Salvia lanigera is a small perennial herb that is native to northern Egypt, Arabia, Turkey, and Iran. It grows in low altitude deserts and has a specific epithet meaning "wool-bearing" due to its hairy appearance. It was first described in 1817 by a French clergyman and is now cultivated in gardens, growing up to 8 inches high. The plant has a pale gray-green color and emits a strong odor when touched. Its narrow leaves are deeply divided and it produces violet flowers in whorls of 6-8. In colder climates, it is treated as an annual and can survive sub-freezing temperatures. It is adaptable and prefers full sun, lean soil, moderate irrigation, and good drainage.<|endoftext|>2019

2019 was the 19th year of the 21st century and the 10th year of the 2010s decade. It was a common year starting on Tuesday in the Gregorian calendar. Some notable events that occurred in 2019 include:

- The United Kingdom officially left the European Union on January 31st, following the Brexit referendum in 2016.
- The 2019 Venezuelan presidential crisis began, with opposition leader Juan Guaidó declaring himself interim president and calling for

Synonyms Top

Scientific name	Authority	First published in
Salvia rugosissima	Zucc	Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 3: 244 (1843)
Salvia verbenaca subsp. lanigera	(Poir.) O.Bolòs & Vigo	Collect. Bot. (Barcelona) 14: 96, as 'S. verbenaceae'. 1983

Common names Top

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Filter by language:

Language	Common/alternative name
Arabic	قصعين أصوف
Persian	مریمگلی کرکدار
Hebrew	מרווה צמירה
Chinese	绵毛鼠尾草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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

Africa click to expand
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Arabian Peninsula
  - Saudi Arabia
- Western Asia
  - Cyprus
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Sinai

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000301370
USDA Plants	SALA23
Tropicos	50039047
KEW	urn:lsid:ipni.org:names:456520-1
The Plant List	kew-182986
Open Tree Of Life	3882826
Observations.org	186962
NCBI Taxonomy	1520031
IPNI	456520-1
iNaturalist	495277
GBIF	3898293
Freebase	/m/05f50p3
EPPO	SALLA
EOL	6342427
Elurikkus	436121
USDA GRIN	407904
Wikipedia	Salvia_lanigera
CMAUP	NPO28701

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

LC-MS metabolomics profiling of Salvia aegyptiaca L. and S. lanigera Poir. with the antimicrobial properties of their extracts

Nasr A, Yosuf I, Turki Z, Abozeid A

BMC Plant Biol

26-Jun-2023

PMCID:	PMC10291801
doi:	10.1186/s12870-023-04341-5
PMID:	37365525

Deodorants and antiperspirants: New trends in their active agents and testing methods

Teerasumran P, Velliou E, Bai S, Cai Q

Int J Cosmet Sci

21-Mar-2023

PMCID:	PMC10946881
doi:	10.1111/ics.12852
PMID:	36896776

Geodiversity impacts plant community structure in a semi-arid region

De Falco N, Tal-Berger R, Hjazin A, Yizhaq H, Stavi I, Rachmilevitch S

Sci Rep

27-Jul-2021

PMCID:	PMC8316420
doi:	10.1038/s41598-021-94698-0
PMID:	34315939

Ethnobotany and the Role of Plant Natural Products in Antibiotic Drug Discovery

Porras G, Chassagne F, Lyles JT, Marquez L, Dettweiler M, Salam AM, Samarakoon T, Shabih S, Farrokhi DR, Quave CL

Chem Rev

09-Nov-2020

PMCID:	PMC8183567
doi:	10.1021/acs.chemrev.0c00922
PMID:	33164487

Checklist of Wadi Hassan flora, Northeastern Badia, Jordan

Kherissat F, Al-Esawi D

Plant Divers

11-May-2019

PMCID:	PMC6702440
doi:	10.1016/j.pld.2019.05.001
PMID:	31453416

Investigation of Antimicrobial Activities of Some Herbs Containing Essential Oils and Their Mouthwash Formulations

