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.

Zanthoxylum simulans, commonly known as Sichuan pepper, has a long history of medicinal use in East Asia. In the Sichuan region of China, the dried fruit (seeds) is steeped in hot water to produce a numbing tea that is traditionally taken to relieve stomach pain, cough, and sore throat, according to the Chinese Pharmacopoeia 2020. The bark and young leaves are also used in decoctions for digestive upset and as a mild analgesic, a practice documented in the ethnobotanical survey of the Yi people in Sichuan (Li et al., 2021). In Korea, Z. simulans is incorporated into decoctions for cough and throat irritation; the Korean Medicine Journal 2018 reports that the fruit’s infusion is used to soothe the upper respiratory tract. Japanese traditional medicine records the use of a decoction made from the fruit to treat stomach discomfort and mild abdominal pain, as noted in the Japanese Traditional Medicine compendium 2019. Across these cultures, the common theme is the use of infusions and decoctions of the fruit, bark, or leaves to address digestive and respiratory ailments.

A simple, safe recipe for a mild Sichuan‑pepper tea uses the fruit’s numbing properties without overwhelming the palate. Take 5 g of dried Z. simulans fruit (the seeds) and add it to 250 ml of boiling water. Let the mixture steep for 5–10 minutes, then strain. Drink one cup in the morning and one in the evening, but limit intake to two cups per day. Pregnant women should avoid this tea because the alkylamides in the fruit can stimulate uterine contractions. The tea is best enjoyed warm, and a pinch of salt or a splash of vinegar can help balance the sharp numbing flavor.

The therapeutic effects of Z. simulans are largely attributed to its well‑characterized phytochemicals. The fruit contains hydroxy‑alkylamides, such as hydroxy‑alkylamides, that produce the characteristic tingling sensation and have documented analgesic and anti‑inflammatory activity. Essential oils—including limonene, linalool, and β‑pinene—contribute to the aroma and possess antimicrobial properties. Flavonoids such as quercetin and kaempferol are also present and are known for their antioxidant effects. These constituents together explain the traditional use of the plant for pain relief, cough suppression, and digestive support.

Today, Zanthoxylum simulans remains a popular spice in Sichuan cuisine and is widely available in Asian markets worldwide. Ongoing research is exploring its essential oil profile for potential pharmaceutical applications, and the plant continues to be used by traditional healers in China, Korea, and Japan, bridging culinary and medicinal traditions.

General Uses Top

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Common products:
• Dried pericarp (Zanthoxylum simulans) used as a spice and flavoring agent, commonly labeled as “Sichuan pepper” or “prickly ash” in food products and seasonings; the oleoresin (alcohol-soluble extract) is used as a standardized flavoring in the food industry.
• Volatile oil produced by hydrodistillation of the fruit pericarp, employed as a natural flavor and fragrance ingredient (香辛料精油).

Industrial and craft applications:
• The volatile oil may be formulated into fragrances (e.g., spicy/herbal accords) and into savory flavor systems for processed foods; use occurs via established flavor houses rather than commodity-scale processing.

Food and beverages (non-medicinal):
• Fruit pericarp is incorporated as a seasoning in regional Chinese cuisine, in marinades, sauces, snacks, and packaged savory products.
• The oleoresin is used as a standardized flavoring in prepared foods (e.g., sauces, spice blends) to deliver consistent sensory properties without health claims.

Colorants and tanning:
• No documented use as a dye or tanning agent.

Wood and fiber:
• No documented timber, fiber, or gum uses.

Fragrance and cosmetics:
• Fruit pericarp essential oil is used in fragrance compositions for spicy/herbal notes; allergen labeling (e.g., EU cosmetic fragrance allergen disclosure) applies to natural components such as limonene and linalool present in the oil.

Properties relevant to use:
• Chemical markers reported in the fruit pericarp volatile oil include linalool, geranyl acetate, limonene, and β-caryophyllene, which provide characteristic floral-spicy and herbal notes; theoleoresin solubility in ethanol facilitates standardized flavor delivery.
• The non-volatile profile includes hydroxy-α-sanshool (capsaicinoid-like), recognized as the primary sensory compound responsible for the characteristic tingling and numbing sensations in culinary contexts.

Standards and regulation:
• In the United States, the pericarp is recognized as a flavoring agent (GRAS) under the broader category of Zanthoxylum spp. fruit (FDA CFR 21 §182.20).
• In the European Union, the pericarp is listed as a food flavoring in the Flavouring Substances Regulation (Regulation (EC) No 1334/2008) and in the UK under the former Flavouring Regulations.
• Fragrance use in cosmetics follows EU cosmetic allergen labeling requirements for naturally occurring fragrance components (Regulation (EC) No 1223/2009); ISO/ASTM/EN timber or fiber standards do not apply.

Sustainability and sourcing:
• Major production originates from cultivation in central and western China; market supply includes both hand-harvested dried pericarp and industrially extracted oleoresin.

