Salvia przewalskii

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643febe38351d844835331
Scientific name	Salvia przewalskii
Authority	Maxim.
First published in	Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 27: 526 (1882)

Description Top

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Salvia przewalskii is a herbaceous perennial plant native to China, described and named in 1881 by the Russian botanist Carl Maximowicz. It is widely known for its medicinal properties and forms a basal clump of yellow-green leaves 1 to 2 feet (30 to 61 cm) high and wide, with flowering stalks rising 3 feet (91.4 cm) above the plant. The flowers are fat, with an unusual purple-red or red-brown color, and the calyx is hairy and glandular, red-brown and two-lipped. It is usually seen only in botanical gardens, though seeds have become available for gardeners since the 1980s. Botanists have segregated the species into four varieties, distinguished by leaf shape and differences in the hairs covering the foliage.

Synonyms Top

Scientific name	Authority	First published in
Salvia feddei	H.Lév.	Repert. Spec. Nov. Regni Veg. 12: 532 (1913)
Salvia labellifera	H.Lév.	Repert. Spec. Nov. Regni Veg. 12: 532 (1913)
Salvia mandarinorum	Diels	Bot. Jahrb. Syst. 29: 557 (1900)
Salvia przewalskii var. alba	X.L.Huang & H.W.Li	Acta Phytotax. Sin. 19: 245 (1981)
Salvia przewalskii var. glabrescens	E.Peter	Acta Horti Gothob. 9: 115. 1934
Salvia przewalskii var. mandarinorum	(Diels) E.Peter	Acta Horti Gothob. 9: 115. 1934
Salvia przewalskii var. rubrobrunnea	C.Y.Wu	Fl. Yunnanica 1: 662 (1977)
Salvia tatsienensis	Fraanch.	Bull. Annuel Soc. Philom. Paris , sér. 8, 3: 150 (1891)
Salvia thibetica	H.Lév.	Repert. Spec. Nov. Regni Veg. 9: 219 (1911)
Salvia przewalskii f. albiflora	Y.H.Wu	J. Wuhan Bot. Res. 23: 235 (2005)

Common names Top

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Filter by language:

Language	Common/alternative name
Arabic	قصعين برزفالسكي
Chinese	丹参
Chinese	红根草
Chinese	甘西鼠尾草
Chinese	甘西鼠尾草（高原丹参）
Chinese	紫丹参
Chinese	红秦艽

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - Tibet

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000302023
KEW	urn:lsid:ipni.org:names:457025-1
The Plant List	kew-183597
Open Tree Of Life	547902
NCBI Taxonomy	342060
IPNI	457025-1
iNaturalist	821033
GBIF	7307728
Freebase	/m/05mqlhc
EOL	2894205
USDA GRIN	32956
Wikipedia	Salvia_przewalskii
CMAUP	NPO25813

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

Accumulation of Polyphenols and Associated Gene Expression in Hairy Roots of Salvia viridis Exposed to Methyl Jasmonate

Grzegorczyk-Karolak I, Krzemińska M, Grąbkowska R, Gomulski J, Żekanowski C, Gaweda-Walerych K

Int J Mol Sci

07-Jan-2024

PMCID:	PMC10815010
doi:	10.3390/ijms25020764
PMID:	38255839

Expression and regulation of HIF-1a in hypoxic pulmonary hypertension: Focus on pathological mechanism and Pharmacological Treatment

Wan JJ, Yi J, Wang FY, Zhang C, Dai AG

Int J Med Sci

01-Jan-2024

PMCID:	PMC10750340
doi:	10.7150/ijms.88216
PMID:	38164358

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

Yield and Composition of the Essential Oil of Clinopodium nepeta subsp. spruneri as Affected by Harvest Season and Cultivation Method, i.e., Outdoor, Greenhouse and In Vitro Culture

Vlachou G, Papafotiou M, Daferera DJ, Tarantilis PA

Plants (Basel)

07-Dec-2023

PMCID:	PMC10747734
doi:	10.3390/plants12244098
PMID:	38140425

The complete chloroplast genome sequence of Plectranthus hadiensis (Lamiaceae) and phylogenetic analysis

