Salvia splendens

Salvia splendens - Leaf — Part: Leaf
Author: Sorin

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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

Contributors

Collections

Details Top

Internal ID	UUID643febf50cbd7405114579
Scientific name	Salvia splendens
Authority	Sellow ex Schult.
First published in	Mant. 1 (Schultes) 1: 185. 1822 [late 1822]

Description Top

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Salvia splendens, also known as scarlet sage, is a tender herbaceous perennial plant native to Brazil. It grows at high elevations with warm temperatures and high humidity. While the wild form can reach up to 1.3 meters tall, smaller cultivars are more commonly seen as bedding plants in shopping malls and public gardens worldwide. This plant was first described in 1822 and has since been selected for dwarf sizes and different colors, ranging from white to dark purple. It is a popular ornamental plant, but does not survive freezing temperatures and is often grown as an annual. Some notable cultivars include 'Alba' with white flowers, 'Atropurpurea' with dark violet to purple flowers, and 'Grandiflora' with large red flowers. Two cultivars, 'Vanguard' and 'Van-Houttei', have received the Royal Horticultural Society's Award of Garden Merit.

Synonyms Top

Scientific name	Authority	First published in
Jungia splendens	(Sellow ex Schult.) Soják	Čas. Nár. Muz. Praze, Rada Přír. 152(1): 21. 1983
Salvia brasiliensis	Spreng.	Syst. Veg. 1: 56 (1824)
Salvia colorans	hort. ex Benth.	Labiat. Gen. Spec. : 287 (1833)
Fenixanthes splendens	Raf.	Autik. Bot. : 122 (1840)

Common names Top

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Filter by language:

Language	Common/alternative name
English	tropical sage
English	scarlet sage
Spanish	fenixanthes splendens
Spanish	jungia splendens
Spanish	salvia brasiliensis
Spanish	salvia colorans
Spanish	salvia issanchou
Spanish	salvia roja
Spanish	salvia tropical
Azerbaijani	salvia vanhouttei
Belarusian	Сальвія
Belarusian	Шалфей цудоўны
Bulgarian	обикновено пламъче
Catalan	coral·lins
Catalan	coral·lí
Czech	šalvěj zářivá
German	feuer-salbei
German	feuersalbei
Estonian	leeksalvei
Persian	سالویا اسپلندنز
Finnish	tulisalvia
Hebrew	מרווה הדורה
Upper Sorbian	pyšna želbija
Armenian	Եղեսպակ փայլուն
Japanese	ヒゴロモソウ
Japanese	サルビア
Japanese	緋衣草
Japanese	サルビア・スプレンデンス
Japanese	スカーレットセージ
Japanese	来路花
Korean	깨꽃
Korean	샐비어
Lithuanian	raudonžiedis šalavijas
Macedonian	жарче
Dutch	vuursalie
Polish	szałwia błyszcząca
Romanian	Salvie
Russian	Шалфей блестящий
Russian	Шалфей тропический
Russian	Шалфей сверкающий
Swedish	praktsalvia
Tonga	teʻekosi sivilaise
Turkish	ateş çiçeği
Chinese	地梗鼠尾
Chinese	象牙红
Chinese	一串紅
Chinese	一串红
Chinese	墙下红
Chinese	炮仔花
Chinese	西洋红
Chinese	象牙海棠
Chinese	鼠尾草
Chinese	赛尔维亚

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000302359
USDA Plants	SASP6
Tropicos	50293092
INPN	639059
Flora of Italy	8605
KEW	urn:lsid:ipni.org:names:60466516-2
The Plant List	kew-183912
Plantarium	33541
Missouri Botanical Garden	281427
Open Tree Of Life	294217
Observations.org	145594
NCBI Taxonomy	180675
NBN Atlas	NHMSYS0000463193
Nature Serve	2.136267
IPNI	60452620-2
iNaturalist	143203
GBIF	2927029
Freebase	/m/06_spk
WisFlora	7626
EPPO	SALSP
EOL	579412
Elurikkus	215082
USDA GRIN	70596
Wikipedia	Salvia_splendens

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCF_004379255.2	SspV2	Chromosome	Beijing Forestry University	2021-05-20	100.0x	768.60 Mb

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

The complete chloroplast genome of Lagochilus ilicifolius Bunge ex Bentham, Labiat. Gen. 1834 (Lamiaceae) and its phylogenetic analysis

