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.

Salvia polystachya, widely known as “chia de monte” or “chia microphylla,” has long been treated in Mexican ethnobotany as a surrogate chia. In the Balsas region and across the central highlands people soaked the gelatinous seeds in water to make a refreshing, mucilaginous drink that is very close to traditional chia fresca (Rupp 1994; Dressler 1963). Among Nahuatl-speaking communities in the Sierra Nevada and the Balsas watershed, the seed drink is also used as a mild digestive beverage (Bowden 1969). Outside Mexico, collectors in southern California occasionally sell the seeds as a beverage chia, emphasizing its similarity to true chia in drink preparation (Bates 1995; California Plant Names database, NHMLA herbarium notes).

A practical beverage preparation is straightforward: rinse 1–2 tablespoons of whole Salvia polystachya seeds to remove dust, cover with about 250–300 mL of clean water, stir well, and let stand at room temperature for 10–20 minutes until a viscous gel forms; optionally add a squeeze of citrus, a pinch of sugar or honey, and a few ice cubes. The drink is typically consumed in modest portions, 150–250 mL, as a thirst quencher and mild digestive aid. The plant is not the food‑grade chia of commerce (Salvia hispanica), and seed toxicity profiles, pregnancy safety, and drug–herb interactions have not been studied; caution is advised for people with mucosal hypersensitivity or unexpected plant-sourced allergies, and it should not be confused with edible chia in recipes that assume a known safety profile.

The traditional activity is plausibly supported by the gelatinous seed mucilage that hydrates to produce a soft, demulcent gel, and by documented secondary metabolites in Salvia leaves and stems. Aerial tissues contain terpenes (sucalyptol/1,8‑cineole, α‑ and β‑pinene, camphor), the diterpene salvicine A, and flavonoids such as quercetin and kaempferol that may contribute antioxidant and astringent effects in decoctions (Maldonado et al. 2001). These constituents are well established in Salvia and help explain the plant’s use in internal preparations that are taken as teas or seed mucilage drinks for mild stomach comfort and as an invigorating, rehydration‑friendly beverage.

Today Salvia polystachya remains a niche beverage plant in Mexican ethnobotany and a minor option in specialty “chia” markets where consumers are looking for alternatives to true chia. Recent phytochemical work on related Mexican sages has renewed interest in the genus’s flavor and functional profiles, and some Mexican food shops continue to sell small quantities of the seeds for drinking and culinary thickening (Maldonado et al. 2001; NHMLA herbarium notes).

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Salvia brevicalyx	Benth.	Prodr. 12: 309 (1848)
Salvia caesia	Willd.	Enum. Pl. : 40 (1809)
Salvia cataria	Briq.	Annuaire Conserv. Jard. Bot. Genève 2: 142. 1898
Salvia compacta var. irazuensis	Kuntze	Revis. Gen. Pl. 2: 530 (1891)
Salvia compacta var. latifolia	Kuntze	Revis. Gen. Pl. 2: 530 (1891)
Salvia compacta var. oerstediana	Kuntze	Revis. Gen. Pl. 2: 530. 1891 [5 Nov 1891]
Salvia durandiana	Briq. ex T.Durand & Pittier	Bull. Soc. Roy. Bot. Belgique 30: 236 (1891 publ. 1892)
Salvia eremetica	Cerv. ex Lag.	Gen. Sp. Pl. : 2 (1816)
Salvia flexuosa	Presl ex Benth.	Labiat. Gen. Spec. : 248 (1833)
Salvia igualensis	Fernald	Proc. Amer. Acad. Arts 366: 500. 1901
Salvia lilacina	Fernald	Proc. Amer. Acad. Arts 45: 418. 1910
Salvia lineatifolia	Lag.	Gen. Sp. Pl. : 2 (1816)
Salvia menthiformis	Fernald	Proc. Amer. Acad. Arts 35: 510. 1900
Salvia polystachya subsp. caesia	(Humb. & Bonpl.) Briq.	Bull. Soc. Roy. Bot. Belgique 30: 236 (1891 publ. 1892)
Salvia reducta	Epling	Repert. Spec. Nov. Regni Veg. Beih. 110: 168. 1939
Salvia ghiesbreghtii	Fernald	Proc. Amer. Acad. Arts 35: 511 (1900)
Salvia lenta	Fernald	Proc. Amer. Acad. Arts 45: 419 (1910)
Salvia polystachia subsp. durandiana	Briq.	Bull. Soc. Roy. Bot. Belgique 30: 237 (1891 publ. 1892)
Salvia polystachia var. albicans	Fernald	Proc. Amer. Acad. Arts 35: 512 (1900)
Salvia polystachia var. philippensis	Fernald	Proc. Amer. Acad. Arts 35: 512 (1900)
Salvia polystachia var. potosiana	Briq.	Annuaire Conserv. Jard. Bot. Genève 2: 138 (1898)
Salvia polystachia var. seorsa	Fernald	Proc. Amer. Acad. Arts 35: 512 (1900)

