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Salvia viridis

Salvia viridis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
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 UUID643fec0212aa2589534008
Scientific name Salvia viridis
Authority L.
First published in Sp. Pl. : 24 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

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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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 schopf-salbei
German buntschopf-salbei
German grüner salbei
German salvia horminum
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

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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
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Turkmenistan
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Europe
    • 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
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
A review of medicinal plant of Middle East and North Africa (MENA) region as source in tuberculosis drug discovery Dehyab AS, Bakar MF, AlOmar MK, Sabran SF Saudi J Biol Sci 10-Jul-2020
PMCID:PMC7451596
doi:10.1016/j.sjbs.2020.07.007
PMID:32884430

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 / 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/10.1016/S0031-9422(03)00225-5
https://doi.org/10.1055/S-2000-8596
> 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/10.1016/S0031-9422(03)00225-5
https://doi.org/10.1055/S-2000-8596
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
1-Oxoferruginol 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/10.1055/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
Salviviridinol 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/10.1016/S0031-9422(03)00225-5
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
Viridone 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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(17alpha,23E)-5alpha-Dammara-20,23-diene-3beta,25-diol 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
Olean-13(18)-ene-2beta,3beta-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
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
(25R)-3beta-[4-O-[4-O-(alpha-L-Rhamnopyranosyl)-alpha-L-rhamnopyranosyl]-beta-D-glucopyranosyloxy]spirosta-5-ene 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)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-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]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 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
Borassoside A 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
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 C 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
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
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
Trigonelloside C 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
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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