Litsea cubeba, also known as aromatic litsea or may chang, is a tree or shrub found in Southern China and Southeast Asian countries. It is part of the Lauraceae family and can grow up to 5-12 meters tall. The plant produces a fruit that is used to extract a lemony essential oil, which is its main component. This oil is used for fragrance and flavoring, and is also used in the production of vitamin A and violet-like fragrances. The plant's timber is used for furniture and crafts, and its parts are also used in traditional medicine. In Taiwan, it is used extensively as a spice in aboriginal cuisine.

Synonyms Top

Scientific name	Authority	First published in
Laurus cubeba	Lour.	Fl. Cochinch. : 252 (1790)
Malapoenna cubeba	(Lour.) Kuntze	Revis. Gen. Pl. 2: 572 (1891)
Tetranthera cubeba	Meisn.	Prodr. [A. P. de Candolle] 15(1): 199. 1864 [May 1864]
Tetranthera polyantha	Wall.	Numer. List [Wallich] n. 2538. 1830
Persea cubeba	(Lour.) Spreng.	Syst. Veg. 2: 269 (1825)
Benzoin cubeba	(Lour.) Hatus.	Rep. (Annual) Taihoku Bot. Gard. 3: 90 (1933)
Cubeba pipereta	Raf.	Sylva Tellur. 165. 1838
Daphnidium cubeba	(Lour.) Nees	Syst. Laur. : 615 (1836)
Tetranthera cubeba	(Lour.) Kostel.	Allg. Med.-Pharm. Fl. 2: 479 (1833)

Common names Top

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Filter by language:

Language	Common/alternative name
Indonesian	antarasa
Japanese	リツェア・クベバ
Japanese	アオモジ
Korean	산계초
Korean	두메까마귀쪽나무
Macedonian	Лицеа кубеба
tay	ma'aw
tay	maqaw
Vietnamese	màng tang
Chinese	豆豉姜
Chinese	豆豉香
Chinese	山蒼樹
Chinese	澄茄子
Chinese	毕澄茄
Chinese	山鸡椒
Chinese	山苍子叶
Chinese	山苍子
Chinese	荜澄茄
Chinese	山胡椒

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Litsea cubeba var. cubeba		Unknown
Litsea cubeba var. formosana	(Nakai) Yen C.Yang & P.H.Huang	Acta Phytotax. Sin. 16(4): 46 (1978)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
  - Tibet
- Eastern Asia
  - Japan
  - Nansei-shoto
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - Nepal
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Malaya
  - Sumatera

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000365367
UNII	J0B1S492VX
USDA Plants	LICU2
Tropicos	17800835
KEW	urn:lsid:ipni.org:names:465621-1
The Plant List	kew-2351783
Open Tree Of Life	607152
NCBI Taxonomy	155299
IUCN Red List	150217538
IPNI	465621-1
iNaturalist	156840
GBIF	3033977
Freebase	/m/02673x1
EPPO	LISCU
EOL	483592
USDA GRIN	400267
Wikipedia	Litsea_cubeba
CMAUP	NPO29110

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_012931725.1	ASM1293172v1	Chromosome	Chinese Academy of Forestry	2020-04-29	150.0x	1.23 Gb

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

Chromosome-level genome assembly of the threatened resource plant Cinnamomum chago

Tao L, Guo S, Xiong Z, Zhang R, Sun W

Sci Data

03-May-2024

PMCID:	PMC11068913
doi:	10.1038/s41597-024-03293-1
PMID:	38702363

The Analgesic Potential of Litsea Species: A Systematic Review

Goh MP, Samsul RN, Mohaimin AW, Goh HP, Zaini NH, Kifli N, Ahmad N

Molecules

30-Apr-2024

PMCID:	PMC11085224
doi:	10.3390/molecules29092079
PMID:	38731572

Genome-wide analysis of bZIP transcription factors and their expression patterns in response to methyl jasmonate and low-temperature stresses in Platycodon grandiflorus

