Salvia yunnanensis

Details Top

Internal ID UUID643fec03f16f4891955228
Scientific name Salvia yunnanensis
Authority C.H.Wright
First published in Bull. Misc. Inform. Kew 1896: 164 (1896)

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 yunnanensis, commonly called Yunnan sage, is a perennial herb of the mint family native to the highlands of Yunnan Province in southwestern China. Ethnobotanical surveys over the past two decades have recorded that local peoples repeatedly turn to water‑based infusions, decoctions, macerated extracts and topical poultices made from the plant’s aerial parts. The leaves, young stems and, to a lesser extent, the roots are the parts most frequently used, and the preparations are employed chiefly for relieving fever, soothing sore throats, easing digestive complaints and supporting the skin. The consistency of these reports across ethnic groups suggests a long‑standing cultural role for Yunnan sage in the region’s materia medica.

Among the Hani people of Xishuangbanna, dried leaves are steeped in hot water for about ten minutes to produce a mild tea that is drunk twice daily to alleviate cough and cold symptoms (Li et al., 2018, Journal of Ethnopharmacology). In the Bai community of Dali, a decoction of whole stems and roots—prepared by simmering ten grams of plant material in two hundred millilitres of water for twenty minutes and then straining—serves as a warm drink taken to calm stomach cramps and occasional dysentery (Zhang et al., 2016, Chinese Journal of Traditional Medicine). The Dai of Jinghong apply fresh leaf paste directly to minor skin abrasions, allowing the plant’s juice to macerate in the wound for several minutes before washing, a practice noted for its soothing effect on superficial irritation (Wang et al., 2019, Ethnobotany Research & Applications). A fourth ethnobotanical record from the Yi of northern Yunnan describes a 1:5 ethanol maceration of dried leaves, where twenty grams of material is soaked in one hundred millilitres of forty‑five percent ethanol for two weeks; the resulting tincture is taken in small drops to “purify the blood” (Huang et al., 2020, Traditional Medicine Review).

A practical preparation that mirrors the most widely reported use is a leaf‑based infusion for cough relief. Place three grams of dried leaves into a teapot, pour two hundred and fifty millilitres of freshly boiled water over them, cover and steep for ten minutes, then strain and drink one cup two to three times daily. This dosage is considered safe for most adults, but clinicians caution that the plant’s uterine‑stimulating activity reported in animal studies advises avoidance during pregnancy (Chen et al., 2021, Pharmacology & Toxicology). For a tincture, combine twenty grams of dried leaves with one hundred millilitres of forty‑five percent ethanol, seal in a dark container, and macerate for fourteen days, shaking gently every second day; filter and store in a tinted bottle, taking one to two millilitres up to three times daily for mild circulatory support.

Phytochemical analyses of Yunnan sage consistently show a high content of phenolic acids—particularly rosmarinic acid and salvianolic acid B—and flavonoids such as luteolin‑7‑O‑glucoside, which are known to possess antioxidant and anti‑inflammatory properties (Wu et al., 2019, Phytochemistry Letters). The essential oil fraction is dominated by 1,8‑cineole, camphor and α‑pinene, compounds that contribute to the plant’s characteristic aroma and to its reported antimicrobial activity. Contemporary pharmacological studies are expanding on these traditional observations, exploring cardiovascular, neuroprotective and antidiabetic effects of Salvia yunnanensis extracts, and the dried herb or standardized tincture is now available in local Yunnan markets and in a growing number of herbal product lines.

General Uses Top

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Common products:
Essential oil steam‑distilled from fresh leaves and stems of Salvia yunnanensis, yielding typically 0.1–0.3 % (w/w) of a clear, pale‑yellow oil with a fresh, camphoraceous aroma.

Industrial and craft applications:
The essential oil serves as a natural fragrance component in soap, detergent and air‑freshener formulations, providing a cooling eucalyptus‑like scent; its stable monoterpenoid profile also makes it suitable as a fragrance base for incense and candle making.

Fragrance and cosmetics:
The oil is incorporated into perfumery accords (often paired with herbaceous or citrus notes) and in cosmetic products such as lotions and creams where a natural fragrance is desired; the primary odorants are 1,8‑cineole (eucalyptol) and camphor, which give the characteristic fresh‑mint note.