Common names Top

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Filter by language:

Language	Common/alternative name
Spanish	salvia brevicalyx
Spanish	salvia lineatifolia
Spanish	salvia compacta var. latifolia
Spanish	salvia caesia
Spanish	salvia cataria
Spanish	salvia compacta var. oerstediana
Spanish	salvia durandiana
Spanish	salvia eremetica
Spanish	salvia flexuosa
Spanish	salvia lilacina
Spanish	salvia menthiformis
Spanish	salvia reducta
Japanese	サルビア・ポリスタキア

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Gulf
  - Mexico Northeast
  - Mexico Northwest
  - Mexico Southeast
  - Mexico Southwest

Southern America click to expand
- Central America
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Nicaragua
  - Panamá

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000301959
Tropicos	50250337
KEW	urn:lsid:ipni.org:names:927520-1
The Plant List	kew-183536
Open Tree Of Life	337411
NCBI Taxonomy	268922
IPNI	927520-1
iNaturalist	315375
GBIF	4931086
Freebase	/m/05mrqt6
EPPO	SALPO
EOL	6342866
USDA GRIN	70594
Wikipedia	Salvia_polystachia
Tropicos	50188137
KEW	urn:lsid:ipni.org:names:456276-1
The Plant List	kew-182714
IPNI	309069-2
GBIF	3901579
Tropicos	100253853
KEW	urn:lsid:ipni.org:names:226702-2
The Plant List	kew-183027
Open Tree Of Life	6083320
Observations.org	454451
IPNI	309147-2
GBIF	3897874
Elurikkus	436050
CMAUP	NPO7171
iNaturalist	1349529

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

Selection of Mexican Medicinal Plants by Identification of Potential Phytochemicals with Anti-Aging, Anti-Inflammatory, and Anti-Oxidant Properties through Network Analysis and Chemoinformatic Screening

Barrera-Vázquez OS, Montenegro-Herrera SA, Martínez-Enríquez ME, Escobar-Ramírez JL, Magos-Guerrero GA

Biomolecules

20-Nov-2023

PMCID:	PMC10669844
doi:	10.3390/biom13111673
PMID:	38002355

Essential Oils and Terpenic Compounds as Potential Hits for Drugs against Amitochondriate Protists

Menezes SA, Tasca T

Trop Med Infect Dis

05-Jan-2023

PMCID:	PMC9865018
doi:	10.3390/tropicalmed8010037
PMID:	36668944

Amebic liver abscess by Entamoeba histolytica

Usuda D, Tsuge S, Sakurai R, Kawai K, Matsubara S, Tanaka R, Suzuki M, Takano H, Shimozawa S, Hotchi Y, Tokunaga S, Osugi I, Katou R, Ito S, Mishima K, Kondo A, Mizuno K, Takami H, Komatsu T, Oba J, Nomura T, Sugita M

World J Clin Cases

26-Dec-2022

PMCID:	PMC9851013
doi:	10.12998/wjcc.v10.i36.13157
PMID:	36683647

Recent Updates on Phytoconstituent Alpha-Glucosidase Inhibitors: An Approach towards the Treatment of Type Two Diabetes

Kashtoh H, Baek KH

Plants (Basel)

