Scientific name	Authority	First published in
Horminum coloratum	Moench	Methodus : 377 (1794)
Horminum sativum	Mill.	Gard. Dict. ed. 8 : n.º 5 (1768)
Horminum viride	Moench	Methodus : 377 (1794)
Ormilis horminum	Raf.	Fl. Tellur. 3: 94 (1837)
Ormilis viridis	Raf.	Fl. Tellur. 3: 94 (1837)
Salvia colorata	Thore	Essai Chloris : 17 (1803)
Salvia comosa	Salisb.	Prodr. Stirp. Chap. Allerton : 73 (1796)
Salvia dolichorrhiza	Caball.	Bol. Soc. Esp. Hist. Nat. 13: 238 (1913)
Salvia horminum	L.	Sp. Pl. : 24 (1753)
Salvia intercedens	Pobed.	Fl. URSS 21: 657 (1954)
Salvia rosani	Ten.	Fl. Napol. 3: 22 (1824)
Salvia spielmannii	Scop.	Delic. Fl. Faun. Insubr. 3: 31 (1788)
Salvia truncata	Willd.	Enum. Pl. : 34 (1809)
Sclarea viridis	(L.) Soják	Cas. Nár. Mus., Odd. Prír. 152: 22 (1983)
Salvia horminum var. viridis	(L.) Briq.	Lab. Alp. Mar. 503 1895
Salvia horminum var. intermedia	Briq.	Lab. Alp. Mar. 503. 1895
Salvia horminum var. hypoleuca	Briq.	Lab. Alp. Mar. 505. 1895
Salvia horminum var. angustifolia	Boiss.	Fl. Orient. 4: 631. 1879
Flipanta ovata	Raf.	Fl. Tellur. 3: 92 (1837)
Salvia viridis var. comata	Heldr.	Fl. Céphalonie : 58 (1882)

Common names Top

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Filter by language:

Language	Common/alternative name
English	annual clary
Arabic	قصعين أخضر
Azerbaijani	yaşıl adaçayı
azb	یاشیل آداچایی
Bulgarian	зелен конски босилек
Czech	šalvěj zahradní
Welsh	clari unflwydd
German	buntschopf-salbei
German	schopf-salbei
German	grüner salbei
Persian	مریمگلی یکساله
Finnish	kirjosalvia
Hebrew	מרווה דגולה
Norwegian Bokmål	spraglesalvie
Norwegian Nynorsk	spreklesalvie
Russian	Шалфей зелёный
Swedish	broksalvia
Chinese	彩苞鼠尾草

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

Suggest a correction or add new data!

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

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

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Middle Asia
  - Turkmenistan
- Western Asia
  - Cyprus
  - East Aegean Islands
  - Lebanon-Syria
  - Palestine
  - Turkey

Europe click to expand
- Eastern Europe
  - Central European Russia
  - Krym
  - South European Russia
- Middle Europe
  - Czechoslovakia
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Portugal
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000302616
USDA Plants	SAVI13
Tropicos	17600315
INPN	120704
Flora of Italy	4680
KEW	urn:lsid:ipni.org:names:457515-1
The Plant List	kew-184146
Open Tree Of Life	499330
Observations.org	150087
NCBI Taxonomy	49221
NBN Atlas	NBNSYS0000034225
IPNI	457515-1
iNaturalist	493015
GBIF	3883959
Freebase	/m/05k60x
EPPO	SALVI
EOL	6342307
USDA GRIN	401827
Wikipedia	Salvia_viridis
CMAUP	NPO15183

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

Visual-, Olfactory-, and Nectar-Taste-Based Flower Aposematism

Lev-Yadun S

Plants (Basel)

29-Jan-2024

PMCID:	PMC10857241
doi:	10.3390/plants13030391
PMID:	38337924

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

Investigation of Volatile Components and Assessment of Antioxidant Potential in Seven Lamiaceae Plant Hydrosols

Xin Z, Wang W, Yang W, Li Y, Niu L, Zhang Y

Molecules

26-Dec-2023

PMCID:	PMC10780048
doi:	10.3390/molecules29010145
PMID:	38202728

Pseudanthia in angiosperms: a review

Baczyński J, Claßen-Bockhoff R

Ann Bot

21-Jul-2023

PMCID:	PMC10583202
doi:	10.1093/aob/mcad103
PMID:	37478306

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

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

Essential Oil Composition Analysis, Antimicrobial Activities, and Biosystematic Studies on Six Species of Salvia

Demirpolat A

Life (Basel)