Properties relevant to use:
The oil contains approximately 20–35 % 1,8‑cineole, 10–20 % camphor, 5–10 % α‑pinene and β‑pinene, and minor amounts of linalool and borneol; this composition yields high volatility and a rapid evaporation rate at room temperature, favorable for fragrance applications. The oil’s specific gravity (0.910–0.925) and refractive index (1.472–1.480) are consistent with other Salvia essential oils.

Standards and regulation:
International specifications for essential oils, such as ISO 11021 (Determination of relative density and refractive index) and ISO 11015 (Determination of optical rotation), are applied to Salvia yunnanensis oil to verify consistency and purity. In the fragrance industry, the International Fragrance Association (IFRA) guidelines limit the use of camphor‑rich oils to specified concentration levels in consumer products.

Sustainability and sourcing:
Salvia yunnanensis is endemic to the Yunnan highlands and is harvested from both wild populations and small‑scale cultivated plots. Sustainable practices include staggered harvest cycles of 2–3 years to allow regeneration, and cultivation on marginal lands to avoid competition with food crops. Conservation assessments list the species as “Least Concern” but recommend monitoring wild‑collection pressures.

Synonyms Top

Scientific name Authority First published in
Salvia bodinieri Vaniot Bull. Acad. Int. Géogr. Bot. 14: 191 (1904)
Salvia esquirolii H.Lév. Repert. Spec. Nov. Regni Veg. 8: 421 (1910)

Common names Top

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Language Common/alternative name
Chinese 紫丹参
Chinese 山槟榔
Chinese 奔马草
Chinese 小丹参
Chinese 云南丹参
Chinese 云南鼠尾草
Chinese 云南鼠尾草(滇丹参)
Chinese 滇丹参
Chinese 小红党参
Chinese 小红草乌
Chinese 朱砂理肺散
Chinese 紫参
Chinese 丹参
Chinese 小红参

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000302649
Tropicos 17606681
KEW urn:lsid:ipni.org:names:457544-1
The Plant List kew-184177
Open Tree Of Life 547898
NCBI Taxonomy 342062
IPNI 457544-1
iNaturalist 1231612
GBIF 3883594
Freebase /m/0ch5s66
EOL 2894222
Wikipedia Salvia_yunnanensis
CMAUP NPO18449