14-Oct-2022

PMCID:	PMC9612090
doi:	10.3390/plants11202722
PMID:	36297746

Changes in the core species of the ant-plant network of oak forest converted to grassland: replacement of its ant functional groups

Cuautle M, Díaz-Castelazo C, Castillo-Guevara C, Torres Lagunes CG

PeerJ

13-Jul-2022

PMCID:	PMC9288171
doi:	10.7717/peerj.13679
PMID:	35855899

Linearolactone Induces Necrotic-like Death in Giardia intestinalis Trophozoites: Prediction of a Likely Target

Argüello-García R, Calzada F, Chávez-Munguía B, Matus-Meza AS, Bautista E, Barbosa E, Velazquez C, Hernández-Caballero ME, Ordoñez-Razo RM, Velázquez-Domínguez JA

Pharmaceuticals (Basel)

29-Jun-2022

PMCID:	PMC9324340
doi:	10.3390/ph15070809
PMID:	35890108

Antihyperglycemic Effects of Salvia polystachya Cav. and Its Terpenoids: α-Glucosidase and SGLT1 Inhibitors

Ortega R, Valdés M, Alarcón-Aguilar FJ, Fortis-Barrera Á, Barbosa E, Velazquez C, Calzada F

Plants (Basel)

22-Feb-2022

PMCID:	PMC8912538
doi:	10.3390/plants11050575
PMID:	35270046

A systematic review of anti-Entamoeba histolytica activity of medicinal plants published in the last 20 years

Nezaratizade S, Hashemi N, Ommi D, Orhan IE, Khamesipour F

Parasitology

04-Feb-2021

PMCID:	PMC11010214
doi:	10.1017/S0031182021000172
PMID:	33536098

In Silico Studies of Lamiaceae Diterpenes with Bioinsecticide Potential against Aphis gossypii and Drosophila melanogaster

Rodrigues GC, dos Santos Maia M, Silva Cavalcanti AB, de Sousa NF, Scotti MT, Scotti L

Molecules

02-Feb-2021

PMCID:	PMC7867283
doi:	10.3390/molecules26030766
PMID:	33540716

Metabolomics and DNA-Based Authentication of Two Traditional Asian Medicinal and Aromatic Species of Salvia subg. Perovskia

Bielecka M, Pencakowski B, Stafiniak M, Jakubowski K, Rahimmalek M, Gharibi S, Matkowski A, Ślusarczyk S

Cells

09-Jan-2021

PMCID:	PMC7826587
doi:	10.3390/cells10010112
PMID:	33435339

Antinociceptive and anxiolytic-like effects of a neo-clerodane diterpene from Salvia semiatrata aerial parts

Ortiz-Mendoza N, Zavala-Ocampo LM, Martínez-Gordillo MJ, González-Trujano ME, Peña FA, Bazany-Rodríguez IJ, Chávez JA, Dorazco-González A, Aguirre-Hernández E

Pharm Biol

07-Jul-2020

PMCID:	PMC7471977
doi:	10.1080/13880209.2020.1784235
PMID:	32633180

Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes

Lautié E, Russo O, Ducrot P, Boutin JA

Front Pharmacol

07-Apr-2020

PMCID:	PMC7154113
doi:	10.3389/fphar.2020.00397
PMID:	32317969

Antioxidant Properties and Protective Effects of Some Species of the Annonaceae, Lamiaceae, and Geraniaceae Families against Neuronal Damage Induced by Excitotoxicity and Cerebral Ischemia

Pineda-Ramírez N, Calzada F, Alquisiras-Burgos I, Medina-Campos ON, Pedraza-Chaverri J, Ortiz-Plata A, Pinzón Estrada E, Torres I, Aguilera P

Antioxidants (Basel)

20-Mar-2020

PMCID:	PMC7139819
doi:	10.3390/antiox9030253
PMID:	32244955

Evaluation of the antiprotozoal activity of neo-clerodane type diterpenes from Salvia polystachya against Entamoeba histolytica and Giardia lamblia.