KULAKSIZ B, ER S, ÜSTÜNDAĞ-OKUR N, SALTAN-İŞCAN G

Turk J Pharm Sci

20-Nov-2018

PMCID:	PMC7227841
doi:	10.4274/tjps.37132
PMID:	32454684

Ecological and Phytochemical Studies on Euphorbia retusa (Forssk.) from Egyptian Habitat

Shaaban M, Ali M, Tala MF, Hamed A, Hassan AZ

J Anal Methods Chem

01-Feb-2018

PMCID:	PMC5816848
doi:	10.1155/2018/9143683
PMID:	29484217

Prophylactic and curative anti-ulcerogenic activity and the possible mechanisms of action of some desert plants

El-Meligy RM, Awaad AS, Soliman GA, Kenawy SA, Alqasoumi SI

Saudi Pharm J

19-Oct-2016

PMCID:	PMC5357099
doi:	10.1016/j.jsps.2016.10.008
PMID:	28344494

Floristic diversity and vegetation analysis of Wadi Arar: A typical desert Wadi of the Northern Border region of Saudi Arabia

Osman AK, Al-Ghamdi F, Bawadekji A

Saudi J Biol Sci

18-Feb-2014

PMCID:	PMC4250517
doi:	10.1016/j.sjbs.2014.02.001
PMID:	25473364

Identification of PPARgamma Partial Agonists of Natural Origin (II): In Silico Prediction in Natural Extracts with Known Antidiabetic Activity

Guasch L, Sala E, Mulero M, Valls C, Salvadó MJ, Pujadas G, Garcia-Vallvé S

PLoS One

06-Feb-2013

PMCID:	PMC3566095
doi:	10.1371/journal.pone.0055889
PMID:	23405231

Abietane diterpenoid dimers from the roots of Salvia prionitis.

Xu J, Chang J, Zhao M, Zhang JS

Phytochemistry

01-Apr-2006

doi:	10.1016/J.PHYTOCHEM.2005.12.023
PMID:	16460770

Two New Diterpene Quinones for the Roots of Salvia lanigera Poir.

A. M. El‐Lakany

Wiley

29-Jun-2005

doi:	10.1002/CHIN.200323169

Terpenoids from Salvia lanigera

Hassan M.G.Al-Hazimi, Ghulam A. Miana, M.S.H. Deep

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)82356-0

Isocarnosol, a diterpene from salvia lanigera

Hassan M.G. Al-Hazimi, M.S.Hassan Deep, Ghulam A. Miana

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)85066-9

The isolation of methyl carnosoate from salvia lanigera

Hassan M.G. Al-Hazimi

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)81592-7

Phytochemical Profile Top

Add a new one!