Synonyms Top

Scientific name	Authority	First published in
Zanthoxylum coreanum	Nakai	Bot. Mag. (Tokyo) 44: 528 (1930)
Fagara podocarpa	Engl.	Nat. Pflanzenfam. 3(4): 118 (1896)
Fagara setosa	Engl.	Nat. Pflanzenfam. 3(4): 118 (1896)
Zanthoxylum acanthophyllum	Hayata	Icon. Pl. Formosan. 6: 7 (1916)
Zanthoxylum setosum	Hemsl. ex F.B.Forbes & Hemsl.	J. Linn. Soc., Bot. 23: 107 (1886)
Zanthoxylum argyi	H.Lév.	Mem. Real Acad. Ci. Barcelona 12(22): 20 (1916)
Zanthoxylum podocarpum	Hemsl.	J. Linn. Soc., Bot. 23: 107 (1886)

Common names Top

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Filter by language:

Language	Common/alternative name
English	chinese-pepper
Arabic	فاغرة بنجية
Azerbaijani	oxşar zantoksilum
azb	زانتوکسیلوم بونقانوم
German	szechuanpfeffer
Japanese	トウザンショウ
Japanese	トゲザンショウ
Japanese	オオザンショウ
Japanese	四川山椒
Japanese	華北山椒
Chinese	黄椒
Chinese	柄果花椒
Chinese	刺椒
Chinese	黄总管
Chinese	香椒
Chinese	天角椒
Chinese	大花椒
Chinese	野花椒皮
Chinese	野花椒叶
Chinese	野花椒（柄果花椒）
Chinese	野花椒
Chinese	刺花椒
Chinese	麻口皮子药

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Zanthoxylum simulans subsp. calcareum	Z.H.Chen, Feng Chen & W.Zhu	J. Hangzhou Norm. Univ., Nat. Sci. Ed. 19(6): [96-102] 2020
Zanthoxylum simulans subsp. simulans

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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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 North-central
  - China South-central
  - China Southeast
  - Qinghai
- Eastern Asia
  - Korea
  - Taiwan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000429371
UNII	62FI768Z5U
USDA Plants	ZASI2
Tropicos	28101583
KEW	urn:lsid:ipni.org:names:776025-1
The Plant List	kew-2469033
PFAF	Zanthoxylum simulans
Open Tree Of Life	889927
NCBI Taxonomy	328402
IPNI	776025-1
iNaturalist	170408
GBIF	3834219
Freebase	/m/088_qn
USDA GRIN	312178
Wikipedia	Zanthoxylum_simulans
CMAUP	NPO26298

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

The complete chloroplast genome sequence of Zanthoxylum ailanthoides Sieb. et. Zucc (Rutaceae): an important medicinal plant

Liang YN, Cui N, Liang XB, Huang XY, Zhang W, Li H

Mitochondrial DNA B Resour

12-Apr-2024

PMCID:	PMC11018064
doi:	10.1080/23802359.2024.2338260
PMID:	38623176

Identification of Novel Quinolone and Quinazoline Alkaloids as Phosphodiesterase 10A Inhibitors for Parkinson’s Disease through a Computational Approach

Ahmad I, Khalid H, Perveen A, Shehroz M, Nishan U, Rahman FU, Sheheryar, Moura AA, Ullah R, Ali EA, Shah M, Ojha SC

ACS Omega

26-Mar-2024

PMCID:	PMC11007772
doi:	10.1021/acsomega.3c10351
PMID:	38617664

Dual COX-2/5-LOX inhibitors from Zanthoxylum simulans inhibit gastric cancer cells by cross-mediating thyroid, estrogen, and oxytocin signaling pathways

Tian YQ, Liu J, Cheng P, Zou J, Xu HF, Shi XH, Zhang YS, Mei L

Front Chem

10-Jan-2024

PMCID:	PMC10805830
doi:	10.3389/fchem.2023.1287570
PMID:	38268762

Editorial: Recent advances in the research and development of kinase-inhibitory anticancer molecules

Al-Karmalawy AA, El-Subbagh HI, Logoyda L, Lesyk RB, El-Gamal MI

Front Chem

09-Nov-2023

PMCID:	PMC10666179
doi:	10.3389/fchem.2023.1328424
PMID:	38025062

Synthesis of tetrahydrofuro[3,2-c]pyridines via Pictet–Spengler reaction

Mendogralo EY, Uchuskin MG

Beilstein J Org Chem

30-Jun-2023

PMCID:	PMC10315887
doi:	10.3762/bjoc.19.74
PMID:	37404803

Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China

Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C

J Ethnobiol Ethnomed

30-May-2023

PMCID:	PMC10230803
doi:	10.1186/s13002-023-00594-4
PMID:	37254191

Assessing the Spontaneous Spread of Climate-Adapted Woody Plants in an Extensively Maintained Collection Garden

Szabó K, Gergely A, Tóth B, Szilágyi K

Plants (Basel)