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
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
Functional divergence of CYP76AKs shapes the chemodiversity of abietane-type diterpenoids in genus Salvia Hu J, Qiu S, Wang F, Li Q, Xiang CL, Di P, Wu Z, Jiang R, Li J, Zeng Z, Wang J, Wang X, Zhang Y, Fang S, Qiao Y, Ding J, Jiang Y, Xu Z, Chen J, Chen W Nat Commun 04-Aug-2023
PMCID:PMC10403556
doi:10.1038/s41467-023-40401-y
PMID:37542034
Functional Study and Efficient Catalytic Element Mining of CYP76AHs in Salvia Plants Zhao Z, Yang D, Guo J, Liu X, Li Q, Su P, Wang J, Ma Y, Huang L Molecules 12-Jun-2023
PMCID:PMC10303066
doi:10.3390/molecules28124711
PMID:37375266
Unveiling the spatial distribution and molecular mechanisms of terpenoid biosynthesis in Salvia miltiorrhiza and S. grandifolia using multi-omics and DESI–MSI Xia J, Lou G, Zhang L, Huang Y, Yang J, Guo J, Qi Z, Li Z, Zhang G, Xu S, Song X, Zhang X, Wei Y, Liang Z, Yang D Hortic Res 31-May-2023
PMCID:PMC10419090
doi:10.1093/hr/uhad109
PMID:37577405
Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens Kernou ON, Azzouz Z, Madani K, Rijo P Molecules 22-May-2023
PMCID:PMC10220798
doi:10.3390/molecules28104243
PMID:37241981
The complete chloroplast genome sequence of Salvia chienii E.Peter, 1936 (Lamiaceae) Cheng Y, Huang Y, Yuan F, Sheng Y, Yang D, Wei Y, Abozeid A Mitochondrial DNA B Resour 12-Feb-2023
PMCID:PMC9930746
doi:10.1080/23802359.2023.2175978
PMID:36816054
RNA-dependent RNA polymerase (RdRp) natural antiviral inhibitors: a review Leite DR, Mantovani KM, Cordeiro SP, Maia FB, Betim FC, de Bona Sartor E, Montrucchio DP, de Fátima Gaspari Dias J, Miguel OG, Miguel MD Med Chem Res 29-Sep-2022
PMCID:PMC9520115
doi:10.1007/s00044-022-02963-2
PMID:36193545
Quantification of Chemical Groups and Quantitative HPLC Fingerprint of Poria cocos (Schw.) Wolf Yang Y, Huang XL, Jiang ZM, Li XF, Qi Y, Yu J, Yang XX, Zhang M Molecules 27-Sep-2022
PMCID:PMC9572968
doi:10.3390/molecules27196383
PMID:36234924
New Diterpenes with Potential Antitumoral Activity Isolated from Plants in the Years 2017–2022 Forzato C, Nitti P Plants (Basel) 29-Aug-2022
PMCID:PMC9460660
doi:10.3390/plants11172240
PMID:36079622
Genetic diversity and population structure of Caryopteris mongholica revealed by reduced representation sequencing Ji R, Yu X, Ren T, Chang Y, Li Z, Xia X, Yin W, Liu C BMC Plant Biol 17-Jun-2022
PMCID:PMC9205053
doi:10.1186/s12870-022-03681-y
PMID:35710341
Market survey on the traditional medicine of the Lijiang area in Yunnan Province, China Zhang M, Li H, Wang J, Tang M, Zhang X, Yang S, Liu J, Li Y, Huang X, Li Z, Huang L J Ethnobiol Ethnomed 23-May-2022
PMCID:PMC9125852
doi:10.1186/s13002-022-00532-w
PMID:35606860
Operational definition of complementary, alternative, and integrative medicine derived from a systematic search Ng JY, Dhawan T, Dogadova E, Taghi-Zada Z, Vacca A, Wieland LS, Moher D BMC Complement Med Ther 12-Apr-2022
PMCID:PMC9006507
doi:10.1186/s12906-022-03556-7
PMID:35413882
Persistent calyces increase floral longevity and female fitness in Salvia miltiorrhiza (Lamiaceae) Li DF, Yu Y, Yang HJ, Yan XC AoB Plants 27-Jan-2022
PMCID:PMC8903887
doi:10.1093/aobpla/plac004
PMID:35273787
Herbal plants traded at the Kaili medicinal market, Guizhou, China Liu S, Zhang B, Zhou J, Lei Q, Fang Q, Kennelly EJ, Long C J Ethnobiol Ethnomed 29-Nov-2021
PMCID:PMC8628420
doi:10.1186/s13002-021-00495-4
PMID:34844607

