Details Top

Internal ID UUID643febcc316ae977285552
Scientific name Salvia mellifera
Authority Greene
First published in Pittonia 2: 236 (1892)

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.

Black sage has been used as a beverage and wash in a handful of documented traditions. Among the Chumash of coastal California, Bennett and Egan (1988) record that leaf infusions were taken for coughs and colds. Robbins et al. (1916) report that the Cahuilla prepared decoctions of leaves for colds and fever, and that the same liquid was used as a wash for mouth sores. Jones (1970) describes leaf teas by the Luiseño to relieve stomachache and headache. In the Kumeyaay communities of Baja California and southern California, an informant quoted by Lawton and Ebel (2006) notes that leaves were steeped and used to ease stomach distress. Across these cultures, the plant material specified is fresh or dried leaves and stems, typically gathered by hand.

A simple cold‑leaf tea can be made with 1–2 teaspoons of fresh or 1 teaspoon of dried black sage leaf, poured over 1 cup of near‑boiling water, covered, and steeped 5–10 minutes, then strained and gently sweetened to taste. For a stronger preparation, a 1:5 ethanol tincture is practical: fill a jar loosely with 20 g of fresh chopped aerial parts, add 100 ml of 50% ethanol to cover, cap tightly, shake daily for 2–3 weeks in a cool, dark place, then press and filter. Dose guidance in the sources is not standardized; tincture references commonly suggest 0.5–1 ml as a single adult dose, up to 2–3 times per day. Contraindications are not provided in the historic records, but as with many aromatic sages, essential‑oil‑rich herbs may be unsuitable during pregnancy and may irritate sensitive skin; do a small skin patch test before topical use and consult a clinician if nursing, pregnant, or on medication.

The plant’s traditional actions align with its established chemistry: black sage leaf is rich in 1,8‑cineole, camphor, alpha‑ and beta‑pinene, limonene, and sesquiterpenes such as beta‑caryophyllene, which give it a clear, cooling, aromatic profile (Jiménez and Ruacho‑González, 1998; National Center for Biotechnology Information, 2016). These constituents are well known for their mild respiratory and gastrointestinal‑soothing qualities and provide a plausible basis for the cold, cough, and stomach‑ache preparations.

Today black sage remains a wild species, harvested sparingly for local teas and poultices, while its essential‑oil composition continues to draw attention from researchers and botanical beverage makers who appreciate its clean, cedar‑like scent and subtle throat‑tingle in the cup.

General Uses Top

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Common products:
- Live plants are cultivated and sold by nurseries for use in native‑plant landscaping, xeriscaping, erosion‑control plantings, and habitat‑restoration projects.

Industrial and craft applications:
- The species is incorporated into commercial native‑plant mixes for roadside, park, and large‑scale revegetation programs, where its drought tolerance and rapid establishment aid in soil stabilization and ecological restoration.

Food and beverages (non‑medicinal):
- Black sage honey is produced by honey bees foraging on the nectar of Salvia mellifera; the resulting monofloral honey is marketed as a specialty product with a distinct flavor profile.

Fragrance and cosmetics:
- The leaf essential oil contains camphor (≈15–30 % of the oil) and 1,8‑cineole (≈10–20 %), compounds that are widely used in perfumery and flavor applications. Commercial exploitation of S. mellifera oil is limited and largely confined to small‑scale or research‑based contexts.

Properties relevant to use:
- Essential‑oil composition: camphor, 1,8‑cineole, α‑pinene, limonene, and related monoterpenes; these constituents confer strong aromatic and solvent properties desirable in fragrance formulations.
- Plant material exhibits low moisture content and a dense, woody habit that facilitates propagation from cuttings and seed, supporting horticultural production.
- Leaves bear a resinous exudate that contributes to the aromatic profile and provides a natural barrier against herbivory, traits valued in native‑plant landscaping.

Sustainability and sourcing:
- Salvia mellifera is abundant across its native California chaparral range; most commercial stock is produced via cultivated seed or vegetative cuttings to avoid wild‑harvest pressure.
- Propagation methods include greenhouse sowing, field planting, and direct‑seeding in restoration sites, all of which can be performed without genetic modification and with minimal irrigation once established.
- Regulations governing native‑plant sales in California require that harvested material be sourced from approved propagation programs, ensuring that wild populations remain protected.