15-May-2023

PMCID:	PMC10224429
doi:	10.3390/plants12101989
PMID:	37653906

Anticancer Potentials of the Lignan Magnolin: A Systematic Review

Bhuia MS, Wilairatana P, Chowdhury R, Rakib AI, Kamli H, Shaikh A, Coutinho HD, Islam MT

Molecules

23-Apr-2023

PMCID:	PMC10180476
doi:	10.3390/molecules28093671
PMID:	37175081

Bioactive Compounds Produced by Endophytic Microorganisms Associated with Bryophytes—The “Bryendophytes”

Stelmasiewicz M, Świątek Ł, Gibbons S, Ludwiczuk A

Molecules

05-Apr-2023

PMCID:	PMC10096483
doi:	10.3390/molecules28073246
PMID:	37050009

Pyrrole-2-carboxaldehydes: Origins and Physiological Activities

Matsugo S, Nakamura Y

Molecules

13-Mar-2023

PMCID:	PMC10058459
doi:	10.3390/molecules28062599
PMID:	36985566

Roles of Essential Oils, Polyphenols, and Saponins of Medicinal Plants as Natural Additives and Anthelmintics in Ruminant Diets: A Systematic Review

Ramdani D, Yuniarti E, Jayanegara A, Chaudhry AS

Animals (Basel)

20-Feb-2023

PMCID:	PMC9951870
doi:	10.3390/ani13040767
PMID:	36830554

Anthelmintic Agents from African Medicinal Plants: Review and Prospects

Jato J, Orman E, Duah Boakye Y, Oppong Bekoe E, Oppong Bekoe S, Asare-Nkansah S, Spiegler V, Hensel A, Liebau E, Agyare C

Evid Based Complement Alternat Med

31-Dec-2022

PMCID:	PMC9825222
doi:	10.1155/2022/8023866
PMID:	36624864

Ethnobotanical study of the wild edible and healthy functional plant resources of the Gelao people in northern Guizhou, China

Xie J, Liu F, Jia X, Zhao Y, Liu X, Luo M, He Y, Liu S, Wu F

J Ethnobiol Ethnomed

19-Dec-2022

PMCID:	PMC9761637
doi:	10.1186/s13002-022-00572-2
PMID:	36536370

Essential Oils as Novel Anthelmintic Drug Candidates

Panda SK, Daemen M, Sahoo G, Luyten W

Molecules

29-Nov-2022

PMCID:	PMC9735941
doi:	10.3390/molecules27238327
PMID:	36500419

Synthesis and Anti-Leishmanial Properties of Quinolones Derived from Zanthosimuline

Jézéquel G, Cardoso LN, Olivon F, Dennemont I, Apel C, Litaudon M, Roussi F, Pomel S, Desrat S

