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Phlomoides umbrosa

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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 UUID643fe71d0a8d7244755065
Scientific name Phlomoides umbrosa
Authority (Turcz.) Kamelin & Makhm.
First published in Bot. Zhurn. (Moscow & Leningrad) 75: 242 (1990)

Description Top

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Synonyms Top

Scientific name Authority First published in
Phlomis stenocalyx Diels Bot. Jahrb. Syst. 29: 555 (1900)
Phlomis umbrosa Turcz. Bull. Soc. Imp. Naturalistes Moscou 13: 76 (1840)
Phlomis umbrosa var. australis Hemsl. J. Linn. Soc., Bot. 26: 306 (1890)
Phlomis umbrosa var. latibrateata Y.Z.Sun Acta Phytotax. Sin. 11(1): 46. 1966 [17 Jan 1966]
Phlomis umbrosa var. ovalifolia C.Y.Wu Fl. Reipubl. Popularis Sin. 65(2): 601 (1977)
Phlomis umbrosa var. stenocalyx (Diels) C.Y.Wu Fl. Reipubl. Popularis Sin. 65(2): 477 (1977)
Phlomis umbrosa var. subaustralis K.T.Fu & J.Q.Fu Fl. Tsinling. 1(4): 398 (1983)
Phlomis umbrosa var. sylvatica K.T.Fu & J.Q.Fu Fl. Tsinling. 1(4): 398 (1983)
Phlomis umbrosa f. villosa C.Y.Wu Fl. Reipubl. Popularis Sin. 65(2): 600 (1977)
Phlomis umbrosa f. albiflora Y.N.Lee Fl. Korea , ed. 3: 1146 (1998)
Phlomis umbrosa var. emarginata S.H.Fu & J.H.Zheng Fl. Hubeiensis 3: 464 (2002)
Phlomoides umbrosa var. australis (Hemsl.) C.L.Xiang & H.Peng Pl. Diversity Resources 36: 554 (2014)
Phlomoides umbrosa var. latibrateata (Y.Z.Sun) C.L.Xiang & H.Peng Pl. Diversity Resources 36: 554 (2014)
Phlomoides umbrosa var. ovalifolia (C.Y.Wu) C.L.Xiang & H.Peng Pl. Diversity Resources 36: 554 (2014)
Phlomoides umbrosa var. stenocalyx (Diels) C.L.Xiang & H.Peng Pl. Diversity Resources 36: 555 (2014)

Common names Top

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Language Common/alternative name
Chinese 糙苏

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Korea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000269721
Tropicos 100241798
KEW urn:lsid:ipni.org:names:947678-1
The Plant List kew-152628
Open Tree Of Life 7054124
NCBI Taxonomy 1986521
IPNI 947678-1
iNaturalist 966514
GBIF 3884849
CMAUP NPO4838

