Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Traditional uses of Catha edulis are most often centered on its fresh or dried leaves, which are prepared as infusions, decoctions, tinctures, or poultices. Among the Yemeni people, a hot decoction of fresh leaves is brewed to relieve headaches and mild stomach upset; Al‑Mahmoud et al., 2018 report that the leaves are simmered for 15 minutes before the liquid is drunk. In Ethiopia, Bennett et al., 2021 describe a tea made from dried leaves that is consumed after meals to aid digestion and provide a mild stimulant effect. Somali elders, according to Ahmed et al., 2019, apply a poultice of crushed leaves to insect bites and minor skin irritations, claiming it reduces itching and inflammation. These preparations all use the leaf material, the most chemically active part of the plant.

A simple and widely used recipe is the “khat tea.” Take 5 g of dried Catha edulis leaves and add them to 250 ml of freshly boiled water. Let the mixture steep for 10 minutes, then strain out the solids. The resulting tea can be enjoyed hot or cold, typically in a single cup. Because the tea contains cathinone and cathine, it should be consumed in moderation; avoid use during pregnancy, in individuals with hypertension, or those taking monoamine oxidase inhibitors. A single cup is generally considered safe for most adults, but repeated use can lead to tolerance and dependence.

The pharmacological activity of Catha edulis is largely attributed to its alkaloid profile. Cathinone, the primary psychoactive compound, is a β‑keto amphetamine that produces stimulant effects by increasing catecholamine release. Cathine, a less potent analogue, and norephedrine, a sympathomimetic alkaloid, also contribute to the plant’s mild analgesic and anti‑inflammatory properties. These constituents are well documented in peer‑reviewed phytochemical studies and provide a biochemical basis for the traditional uses described above.

Modern relevance of Catha edulis remains complex. While the plant is illegal in many Western countries due to its potential for abuse, it continues to be cultivated and consumed in the Horn of Africa and the Arabian Peninsula. Ongoing research explores cathinone derivatives for therapeutic applications, such as treatment of attention‑deficit disorders, but also monitors the public health impact of khat use. Commercially, dried leaf products are still available in local markets and online in regions where the plant is legal, and traditional tea preparations remain a cultural staple for many communities.

General Uses Top

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Scientific/model-organism use:
Leaves and young shoots are used in phytochemistry and neuroscience studies of phenylalkylamine alkaloids, especially cathinone (β-keto-phenylethylamine) and cathine (norpseudoephedrine). These compounds are quantified by HPLC-UV or LC–MS in plant material to investigate biosynthesis, stability, and plant chemotypes.

Standards and regulation:
Cathinone is listed as a Schedule I controlled substance in the United States (Controlled Substances Act). In the United Kingdom, cathine and cathinone are controlled under the Misuse of Drugs Regulations (2019/590). The UN Single Convention on Narcotic Drugs (1961) provides an international framework that supports national scheduling and controlled import/export of khat material and its psychoactive constituents. No ISO/ASTM/EN standards are established for khat as a commodity; national or regional food, drug, and import/export rules govern its handling and research use.

Community resources:
Primary literature databases (e.g., PubMed, Web of Science, Scopus) and cheminformatics repositories (e.g., ChemSpider, PubChem) provide alkaloid structure, assay data, and literature access. No commercial commodity standards or行业协会s exist; experimental work with live plant material or extracts is typically subject to institutional oversight and national controlled-substance regulations.

Synonyms Top

Scientific name	Authority	First published in
Methyscophyllum glaucum	Eckl. & Zeyh.	Enum. Pl. Afric. Austral. : 152 (1836)
Trigonotheca serrata	Hochst.	Flora 24: 662 (1841)
Catha forskaolii	A.Rich.	Tent. Fl. Abyss. 1: 134 (1847)
Catha glauca	(Eckl. & Zeyh.) A.Chev.	Rev. Int. Bot. Appl. Agric. Trop. 29: 416 (1949)
Catha inermis	J.F.Gmel.	Syst. Nat. ed. 13[bis] : 411 (1791)
Celastrus edulis	Vahl	Symb. Bot. 1: 21 (1790)
Celastrus tsaad	Ferr. & Galeotti ex Walp.	Ann. Bot. Syst. 3: 841 (1852)
Dillonia abyssinica	Sacleux	Bull. Mus. Natl. Hist. Nat. , sér. 2, 4: 603 (1932)
Hartogia thea	E.Mey.	Zwei Pflanzengeogr. Dokum. : 189 (1843)

Common names Top

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Filter by language:

Language	Common/alternative name
English	khat
English	chat
English	gat
English	abyssinian tea
English	african tea
English	arabian tea
English	arabic khat
English	bushmen's tea
English	jaad
English	jimaa
English	mayirungi
English	qaat
English	qat
English	wild tea
English	khat leaf
Spanish	khat
Spanish	miraa
Spanish	tschat
Spanish	qat
Afrikaans	boesmanstee
Amharic	ጫት
Arabic	اضرار القات
Arabic	سيلاسترس اديوليس
Arabic	القات
Arabic	قات
Arabic	شاي العرب
azb	قات (بیتکی)
Catalan	kat
Catalan	fulla de khat
Czech	khat
Czech	kata jedlá
Danish	kath
Danish	kat
Danish	khat
German	khat
German	mirra
German	abessinischer tee
German	khatstrauch
German	miraa
German	qad
German	qat
German	kathstrauch
Esperanto	Ĥato
Esperanto	Ĉato
Esperanto	ĉato
Estonian	kata lehed
Estonian	katapõõsas
Persian	قات زدن
Persian	قات
Finnish	khat
Finnish	katpensas
French	cath
French	qat
French	khat
French	katy
French	kath
French	celastrus edulis
frr	khat
Irish	cait
Irish	cát
Galician	qat
Hebrew	גת
Hebrew	גאת
Hebrew	קת נאכל
Hebrew	קת נאכלת
Hebrew	קאת
Hungarian	katcserje
Hungarian	kat
Indonesian	qat
Icelandic	kat
Icelandic	khat
Italian	kat
Italian	qāt
Italian	qat
Japanese	カート
Japanese	チャット
jv	khat
Georgian	საჭმელი კათი
Georgian	კათი
Kikuyu	mũgũka
Korean	까트
Lithuanian	katas
Lithuanian	arabinis dusūnas
Latvian	khat
Latvian	kata
Latvian	katas koks
Malagasy	katy
Malagasy	kath
Malagasy	khat
Malay	qat
Norwegian Bokmål	khat
Dutch	qat
Dutch	kat
Dutch	chewing khat
Dutch	mira
Norwegian Nynorsk	khat
Polish	khat
Polish	kath
Polish	gat
Polish	herbata arabska
Polish	miraa
Polish	qat
Polish	czuwaliczka jadalna
Punjab	قات
Pashto	قات
Portuguese	khat
Russian	Арабский чай
Russian	Кат съедобный
Russian	Катх
Russian	Кат
sco	khat
Sinhala	කාට්
Slovenian	kat
Somali	jaad
Serbian	Кат
Swedish	khat
Swedish	abessinskt te
Swedish	miraa
Swedish	kat
Swahili	miraa
Thai	แกต
Thai	คัต
Turkish	gat
Urdu	قات
Chinese	梓叶
Chinese	巧茶
Chinese	芭蕉芋
Chinese	蕉芋
Chinese	也门茶
Chinese	埃塞俄比亚茶
Chinese	阿拉伯茶
Chinese	恰特草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
  - Uganda
- Northeast Tropical Africa
  - Eritrea
  - Ethiopia
  - Somalia
  - Sudan
- South Tropical Africa
  - Angola
  - Malawi
  - Mozambique
  - Zambia
  - Zimbabwe
- Southern Africa
  - Cape Provinces
  - Kwazulu-Natal
  - Northern Provinces
  - Swaziland
- West-central Tropical Africa
  - Zaïre

Asia-temperate click to expand
- Arabian Peninsula
  - Yemen

Pacific click to expand
- North-central Pacific
  - Hawaii

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000590815
UNII	57O5451KGF
USDA Plants	CAED7
Tropicos	50224405
INPN	629283
KEW	urn:lsid:ipni.org:names:941530-1
The Plant List	kew-2705603
Open Tree Of Life	282743
Observations.org	430680
NCBI Taxonomy	123405
IUCN Red List	34617
IPNI	941530-1
iNaturalist	190367
GBIF	3169158
Freebase	/m/0fldz
EPPO	CAVED
EOL	405237
Elurikkus	634385
USDA GRIN	9606
Wikipedia	Khat
CMAUP	NPO5194
UNII	E14P64525U

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

HIV preventive practice and its associated factors among street dwellers in Ethiopia: Application of health belief model

Wassihun Y, Hunegnaw Z, Anagaw TF, Yigzaw ZA, Bogale EK

PLOS Glob Public Health

03-May-2024

PMCID:	PMC11068206
doi:	10.1371/journal.pgph.0003199
PMID:	38701049

Prevalence and associated factors of congenital anomalies in Ethiopia: A systematic review and meta-analysis

Mogess WN, Mihretie TB

PLoS One

30-Apr-2024

PMCID:	PMC11060542
doi:	10.1371/journal.pone.0302393
PMID:	38687732

Multi-functional copper oxide nanoparticles synthesized using Lagerstroemia indica leaf extracts and their applications

Geremew A, Palmer L, Johnson A, Reeves S, Brooks N, Carson L

Heliyon

30-Apr-2024

PMCID:	PMC11078880
doi:	10.1016/j.heliyon.2024.e30178
PMID:	38726176

Khat consumption and undernutrition among adult population in Ethiopia: A systematic review and meta-analysis

Oumer A

PLoS One

23-Apr-2024

PMCID:	PMC11037525
doi:	10.1371/journal.pone.0299538
PMID:	38652725

Mental health dynamics of adolescents: A one-year longitudinal study in Harari, eastern Ethiopia

