org/10.1002/CJOC.201180379
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1002/CJOC.201180379
https://doi.org/10.4268/CJCMM20111319
Thymol acetate 68252 Click to see CC1=CC(=C(C=C1)C(C)C)OC(=O)C 192.25 unknown https://doi.org/10.1002/CJOC.201180379
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-(1S,4S)-Borneol 6850744 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
(-)-3-Carene 442461 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
(-)-alpha-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(-)-beta-Pinene 440967 Click to see 136.23 unknown https://doi.org/10.1002/CJOC.201180379
(-)-Camphene 440966 Click to see 136.23 unknown https://doi.org/10.1002/CJOC.201180379
(-)-Sabinene 11051711 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1002/CJOC.201180379
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.4268/CJCMM20111319
https://doi.org/10.1002/CJOC.201180379
(+)-3-Carene 443156 Click to see 136.23 unknown https://doi.org/10.1002/CJOC.201180379
(+)-Bornyl acetate 6950274 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
(+)-Camphene 92221 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(1R,2S,4R)-(+)-Bornyl acetate 443131 Click to see 196.29 unknown via CMAUP database
(1R,2S,4S)-1,7,7-trimethylbicyclo(2.2.1)heptan-2-ol 10492 Click to see 154.25 unknown via CMAUP database
(1R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol 12242824 Click to see 154.25 unknown via CMAUP database
(1R)-Camphor 230921 Click to see 152.23 unknown via CMAUP database
(1S,2R,4S)-(-)-Bornyl acetate 442460 Click to see 196.29 unknown via CMAUP database
(1S,2S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol 12242815 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
(1S,4S,5S)-4-methyl-1-propan-2-ylbicyclo[3.1.0]hex-2-ene 12444328 Click to see 136.23 unknown https://doi.org/10.1002/CJOC.201180379
(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene 12223113 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(2Z)-5-[(1S,5S,6R)-2,6-dimethylbicyclo[3.1.1]hept-2-en-6-yl]-2-methylpent-2-en-1-ol 73555482 Click to see 220.35 unknown https://doi.org/10.1002/CJOC.201180379
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1002/CJOC.201180379
3-Thujanone 11027 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown via CMAUP database
3-Thujanone, (-)- 12304613 Click to see 152.23 unknown via CMAUP database
4-Thujanol, cis-(+-)- 20055523 Click to see 154.25 unknown https://doi.org/10.1002/CJOC.201180379
5-[(1S,5S,6R)-2,6-dimethyl-6-bicyclo[3.1.1]hept-2-enyl]-2-methylpent-2-en-1-ol 90903449 Click to see 220.35 unknown https://doi.org/10.1002/CJOC.201180379
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester 6448 Click to see 196.29 unknown via CMAUP database
alpha-Bergamotene 86608 Click to see 204.35 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown https://doi.org/10.1002/CJOC.201180379
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1002/CJOC.201180379
alpha-THUJENE, (+/-)- 12444324 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1002/CJOC.201180379
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1002/CJOC.201180379
beta-Thujene 520384 Click to see CC1C=CC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1002/CJOC.201180379
Bicyclo(3.1.1)hept-3-en-2-ol, 4,6,6-trimethyl-, (1R,2S,5R)-rel- 89664 Click to see 152.23 unknown https://doi.org/10.1002/CJOC.201180379
Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, exo- 439569 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1002/CJOC.201180379
Borneol, (-)- 1201518 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1002/CJOC.201180379
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown via CMAUP database
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1002/CJOC.201180379
Camphor 2537 Click to see 152.23 unknown via CMAUP database
Camphor, (-)- 444294 Click to see 152.23 unknown via CMAUP database
Camphor, (1S)- 10050 Click to see 152.23 unknown via CMAUP database
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
D-Borneol 6552009 Click to see 154.25 unknown via CMAUP database
D-Camphor 159055 Click to see 152.23 unknown via CMAUP database
d-Isothujone 249286 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown via CMAUP database
Isobornyl formate 23623868 Click to see 182.26 unknown https://doi.org/10.1002/CJOC.201180379
Npc126240 44630108 Click to see 196.29 unknown via CMAUP database
Npc189036 10049 Click to see 154.25 unknown via CMAUP database
Npc308218 439568 Click to see 154.25 unknown via CMAUP database
Npc54264 9543187 Click to see 152.23 unknown via CMAUP database
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1002/CJOC.201180379
Sumatra camphor 657014 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
trans-alpha-Bergaptene 6428986 Click to see CC1=CCC2CC1C2(C)CCC=C(C)C 204.35 unknown via CMAUP database