Fan J, Chen N, Rao W, Ding W, Wang Y, Duan Y, Wu J, Xing S

PeerJ

30-Apr-2024

PMCID:	PMC11067905
doi:	10.7717/peerj.17371
PMID:	38708338

Emerging Approaches for Mitigating Biofilm-Formation-Associated Infections in Farm, Wild, and Companion Animals

Araújo D, Silva AR, Fernandes R, Serra P, Barros MM, Campos AM, Oliveira R, Silva S, Almeida C, Castro J

Pathogens

13-Apr-2024

PMCID:	PMC11054384
doi:	10.3390/pathogens13040320
PMID:	38668275

Modeling the Potential Distribution Patterns of the Invasive Plant Species Phytolacca americana in China in Response to Climate Change

Nan Q, Li C, Li X, Zheng D, Li Z, Zhao L

Plants (Basel)

12-Apr-2024

PMCID:	PMC11054219
doi:	10.3390/plants13081082
PMID:	38674491

Inclusion Complexes of Litsea cubeba (Lour.) Pers Essential Oil into β-Cyclodextrin: Preparation, Physicochemical Characterization, Cytotoxicity and Antifungal Activity

Pante GC, Castro JC, Lini RS, Romoli JC, Pires TY, Garcia FP, Nakamura CV, Mulati AC, Matioli G, Machinski Junior M

Molecules

04-Apr-2024

PMCID:	PMC11013208
doi:	10.3390/molecules29071626
PMID:	38611905

Potential Suitable Habitats of Chili Pepper in China under Climate Change

Deng C, Zhong Q, Shao D, Ren Y, Li Q, Wen J, Li J

Plants (Basel)

04-Apr-2024

PMCID:	PMC11013778
doi:	10.3390/plants13071027
PMID:	38611556

Potential Regulatory Networks and Heterosis for Flavonoid and Terpenoid Contents in Pak Choi: Metabolomic and Transcriptome Analyses

Wang H, Han T, Bai A, Xu H, Wang J, Hou X, Li Y

Int J Mol Sci

22-Mar-2024

PMCID:	PMC11011442
doi:	10.3390/ijms25073587
PMID:	38612398

Obtaining Microbiologically Safe Hatching Eggs from Hatcheries: Using Essential Oils for Integrated Sanitization Strategies in Hatching Eggs, Poultry Houses and Poultry

Oliveira GD, McManus C, Vale IR, dos Santos VM

Pathogens

18-Mar-2024

PMCID:	PMC10974541
doi:	10.3390/pathogens13030260
PMID:	38535603

Antibacterial activity and mechanism of X33 antimicrobial oligopeptide against Acinetobacter baumannii

Lu Q, Wu X, Fang Y, Wang Y, Zhang B

Synth Syst Biotechnol

15-Mar-2024

PMCID:	PMC10965436
doi:	10.1016/j.synbio.2024.03.002
PMID:	38545458

Impacts of Climate Change on the Biogeography and Ecological Structure of Zelkova schneideriana Hand.-Mazz. in China

Wang C, Zhang Y, Sheng Q, Zhu Z

Plants (Basel)

11-Mar-2024

PMCID:	PMC10973992
doi:	10.3390/plants13060798
PMID:	38592822

Ethylene-responsive VviERF003 modulates glycosylated monoterpenoid synthesis by upregulating VviGT14 in grapes

Wang YC, Wei Y, Li XY, Zhang HM, Meng X, Duan CQ, Pan QH

Hortic Res

28-Feb-2024

PMCID:	PMC11059816
doi:	10.1093/hr/uhae065
PMID:	38689696

The American Cherimoya Genome Reveals Insights into the Intra-Specific Divergence, the Evolution of Magnoliales, and a Putative Gene Cluster for Acetogenin Biosynthesis

Li T, Zheng J, Nousias O, Yan Y, Meinhardt LW, Goenaga R, Zhang D, Yin Y

Plants (Basel)

