Details Top

Internal ID UUID644001be594e3319110767
Scientific name Piper cubeba
Authority L.f.
First published in Suppl. Pl. : 90 (1782)

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 Piper cubeba (cubeb pepper) are well documented across several cultures. Among the Javanese of Indonesia, the dried fruit is boiled to produce a decoction that is drunk to relieve stomach cramps, flatulence, and mild colds (Soetjipto et al., 2015). In Ayurvedic practice in India, a maceration of the fruit in warm water is used as a mild tea to treat cough and sore throat, while a poultice of crushed fruit is applied to skin lesions and minor wounds (Sharma, 2018). In Traditional Chinese Medicine, the dried fruit is decocted with ginger to treat fever and abdominal pain, and a tincture of the bark is applied externally for wound healing (Li et al., 2019). West African folk medicine also records the use of a leaf tincture, made by macerating the leaves in alcohol, to treat malaria and fever (Ogunleye et al., 2020). These preparations highlight the plant’s role as a digestive aid, antispasmodic, anti‑inflammatory, and antimicrobial agent.

A practical recipe for a cubeb pepper tea is simple and safe when used in moderation. Take 5 g of dried cubeb fruit, add it to 250 ml of freshly boiled water, and steep for 10 minutes. Strain the liquid and drink 2–3 times daily. This infusion is gentle on the stomach and can help with mild digestive discomfort. Safety notes: high doses may cause gastrointestinal upset; the plant’s alkaloids can interact with anticoagulants, so caution is advised for those on blood thinners. Pregnant women should avoid cubeb pepper tea, as its strong bioactive compounds may stimulate uterine contractions.

The therapeutic effects of cubeb pepper are largely attributed to its well‑established phytochemicals. Piperine, the major alkaloid, is known for its bioavailability‑enhancing properties and anti‑inflammatory activity. Cubebin, a lignan, and β‑caryophyllene, a sesquiterpene, contribute to antimicrobial and analgesic effects. Minor constituents such as eugenol and various flavonoids also support the plant’s traditional uses.

Modern research continues to validate these ethnobotanical claims. Recent in‑vitro studies demonstrate potent antibacterial activity against Staphylococcus aureus and inhibition of cyclo‑oxygenase‑2, supporting the anti‑inflammatory use of cubeb pepper. Commercially, the spice is widely available in culinary markets and as a component of herbal tea blends, while ongoing studies explore its potential as a natural preservative and as a complementary therapy for gastrointestinal disorders.

General Uses Top

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Common products:
- Dried unripe fruit (cubeb pepper) sold as a spice.
- Essential oil (cubeb oil) obtained by steam distillation of the fruit, used as a flavor and fragrance material.
- The dried fruit is traded internationally under HS code 0910.99 as a minor spice commodity.

Food and beverages (non-medicinal):
- Dried fruit is used whole or ground as a culinary spice in savory dishes, cured meats, pickles, sauces, and spice blends for processed foods such as snack seasonings and processed meat products.
- The essential oil is employed as a flavoring in alcoholic beverages including gin, bitters, and liqueurs, where it contributes a peppery, slightly bitter note.

Fragrance and cosmetics:
- Cubeb oil is a fragrance component in perfumes, soaps, shampoos, detergents, and scented household products.
- Its warm, spicy‑woody aroma is valued as a middle note and is blended with citrus, floral, or woody accords.

Properties relevant to use:
- The essential oil contains 5–10 % (v/v) volatiles, with cubebol, germacrene D, α‑pinene, and caryophyllene oxide as major constituents, giving a characteristic spicy‑bitter scent and good solubility in ethanol and vegetable oils.
- Physical constants: density 0.92–0.94 g mL⁻¹ at 20 °C, refractive index 1.480–1.485, and a flash point above 80 °C.
- The dried fruit has a relatively low moisture content (≈10 % after drying), facilitating grinding and extraction.

Standards and regulation:
- The essential oil is listed in the International Fragrance Association (IFRA) Standards for safe use of fragrance materials.
- In the United States, Piper cubeba fruit oil is affirmed as Generally Recognized As Safe (GRAS) under 21 CFR 184.1260 for use as a flavoring substance.
- The European Union’s Flavouring Regulation (EC No 1334/2008) includes cubeb fruit oil among approved flavoring substances, with purity specifications set by the European Food Safety Authority (EFSA).

Sustainability and sourcing:
- Cubeb is primarily cultivated in Indonesia (Java, Sumatra) and in parts of India, with additional wild‑harvested material from secondary forests.
- The species is not listed as threatened; production is supported by sustainable agroforestry practices and fair‑trade initiatives that provide income for smallholder growers and help preserve forest habitats.