trans-Thujone 6432452 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown via CMAUP database
Verbenol 61126 Click to see 152.23 unknown https://doi.org/10.1002/CJOC.201180379
> 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 via CMAUP database
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown via CMAUP database
(+-)-Piperitone 6987 Click to see 152.23 unknown via CMAUP database
(+) Menthol 12285346 Click to see CC1CCC(C(C1)O)C(C)C 156.26 unknown via CMAUP database
(+)-alpha-Phellandrene 443160 Click to see 136.23 unknown https://doi.org/10.1002/CJOC.201180379
(+)-cis-Isopulegone 443529 Click to see CC1CCC(C(=O)C1)C(=C)C 152.23 unknown https://doi.org/10.1002/CJOC.201180379
(+)-Limonene 440917 Click to see 136.23 unknown https://doi.org/10.1002/CJOC.201180379
(+)-Menthol 165675 Click to see CC1CCC(C(C1)O)C(C)C 156.26 unknown via CMAUP database
(+)-Neomenthol 439263 Click to see 156.26 unknown via CMAUP database
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1002/CJOC.201180379
(+)-trans-Carveol 443178 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown via CMAUP database
(L)-alpha-terpineol 443162 Click to see 154.25 unknown via CMAUP database
2-Methyl-5-prop-1-en-2-ylcyclohexa-2,4-dien-1-ol 527142 Click to see 150.22 unknown via CMAUP database
4-Methyl-beta-methylenecyclohex-3-ene-1-ethanol 527143 Click to see CC1=CCC(CC1)C(=C)CO 152.23 unknown via CMAUP database
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1002/CJOC.201180379
https://doi.org/10.4268/CJCMM20111319
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1002/CJOC.201180379
alpha-PHELLANDRENE, (-)- 442482 Click to see 136.23 unknown via CMAUP database
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1002/CJOC.201180379
https://doi.org/10.4268/CJCMM20111319
Alpha-Terpineol 17100 Click to see 154.25 unknown via CMAUP database
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown via CMAUP database
beta-Terpinene 66841 Click to see CC(C)C1=CCC(=C)CC1 136.23 unknown via CMAUP database
Carvone, (-)- 439570 Click to see 150.22 unknown via CMAUP database
Carvone, (+-)- 7439 Click to see 150.22 unknown via CMAUP database
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown via CMAUP database
Isopulegone 34645 Click to see CC1CCC(C(=O)C1)C(=C)C 152.23 unknown https://doi.org/10.1002/CJOC.201180379
l-Menthol 16666 Click to see CC1CCC(C(C1)O)C(C)C 156.26 unknown via CMAUP database
l-Menthyl propionate 221455 Click to see CCC(=O)OC1CC(CCC1C(C)C)C 212.33 unknown via CMAUP database
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1002/CJOC.201180379
Menthol 1254 Click to see 156.26 unknown via CMAUP database
Perilla alcohol 369312 Click to see CC(=C)C1CCC(=CC1)CO 152.23 unknown via CMAUP database
Perillyl acetate 61780 Click to see CC(=C)C1CCC(=CC1)COC(=O)C 194.27 unknown via CMAUP database
Perillyl alcohol 10819 Click to see CC(=C)C1CCC(=CC1)CO 152.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1002/CJOC.201180379
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Amorphene 12306052 Click to see 204.35 unknown via CMAUP database
(-)-Isocaryophyllene 5281522 Click to see 204.35 unknown via CMAUP database
(+)-beta-Caryophyllene 20831623 Click to see 204.35 unknown via CMAUP database
(+)-Delta-cadinol 11990360 Click to see 222.37 unknown via CMAUP database
(+)-Longifolene 1796220 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown https://doi.org/10.1002/CJOC.201180379
(+)-Nerolidol 5356544 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
(1S,2S,7S,8S)-2,6,6,9-tetramethyltricyclo[5.4.0.02,8]undec-9-ene 91753627 Click to see 204.35 unknown via CMAUP database
(1Z,5E)-1,4,4-trimethyl-8-methylidenecycloundeca-1,5-diene 5879124 Click to see 204.35 unknown via CMAUP database
(2-cis,6-trans)-Farnesol 1549108 Click to see 222.37 unknown via CMAUP database
(2S)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol 6097621 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
(3R,6E)-Nerolidol 11241545 Click to see 222.37 unknown via CMAUP database
(3S,6E)-Nerolidol 5281525 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
(4Z)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene 5322111 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
(Z)-caryophyllene 6429301 Click to see 204.35 unknown via CMAUP database
1-Methyl-4-(6-methylhepta-1,5-dien-2-yl)cyclohex-1-ene 403919 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown via CMAUP database
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl- 8888 Click to see 222.37 unknown via CMAUP database
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-, (3R,6Z)- 12227246 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
2,6,10-Trimethyldodeca-2,6,9,11-tetraenal 21064 Click to see CC(=CCC=C(C)C=C)CCC=C(C)C=O 218.33 unknown via CMAUP database