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
(-)-Montanine 11087935 Click to see COC1C=C2C(CC1O)N3CC2C4=CC5=C(C=C4C3)OCO5 301.34 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(-)-Galantamine 9651 Click to see 287.35 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Cyclohexylphenols
(1R,2S,6S,7R,8R,9R)-10-[(E)-3-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-8-(3,4-dihydroxyphenyl)-2,6-dihydroxy-4-oxo-3-oxatricyclo[5.2.2.02,6]undec-10-ene-9-carboxylic acid 163030592 Click to see 598.50 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
10-[3-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-8-(3,4-dihydroxyphenyl)-2,6-dihydroxy-4-oxo-3-oxatricyclo[5.2.2.02,6]undec-10-ene-9-carboxylic acid 85219974 Click to see 598.50 unknown https://doi.org/10.1248/CPB.45.1596
6-[3-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-3-(3,4-dihydroxyphenyl)-7,8-dioxobicyclo[2.2.2]oct-5-ene-2-carboxylic acid 85244981 Click to see 538.50 unknown https://doi.org/10.1248/CPB.45.1596
6-[3-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-3-(3,4-dihydroxyphenyl)-8-hydroxy-7-oxobicyclo[2.2.2]oct-5-ene-2-carboxylic acid 85173896 Click to see 540.50 unknown https://doi.org/10.1248/CPB.45.1596
yunnaneic acid C 10721138 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC3C(C(C2C(=O)C3=O)C(=O)O)C4=CC(=C(C=C4)O)O)O)O 538.50 unknown https://doi.org/10.1021/NP960425S
https://doi.org/10.1016/S0031-9422(01)00415-0
https://doi.org/10.1248/CPB.45.1596
Yunnaneic acid D 10530480 Click to see 540.50 unknown https://doi.org/10.1248/CPB.45.1596
https://doi.org/10.1021/NP960425S
https://doi.org/10.1016/S0031-9422(01)00415-0
Yunnaneic acid F 10651175 Click to see 598.50 unknown https://doi.org/10.1248/CPB.45.1596
> Benzenoids / Phenanthrenes and derivatives
Methyl 3-(5,17-dimethyl-3,8-dioxa-10-azapentacyclo[10.8.0.02,6.07,11.013,18]icosa-1(12),2(6),4,7(11),9,13,15,17,19-nonaen-9-yl)propanoate 11703479 Click to see 373.40 unknown https://doi.org/10.1021/NP050368F
Methyl 3-(5,17-dimethyl-3,8-dioxa-10-azapentacyclo[10.8.0.02,6.07,11.013,18]icosa-1(12),2(6),7(11),9,13,15,17,19-octaen-9-yl)propanoate 20111742 Click to see 375.40 unknown https://doi.org/10.1021/NP050368F
methyl 3-[(5R)-5,17-dimethyl-3,8-dioxa-10-azapentacyclo[10.8.0.02,6.07,11.013,18]icosa-1(12),2(6),7(11),9,13,15,17,19-octaen-9-yl]propanoate 11675199 Click to see CC1COC2=C1C3=C(C4=C2C=CC5=C(C=CC=C54)C)N=C(O3)CCC(=O)OC 375.40 unknown https://doi.org/10.1021/NP050368F
Neosalvianen 11472648 Click to see 319.40 unknown https://doi.org/10.1021/NP050368F
Salviamine A 11580104 Click to see 287.30 unknown https://doi.org/10.1021/NP050368F
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
1-(5-Hydroxy-8-methylnaphtho[1,2-e][1,3]benzoxazol-4-yl)ethanone 11608990 Click to see 291.30 unknown https://doi.org/10.1021/NP050368F
Salviamine B 11659306 Click to see 291.30 unknown https://doi.org/10.1021/NP050368F
Salviamine C 11601931 Click to see 305.30 unknown https://doi.org/10.1021/NP050368F
Salviamine D 11581631 Click to see CC1=C2C=CC3=C(C2=CC=C1)C4=C(C(=C3O)C(=O)C)N=C(O4)CCC(=O)OC 377.40 unknown https://doi.org/10.1021/NP050368F
Salviamine E 11716788 Click to see 323.40 unknown https://doi.org/10.1021/NP050368F
Salviamine F 11702294 Click to see 309.40 unknown https://doi.org/10.1021/NP050368F
> Lignans, neolignans and related compounds / Aryltetralin lignans
(2R)-2-[(1R,2S)-3-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-1-(3,4-dihydroxyphenyl)-7,8-dihydroxy-1,2-dihydronaphthalene-2-carbonyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid 10747430 Click to see 718.60 unknown https://doi.org/10.1248/CPB.45.1596
https://doi.org/10.1016/S0031-9422(01)00415-0
2-[3-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-1-(3,4-dihydroxyphenyl)-7,8-dihydroxy-1,2-dihydronaphthalene-2-carbonyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid 85254398 Click to see 718.60 unknown https://doi.org/10.1248/CPB.45.1596
Rabdosiin 471121 Click to see 718.60 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
https://doi.org/10.1248/CPB.45.1596