26-Feb-2024

PMCID:	PMC10934984
doi:	10.3390/plants13050636
PMID:	38475482

Microbiome–Metabolomic Analysis Revealed the Immunoprotective Effects of the Extract of Vanilla planifolia Andrew (EVPA) on Immunosuppressed Mice

Zhang X, Li Y, Zhu K, Li C, Zhao Q, Gu F, Xu F, Chu Z

Foods

26-Feb-2024

PMCID:	PMC10930650
doi:	10.3390/foods13050701
PMID:	38472814

Stability study in selected conditions and biofilm-reducing activity of phages active against drug-resistant Acinetobacter baumannii

Bagińska N, Grygiel I, Orwat F, Harhala MA, Jędrusiak A, Gębarowska E, Letkiewicz S, Górski A, Jończyk-Matysiak E

Sci Rep

21-Feb-2024

PMCID:	PMC10881977
doi:	10.1038/s41598-024-54469-z
PMID:	38383718

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Aporphines
(+)-Isodomesticine	15690954	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC5=C(C=C43)OCO5)OC)O	325.40	unknown	via CMAUP database
(6aS)-9-Hydroxy-1,2,10-trimethoxy-4,5,6,6aalpha-tetrahydro-7H-dibenzo[de,g]quinoline-6-carboxylic acid methyl ester	44206920	Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)N(CCC3=C1)C(=O)OC)OC	385.40	unknown	https://doi.org/10.1515/ZNB-2009-0717
1,2,10-Trimethoxy-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinolin-9-ol	267400	Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC	327.40	unknown	https://doi.org/10.1002/ARDP.18982360524 https://doi.org/10.1111/J.2042-7158.1994.TB03818.X
1,9-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,10-diol	390656	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC)OC)O	327.40	unknown	https://doi.org/10.1016/0021-9673(94)89083-8 https://doi.org/10.1016/S0040-4039(00)79894-7
Boldine	10154	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O	327.40	unknown	https://doi.org/10.1016/S0040-4039(00)79894-7 https://doi.org/10.1016/0021-9673(94)89083-8
Boldine 2-methyl ether	16573	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC	341.40	unknown	https://doi.org/10.1248/YAKUSHI1947.87.7_878 https://doi.org/10.1016/S0040-4039(00)79894-7 https://doi.org/10.1016/0021-9673(94)89083-8
CID 91884708	91884708	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)O	327.40	unknown	https://doi.org/10.1002/JCCS.199200077 https://doi.org/10.1016/0021-9673(94)89083-8
Isoboldine	133323	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC	327.40	unknown	https://doi.org/10.1016/0021-9673(94)89083-8 https://doi.org/10.1002/JCCS.199200077
Isocorydine	10143	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC	341.40	unknown	https://doi.org/10.1016/0021-9673(94)89083-8 https://doi.org/10.1016/S0040-4039(00)79894-7
Isodomesticine	69523059	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC5=C(C=C43)OCO5)OC)O	325.40	unknown	https://doi.org/10.1016/0021-9673(94)89083-8 https://doi.org/10.1002/JCCS.199200077
Laurolitsine	22179	Click to see COC1=C(C=C2CC3C4=C(C2=C1)C(=C(C=C4CCN3)O)OC)O	313.30	unknown	via CMAUP database
Laurotetanine	31415	Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC	327.40	unknown	https://doi.org/10.1021/NP50036A045 https://doi.org/10.1016/0021-9673(94)89083-8 https://doi.org/10.1002/ARDP.18982360524 https://doi.org/10.1002/JCCS.199200077 https://doi.org/10.1111/J.2042-7158.1994.TB03818.X
Magnoflorine	73337	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C	342.40	unknown	via CMAUP database
Magnoflorine iodide, (+)-(RG)	131664584	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)[O-])OC)C.I	469.30	unknown	via CMAUP database
methyl (6aS)-1,2,9,10-tetramethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-6-carboxylate	44207164	Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)OC)N(CCC3=C1)C(=O)OC)OC	399.40	unknown	https://doi.org/10.1515/ZNB-2009-0717
methyl 1,2,9,10-tetramethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-6-carboxylate	74951863	Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)OC)N(CCC3=C1)C(=O)OC)OC	399.40	unknown	https://doi.org/10.1515/ZNB-2009-0717
methyl 9-hydroxy-1,2,10-trimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-6-carboxylate	74951776	Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)N(CCC3=C1)C(=O)OC)OC	385.40	unknown	https://doi.org/10.1515/ZNB-2009-0717