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown via CMAUP database
4,11,11-Trimethyl-8-methylene-5-oxatricyclo(8.2.0.0(4,6))dodecane, (1R,4R,6R,10S)- 6604672 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
4,11,11-Trimethyl-8-methylenebicyclo(7.2.0)undec-4-ene 26318 Click to see 204.35 unknown https://doi.org/10.1002/CJOC.201180379
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown via CMAUP database
4,8,8-Trimethyl-9-methylidenedecahydro-1,4-methanoazulene 289151 Click to see 204.35 unknown https://doi.org/10.1002/CJOC.201180379
7,11-Dimethyl-3-methylene-1,6,10-dodecatriene 10407 Click to see 204.35 unknown https://doi.org/10.1002/CJOC.201180379
alpha-Bisabolol 10586 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
Beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown via CMAUP database
beta-Bourbonene 62566 Click to see 204.35 unknown via CMAUP database
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1002/CJOC.201180379
beta-Farnesene, (6Z)- 5317319 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown via CMAUP database
Bisabolol 1549992 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
Cadin-4-en-10-ol 519662 Click to see 222.37 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1002/CJOC.201180379
Caryophyllene oxide 1742210 Click to see 220.35 unknown via CMAUP database
Caryophyllene,alpha + beta mixt. 5354499 Click to see 204.35 unknown via CMAUP database
cis-Nerolidol 5320128 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
Cubebene 518814 Click to see CC1CCC(C2C13C2C(=C)CC3)C(C)C 204.35 unknown via CMAUP database
delta-Cadinene 441005 Click to see 204.35 unknown via CMAUP database
Farnesene 5281516 Click to see 204.35 unknown via CMAUP database
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1002/CJOC.201180379
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.1002/CJOC.201180379
Humulene 5281520 Click to see 204.35 unknown via CMAUP database
I2-Ionone 638014 Click to see 192.30 unknown via CMAUP database
Levomenol 442343 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
Neophytadiene 10446 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=C)C=C 278.50 unknown via CMAUP database
Nerolidol 5284507 Click to see 222.37 unknown via CMAUP database
Npc14576 6432083 Click to see 204.35 unknown via CMAUP database
Npc225463 520957 Click to see 204.35 unknown via CMAUP database
Npc294136 14757966 Click to see 204.35 unknown via CMAUP database
Npc57877 6431302 Click to see 222.37 unknown via CMAUP database
Sesquiphellandrene 519764 Click to see 204.35 unknown via CMAUP database
tau-Muurolol 6432221 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
1H-Cyclopropa(a)naphthalene, 1a,2,3,5,6,7,7a,7b-octahydro-1,1,7,7a-tetramethyl-, (1aR-(1aalpha,7alpha,7aalpha,7balpha))- 15560278 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C 204.35 unknown via CMAUP database
Calarene 28481 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C 204.35 unknown via CMAUP database
Npc30025 6432176 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see 222.37 unknown via CMAUP database
(1aS,4S,4aS,7S,7aR,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 12304982 Click to see 222.37 unknown via CMAUP database
1H-Cycloprop[e]azulen-7-ol, decahydro-1,1,7-trimethyl-4-methylene-, [1ar-(1aalpha,4aalpha,7beta,7abeta,7balpha)]- 6432640 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown via CMAUP database
beta-Spathulenol 522266 Click to see 220.35 unknown via CMAUP database
Globulol 12304985 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
Npc123229 6432543 Click to see 222.37 unknown via CMAUP database
Npc143639 6432706 Click to see 220.35 unknown via CMAUP database
Npc239037 101716 Click to see 222.37 unknown via CMAUP database
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown via CMAUP database
Spathulenol, (-)- 13854255 Click to see 220.35 unknown via CMAUP database
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(-)-Cedrene 6431015 Click to see 204.35 unknown via CMAUP database
Cedran-8-ol 522667 Click to see 222.37 unknown https://doi.org/10.1002/CJOC.201180379
Cedrenol 119831 Click to see CC1CCC2C13CC(C2(C)C)C(=C)C(C3)O 220.35 unknown via CMAUP database
Cedrol 65575 Click to see 222.37 unknown https://doi.org/10.1002/CJOC.201180379
CID 21119906 21119906 Click to see CC1CCC2C13CC(C2(C)C)C(=C)C(C3)O 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
alpha-Elemol 6429032 Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O 222.37 unknown via CMAUP database
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)- 9859094 Click to see 204.35 unknown via CMAUP database
Elemol 92138 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-(4a-Methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)propan-2-ol 521215 Click to see 222.37 unknown via CMAUP database
