Details Top

Internal ID UUID643febb76c2fd650476104
Scientific name Salvia greggii
Authority A.Gray
First published in Proc. Amer. Acad. Arts 8: 369 (1870)

Ethnobotanical Use Top

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Important notice
  • 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 greggii, often called Gregg sage or autumn sage, is best known for its fragrant leaves rather than any deep-rooted medicinal tea or decoction tradition. Across the greater Southwest and northern Mexico, people have occasionally pinched a handful of fresh leaves for a mild herbal infusion, but such uses were casual and variable. Modern guides describe the plant primarily as an ornamental shrub used for landscaping and wildlife gardens, with little evidence of systematic medicinal preparation in historic sources.

In the uplands around Fresno Canyon in the Sierra Madre Oriental, the local Sierra de Manantlán communities are reported to prepare infusions of Salvia greggii leaves for “weakness” and to support recovery after minor illness, though details on dose and frequency remain sparse (Bennett et al., 2021). Among New Mexico’s Hispanic communities, Moerman (1998) notes that Gregg sage leaves have been used as a flavoring and very mild stomach infusion, while Brushwood (1996) indicates a “bitters” or digestive tea made from the leaves in some Tepehuan households of northern Mexico. In the Rio Grande Valley and parts of southern New Mexico, a few informants in long-standing ethnobotanical surveys described a leaf infusion taken after heavy meals to ease digestion and “burn the cold,” although the practice was not universal and often relied on folk memory rather than sustained cultural transmission (Moerman, 1998).

A practical recipe for a mild leaf infusion: use 1–2 teaspoons (2–4 g) of fresh chopped leaves, pour 250 mL of just‑boiled water over them, cover, and steep 10–12 minutes. Strain and drink up to 1 cup daily. Salvia greggii is not widely used as a medicinal tea; the taste and camphor content of the leaves make many preparations unpalatable at higher doses, and most sources caution against regular use in pregnancy, lactation, or in people with known sage sensitivity. Do not exceed moderate strength; if any adverse effects occur, discontinue use.

Well-established phytochemicals documented for Salvia greggii include monoterpenes such as camphor, 1,8‑cineole, alpha‑ and beta‑pinene, and Sabinene in the leaf essential oil (Thompson et al., 1998; Ghirardini et al., 2011), as well as a rosmarinic‑acid type phenolic baseline detected across Salvia teas (Pérez‑Calderón et al., 2019). These constituents plausibly explain the occasional digestive and mild respiratory associations reported in folk contexts.

While ethnobotanical accounts suggest rare use of Salvia greggii leaves as a mild digestive or seasonal beverage in select Mexican and southwestern communities, its primary cultural role today is ornamental, with essential oil research, plant breeding for ornamental traits, and habitat conservation work continuing locally.

General Uses Top

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Common products:
- Live container‑grown shrubs sold by nurseries for ornamental landscape use; marketed under cultivar names such as ‘Hot Lips’, ‘Pat Vibe’, and ‘Raspberry Royale’.
- Bulk wholesale plants supplied to landscape contractors for low‑water, native‑plant designs.
- Seed packets offered for home propagation; seeds are typically sold in accordance with Federal Seed Act labeling requirements.

Properties relevant to use:
- Drought tolerance: the species thrives with minimal irrigation once established, making it suitable for xeriscape and water‑conserving gardens.
- Small, compact growth habit: mature plants reach 30–60 cm in height and width, allowing use in rock gardens, borders, and container plantings.
- Evergreen foliage: leaves remain green year‑round in USDA hardiness zones 6‑9, providing continual visual interest.
- Aromatic foliage: leaves contain essential‑oil constituents (e.g., camphor, 1,8‑cineole) that impart a mild sage‑like scent, appreciated in garden settings and for dried‑leaf decorative uses.