24-Feb-2023

PMCID:	PMC10054517
doi:	10.3390/life13030634
PMID:	36983789

Leucosceptosides A and B: Two Phenyl-Ethanoid Glycosides with Important Occurrence and Biological Activities

Frezza C, De Vita D, Toniolo C, Sciubba F, Tomassini L, Venditti A, Bianco A, Serafini M, Foddai S

Biomolecules

02-Dec-2022

PMCID:	PMC9775335
doi:	10.3390/biom12121807
PMID:	36551235

The phenomenon of red and yellow autumn leaves: Hypotheses, agreements and disagreements

Lev‐Yadun S

J Evol Biol

16-Aug-2022

PMCID:	PMC9804425
doi:	10.1111/jeb.14069
PMID:	35975328

In Vitro Strategy for the Enhancement of the Production of Bioactive Polyphenols in Transformed Roots of Salvia bulleyana

Krzemińska M, Owczarek A, Olszewska MA, Grzegorczyk-Karolak I

Int J Mol Sci

14-Jul-2022

PMCID:	PMC9322094
doi:	10.3390/ijms23147771
PMID:	35887119

A Comprehensive Review of Rosmarinic Acid: From Phytochemistry to Pharmacology and Its New Insight

Guan H, Luo W, Bao B, Cao Y, Cheng F, Yu S, Fan Q, Zhang L, Wu Q, Shan M

Molecules

20-May-2022

PMCID:	PMC9143754
doi:	10.3390/molecules27103292
PMID:	35630768

Secondary metabolites: a boon from plants, the best chemist in nature: preface from the editors

Ochatt S, Alan AR, Bhattacharya A, Hano C, Kiselev KV, Marconi PL, Otoni WC, Park SY, Tang KX, Weathers PJ

Plant Cell Tissue Organ Cult

28-Mar-2022

PMCID:	PMC8959786
doi:	10.1007/s11240-022-02289-2
PMID:	35369037

An Ethnobotanical Study of Medicinal Plants in Mersin (Turkey)

Emre G, Dogan A, Haznedaroglu MZ, Senkardes I, Ulger M, Satiroglu A, Can Emmez B, Tugay O

Front Pharmacol

07-Jul-2021

PMCID:	PMC8294455
doi:	10.3389/fphar.2021.664500
PMID:	34305586

Potential anti-influenza effective plants used in Turkish folk medicine: A review

Sargin SA

J Ethnopharmacol

31-Aug-2020

PMCID:	PMC7458060
doi:	10.1016/j.jep.2020.113319
PMID:	32882361

HPLC profiling of selected phenolic acids and flavonoids in Salvia eigii, Salvia hierosolymitana and Salvia viridis growing wild in Jordan and their in vitro antioxidant activity