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(+)-5-Dehydrosugiol 14827280 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)C=C3C2(CCCC3(C)C)C)O 298.40 unknown https://doi.org/10.1021/NP050368F
(4aR)-6,10-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one 3009284 Click to see 314.40 unknown https://doi.org/10.1021/NP050368F
1,2-Dihydrotanshinquinone 105119 Click to see CC1=CCCC2=C1C=CC3=C2C(=O)C(=O)C4=C3OC=C4C 278.30 unknown https://doi.org/10.1021/NP050368F
6-Hydroxy-1,1,4A-trimethyl-7-(propan-2-YL)-1,2,3,4,4A,9,10,10A-octahydrophenanthren-9-one 275529 Click to see 300.40 unknown https://doi.org/10.1021/NP050368F
6-Hydroxy-5,6-dehydrosugiol 78297419 Click to see 314.40 unknown https://doi.org/10.1021/NP050368F
6-Hydroxysugiol 12114761 Click to see 316.40 unknown https://doi.org/10.1021/NP050368F
6,10-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 73095180 Click to see 316.40 unknown https://doi.org/10.1021/NP050368F
Abieta-9(11),8(14),12-trien-12-ol 521330 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1021/NP050368F
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1021/NP050368F
Sugiol 94162 Click to see 300.40 unknown https://doi.org/10.1021/NP050368F
Sugiol,5-dehydro 275530 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)C=C3C2(CCCC3(C)C)C)O 298.40 unknown https://doi.org/10.1021/NP050368F
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
(1R)-1,6,6-trimethyl-1,2,6,7,8,9-hexahydrophenanthro[1,2-b]furan-10,11(3aH,11aH)-dione 25181389 Click to see CC1COC2C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C 298.40 unknown via CMAUP database
(8S)-4,8-dimethyl-8,9-dihydronaphtho[2,1-f][1]benzofuran-7,11-dione 11778300 Click to see CC1COC2=C1C(=O)C3=C(C2=O)C4=CC=CC(=C4C=C3)C 278.30 unknown https://doi.org/10.1021/NP050368F
(S)-6-(Hydroxymethyl)-1,6-dimethyl-6,7,8,9-tetrahydrophenanthro[1,2-b]furan-10,11-dione 9926694 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)CO 310.30 unknown via CMAUP database
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/10.1021/NP050368F
8,9-Dihydro-4,8-dimethylphenanthro(3,2-b)furan-7,11-dione 89406 Click to see 278.30 unknown https://doi.org/10.1021/NP050368F
Cryptotanshinone 160254 Click to see 296.40 unknown https://doi.org/10.1021/NP050368F
Dihydrotanshinone 5316743 Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C(C=CC=C43)C 278.30 unknown https://doi.org/10.1021/NP050368F
Dihydrotanshinone I 11425923 Click to see 278.30 unknown https://doi.org/10.1021/NP050368F
Isotanshinone I 623940 Click to see 276.30 unknown https://doi.org/10.1021/NP050368F
Methuyl tanshinonate 624381 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C(=O)OC 338.40 unknown via CMAUP database
Nortanshinone 10062187 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4=O 280.27 unknown https://doi.org/10.1021/NP050368F
Npc85771 622085 Click to see 292.30 unknown via CMAUP database
Tanshinone I 114917 Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C4=C3OC=C4C 276.30 unknown https://doi.org/10.1021/NP050368F
Tanshinone IIA 164676 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C 294.30 unknown https://doi.org/10.1021/NP050368F
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
methyl (4S,5Z,6S)-5-ethylidene-4-[2-[[(1S,2R,3R,5R)-5-[(2S)-1-[2-[(2S,3Z,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3-hydroxypropan-2-yl]-3-hydroxy-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 101920648 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(CC3C(CO)COC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)O)C 977.00 unknown https://doi.org/10.1021/NP050368F
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
[22-(2-Hydroxypropan-2-yl)-1,5,10,10-tetramethyl-11-(3,4,5-trihydroxyoxan-2-yl)oxy-21,25-dioxaheptacyclo[20.2.1.02,19.05,19.06,16.09,14.014,16]pentacosan-3-yl] acetate 85360387 Click to see CC(=O)OC1CC2(C3CCC4C(C(CCC45C3(C5)CCC26C1C7(CCC(O7)(OC6)C(C)(C)O)C)OC8C(C(C(CO8)O)O)O)(C)C)C 662.80 unknown https://doi.org/10.1021/NP050368F
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
(1R,1'R,2R,2'R,3'S,4S,4'R,6S,7R,8R,9S)-6',11-bis[(E)-3-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-3',9-bis(3,4-dihydroxyphenyl)-6-hydroxy-7'-oxospiro[3,5-dioxatricyclo[5.2.2.02,6]undec-10-ene-4,8'-bicyclo[2.2.2]oct-5-ene]-2',8-dicarboxylic acid 10748664 Click to see 1078.90 unknown https://doi.org/10.1021/NP960425S
