Scientific name	Authority	First published in
Uvaria fluminensis	Vell.	Fl. Flumin. : 238 (1829)
Xylopia carminativa	R.E.Fr.	Kongl. Svenska Vetensk.-Akad. Handl. 34(5): 32. 1900
Xylopia intermedia	R.E.Fr.	Kongl. Svenska Vetensk. Acad. Handl. , n.s., 34(5): 32 (1900)
Mayna sericea	Spreng.	Neue Entdeck. Pflanzenk. 2: 153 (1821)
Unona carminativa	Arruda	Diss. Pl. Brazil : 48 (1810)
Xylopicrum carminativum	Kuntze	Revis. Gen. Pl. 1: 8 (1891)
Unona fluminensis	Vell.	Fl. Flumin. 5: t. 121 (1829)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Central America
  - Costa Rica
  - Nicaragua
  - Panamá
- Northern South America
  - French Guiana
  - Guyana
  - Suriname
  - Venezuela
- Western South America
  - Bolivia
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000428724
Tropicos	1600524
INPN	732569
KEW	urn:lsid:ipni.org:names:76256-1
The Plant List	kew-2467939
Open Tree Of Life	3868026
NCBI Taxonomy	1005659
IUCN Red List	143325219
IPNI	76256-1
GBIF	3157040
Freebase	/m/04z_tcc
EOL	1054966
USDA GRIN	405760
Wikipedia	Xylopia_sericea

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

Fissistigma oldhamii (Hemsl.) Merr.: Ethnomedicinal, Phytochemistry, and Pharmacological Aspects

Bailly C

Plants (Basel)

07-Dec-2023

PMCID:	PMC10748316
doi:	10.3390/plants12244094
PMID:	38140421

Rust Fungi on Medicinal Plants in Guizhou Province with Descriptions of Three New Species

Wu Q, He M, Liu T, Hu H, Liu L, Zhao P, Li Q

J Fungi (Basel)

21-Sep-2023

PMCID:	PMC10532644
doi:	10.3390/jof9090953
PMID:	37755061

Phytochemical Profile, Antioxidant Potential and Toxicity Evaluation of the Essential Oils from Duguetia and Xylopia Species (Annonaceae) from the Brazilian Amazon

Cascaes MM, De Moraes ÂA, Cruz JN, Franco CD, E Silva RC, do Nascimento LD, Ferreira OO, dos Anjos TO, de Oliveira MS, Guilhon GM, Andrade EH

Antioxidants (Basel)

30-Aug-2022

PMCID:	PMC9495368
doi:	10.3390/antiox11091709
PMID:	36139777

Essential Oils from Annonaceae Species from Brazil: A Systematic Review of Their Phytochemistry, and Biological Activities

Cascaes MM, Carneiro OD, do Nascimento LD, de Moraes ÂA, de Oliveira MS, Cruz JN, Guilhon GM, Andrade EH

Int J Mol Sci

09-Nov-2021

PMCID:	PMC8623146
doi:	10.3390/ijms222212140
PMID:	34830022

Multi-Gene Phylogeny and Morphology Reveal Haplohelminthosporium gen. nov. and Helminthosporiella gen. nov. Associated with Palms in Thailand and A Checklist for Helminthosporium Reported Worldwide

Konta S, Hyde KD, Karunarathna SC, Mapook A, Senwanna C, Dauner LA, Nanayakkara CM, Xu J, Tibpromma S, Lumyong S

Life (Basel)

19-May-2021

PMCID:	PMC8161214
doi:	10.3390/life11050454
PMID:	34069619

Directional change in leaf dry matter δ 13C during leaf development is widespread in C3 plants

Vogado NO, Winter K, Ubierna N, Farquhar GD, Cernusak LA

Ann Bot

24-Jun-2020

PMCID:	PMC7596372
doi:	10.1093/aob/mcaa114
PMID:	32577724

Consequences of removal of exotic species (eucalyptus) on carbon and nitrogen cycles in the soil-plant system in a secondary tropical Atlantic forest in Brazil with a dual-isotope approach

Teixeira MC, Vitória AP, de Rezende CE, de Almeida MG, Nardoto GB

PeerJ

28-May-2020

PMCID:	PMC7261475
doi:	10.7717/peerj.9222
PMID:	32523812

Alkaloids from Plants with Antimalarial Activity: A Review of Recent Studies

Uzor PF

Evid Based Complement Alternat Med

12-Feb-2020

PMCID:	PMC7037883
doi:	10.1155/2020/8749083
PMID:	32104196

Prenylated flavonoid-enriched fraction from Maclura tinctoria shows biological activity against Staphylococcus aureus and protects Galleria mellonella larvae from bacterial infection

das Chagas Almeida A, Azevedo Rodrigues L, dos Santos Paulino G, Pereira Aguilar A, Andrade Almeida A, Olavo Ferreira S, Brandão GC, Viana Leite JP, de Oliveira Barros Ribon A

