Salvia nemorosa, also known as woodland sage, Balkan clary, blue sage or wild sage, is a hardy herbaceous perennial plant native to central Europe and Western Asia. It is a popular plant among gardeners due to its attractive appearance and ease of growth and propagation. This has resulted in the development of numerous cultivars and hybrids, making it difficult to distinguish them from the original species. The plant was first described by Carl Linnaeus in 1762 and is named after its typical habitat in woods and groves. In northern Britain, both Salvia nemorosa and Salvia pratensis are at risk of disappearing due to damage from slugs. The plant produces multiple inflorescences with small flowers in vibrant colors. It is hardy to USDA Hardiness Zones 4-8 and prefers full sun, good drainage, and moderate watering. Several cultivars of Salvia nemorosa have received the Royal Horticultural Society's Award of Garden Merit in the UK. The plant has also been used in Turkish medicine for its ability to stop bleeding. Phytochemical studies have identified various compounds in the plant, including diterpenes, triterpenes, and flavonoids.

Synonyms Top

Scientific name	Authority	First published in
Salvia collina	Schur	Enum. Pl. Transsilv. : 522 (1866)
Sclarea nemorosa	Mill.	Gard. Dict. ed. 8 : n.º 6 (1768)
Sclarea punctata	Moench	Methodus : 374 (1794)
Salvia sylvestris var. nemorosa	(L.) Nyman	Consp. Fl. Eur. 570. 1881
Salvia nemorosa var. latifolia	K.Koch	Linnaea 21: 658. 1849
Salvia nemorosa subsp. illuminata	Soó
Salvia nemorosa subsp. jailicola	Soó
Salvia nemorosa subsp. moldavica	Soó

Common names Top

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Filter by language:

Language	Common/alternative name
English	woodland sage
English	wild sage
English	balkan clary
English	blue sage
Belarusian	шалфей лясны
Bulgarian	горски конски босилек
Czech	šalvěj hajní
Danish	småblomstret salvie
Danish	steppe-salvie
German	steppen-salbei
German	hain-salbei
Estonian	metssalvei
Finnish	lehtosalvia
Upper Sorbian	stepowa želbija
Norwegian Bokmål	steppesalvie
Norwegian Bokmål	solbærsalvie
Dutch	bossalie
Norwegian Nynorsk	steppesalvie
Polish	szałwia omszona
Romanian	jaleș de cîmp
Romanian	jaleș de câmp
Russian	шалфей яйлинский
Russian	шалфей дубравный
Russian	шалфей молдавский
Slovak	šalvia hájna
Swedish	stäppsalvia
Turkish	orman adaçayı
Chinese	林地鼠尾草

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Salvia nemorosa subsp. nemorosa	L.	Unknown
Salvia nemorosa subsp. pseudosylvestris	(Stapf) Bornm.	Beih. Bot. Centralbl. 22(2): 123 (1907)

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

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Middle Asia
  - Kazakhstan
  - Tadzhikistan
  - Uzbekistan
- Siberia
  - West Siberia
- Western Asia
  - Afghanistan
  - Iran

Australasia click to expand
- New Zealand
  - New Zealand South

Europe click to expand
- Eastern Europe
  - Central European Russia
  - East European Russia
  - Krym
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Czechoslovakia
  - Hungary
  - Poland
  - Switzerland
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Yugoslavia
- Southwestern Europe
  - France
  - Spain

Northern America click to expand
- North-central U.S.A.
  - Wisconsin
- Northeastern U.S.A.
  - New York

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000301687
Canadensys	6446
Tropicos	17600301
INPN	120673
KEW	urn:lsid:ipni.org:names:456774-1
The Plant List	kew-183282
Plantarium	33515
Missouri Botanical Garden	281423
Open Tree Of Life	1025149
Observations.org	9168
NCBI Taxonomy	49215
NBN Atlas	NBNSYS0000004221
Nature Serve	2.158871
IPNI	456774-1
iNaturalist	168387
GBIF	2927028
Freebase	/m/05f9flq
WisFlora	4966
EPPO	SALNE
Elurikkus	7047
USDA GRIN	70593
Wikipedia	Salvia_nemorosa

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

Cyanobacterial elicitor enhances the biomass of Mentha piperita L. and improves the production of high-value rosmarinic acid under in vitro culture of apical meristem