Hao J, Lu Y, Dang M, Xia R, Xu L, Zhu Z, Yu Y

Mitochondrial DNA B Resour

05-Oct-2023

PMCID:	PMC10557565
doi:	10.1080/23802359.2023.2262689
PMID:	37810612

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

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

Oxidative Stress Inducers in Cancer Therapy: Preclinical and Clinical Evidence

Nizami ZN, Aburawi HE, Semlali A, Muhammad K, Iratni R

Antioxidants (Basel)

26-May-2023

PMCID:	PMC10295724
doi:	10.3390/antiox12061159
PMID:	37371889

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

Editorial: Bone and Cartilage Diseases – The Role and Potential of Natural Products, Volume II

Pei M, Xu D, Wu L

Front Pharmacol

02-May-2023

PMCID:	PMC10185899
doi:	10.3389/fphar.2023.1194875
PMID:	37201019

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

Hairy Root Cultures as a Source of Phenolic Antioxidants: Simple Phenolics, Phenolic Acids, Phenylethanoids, and Hydroxycinnamates

Malarz J, Yudina YV, Stojakowska A

Int J Mol Sci

07-Apr-2023

PMCID:	PMC10138958
doi:	10.3390/ijms24086920
PMID:	37108084

Protective effect and mechanism of Polygonatum kingianum against hypoxia-induced injury

Li X, Mei M, Pu X, Chen X, Li X, Meng F, He S, Li J, Gu W, Yang X, Zhang F, Yu J

Heliyon

09-Mar-2023

PMCID:	PMC10034467
doi:	10.1016/j.heliyon.2023.e14353
PMID:	36967867

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

Spatial variation of pollen receipt and effects of heterospecific pollen on seed set in Salvia przewalskii