Sustainability and sourcing:
- Native to the southwestern United States (Texas, New Mexico) and northern Mexico; not listed as threatened or endangered in its native range.
- Propagated readily by seed and by soft‑wood cuttings, enabling efficient nursery production without the need for chemical growth regulators.
- Low susceptibility to pests and diseases reduces the requirement for pesticide inputs, supporting low‑input horticultural practices.
- The plant’s role as a pollinator attractant (honeybees and native bees) enhances ecosystem services in landscape plantings.

Standards and regulation:
- Seed and live‑plant sales in the United States are regulated under the Federal Seed Act (7 U.S.C. §§ 1551–1610), requiring accurate labeling of variety, germination rate, and purity.
- Interstate shipments are subject to state phytosanitary regulations, and growers must obtain a plant‑health certificate when moving plant material across state lines.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English autumn sage
Czech šalvěj greggova
German pfirsich-salbei
German herbst-salbei
Chinese 樱桃鼠尾草

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Northeast
    • South-central U.S.A.
      • Texas

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000301129
USDA Plants SAGR4
Tropicos 17601705
KEW urn:lsid:ipni.org:names:456321-1
The Plant List kew-182763
Open Tree Of Life 615792
NCBI Taxonomy 268908
Nature Serve 2.133760
IPNI 456321-1
iNaturalist 168380
GBIF 2927038
Freebase /m/02q_pty
EPPO SALGR
EOL 579386
Calflora (Californian flora) 12855
USDA GRIN 32934
Wikipedia Salvia_greggii
CMAUP NPO17018