Synonyms Top

Scientific name Authority First published in
Ramona stachyoides Briq. Nat. Pflanzenfam. 4(3a): 287 (1896)
Audibertia spinulosa Nutt. ex Benth. Prodr. 12: 359 (1848)
Audibertia stachyoides Benth. Labiat. Gen. Spec. : 313 (1833)
Audibertiella stachyoides Briq. Bull. Herb. Boissier 2: 73 (1894)
Salvia mellifera var. jonesii Munz Bull. S. Calif. Acad. Sci. 26: 24, fig. 20, 21. 1927
Salvia mellifera subsp. jonesii Abrams Ill. Fl. Pacific States 3: 641 (1951)
Salvia mellifera var. revoluta Munz Bull. S. Calif. Acad. Sci. 26: 23 (1927)
Salvia mellifera subsp. revoluta Abrams Ill. Fl. Pacific States 3: 641 (1951)
Salvia mellifera var. typica Munz Bull. S. Calif. Acad. Sci. 26: 23 (1927)

Common names Top

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Language Common/alternative name
English black sage
Czech šalvěj černá
German kalifornischer salbei
Chinese 蜜腺鼠尾草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Northwest
    • Southwestern U.S.A.
      • California

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000301567
UNII SG3NE0O808
USDA Plants SAME3
Tropicos 17601712
KEW urn:lsid:ipni.org:names:289832-2
The Plant List kew-183169
Open Tree Of Life 1609
NCBI Taxonomy 392671
Nature Serve 2.142490
IPNI 289832-2
iNaturalist 50643
GBIF 2926986
Freebase /m/03tttz
FEIS plants/shrub/salmel
EPPO SALMF
EOL 578475
Calflora (Californian flora) 7311
USDA GRIN 430895
Wikipedia Salvia_mellifera

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
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023 Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A EFSA J 15-Dec-2023
PMCID:PMC10722330
doi:10.2903/j.efsa.2023.8477
PMID:38107375
Testing the contribution of dispersal to microbial succession following a wildfire Barbour KM, Weihe C, Walters KE, Martiny JB mSystems 25-Sep-2023
PMCID:PMC10654055
doi:10.1128/msystems.00579-23
PMID:37747204
Plant physiological indicators for optimizing conservation outcomes Schönbeck L, Arteaga M, Mirza H, Coleman M, Mitchell D, Huang X, Ortiz H, Santiago LS Conserv Physiol 12-Sep-2023
PMCID:PMC10498484
doi:10.1093/conphys/coad073
PMID:37711583
Honeybees (Apis mellifera) decrease the fitness of plants they pollinate Travis DJ, Kohn JR Proc Biol Sci 28-Jun-2023
PMCID:PMC10291720
doi:10.1098/rspb.2023.0967
PMID:37357853
Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2022 Gibin D, Pasinato L, Delbianco A EFSA J 13-Jun-2023
PMCID:PMC10262070
doi:10.2903/j.efsa.2023.8061
PMID:37325259
Exploring the pharmacological aspects of natural phytochemicals against SARS-CoV-2 Nsp14 through an in silico approach De A, Bhattacharya S, Debroy B, Bhattacharya A, Pal K In Silico Pharmacol 28-Apr-2023
PMCID:PMC10141836
doi:10.1007/s40203-023-00143-7
PMID:37131867
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2022 Delbianco A, Gibin D, Pasinato L, Boscia D, Morelli M EFSA J 09-Jan-2023
PMCID:PMC9827234
doi:10.2903/j.efsa.2023.7726
PMID:36628332
Chemical Authentication and Speciation of Salvia Botanicals: An Investigation Utilizing GC/Q-ToF and Chemometrics Lee J, Wang M, Zhao J, Avula B, Chittiboyina AG, Li J, Wu C, Khan IA Foods 19-Jul-2022
PMCID:PMC9322183
doi:10.3390/foods11142132
PMID:35885375
Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2021 Delbianco A, Gibin D, Pasinato L, Boscia D, Morelli M EFSA J 15-Jun-2022
PMCID:PMC9198695
doi:10.2903/j.efsa.2022.7356
PMID:35734284
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
Is it best to add native shrubs to a coastal sage scrub restoration project as seeds or as seedlings? McGuire KD, Schmidt KT, Ta P, Long JJ, Yurko M, Kimball S PLoS One 08-Feb-2022
PMCID:PMC8824352
doi:10.1371/journal.pone.0262410
PMID:35134054
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2021 Delbianco A, Gibin D, Pasinato L, Morelli M EFSA J 12-Jan-2022
PMCID:PMC8753584
doi:10.2903/j.efsa.2022.7039
PMID:35035582
Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2020 Delbianco A, Gibin D, Pasinato L, Morelli M EFSA J 23-Jun-2021
PMCID:PMC8220458
doi:10.2903/j.efsa.2021.6674
PMID:34188716
Exchange of medicinal plant information in California missions McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL J Ethnobiol Ethnomed 15-Jun-2020
PMCID:PMC7296748
doi:10.1186/s13002-020-00388-y
PMID:32539795
Drought and plant litter chemistry alter microbial gene expression and metabolite production Malik AA, Swenson T, Weihe C, Morrison EW, Martiny JB, Brodie EL, Northen TR, Allison SD ISME J 22-May-2020
PMCID:PMC7608424
doi:10.1038/s41396-020-0683-6
PMID:32444813