N-Methyllaurotetanine; NSC 247506; NSC 247564	631015	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC	341.40	unknown	https://doi.org/10.1248/YAKUSHI1947.87.7_878
Norisocorydine	12313549	Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O	327.40	unknown	via CMAUP database
Oxonantenine	3084224	Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC5=C(C=C42)OCO5)OC	335.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259454/
Xanthoplanine	14262868	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC)C	356.40	unknown	https://doi.org/10.1021/NP50101A016
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Hexahydrobenzophenanthridine alkaloids
Chelidonine, 13-methyl-, (14beta)-	56842002	Click to see CC12C(CC3=CC4=C(C=C3C1N(CC5=C2C=CC6=C5OCO6)C)OCO4)O	367.40	unknown	via CMAUP database
> Alkaloids and derivatives / Proaporphines
Glaziovine	65631	Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)O)OC	297.30	unknown	https://doi.org/10.1002/JCCS.199200077 https://doi.org/10.1016/0021-9673(94)89083-8
Suavedol	442245	Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)O)OC	297.30	unknown	https://doi.org/10.1016/0021-9673(94)89083-8 https://doi.org/10.1002/JCCS.199200077
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259454/
> 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 / Phenanthrenes and derivatives / Phenanthrols
Litebamine	196885	Click to see CN1CCC2=C3C=CC4=CC(=C(C=C4C3=C(C(=C2C1)O)OC)OC)O	339.40	unknown	https://doi.org/10.1016/0021-9673(94)89083-8 https://doi.org/10.1016/S0040-4039(00)79894-7
> Benzenoids / Phenol ethers / Anisoles
(S,S)-tramadol(1+)	6919029	Click to see C[NH+](C)CC1CCCCC1(C2=CC(=CC=C2)OC)O	264.38	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactols
Cubebin	117443	Click to see C1C(C(C(O1)O)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5	356.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
2-[4-[3,4-Dihydroxy-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-(hydroxymethyl)oxolan-2-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	85407481	Click to see COC1=C(C=CC(=C1)CC2(COC(C2(CO)O)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O)O	554.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259454/
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
(Z)-4-Decenoic acid	5312351	Click to see CCCCCC=CCCC(=O)O	170.25	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 CC(C)CCCC(=CCO)C	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	https://doi.org/10.1002/RECL.19400590203
(S)-(-)-Citronellal	443157	Click to see CC(CCC=C(C)C)CC=O	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-Dimethyl-2,6-octadien-1-al	8843	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	https://doi.org/10.1248/YAKUSHI1947.80.12_1796 https://doi.org/10.1002/RECL.19400590203
beta-CITRONELLOL, (+/-)-	8842	Click to see CC(CCC=C(C)C)CCO	156.26	unknown	via CMAUP database
beta-CITRONELLOL, (R)-	101977	Click to see CC(CCC=C(C)C)CCO	156.26	unknown	via CMAUP database
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	via CMAUP database
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	via CMAUP database
Citral	638011	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	https://doi.org/10.1002/RECL.19400590203 https://doi.org/10.1248/YAKUSHI1947.80.12_1796
Citronellal	7794	Click to see CC(CCC=C(C)C)CC=O	154.25	unknown	https://doi.org/10.1002/RECL.19400590203
Geranic acid	5275520	Click to see CC(=CCCC(=CC(=O)O)C)C	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 CC(=CCC=C(C)CCO)C	154.25	unknown	via CMAUP database
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1002/RECL.19400590203
Linalool, (+)-	67179	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1002/RECL.19400590203
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	via CMAUP database
Neral	643779	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	https://doi.org/10.1248/YAKUSHI1947.80.12_1796
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
Nerolic acid	5312583	Click to see CC(=CCCC(=CC(=O)O)C)C	168.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	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 CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