7-Isopropenyl-4a-methyl-1-methylenedecahydronaphthalene 519361 Click to see 204.35 unknown via CMAUP database
Beta-Eudesmol 91457 Click to see 222.37 unknown via CMAUP database
Beta-Selinene 442393 Click to see 204.35 unknown via CMAUP database
gamma-EUDESMOL 6432005 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown via CMAUP database
Npc53720 6432456 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(+)-Germacrene D 24771782 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
(1E)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene 74764030 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
(1Z)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene 92003564 Click to see 204.35 unknown via CMAUP database
(6E,8S)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene 49796490 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
1-Methyl-5-methylene-8-(1-methylethyl)-1,6-cyclodecadiene 6436582 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)- 5373727 Click to see 204.35 unknown via CMAUP database
1,6-Germacradien-5-ol 91748908 Click to see 222.37 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 / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
(S)-beta-himachalene 24798710 Click to see CC1=CC2C(=C(CCCC2(C)C)C)CC1 204.35 unknown https://doi.org/10.1002/CJOC.201180379
3,5,5,9-Tetramethyl-2,4a,5,6,7,8-hexahydro-1H-benzo(7)annulene 15095 Click to see 204.35 unknown https://doi.org/10.1002/CJOC.201180379
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(10R)-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 45358157 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
(1S,2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-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 45483617 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
[(3S)-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-yl] acetate 6432446 Click to see 456.70 unknown via CMAUP database
Bayogenin 12305221 Click to see 488.70 unknown https://doi.org/10.1055/S-2007-969052
Beta-Sitosteryl Acetate 5354503 Click to see 456.70 unknown via CMAUP database
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1055/S-2007-969052
Npc155187 521199 Click to see 456.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1055/S-2007-969052
Oleanolic acid acetate 6708573 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1055/S-2007-969052
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
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 via CMAUP database
gamma-Sitosterol 457801 Click to see 414.70 unknown via CMAUP database
Npc29 6432744 Click to see 414.70 unknown via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Ammoniohexanoate 517543 Click to see 131.17 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Alpha,beta-unsaturated carboxylic esters / Enoate esters
Butyl methacrylate 7354 Click to see CCCCOC(=O)C(=C)C 142.20 unknown https://doi.org/10.1002/CJOC.201180379
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
2-Pentyl propionate 521483 Click to see 144.21 unknown via CMAUP database
Butyl isobutyrate 7353 Click to see 144.21 unknown https://doi.org/10.1002/CJOC.201180379
Butyl propionate 11529 Click to see CCCCOC(=O)CC 130.18 unknown via CMAUP database
Heptyl acetate 8159 Click to see CCCCCCCOC(=O)C 158.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Enol esters
1-Octenyl acetate 5352540 Click to see 170.25 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Methyl esters
(Z)-Methyl jasmonate 6430765 Click to see 210.27 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Oct-1-en-1-ol;acetate 53438751 Click to see 187.26 unknown via CMAUP database
> Organic acids and derivatives / Organic carbonic acids and derivatives / Carbonic acid diesters
4,5-Dimethyl-1,3-dioxolan-2-one 536113 Click to see CC1C(OC(=O)O1)C 116.11 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Organic cyanides / Nitriles
2-Pentenenitrile 5364360 Click to see CCC=CC#N 81.12 unknown via CMAUP database
2-Pentenenitrile, (Z)- 6433944 Click to see 81.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Myrcenol 10975 Click to see CC(C)(CCCC(=C)C=C)O 154.25 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
3-Methylbutanal 11552 Click to see 86.13 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2,4-Hexadienal 637564 Click to see 96.13 unknown via CMAUP database
cis-3-Hexenal 643941 Click to see CCC=CCC=O 98.14 unknown via CMAUP database
Hexanal 6184 Click to see 100.16 unknown via CMAUP database
Octanal 454 Click to see 128.21 unknown via CMAUP database
trans-2-Hexenal 5281168 Click to see 98.14 unknown via CMAUP database
Undecanal 8186 Click to see CCCCCCCCCCC=O 170.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones
Dehydroelsholtzia ketone 564412 Click to see 164.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