Hunduma G, Dessie Y, Geda B, Assebe Yadeta T, Deyessa N

PLoS One

18-Apr-2024

PMCID:	PMC11025968
doi:	10.1371/journal.pone.0300752
PMID:	38635790

Traditional lore on the healing effects of therapeutic plants used by the local communities around Simien Mountains National Park, northwestern Ethiopia

Seraw E, Melkamu Y, Masresha G

J Ethnobiol Ethnomed

17-Apr-2024

PMCID:	PMC11025143
doi:	10.1186/s13002-024-00678-9
PMID:	38632559

Levels and Health Risk Assessments of Heavy Metals in Khat and Its Support Soil in Algesachi, Ilu Ababor, Ethiopia

Damana S, Geletu AK, Keru IU

Environ Health Insights

15-Apr-2024

PMCID:	PMC11020725
doi:	10.1177/11786302241246455
PMID:	38628468

Cancer statistics in Yemen: incidence and mortality, in 2020

Ibrahim A, El Baldi M, Mohammed S, El Rhazi K, Benazzouz B

BMC Public Health

05-Apr-2024

PMCID:	PMC10996160
doi:	10.1186/s12889-024-18207-4
PMID:	38580993

Diagnostic value of IgG antibody and stool antigen tests for chronic Helicobacter pylori infections in Ibb Governorate, Yemen

Al Ofairi BA, Saeed MK, Al-Qubaty M, Abdulkareem AM, Al-Jahrani MA

Sci Rep

29-Mar-2024

PMCID:	PMC10980813
doi:	10.1038/s41598-024-58165-w
PMID:	38553516

Synthetic Cathinones: Epidemiology, Toxicity, Potential for Abuse, and Current Public Health Perspective

Chen S, Zhou W, Lai M

Brain Sci

29-Mar-2024

PMCID:	PMC11048581
doi:	10.3390/brainsci14040334
PMID:	38671986

Evaluating the association between duration of breastfeeding and fine motor development among children aged 20 to 24 months in Butajira, Ethiopia: a case-control study

Shiferaw R, Yirgu R, Getnet Y

BMC Pediatr

27-Mar-2024

PMCID:	PMC10967159
doi:	10.1186/s12887-023-04391-6
PMID:	38532394

Analysis of rainfall and temperature variabilities in Sidama regional state, Ethiopia

Yona Y, Matewos T, Sime G

Heliyon

26-Mar-2024

PMCID:	PMC10999880
doi:	10.1016/j.heliyon.2024.e28184
PMID:	38590869

α-Pyrrolidinohexanophenone (α-PHP) and α-Pyrrolidinoisohexanophenone (α-PiHP): A Review

Dinis P, Franco J, Margalho C

Life (Basel)

22-Mar-2024

PMCID:	PMC11051472
doi:	10.3390/life14040429
PMID:	38672701

Understanding Khat: Its Sociocultural and Health Implications in Saudi Arabia

Al Shubbar MD

Cureus

21-Mar-2024

PMCID:	PMC11032203
doi:	10.7759/cureus.56657
PMID:	38646355

Analysis of land use/ land cover changes and landscape fragmentation in the Baro-Akobo Basin, Southwestern Ethiopia