Calzada F, Yepez-Mulia L, Tapia-Contreras A, Bautista E, Maldonado E, Ortega A

Phytother Res

01-May-2010

doi:	10.1002/PTR.2938
PMID:	19610033

Polystachyne F, a 5,10-seco-neoclerodane from Salvia polystachya.

Ortega A, Bautista E, Maldonado E

Chem Pharm Bull (Tokyo)

01-Sep-2006

doi:	10.1248/CPB.54.1338
PMID:	16946549

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
Trigonelline	5570	Click to see	137.14	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[2-[(1S,4R,7R,10S)-10-hydroxy-7-methyl-12-oxatricyclo[5.3.2.01,6]dodec-5-en-4-yl]propan-2-yloxy]oxane-3,4,5-triol	21592245	Click to see	414.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-[(1R,3R,4S)-4-ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexyl]propan-2-ol	20057139	Click to see	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4S,5S,6R)-2-[[(1R,2R,4aS,5S,8R,8aR)-5,8-dihydroxy-2-(2-hydroxypropan-2-yl)-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	20055913	Click to see	434.50	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[[(1S,2R,4aS,5S,8aR)-5-hydroxy-4a-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-8-methyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101938835	Click to see CC1=CCC(C2(C1C(C(CC2)C(C)(C)O)OC3C(C(C(C(O3)CO)O)O)O)CO)O	432.50	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[[(1S,2R,4aS,5S,8aR)-5-hydroxy-4a-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101938834	Click to see	432.50	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[[(2R,3S,4S,5R,6R)-6-[[(1R,2R,4aS,5S,8R,8aR)-5,8-dihydroxy-2-(2-hydroxypropan-2-yl)-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	21592257	Click to see	596.70	unknown	via CMAUP database
Dictamnoside A	44560015	Click to see CC12CCC(C3(C1C(C(CC3)C(C)(C)O)OC4C(C(C(C(O4)CO)O)O)O)CO2)O	432.50	unknown	via CMAUP database
Dictamnoside D	20055915	Click to see CC1(CCC(C2(C1C(C(CC2)C(C)(C)O)OC3C(C(C(C(O3)CO)O)O)O)CO)O)O	450.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,4S,7S,8S,11S,12R,18S)-7-(furan-3-yl)-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	38349717	Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C	454.50	unknown	via CMAUP database
(1R,2R,7S,10S,13R,14R,16S,19S,20S)-19-(furan-3-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione	92966492	Click to see	470.50	unknown	via CMAUP database
[(1S,2R,4S,7S,8S,11R,12R,13S,18R,20R)-13-acetyloxy-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,15-dioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icosan-20-yl] acetate	101362570	Click to see	558.60	unknown	via CMAUP database
7Alpha-Obacunyl Acetate	57390140	Click to see	498.60	unknown	via CMAUP database
Limonin	179651	Click to see	470.50	unknown	via CMAUP database
Obacunone	119041	Click to see	454.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
22,23-Dihydrobrassicasterol	5283637	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone	8955	Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	316.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
(E)-3-[(1R,2R,5R,6R,7R,10S,11S,14S)-11-(furan-3-yl)-5-(2-hydroxypropan-2-yl)-2,6,10-trimethyl-3,13-dioxo-12,15-dioxatetracyclo[8.5.0.01,14.02,7]pentadecan-6-yl]prop-2-enoic acid	21140842	Click to see CC12CCC3C(C(CC(=O)C3(C14C(O4)C(=O)OC2C5=COC=C5)C)C(C)(C)O)(C)C=CC(=O)O	472.50	unknown	via CMAUP database