BMC Complement Altern Med

29-Jul-2019

PMCID:	PMC6664575
doi:	10.1186/s12906-019-2600-y
PMID:	31357964

Persistence of Coffea arabica and its relationship with the structure, species diversity and composition of a secondary forest in Brazil

Raymundo D, Prado-Junior J, de Oliveira-Neto NE, Santana LD, do Vale VS, Jacobson TB, de Oliveira PE, Carvalho FA

PLoS One

14-Mar-2018

PMCID:	PMC5851612
doi:	10.1371/journal.pone.0194032
PMID:	29538468

Local ecological knowledge and its relationship with biodiversity conservation among two Quilombola groups living in the Atlantic Rainforest, Brazil

Conde BE, Ticktin T, Fonseca AS, Macedo AL, Orsi TO, Chedier LM, Rodrigues E, Pimenta DS

PLoS One

28-Nov-2017

PMCID:	PMC5705149
doi:	10.1371/journal.pone.0187599
PMID:	29182637

Leaf epidermis images for robust identification of plants

da Silva NR, Oliveira MW, Filho HA, Pinheiro LF, Rossatto DR, Kolb RM, Bruno OM

Sci Rep

24-May-2016

PMCID:	PMC4877573
doi:	10.1038/srep25994
PMID:	27217018

A new species of the lenticel fungal genus Claviradulomyces (Ostropales) from the Brazilian Atlantic forest tree Xylopia sericea (Annonaceae)

Barreto RW, Johnston PR, Crous PW, Evans HC

IMA Fungus

15-Nov-2012

PMCID:	PMC3539316
doi:	10.5598/imafungus.2012.03.02.05
PMID:	23355966

Evidence for conservation and sustainable use in a fragment of the Atlantic forest in southeastern Brazil by a traditional human group

Christo AG, Guedes-Bruni RR, Sobrinho F, da Silva AG, Peixoto AL

Springerplus

28-Sep-2012

PMCID:	PMC3725884
doi:	10.1186/2193-1801-1-21
PMID:	23961351

Chemical composition and antibacterial activity of essential oils from six Moroccan plants