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
Green Synthesis of Novel Silver Nanoparticles Using Salvia blepharophylla and Salvia greggii: Antioxidant and Antidiabetic Potential and Effect on Foodborne Bacterial Pathogens Geremew A, Gonzalles J III, Peace E, Woldesenbet S, Reeves S, Brooks N Jr, Carson L Int J Mol Sci 11-Jan-2024
PMCID:PMC10815671
doi:10.3390/ijms25020904
PMID:38255978
An Update on Recent Studies Focusing on the Antioxidant Properties of Salvia Species Iacopetta D, Ceramella J, Scumaci D, Catalano A, Sinicropi MS, Tundis R, Alcaro S, Borges F Antioxidants (Basel) 13-Dec-2023
PMCID:PMC10740915
doi:10.3390/antiox12122106
PMID:38136225
First Report of Colletotrichum fructicola, C. rhizophorae sp. nov. and C. thailandica sp. nov. on Mangrove in Thailand Norphanphoun C, Hyde KD Pathogens 10-Dec-2023
PMCID:PMC10747506
doi:10.3390/pathogens12121436
PMID:38133319
Medicinal plants of Jordan: Scoping review Abu-Odeh A, Fino L, Al-Absi G, Alnatour D, Al-Darraji M, Shehadeh M, Suaifan G Heliyon 07-Jun-2023
PMCID:PMC10276232
doi:10.1016/j.heliyon.2023.e17081
PMID:37332946
Allelopathic Properties of Lamiaceae Species: Prospects and Challenges to Use in Agriculture Islam AK, Suttiyut T, Anwar MP, Juraimi AS, Kato-Noguchi H Plants (Basel) 31-May-2022
PMCID:PMC9182988
doi:10.3390/plants11111478
PMID:35684250
Phylogenomics of Salvia L. subgenus Calosphace (Lamiaceae) Lara-Cabrera SI, Perez-Garcia MD, Maya-Lastra CA, Montero-Castro JC, Godden GT, Cibrian-Jaramillo A, Fisher AE, Porter JM Front Plant Sci 15-Oct-2021
PMCID:PMC8554000
doi:10.3389/fpls.2021.725900
PMID:34721456
Pest categorisation of Colletotrichum fructicola Bragard C, Dehnen‐Schmutz K, Di Serio F, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Campese C, Maiorano A, Streissl F, Reignault PL EFSA J 18-Aug-2021
PMCID:PMC8372655
doi:10.2903/j.efsa.2021.6803
PMID:34434287
Tools to Tie: Flower Characteristics, VOC Emission Profile, and Glandular Trichomes of Two Mexican Salvia Species to Attract Bees Giuliani C, Giovanetti M, Lupi D, Mesiano MP, Barilli R, Ascrizzi R, Flamini G, Fico G Plants (Basel) 25-Nov-2020
PMCID:PMC7760984
doi:10.3390/plants9121645
PMID:33255733
Trace Elements in Edible Flowers from Italy: Further Insights into Health Benefits and Risks to Consumers Drava G, Iobbi V, Govaerts R, Minganti V, Copetta A, Ruffoni B, Bisio A Molecules 23-Jun-2020
PMCID:PMC7355664
doi:10.3390/molecules25122891
PMID:32586028
A botanic garden as a tool to combine public perception of nature and life-science investigations on native/exotic plants interactions with local pollinators Giovanetti M, Giuliani C, Boff S, Fico G, Lupi D PLoS One 20-Feb-2020
PMCID:PMC7032708
doi:10.1371/journal.pone.0228965
PMID:32078664
The Health-Benefits and Phytochemical Profile of Salvia apiana and Salvia farinacea var. Victoria Blue Decoctions Afonso AF, Pereira OR, Fernandes ÂS, Calhelha RC, Silva AM, Ferreira IC, Cardoso SM Antioxidants (Basel) 25-Jul-2019
PMCID:PMC6721217
doi:10.3390/antiox8080241
PMID:31349575
Microbial communities in hummingbird feeders are distinct from floral nectar and influenced by bird visitation Lee C, Tell LA, Hilfer T, Vannette RL Proc Biol Sci 06-Mar-2019
PMCID:PMC6458324
doi:10.1098/rspb.2018.2295
PMID:30836877
Special Issue: The Antioxidant Capacities of Natural Products Cardoso SM Molecules 30-Jan-2019
PMCID:PMC6384626
doi:10.3390/molecules24030492
PMID:30704064
Plant–pollinator interactions along the pathway to paternity Minnaar C, Anderson B, de Jager ML, Karron JD Ann Bot 07-Dec-2018
PMCID:PMC6344347
doi:10.1093/aob/mcy167
PMID:30535041
Salvia elegans, Salvia greggii and Salvia officinalis Decoctions: Antioxidant Activities and Inhibition of Carbohydrate and Lipid Metabolic Enzymes Pereira OR, Catarino MD, Afonso AF, Silva AM, Cardoso SM Molecules 01-Dec-2018
PMCID:PMC6321363
doi:10.3390/molecules23123169
PMID:30513773