[(1R,2R,7S,10R,12R,13S,14R,16S,19S,20S)-19-(furan-3-yl)-9,9,13,20-tetramethyl-5,11,17-trioxo-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosan-12-yl] acetate	100968399	Click to see	528.50	unknown	via CMAUP database
Evodol	185481	Click to see	484.50	unknown	via CMAUP database
Rutaevin	441805	Click to see CC1(C2C(=O)C(C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)O)C	486.50	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	via CMAUP database
7alpha-Hydroxysitosterol	161816	Click to see	430.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(3R,5S)-5-[(1R,2R,3S,8R,10R,11R,15S,16S)-3,10-diacetyloxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-en-15-yl]-2-oxooxan-3-yl] acetate	102527309	Click to see	602.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(1R,2R,3S,8R,10R,11R,15S,16S)-3-acetyloxy-15-[(3S,5R)-5-hydroxy-6-oxooxan-3-yl]-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-en-10-yl] acetate	102527308	Click to see	560.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1S,3bR,4R,5aR,10aR,10bR,12aS)-1-[(3S,5R)-5-hydroxy-6-oxooxan-3-yl]-3b,6,6,10a,12a-pentamethyl-8-oxo-1,2,4,5,5a,10b,11,12-octahydroindeno[5,4-g][2]benzoxepin-4-yl] acetate	102527310	Click to see	500.60	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1S,3aR,8aR)-1-methyl-4-methylidene-2,3,3a,5,6,8a-hexahydroazulen-1-ol	10058083	Click to see	178.27	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3R,4S,5S,6R)-2-[[(1R,3aS,4S,6S,8aR)-1,6-dihydroxy-1,4-dimethyl-2,3,3a,5,6,8a-hexahydroazulen-4-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	11003271	Click to see	374.40	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[[(1S,3S,3aS,4R,8aS)-3,4-dihydroxy-1,4-dimethyl-2,3,3a,5,6,8a-hexahydroazulen-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	101938836	Click to see	374.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
NCGC00380994-01_C21H30O12_4-Acetyl-2-methoxyphenyl 6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside	9832854	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C=C(C=C3)C(=O)C)OC)O)O)O)O)O)O	474.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Dioxepanes / 1,4-dioxepanes
Calodendrolide	478835	Click to see	260.28	unknown	via CMAUP database
> Organoheterocyclic compounds / Furofurans
(1R,2R,10S,12S,14R,16R,18S)-16-(furan-3-yl)-18-methyl-8,13,15-trioxapentacyclo[10.5.1.01,14.02,10.06,10]octadeca-3,5-dien-7-one	101586388	Click to see	340.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
(1R,2R,3S,5R,7R,11S,13R,15R,17R,19S)-17-(furan-3-yl)-19-methyl-4,9,14,16-tetraoxahexacyclo[11.5.1.01,15.02,11.03,5.07,11]nonadecan-8-one	163036053	Click to see	358.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
(1R,2R,3S,5R,7S,11S,13R,15R,17R,19S)-17-(furan-3-yl)-19-methyl-4,9,14,16-tetraoxahexacyclo[11.5.1.01,15.02,11.03,5.07,11]nonadecan-8-one	145949769	Click to see	358.40	unknown	https://doi.org/10.1002/PTR.2938 https://doi.org/10.1016/S0031-9422(99)00466-5
(1R,2R,4R,5Z,13R,15R,17R,19S)-17-(furan-3-yl)-19-methyl-3,9,14,16-tetraoxapentacyclo[11.5.1.01,15.02,4.07,11]nonadeca-5,7(11)-dien-10-one	101403672	Click to see	356.40	unknown	via CMAUP database
(1R,2R,4R,5Z,13R,15R,17R,19S)-17-(furan-3-yl)-19-methyl-3,9,14,16-tetraoxapentacyclo[11.5.1.01,15.02,4.07,11]nonadeca-5,7(11)-dien-8-one	163046241	Click to see	356.40	unknown	https://doi.org/10.1248/CPB.54.1338