Molecules

15-Nov-2022

PMCID:	PMC9693141
doi:	10.3390/molecules27227892
PMID:	36431992

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 / Aporphines
1-((7aR)-5,6,7a,8-Tetrahydro-7H-benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-7-yl)ethanone	6453733	Click to see	307.30	unknown	https://doi.org/10.1021/NP50111A003 https://doi.org/10.1016/0031-9422(95)00856-X https://doi.org/10.1016/S0031-9422(00)97045-6 https://doi.org/10.1016/S0031-9422(00)90870-7
1-[(6aR)-2-hydroxy-1-methoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-yl]ethanone	101664493	Click to see CC(=O)N1CCC2=CC(=C(C3=C2C1CC4=CC=CC=C43)OC)O	309.40	unknown	https://doi.org/10.1016/S0031-9422(00)97045-6 https://doi.org/10.1016/0031-9422(95)00856-X
Liriodenine	10144	Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53	275.26	unknown	https://doi.org/10.1021/NP50111A003
N-Acetyldehydroanonaine	5315739	Click to see CC(=O)N1CCC2=CC3=C(C4=C2C1=CC5=CC=CC=C54)OCO3	305.30	unknown	https://doi.org/10.1016/0031-9422(95)00856-X
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
(2S)-2-[[(13R)-1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl]methyl]-7-methoxy-2,6-dimethylpyrano[3,2-c]quinolin-5-one	102236946	Click to see	618.70	unknown	https://doi.org/10.1016/S0031-9422(00)90870-7
[(13R)-1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-yl]methanol	154496264	Click to see	379.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
Bocconoline	181121	Click to see	379.40	unknown	https://doi.org/10.1016/S0031-9422(00)97045-6 https://doi.org/10.1016/S0031-9422(02)00268-6 https://doi.org/10.1021/NP50111A003 https://doi.org/10.1016/0031-9422(95)00856-X https://doi.org/10.1016/S0031-9422(00)90870-7
Dihydrochelerythrine	485077	Click to see	349.40	unknown	https://doi.org/10.1021/NP50111A003 https://doi.org/10.1016/0031-9422(95)00856-X https://doi.org/10.1016/S0031-9422(00)97045-6
Simulanoquinoline	5321314	Click to see	618.70	unknown	https://doi.org/10.1016/S0031-9422(00)90870-7 https://doi.org/10.1016/0031-9422(95)00856-X https://doi.org/10.1021/NP50111A003
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Chelerythrine	2703	Click to see	348.40	unknown	https://doi.org/10.1016/0031-9422(95)00856-X https://doi.org/10.1016/S0031-9422(00)90870-7 https://doi.org/10.1021/NP50111A003 https://doi.org/10.1016/S0031-9422(00)97045-6
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
Arnottianamide	3085181	Click to see CN(C=O)C1=C(C=CC2=CC3=C(C=C21)OCO3)C4=C(C(=C(C=C4)OC)OC)O	381.40	unknown	https://doi.org/10.1016/S0031-9422(00)97045-6 https://doi.org/10.1016/S0031-9422(97)00280-X https://doi.org/10.1016/0031-9422(95)00856-X https://doi.org/10.1016/S0031-9422(00)90870-7 https://doi.org/10.1021/NP50111A003
Simulansamide	5321312	Click to see	397.40	unknown	https://doi.org/10.1002/JCCS.199600028
> 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/10.1016/S0031-9422(02)00268-6
> 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://doi.org/10.1016/S0031-9422(02)00268-6
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(3S,3aR,6S,6aR)-3-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro(3,4-c)furan-6-ol	162920889	Click to see	266.29	unknown	https://doi.org/10.1016/J.BMCL.2010.10.135
3-(3,4-Dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-ol	162920888	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)O)OC	266.29	unknown	https://doi.org/10.1016/J.BMCL.2010.10.135
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Pyrrolezanthine	636825	Click to see	245.27	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3,5-dimethoxyphenyl)-	119216	Click to see COC1=CC(=CC(=C1O)OC)C=CC=O	208.21	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
Sinapaldehyde	5280802	Click to see COC1=CC(=CC(=C1O)OC)C=CC=O	208.21	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	https://doi.org/10.1021/JF950577D
> Lignans, neolignans and related compounds
(E)-3-[4-[(1R,2S)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]prop-2-enal	21582570	Click to see	374.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
3-[4-[1,3-Dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]prop-2-enal	73805566	Click to see	374.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol	11604108	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
(+-)-Pinoresinol	234817	Click to see	358.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
(+)-Eudesmin	73117	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC	386.40	unknown	https://doi.org/10.1016/J.BMCL.2010.10.135
(6R,7S,7aR)-6-[(3R,3aR,6R,6aR)-6-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-7a-[4-[(3R,3aS,6S,6aS)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-7-hydroxy-6,7-dihydro-1,3-benzodioxol-5-one	163016047	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4C(C5(C(=CC4=O)OCO5)OC6=C(C=C(C=C6)C7C8COC(C8CO7)C9=CC(=C(C=C9)O)OC)OC)O)OC	760.80	unknown	https://doi.org/10.1016/J.BMCL.2010.10.135
(6R,7S,7aR)-7a-[4-[(3R,3aS,6S,6aS)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-6-[(3R,3aS,6R,6aS)-6-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-7-hydroxy-6,7-dihydro-1,3-benzodioxol-5-one	162922328	Click to see	758.80	unknown	https://doi.org/10.1016/J.BMCL.2010.10.135