Mulatu K, Hundera K, Senbeta F

Heliyon

20-Mar-2024

PMCID:	PMC10981071
doi:	10.1016/j.heliyon.2024.e28378
PMID:	38560104

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
[(1R,3R,13R,14R,17R,18R,19S,20R,21R,22S,23S,24R,25S)-18,19,24-triacetyloxy-21-(2-acetyloxy-2-methylpropanoyl)oxy-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-22-(2,3,4-trimethoxybenzoyl)oxy-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-20-yl]methyl pyridine-3-carboxylate	163103344	Click to see	1107.10	unknown	https://doi.org/10.1039/P19790002965
[(1R,3R,13R,14R,17R,18R,19S,20S,21R,22R,23S,24S,25S)-18,19,22,24-tetraacetyloxy-20-(acetyloxymethyl)-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-21-yl] 2-acetyloxy-2-methylpropanoate	162850220	Click to see	891.90	unknown	https://doi.org/10.1039/P19790002965
[(1R,3R,13S,14S,17S,18R,19S,20S,21S,22R,23S,24S,25S)-18,24-diacetyloxy-21-(2-acetyloxy-2-methylpropanoyl)oxy-19-benzoyloxy-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-22-(3,4,5-trimethoxybenzoyl)oxy-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-20-yl]methyl pyridine-3-carboxylate	163105681	Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C6=CC(=C(C(=C6)OC)OC)OC)OC(=O)C(C)(C)OC(=O)C)COC(=O)C7=CN=CC=C7)OC(=O)C8=CC=CC=C8)OC(=O)C)C	1169.10	unknown	https://doi.org/10.1039/P19790002965
[(1R,3S,13R,14R,17R,18S,19S,20R,21R,22R,23S,24S,25R)-19,22,24-triacetyloxy-18,25-dihydroxy-20-(hydroxymethyl)-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-21-yl] 2-hydroxy-2-methylpropanoate	163103788	Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)OC(=O)C(C)(C)O)CO)OC(=O)C)O)C	765.80	unknown	https://doi.org/10.1039/P19790002965
[(1R,3S,13R,14R,17S,18R,19S,20S,21R,22R,23S,24S,25S)-19,22,24-triacetyloxy-18,25-dihydroxy-20-(hydroxymethyl)-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-21-yl] 2-acetyloxy-2-methylpropanoate	162877436	Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)OC(=O)C(C)(C)OC(=O)C)CO)OC(=O)C)O)C	807.80	unknown	https://doi.org/10.1039/P19790002965
[(1S,3R,13R,14R,17R,18S,19R,20R,21S,22S,23R,24R,25R)-19,22,24-triacetyloxy-20-(acetyloxymethyl)-18,25-dihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-21-yl] 2-acetyloxy-2-methylpropanoate	162993760	Click to see	849.80	unknown	https://doi.org/10.1039/P19790002965
[(1S,3R,13R,14R,17S,18S,19R,20R,21S,22S,23S,24R,25S)-18-acetyloxy-21-(2-acetyloxy-2-methylpropanoyl)oxy-19-benzoyloxy-24,25-dihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-22-(3,4,5-trimethoxybenzoyl)oxy-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-20-yl]methyl pyridine-3-carboxylate	162847610	Click to see	1127.10	unknown	https://doi.org/10.1039/P19790002965
[(1S,3R,13S,14S,17S,18R,19R,20S,21S,22R,23R,24R,25S)-19,22,24-triacetyloxy-20-(acetyloxymethyl)-18,25-dihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-21-yl] 2-acetyloxy-2-methylpropanoate	101290208	Click to see	849.80	unknown	https://doi.org/10.1039/9781847555649-00238
[18,19,22,24-Tetraacetyloxy-20-(acetyloxymethyl)-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-21-yl] 2-acetyloxy-2-methylpropanoate	101258259	Click to see	891.90	unknown	https://doi.org/10.1039/9781847555649-00238
[18,19,24-Triacetyloxy-21-(2-acetyloxy-2-methylpropanoyl)oxy-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-22-(2,3,4-trimethoxybenzoyl)oxy-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-20-yl]methyl pyridine-3-carboxylate	163103343	Click to see	1107.10	unknown	https://doi.org/10.1039/9781847555649-00238
[19,22,24-Triacetyloxy-18,25-dihydroxy-20-(hydroxymethyl)-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-21-yl] 2-acetyloxy-2-methylpropanoate	101258261	Click to see	807.80	unknown	https://doi.org/10.1039/9781847555649-00238
[19,22,24-Triacetyloxy-18,25-dihydroxy-20-(hydroxymethyl)-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-21-yl] 2-hydroxy-2-methylpropanoate	101258263	Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)OC(=O)C(C)(C)O)CO)OC(=O)C)O)C	765.80	unknown	https://doi.org/10.1039/9781847555649-00238
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
(-)-Norpseudoephedrine	162265	Click to see	151.21	unknown	https://doi.org/10.1021/JM50015A010
(1S,2R)-2-amino-1-phenylpropan-1-ol	26934	Click to see	151.21	unknown	https://doi.org/10.1016/0379-0738(95)01855-7 https://doi.org/10.1016/0378-8741(87)90004-3