Shariatmadari Z, Zarezadeh S, Riahi H, Ghotbi-Ravandi AA, Seyed Hashtroudi M, Shahroudi E

BMC Plant Biol

15-Mar-2024

PMCID:	PMC10941488
doi:	10.1186/s12870-024-04876-1
PMID:	38486151

Does increasing biodiversity in an urban woodland setting promote positive emotional responses in humans? A stress recovery experiment using 360-degree videos of an urban woodland

Farris S, Dempsey N, McEwan K, Hoyle H, Cameron R

PLoS One

07-Feb-2024

PMCID:	PMC10849218
doi:	10.1371/journal.pone.0297179
PMID:	38324517

Integrative effects of phytohormones in the phenolic acids production in Salvia verticillata L. under multi-walled carbon nanotubes and methyl jasmonate elicitation

Rahmani N, Radjabian T

BMC Plant Biol

19-Jan-2024

PMCID:	PMC10797988
doi:	10.1186/s12870-023-04719-5
PMID:	38238679

Genome-Wide Identification and Expression Analysis of the MYB Transcription Factor Family in Salvia nemorosa

Yang H, Chen C, Han L, Zhang X, Yue M

Genes (Basel)

17-Jan-2024

PMCID:	PMC10815335
doi:	10.3390/genes15010110
PMID:	38254999

A Possible Perspective of Recultivation with Arbuscular Mycorrhiza-Inoculated Drought-Tolerant Herbaceous Plants

Papp L, Habtemariam AA, Brandt S, Cseh P, Heller Á, Péter B, Szakály ÁP, Kiszel P, Codogno B, Bratek Z, Tóth Z

Plants (Basel)

06-Dec-2023

PMCID:	PMC10747347
doi:	10.3390/plants12244088
PMID:	38140415

In Vitro Antibacterial, Antioxidant, Anticholinesterase, and Antidiabetic Activities and Chemical Composition of Salvia balansae

Mokhtar A, Souhila T, Nacéra B, Amina B, Alghonaim MI, Öztürk M, Alsalamah SA, Miara MD, Boufahja F, Bendif H

Molecules

27-Nov-2023

PMCID:	PMC10708212
doi:	10.3390/molecules28237801
PMID:	38067531

The effects of precipitation change on urban meadows in different design models and substrates

Jiang Y, Yuan T

Sci Rep

23-Nov-2023

PMCID:	PMC10667351
doi:	10.1038/s41598-023-44974-y
PMID:	37996501

Natural Antimicrobials: A Reservoir to Contrast Listeria monocytogenes

Ricci A, Lazzi C, Bernini V

Microorganisms

15-Oct-2023

PMCID:	PMC10609241
doi:	10.3390/microorganisms11102568
PMID:	37894226

The genome sequence of a leaf beetle, Cryptocephalus moraei (Linnaeus, 1758)

Sivell O, Sivell D, Mitchell R

Wellcome Open Res

13-Oct-2023

PMCID:	PMC11053346
doi:	10.12688/wellcomeopenres.19522.1
PMID:	38680651

Screening of 20 species from Lamiaceae family based on phytochemical analysis, antioxidant activity and HPLC profiling

Moshari-Nasirkandi A, Alirezalu A, Alipour H, Amato J

Sci Rep

09-Oct-2023

PMCID:	PMC10562417
doi:	10.1038/s41598-023-44337-7
PMID:	37813985

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

Comparing Non-Thermal Plasma and Cold Stratification: Which Pre-Sowing Treatment Benefits Wild Plant Emergence?

Gudyniene V, Juzenas S, Stukonis V, Mildaziene V, Ivankov A, Norkeviciene E

Plants (Basel)

10-Sep-2023

PMCID:	PMC10534388
doi:	10.3390/plants12183220
PMID:	37765384

Chemical Profile and Bioactivity Evaluation of Salvia Species from Eastern Europe

Luca SV, Skalicka-Woźniak K, Mihai CT, Gradinaru AC, Mandici A, Ciocarlan N, Miron A, Aprotosoaie AC

Antioxidants (Basel)

28-Jul-2023

PMCID:	PMC10451821
doi:	10.3390/antiox12081514
PMID:	37627509

Production of secondary metabolites using tissue culture-based biotechnological applications

Ozyigit II, Dogan I, Hocaoglu-Ozyigit A, Yalcin B, Erdogan A, Yalcin IE, Cabi E, Kaya Y