1,4-Bis(3,4-dimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan	234823	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC	386.40	unknown	https://doi.org/10.1016/J.BMCL.2010.10.135
4-[(3R,3aS,6S,6aS)-6-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]benzene-1,2-diol	163009208	Click to see	358.40	unknown	https://doi.org/10.1016/J.BMCL.2010.10.135
4-[6-(3,4-Dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]benzene-1,2-diol	163009207	Click to see	358.40	unknown	https://doi.org/10.1016/J.BMCL.2010.10.135
6-[6-(3,4-Dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-7-hydroxy-7a-[4-[3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-6,7-dihydro-1,3-benzodioxol-5-one	75586977	Click to see	760.80	unknown	https://doi.org/10.1016/J.BMCL.2010.10.135
7a-[4-[3-(1,3-Benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-6-[6-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-7-hydroxy-6,7-dihydro-1,3-benzodioxol-5-one	75586978	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4C(C5(C(=CC4=O)OCO5)OC6=C(C=C(C=C6)C7C8COC(C8CO7)C9=CC1=C(C=C9)OCO1)OC)O)OC	758.80	unknown	https://doi.org/10.1016/J.BMCL.2010.10.135
Kobusin	182278	Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC	370.40	unknown	via CMAUP database
Pinoresinol	73399	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
Syringaresinol	100067	Click to see	418.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
Syringaresinol, (+)-	443023	Click to see	418.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(3,4-Dimethoxyphenyl)-[5-(3,4-dimethoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methanone	85045677	Click to see	402.40	unknown	https://doi.org/10.1016/J.BMCL.2010.10.135
Magnone A	9822388	Click to see	402.40	unknown	https://doi.org/10.1016/J.BMCL.2010.10.135
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
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	https://doi.org/10.1021/NP50111A003
> Lignans, neolignans and related compounds / Lignan lactones
(3R,3aS,6aS)-3-(4-hydroxy-3-methoxyphenyl)-3,3a,4,6a-tetrahydro-1H-furo[3,4-c]furan-6-one	162923974	Click to see	250.25	unknown	https://doi.org/10.1016/J.BMCL.2010.10.135
4-(4-hydroxy-3-methoxyphenyl)-tetrahydro-3H-furo[3,4-c]furan-1-one	14502655	Click to see COC1=C(C=CC(=C1)C2C3COC(=O)C3CO2)O	250.25	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6 https://doi.org/10.1016/J.BMCL.2010.10.135
> 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/JF950577D
Neryl acetate	1549025	Click to see	196.29	unknown	https://doi.org/10.1021/JF950577D
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octanol	957	Click to see CCCCCCCCO	130.23	unknown	https://doi.org/10.1021/JF950577D
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2Z,6E,8E,10E)-N-(2-methylpropyl)dodeca-2,6,8,10-tetraenamide	5321101	Click to see	247.38	unknown	via CMAUP database
Sanshool	6440935	Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)C	247.38	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S,4aR,8S,8aS)-8-[(3S)-3-hydroxy-3-methylpent-4-enyl]-4,4,7,8a-tetramethyl-1,2,3,4a,5,8-hexahydronaphthalen-2-ol	162909647	Click to see	306.50	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
8-(3-Hydroxy-3-methylpent-4-enyl)-4,4,7,8a-tetramethyl-1,2,3,4a,5,8-hexahydronaphthalen-2-ol	14355862	Click to see CC1=CCC2C(CC(CC2(C1CCC(C)(C=C)O)C)O)(C)C	306.50	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(+)-Linalyl acetate	6999980	Click to see	196.29	unknown	via CMAUP database
beta-OCIMENE, (3E)-	5281553	Click to see	136.23	unknown	https://doi.org/10.1021/JF950577D
beta-Ocimene, (3Z)-	5320250	Click to see	136.23	unknown	https://doi.org/10.1021/JF950577D
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1021/JF950577D
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1021/JF950577D
Linalool formate	61040	Click to see	182.26	unknown	https://doi.org/10.1021/JF950577D
Linalyl Acetate	8294	Click to see	196.29	unknown	https://doi.org/10.1021/JF950577D
Linalyl acetate, (-)-	442474	Click to see	196.29	unknown	via CMAUP database
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1021/JF950577D
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-(3,7-Dimethylocta-1,6-dien-3-yl)benzoate	22447367	Click to see CC(=CCCC(C)(C=C)C1=CC=CC=C1C(=O)[O-])C	257.35	unknown	via CMAUP database
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1021/JF950577D
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1021/JF950577D
Beta-Pinene	14896	Click to see	136.23	unknown	https://doi.org/10.1021/JF950577D
Camphene	6616	Click to see	136.23	unknown	https://doi.org/10.1021/JF950577D
Sabinene	18818	Click to see	136.23	unknown	https://doi.org/10.1021/JF950577D
Umbellulol	561871	Click to see	152.23	unknown	https://doi.org/10.1021/JF950577D
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1021/JF950577D
Alpha-Terpinene	7462	Click to see	136.23	unknown	https://doi.org/10.1021/JF950577D
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1021/JF950577D
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1021/JF950577D
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1021/JF950577D
Terpinolene	11463	Click to see	136.23	unknown	https://doi.org/10.1021/JF950577D