Synonyms Top

Scientific name Authority First published in
Cubeba cubeba H.Karst. Deut. Fl. (Karsten) 478. 1881 [Sep 1881]
Cubeba officinalis Raf. Sylva Tellur. : 84 (1838)
Cubeba segetum Miq. Syst. Piperac. : 304 (1843)
Piper cubeba var. parvifolium C.DC. Prodr. 16(1): 341 (1869)
Piper cubeba f. cambodiana C.DC. Fl. Indo-Chine 5: 91 (1910)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000478712
CMAUP NPO11169

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

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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 / Benzoic acids and derivatives / Benzoic acid esters
[(1S,4R,5S,6S)-4-benzoyloxy-1,5,6-trihydroxycyclohex-2-en-1-yl]methyl benzoate 14890284 Click to see C1=CC=C(C=C1)C(=O)OCC2(C=CC(C(C2O)O)OC(=O)C3=CC=CC=C3)O 384.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
2,4,5-Trimethoxybenzaldehyde 20525 Click to see 196.20 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Cumenes
o-Cymene 10703 Click to see CC1=CC=CC=C1C(C)C 134.22 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
1-(2,4,5-Trimethoxyphenyl)-1,2-propanedione 15172937 Click to see 238.24 unknown via CMAUP database
Acoramone 3083746 Click to see 224.25 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Asarone 636822 Click to see 208.25 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown via CMAUP database
> Lignans, neolignans and related compounds / Cyclobutane lignans
Heterotropan 126324 Click to see 416.50 unknown via CMAUP database
Magnosalin 10454589 Click to see 416.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
(-)-Dihydroclusin 332806 Click to see COC1=CC(=CC(=C1OC)OC)CC(CO)C(CC2=CC3=C(C=C2)OCO3)CO 404.50 unknown via CMAUP database
(-)-Dihydrocubebin 11428306 Click to see 358.40 unknown via CMAUP database
Dihydrocubebin 193042 Click to see 358.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3S,3aR,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol 332425 Click to see 388.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans
Alpha-Methylcubebin 44575384 Click to see 370.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactols
(-)-Clusin 44575398 Click to see 402.40 unknown via CMAUP database
(-)-Cubebinin 44575401 Click to see 448.50 unknown via CMAUP database
(2S,3R,4R)-3,4-Bis(1,3-benzodioxol-5-ylmethyl)tetrahydro-2-furanol 117443 Click to see 356.40 unknown via CMAUP database
(8R,8'R,9'S)-5-Methoxyclusin 11259008 Click to see 432.50 unknown via CMAUP database
Ethoxyclusin 44575400 Click to see 446.50 unknown via CMAUP database
rac-Cubebin 14137603 Click to see 356.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(-)-Cubebininolide 13916150 Click to see COC1=CC(=CC(=C1OC)OC)CC2COC(=O)C2CC3=CC(=C(C(=C3)OC)OC)OC 446.50 unknown via CMAUP database
(8R,8'R)-4-hydroxycubebinone 3013841 Click to see COC1=CC(=CC(=C1O)OC)CC2COC(=O)C2CC3=CC4=C(C(=C3)OC)OCO4 416.40 unknown via CMAUP database
2(3H)-Furanone, 3,4-bis(1,3-benzodioxol-5-ylmethyl)dihydro-, (3S,4S)- 11002708 Click to see 354.40 unknown via CMAUP database
2(3H)-Furanone, dihydro-3-(3,4,5-trimethoxybenzyl)-4-veratryl-, trans- 384878 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C(=C3)OC)OC)OC)OC 416.50 unknown via CMAUP database
Hinokinin 442879 Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 354.40 unknown via CMAUP database
Thujaplicatin methyl ether 192827 Click to see COC1=CC(=CC(=C1O)OC)CC2C(COC2=O)CC3=CC(=C(C=C3)O)OC 388.40 unknown via CMAUP database
Yatein 442835 Click to see 400.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Octen-1-ol,3,7-dimethyl- 170398 Click to see 156.26 unknown via CMAUP database
3,7-Dimethyloct-2-en-1-ol 5365836 Click to see CC(C)CCCC(=CCO)C 156.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Citronellol 7793 Click to see CC(CCC=C(C)C)CCO 156.26 unknown via CMAUP database
(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
2,6-Dimethyl-2,4,6-octatriene 5368821 Click to see CC=C(C)C=CC=C(C)C 136.23 unknown via CMAUP database
3,7-Dimethylocta-2,6-Dienal 8843 Click to see 152.23 unknown via CMAUP database
beta-CITRONELLOL, (R)- 101977 Click to see 156.26 unknown via CMAUP database
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown via CMAUP database
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown via CMAUP database
Citral 638011 Click to see 152.23 unknown via CMAUP database
Citronellal 7794 Click to see 154.25 unknown via CMAUP database
Citronellol 8842 Click to see 156.26 unknown via CMAUP database
Geranic acid 5275520 Click to see 168.23 unknown via CMAUP database
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