Hou WJ, Men WX, Xing YP, Yang YY, Xu L, Kang TG, Song YY

Mitochondrial DNA B Resour

02-Apr-2024

PMCID:	PMC10993758
doi:	10.1080/23802359.2024.2334013
PMID:	38586511

Chromosome-level genome assembly provides insights into the genome evolution and functional importance of the phenylpropanoid–flavonoid pathway in Thymus mongolicus

Dang Z, Xu Y, Zhang X, Mi W, Chi Y, Tian Y, Liu Y, Ren W

BMC Genomics

19-Mar-2024

PMCID:	PMC10949689
doi:	10.1186/s12864-024-10202-8
PMID:	38504151

Chromosome-level genome of Thymus mandschuricus reveals molecular mechanism of aroma compounds biosynthesis

Jia L, Xu N, Xia B, Gao W, Meng Q, Li Q, Sun Y, Xu S, He M, Gu H

Front Plant Sci

13-Mar-2024

PMCID:	PMC10965588
doi:	10.3389/fpls.2024.1368869
PMID:	38545395

Integrating Transcriptome and Chemical Analyses to Provide Insights into Biosynthesis of Terpenoids and Flavonoids in the Medicinal Industrial Crop Andrographis paniculate and Its Antiviral Medicinal Parts

Yu K, Liang P, Yu H, Liu H, Guo J, Yan X, Li Z, Li G, Wang Y, Wang C

Molecules

14-Feb-2024

PMCID:	PMC10893308
doi:	10.3390/molecules29040852
PMID:	38398604

A haplotype-resolved gap-free genome assembly provides novel insight into monoterpenoid diversification in Mentha suaveolens ‘Variegata’

Yang H, Wang C, Zhou G, Zhang Y, He T, Yang L, Wu Y, Wang Z, Tang X, Chen G, Liu Z, Tang H, Zhou H, Kang X, Zhang S, Leng L, Chen S, Song C

Hortic Res

17-Jan-2024

PMCID:	PMC10925848
doi:	10.1093/hr/uhae022
PMID:	38469381

Subgenome phasing for complex allopolyploidy: case-based benchmarking and recommendations

Zhang RG, Shang HY, Jia KH, Ma YP

Brief Bioinform

06-Jan-2024

PMCID:	PMC10772947
doi:	10.1093/bib/bbad513
PMID:	38189536

Reference genome of the nutrition-rich orphan crop chia (Salvia hispanica) and its implications for future breeding

Gupta P, Geniza M, Elser J, Al-Bader N, Baschieri R, Phillips JL, Haq E, Preece J, Naithani S, Jaiswal P

Front Plant Sci

14-Dec-2023

PMCID:	PMC10757625
doi:	10.3389/fpls.2023.1272966
PMID:	38162307

Identification of the CDPK gene family in patchouli and functional analysis in response to continuous cropping stress

Liu X, Zeeshan Ul Haq M, Yu J, Liu Y, Yang H, Cui H, Yang D, Wu Y

Front Plant Sci

22-Nov-2023

PMCID:	PMC10702526
doi:	10.3389/fpls.2023.1300073
PMID:	38078089

Gap-free genome assembly and CYP450 gene family analysis reveal the biosynthesis of anthocyanins in Scutellaria baicalensis

Pei T, Zhu S, Liao W, Fang Y, Liu J, Kong Y, Yan M, Cui M, Zhao Q

Hortic Res

17-Nov-2023

PMCID:	PMC10753160
doi:	10.1093/hr/uhad235
PMID:	38156283

Structural identification of catalytic His158 of PtMAC2p from Pseudozyma tsukubaensis, an acyltransferase involved in mannosylerythritol lipids formation

Nakamichi Y, Saika A, Watanabe M, Fujii T, Morita T

Front Bioeng Biotechnol

18-Oct-2023

PMCID:	PMC10619693
doi:	10.3389/fbioe.2023.1243595
PMID:	37920243

Overexpression of ApHIPP26 from the Hyperaccumulator Arabis paniculata Confers Enhanced Cadmium Tolerance and Accumulation to Arabidopsis thaliana

Zhou L, Ye L, Pang B, Hou Y, Yu J, Du X, Gu L, Wang H, Zhu B

Int J Mol Sci

10-Oct-2023

PMCID:	PMC10606507
doi:	10.3390/ijms242015052
PMID:	37894733

Family characteristics, phylogenetic reconstruction, and potential applications of the plant BAHD acyltransferase family