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
Evaluation of Efficacy and Safety of EstroG-100® in Alleviating Menopausal Symptoms in Postmenopausal Women in India: A Prospective, Single-center, Single-arm, Interventional Study Kirubamani H, Ahire P, Stalin C J Midlife Health 23-Feb-2024
PMCID:PMC10946679
doi:10.4103/jmh.jmh_220_23
PMID:38504729
Medical treatment of osteoarthritis: botanical pharmacologic aspect Park J, Lee SW J Rheum Dis 01-Feb-2024
PMCID:PMC10973355
doi:10.4078/jrd.2023.0084
PMID:38559799
Effect of grazing and climatic factors on biodiversity-ecosystem functioning relationships in grassland ecosystems - a case study of typical steppe in Inner Mongolia, China Zhang Y, Wuriliga, Liu P, Fan R, Guo J, Liu L, Ding Y Front Plant Sci 22-Dec-2023
PMCID:PMC10770857
doi:10.3389/fpls.2023.1297061
PMID:38186605
Rhizocompartmental microbiomes of arrow bamboo (Fargesia nitida) and their relation to soil properties in Subalpine Coniferous Forests Zhang NN, Chen XX, Liang J, Zhao C, Xiang J, Luo L, Wang ET, Shi F PeerJ 29-Nov-2023
PMCID:PMC10693234
doi:10.7717/peerj.16488
PMID:38047031
Plant-derived natural medicines for the management of osteoporosis: A comprehensive review of clinical trials Karimi SM, Bayat M, Rahimi R J Tradit Complement Med 05-Aug-2023
PMCID:PMC10785263
doi:10.1016/j.jtcme.2023.08.001
PMID:38223808
Density-Dependent Seed Predation of Quercus wutaishanica by Rodents in Response to Different Seed States Luo Y, Cheng J, Yan X, Yang H, Shen Y, Ge J, Zhang M, Zhang J, Xu Z Animals (Basel) 24-May-2023
PMCID:PMC10251812
doi:10.3390/ani13111732
PMID:37889661
New insights of the application of water or ethanol-water plant extract rich in active compounds in food Plaskova A, Mlcek J Front Nutr 28-Mar-2023
PMCID:PMC10086256
doi:10.3389/fnut.2023.1118761
PMID:37057062
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
Endophytic Fungi: An Effective Alternative Source of Plant-Derived Bioactive Compounds for Pharmacological Studies Wen J, Okyere SK, Wang S, Wang J, Xie L, Ran Y, Hu Y J Fungi (Basel) 20-Feb-2022
PMCID:PMC8877053
doi:10.3390/jof8020205
PMID:35205959
Potential Roles of Iridoid Glycosides and Their Underlying Mechanisms against Diverse Cancer Growth and Metastasis: Do They Have an Inhibitory Effect on Cancer Progression? Kim CW, Choi KC Nutrients 26-Aug-2021
PMCID:PMC8466600
doi:10.3390/nu13092974
PMID:34578851
Subcritical Water Extraction of Natural Products Cheng Y, Xue F, Yu S, Du S, Yang Y Molecules 30-Jun-2021
PMCID:PMC8271798
doi:10.3390/molecules26134004
PMID:34209151
An In Vitro Evaluation of the Molecular Mechanisms of Action of Medical Plants from the Lamiaceae Family as Effective Sources of Active Compounds against Human Cancer Cell Lines Sitarek P, Merecz-Sadowska A, Śliwiński T, Zajdel R, Kowalczyk T Cancers (Basel) 13-Oct-2020
PMCID:PMC7601952
doi:10.3390/cancers12102957
PMID:33066157
Lamiaceae: An Insight on Their Anti-Allergic Potential and Its Mechanisms of Action Sim LY, Abd Rani NZ, Husain K Front Pharmacol 19-Jun-2019
PMCID:PMC6594199
doi:10.3389/fphar.2019.00677
PMID:31275149
Osteogenic effects of Phlomis umbrosa via up-regulation of Runx2 in osteoporosis Lee JE, Lee H, Kim MH, Yang WM Biomed Rep 20-Nov-2018
PMCID:PMC6299205
doi:10.3892/br.2018.1172
PMID:30588298
A preliminary review of studies on adaptogens: comparison of their bioactivity in TCM with that of ginseng-like herbs used worldwide Liao LY, He YF, Li L, Meng H, Dong YM, Yi F, Xiao PG Chin Med 16-Nov-2018
PMCID:PMC6240259
doi:10.1186/s13020-018-0214-9
PMID:30479654