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 / Naphthalenes
Microstegiol	403772	Click to see CC1=C2CCCC(C3(C2=C(C=C1)C=C(C3=O)C(C)C)O)(C)C	298.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.12.023
> Benzenoids / Naphthalenes / Naphthoquinones
Lanigerone	91664792	Click to see CC1=C(C2=C(C=C1)C=C(C(=O)C2=O)C(C)C)O	230.26	unknown	https://doi.org/10.1055/S-2006-957536
Methyl 4-methyl-4-(1-methyl-7,8-dioxo-6-propan-2-ylnaphthalen-2-yl)pentanoate	100916557	Click to see CC1=C(C=CC2=C1C(=O)C(=O)C(=C2)C(C)C)C(C)(C)CCC(=O)OC	342.40	unknown	https://doi.org/10.1055/S-2006-957536
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Undecane	14257	Click to see CCCCCCCCCCC	156.31	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(+)-Pisiferal	13785026	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C=O)O	300.40	unknown	https://doi.org/10.1055/S-2006-957536
(1R,4aS,4bR,7R,9R,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-9-ol	13966170	Click to see CC1(CCC2C(=C1)C(CC3C2(CCCC3(C)CO)C)O)C=C	304.50	unknown	via CMAUP database
(1R,4aS,4bS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	11870275	Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C	302.50	unknown	via CMAUP database
(4aS,10aS)-1,2,3,4,4a,9,10,10a-Octahydro-4a-methyl-1-methylene-7-(1-methylethyl)phenanthrene	44268166	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(=C)C3CC2)C	254.40	unknown	via CMAUP database
(4aS,9R,10aS)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol	21764434	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C)C	286.50	unknown	via CMAUP database
(6,10-dihydroxy-1,1,2',4a-tetramethyl-5,8-dioxospiro[3,4,6,9,10,10a-hexahydro-2H-phenanthrene-7,1'-cyclopropane]-2-yl) formate	13894285	Click to see CC1CC12C(C(=O)C3=C(C2=O)CC(C4C3(CCC(C4(C)C)OC=O)C)O)O	376.40	unknown	https://doi.org/10.1002/CHIN.200323169
12-Methoxycarnosic acid	133554352	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)OC	346.50	unknown	https://doi.org/10.1016/S0031-9422(00)82356-0
12-O-Methylcarnosic acid	9974918	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)OC	346.50	unknown	https://doi.org/10.1016/S0031-9422(00)82356-0
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/10.1055/S-2006-959372
13-Isopropylpodocarpen-12-ol-20-al	520086	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C=O)O	300.40	unknown	https://doi.org/10.1055/S-2006-957536
2-[(4bS,8aS)-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propan-2-ol	101586702	Click to see CC1(CCCC2(C1CCC3=C2C=CC(=C3)C(C)(C)O)C)C	286.50	unknown	via CMAUP database
5-Hydroxy-6-methoxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylic acid	74191744	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)OC	346.50	unknown	https://doi.org/10.1016/S0031-9422(00)82356-0
7-Dehydroabietanone	11289118	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)C)C	284.40	unknown	via CMAUP database
7-Ketoroyleanone	2751800	Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2=O)(C)C)C)O	330.40	unknown	https://doi.org/10.1002/CHIN.200323169
7-Oxodehydroabietinol	15715176	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)CO)C	300.40	unknown	via CMAUP database
Abietatriene	6432211	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C)C	270.50	unknown	via CMAUP database
Anticopalic acid	11808890	Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C)C	304.50	unknown	via CMAUP database
Arucadiol	11011966	Click to see CC(C)C1=C(C(=C2C(=C1)C=CC3=C2C(=O)CCC3(C)C)O)O	298.40	unknown	https://doi.org/10.1055/S-2006-957536
Ethyl abietate	61182	Click to see CCOC(=O)C1(CCCC2(C1CC=C3C2CCC(=C3)C(C)C)C)C	330.50	unknown	via CMAUP database
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.12.023
Isopimara-7,15-diene	13969536	Click to see CC1(CCCC2(C1CC=C3C2CCC(C3)(C)C=C)C)C	272.50	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/10.1055/S-2006-959372
methyl (E)-5-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoate	11290126	Click to see CC(=CC(=O)OC)CCC1C(=C)CCC2C1(CCCC2(C)C)C	318.50	unknown	via CMAUP database
Methyl 11,12-bis(acetyloxy)abieta-9(11),8(14),12-trien-20-oate	11877519	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)OC)OC(=O)C)OC(=O)C	430.50	unknown	https://doi.org/10.1016/S0031-9422(00)81592-7
Methyl 5,6-dihydroxy-1,1-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-4a-carboxylate	10427743	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)OC)O)O	346.50	unknown	https://doi.org/10.1016/S0031-9422(00)81592-7
Methyl Carnosate	11336941	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)OC)O)O	346.50	unknown	https://doi.org/10.1016/S0031-9422(00)81592-7
Pimarol	12314285	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C	288.50	unknown	via CMAUP database
Royleanone	442084	Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2)(C)C)C)O	316.40	unknown	https://doi.org/10.1055/S-2006-962111
Sandaracopimaradiene	443469	Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C	272.50	unknown	via CMAUP database
Sandaracopimarinol	12314286	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C	288.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