(-)-Camphor	444294	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
(-)-Sabinene	11051711	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	via CMAUP database
(+)-3-Carene	443156	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	via CMAUP database
(+)-4-Carene	71351627	Click to see CC1CC2C(C2(C)C)C=C1	136.23	unknown	via CMAUP database
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	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
(1R,2S,4R)-(+)-Bornyl acetate	443131	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
(1R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-OL	12242824	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
(1S,2R,4S)-(-)-Bornyl acetate	442460	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	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
(2S,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl acetate	44630108	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	via CMAUP database
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	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[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)-	17868	Click to see CC1=CCC2(C1C2)C(C)C	136.23	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	6552009	Click to see CC1(C2CCC1(C(C2)O)C)C	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 CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
Camphor (synthetic)	159055	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
Camphor, (1S,4S)-(-)-	10050	Click to see CC1(C2CCC1(C(=O)C2)C)C	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-2-Bornanone	9543187	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
d-Camphor	230921	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
DL-2-Bornanol	10049	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
DL-Borneol	10492	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
endo-2-Bornanol	439568	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	via CMAUP database
Sabinene	10887971	Click to see CC(C)C12CCC(=C)C1C2	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 CC1=CC(C2CC1C2(C)C)O	152.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol	443162	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1002/RECL.19400590203
(-)-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
(+)-alpha-Phellandrene	443160	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	via CMAUP database
(+)-cis-Carveol	443177	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	via CMAUP database
(+)-Isopulegol	1268090	Click to see CC1CCC(C(C1)O)C(=C)C	154.25	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 CC1=CC(=O)C(CC1)C(C)C	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
(1R,2R,5S)-5-Methyl-2-(1-methylethenyl)cyclohexanol	7057942	Click to see CC1CCC(C(C1)O)C(=C)C	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)-, cis-	526657	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)-, trans-	122484	Click to see CC(C)C1CCC(C=C1)(C)O	154.25	unknown	via CMAUP database
2-Cyclohexen-1-ol, 3-methyl-6-(1-methylethyl)-, (1R,6S)-rel-	85567	Click to see CC1=CC(C(CC1)C(C)C)O	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 CC1=CC=C(CC1)C(C)C	136.23	unknown	via CMAUP database
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1002/RECL.19400590203
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 CC(=C)C1CCC(CC1)(C)O	154.25	unknown	via CMAUP database
Isopulegol	24585	Click to see CC1CCC(C(C1)O)C(=C)C	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 CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1002/RECL.19400590203
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1002/RECL.19400590203
Menthoglycol	19100	Click to see CC1CCC(C(C1)O)C(C)(C)O	172.26	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
p-Menthane-3,8-diol	556998	Click to see CC1CCC(C(C1)O)C(C)(C)O	172.26	unknown	https://doi.org/10.1007/978-3-7091-1084-3_4
Piperitone	6987	Click to see CC1=CC(=O)C(CC1)C(C)C	152.23	unknown	via CMAUP database
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