Xu D, Wang Z, Zhuang W, Wang T, Xie Y

Front Plant Sci

05-Oct-2023

PMCID:	PMC10585174
doi:	10.3389/fpls.2023.1218914
PMID:	37868312

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

In vitro Antimicrobial Activity of Some Extracts of Salvia spp Harvested from the Oltenia Flora Using Different Solvents

BĂLĂȘOIU RM, BIȚĂ A, STĂNCIULESCU EC, BĂLĂȘOIU M, BEJENARU C, BEJENARU LE, PISOSCHI CG

Curr Health Sci J

30-Sep-2023

PMCID:	PMC10832872
doi:	10.12865/CHSJ.49.03.12
PMID:	38314220

Ethnobotanical study on edible flowers in Xishuangbanna, China

Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C

J Ethnobiol Ethnomed

30-Sep-2023

PMCID:	PMC10542681
doi:	10.1186/s13002-023-00608-1
PMID:	37777741

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
[(1R)-2-[(6aR,7R,8S,9R,10aS)-9-[(2R,3S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-oxooxan-2-yl]oxy-7,8-dimethyl-3-oxo-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-7-yl]-1-(furan-3-yl)ethyl] acetate	53348973	Click to see CC1C(CC23COC(=O)C2=CCCC3C1(C)CC(C4=COC=C4)OC(=O)C)OC5C(C(=O)C(C(O5)CO)O)O	548.60	unknown	https://doi.org/10.1002/HLCA.201000203
[2-[9-[3,5-dihydroxy-6-(hydroxymethyl)-4-oxooxan-2-yl]oxy-7,8-dimethyl-3-oxo-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-7-yl]-1-(furan-3-yl)ethyl] acetate	76019168	Click to see CC1C(CC23COC(=O)C2=CCCC3C1(C)CC(C4=COC=C4)OC(=O)C)OC5C(C(=O)C(C(O5)CO)O)O	548.60	unknown	https://doi.org/10.1002/HLCA.201000203
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(6aR,7S,8R,10aS)-7-[(2R)-2-hydroxy-2-(5-oxo-2H-furan-3-yl)ethyl]-7,8-dimethyl-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-3-one	162906744	Click to see CC1CCC23COC(=O)C2=CCCC3C1(C)CC(C4=CC(=O)OC4)O	346.40	unknown	https://doi.org/10.1021/NP068036D
[(1R)-2-[(6aR,7S,8S,9R,10aS)-9-hydroxy-7,8-dimethyl-3-oxo-5,6,6a,8,9,10-hexahydro-1H-benzo[d][2]benzofuran-7-yl]-1-(furan-3-yl)ethyl] acetate	163106183	Click to see CC1C(CC23COC(=O)C2=CCCC3C1(C)CC(C4=COC=C4)OC(=O)C)O	388.50	unknown	https://doi.org/10.1021/NP068036D
CID 12313706	12313706	Click to see CC1CCC23COC(=O)C2=CCCC3C1(C)CC(C4=CC(=O)OC4)O	346.40	unknown	https://doi.org/10.1021/NP068036D
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1S,4S,7S,8R,9R,10S,11R,14R)-8-acetyloxy-7-[(2S)-2-hydroxy-5-oxo-2H-furan-4-yl]-9-methyl-5,15-dioxo-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-en-11-yl] acetate	162983118	Click to see CC(=O)OC1C=CC2C(=O)OCC23C1C4(C(CC3)C(=O)OC(C4OC(=O)C)C5=CC(OC5=O)O)C	490.50	unknown	https://doi.org/10.1016/S0031-9422(97)00180-5
[8-acetyloxy-7-(2-hydroxy-5-oxo-2H-furan-4-yl)-9-methyl-5,15-dioxo-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-en-11-yl] acetate	162983117	Click to see CC(=O)OC1C=CC2C(=O)OCC23C1C4(C(CC3)C(=O)OC(C4OC(=O)C)C5=CC(OC5=O)O)C	490.50	unknown	https://doi.org/10.1016/S0031-9422(97)00180-5
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,8-Dihydroxy-2,6-dimethoxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one	163014324	Click to see COC1=C(C2=C(C=C1)OC3=C(C2=O)C(=CC(=C3OC4C(C(C(C(O4)CO)O)O)O)OC)O)O	466.40	unknown	https://doi.org/10.1016/S0031-9422(97)00180-5 https://doi.org/10.1021/NP068036D https://doi.org/10.1002/HLCA.201000203 https://doi.org/10.1002/MRC.1869
> Organoheterocyclic compounds / Naphthofurans