Al-Jaber HI, Shakya AK, Elagbar ZA

PeerJ

26-Aug-2020

PMCID:	PMC7456256
doi:	10.7717/peerj.9769
PMID:	32913677

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
1-Hydroxy-8,13,13-trimethyl-3-propan-2-yltricyclo[7.4.1.05,14]tetradeca-3,5(14),6,8-tetraen-2-one	50907654	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/10.1055/S-2000-8596
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/10.1055/S-2000-8596 https://doi.org/10.1016/S0031-9422(03)00225-5
> Benzenoids / Naphthalenes / Naphthoquinones
Aethiopinone	157301	Click to see CC1=C(C2=C(C=C1)C=C(C(=O)C2=O)C(C)C)CCCC(=C)C	296.40	unknown	https://doi.org/10.1055/S-2000-8596 https://doi.org/10.1016/S0031-9422(03)00225-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aS,10aS)-6-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,9,10,10a-tetrahydro-2H-phenanthren-4-one	15241260	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(C(=O)CCC3(C)C)C)O	300.40	unknown	https://doi.org/10.1016/S0031-9422(03)00225-5 https://doi.org/10.1055/S-2000-8596
(4bR)-4-hydroxy-9-methoxy-4b,8,8-trimethyl-2-propan-2-yl-6,7-dihydro-5H-phenanthren-3-one	102005792	Click to see CC(C)C1=CC2=CC(=C3C(CCCC3(C2=C(C1=O)O)C)(C)C)OC	328.40	unknown	https://doi.org/10.1055/S-2000-8596
(4bS,8aS,9R,10R)-3-methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-4,9,10-triol	102005790	Click to see CC(C)C1=C(C(=C2C(=C1)C(C(C3C2(CCCC3(C)C)C)O)O)O)OC	348.50	unknown	https://doi.org/10.1055/S-2000-8596 https://doi.org/10.1016/S0031-9422(03)00225-5
3-Methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-4,9,10-triol	163033166	Click to see CC(C)C1=C(C(=C2C(=C1)C(C(C3C2(CCCC3(C)C)C)O)O)O)OC	348.50	unknown	https://doi.org/10.1055/S-2000-8596
4-hydroxy-9-methoxy-4b,8,8-trimethyl-2-propan-2-yl-6,7-dihydro-5H-phenanthren-3-one	162882186	Click to see CC(C)C1=CC2=CC(=C3C(CCCC3(C2=C(C1=O)O)C)(C)C)OC	328.40	unknown	https://doi.org/10.1055/S-2000-8596
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/10.1055/S-2000-8596
6-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,9,10,10a-tetrahydro-2H-phenanthren-4-one	85093918	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(C(=O)CCC3(C)C)C)O	300.40	unknown	https://doi.org/10.1055/S-2000-8596
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/10.1055/S-2000-8596
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1055/S-2000-8596
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/10.1055/S-2000-8596
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,3R,4aR,6aR,6bS,8aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,13,14,14a-tetradecahydropicene-2,3-diol	101686479	Click to see CC1(CCC2(CCC3(C(=C2C1)CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C)C)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(00)89266-3
(3S,5R,8R,9R,10R,13R,14R,17R)-17-[(4E)-6-hydroxy-6-methylhepta-1,4-dien-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	9955042	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C(=C)CC=CC(C)(C)O)C)C)C	442.70	unknown	via CMAUP database
3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,10-diol	72745631	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(00)89266-3
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,13,14,14a-tetradecahydropicene-2,3-diol	23132194	Click to see CC1(CCC2(CCC3(C(=C2C1)CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C)C)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(00)89266-3
Diosgenin	99474	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	via CMAUP database
Lup-20(29)-en-3-ol, (3beta)-	521518	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)89266-3
Lup-20(29)-ene-2alpha,3beta-diol	15127233	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(00)89266-3
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)89266-3
Yamogenin	441900	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(4bS,8aS,9R)-4,9-dihydroxy-1-methoxy-4b,8,8-trimethyl-2-propan-2-yl-6,7,8a,9-tetrahydro-5H-phenanthren-3-one	154497675	Click to see CC(C)C1=C(C2=CC(C3C(CCCC3(C2=C(C1=O)O)C)(C)C)O)OC	346.50	unknown	https://doi.org/10.1016/S0031-9422(03)00225-5
4,9-dihydroxy-1-methoxy-4b,8,8-trimethyl-2-propan-2-yl-6,7,8a,9-tetrahydro-5H-phenanthren-3-one	162992044	Click to see CC(C)C1=C(C2=CC(C3C(CCCC3(C2=C(C1=O)O)C)(C)C)O)OC	346.50	unknown	https://doi.org/10.1055/S-2000-8596
Viridinol	102005791	Click to see CC(C)C1=C(C2=CC(C3C(CCCC3(C2=C(C1=O)O)C)(C)C)O)OC	346.50	unknown	https://doi.org/10.1055/S-2000-8596
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-6-[(1S,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S)-3'-hydroxy-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	102155845	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O	901.00	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol	21603983	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'S,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol	16204068	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
Asparasaponin I	441899	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1049.20	unknown	via CMAUP database
Borassoside B	102155844	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O	901.00	unknown	via CMAUP database
Borassoside D	16204180	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
Borassoside E	16204181	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
Borassoside F	16204183	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1	1015.20	unknown	via CMAUP database
Collettinside III	10653210	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
Dioscin	119245	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
Disogluside	11827970	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)C)C)OC1	576.80	unknown	via CMAUP database
Methylprotodioscin	11263254	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC	1063.20	unknown	via CMAUP database
Pennogenin Rahamnosyl Chacotrioside	21603986	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1	1015.20	unknown	via CMAUP database
Progenin II	44429638	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
Prosapogenin A	11061578	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
Protodioscin	441891	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O	1049.20	unknown	via CMAUP database
Pseudoprotodioscin	21637110	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC8C7C(=C(O8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O	1031.20	unknown	via CMAUP database
Yamogenin 3-O-neohesperidoside	441901	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-O-beta-D-mannopyranosyl-alpha-D-mannopyranose	5288769	Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
Gal(a1-6)a-Man	11724912	Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O	342.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
beta-D-Manp-(1->4)-beta-D-Manp-(1->4)-beta-D-Manp	5287808	Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O	504.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	154496936	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1016/S0031-9422(01)00415-0
5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	139031083	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O	578.50	unknown	https://doi.org/10.1016/S0031-9422(01)00415-0

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Salvia viridis

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