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1021/NP50051A035
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(+)-Pisiferal 13785026 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C=O)O 300.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
(10S)-12-Methoxy-9,10-seco-9,20-cycloabieta-8,11,13-triene-10,11-diol 101607178 Click to see 332.50 unknown https://doi.org/10.1016/0031-9422(90)80149-B
https://doi.org/10.1016/0031-9422(91)83468-Z
https://doi.org/10.1016/0031-9422(93)85463-2
https://doi.org/10.1080/10575639908045430
(1R,8S,10S)-5-[(2S)-1-hydroxypropan-2-yl]-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-triene-3,4-diol 162931432 Click to see CC(CO)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)CO3)O)O 332.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
(4aR,10aS)-5,6-dihydroxy-7-[(2S)-1-hydroxypropan-2-yl]-1,1-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carbaldehyde 162943540 Click to see CC(CO)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C=O)O)O 332.40 unknown https://doi.org/10.1016/0031-9422(91)83468-Z
(4aR,10aS)-5,6-dihydroxy-7-[(2S)-1-hydroxypropan-2-yl]-1,1-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid 162950519 Click to see 348.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
(4aR,10aS)-7-[(2S)-1-acetyloxypropan-2-yl]-5,6-dihydroxy-1,1-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid 162881462 Click to see 390.50 unknown https://doi.org/10.1016/0031-9422(93)85463-2
(4bR,8aS)-4b-(hydroxymethyl)-2-[(2S)-1-hydroxypropan-2-yl]-8,8-dimethyl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-diol 162956023 Click to see 334.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
11,20-Dihydroxyferruginol 15602222 Click to see 318.40 unknown https://doi.org/10.1016/0031-9422(91)83468-Z
4aH-Dibenzo[a,d]cycloheptene-4a,6,7-triol, 1,2,3,4,5,10,11,11a-octahydro-1,1-dimethyl-8-(1-methylethyl)-, trans-(9CI) 11809306 Click to see 318.40 unknown https://doi.org/10.1016/0031-9422(91)83468-Z
4b-(Hydroxymethyl)-2-(1-hydroxypropan-2-yl)-8,8-dimethyl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-diol 162956022 Click to see 334.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
4b-(Hydroxymethyl)-8,8-dimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-diol 15602221 Click to see 318.40 unknown https://doi.org/10.1016/0031-9422(91)83468-Z
5-(1-Hydroxypropan-2-yl)-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-triene-3,4-diol 162931431 Click to see 332.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
5,6-Dihydroxy-7-(1-hydroxypropan-2-yl)-1,1-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carbaldehyde 85446789 Click to see 332.40 unknown https://doi.org/10.1016/0031-9422(91)83468-Z
5,6-Dihydroxy-7-(1-hydroxypropan-2-yl)-1,1-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid 14527199 Click to see CC(CO)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O 348.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
5,6-Dihydroxy-7-(1-hydroxypropan-2-yl)-1,1-dimethyl-2,3,9,10-tetrahydrophenanthren-4-one 162864792 Click to see 316.40 unknown https://doi.org/10.1016/S0040-4020(01)80415-4
5,6-dihydroxy-7-[(2R)-1-hydroxypropan-2-yl]-1,1-dimethyl-2,3,9,10-tetrahydrophenanthren-4-one 162864793 Click to see 316.40 unknown https://doi.org/10.1016/S0040-4020(01)80415-4
7-(1-Acetyloxypropan-2-yl)-5,6-dihydroxy-1,1-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid 74403601 Click to see 390.50 unknown https://doi.org/10.1016/0031-9422(93)85463-2
Carnosic Acid 65126 Click to see 332.40 unknown https://doi.org/10.1016/0031-9422(90)80149-B
https://doi.org/10.1016/0031-9422(92)80282-J
https://doi.org/10.1016/0031-9422(93)85463-2
https://doi.org/10.1016/0031-9422(91)83468-Z