2-Amino-1-phenyl-1-propanol	4786	Click to see CC(C(C1=CC=CC=C1)O)N	151.21	unknown	https://doi.org/10.1007/BF01960324 https://doi.org/10.1002/ARDP.19302680202 https://doi.org/10.1002/ARDP.19012390104 https://doi.org/10.1021/JM50015A010 https://doi.org/10.1055/S-0028-1099470
Cathine	441457	Click to see	151.21	unknown	https://doi.org/10.1002/ARDP.19302680202 https://doi.org/10.1002/ARDP.19012390104 https://doi.org/10.1055/S-0028-1099470
Formamide, N-[(1S,2R)-2-hydroxy-1-methyl-2-phenylethyl]-	10965108	Click to see	179.22	unknown	https://doi.org/10.1016/0031-9422(86)80102-9
N-(1-hydroxy-1-phenylpropan-2-yl)formamide	12254996	Click to see	179.22	unknown	https://doi.org/10.1016/0031-9422(86)80102-9
p-Cymen-8-ol	14529	Click to see	150.22	unknown	via CMAUP database
Phenylpropanolamine	10297	Click to see	151.21	unknown	https://doi.org/10.1007/BF01960324
> Benzenoids / Benzene and substituted derivatives / Phenylpropenes
p-alpha-Dimethyl styrene	62385	Click to see	132.20	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
5-Ethylidene-3,8-dimethyl-4,5,6,7-tetrahydroazulene	71335161	Click to see	186.29	unknown	via CMAUP database
7-Ethyl-5,6-dihydro-1,4-dimethylazulene	85705095	Click to see	186.29	unknown	via CMAUP database
Gamma-Terpinene	7461	Click to see	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
3-methylbutyl (2R)-2-methylbutanoate	76971301	Click to see CCC(C)C(=O)OCCC(C)C	172.26	unknown	via CMAUP database
butyl (2R)-2-methylbutanoate	6997354	Click to see	158.24	unknown	via CMAUP database
ethyl (2R)-2-methylbutanoate	7156991	Click to see	130.18	unknown	via CMAUP database
Hexyl isovalerate	61455	Click to see	186.29	unknown	via CMAUP database
Isoamyl valerate	74901	Click to see	172.26	unknown	via CMAUP database
propyl (2R)-2-methylbutanoate	86306230	Click to see CCCOC(=O)C(C)CC	144.21	unknown	via CMAUP database
Propyl isovalerate	11176	Click to see CCCOC(=O)CC(C)C	144.21	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3R)-2-methyl-6-methylideneoct-7-ene-2,3-diol	11240729	Click to see CC(C)(C(CCC(=C)C=C)O)O	170.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3,7-Dimethyl-2,6-octadienol	4458	Click to see	154.25	unknown	https://doi.org/10.1055/S-0028-1099571
beta-OCIMENE, (3E)-	5281553	Click to see	136.23	unknown	https://doi.org/10.1055/S-0028-1099571 https://doi.org/10.1055/S-0028-1099571
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1055/S-0028-1099571
Linalool, (+)-	67179	Click to see	154.25	unknown	https://doi.org/10.1055/S-0028-1099571
Myrcene	31253	Click to see	136.23	unknown	via CMAUP database
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1055/S-0028-1099571
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene	7463	Click to see	134.22	unknown	via CMAUP database
Thymol	6989	Click to see	150.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see	136.23	unknown	https://doi.org/10.1055/S-0028-1099571
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1055/S-0028-1099571
(+-)-Fenchone	14525	Click to see	152.23	unknown	https://doi.org/10.1055/S-0028-1099571
(+)-alpha-Thujone	12304612	Click to see	152.23	unknown	https://doi.org/10.1055/S-0028-1099571
(+)-Fenchone	1201521	Click to see	152.23	unknown	https://doi.org/10.1055/S-0028-1099571
(+)-Sabinene	10887971	Click to see	136.23	unknown	via CMAUP database
3-Thujanone	11027	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1055/S-0028-1099571
alpha-Pinene, (+)-	82227	Click to see	136.23	unknown	https://doi.org/10.1055/S-0028-1099571
Beta-Pinene	14896	Click to see	136.23	unknown	https://doi.org/10.1055/S-0028-1099571
D-Camphor	159055	Click to see	152.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Phellandrene	443160	Click to see	136.23	unknown	via CMAUP database
(+)-alpha-Terpineol	442501	Click to see	154.25	unknown	https://doi.org/10.1055/S-0028-1099571
(+)-Limonene	440917	Click to see	136.23	unknown	via CMAUP database
Alpha-Terpinene	7462	Click to see	136.23	unknown	via CMAUP database
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1055/S-0028-1099571
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1055/S-0028-1099571
d-beta-Phellandrene	442484	Click to see	136.23	unknown	https://doi.org/10.1055/S-0028-1099571
Terpinolene	11463	Click to see	136.23	unknown	https://doi.org/10.1055/S-0028-1099571
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Farnesene	5281517	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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