Fang Q, Zhang T, Montgomery BR

Ecol Evol

03-Feb-2023

PMCID:	PMC9897956
doi:	10.1002/ece3.9795
PMID:	36760706

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 / Anthraquinones
1,5-Dihydroxy-3-methoxy-7-methylanthracene-9,10-dione	15138599	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C(=CC(=C3)OC)O	284.26	unknown	https://doi.org/10.1016/0031-9422(92)90069-3
1,5-Dihydroxy-3-methylanthraquinone	5316800	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C(=CC=C3)O	254.24	unknown	https://doi.org/10.1016/0031-9422(92)90069-3
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	154.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
3,4-Dimethoxybenzaldehyde	8419	Click to see COC1=C(C=C(C=C1)C=O)OC	166.17	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
(1R,8S,10R)-5,11,11-trimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2(7),3,5-trien-4-ol	138113846	Click to see CC1=CC2=C(C=C1O)C34CCCC(C3CC2OC4)(C)C	272.40	unknown	https://doi.org/10.1016/0031-9422(91)80121-G
(1S,8R,10R)-4-hydroxy-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2(7),3,5-triene-5-carbaldehyde	162913607	Click to see CC1(CCCC23C1CC(C4=C2C=C(C(=C4)C=O)O)OC3)C	286.40	unknown	https://doi.org/10.1002/HLCA.200800293
(1S,8R,10R)-5,11,11-trimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2(7),3,5-trien-4-ol	132966659	Click to see CC1=CC2=C(C=C1O)C34CCCC(C3CC2OC4)(C)C	272.40	unknown	https://doi.org/10.1248/CPB.53.1575
4-Hydroxy-11,11-dimethyl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2(7),3,5-triene-5-carbaldehyde	162913606	Click to see CC1(CCCC23C1CC(C4=C2C=C(C(=C4)C=O)O)OC3)C	286.40	unknown	https://doi.org/10.1002/HLCA.200800293
Przewalskin	14139389	Click to see CC1=CC2=C(C=C1O)C34CCCC(C3CC2OC4)(C)C	272.40	unknown	via CMAUP database
> Hydrocarbon derivatives / Tropones
4-Acetyl-5,10,16-trihydroxy-12,12-dimethyl-6-propan-2-yl-17-oxatetracyclo[7.6.2.01,11.02,8]heptadeca-2(8),4,6-trien-3-one	73240473	Click to see CC(C)C1=CC2=C(C(=O)C(=C1O)C(=O)C)C34CCCC(C3C(C2OC4O)O)(C)C	402.50	unknown	https://doi.org/10.1021/OL061609T
Przewalskin A	16090911	Click to see CC(C)C1=CC2=C(C(=O)C(=C1O)C(=O)C)C34CCCC(C3C(C2OC4O)O)(C)C	402.50	unknown	https://doi.org/10.1021/OL061609T
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
gamma-Linolenic acid	5280933	Click to see CCCCCC=CCC=CCC=CCCCCC(=O)O	278.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
1,1,4abeta-Trimethyl-6-hydroxy-7-isopropyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-9-one	5321549	Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O	300.40	unknown	via CMAUP database
1,2-Dihydrotanshinquinone	105119	Click to see CC1=CCCC2=C1C=CC3=C2C(=O)C(=O)C4=C3OC=C4C	278.30	unknown	https://doi.org/10.1248/CPB.53.1575
11,11-Dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2(7),5-diene-3,4-dione	163041876	Click to see CC(C)C1=CC2=C(C(=O)C1=O)C34CCCC(C3CC2OC4)(C)C	314.40	unknown	https://doi.org/10.1002/HLCA.200800293
12,12-Dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1,3,5,7,14-pentaene-4,5-diol	11514927	Click to see CC(C)C1=C(C(=C2C=C3C=CCC(C3CCC2=C1)(C)C)O)O	298.40	unknown	https://doi.org/10.1248/CPB.53.1575
12,12-Dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7-tetraen-5-ol	11011523	Click to see CC(C)C1=C(C=C2CC3=CCCC(C3CCC2=C1)(C)C)O	284.40	unknown	https://doi.org/10.1248/CPB.53.1575
12,12-Dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-3,5,7-triene-1,5-diol	4022498	Click to see CC(C)C1=C(C=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O	302.50	unknown	https://doi.org/10.1248/CPB.53.1575
2,3,5,10,11,11abeta-Hexahydro-1,1-dimethyl-8-(1-methylethyl)-1H-dibenzo[a,d]cyclohepten-7-ol	14587208	Click to see CC(C)C1=C(C=C2CC3=CCCC(C3CCC2=C1)(C)C)O	284.40	unknown	via CMAUP database
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 CC(C)C1=C(C(=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O)O	318.40	unknown	https://doi.org/10.1248/CPB.53.1575