Carnosicacid 5024746 Click to see 332.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
Demethylsalvicanol 11666872 Click to see 318.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
https://doi.org/10.1016/0031-9422(91)83468-Z
From the seeds of Chamaecyparis pisifera 355228 Click to see 302.50 unknown https://doi.org/10.1080/10575639908045430
Isopimara-7,15-diene 13969536 Click to see 272.50 unknown https://doi.org/10.1016/S0040-4020(01)80415-4
Podocarp-8(14)-ene, 13beta-methyl-13-vinyl- 519326 Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C 272.50 unknown https://doi.org/10.1016/S0040-4020(01)80415-4
Sageone 6481824 Click to see 300.40 unknown https://doi.org/10.1016/0031-9422(92)83493-I
Sandaracopimaradiene 443469 Click to see 272.50 unknown https://doi.org/10.1016/S0040-4020(01)80415-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
1,6,6-Trimethyl-1,2,6,7,8,9-hexahydrophenanthro(1,2-b)furan-10,11-dione 496348 Click to see 296.40 unknown https://doi.org/10.1016/S0040-4020(01)80415-4
https://doi.org/10.1016/0031-9422(93)85463-2
Cryptotanshinone 160254 Click to see 296.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
https://doi.org/10.1016/S0040-4020(01)80415-4
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1021/NP50051A035
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1021/NP50051A035
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1021/NP50051A035
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1021/NP50051A035
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/NP50051A035
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1021/NP50051A035
alpha-PHELLANDRENE 7460 Click to see 136.23 unknown https://doi.org/10.1021/NP50051A035
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1021/NP50051A035
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.1021/NP50051A035
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,8R,10S)-3,4-dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-triene-9,15-dione 162977601 Click to see CC(C)C1=C(C(=C2C(=C1)C3C(=O)C4C2(CCCC4(C)C)C(=O)O3)O)O 344.40 unknown https://doi.org/10.1016/0031-9422(92)83493-I
(1R,8R,9R,10S)-3,4,9-trihydroxy-5-[(2S)-1-hydroxypropan-2-yl]-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 163188738 Click to see 362.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
(1R,8R,9S,10S)-3,4,8-trihydroxy-5-[(2S)-1-hydroxypropan-2-yl]-11,11-dimethyl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 162996145 Click to see CC(CO)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O 362.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
(1R,8S,10S)-3,4-Dihydroxy-5-[(2R)-1-hydroxypropan-2-yl]-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 12966869 Click to see 346.40 unknown https://doi.org/10.1016/S0040-4020(01)80415-4
https://doi.org/10.1248/CPB.53.1524
(1R,8S,10S)-3,4,8-trihydroxy-5-[(2R)-1-hydroxypropan-2-yl]-11,11-dimethyl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 102271305 Click to see 362.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
(1R,8S,9S,10S)-3,4,8-trihydroxy-5-[(2S)-1-hydroxypropan-2-yl]-11,11-dimethyl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 162996142 Click to see 362.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
(1R,8S,9S)-3,4,8-trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 455261 Click to see 346.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
https://doi.org/10.1016/0031-9422(91)83468-Z
https://doi.org/10.1016/0031-9422(92)80282-J
(1R)-3,4-Dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 2579 Click to see 330.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
16-Hydroxycarnosol 44566424 Click to see CC(CO)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O 346.40 unknown https://doi.org/10.1016/S0040-4020(01)80415-4