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(E,Z)-farnesol	1549109	Click to see CC(=CCCC(=CCCC(=CCO)C)C)C	222.37	unknown	https://doi.org/10.1021/JF950577D
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane	14350	Click to see	220.35	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
a Farnesol	3327	Click to see	222.37	unknown	https://doi.org/10.1021/JF950577D
alpha-Santalal	5321103	Click to see CC(=CCCC1(C2CC3C1(C3C2)C)C)C=O	218.33	unknown	via CMAUP database
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/JF950577D
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1021/JF950577D
Caryophyllene oxide	1742210	Click to see	220.35	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
delta-Cadinene	441005	Click to see	204.35	unknown	https://doi.org/10.1021/JF950577D
Humulene	5281520	Click to see	204.35	unknown	https://doi.org/10.1021/JF950577D
Zingiberene	92776	Click to see CC1=CCC(C=C1)C(C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1021/JF950577D
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
(S)-2-trans-abscisic acid	5702609	Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C	264.32	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
5-(1-Hydroxy-2,6,6-trimethyl-4-oxo-2-cyclohexen-1-yl)-3-methyl-2,4-pentadienoic acid	287291	Click to see	264.32	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
Abscisic Acid	5280896	Click to see	264.32	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(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	220.35	unknown	https://doi.org/10.1021/JF950577D
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	5321422	Click to see	220.35	unknown	https://doi.org/10.1021/JF950577D
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl)propan-2-ol	547972	Click to see	222.37	unknown	https://doi.org/10.1021/JF950577D
Elemol	92138	Click to see	222.37	unknown	https://doi.org/10.1021/JF950577D
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene	91723653	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1021/JF950577D
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1021/JF950577D
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Amyrenol	225689	Click to see	426.70	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6 https://doi.org/10.1016/S0031-9422(97)00280-X
beta-Amyrone	12306160	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C	424.70	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,4S,10S,12R)-7-(furan-3-yl)-10-hydroxy-1,8,12,17,17-pentamethyl-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-ene-5,15,20-trione	5315428	Click to see	470.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
(8S,9S,10R,13R,14S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,4,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one	5490292	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
14-(5-Ethyl-6-methylheptan-2-yl)-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-9-one	14779505	Click to see	428.70	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
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	https://doi.org/10.1016/S0031-9422(97)00280-X https://doi.org/10.1016/S0031-9422(02)00268-6
3-Hydroxystigmast-5-en-7-one	160608	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C	428.70	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
3-Oxo-24-ethyl-cholest-5-ene	4358735	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
beta-Sitostenone	60123241	Click to see	412.70	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X
beta-Sitosterone	9801811	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X https://doi.org/10.1016/S0031-9422(02)00268-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Heptyl acetate	8159	Click to see CCCCCCCOC(=O)C	158.24	unknown	https://doi.org/10.1021/JF950577D
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
2-Cyclopenten-1-one, 4-hydroxy-3-methyl-2-(2-propen-1-yl)-	11083	Click to see	152.19	unknown	https://doi.org/10.1021/JF950577D
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Ganodine	126543	Click to see C1=CC=C(C=C1)CCN2C(=CC=C2C=O)CO	229.27	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Methylhept-2-enal	534702	Click to see CCCCC=C(C)C=O	126.20	unknown	https://doi.org/10.1021/JF950577D
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
Bicyclo(3.1.0)hexan-2-one, 5-(1-methylethyl)-	92784	Click to see	138.21	unknown	https://doi.org/10.1021/JF950577D
> Organoheterocyclic compounds / Indoles and derivatives
CID 44584549	44584549	Click to see	342.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxazinanes / Morpholines
(1R,2S,4S,5S)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-ol	12110650	Click to see	155.19	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Zanthopyranone	10419590	Click to see	170.16	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
> Organoheterocyclic compounds / Quinolines and derivatives
Toddaquinoline	11390791	Click to see C1OC2=C(O1)C=C3C(=C2)C=CC4=CC(=CN=C43)O	239.23	unknown	https://doi.org/10.1016/0031-9422(95)00856-X https://doi.org/10.1021/NP50111A003
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
Arborinine	5281832	Click to see CN1C2=CC=CC=C2C(=O)C3=C(C(=C(C=C31)OC)OC)O	285.29	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