(1S,4S,6R,8R,9S,11R)-6-(furan-3-yl)-11-hydroxy-4,8-dimethyl-5,15-dioxatetracyclo[7.7.0.01,13.04,8]hexadec-12-en-14-one	16099457	Click to see CC12CCC34COC(=O)C3=CC(CC4C1(CC(O2)C5=COC=C5)C)O	344.40	unknown	https://doi.org/10.1002/HLCA.201000203 https://doi.org/10.1021/NP068036D
(1S,4S,6S,8R,9S,11R)-6-(furan-3-yl)-11-hydroxy-4,8-dimethyl-5,15-dioxatetracyclo[7.7.0.01,13.04,8]hexadec-12-en-14-one	162975323	Click to see CC12CCC34COC(=O)C3=CC(CC4C1(CC(O2)C5=COC=C5)C)O	344.40	unknown	https://doi.org/10.1021/NP068036D
6-(Furan-3-yl)-11-hydroxy-4,8-dimethyl-5,15-dioxatetracyclo[7.7.0.01,13.04,8]hexadec-12-en-14-one	162975322	Click to see CC12CCC34COC(=O)C3=CC(CC4C1(CC(O2)C5=COC=C5)C)O	344.40	unknown	https://doi.org/10.1002/HLCA.201000203 https://doi.org/10.1021/NP068036D
> Organoheterocyclic compounds / Naphthopyrans
(1S,4S,7R,9R,10R,11R,14R)-7-(furan-3-yl)-11-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione	73350928	Click to see CC12CC(OC(=O)C1CCC34C2C(C=CC3C(=O)OC4)O)C5=COC=C5	358.40	unknown	https://doi.org/10.1021/NP068036D https://doi.org/10.1002/HLCA.201000203 https://doi.org/10.1016/S0031-9422(97)00180-5 https://doi.org/10.1002/MRC.1869
(1S,4S,7S,8R,9R,10S,11R,14R)-7-(furan-3-yl)-8,11-dihydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione	52914116	Click to see CC12C(CCC34C1C(C=CC3C(=O)OC4)O)C(=O)OC(C2O)C5=COC=C5	374.40	unknown	https://doi.org/10.1002/HLCA.201000203
(1S,4S,7S,8R,9R,10S,14R)-7-(furan-3-yl)-8-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione	16099452	Click to see CC12C(CCC34C1CC=CC3C(=O)OC4)C(=O)OC(C2O)C5=COC=C5	358.40	unknown	https://doi.org/10.1021/NP068036D https://doi.org/10.1002/HLCA.201000203
(1S,4S,7S,8R,9R,10S)-7-(furan-3-yl)-8-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione	163186470	Click to see CC12C(CCC34C1CC=CC3C(=O)OC4)C(=O)OC(C2O)C5=COC=C5	358.40	unknown	https://doi.org/10.1021/NP068036D
(1S,7S,8R,9R,10S,14R)-7-(furan-3-yl)-8-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadeca-3,12-diene-5,15-dione	16099456	Click to see CC12C3CC=CC4C3(CC=C1C(=O)OC(C2O)C5=COC=C5)COC4=O	356.40	unknown	https://doi.org/10.1021/NP068036D
[(1S,4S,7S,8R,9R,10S,11R,14R)-8-acetyloxy-7-(furan-3-yl)-9-methyl-5,15-dioxo-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-en-11-yl] acetate	101939043	Click to see CC(=O)OC1C=CC2C(=O)OCC23C1C4(C(CC3)C(=O)OC(C4OC(=O)C)C5=COC=C5)C	458.50	unknown	https://doi.org/10.1002/HLCA.201000203 https://doi.org/10.1002/MRC.1869 https://doi.org/10.1016/S0031-9422(97)00180-5 https://doi.org/10.1021/NP068036D
[(1S,4S,7S,8R,9R,10S,14R)-7-(furan-3-yl)-9-methyl-5,15-dioxo-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-en-8-yl] acetate	102589440	Click to see CC(=O)OC1C(OC(=O)C2C1(C3CC=CC4C3(CC2)COC4=O)C)C5=COC=C5	400.40	unknown	https://doi.org/10.1002/MRC.1869 https://doi.org/10.1002/HLCA.201000203 https://doi.org/10.1021/NP068036D https://doi.org/10.1016/S0031-9422(97)00180-5
[(1S,7S,8R,9R,10S,11R,14R)-7-(furan-3-yl)-8-hydroxy-9-methyl-5,15-dioxo-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadeca-3,12-dien-11-yl] acetate	53348972	Click to see CC(=O)OC1C=CC2C(=O)OCC23C1C4(C(C(OC(=O)C4=CC3)C5=COC=C5)O)C	414.40	unknown	https://doi.org/10.1002/HLCA.201000203
[7-(Furan-3-yl)-8-hydroxy-9-methyl-5,15-dioxo-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadeca-3,12-dien-11-yl] acetate	76019167	Click to see CC(=O)OC1C=CC2C(=O)OCC23C1C4(C(C(OC(=O)C4=CC3)C5=COC=C5)O)C	414.40	unknown	https://doi.org/10.1002/HLCA.201000203