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoate 54675866 Click to see C1=CC(=C(C=C1C(=O)O)O)[O-] 153.11 unknown via CMAUP database
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols
[1-hydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl] (Z)-icos-9-enoate 5317678 Click to see CCCCCCCCCCC=CCCCCCCCC(=O)OC(CO)COC1C(C(C(C(O1)CO)O)O)O 546.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
7-Epiphlomiol 24721557 Click to see CC1(C(C(C2(C1(C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O)O)O)O 454.40 unknown via CMAUP database
8-O-Acetyl shanzhiside methyl ester 162823 Click to see CC(=O)OC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)C 448.40 unknown https://doi.org/10.1021/NP060499W
methyl (1S,4aS,5R,7S,7aS)-5,7-dihydroxy-7-methyl-1-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 49775358 Click to see CC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown via CMAUP database
methyl (1S,5R,7S)-5,7-dihydroxy-7-methyl-1-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 17751041 Click to see CC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown via CMAUP database
methyl (4aS,7aS)-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,4a,5,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 6325240 Click to see COC(=O)C1COC(C2C1CC=C2CO)OC3C(C(C(C(O3)CO)O)O)O 390.40 unknown via CMAUP database
Phloyoside I 70688398 Click to see CC1(C2C(OC=C(C2(C(C1O)O)O)C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 438.40 unknown https://doi.org/10.1021/NP060499W
Phloyoside II 101667556 Click to see CC1(C2C(OC=C(C2(C(C1Cl)O)O)C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 456.80 unknown https://doi.org/10.1021/NP060499W
Shanzhiside methyl ester 13892722 Click to see CC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1021/NP060499W
Shanzhiside-methylester 3085296 Click to see CC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Sculponeatin A 15922655 Click to see CC12CCC3C4(C1C(OC2)OC4)C5C(CC6CC5(C(=O)C6=C)C(=O)O3)O 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(-)-Butyrospermol 12302182 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown via CMAUP database
(3S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 102004740 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown via CMAUP database
(3S,5R,10R,13S,14S)-17-[(1R)-1,5-dimethylhex-4-enyl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 472759 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown via CMAUP database
(4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 45483610 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 via CMAUP database
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
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 via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 12-hydroxysteroids
1,1-bis(hydroxymethyl)-1',1',4a,10a,10b-pentamethylspiro[3,4,4b,5,7,9,10,11,12,12a-decahydro-2H-chrysene-8,3'-cyclopentane]-2,3-diol 74371139 Click to see CC1(CCC2(C1)CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)C2)C)C 460.70 unknown https://doi.org/10.1248/CPB.56.951
1,1-bis(hydroxymethyl)-6-methoxy-1',1',4a,10a,10b-pentamethylspiro[3,4,4b,5,6,9,10,11,12,12a-decahydro-2H-chrysene-8,3'-cyclopentane]-2,3-diol 162968916 Click to see CC1(CCC2(C1)CCC3(C(=C2)C(CC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)OC)C)C 490.70 unknown https://doi.org/10.1002/HLCA.200790061
1,1,1'-tris(hydroxymethyl)-6-methoxy-1',4a,10a,10b-tetramethylspiro[3,4,4b,5,6,9,10,11,12,12a-decahydro-2H-chrysene-8,3'-cyclopentane]-2,3-diol 162900130 Click to see CC1(CCC2(C1)CCC3(C(=C2)C(CC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)OC)C)CO 506.70 unknown https://doi.org/10.1002/HLCA.200790061
1,8,9-trihydroxy-7,7-bis(hydroxymethyl)-2',2',4a,4b,10a-pentamethylspiro[3,4,5,6,6a,8,9,10,10b,11-decahydro-1H-chrysene-2,4'-cyclopentane]-1'-one 74371224 Click to see CC1(CC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)C2O)C)CC1=O)C 490.70 unknown https://doi.org/10.1248/CPB.56.951