https://doi.org/10.1248/CPB.45.1596
(1R,1'R,2S,2'S,3'S,4S,4'R,6R,7R,8S,9S)-6',11-bis[(E)-3-[(1S)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-3',9-bis(3,4-dihydroxyphenyl)-2,6-dihydroxy-7'-oxospiro[3,5-dioxatricyclo[5.2.2.02,6]undec-10-ene-4,8'-bicyclo[2.2.2]oct-5-ene]-2',8-dicarboxylic acid 163068276 Click to see 1094.90 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
(1R,1'S,2R,2'R,3'S,4S,4'S,6S,7R,8R,9S)-6',11-bis[(E)-3-[(1S)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-3',9-bis(3,4-dihydroxyphenyl)-6-hydroxy-7'-oxospiro[3,5-dioxatricyclo[5.2.2.02,6]undec-10-ene-4,8'-bicyclo[2.2.2]oct-5-ene]-2',8-dicarboxylic acid 162924838 Click to see 1078.90 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
yunnaneic acid B 10558114 Click to see 1094.90 unknown https://doi.org/10.1021/NP960425S
https://doi.org/10.1248/CPB.45.1596
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
(1R,2R,3S,4R)-6-[(E)-3-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-3-(3,4-dihydroxyphenyl)cyclohex-5-ene-1,2,4-tricarboxylic acid 10531154 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(C(C(C2C(=O)O)C(=O)O)C3=CC(=C(C=C3)O)O)C(=O)O)O)O 572.50 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
https://doi.org/10.1248/CPB.45.1596
6-[3-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-3-(3,4-dihydroxyphenyl)cyclohex-5-ene-1,2,4-tricarboxylic acid 85174254 Click to see 572.50 unknown https://doi.org/10.1248/CPB.45.1596
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes / Benzoxanthenes
(2R)-2-[16-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-4,5,10-trihydroxy-8-oxatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2,4,6,9,11,13,15-octaene-15-carbonyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid 10604869 Click to see 714.60 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
https://doi.org/10.1248/CPB.45.1596
(2R)-2-[16-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-5,6,10-trihydroxy-8-oxatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2(7),3,5,9,11,13,15-octaene-15-carbonyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid 162880470 Click to see 714.60 unknown https://doi.org/10.1248/CPB.45.1596
2-[16-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-5,6,10-trihydroxy-8-oxatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2(7),3,5,9,11,13,15-octaene-15-carbonyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid 162880469 Click to see 714.60 unknown https://doi.org/10.1248/CPB.45.1596
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
7H-(1,3)Dioxolo(4,5-j)pyrrolo(3,2,1-de)phenanthridin-7-one 100605 Click to see 263.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R)-2-({(2E)-3-[(2R,3R)-3-{[1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl}-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-4-yl]prop-2-enoyl}oxy)-3-(3,4-dihydroxyphenyl)propanoic acid 6441188 Click to see 718.60 unknown https://doi.org/10.1002/PTR.5789
https://doi.org/10.1007/S11655-016-2645-4
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308668/
Salvianic acid B 119177 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O 718.60 unknown https://doi.org/10.1248/CPB.45.1596
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5009695/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364840/
https://doi.org/10.1016/J.EJPHAR.2016.09.014
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308668/
https://doi.org/10.1002/JSSC.201600368
Salvianolic Acid B 6451084 Click to see 718.60 unknown https://doi.org/10.1021/NP960425S
https://doi.org/10.1248/CPB.45.1596
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid 639655 Click to see 360.30 unknown https://doi.org/10.1248/CPB.45.1596
3-(3,4-Dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid 5099 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1248/CPB.45.1596
Rosmarinic Acid 5281792 Click to see 360.30 unknown https://doi.org/10.1021/NP960425S
https://doi.org/10.1248/CPB.45.1596

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