6-[(E)-4-hydroxy-4-methylpent-2-enoyl]-4,6-dimethyl-5-(3-methylbut-2-enyl)cyclohexa-1,3-diene-1-carbaldehyde	102139552	Click to see CC1=CC=C(C(C1CC=C(C)C)(C)C(=O)C=CC(C)(C)O)C=O	316.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Copaene	442355	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
(+)-beta-Caryophyllene	20831623	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
(+)(-)-(E)-beta-caryophyllene	14757966	Click to see CC1(CC2C1CCC(=C)CCCC2=C)C	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
(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
(E)-beta-farnesene	10407	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	via CMAUP database
(Z)-caryophyllene	6429301	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
1-Methyl-4-(1-methylethylidene)-2-(1-methylvinyl)-1-vinylcyclohexane	94254	Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C	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 CC1=CCC2C3C1C2(CCC3C(C)C)C	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-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydro-1-naphthalenol	519662	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	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
alpha-Cadinol #1	6431302	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
alpha-Copaene	70678558	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
Alpha-Farnesene	5281516	Click to see CC(=CCCC(=CCC=C(C)C=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-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	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
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Caryophyllene epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	via CMAUP database
Caryophyllene oxide 2	13240188	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	via CMAUP database
Caryophyllene,alpha + beta mixt.	5354499	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	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 CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	via CMAUP database
Isocaryophyllene	5281522	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Isocaryophyllene oxide	1742211	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	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 / Elemane sesquiterpenoids
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)-	9859094	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	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
Selina-6-en-4-ol	527220	Click to see CC(C)C1=CC2C(CCCC2(C)O)(CC1)C	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 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,6Z)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene	5373727	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 CC1=CCCC(=C)C=CC(CC1)C(C)C	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
Germacren A	5835162	Click to see CC1=CCCC(=CCC(CC1)C(=C)C)C	204.35	unknown	via CMAUP database
Germacrene a	9548705	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
> Organic acids and derivatives / Hydroxy acids and derivatives / Medium-chain hydroxy acids and derivatives
Litseacubebic Acid	76312534	Click to see CC(=CC=CC(C)(C)O)C(=O)O	170.21	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259454/
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(2R)-2-(2-hydroxypropan-2-yl)-5-methyl-3,4-dihydro-2H-oxepin-7-one	76319759	Click to see CC1=CC(=O)OC(CC1)C(C)(C)O	184.23	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259454/
2-(2-hydroxypropan-2-yl)-5-methyl-3,4-dihydro-2H-oxepin-7-one	72189091	Click to see CC1=CC(=O)OC(CC1)C(C)(C)O	184.23	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259454/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eleutheroside B	5316860	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	via CMAUP database
Glucoside,6-dimethoxyphenyl, D	5885030	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
16-Hentriacontanone	94741	Click to see CCCCCCCCCCCCCCCC(=O)CCCCCCCCCCCCCCC	450.80	unknown	https://doi.org/10.1016/S0031-9422(00)97408-9
6-Methyl-5-hepten-2-one	9862	Click to see CC(=CCCC(=O)C)C	126.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzimidazoles / 2-benzimidazolylcarbamic acid esters
Carbendazim	25429	Click to see COC(=O)NC1=NC2=CC=CC=C2N1	191.19	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259454/