1',7,7-tris(hydroxymethyl)-1',4a,4b,10a-tetramethylspiro[3,4,5,6,6a,8,9,10,10b,11-decahydro-1H-chrysene-2,3'-cyclopentane]-1,8,9-triol 78101530 Click to see CC1(CCC2(C1)CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)C2O)C)CO 492.70 unknown https://doi.org/10.1002/HLCA.200790061
11,11-Bis(hydroxymethyl)-7,15,16,21-tetramethyl-19-oxahexacyclo[19.2.1.01,18.03,16.06,15.07,12]tetracos-3-ene-9,10,20-triol 74371308 Click to see CC12CCC3(C1)CC4=CCC5C(C4(CC3OC2O)C)(CCC6C5(CC(C(C6(CO)CO)O)O)C)C 490.70 unknown https://doi.org/10.1007/S10600-010-9676-4
https://doi.org/10.1248/CPB.56.951
7-(hydroxymethyl)-1',1',4a,4b,7,10a-hexamethylspiro[3,4,5,6,6a,8,9,10,10b,11-decahydro-1H-chrysene-2,3'-cyclopentane]-1,8,9-triol 74371138 Click to see CC1(CCC2(C1)CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2O)C)C 460.70 unknown https://doi.org/10.1248/CPB.56.951
7,7-bis(hydroxymethyl)-1',1',4a,4b,10a-pentamethylspiro[3,4,5,6,6a,8,9,10,10b,11-decahydro-1H-chrysene-2,3'-cyclopentane]-1,8,9-triol 74371225 Click to see CC1(CCC2(C1)CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)C2O)C)C 476.70 unknown https://doi.org/10.1002/HLCA.200790061
https://doi.org/10.1248/CPB.56.951
7,7-bis(hydroxymethyl)-2',2',4a,4b,10a-pentamethylspiro[3,4,5,6,6a,8,9,10,10b,11-decahydro-1H-chrysene-2,4'-cyclopentane]-1,1',8,9-tetrol 74371226 Click to see CC1(CC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)C2O)C)CC1O)C 492.70 unknown https://doi.org/10.1248/CPB.56.951
7,7-bis(hydroxymethyl)-4a,4b,5',5',10a-pentamethylspiro[3,4,5,6,6a,8,9,10,10b,11-decahydro-1H-chrysene-2,2'-cyclopentane]-1,1',8,9-tetrol 74371223 Click to see CC1(CCC2(C1O)CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)C2O)C)C 492.70 unknown https://doi.org/10.1248/CPB.56.951
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 12-hydroxysteroids / 12-beta-hydroxysteroids
(1'R,2S,3R,4aR,4bR,6S,8R,10aS,10bR,12aR)-1,1,1'-tris(hydroxymethyl)-6-methoxy-1',4a,10a,10b-tetramethylspiro[3,4,4b,5,6,9,10,11,12,12a-decahydro-2H-chrysene-8,3'-cyclopentane]-2,3-diol 163194565 Click to see CC1(CCC2(C1)CCC3(C(=C2)C(CC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)OC)C)CO 506.70 unknown https://doi.org/10.1002/HLCA.200790061
(1R,1'R,2R,4aS,4bR,6aR,8S,9R,10aR,10bR)-7,7-bis(hydroxymethyl)-4a,4b,5',5',10a-pentamethylspiro[3,4,5,6,6a,8,9,10,10b,11-decahydro-1H-chrysene-2,2'-cyclopentane]-1,1',8,9-tetrol 24950517 Click to see CC1(CCC2(C1O)CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)C2O)C)C 492.70 unknown https://doi.org/10.1248/CPB.56.951
(1R,6R,7R,9R,10R,12R,15R,16R,18S,20R,21R)-11,11-bis(hydroxymethyl)-7,15,16,21-tetramethyl-19-oxahexacyclo[19.2.1.01,18.03,16.06,15.07,12]tetracos-3-ene-9,10,20-triol 162919486 Click to see CC12CCC3(C1)CC4=CCC5C(C4(CC3OC2O)C)(CCC6C5(CC(C(C6(CO)CO)O)O)C)C 490.70 unknown https://doi.org/10.1007/S10600-010-9676-4
(1R,6R,7R,9R,10S,12R,15R,16R,18S,20S,21R)-11,11-bis(hydroxymethyl)-7,15,16,21-tetramethyl-19-oxahexacyclo[19.2.1.01,18.03,16.06,15.07,12]tetracos-3-ene-9,10,20-triol 24950678 Click to see CC12CCC3(C1)CC4=CCC5C(C4(CC3OC2O)C)(CCC6C5(CC(C(C6(CO)CO)O)O)C)C 490.70 unknown https://doi.org/10.1248/CPB.56.951
(1S,1'S,2R,4aS,4bR,6aR,8S,9R,10aR,10bR)-1',7,7-tris(hydroxymethyl)-1',4a,4b,10a-tetramethylspiro[3,4,5,6,6a,8,9,10,10b,11-decahydro-1H-chrysene-2,3'-cyclopentane]-1,8,9-triol 163045426 Click to see CC1(CCC2(C1)CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)C2O)C)CO 492.70 unknown https://doi.org/10.1002/HLCA.200790061
(1S,1'S,2S,4aS,4bR,6aR,8S,9R,10aR,10bR)-7,7-bis(hydroxymethyl)-2',2',4a,4b,10a-pentamethylspiro[3,4,5,6,6a,8,9,10,10b,11-decahydro-1H-chrysene-2,4'-cyclopentane]-1,1',8,9-tetrol 24950521 Click to see CC1(CC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)C2O)C)CC1O)C 492.70 unknown https://doi.org/10.1248/CPB.56.951
(1S,2S,4aS,4bR,6aR,7R,8S,9R,10aR,10bR)-7-(hydroxymethyl)-1',1',4a,4b,7,10a-hexamethylspiro[3,4,5,6,6a,8,9,10,10b,11-decahydro-1H-chrysene-2,3'-cyclopentane]-1,8,9-triol 24950359 Click to see CC1(CCC2(C1)CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2O)C)C 460.70 unknown https://doi.org/10.1248/CPB.56.951