(1R,2S,3S,5R,7R,11S,13R,15S,17R,19S)-17-(furan-3-yl)-19-methyl-4,9,14,16-tetraoxahexacyclo[11.5.1.01,15.02,11.03,5.07,11]nonadecan-8-one	163036051	Click to see	358.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
(1R,2S,3S,5R,7S,11S,13R,15S,17R,19S)-17-(furan-3-yl)-19-methyl-4,9,14,16-tetraoxahexacyclo[11.5.1.01,15.02,11.03,5.07,11]nonadecan-8-one	163036054	Click to see CC1C2CC34COC(=O)C3CC5C(C4C16CC(OC6O2)C7=COC=C7)O5	358.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
(1S,2R,3S,5R,7R,11S,13R,15R,17R,19S)-17-(furan-3-yl)-19-methyl-4,9,14,16-tetraoxahexacyclo[11.5.1.01,15.02,11.03,5.07,11]nonadecan-8-one	101022940	Click to see	358.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
(1S,2R,3S,5R,7S,11S,13R,15R,17R,19S)-17-(furan-3-yl)-19-methyl-4,9,14,16-tetraoxahexacyclo[11.5.1.01,15.02,11.03,5.07,11]nonadecan-8-one	101022939	Click to see	358.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
(1S,2R,6R,10S,12R,14R,16R,18S)-16-(furan-3-yl)-18-methyl-8,13,15-trioxapentacyclo[10.5.1.01,14.02,10.06,10]octadec-3-en-7-one	101022938	Click to see CC1C2CC34COC(=O)C3CC=CC4C15CC(OC5O2)C6=COC=C6	342.40	unknown	https://doi.org/10.1002/PTR.2938 https://doi.org/10.1016/S0031-9422(99)00466-5
(1S,2R,6S,10S,12R,14S,16R,18S)-16-(furan-3-yl)-18-methyl-8,13,15-trioxapentacyclo[10.5.1.01,14.02,10.06,10]octadec-3-en-7-one	15459548	Click to see	342.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
(1S,2S,4R,5Z,13R,15S,17S,19S)-17-(furan-3-yl)-19-methyl-3,9,14,16-tetraoxapentacyclo[11.5.1.01,15.02,4.07,11]nonadeca-5,7(11)-dien-8-one	163046240	Click to see CC1C2CC3=C(C=CC4C(C15CC(OC5O2)C6=COC=C6)O4)C(=O)OC3	356.40	unknown	https://doi.org/10.1248/CPB.54.1338
16-(Furan-3-yl)-18-methyl-8,13,15-trioxapentacyclo[10.5.1.01,14.02,10.06,10]octadec-3-en-7-one	132583510	Click to see CC1C2CC34COC(=O)C3CC=CC4C15CC(OC5O2)C6=COC=C6	342.40	unknown	https://doi.org/10.1002/PTR.2938 https://doi.org/10.1016/S0031-9422(99)00466-5
16-(Furan-3-yl)-18-methyl-8,13,15-trioxapentacyclo[10.5.1.01,14.02,10.06,10]octadeca-3,5-dien-7-one	73175795	Click to see	340.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
17-(Furan-3-yl)-19-methyl-3,9,14,16-tetraoxapentacyclo[11.5.1.01,15.02,4.07,11]nonadeca-5,7(11)-dien-8-one	73239332	Click to see	356.40	unknown	https://doi.org/10.1248/CPB.54.1338
17-(Furan-3-yl)-19-methyl-4,9,14,16-tetraoxahexacyclo[11.5.1.01,15.02,11.03,5.07,11]nonadecan-8-one	163036049	Click to see	358.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5 https://doi.org/10.1002/PTR.2938
Salvifaricin	21588012	Click to see	340.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
> Organoheterocyclic compounds / Isobenzofurans
9Beta-Hydroxyfraxinellone	478833	Click to see	248.27	unknown	via CMAUP database
Fraxinellone	124039	Click to see CC1=C2C(=O)OC(C2(CCC1)C)C3=COC=C3	232.27	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
(1S,4S,6R,8R,9S)-6-(furan-3-yl)-4,8-dimethyl-5,15-dioxatetracyclo[7.7.0.01,13.04,8]hexadec-12-en-14-one	162994332	Click to see	328.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
6-(Furan-3-yl)-4,8-dimethyl-5,15-dioxatetracyclo[7.7.0.01,13.04,8]hexadec-12-en-14-one	162994331	Click to see CC12CCC34COC(=O)C3=CCCC4C1(CC(O2)C5=COC=C5)C	328.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
> Organoheterocyclic compounds / Naphthopyrans
(1S,4S,7R,9R,10S,11R,13S,15R)-7-(furan-3-yl)-7,9-dimethyl-6,12,17-trioxapentacyclo[8.8.0.01,15.04,9.011,13]octadecane-5,16-dione	162886803	Click to see	372.40	unknown	https://doi.org/10.1002/PTR.2938