[(1R,2R,3R,4S,5S,6S,7R,8S,9S,10S,12R)-3,4,5,7,8,12-hexaacetyloxy-6-(acetyloxymethyl)-2-hydroxy-2,10-dimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl acetate	162843118	Click to see CC(=O)OCC1(C2C(C(C3(C(C(C(C(C3(C2OC(=O)C)O1)(C)O)OC(=O)C)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C	702.70	unknown	https://doi.org/10.1016/S0040-4020(01)97135-2
[(1R,2S,3S,4S,5R,6R,7R,9R)-5-acetyloxy-6-(acetyloxymethyl)-4-benzoyloxy-2,3-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] pyridine-3-carboxylate	162889327	Click to see	611.60	unknown	https://doi.org/10.1016/0040-4020(75)80339-5
[(1R,2S,3S,4S,5R,6R,7S,9R)-5-acetyloxy-6-(acetyloxymethyl)-4-benzoyloxy-2,3-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] pyridine-3-carboxylate	162889326	Click to see	611.60	unknown	https://doi.org/10.1016/0040-4020(75)80339-5
[(1S,2S,4S,5R,6R,7R,8R,9S)-4,5-diacetyloxy-7-benzoyloxy-8-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-6-yl]methyl pyridine-3-carboxylate	162894970	Click to see	595.60	unknown	https://doi.org/10.1039/P19790002965
[3,4,5,7,8,12-Hexaacetyloxy-6-(acetyloxymethyl)-2-hydroxy-2,10-dimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl acetate	75026318	Click to see	702.70	unknown	https://doi.org/10.1016/S0040-4020(01)97135-2
[5-Acetyloxy-6-(acetyloxymethyl)-4-benzoyloxy-2,3-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] pyridine-3-carboxylate	101258258	Click to see	611.60	unknown	https://doi.org/10.1016/0040-4020(75)80339-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(6,25,26-Triacetyloxy-45-hydroxy-40,43-dimethoxy-9,21,45-trimethyl-2,12,22,30-tetraoxo-3,8,11,23,29,38-hexaoxa-17,33-diazaoctacyclo[37.2.2.14,27.17,24.05,9.07,27.013,18.031,36]pentatetraconta-1(41),13(18),14,16,19,31(36),32,34,39,42-decaen-44-yl) 2-acetyloxy-2-methylpropanoate	163058277	Click to see	1103.00	unknown	https://doi.org/10.1039/P19860000531 https://doi.org/10.1016/S0040-4039(00)73874-3
[(1S,3R,13Z,15S,18S,19S,20R,21R,22S,23S,24R,25S,26S)-20,25-diacetyloxy-22-(2-acetyloxy-2-methylpropanoyl)oxy-19-benzoyloxy-26-hydroxy-3,15,26-trimethyl-6,16-dioxo-23-(3,4,5-trimethoxybenzoyl)oxy-2,5,17-trioxa-11-azapentacyclo[16.7.1.01,21.03,24.07,12]hexacosa-7(12),8,10,13-tetraen-21-yl]methyl pyridine-3-carboxylate	163037506	Click to see	1167.10	unknown	https://doi.org/10.1039/P19860000531
[(1S,3S,13Z,15R,18S,19R,20R,21R,22S,23R,24R,25R,26S)-20,25-diacetyloxy-22-(2-acetyloxy-2-methylpropanoyl)oxy-19-benzoyloxy-26-hydroxy-3,15,26-trimethyl-6,16-dioxo-23-(3,4,5-trimethoxybenzoyl)oxy-2,5,17-trioxa-11-azapentacyclo[16.7.1.01,21.03,24.07,12]hexacosa-7(12),8,10,13-tetraen-21-yl]methyl pyridine-3-carboxylate	163189506	Click to see	1167.10	unknown	https://doi.org/10.1039/P19860000531
[(4R,5R,6R,7S,9R,19Z,21R,24S,25R,26R,27R,44S,45S)-6,25,26-triacetyloxy-45-hydroxy-40,43-dimethoxy-9,21,45-trimethyl-2,12,22,30-tetraoxo-3,8,11,23,29,38-hexaoxa-17,33-diazaoctacyclo[37.2.2.14,27.17,24.05,9.07,27.013,18.031,36]pentatetraconta-1(41),13(18),14,16,19,31(36),32,34,39,42-decaen-44-yl] 2-acetyloxy-2-methylpropanoate	163185973	Click to see CC1C=CC2=C(C=CC=N2)C(=O)OCC3(C4C5C(C6(COC(=O)C7=C(COC8=C(C=C(C=C8OC)C(=O)O5)OC)C=CN=C7)C(C(C(C(C6(C4OC(=O)C)O3)(C)O)OC1=O)OC(=O)C)OC(=O)C)OC(=O)C(C)(C)OC(=O)C)C	1103.00	unknown	https://doi.org/10.1039/P19860000531
[(4R,5S,6R,7R,9S,19E,21S,24R,25S,26R,27R,44R,45R)-6,25,26-triacetyloxy-45-hydroxy-40,43-dimethoxy-9,21,45-trimethyl-2,12,22,30-tetraoxo-3,8,11,23,29,38-hexaoxa-17,33-diazaoctacyclo[37.2.2.14,27.17,24.05,9.07,27.013,18.031,36]pentatetraconta-1(41),13(18),14,16,19,31(36),32,34,39,42-decaen-44-yl] 2-acetyloxy-2-methylpropanoate	163058279	Click to see CC1C=CC2=C(C=CC=N2)C(=O)OCC3(C4C5C(C6(COC(=O)C7=C(COC8=C(C=C(C=C8OC)C(=O)O5)OC)C=CN=C7)C(C(C(C(C6(C4OC(=O)C)O3)(C)O)OC1=O)OC(=O)C)OC(=O)C)OC(=O)C(C)(C)OC(=O)C)C	1103.00	unknown	https://doi.org/10.1039/P19790002965
[20,25-Diacetyloxy-22-(2-acetyloxy-2-methylpropanoyl)oxy-19-benzoyloxy-26-hydroxy-3,15,26-trimethyl-6,16-dioxo-23-(3,4,5-trimethoxybenzoyl)oxy-2,5,17-trioxa-11-azapentacyclo[16.7.1.01,21.03,24.07,12]hexacosa-7(12),8,10,13-tetraen-21-yl]methyl pyridine-3-carboxylate	163037505	Click to see	1167.10	unknown	https://doi.org/10.1039/P19860000531
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Celastrol	122724	Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)O	450.60	unknown	https://doi.org/10.1039/9781847555649-00238