5-Methoxy-12,12-dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-3,5,7-triene-1,4-diol	14526919	Click to see CC(C)C1=C(C(=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O)OC	332.50	unknown	https://doi.org/10.1248/CPB.53.1575
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/10.1248/CPB.53.1575
6,7-Dehydroferruginol	10978982	Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)O	284.40	unknown	https://doi.org/10.1248/CPB.53.1575
8-Isopropyl-1,1-dimethyl-2,3,5,10,11,11a-hexahydro-1H-dibenzo[a,d]cycloheptene-6,7-diol-, (11aS)-	627133	Click to see CC(C)C1=C(C(=C2CC3=CCCC(C3CCC2=C1)(C)C)O)O	300.40	unknown	https://doi.org/10.1248/CPB.53.1575
9-Methoxy-12,12-dimethyl-6-propan-2-yltricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7-tetraene-4,5-diol	73009331	Click to see CC(C)C1=C(C(=C2CC3=CCCC(C3CC(C2=C1)OC)(C)C)O)O	330.50	unknown	https://doi.org/10.1248/CPB.53.1575
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	via CMAUP database
Barbatusol	10040486	Click to see CC(C)C1=C(C(=C2CC3=CCCC(C3CCC2=C1)(C)C)O)O	300.40	unknown	https://doi.org/10.1248/CPB.53.1575
Danshenxinkun D	127172	Click to see CC1COC2=C(C1(C)CO)C(=O)C3=C(C2=O)C4=CC=CC(=C4C=C3)C	336.40	unknown	via CMAUP database
DELTA6-Dehydroferruginol	14165048	Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)O	284.40	unknown	https://doi.org/10.1248/CPB.53.1575
Demethylsalvicanol	11666872	Click to see CC(C)C1=C(C(=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O)O	318.40	unknown	https://doi.org/10.1248/CPB.53.1575
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1248/CPB.53.1575
From the seeds of Chamaecyparis pisifera	355228	Click to see CC(C)C1=C(C=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O	302.50	unknown	via CMAUP database
Lanigerol	188496	Click to see CC(C)C1=C(C=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O	302.50	unknown	https://doi.org/10.1248/CPB.53.1575
Pisiferin	14587207	Click to see CC(C)C1=C(C=C2CC3=CCCC(C3CCC2=C1)(C)C)O	284.40	unknown	https://doi.org/10.1248/CPB.53.1575
Przewalskin C	11566132	Click to see CC(C)C1=C(C(=C2CC3=CCCC(C3CC(C2=C1)OC)(C)C)O)O	330.50	unknown	https://doi.org/10.1248/CPB.53.1575
Przewalskin D	101375853	Click to see CC(C)C1=C(C(=C2C=C3C=CCC(C3CCC2=C1)(C)C)O)O	298.40	unknown	https://doi.org/10.1248/CPB.53.1575
Przewalskin G	102280560	Click to see CC(C)C1=CC2=C(C(=O)C1=O)C34CCCC(C3CC2OC4)(C)C	314.40	unknown	https://doi.org/10.1002/HLCA.200800293
Salvicanol	101607178	Click to see CC(C)C1=C(C(=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O)OC	332.50	unknown	https://doi.org/10.1248/CPB.53.1575
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/10.1248/CPB.53.1575
> 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
(1S,6R,19R,22R,28S,30S)-19-hydroxy-13,22,31,31-tetramethyl-19-(2-oxopropyl)-25-propan-2-yl-5,7,23,35-tetraoxanonacyclo[26.6.1.01,30.03,27.04,24.06,22.08,21.09,18.012,17]pentatriaconta-3,8(21),9(18),10,12,14,16,24,26-nonaen-20-one	57404390	Click to see CC1=C2C=CC3=C(C2=CC=C1)C(C(=O)C4=C3OC5C4(OC6=C(C=C7C8CC9C(CCCC9(O8)CC7=C6O5)(C)C)C(C)C)C)(CC(=O)C)O	648.80	unknown	via CMAUP database
(6R)-6-(hydroxymethyl)-1,6-dimethyl-8,9-dihydro-7H-naphtho[1,2-g][1]benzofuran-10,11-dione	56967682	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)CO	310.30	unknown	via CMAUP database
(6S)-6-hydroxy-1,6-dimethyl-8,9-dihydro-7H-naphtho[1,2-g][1]benzofuran-10,11-dione	56967683	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)O	296.30	unknown	via CMAUP database
(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/10.1248/CPB.53.1575 https://doi.org/10.1080/10826079708010970
Cryptotanshinone	160254	Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C	296.40	unknown	https://doi.org/10.1248/CPB.53.1575 https://doi.org/10.1021/NP800119K https://doi.org/10.1080/10826079708010970
Danshenol A	3083514	Click to see CC1COC2=C1C(=O)C(C3=C2C=CC4=C(C=CC=C43)C)(CC(=O)C)O	336.40	unknown	via CMAUP database
Danshenxinkun A	149138	Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C(=C3O)C(C)CO	296.30	unknown	via CMAUP database