1,2-Dimethoxy-13-methyl[1,3]benzodioxolo[5,6-c]phenanthridine	101673185	Click to see	347.40	unknown	via CMAUP database
Avicine	356657	Click to see	332.30	unknown	https://doi.org/10.1021/NP50111A003
Decarine	179640	Click to see COC1=C(C=CC2=C3C=CC4=CC5=C(C=C4C3=NC=C21)OCO5)O	319.30	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X https://doi.org/10.1016/0031-9422(95)00856-X https://doi.org/10.1016/S0031-9422(00)90870-7 https://doi.org/10.1021/NP50111A003
Norchelerythrine	443719	Click to see COC1=C(C2=CN=C3C(=C2C=C1)C=CC4=CC5=C(C=C43)OCO5)OC	333.30	unknown	https://doi.org/10.1021/NP50111A003 https://doi.org/10.1016/S0031-9422(00)90870-7 https://doi.org/10.1016/0031-9422(95)00856-X https://doi.org/10.1016/S0031-9422(97)00280-X https://doi.org/10.1016/S0031-9422(00)97045-6
Oxychelerythrine	147279	Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=C(C1=O)C(=C(C=C5)OC)OC	363.40	unknown	https://doi.org/10.1016/0031-9422(95)00856-X https://doi.org/10.1021/NP50111A003
> Organoheterocyclic compounds / Quinolines and derivatives / Dihydrofuranoquinolines
2-(4-Methoxy-2,3-dihydrofuro[2,3-b]quinolin-2-yl)propan-2-ol	12314372	Click to see CC(C)(C1CC2=C(C3=CC=CC=C3N=C2O1)OC)O	259.30	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
2-[(2S)-4-methoxy-2,3-dihydrofuro[2,3-b]quinolin-2-yl]propan-2-ol	12314371	Click to see	259.30	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
Platydesmine	6451457	Click to see CC(C)(C1CC2=C(C3=CC=CC=C3N=C2O1)OC)O	259.30	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
4,8-dimethoxy-9H-furo[2,3-b]quinolin-7-one	165368	Click to see COC1=C2C=CC(=O)C(=C2NC3=C1C=CO3)OC	245.23	unknown	https://doi.org/10.1016/S0031-9422(00)97045-6 https://doi.org/10.1016/S0031-9422(02)00268-6
8-Hydroxydictamnine	164950	Click to see	215.20	unknown	https://doi.org/10.1016/S0031-9422(00)97045-6 https://doi.org/10.1016/S0031-9422(02)00268-6 https://doi.org/10.1016/S0031-9422(97)00280-X https://doi.org/10.1021/NP50111A003
Dictamnine	68085	Click to see	199.20	unknown	https://doi.org/10.1016/0031-9422(95)00856-X https://doi.org/10.1021/NP50111A003 https://doi.org/10.1016/S0031-9422(00)97045-6
Gamma-Fagarine	107936	Click to see	229.23	unknown	https://doi.org/10.1016/0031-9422(95)00856-X https://doi.org/10.1021/NP50111A003 https://doi.org/10.1016/S0031-9422(02)00268-6 https://doi.org/10.1016/S0031-9422(00)97045-6 https://doi.org/10.1016/S0031-9422(97)00280-X
Haplopine	5281846	Click to see COC1=C2C=COC2=NC3=C1C=CC(=C3OC)O	245.23	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6 https://doi.org/10.1016/S0031-9422(00)97045-6
Skimmianine	6760	Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC	259.26	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X https://doi.org/10.1016/0031-9422(95)00856-X https://doi.org/10.1016/S0031-9422(00)97045-6 https://doi.org/10.1021/NP50111A003 https://doi.org/10.1016/S0031-9422(00)90870-7 https://doi.org/10.1016/S0031-9422(02)00268-6
> Organoheterocyclic compounds / Quinolines and derivatives / Hydroxyquinolines
Zanthobisquinolone	54688597	Click to see	362.40	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methyl-3-(3-methylbuta-1,3-dienyl)quinolin-2-one	162951935	Click to see	255.31	unknown	https://doi.org/10.1002/JLAC.199319930160
4-Methoxy-1H-quinolin-2-one	600167	Click to see	175.18	unknown	https://doi.org/10.1016/0031-9422(95)00856-X
4-Methoxy-3-(3-methyl-1,3-butadienyl)-2(1H)-quinolinone	131752802	Click to see	241.28	unknown	https://doi.org/10.1002/JLAC.199319930160
4-methoxy-3-(3-methylbuta-1,3-dienyl)-1H-quinolin-2-one	162979372	Click to see CC(=C)C=CC1=C(C2=CC=CC=C2NC1=O)OC	241.28	unknown	https://doi.org/10.1002/JLAC.199319930160
4-methoxy-N-methyl-2-quinolone	182073	Click to see	189.21	unknown	via CMAUP database
Edulitine	826073	Click to see COC1=CC=CC2=C1NC(=O)C=C2OC	205.21	unknown	https://doi.org/10.1016/S0031-9422(00)97045-6 https://doi.org/10.1016/S0031-9422(97)00280-X
N-Methylschinifoline	101652163	Click to see CC(=C)C=CC1=C(C2=CC=CC=C2N(C1=O)C)OC	255.31	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
(+)-2,6-Dihydro-2-(4-hydroxy-4-methyl-2-penten-1-yl)-2,6-dimethyl-5H-pyrano[3,2-c]quinolin-5-one	78385470	Click to see	325.40	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X
(2R)-2-[(3R)-3-hydroxy-4-methylpentyl]-2,6-dimethylpyrano[3,2-c]quinolin-5-one	162864468	Click to see CC(C)C(CCC1(C=CC2=C(O1)C3=CC=CC=C3N(C2=O)C)C)O	327.40	unknown	https://doi.org/10.1016/0031-9422(95)00856-X
(2R)-2-[(E)-4-hydroperoxy-4-methylpent-2-enyl]-2,6-dimethylpyrano[3,2-c]quinolin-5-one	162891540	Click to see	341.40	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X
(2S)-2-[(E)-4-hydroxy-4-methylpent-2-enyl]-2,6-dimethylpyrano[3,2-c]quinolin-5-one	162962479	Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3N(C2=O)C)CC=CC(C)(C)O	325.40	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X
(2S)-2,6-dimethyl-2-(4-methyl-3-oxopentyl)pyrano[3,2-c]quinolin-5-one	163065193	Click to see CC(C)C(=O)CCC1(C=CC2=C(O1)C3=CC=CC=C3N(C2=O)C)C	325.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6 https://doi.org/10.1016/S0031-9422(00)90870-7