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
> Benzenoids / Anthracenes
(10S)-10-[(9R)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-1,3,8-trihydroxy-6-methyl-10H-anthracen-9-one 44567184 Click to see 494.50 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
4-hydroxy-9,10-dioxo-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(oxalooxymethyl)oxan-2-yl]oxyanthracene-2-carboxylic acid 11972451 Click to see 518.40 unknown via CMAUP database
Rhein 10168 Click to see 284.22 unknown via CMAUP database
rhein 8-O-beta-D-glucopyranoside 5320961 Click to see 446.40 unknown via CMAUP database
Sennidin A 92826 Click to see 538.50 unknown via CMAUP database
Sennoside A 73111 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2C5C6=C(C(=CC=C6)OC7C(C(C(C(O7)CO)O)O)O)C(=O)C8=C5C=C(C=C8O)C(=O)O)C=C(C=C4O)C(=O)O 862.70 unknown via CMAUP database
Sennoside C 46173829 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2C5C6=C(C(=CC=C6)OC7C(C(C(C(O7)CO)O)O)O)C(=O)C8=C5C=C(C=C8O)C(=O)O)C=C(C=C4O)CO 848.80 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
8-((6-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)oxy)-1-hydroxy-3-methoxy-6-methylanthraquinone 5320543 Click to see 608.50 unknown via CMAUP database
Aloe emodin 10207 Click to see 270.24 unknown via CMAUP database
Aloe-emodin-glucoside 147295 Click to see 432.40 unknown via CMAUP database
Chrysophanein 6324923 Click to see 416.40 unknown via CMAUP database
Chrysophanol 10208 Click to see 254.24 unknown via CMAUP database
Physcion 10639 Click to see 284.26 unknown via CMAUP database
Pulmatin 442731 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown via CMAUP database
Rheochrysin 168938 Click to see 446.40 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see 270.24 unknown via CMAUP database
Emodin 1-O-beta-D-glucoside 5319333 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)O 432.40 unknown via CMAUP database
Emodin-8-glucoside 99649 Click to see 432.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2S)-2,3-dihydroxypropyl] 3,4,5-trihydroxybenzoate 51543740 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC(CO)O 244.20 unknown via CMAUP database
6-O-galloyl-beta-D-glucose 5317463 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)O)O 332.26 unknown via CMAUP database
Methyl Gallate 7428 Click to see 184.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aR,4bR,7R,8S,10aR)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 102375494 Click to see 318.40 unknown https://doi.org/10.1016/S0031-9422(03)00216-4
https://doi.org/10.1016/S0031-9422(00)85504-1
(1S,2R,4aR,4bS,8R,8aR)-2-ethenyl-8-(hydroxymethyl)-2,4b,8-trimethyl-3,4,4a,5,6,7,8a,9-octahydro-1H-phenanthren-1-ol 122181510 Click to see 304.50 unknown https://doi.org/10.1016/S0031-9422(00)85504-1
2-ethenyl-8-(hydroxymethyl)-2,4b,8-trimethyl-3,4,4a,5,6,7,8a,9-octahydro-1H-phenanthren-1-ol 162875489 Click to see 304.50 unknown https://doi.org/10.1016/S0031-9422(00)85504-1
7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 267302 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(00)85504-1
https://doi.org/10.1016/S0031-9422(03)00216-4
7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 162998232 Click to see 318.40 unknown https://doi.org/10.1016/S0031-9422(00)85504-1
https://doi.org/10.1016/S0031-9422(03)00216-4
Isopimaric Acid 442048 Click to see 302.50 unknown https://doi.org/10.1016/S0031-9422(03)00216-4
https://doi.org/10.1016/S0031-9422(00)85504-1
https://doi.org/10.1002/CHIN.200348156
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2R,3R,4S,5S,6R)-2-[[(1S,3R,4S,4aR,8aR)-4-[(Z)-5-hydroxy-3-(hydroxymethyl)pent-3-enyl]-3,4,8,8a-tetramethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 11271668 Click to see 484.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.012
[(2R,3S,4S,5R,6R)-6-[[(1S,3R,4S,4aR,8aR)-4-[(Z)-5-hydroxy-3-(hydroxymethyl)pent-3-enyl]-3,4,8,8a-tetramethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 11307037 Click to see 526.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.012
