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

Description Top

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Salvia yunnanensis is a hardy plant that is easy to grow in a sunny location with well-drained soil. It is drought tolerant and can tolerate temperatures as low as -10°C (14°F).

Salvia yunnanensis is a perennial plant native to Yunnan, Guizhou, and Sichuan provinces in China. It grows on grassy hillsides, forest margins, and dry forests at 1,800 to 2,900 m elevation. It has tuberous roots and grows on erect stems to 30 cm tall, with simple oblong-elliptic leaves that are 2 to 8 cm long and 1.5 to 3.5 cm wide. The inflorescences are widely spaced 4-6-flowered verticillasters in terminal racemes or panicles, with a 2.5 to 3.0 cm blue-purple corolla. It is a hardy plant that is easy to grow in a sunny location with well-drained soil and is drought tolerant and can tolerate temperatures as low as -10°C (14°F).

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!
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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 CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 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 C1C(=O)OC2(C1(C3C=C(C2C(C3C4=CC(=C(C=C4)O)O)C(=O)O)C=CC(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O 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 C1C(=O)OC2(C1(C3C=C(C2C(C3C4=CC(=C(C=C4)O)O)C(=O)O)C=CC(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O 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 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/10.1248/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 C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC3C(C(C2C(=O)C3O)C(=O)O)C4=CC(=C(C=C4)O)O)O)O 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/10.1016/S0031-9422(01)00415-0
https://doi.org/10.1021/NP960425S
https://doi.org/10.1248/CPB.45.1596
Yunnaneic acid D 10530480 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC3C(C(C2C(=O)C3O)C(=O)O)C4=CC(=C(C=C4)O)O)O)O 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 C1C(=O)OC2(C1(C3C=C(C2C(C3C4=CC(=C(C=C4)O)O)C(=O)O)C=CC(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O 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 CC1=C2C=CC3=C(C2=CC=C1)C4=C(C5=C3OC=C5C)OC(=N4)CCC(=O)OC 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 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
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 CC1=COC2=C1C3=C(C4=C2C=CC5=C4CCCC5(C)C)OC(=N3)C 319.40 unknown https://doi.org/10.1021/NP050368F
Salviamine A 11580104 Click to see CC1=C2C=CC3=C(C2=CC=C1)C4=C(C5=C3OC=C5C)N=CO4 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 CC1=C2C=CC3=C(C2=CC=C1)C4=C(C(=C3O)C(=O)C)OC=N4 291.30 unknown https://doi.org/10.1021/NP050368F
Salviamine B 11659306 Click to see CC1=C2C=CC3=C(C2=CC=C1)C4=C(C(=C3O)C(=O)C)N=CO4 291.30 unknown https://doi.org/10.1021/NP050368F
Salviamine C 11601931 Click to see CC1=C2C=CC3=C(C2=CC=C1)C4=C(C(=C3O)C(=O)C)N=C(O4)C 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 CC1=NC2=C(O1)C3=C(C=CC4=C3CCCC4(C)C)C(=C2C(=O)C)O 323.40 unknown https://doi.org/10.1021/NP050368F
Salviamine F 11702294 Click to see CC(=O)C1=C(C2=C(C3=C(C=C2)C(CCC3)(C)C)C4=C1N=CO4)O 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 C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C2C(C3=C(C=CC(=C3O)O)C=C2C(=O)OC(CC4=CC(=C(C=C4)O)O)C(=O)O)C5=CC(=C(C=C5)O)O)O)O 718.60 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
https://doi.org/10.1248/CPB.45.1596
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 C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C2C(C3=C(C=CC(=C3O)O)C=C2C(=O)OC(CC4=CC(=C(C=C4)O)O)C(=O)O)C5=CC(=C(C=C5)O)O)O)O 718.60 unknown https://doi.org/10.1248/CPB.45.1596
Rabdosiin 471121 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C2C(C3=CC(=C(C=C3C=C2C(=O)OC(CC4=CC(=C(C=C4)O)O)C(=O)O)O)O)C5=CC(=C(C=C5)O)O)O)O 718.60 unknown https://doi.org/10.1248/CPB.45.1596
https://doi.org/10.1016/S0031-9422(01)00415-0
> 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
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 CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O 300.40 unknown https://doi.org/10.1021/NP050368F
6-Hydroxy-5,6-dehydrosugiol 3009284 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)C(=C3C2(CCCC3(C)C)C)O)O 314.40 unknown https://doi.org/10.1021/NP050368F