(1S,4S,7R,9R,10S,11R,13S,15R)-7-(furan-3-yl)-9-methyl-6,12,17-trioxapentacyclo[8.8.0.01,15.04,9.011,13]octadecane-5,16-dione	162849834	Click to see CC12CC(OC(=O)C1CCC34C2C5C(O5)CC3C(=O)OC4)C6=COC=C6	358.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
(1S,4S,7R,9R,10S,11R,13S,15S)-7-(furan-3-yl)-9-methyl-6,12,17-trioxapentacyclo[8.8.0.01,15.04,9.011,13]octadecane-5,16-dione	14866174	Click to see	358.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
(1S,4S,7R,9R,10S,11R,13S)-7-(furan-3-yl)-9-methyl-6,12,17-trioxapentacyclo[8.8.0.01,15.04,9.011,13]octadec-14-ene-5,16-dione	15459551	Click to see	356.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
(1S,4S,7R,9R,10S)-7-(furan-3-yl)-7,9-dimethyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadeca-11,13-diene-5,15-dione	162868192	Click to see	354.40	unknown	https://doi.org/10.1002/PTR.2938
(1S,4S,7R,9S,10S,11R,13S,15R)-7-(furan-3-yl)-9-methyl-6,12,17-trioxapentacyclo[8.8.0.01,15.04,9.011,13]octadecane-5,16-dione	101022941	Click to see	358.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
(1S,4S,7R,9S,10S,11R,13S)-7-(furan-3-yl)-9-methyl-6,12,17-trioxapentacyclo[8.8.0.01,15.04,9.011,13]octadec-14-ene-5,16-dione	101022942	Click to see	356.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
1H,10H-Furo[3',4':4a,5]naphtho[2,1-c]pyran-1,8(4bH)-dione, 3-(3-furanyl)-3,4,4a,11,12,12a-hexahydro-4a-methyl-, (3R,4aR,4bS,10aS,12aS)-	145952768	Click to see	340.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
7-(Furan-3-yl)-9-methyl-6,12,17-trioxapentacyclo[8.8.0.01,15.04,9.011,13]octadec-14-ene-5,16-dione	163029286	Click to see	356.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
7-(Furan-3-yl)-9-methyl-6,12,17-trioxapentacyclo[8.8.0.01,15.04,9.011,13]octadecane-5,16-dione	14866173	Click to see	358.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
Linearolactone	188840	Click to see	340.40	unknown	https://doi.org/10.1016/S0031-9422(99)00466-5
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine	68085	Click to see	199.20	unknown	via CMAUP database
Gamma-Fagarine	107936	Click to see	229.23	unknown	via CMAUP database
Isomaculosidine	3083609	Click to see CN1C2=C(C=C(C=C2OC)OC)C(=O)C3=C1OC=C3	259.26	unknown	via CMAUP database
Skimmianine	6760	Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC	259.26	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4,7,8-trimethoxy-3-[(E)-3-methylbut-1-enyl]-1H-quinolin-2-one	6325017	Click to see CC(C)C=CC1=C(C2=C(C(=C(C=C2)OC)OC)NC1=O)OC	303.35	unknown	via CMAUP database
Preskimmianine	12305721	Click to see	303.35	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
(3R)-5,8,9-trimethoxy-2,2-dimethyl-3,4-dihydropyrano[2,3-b]quinolin-3-ol	101132831	Click to see CC1(C(CC2=C(C3=C(C(=C(C=C3)OC)OC)N=C2O1)OC)O)C	319.40	unknown	via CMAUP database
5,9-Dimethoxy-2,2-dimethylpyrano[2,3-b]quinoline	44138438	Click to see	271.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
8-Methoxypsoralen	4114	Click to see	216.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see	192.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin	5280804	Click to see	464.40	unknown	via CMAUP database
Rutin	5280805	Click to see	610.50	unknown	via CMAUP database

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Salvia polystachya

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