Front Plant Sci

29-Jun-2023

PMCID:	PMC10339834
doi:	10.3389/fpls.2023.1132555
PMID:	37457343

Reproductive Capacity and Scanning Electron Microscopy (SEM) Analyses of the Micromorphological Surfaces of Three Endemic Satureja Species from Bulgaria

Semerdjieva I, Yankova-Tsvetkova E, Zheljazkov VD, Koleva-Valkova LH, Nikolova R

Plants (Basel)

24-Jun-2023

PMCID:	PMC10346649
doi:	10.3390/plants12132436
PMID:	37446998

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 / Ibogan-type alkaloids
methyl (1S,15R,17R,18S)-17-[(1R)-1-hydroxyethyl]-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate	162988186	Click to see CC(C1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC)O	354.40	unknown	https://doi.org/10.1007/BF00568696
> Benzenoids / Fluorenes
Veratramine	6070	Click to see CC1CC(C(NC1)C(C)C2=C(C3=C(C=C2)C4CC=C5CC(CCC5(C4C3)C)O)C)O	409.60	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
> Benzenoids / Naphthalenes / Naphthoquinones
4-Hydroxy-7-methyl-8-(4-methylpent-4-enyl)-3-propan-2-ylnaphthalene-1,2-dione	821448	Click to see CC1=C(C2=C(C=C1)C(=C(C(=O)C2=O)C(C)C)O)CCCC(=C)C	312.40	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(4R)-4-[(3S)-3-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one	102446069	Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)OC3C(C(CO3)(CO)O)O)(C)C	504.60	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
(4R)-4-[(E,3R)-3-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]-3,5,5-trimethylcyclohex-2-en-1-one	95224721	Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)OC3C(C(CO3)(CO)O)O)(C)C	502.60	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
(4R)-4-[(E,3S)-3-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]-3,5,5-trimethylcyclohex-2-en-1-one	95224723	Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)OC3C(C(CO3)(CO)O)O)(C)C	502.60	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
(6R,9S)-3-Oxo-alpha-ionol glucoside	73815024	Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C	370.40	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
3Eec4Q65S4	21630888	Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C	370.40	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
4-[3-[3-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]-3,5,5-trimethylcyclohex-2-en-1-one	75614565	Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)OC3C(C(CO3)(CO)O)O)(C)C	502.60	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
4-[3-[3-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one	73106837	Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)OC3C(C(CO3)(CO)O)O)(C)C	504.60	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
4-Hydroxy-3,5,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one	73815023	Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	386.40	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
Blumenol C glucoside	14135394	Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C	372.50	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
Byzantionoside B	14135395	Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C	372.50	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
Corchoionoside C	10317980	Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	386.40	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
Roseoside	9930064	Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	386.40	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,3R,4aS,10aR)-3,8-dihydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	163056588	Click to see CC(C)C1=C(C2=C(C=C1)C3(CC(CC(C3CC2)(C)C(=O)O)O)C)O	332.40	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
3,8-Dihydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	163056587	Click to see CC(C)C1=C(C2=C(C=C1)C3(CC(CC(C3CC2)(C)C(=O)O)O)C)O	332.40	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
7-Acetylhorminone	2751796	Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2OC(=O)C)(C)C)C)O	374.50	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
Horminone	2751795	Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C)O	332.40	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
Taxoquinone	99965	Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C)O	332.40	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(199907/08)14:4<230::AID-FFJ816>3.0.CO;2-L
beta-Farnesene, (6Z)-	5317319	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(199907/08)14:4<230::AID-FFJ816>3.0.CO;2-L
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(199907/08)14:4<230::AID-FFJ816>3.0.CO;2-L
Caryophyllene epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(199907/08)14:4<230::AID-FFJ816>3.0.CO;2-L
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene	91723653	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(199907/08)14:4<230::AID-FFJ816>3.0.CO;2-L
Germacrene B	5281519	Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C	204.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(199907/08)14:4<230::AID-FFJ816>3.0.CO;2-L
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(199907/08)14:4<230::AID-FFJ816>3.0.CO;2-L