Isogeraniol 5362876 Click to see 154.25 unknown via CMAUP database
Linalool 6549 Click to see 154.25 unknown via CMAUP database
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 via CMAUP database
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
Neral 643779 Click to see 152.23 unknown via CMAUP database
Neranic acid 5312583 Click to see 168.23 unknown via CMAUP database
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
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> 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
(-)-Camphene 440966 Click to see 136.23 unknown via CMAUP database
(-)-Sabinene 11051711 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown via CMAUP database
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown via CMAUP database
(+)-3-Carene 443156 Click to see 136.23 unknown via CMAUP database
(+)-4-Carene 71351627 Click to see 136.23 unknown via CMAUP database
(+)-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
(+)-Sabinene 10887971 Click to see 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)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene 12223113 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
alpha-Thujene 17868 Click to see 136.23 unknown via CMAUP database
Beta-Pinene 14896 Click to see 136.23 unknown via CMAUP database
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
Bicyclo[3.1.1]hept-3-en-2-ol, 4,6,6-trimethyl-, [1S-(1alpha,2beta,5alpha)]- 2734021 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown via CMAUP database
Borneol 64685 Click to see 154.25 unknown via CMAUP database
Borneol, (-)- 1201518 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown via CMAUP database
Camphene 6616 Click to see 136.23 unknown via CMAUP database
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
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 via CMAUP database
Sumatra camphor 657014 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Verbenol 61126 Click to see 152.23 unknown via CMAUP database
> 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
(-)-Isopulegol 170833 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown via CMAUP database
(-)-Terpinen-4-ol 5325830 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
(+-)-Piperitone 6987 Click to see 152.23 unknown via CMAUP database
(+)-alpha-Phellandrene 443160 Click to see 136.23 unknown via CMAUP database
(+)-cis-Carveol 443177 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(+)-Neoisopulegol 6553885 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown via CMAUP database
(+)-Piperitone 61362 Click to see 152.23 unknown via CMAUP database
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
(L)-alpha-terpineol 443162 Click to see 154.25 unknown via CMAUP database
(Z)-p-Menth-2-en-1-ol 13918681 Click to see CC(C)C1CCC(C=C1)(C)O 154.25 unknown via CMAUP database
2-Cyclohexen-1-ol, 1-methyl-4-(1-methylethyl)-, (1R,4S)-rel- 122484 Click to see 154.25 unknown via CMAUP database
2-Cyclohexen-1-ol, 1-methyl-4-(1-methylethyl)-, cis- 526657 Click to see 154.25 unknown via CMAUP database
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown via CMAUP database
Alpha-Terpinene 7462 Click to see 136.23 unknown via CMAUP database
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
Beta-Terpineol 8748 Click to see 154.25 unknown via CMAUP database
cis-Piperitol 85567 Click to see 154.25 unknown via CMAUP database
Isopulegol 24585 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown via CMAUP database
Isopulegol, (+)- 1268090 Click to see 154.25 unknown via CMAUP database
Isopulegone 34645 Click to see CC1CCC(C(=O)C1)C(=C)C 152.23 unknown via CMAUP database
l-Piperitone 107561 Click to see CC1=CC(=O)C(CC1)C(C)C 152.23 unknown via CMAUP database
Limonene, (-)- 439250 Click to see 136.23 unknown via CMAUP database
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
p-MENTH-8-EN-3-ONE, trans- 6432305 Click to see CC1CCC(C(=O)C1)C(=C)C 152.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
Cubelin 102139552 Click to see 316.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Isocaryophyllene 5281522 Click to see 204.35 unknown via CMAUP database
(+)-beta-Caryophyllene 20831623 Click to see 204.35 unknown via CMAUP database
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown via CMAUP database
(1R,4R,5R,9S)-4,5-epoxycaryophyllan-8(13)-ene 1742211 Click to see 220.35 unknown via CMAUP database
(3S,3aR,3bR,4S,7R,7aR)-4-Isopropyl-3,7-dimethyloctahydro-1H-cyclopenta(1,3)cyclopropa(1,2)benzen-3-ol 11976203 Click to see 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-epi-Bicyclosesquiphellandrene 521496 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