(1S,2S,4aS,4bR,6aR,8R,9R,10aR,10bR)-7,7-bis(hydroxymethyl)-1',1',4a,4b,10a-pentamethylspiro[3,4,5,6,6a,8,9,10,10b,11-decahydro-1H-chrysene-2,3'-cyclopentane]-1,8,9-triol 24950520 Click to see CC1(CCC2(C1)CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)C2O)C)C 476.70 unknown https://doi.org/10.1248/CPB.56.951
(1S,2S,4aS,4bR,6aR,8S,9R,10aR,10bR)-7,7-bis(hydroxymethyl)-1',1',4a,4b,10a-pentamethylspiro[3,4,5,6,6a,8,9,10,10b,11-decahydro-1H-chrysene-2,3'-cyclopentane]-1,8,9-triol 102078895 Click to see CC1(CCC2(C1)CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)C2O)C)C 476.70 unknown https://doi.org/10.1002/HLCA.200790061
(2R,3R,4aR,4bR,8S,10aR,10bR,12aR)-1,1-bis(hydroxymethyl)-1',1',4a,10a,10b-pentamethylspiro[3,4,4b,5,7,9,10,11,12,12a-decahydro-2H-chrysene-8,3'-cyclopentane]-2,3-diol 24950360 Click to see CC1(CCC2(C1)CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)C2)C)C 460.70 unknown https://doi.org/10.1248/CPB.56.951
(2S,3R,4aR,4bR,6S,8S,10aS,10bR,12aR)-1,1-bis(hydroxymethyl)-6-methoxy-1',1',4a,10a,10b-pentamethylspiro[3,4,4b,5,6,9,10,11,12,12a-decahydro-2H-chrysene-8,3'-cyclopentane]-2,3-diol 102078896 Click to see CC1(CCC2(C1)CCC3(C(=C2)C(CC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)OC)C)C 490.70 unknown https://doi.org/10.1002/HLCA.200790061
19,28-Cyclo-18,19-seco-22-noroleana-12-ene-2alpha,3beta,18beta,23-tetraol 24950519 Click to see CC1(CCC2(C1)CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2O)C)C 460.70 unknown https://doi.org/10.1248/CPB.56.951
Phlomisone 24950518 Click to see CC1(CC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)CO)O)O)C)C)C2O)C)CC1=O)C 490.70 unknown https://doi.org/10.1248/CPB.56.951
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 6432744 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
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 via CMAUP database
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
Sesamoside 3082856 Click to see CC12C3C(OC=C(C3(C(C1O2)O)O)C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O 420.40 unknown https://doi.org/10.1021/NP060499W
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4R,5R,6R)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 23955868 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 770.70 unknown via CMAUP database
[(2R,3R,4R,5R,6R)-2-[[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 45027864 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 770.70 unknown via CMAUP database
Alyssonoside 6444250 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 770.70 unknown via CMAUP database
Forsythoside B 23928102 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1021/NP060499W
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
4-(Hydroxymethyl)furan-2-carbaldehyde 5318289 Click to see C1=C(OC=C1CO)C=O 126.11 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrazines
2,5-Dimethylpyrazine 31252 Click to see CC1=CN=C(C=N1)C 108.14 unknown via CMAUP database
5-Ethyl-2,3-dimethylpyrazine 27460 Click to see CCC1=CN=C(C(=N1)C)C 136.19 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
(3,9,10-Trihydroxy-12-methyl-6-methylidene-7-oxo-16,17-dioxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl)methyl acetate 162909324 Click to see CC(=O)OCC1(CCCC23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OO3)O)O)C 408.40 unknown https://doi.org/10.1007/S10600-010-9573-X
[(1R,2S,3R,5S,8S,9S,10S,11S,12R)-3,9,10-trihydroxy-12-methyl-6-methylidene-7-oxo-16,17-dioxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl]methyl acetate 162909325 Click to see CC(=O)OCC1(CCCC23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OO3)O)O)C 408.40 unknown https://doi.org/10.1007/S10600-010-9573-X
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-5-heptyloxolan-2-one 441644 Click to see CCCCCCCC1CCC(=O)O1 184.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Isoacteoside 6476333 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Scutamoenin 5321200 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=C(C=CC=C3O)O)O 302.28 unknown via CMAUP database

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