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
2,2,4a,6a,6b,9,9,12a-Octamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-3,10,13-triol	74323912	Click to see CC1(CC2C3=CC(C4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C)C)C)(C)C)O)C)O)C	458.70	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol	225688	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
alpha-Amyrin	73170	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
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/S0031-9422(00)90672-1
Salvinemorol	44575230	Click to see CC1(CC2C3=CC(C4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C)C)C)(C)C)O)C)O)C	458.70	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
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)90672-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
24-Methylenecycloartanol	94204	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
CID 9547213	9547213	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R)-6-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,16-trimethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol	162887483	Click to see CC(CCC(=C)C(C)(C)O)C1CCC2C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
15-(6-Hydroxy-6-methyl-5-methylideneheptan-2-yl)-7,7,16-trimethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol	162887482	Click to see CC(CCC(=C)C(C)(C)O)C1CCC2C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
1-(5a,5b,8,8,11a,13b-Hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-3-yl)ethanone	15558362	Click to see CC(=O)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C	412.70	unknown	https://doi.org/10.1007/BF00683848
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
(4alpha,5xi,7alpha,13xi,15alpha)-4,9-Epoxycevane-3,4,7,14,15,16,20-heptol	139292053	Click to see CC1CCC2C(C3C(CN2C1)C4CC56C(C4(C(C3O)O)O)C(CC7C5(CCC(C7(O6)O)O)C)O)(C)O	509.60	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
Angeloylzygadenine	6441115	Click to see CC=C(C)C(=O)OC1CCC2(C3C1(OC24CC5C6CN7CC(CCC7C(C6C(C(C5(C4CC3)O)O)O)(C)O)C)O)C	575.70	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
Zygadenine	442987	Click to see CC1CCC2C(C3C(CN2C1)C4CC56C(C4(C(C3O)O)O)CCC7C5(CCC(C7(O6)O)O)C)(C)O	493.60	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Jerveratrum-type alkaloids
Jervine	10098	Click to see CC1CC2C(C(C3(O2)CCC4C5CC=C6CC(CCC6(C5C(=O)C4=C3C)C)O)C)NC1	425.60	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
Isorubijervine	99473	Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)CO)C	413.60	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
Rubijervine	253295	Click to see CC1CCC2C(C3C(N2C1)CC4C3(C(CC5C4CC=C6C5(CCC(C6)O)C)O)C)C	413.60	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
Pseudojervine	16398499	Click to see CC1CC2C(C(C3(O2)CCC4C5CC=C6CC(CCC6(C5C(=O)C4=C3C)C)OC7C(C(C(C(O7)CO)O)O)O)C)NC1	587.70	unknown	https://doi.org/10.1016/S0031-9422(96)00359-7
> 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/S0031-9422(00)90672-1
22,23-Dihydro-alpha-spinasterone	14160308	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(=O)C4)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
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/S0031-9422(00)90672-1
delta7Stigmastenol	521367	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
Schottenol	441837	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
Schottenone	129681578	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(=O)C4)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
Stigmast-4-en-3-one	5484202	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
Stigmast-4-en-3-one, (24S)-	579897	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
Stigmast-7-en-3-one	5748344	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(=O)C4)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
5-[[4-Amino-5-[[1-[[1-carboxy-4-[(4-carboxy-3-methylbut-2-enoyl)-hydroxyamino]butyl]amino]-5-[(4-carboxy-3-methylbut-2-enoyl)-hydroxyamino]-1-oxopentan-2-yl]amino]-5-oxopentyl]-hydroxyamino]-3-methyl-5-oxopent-3-enoic acid	163059045	Click to see CC(=CC(=O)N(CCCC(C(=O)NC(CCCN(C(=O)C=C(C)CC(=O)O)O)C(=O)NC(CCCN(C(=O)C=C(C)CC(=O)O)O)C(=O)O)N)O)CC(=O)O	786.80	unknown	https://doi.org/10.1007/BF00683848
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
(16S)-16-(2-hydroperoxypropan-2-yl)-11,20-dihydroxy-7,7-dimethyl-2,8,17-trioxapentacyclo[12.9.0.03,12.04,9.018,23]tricosa-1(14),3(12),4(9),5,10,18(23),19,21-octaen-13-one	162957955	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)CC(OC5=C4C=CC(=C5)O)C(C)(C)OO)O)C	452.50	unknown	https://doi.org/10.1007/BF00568696
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupatilin	5273755	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC	344.30	unknown	https://doi.org/10.1016/S0031-9422(00)90672-1
> 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)90672-1

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Salvia nemorosa

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