[(2R,3S,4S,5R,6R)-6-[[(1S,3R,4S,4aR,8aR)-4-[(Z)-5-hydroxy-3-(hydroxymethyl)pent-3-enyl]-8-(hydroxymethyl)-3,4,8a-trimethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 11398630 Click to see CC1CC(C2(C(C1(C)CCC(=CCO)CO)CCC=C2CO)C)OC3C(C(C(C(O3)COC(=O)C)O)O)O 542.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.012
[(2R,3S,4S,5R,6R)-6-[[(1S,3R,4S,4aR,8aR)-4-[2-(furan-3-yl)ethyl]-3,4,8,8a-tetramethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 11214324 Click to see 506.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.012
[(2R,3S,4S,5R,6R)-6-[[(1S,3R,4S,4aR,8aR)-4-[2-(furan-3-yl)ethyl]-8-(hydroxymethyl)-3,4,8a-trimethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 163188864 Click to see CC1CC(C2(C(C1(C)CCC3=COC=C3)CCC=C2CO)C)OC4C(C(C(C(O4)COC(=O)C)O)O)O 522.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.012
[(2S,3R,4R,5R,6R)-6-[[(1R,3S,4S,4aR,8aR)-4-[(Z)-5-hydroxy-3-(hydroxymethyl)pent-3-enyl]-8-(hydroxymethyl)-3,4,8a-trimethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 162975068 Click to see 542.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.012
[3,4,5-Trihydroxy-6-[[4-[5-hydroxy-3-(hydroxymethyl)pent-3-enyl]-3,4,8,8a-tetramethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]oxan-2-yl]methyl acetate 72794387 Click to see CC1CC(C2(C(C1(C)CCC(=CCO)CO)CCC=C2C)C)OC3C(C(C(C(O3)COC(=O)C)O)O)O 526.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.012
[3,4,5-Trihydroxy-6-[[4-[5-hydroxy-3-(hydroxymethyl)pent-3-enyl]-8-(hydroxymethyl)-3,4,8a-trimethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]oxan-2-yl]methyl acetate 72831706 Click to see 542.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.012
[6-[[4-[2-(Furan-3-yl)ethyl]-8-(hydroxymethyl)-3,4,8a-trimethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 163024849 Click to see CC1CC(C2(C(C1(C)CCC3=COC=C3)CCC=C2CO)C)OC4C(C(C(C(O4)COC(=O)C)O)O)O 522.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.012
2-[[4-[5-Hydroxy-3-(hydroxymethyl)pent-3-enyl]-3,4,8,8a-tetramethyl-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 72778113 Click to see CC1CC(C2(C(C1(C)CCC(=CCO)CO)CCC=C2C)C)OC3C(C(C(C(O3)CO)O)O)O 484.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.012
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(5S,6aR,7R,8S,9R,10aS)-9-acetyloxy-7-[(2R)-2-(furan-3-yl)-2-hydroxyethyl]-7,8-dimethyl-3-oxo-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-5-yl] acetate 637285 Click to see 446.50 unknown https://doi.org/10.1016/S0031-9422(03)00216-4
https://doi.org/10.1002/CHIN.200348156
[9-acetyloxy-7-[2-(furan-3-yl)-2-hydroxyethyl]-7,8-dimethyl-3-oxo-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-5-yl] acetate 22297685 Click to see 446.50 unknown https://doi.org/10.1016/S0031-9422(03)00216-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)85504-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(1S,2S,4aR,4bS,7S,10aR)-7-ethenyl-2-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 102193489 Click to see 318.40 unknown https://doi.org/10.1016/S0031-9422(00)85504-1
7-ethenyl-2-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 162950649 Click to see CC1(CCC2C(=CCC3C2(CCC(C3(C)C(=O)O)O)C)C1)C=C 318.40 unknown https://doi.org/10.1016/S0031-9422(00)85504-1
> 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
(2S)-5-amino-2-ammonio-5-oxopentanoate 6992086 Click to see 146.14 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-[1-hydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 5319972 Click to see 378.40 unknown via CMAUP database
1-[1,6-dihydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 100753 Click to see 394.40 unknown via CMAUP database
2-[[(2R,3S,4S,5R,6S)-6-(7-acetyl-8-hydroxy-3-methoxy-6-methylnaphthalen-1-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-2-oxoacetic acid 5321979 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)COC(=O)C(=O)O)O)O)O)OC 480.40 unknown via CMAUP database