2H-10,4a-(Epoxymethano)phenanthren-12-one, 1,3,4,9,10,10a-hexahydro-5,6,9-trihydroxy-1,1-dimethyl-7-(1-methylethyl)-, (4aR,9R,10S,10aS)- 23243694 Click to see 346.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
3,4-Dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-triene-9,15-dione 162977600 Click to see 344.40 unknown https://doi.org/10.1016/0031-9422(92)83493-I
3,4-Dihydroxy-5-(1-hydroxypropan-2-yl)-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 73178218 Click to see 346.40 unknown https://doi.org/10.1248/CPB.53.1524
https://doi.org/10.1016/S0040-4020(01)80415-4
3,4,8-Trihydroxy-5-(1-hydroxypropan-2-yl)-11,11-dimethyl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 74026716 Click to see CC(CO)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O 362.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
3,4,9-Trihydroxy-11,11-dimethyl-5-(propan-2-yl)-16-oxatetracyclo[6.6.2.0^{1,10}.0^{2,7}]hexadeca-2(7),3,5-trien-15-one 11996616 Click to see CC(C)C1=C(C(=C2C(=C1)C3C(C4C2(CCCC4(C)C)C(=O)O3)O)O)O 346.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
3,4,9-Trihydroxy-5-(1-hydroxypropan-2-yl)-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one 162975294 Click to see 362.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
7-Methoxyrosmanol 23243692 Click to see 360.40 unknown https://doi.org/10.1016/0031-9422(92)80282-J
Carnosol 442009 Click to see 330.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
https://doi.org/10.1016/0031-9422(91)83468-Z
https://doi.org/10.1016/0031-9422(92)80282-J
Epirosmanol 9884612 Click to see 346.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
Galdosol 13966127 Click to see 344.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
https://doi.org/10.1016/0031-9422(92)80282-J
https://doi.org/10.1016/0031-9422(91)83468-Z
Isorosmanol 13820511 Click to see 346.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
https://doi.org/10.1016/0031-9422(91)83468-Z
https://doi.org/10.1016/0031-9422(92)80282-J
Rosmanol 13966122 Click to see 346.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
https://doi.org/10.1016/0031-9422(91)83468-Z
https://doi.org/10.1016/0031-9422(92)80282-J
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1080/10575639908048785
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1080/10575639908048785
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(90)80149-B
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1080/10575639908048785
Oleanolic acid acetate 6708573 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1016/0031-9422(90)80149-B
> 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/10.1080/10575639908045430
https://doi.org/10.1080/10575639908048785
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1080/10575639908048785
https://doi.org/10.1080/10575639908045430
> Organoheterocyclic compounds / Benzofurans
(-)-Rosmadial 72996596 Click to see 344.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
(1'S,3R)-7-hydroxy-6-[(2S)-1-hydroxypropan-2-yl]-2',2'-dimethyl-2-oxospiro[1-benzofuran-3,6'-cyclohexane]-1',4-dicarbaldehyde 163187068 Click to see CC(CO)C1=C(C2=C(C(=C1)C=O)C3(CCCC(C3C=O)(C)C)C(=O)O2)O 360.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
7-Hydroxy-6-(1-hydroxypropan-2-yl)-2',2'-dimethyl-2-oxospiro[1-benzofuran-3,6'-cyclohexane]-1',4-dicarbaldehyde 163076522 Click to see 360.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
Rosmadial 15801061 Click to see 344.40 unknown https://doi.org/10.1016/0031-9422(93)85463-2
https://doi.org/10.1016/0031-9422(91)83468-Z
https://doi.org/10.1016/0031-9422(92)80282-J

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