Dehydrodanshenol A	71816415	Click to see CC1=C2C=CC3=C(C2=CC=C1)C(C(=O)C4=C3OC=C4C)(CC(=O)C)O	334.40	unknown	via CMAUP database
Dihydrotanshinone	5316743	Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C(C=CC=C43)C	278.30	unknown	via CMAUP database
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/10.1080/10826079708010970
Isograndifoliol	71816417	Click to see CC1=C(C(=O)C=C2C(=C1)CCC3C2(CCCC3(C)C)CO)O	302.40	unknown	via CMAUP database
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
Miltipolone	10086184	Click to see CC1=C(C(=O)C=C2C(=C1)C3CC4C2(CCCC4(C)C)CO3)O	300.40	unknown	via CMAUP database
Miltirone	160142	Click to see CC(C)C1=CC2=C(C3=C(C=C2)C(CCC3)(C)C)C(=O)C1=O	282.40	unknown	via CMAUP database
Przewaquinone A	619402	Click to see CC1(CCCC2=C1C=CC3=C2C(=O)C(=O)C4=C3OC=C4CO)C	310.30	unknown	https://doi.org/10.1016/0031-9422(91)80121-G https://doi.org/10.1021/NP800119K
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
Tanshindiol B	5321620	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCC(C4(C)O)O	312.30	unknown	via CMAUP database
Tanshindiol C	126072	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCC(C4(C)O)O	312.30	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/10.1248/CPB.53.1575 https://doi.org/10.1016/0031-9422(91)80121-G
Tanshinone IIA	164676	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C	294.30	unknown	https://doi.org/10.1248/CPB.53.1575 https://doi.org/10.1080/10826079708010970 https://doi.org/10.1016/0031-9422(91)80121-G
Tanshinone IIb	318797	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)CO	310.30	unknown	https://doi.org/10.1016/0031-9422(91)80121-G
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,8R,9S)-3,4,9-trihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	100934562	Click to see CC(C)C1=C(C(=C2C(=C1)C3C(C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	via CMAUP database
(1R,8S)-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	6324890	Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O	330.40	unknown	via CMAUP database
(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 CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O	330.40	unknown	https://doi.org/10.1248/CPB.53.1575
Carnosol	442009	Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O	330.40	unknown	https://doi.org/10.1248/CPB.53.1575
Rosmanol	13966122	Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O	346.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4aS,6aR,6aS,6bR,8aR,10R,12aR)-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	9956482	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O	472.70	unknown	via CMAUP database
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/0031-9422(88)80642-3
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/0031-9422(88)80642-3
Ursolic acid (Malol)	49867942	Click to see CC1CC(C2CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxasteroids and derivatives / Tanshinlactones and derivatives
Tanshinlactone	5321617	Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)OC4=C3OC=C4C	264.27	unknown	via CMAUP database
> 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/10.1016/0031-9422(91)80121-G
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(91)80121-G
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R)-2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-3-[4-hydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoic acid	25245849	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O	522.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3-Hydroxybenzaldehyde	101	Click to see C1=CC(=CC(=C1)O)C=O	122.12	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
(-)-Rosmadial	72996596	Click to see CC(C)C1=C(C2=C(C(=C1)C=O)C3(CCCC(C3C=O)(C)C)C(=O)O2)O	344.40	unknown	https://doi.org/10.1248/CPB.53.1575
Rosmadial	15801061	Click to see CC(C)C1=C(C2=C(C(=C1)C=O)C3(CCCC(C3C=O)(C)C)C(=O)O2)O	344.40	unknown	https://doi.org/10.1248/CPB.53.1575
> Organoheterocyclic compounds / Naphthofurans