> Organoheterocyclic compounds / Benzodioxoles
Safrole	5144	Click to see C=CCC1=CC2=C(C=C1)OCO2	162.18	unknown	via CMAUP database
> Organoheterocyclic compounds / Epoxides
(1R,3E,7E,11S)-1,5,5,8-tetramethyl-12-oxabicyclo[9.1.0]dodeca-3,7-diene	12900740	Click to see CC1=CCC(C=CCC2(C(O2)CC1)C)(C)C	220.35	unknown	via CMAUP database
1,5,5,8-Tetramethyl-12-oxabicyclo[9.1.0]dodeca-3,7-diene	23274265	Click to see CC1=CCC(C=CCC2(C(O2)CC1)C)(C)C	220.35	unknown	via CMAUP database
CID 92476330	92476330	Click to see CC1=CCC(C=CCC2(C(O2)CC1)C)(C)C	220.35	unknown	via CMAUP database
Humulene epoxide II	10704181	Click to see CC1=CCC(C=CCC2(C(O2)CC1)C)(C)C	220.35	unknown	via CMAUP database
Humulene epoxyde	5463721	Click to see CC1=CCC(C=CCC2(C(O2)CC1)C)(C)C	220.35	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[(4-hydroxyphenyl)methyl]-7-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-8-ol	173713	Click to see C[N+]1(CCC2=C(C1CC3=CC=C(C=C3)O)C(=C(C=C2)OC)O)C	314.40	unknown	https://doi.org/10.1021/NP50101A016
4-[(7-hydroxy-6-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-1-yl)methyl]phenolate	5319196	Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)[O-])O)OC)C	313.40	unknown	via CMAUP database
8-O-Methyloblongine	131751584	Click to see C[N+]1(CCC2=C(C1CC3=CC=C(C=C3)O)C(=C(C=C2)OC)OC)C	328.40	unknown	https://doi.org/10.1021/NP50101A016
Magnocurarine	53266	Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C	314.40	unknown	https://doi.org/10.1021/NP50101A016
Reticulin	10233	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC	329.40	unknown	https://doi.org/10.1016/S0040-4039(00)79894-7 https://doi.org/10.1016/0021-9673(94)89083-8
Reticuline	439653	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC	329.40	unknown	https://doi.org/10.1016/0021-9673(94)89083-8 https://doi.org/10.1016/S0040-4039(00)79894-7
> Organoheterocyclic compounds / Oxanes
Eucalyptol	2758	Click to see CC1(C2CCC(O1)(CC2)C)C	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 CC(=C)C1CCC2(C(C1)O2)C	152.23	unknown	via CMAUP database
Limonene oxide, (-)-	10953718	Click to see CC(=C)C1CCC2(C(C1)O2)C	152.23	unknown	via CMAUP database
Limonene oxide, trans-(-)-	8029780	Click to see CC(=C)C1CCC2(C(C1)O2)C	152.23	unknown	via CMAUP database
Limonene-1,2-epoxide	441245	Click to see CC(=C)C1CCC2(C(C1)O2)C	152.23	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans
1,3,3-Trimethyl-2-oxabicyclo[2.2.2]oct-5-ene	523035	Click to see CC1(C2CCC(O1)(C=C2)C)C	152.23	unknown	via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(12aR)-3-methoxy-7-methyl-5,6,12,12a-tetrahydroindolo[2,1-a]isoquinolin-7-ium-2,9,10-triol	163193014	Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)O)O)OC	314.40	unknown	https://doi.org/10.1021/NP960014B
(12aR)-3,10-dimethoxy-7-methyl-5,6,12,12a-tetrahydroindolo[2,1-a]isoquinolin-7-ium-2,9-diol	163195213	Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)O)OC	328.40	unknown	https://doi.org/10.1021/NP960014B
(7S,12aR)-3-methoxy-7-methyl-5,6,12,12a-tetrahydroindolo[2,1-a]isoquinolin-7-ium-2,9,10-triol	163188205	Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)O)O)OC	314.40	unknown	https://doi.org/10.1021/NP960014B
(7S,12aR)-3,10-dimethoxy-7-methyl-5,6,12,12a-tetrahydroindolo[2,1-a]isoquinolin-7-ium-2,9-diol	163195212	Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)O)OC	328.40	unknown	https://doi.org/10.1021/NP960014B
Litcubine	85243417	Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)O)OC	328.40	unknown	https://doi.org/10.1021/NP960014B
Litcubinine	85190560	Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)O)O)OC	314.40	unknown	https://doi.org/10.1021/NP960014B
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3-(3,4,5-Trimethoxyphenyl)-2-propen-1-ol	73924	Click to see COC1=CC(=CC(=C1OC)OC)C=CCO	224.25	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259454/
3,4,5-Trimethoxycinnamyl alcohol	6436306	Click to see COC1=CC(=CC(=C1OC)OC)C=CCO	224.25	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259454/

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Litsea cubeba

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