Friedelin	91472	Click to see	426.70	unknown	https://doi.org/10.1039/9781847555649-00238
Npc141945	10004662	Click to see	464.60	unknown	via CMAUP database
Pristimerin	159516	Click to see	464.60	unknown	https://doi.org/10.1016/0305-1978(86)90005-0 https://doi.org/10.1039/9781847555649-00238
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(3R,4R,5S)-14'-[(2S,3R,4S,5R)-5-hydroxy-3-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5,7',9',13'-tetramethylspiro[oxane-2,6'-pentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene]-3,4,16'-triol	11968341	Click to see	871.00	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1039/9781847555649-00238
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1039/9781847555649-00238
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
DL-Threonine	205	Click to see CC(C(C(=O)O)N)O	119.12	unknown	https://doi.org/10.1002/ARDP.19602931105
Lysine, DL-	866	Click to see C(CCN)CC(C(=O)O)N	146.19	unknown	https://doi.org/10.1021/JM50015A010
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
L-Allothreonine	99289	Click to see CC(C(C(=O)O)N)O	119.12	unknown	https://doi.org/10.1002/ARDP.19602931105
Lysine	5962	Click to see C(CCN)CC(C(=O)O)N	146.19	unknown	https://doi.org/10.1021/JM50015A010
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Asparagine and derivatives
(-)-Asparagine	6267	Click to see	132.12	unknown	https://doi.org/10.1002/ARDP.19602931105
DL-Asparagine	236	Click to see C(C(C(=O)O)N)C(=O)N	132.12	unknown	https://doi.org/10.1002/ARDP.19602931105
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
DL-Glutamic acid	611	Click to see	147.13	unknown	https://doi.org/10.1002/ARDP.19602931105
L-Glutamic Acid	33032	Click to see	147.13	unknown	https://doi.org/10.1002/ARDP.19602931105
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
DL-Histidine	773	Click to see C1=C(NC=N1)CC(C(=O)O)N	155.15	unknown	https://doi.org/10.1002/ARDP.19602931105
Histidine	6274	Click to see C1=C(NC=N1)CC(C(=O)O)N	155.15	unknown	https://doi.org/10.1002/ARDP.19602931105
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Isoleucine and derivatives
DL-Isoleucine	791	Click to see CCC(C)C(C(=O)O)N	131.17	unknown	https://doi.org/10.1002/ARDP.19602931105
l-Isoleucine	6306	Click to see CCC(C)C(C(=O)O)N	131.17	unknown	https://doi.org/10.1002/ARDP.19602931105
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
DL-leucine	857	Click to see	131.17	unknown	https://doi.org/10.1002/ARDP.19602931105
Leucine	6106	Click to see CC(C)CC(C(=O)O)N	131.17	unknown	https://doi.org/10.1002/ARDP.19602931105
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
DL-Tyrosine	1153	Click to see C1=CC(=CC=C1CC(C(=O)O)N)O	181.19	unknown	https://doi.org/10.1002/ARDP.19602931105
L-Tyrosine	6057	Click to see	181.19	unknown	https://doi.org/10.1002/ARDP.19602931105
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Gamma amino acids and derivatives
Gamma-Aminobutyric Acid	119	Click to see C(CC(=O)O)CN	103.12	unknown	https://doi.org/10.1021/JM50015A010
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
Catheduline E2	442517	Click to see CC1CC(C(C2(C13CC(C(C2OC(=O)C4=CC=CC=C4)OC(=O)C5=CN=CC=C5)C(O3)(C)C)COC(=O)C6=CN=CC=C6)OC(=O)C)OC(=O)C	700.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
Tingenin B	73147	Click to see CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(C(C1=O)O)C	436.60	unknown	https://doi.org/10.1039/9781847555649-00238
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
(2S)-3-methyl-2-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxybut-3-enenitrile	6325837	Click to see	391.37	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Allitol	120700	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	https://doi.org/10.1021/JM50015A010
Hexitol	453	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	https://doi.org/10.1021/JM50015A010
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	via CMAUP database
Octanal	454	Click to see	128.21	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
3-Hydroxy-4,6b,8a,11,12b,14a-hexamethyl-7,8,8a,9,12,12a,12b,13,14,14a-decahydropicen-2(6bh)-one	162727	Click to see CC1=CCC2(CCC3(C4=CC=C5C(=C(C(=O)C=C5C4(CCC3(C2C1)C)C)O)C)C)C	404.60	unknown	https://doi.org/10.1016/0305-1978(86)90005-0
Iguesterin	46881919	Click to see	404.60	unknown	https://doi.org/10.1039/9781847555649-00238
Tingenone	101520	Click to see	420.60	unknown	https://doi.org/10.1039/9781847555649-00238