6-Hydroxysugiol 12114761 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)C(C3C2(CCCC3(C)C)C)O)O 316.40 unknown https://doi.org/10.1021/NP050368F
6,10-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one 78297419 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)C(=C3C2(CCCC3(C)C)C)O)O 314.40 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 CC(C)C1=C(C=C2C(=C1)C(=O)C(C3C2(CCCC3(C)C)C)O)O 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 CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O 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 CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C 296.40 unknown https://doi.org/10.1021/NP050368F
Cryptotanshinone 160254 Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C 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 CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C(C=CC=C43)C 278.30 unknown https://doi.org/10.1021/NP050368F
Isotanshinone I 623940 Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C4=C(C3=O)C(=CO4)C 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
Phenanthro[3,2-b]furan-7,11-dione, 8,9-dihydro-4,8-dimethyl- 89406 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
Przewaquinone B 622085 Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C4=C3OC=C4CO 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 C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC3C(C(C2C(=O)C34OC5C6C=C(C(C5(O4)O)C(C6C7=CC(=C(C=C7)O)O)C(=O)O)C=CC(=O)OC(CC8=CC(=C(C=C8)O)O)C(=O)O)C(=O)O)C9=CC(=C(C=C9)O)O)O)O 1078.90 unknown https://doi.org/10.1248/CPB.45.1596
https://doi.org/10.1021/NP960425S
(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 C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC3C(C(C2C(=O)C34OC5(C6C=C(C(C5(O4)O)C(C6C7=CC(=C(C=C7)O)O)C(=O)O)C=CC(=O)OC(CC8=CC(=C(C=C8)O)O)C(=O)O)O)C(=O)O)C9=CC(=C(C=C9)O)O)O)O 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 C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC3C(C(C2C(=O)C34OC5C6C=C(C(C5(O4)O)C(C6C7=CC(=C(C=C7)O)O)C(=O)O)C=CC(=O)OC(CC8=CC(=C(C=C8)O)O)C(=O)O)C(=O)O)C9=CC(=C(C=C9)O)O)O)O 1078.90 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
Yunnaneic acid B 10558114 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC3C(C(C2C(=O)C34OC5(C6C=C(C(C5(O4)O)C(C6C7=CC(=C(C=C7)O)O)C(=O)O)C=CC(=O)OC(CC8=CC(=C(C=C8)O)O)C(=O)O)O)C(=O)O)C9=CC(=C(C=C9)O)O)O)O 1094.90 unknown https://doi.org/10.1248/CPB.45.1596
https://doi.org/10.1021/NP960425S
> 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 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/10.1248/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 C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C2=C(C3=C4C(=C2)C=CC(=C4OC5=CC(=C(C=C53)O)O)O)C(=O)OC(CC6=CC(=C(C=C6)O)O)C(=O)O)O)O 714.60 unknown https://doi.org/10.1248/CPB.45.1596
https://doi.org/10.1016/S0031-9422(01)00415-0
(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 C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C2=C(C3=C4C(=C2)C=CC(=C4OC5=C3C=CC(=C5O)O)O)C(=O)OC(CC6=CC(=C(C=C6)O)O)C(=O)O)O)O 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 C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C2=C(C3=C4C(=C2)C=CC(=C4OC5=C3C=CC(=C5O)O)O)C(=O)OC(CC6=CC(=C(C=C6)O)O)C(=O)O)O)O 714.60 unknown https://doi.org/10.1248/CPB.45.1596
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Hippadine 100605 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC5=C4N(C3=O)C=C5 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 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/10.1002/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://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308668/
https://doi.org/10.1016/J.EJPHAR.2016.09.014
https://doi.org/10.1248/CPB.45.1596
https://doi.org/10.1002/JSSC.201600368
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5009695/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364840/
Salvianolic acid B 6451084 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://doi.org/10.1021/NP960425S
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid 639655 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
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 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/10.1021/NP960425S
https://doi.org/10.1248/CPB.45.1596

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