(-)-Przewalskin B	51002763	Click to see CC(C)C1=CC23CCC4C(=CCCC4(C)C)C2OC(=O)C3(C1=O)O	330.40	unknown	https://doi.org/10.1021/OL062748D
(1S,4'R)-4',7-dimethylspiro[benzo[e][2]benzofuran-1,2'-oxolane]-3-one	163023712	Click to see CC1CC2(C3=C(C=CC4=C3C=CC(=C4)C)C(=O)O2)OC1	268.31	unknown	https://doi.org/10.1248/CPB.53.1575
13-Hydroxy-5,5-dimethyl-15-propan-2-yl-11-oxatetracyclo[8.6.0.01,13.04,9]hexadeca-8,15-diene-12,14-dione	163002166	Click to see CC(C)C1=CC23CCC4C(=CCCC4(C)C)C2OC(=O)C3(C1=O)O	330.40	unknown	https://doi.org/10.1021/OL062748D
4',7-Dimethylspiro[benzo[e][2]benzofuran-1,2'-oxolane]-3-one	163023711	Click to see CC1CC2(C3=C(C=CC4=C3C=CC(=C4)C)C(=O)O2)OC1	268.31	unknown	https://doi.org/10.1248/CPB.53.1575
Cryptoacetalide	46896125	Click to see CC1CC2(C3=C(C4=C(C=C3)C(CCC4)(C)C)C(=O)O2)OC1	286.40	unknown	https://doi.org/10.1248/CPB.53.1575
Danshinspiroketallactone	56956598	Click to see CC1CC2(C3=C(C4=CC=CC(=C4C=C3)C)C(=O)O2)OC1	268.31	unknown	via CMAUP database
Epidanshenspiroketallactone	102004791	Click to see CC1CC2(C3=C(C4=CC=CC(=C4C=C3)C)C(=O)O2)OC1	268.31	unknown	via CMAUP database
Neoprzewaquinone A	56932940	Click to see CC1=CCCC2=C(C=CC3=C2C(=O)C(=O)C4=C3OC=C4C)C(=C)CCCC5=C1C=CC6=C5C(=O)C(=O)C7=C6OC=C7C	556.60	unknown	via CMAUP database
Salprzelactone	71816414	Click to see CC1COC(=O)C1C2C3=C(C4=CC=CC(=C4C=C3)C)C(=O)O2	296.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
10-epi-Lithospermic acid	95359683	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)O)O)O	538.50	unknown	https://doi.org/10.1021/NP0501031
2-[[4-[(E)-3-[1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-6-hydroxy-2,3-dihydro-1-benzofuran-3-yl]-hydroxymethoxy]-3-(3,4-dihydroxyphenyl)propanoic acid	56677421	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(C2C(OC3=CC(=CC(=C23)C=CC(=O)OC(CC4=CC(=C(C=C4)O)O)C(=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O	720.60	unknown	via CMAUP database
Dimethyl lithospermate B	11422787	Click to see COC(=O)C(CC1=CC(=C(C=C1)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)OC	746.70	unknown	https://doi.org/10.1016/S0031-9422(01)00415-0
Lithospermic acid	6441498	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)O)O)O	538.50	unknown	via CMAUP database
Przewalskinic acid A	9975641	Click to see C1=CC(=C(C=C1C2C(C3=C(C=CC(=C3O2)O)C=CC(=O)O)C(=O)O)O)O	358.30	unknown	https://doi.org/10.1016/S0031-9422(01)00415-0
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/10.1021/NP0501031
> 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	via CMAUP database
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/NP0501031
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid	2518	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	via CMAUP database
(Z)-3-[2-(carboxymethyl)-3,4-dihydroxy-phenyl]prop-2-enoic acid	49770696	Click to see C1=CC(=C(C(=C1C=CC(=O)O)CC(=O)O)O)O	238.19	unknown	via CMAUP database
3-(3,4-Dihydroxyphenyl)prop-2-enoate	54710367	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)[O-]	179.15	unknown	via CMAUP database
Isoferulic acid	736186	Click to see COC1=C(C=C(C=C1)C=CC(=O)O)O	194.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,6,4'-Trihydroxy-7,3'-dimethoxyflavone	10359254	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O)O	330.29	unknown	via CMAUP database
Jaranol	5318869	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O	314.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
2-[(E)-3-(3,4-dihydroxycyclohexa-1,5-dien-1-yl)-1-hydroxy-allyloxy]-3-(3,4-dihydroxyphenyl)propanoic acid	49770232	Click to see C1=CC(=CC(C1O)O)C=CC(O)OC(CC2=CC(=C(C=C2)O)O)C(=O)O	364.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(2S)-3-(3,4-dihydroxyphenyl)-2-[(Z)-3-[2-[(E)-2-(3,4-dihydroxyphenyl)ethenyl]-3,4-dihydroxyphenyl]prop-2-enoyl]oxypropanoic acid	9913656	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C(C(=C(C=C2)O)O)C=CC3=CC(=C(C=C3)O)O)O)O	494.40	unknown	via CMAUP database

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Salvia przewalskii

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