7-(Furan-3-yl)-11-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione	162845576	Click to see CC12CC(OC(=O)C1CCC34C2C(C=CC3C(=O)OC4)O)C5=COC=C5	358.40	unknown	https://doi.org/10.1002/MRC.1869 https://doi.org/10.1002/HLCA.201000203 https://doi.org/10.1021/NP068036D https://doi.org/10.1016/S0031-9422(97)00180-5
7-(Furan-3-yl)-8-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione	162892325	Click to see CC12C(CCC34C1CC=CC3C(=O)OC4)C(=O)OC(C2O)C5=COC=C5	358.40	unknown	https://doi.org/10.1002/HLCA.201000203 https://doi.org/10.1021/NP068036D
7-(Furan-3-yl)-8-hydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadeca-3,12-diene-5,15-dione	162843560	Click to see CC12C3CC=CC4C3(CC=C1C(=O)OC(C2O)C5=COC=C5)COC4=O	356.40	unknown	https://doi.org/10.1021/NP068036D
7-(Furan-3-yl)-8,11-dihydroxy-9-methyl-6,16-dioxatetracyclo[8.7.0.01,14.04,9]heptadec-12-ene-5,15-dione	75952095	Click to see CC12C(CCC34C1C(C=CC3C(=O)OC4)O)C(=O)OC(C2O)C5=COC=C5	374.40	unknown	https://doi.org/10.1002/HLCA.201000203
Salviarin	329251	Click to see CC12CC(OC(=O)C1CCC34C2CC=CC3C(=O)OC4)C5=COC=C5	342.40	unknown	https://doi.org/10.1016/S0031-9422(97)00180-5 https://doi.org/10.1021/NP068036D https://doi.org/10.1002/HLCA.201000203 https://doi.org/10.1002/MRC.1869
Splendidin	433422	Click to see CC(=O)OC1C=CC2C(=O)OCC23C1C4(C(CC3)C(=O)OC(C4OC(=O)C)C5=COC=C5)C	458.50	unknown	https://doi.org/10.1002/HLCA.201000203 https://doi.org/10.1016/S0031-9422(97)00180-5 https://doi.org/10.1021/NP068036D https://doi.org/10.1002/MRC.1869
ZT72DJ66LU	15705466	Click to see CC12CC(OC(=O)C1CCC34C2CC=CC3C(=O)OC4)C5=COC=C5	342.40	unknown	https://doi.org/10.1002/HLCA.201000203 https://doi.org/10.1002/MRC.1869 https://doi.org/10.1021/NP068036D https://doi.org/10.1016/S0031-9422(97)00180-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanidin 3-O-p-coumaroyl glycosides / Anthocyanidin 3-O-6-p-coumaroyl glycosides
[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	154496255	Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O)O	789.70	unknown	https://doi.org/10.1016/S0040-4039(00)70662-9
[(2R,3S,4S,5S,6S)-3,4,5-trihydroxy-6-[7-hydroxy-5-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate	154496223	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O	773.70	unknown	https://doi.org/10.1016/S0031-9422(01)00415-0
3-[[(2S,3S,4R,5R,6S)-3-(2-carboxyacetyl)oxy-6-[3-[(2S,3S,4S,5S,6S)-6-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-7-hydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-5-yl]oxy-4,5-dihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid	154497407	Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)COC(=O)CC(=O)O)OC(=O)CC(=O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O)O	961.80	unknown	https://doi.org/10.1016/S0040-4039(00)70662-9
3-[[(2S,3S,4S,5S,6S)-6-[3-[(2S,3R,4R,5S,6R)-6-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-7-hydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-5-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid	154497021	Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)COC(=O)CC(=O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O)O	875.70	unknown	https://doi.org/10.1016/S0040-4039(00)70662-9

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Salvia splendens

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