Ahmed Talbaoui,

Academic Journals

29-Aug-2012

doi:	10.5897/JMPR10.078

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
> Benzenoids / Benzene and substituted derivatives / Cumenes
1-Isopropyl-2-methoxybenzene	270623	Click to see CC(C)C1=CC=CC=C1OC	150.22	unknown	https://doi.org/10.1021/NP50048A039
> Hydrocarbons / Polycyclic hydrocarbons
Bornylene	10047	Click to see CC1(C2CCC1(C=C2)C)C	136.23	unknown	https://doi.org/10.5897/JMPR10.078
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hexadecane	11006	Click to see CCCCCCCCCCCCCCCC	226.44	unknown	https://doi.org/10.1021/NP50048A039
Pentadecane	12391	Click to see CCCCCCCCCCCCCCC	212.41	unknown	https://doi.org/10.1021/NP50048A039
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
> 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	https://doi.org/10.1021/NP50048A039
Neryl acetate	1549025	Click to see CC(=CCCC(=CCOC(=O)C)C)C	196.29	unknown	https://doi.org/10.1021/NP50048A039
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,9R,13S)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane	91746569	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)C	272.50	unknown	https://doi.org/10.1080/10412905.1996.9700559
Kaur-16-ene	520687	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)C	272.50	unknown	https://doi.org/10.1080/10412905.1996.9700559
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559 https://doi.org/10.5897/JMPR10.078
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1021/NP50048A039
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
> 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/10.1021/NP50048A039
Cuminaldehyde	326	Click to see CC(C)C1=CC=C(C=C1)C=O	148.20	unknown	https://doi.org/10.1021/NP50048A039
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1021/NP50048A039
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-Isoborneol	6973640	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1021/NP50048A039
(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one	6973628	Click to see CC1=CC(=O)C2CC1C2(C)C	150.22	unknown	https://doi.org/10.1021/NP50048A039
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene	6451618	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1021/NP50048A039
(1S,3R,5S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol	12314318	Click to see CC1(C2CC1C(=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1021/NP50048A039
(3R)-4-methylidene-1-(propan-2-yl)bicyclo[3.1.0]hexan-3-ol	42626428	Click to see CC(C)C12CC1C(=C)C(C2)O	152.23	unknown	https://doi.org/10.1080/10412905.1996.9700559
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.1021/NP50048A039
3-Thujanone	11027	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1021/NP50048A039
alpha-Bergamotene	86608	Click to see CC1=CCC2CC1C2(C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.5897/JMPR10.078 https://doi.org/10.1080/10412905.1996.9700559
alpha-Thujone	12304613	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1021/NP50048A039
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
beta-Thujone	91456	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1021/NP50048A039
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	https://doi.org/10.1021/NP50048A039
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1080/10412905.1996.9700559
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.1021/NP50048A039
CID 44630107	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1021/NP50048A039
Fenchone	14525	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	unknown	https://doi.org/10.1021/NP50048A039
Myrtenal	61130	Click to see CC1(C2CC=C(C1C2)C=O)C	150.22	unknown	https://doi.org/10.1021/NP50048A039
Myrtenol	10582	Click to see CC1(C2CC=C(C1C2)CO)C	152.23	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
Pinocarveol	102667	Click to see CC1(C2CC1C(=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1021/NP50048A039
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1021/NP50048A039
Tricyclene	79035	Click to see CC1(C2CC3C1(C3C2)C)C	136.23	unknown	https://doi.org/10.1021/NP50048A039
Verbenone	29025	Click to see CC1=CC(=O)C2CC1C2(C)C	150.22	unknown	https://doi.org/10.1021/NP50048A039
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol	94221	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	https://doi.org/10.1021/NP50048A039
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.5897/JMPR10.078 https://doi.org/10.1021/NP50048A039
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1021/NP50048A039
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
alpha-Terpinyl acetate	111037	Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C	196.29	unknown	https://doi.org/10.1021/NP50048A039
Carveol	7438	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	https://doi.org/10.1021/NP50048A039
Carvone, (+)-	16724	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1021/NP50048A039
Carvone, (+/-)-	7439	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1021/NP50048A039
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1021/NP50048A039
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
(S)-2,2,3-Trimethylcyclopent-3-ene-1-acetaldehyde	90969	Click to see CC1=CCC(C1(C)C)CC=O	152.23	unknown	https://doi.org/10.1021/NP50048A039
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Cyperene	12308843	Click to see CC1CCC2CC3=C(CCC13C2(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
(+)-Gamma-cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039
(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	https://doi.org/10.1021/NP50048A039
(1R,4aR)-4,7-dimethyl-1-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalene	5315589	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	5315592	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1080/10412905.1996.9700559
(1S,2R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	145994486	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039
(1S,2S,6S,7R,8R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	101607926	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1996.9700559 https://doi.org/10.1080/10412905.1996.9700559
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene	134779875	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
(1S,6R,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	84690	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039
(1Z,6E)-gamma-humulene	14038477	Click to see CC1=CCCC(=C)C=CC(CCC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane	5317024	Click to see CC(=C1CCC(C(C1)(C)C(=C)C)(C)C=C)C	218.38	unknown	https://doi.org/10.1080/10412905.1996.9700559
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene	101708	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039
1,6-Dimethyl-4-isopropyltetralin	10224	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1021/NP50048A039
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	https://doi.org/10.1080/10412905.1996.9700559
3H-3a,7-Methanoazulene, 2,4,5,6,7,8-hexahydro-1,4,9,9-tetramethyl-, [3aR-(3aalpha,4beta,7alpha)]-	99856	Click to see CC1CCC2CC3=C(CCC13C2(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
alpha-Cadinene, (+)-	12306048	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1080/10412905.1996.9700559
alpha-Cubebene	442359	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
alpha-Elemene	80048	Click to see CC(C)C1=CC(=C(C)C)CCC1(C)C=C	204.35	unknown	https://doi.org/10.1021/NP50048A039
alpha-Muurolene	12306047	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039
beta-Cubebene	93081	Click to see CC1CCC(C2C13C2C(=C)CC3)C(C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
Calamenene	6429077	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1021/NP50048A039
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)-	89316	Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
delta-Elemene	12309449	Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039
gamma-Muurolene	12313020	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039 https://doi.org/10.1080/10412905.1996.9700559
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039
Rimuene	12314971	Click to see CC1(CCCC2C1=CCC3C2(CCC(C3)(C)C=C)C)C	272.50	unknown	https://doi.org/10.1080/10412905.1996.9700559
trans-Nerolidol	5284507	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1080/10412905.1996.9700559
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene	91746456	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	97032059	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	5321422	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
Alloaromadendren	91746537	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
alpha-Gurjunene	15560276	Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C	204.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
Aromadendrene	91354	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexyl)propan-2-ol	547972	Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O	222.37	unknown	https://doi.org/10.1080/10412905.1996.9700559
Beta-Elemene	6918391	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
Elemol	92138	Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O	222.37	unknown	https://doi.org/10.1080/10412905.1996.9700559
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
4a,5-Dimethyl-3-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,7-octahydronaphthalene	288227	Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
Valencene	9855795	Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1996.9700559
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrene a	9548705	Click to see CC1=CCCC(=CCC(CC1)C(=C)C)C	204.35	unknown	https://doi.org/10.1021/NP50048A039

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Xylopia sericea

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