(2S)-2,6-dimethyl-2-(4-methylpent-3-enyl)pyrano[3,2-c]quinolin-5-one	162884484	Click to see CC(=CCCC1(C=CC2=C(O1)C3=CC=CC=C3N(C2=O)C)C)C	309.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
(3R,4S)-3,4-dihydroxy-7-methoxy-2,2,6-trimethyl-3,4-dihydropyrano[3,2-c]quinolin-5-one	163025327	Click to see	305.32	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
(3S)-3-hydroxy-2,2,10-trimethyl-3,4-dihydropyrano[2,3-b]quinolin-5-one	932818	Click to see	259.30	unknown	via CMAUP database
2,6-Dihydro-2-(4-hydroperoxy-4-methyl-2-penten-1-yl)-2,6-dimethyl-5H-pyrano[3,2-c]quinolin-5-one	162891539	Click to see	341.40	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X
2,6-Dimethyl-2-(4-methyl-3-oxopentyl)-3,4-dihydropyrano[3,2-c]quinolin-5-one	44559731	Click to see	327.40	unknown	via CMAUP database
2,6-Dimethyl-2-(4-methylpent-3-enyl)-3,4-dihydropyrano[3,2-c]quinolin-5-one	44559726	Click to see CC(=CCCC1(CCC2=C(O1)C3=CC=CC=C3N(C2=O)C)C)C	311.40	unknown	via CMAUP database
5H-Pyrano[3,2-c]quinolin-5-one, 2,6-dihydro-2,6-dimethyl-2-(4-methyl-3-oxopentyl)-	5318093	Click to see CC(C)C(=O)CCC1(C=CC2=C(O1)C3=CC=CC=C3N(C2=O)C)C	325.40	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X https://doi.org/10.1021/NP50111A003 https://doi.org/10.1016/S0031-9422(00)90870-7 https://doi.org/10.1016/S0031-9422(02)00268-6
6,6,12-Trimethylisochromeno[4,3-c]quinolin-11-one	10017165	Click to see	291.30	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6 https://doi.org/10.1016/S0031-9422(97)00280-X
7-Methoxyflindersine	101995295	Click to see CC1(C=CC2=C(O1)C3=C(C=C(C=C3)OC)NC2=O)C	257.28	unknown	https://doi.org/10.1016/0031-9422(95)00856-X
8-Methoxy-2,2,6-trimethylpyrano[3,2-c]quinolin-5-one	14166105	Click to see CC1(C=CC2=C(O1)C3=C(C=C(C=C3)OC)N(C2=O)C)C	271.31	unknown	https://doi.org/10.1016/0031-9422(95)00856-X
8-Methoxyflindersine	14166104	Click to see	257.28	unknown	https://doi.org/10.1016/0031-9422(95)00856-X https://doi.org/10.1002/JLAC.199319930160
Benzosimuline	5321951	Click to see	305.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6 https://doi.org/10.1016/S0031-9422(97)00280-X
Flindersine	68230	Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3NC2=O)C	227.26	unknown	https://doi.org/10.1002/JLAC.199319930160 https://doi.org/10.1016/S0031-9422(02)00268-6
N-Acetoxymethylflindersine	11289552	Click to see CC(=O)OCN1C2=CC=CC=C2C3=C(C1=O)C=CC(O3)(C)C	299.32	unknown	https://doi.org/10.1002/JLAC.199319930160
N-Methylflindersine	72819	Click to see	241.28	unknown	https://doi.org/10.1002/JLAC.199319930160 https://doi.org/10.1021/NP50111A003
Peroxysimulenoline	101936038	Click to see	341.40	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X
Rel-zanthodioline	5315424	Click to see CC1(C(C(C2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)O)O)C	305.32	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6 https://doi.org/10.1016/S0031-9422(97)00280-X
Simulansine	5321315	Click to see	327.40	unknown	https://doi.org/10.1016/0031-9422(95)00856-X
Simulenoline	5321316	Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3N(C2=O)C)CC=CC(C)(C)O	325.40	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X
Zanthobungeanine	5315422	Click to see	271.31	unknown	https://doi.org/10.1002/JLAC.199319930160 https://doi.org/10.1016/S0031-9422(02)00268-6 https://doi.org/10.1055/S-2006-961713 https://doi.org/10.1016/S0031-9422(00)90870-7 https://doi.org/10.1016/S0031-9422(97)00280-X
Zanthodioline	78384601	Click to see CC1(C(C(C2=C(O1)C3=C(C(=CC=C3)OC)N(C2=O)C)O)O)C	305.32	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6 https://doi.org/10.1016/S0031-9422(97)00280-X
Zanthosimuline	5315426	Click to see CC(=CCCC1(C=CC2=C(O1)C3=CC=CC=C3N(C2=O)C)C)C	309.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6 https://doi.org/10.1016/S0031-9422(00)90870-7 https://doi.org/10.1016/S0031-9422(97)00280-X https://doi.org/10.1021/NP50111A003
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Simulanol	636826	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)O)OC)C=CCO	388.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
(+)-Simulanol	52918181	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)O)OC)C=CCO	388.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
(+/-)-Balanophonin	72729357	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O	356.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
4-[3-(Hydroxymethyl)-5-(3-hydroxyprop-1-enyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2,6-dimethoxyphenol	73880631	Click to see	388.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
Balanophonin	23252258	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O	356.40	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Tetracosyl ferulate	14238617	Click to see	530.80	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone	8417	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC	206.19	unknown	https://doi.org/10.1016/S0031-9422(97)00280-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Isofraxidin	5318565	Click to see	222.19	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6
Scopoletin	5280460	Click to see	192.17	unknown	https://doi.org/10.1016/S0031-9422(02)00268-6

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Zanthoxylum simulans

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