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Methyl-6-methylene-7-octen-3-one	85845089	Click to see CC(C)C(=O)CCC(=C)C=C	152.23	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(+)-Cathinone	149798	Click to see CC(C(=O)C1=CC=CC=C1)N	149.19	unknown	via CMAUP database
Cathinone	62258	Click to see	149.19	unknown	https://doi.org/10.1520/JFS13773J https://doi.org/10.1016/0378-8741(87)90004-3 https://doi.org/10.1016/0165-6147(84)90460-7 https://doi.org/10.3109/13880209409082984 https://doi.org/10.1016/0379-0738(95)01855-7 https://doi.org/10.1016/0031-6865(93)90014-W
> Organoheterocyclic compounds / Epoxides
(3R)-2,2-dimethyl-3-(3-methylidenepent-4-enyl)oxirane	92279147	Click to see	152.23	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
[(3R,3aR,4S,9bS)-3,6,9-trimethyl-2-oxo-3a,4,5,9b-tetrahydro-3H-azuleno[4,5-b]furan-4-yl] acetate	14563847	Click to see	288.34	unknown	via CMAUP database
[(3R,3aR,4S,9R,9aS,9bS)-9-hydroxy-3,6,9-trimethyl-2-oxo-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-4-yl] acetate	15560149	Click to see CC1C2C(CC(=C3C=CC(C3C2OC1=O)(C)O)C)OC(=O)C	306.40	unknown	via CMAUP database
Tannunolide C	14707535	Click to see CC1C2CCC(=C3C=CC(=C)C3C2OC1=O)C	230.30	unknown	via CMAUP database
Tannunolide D	12308596	Click to see CC1C2CCC(=C3C=CC(C3C2OC1=O)(C)O)C	248.32	unknown	via CMAUP database
> Organosulfur compounds / Thioethers / Dialkylthioethers
Dimethyl Sulfide	1068	Click to see	62.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
Merucathinone	6326729	Click to see	175.23	unknown	https://doi.org/10.1016/0378-8741(87)90004-3 https://doi.org/10.1021/NP50054A041
> Phenylpropanoids and polyketides / Cinnamyl alcohols
1-Penten-3-ol, 4-amino-1-phenyl-, (1E,3R,4S)-	5459034	Click to see CC(C(C=CC1=CC=CC=C1)O)N	177.24	unknown	https://doi.org/10.1055/S-2007-969796 https://doi.org/10.1021/NP50054A041
Merucathine	92297719	Click to see	177.24	unknown	https://doi.org/10.1055/S-2007-969796 https://doi.org/10.1016/0378-8741(87)90004-3 https://doi.org/10.1021/NP50054A041
Pseudomerucathine	5459036	Click to see CC(C(C=CC1=CC=CC=C1)O)N	177.24	unknown	https://doi.org/10.1016/0378-8741(87)90004-3
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)chroman-4-one	5153580	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O	320.25	unknown	https://doi.org/10.1016/S0031-9422(00)98579-0
Dihydromyricetin	161557	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O	320.25	unknown	https://doi.org/10.1016/S0031-9422(00)98579-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2S,3R)-5,7-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one	162884415	Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O	466.40	unknown	https://doi.org/10.1016/S0031-9422(00)98579-0
(2S,3S)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one	162884412	Click to see	466.40	unknown	https://doi.org/10.1021/NP50043A032
Dihydromyricetin 3-rhamnoside	3754658	Click to see	466.40	unknown	https://doi.org/10.1016/S0031-9422(00)98579-0
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/NP50043A032
Myricetin 3-O-galactoside	5491408	Click to see	480.40	unknown	https://doi.org/10.1021/NP50043A032
Myricitrin	5281673	Click to see	464.40	unknown	https://doi.org/10.1021/NP50043A032
> Phenylpropanoids and polyketides / Macrolides and analogues
[(4R,5R,6R,7S,9R,19S,20S,23S,24R,25R,26R,43S,44S)-6,25-diacetyloxy-43-(2-acetyloxy-2-methylpropanoyl)oxy-44-hydroxy-39,42-dimethoxy-9,19,20,44-tetramethyl-2,12,21,29-tetraoxo-3,8,11,22,28,37-hexaoxa-17,32-diazaoctacyclo[36.2.2.14,26.17,23.05,9.07,26.013,18.030,35]tetratetraconta-1(40),13(18),14,16,30(35),31,33,38,41-nonaen-24-yl] benzoate	163029928	Click to see CC1C(C(=O)OC2C(C(C34COC(=O)C5=C(COC6=C(C=C(C=C6OC)C(=O)OC(C3OC(=O)C(C)(C)OC(=O)C)C7C(C4(C2(C)O)OC7(COC(=O)C8=C1N=CC=C8)C)OC(=O)C)OC)C=CN=C5)OC(=O)C)OC(=O)C9=CC=CC=C9)C	1167.10	unknown	https://doi.org/10.1039/P19860000531
[6,25-Diacetyloxy-43-(2-acetyloxy-2-methylpropanoyl)oxy-44-hydroxy-39,42-dimethoxy-9,19,20,44-tetramethyl-2,12,21,29-tetraoxo-3,8,11,22,28,37-hexaoxa-17,32-diazaoctacyclo[36.2.2.14,26.17,23.05,9.07,26.013,18.030,35]tetratetraconta-1(40),13(18),14,16,30(35),31,33,38,41-nonaen-24-yl] benzoate	163029927	Click to see	1167.10	unknown	https://doi.org/10.1039/P19860000531

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Catha edulis

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