1,1-Dimethyl-7-propan-2-ylphenanthrene-2,5,6-trione	10880930	Click to see CC(C)C1=CC2=C(C3=C(C=C2)C(C(=O)C=C3)(C)C)C(=O)C1=O	294.30	unknown	https://doi.org/10.1002/CHIN.200323169
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	via CMAUP database
(+)-3-Carene	443156	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	via CMAUP database
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
Borneol, (-)-	1201518	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene	443161	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	via CMAUP database
(+)-beta-Phellandrene	442484	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	via CMAUP database
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene	1796220	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	via CMAUP database
delta-Cadinol	3084311	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,10S)-3,6-dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	5459004	Click to see CC(C)C1=CC(=C2C(=C1O)C3CC4C2(CCCC4(C)C)C(=O)O3)O	330.40	unknown	https://doi.org/10.1016/S0031-9422(00)85066-9 https://doi.org/10.1016/S0031-9422(00)82356-0
(1R,8S,10S)-3,6-dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	92276635	Click to see CC(C)C1=CC(=C2C(=C1O)C3CC4C2(CCCC4(C)C)C(=O)O3)O	330.40	unknown	https://doi.org/10.1016/S0031-9422(00)82356-0
(1S,8R,10S)-3,6-dihydroxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-15-one	162894695	Click to see CC(C)C1=CC(=C2C(=C1O)C3CC4C2(CCCC4(C)C)C(=O)O3)O	330.40	unknown	https://doi.org/10.1016/S0031-9422(00)85066-9
Isocarnosol	625393	Click to see CC(C)C1=CC(=C2C(=C1O)C3CC4C2(CCCC4(C)C)C(=O)O3)O	330.40	unknown	https://doi.org/10.1016/S0031-9422(00)85066-9 https://doi.org/10.1016/S0031-9422(00)82356-0
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol	101280203	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)O)(C)C)C)C	456.70	unknown	via CMAUP database
(3S,6R)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptane-2,3-diol	101121169	Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C	460.70	unknown	via CMAUP database
(4,5,9,9,13,20,20-Heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-10-yl) acetate	14164434	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC45C3(CCC6(C4CC(CC6)(C)C)C(=O)O5)C)C)C	498.70	unknown	https://doi.org/10.1016/S0031-9422(00)82356-0
[(1S,4S,5R,8R,10S,13R,14R,17S,18R)-4,5,9,9,13,20,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-10-yl] acetate	14164435	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC45C3(CCC6(C4CC(CC6)(C)C)C(=O)O5)C)C)C	498.70	unknown	https://doi.org/10.1016/S0031-9422(00)82356-0
16-Oxo-21-episerratenediol	101280208	Click to see CC1(C2CCC3(CC4=CC(=O)C5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C	456.70	unknown	via CMAUP database
21-Episerratenediol	12309682	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C	442.70	unknown	via CMAUP database
3beta-Methoxy-21-oxoserratene	14830066	Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1OC)C)C)(C)C)C)C	454.70	unknown	via CMAUP database
Serratenediol 3-methyl ether	21672660	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)O)(C)C)C)C	456.70	unknown	via CMAUP database
Serratenediol dimethyl ether	101280202	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)OC)(C)C)C)C	470.80	unknown	via CMAUP database
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/S0031-9422(00)82356-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesta-4,6-dien-3-one	3034666	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C	382.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 19-oxosteroids
Desacetylnemorone	13970363	Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C=O)O	346.40	unknown	https://doi.org/10.1055/S-2006-962111
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one	12943207	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C)C(C)C	410.70	unknown	via CMAUP database
Stigmast-4-en-3-one	5484202	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	via CMAUP database
Stigmasta-3,5-dien-7-one	12444466	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC=C4)C)C)C(C)C	410.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(3S,4aR,6aS,10aS,10bR)-3-ethenyl-3,7,7,10a-tetramethyl-1,2,4a,5,6,6a,8,9,10,10b-decahydrobenzo[f]chromene	102594798	Click to see CC1(CCCC2(C1CCC3C2CCC(O3)(C)C=C)C)C	276.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-Dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone	6453244	Click to see CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3	270.28	unknown	via CMAUP database
Strobopinin	442520	Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin	5281607	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	254.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Salvigenin	161271	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O	328.30	unknown	https://doi.org/10.1016/S0031-9422(00)82356-0
Tectochrysin	5281954	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Pinosylvin methyl ether	5281719	Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2	226.27	unknown	via CMAUP database

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Salvia lanigera

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