2-Acetyl-5-Methylfuran 14514 Click to see CC1=CC=C(O1)C(=O)C 124.14 unknown via CMAUP database
Elsholtziaketone 521240 Click to see 166.22 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
Thymoquinone 10281 Click to see CC1=CC(=O)C(=CC1=O)C(C)C 164.20 unknown https://doi.org/10.1002/CJOC.201180379
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Jasmone 1549018 Click to see 164.24 unknown via CMAUP database
trans-Jasmone 1549019 Click to see 164.24 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1aR,4aS,8aS)-4a,8,8-trimethyl-1a,5,6,7-tetrahydro-1H-cyclopropa[j]naphthalen-2-one 15560170 Click to see CC1(CCCC2(C13CC3C(=O)C=C2)C)C 204.31 unknown via CMAUP database
Mayurone 538435 Click to see CC1(CCCC2(C13CC3C(=O)C=C2)C)C 204.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(+)-Mayurone 13154078 Click to see CC1(CCCC2(C13CC3C(=O)CC2)C)C 206.32 unknown via CMAUP database
(S)-3-Methyl-2-pentanone 6994393 Click to see CCC(C)C(=O)C 100.16 unknown via CMAUP database
2,6-Dimethyloct-7-en-4-one 102706 Click to see 154.25 unknown via CMAUP database
3-Methylpentan-2-One 11262 Click to see 100.16 unknown via CMAUP database
3-Octanone 246728 Click to see CCCCCC(=O)CC 128.21 unknown via CMAUP database
6-Methyl-5-hepten-2-one 9862 Click to see 126.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetophenone 7410 Click to see CC(=O)C1=CC=CC=C1 120.15 unknown via CMAUP database
Paeonol 11092 Click to see CC(=O)C1=C(C=C(C=C1)OC)O 166.17 unknown https://doi.org/10.4268/CJCMM20111319
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals
1,1-Dibutoxy-isobutane 545177 Click to see 202.33 unknown https://doi.org/10.1002/CJOC.201180379
1,1-Dibutoxybutane 22210 Click to see 202.33 unknown https://doi.org/10.1002/CJOC.201180379
Acetaldehyde, dibutyl acetal 79117 Click to see 174.28 unknown https://doi.org/10.1002/CJOC.201180379
> Organic oxygen compounds / Organooxygen compounds / Ethers / Dialkyl ethers
Butylpentyl ether 29161 Click to see 144.25 unknown https://doi.org/10.1002/CJOC.201180379
> Organoheterocyclic compounds / Benzimidazoles
2-Ethylbenzimidazole 15807 Click to see 146.19 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Safrole 5144 Click to see 162.18 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrazoles / Indazoles
5,7-Dimethyl-1H-indazole 589751 Click to see 146.19 unknown via CMAUP database
> Organoheterocyclic compounds / Benzothiazoles
Benzothiazole 7222 Click to see C1=CC=C2C(=C1)N=CS2 135.19 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrazines
2,3-Diethyl-5-Methylpyrazine 28905 Click to see 150.22 unknown via CMAUP database
> Organoheterocyclic compounds / Epoxides
2,2-Dimethyl-3-(3-methylenepent-4-enyl)oxirane 122371 Click to see CC1(C(O1)CCC(=C)C=C)C 152.23 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
1,8-Cineole 2758 Click to see 154.25 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
Carvone-5,6-oxide, trans-(-)- 11829800 Click to see CC(=C)C1CC2C(O2)(C(=O)C1)C 166.22 unknown via CMAUP database
Carvone-5,6-oxide, trans-(+)- 442462 Click to see 166.22 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
Linalool oxide 22310 Click to see CC1(CCC(O1)C(C)(C)O)C=C 170.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Octadecyl ferulate 5320256 Click to see 446.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1248/CPB.17.124
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1248/CPB.17.124
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol 73160 Click to see 290.27 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown via CMAUP database
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> 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/10.1248/CPB.17.124
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1248/CPB.17.124
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1248/CPB.17.124
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown via CMAUP database
Luteolin 7-O-glucoside 5280637 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 via CMAUP database
Npc85473 5385553 Click to see 432.40 unknown via CMAUP database
Tilianin 5321954 Click to see 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol 5280666 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown via CMAUP database
Mosloflavone 471722 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O)OC 298.29 unknown via CMAUP database
Negletein 471719 Click to see 284.26 unknown https://doi.org/10.1248/CPB.17.124
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Hydroxy-7,8-dimethoxyflavone 188316 Click to see 298.29 unknown via CMAUP database
Xanthomicrol 73207 Click to see 344.30 unknown via CMAUP database
> Uncategorized
Pent-2-enenitrile 25833 Click to see 81.12 unknown via CMAUP database

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