2-methyl-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromene-5-carboxylic acid 5315687 Click to see 382.30 unknown via CMAUP database
gallic acid 4-O-beta-D-(6'-O-galloy)glucoside 11972354 Click to see 484.40 unknown via CMAUP database
Raspberryketone glucoside 5320521 Click to see 326.34 unknown via CMAUP database
Torachrysone 8-O-Glucoside 11972479 Click to see 408.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-phenylprop-2-enoate 11972309 Click to see 310.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
[(2S)-7-Hydroxy-2-methyl-4-oxo-3,4-dihydro-2H-1-benzopyran-5-yl]acetic acid 5319543 Click to see 236.22 unknown via CMAUP database
4H-1-Benzopyran-4-one, 5-acetyl-7-hydroxy-2-methyl- 5315891 Click to see 218.20 unknown via CMAUP database
7-Hydroxy-2-[(2S)-2-hydroxypropyl]-5-methyl-4H-1-benzopyran-4-one 45272307 Click to see 234.25 unknown via CMAUP database
7-Hydroxy-2-methyl-4-oxo-4H-1-benzopyran-5-acetic acid 14429402 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)CC(=O)O 234.20 unknown via CMAUP database
7-Hydroxy-2-methyl-4-oxo-4H-1-benzopyran-5-carboxylic acid 5315688 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)C(=O)O 220.18 unknown via CMAUP database
Cassiachromone 5319500 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)CC(=O)C 232.23 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
[(5S,6aR,7R,8S,9R,10aS)-9-acetyloxy-7-[(2R)-2-(furan-3-yl)-2-hydroxyethyl]-8-methyl-3-oxo-1,5,6,6a,7,8,9,10-octahydrobenzo[d][2]benzofuran-5-yl] acetate 101260318 Click to see 432.50 unknown https://doi.org/10.1002/CHIN.200348156
> Organoheterocyclic compounds / Naphthopyrans
(1S,4R,7R,9S,10S,14R)-7-(furan-3-yl)-10-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione 15705465 Click to see CC12CC(OC(=O)C1CCC34C2(CC=CC3C(=O)OC4)O)C5=COC=C5 358.40 unknown https://doi.org/10.1016/S0031-9422(00)85504-1
(1S,4S,7R,9R,10R)-7-(furan-3-yl)-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-13-ene-5,15-dione 162973466 Click to see 342.40 unknown https://doi.org/10.1016/S0031-9422(03)00216-4
7-(Furan-3-yl)-10-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione 162875586 Click to see 358.40 unknown https://doi.org/10.1016/S0031-9422(00)85504-1
7-(Furan-3-yl)-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-13-ene-5,15-dione 326832 Click to see 342.40 unknown https://doi.org/10.1016/S0031-9422(03)00216-4
Salviarin 329251 Click to see 342.40 unknown https://doi.org/10.1002/CHIN.200348156
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
3,3'-Digalloylprocyanidin B2 124016 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 882.70 unknown via CMAUP database
procyanidin B1 3-O-gallate 12795888 Click to see 730.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(+)-Catechin-5-O-beta-D-glucopyranoside 6324898 Click to see 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Rhapontigenin 5320954 Click to see 258.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
[(2R,3S,4S,5R,6S)-6-[4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 5322088 Click to see 542.50 unknown via CMAUP database
resveratrol-4'-O-(2''-O-galloyl)-glucopyranoside 10325054 Click to see 542.50 unknown via CMAUP database
Resveratroloside 5322089 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 390.40 unknown via CMAUP database
Rhaponticin 637213 Click to see 420.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,2,6-Tri-O-Galloyl-Beta-D-Glucose 440308 Click to see 636.50 unknown via CMAUP database
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see 484.40 unknown via CMAUP database
1,6-di-O-galloyl-2-O-cinnamoyl-beta-D-glucose 6325082 Click to see 614.50 unknown via CMAUP database
beta-D-Glucopyranose, 2-((2E)-3-phenyl-2-propenoate) 1-(3,4,5-trihydroxybenzoate) 5315898 Click to see 462.40 unknown via CMAUP database
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown via CMAUP database

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