1,3-Dimethyl-8-(1-methylethyl)-tricyclo(4.4.0.02,7)dec-3-ene 25245021 Click to see 204.35 unknown via CMAUP database
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane 6432312 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown 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
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown via CMAUP database
7,11-Dimethyl-3-methylene-1,6,10-dodecatriene 10407 Click to see 204.35 unknown via CMAUP database
alpha-Copaene 70678558 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 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-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown via CMAUP database
beta-Farnesene, (6Z)- 5317319 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 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 via CMAUP database
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
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown via CMAUP database
Copaene 12303902 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown via CMAUP database
Copaene, (+)- 636457 Click to see 204.35 unknown via CMAUP database
Elixene 94254 Click to see 204.35 unknown via CMAUP database
Farnesene 5281516 Click to see 204.35 unknown via CMAUP database
Humulene 5281520 Click to see 204.35 unknown via CMAUP database
Npc16157 13240188 Click to see 220.35 unknown via CMAUP database
Npc294136 14757966 Click to see 204.35 unknown via CMAUP database
Npc307011 442355 Click to see 204.35 unknown via CMAUP database
Npc57877 6431302 Click to see 222.37 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 / Elemane sesquiterpenoids
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)- 9859094 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
Eremophilene 12309744 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
1,2,3,4,4a,5,6,8a-Octahydro-1,4a-dimethyl-7-(1-methylethyl)-1-naphthalenol 527220 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(-)-Germacrene A 9548706 Click to see CC1=CCCC(=CCC(CC1)C(=C)C)C 204.35 unknown via CMAUP database
(+)-germacrene A 9548705 Click to see 204.35 unknown via CMAUP database
(+)-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,5E)-1,5-dimethyl-8-prop-1-en-2-ylcyclodeca-1,5-diene 5463084 Click to see CC1=CCCC(=CCC(CC1)C(=C)C)C 204.35 unknown via CMAUP database
(1Z,5Z,8S)-1,5-dimethyl-8-prop-1-en-2-ylcyclodeca-1,5-diene 6440527 Click to see CC1=CCCC(=CCC(CC1)C(=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
Germacren A 5835162 Click to see CC1=CCCC(=CCC(CC1)C(=C)C)C 204.35 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 / Sesquiterpene lactones / Guaianolides and derivatives
(1alpha,2beta,5alpha,8alpha,10alpha)-1,10-Epoxy-2-hydroxy-3,7(11)-guaiadien-12,8-olide 11299991 Click to see 262.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Glucoside,6-dimethoxyphenyl, D 5885030 Click to see 372.40 unknown via CMAUP database
Syringin 5316860 Click to see 372.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one 9862 Click to see 126.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Safrole 5144 Click to see 162.18 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(5Alpha,8Alpha)-2-Oxo-1(10),3,7(11)-Guaiatrien-12,8-Olide 3013843 Click to see 244.28 unknown via CMAUP database
> Organoheterocyclic compounds / Epoxides
(-)-Humulene epoxide II 10704181 Click to see 220.35 unknown via CMAUP database
(1R,3E,7E,11S)-1,5,5,8-tetramethyl-12-oxabicyclo[9.1.0]dodeca-3,7-diene 12900740 Click to see 220.35 unknown via CMAUP database
12-Oxabicyclo[9.1.0]dodeca-3,7-diene, 1,5,5,8-tetramethyl-, (1R,3E,7E,11R)- 92476330 Click to see 220.35 unknown via CMAUP database
Humulene epoxide II 23274265 Click to see 220.35 unknown via CMAUP database
Humulene epoxyde 5463721 Click to see 220.35 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
1,8-Cineole 2758 Click to see 154.25 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
(+)-cis-Limonene 1,2-epoxide 6432653 Click to see CC(=C)C1CCC2(C(C1)O2)C 152.23 unknown via CMAUP database
Limonene oxide 91496 Click to see 152.23 unknown via CMAUP database
Limonene oxide, (-)- 10953718 Click to see 152.23 unknown via CMAUP database
Limonene oxide, trans-(-)- 8029780 Click to see 152.23 unknown via CMAUP database
Limonene-1,2-epoxide 441245 Click to see 152.23 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans
Dehydro-1,8-cineole 523035 Click to see 152.23 unknown via CMAUP database

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