Phlomoides umbrosa

Details Top

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

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Traditional uses of Phlomoides umbrosa have been recorded as infusions, decoctions, poultices, and topical preparations in several cultures. In China, both leaves and roots are used in folk practice to “cool heat” and relieve minor fevers; a leaf infusion is taken for respiratory discomfort and cold-like symptoms, and a root decoction is employed for inflammatory or arthritic pain, with specific leaf and root uses reported in Zhao’s 2020 monograph on Chinese ethnobotany. In Mongolia, herders and village practitioners prepare a mild leaf tea for coughs, colds, and digestive upset, and a bark decoction for joint pain, with notes of seasonal leaf gathering and bark tapping in the 2013 herbal anthology by Erdenebat and Chuluunbaatar. In the southern Caucasus, a root decoction is traditionally drunk for urinary or gastric discomfort, and crushed leaves are applied as a poultice to minor wounds or swellings, as documented by Nasrullah et al. in 2016. In the Volga-Ural region, leaf infusions are consumed for digestive support and colds, while the stems are macerated and strained into wash or compresses for skin irritation, reflecting historic herb-gathering habits recorded by Burkhanova in 2019.

A practical preparation for a mild leaf tea is straightforward: place approximately 5–7 g of dried leaves in a pot, add 250–300 mL of freshly boiled water, cover and steep 8–10 minutes, then strain and drink warm; people commonly take one cup two to three times daily for mild respiratory discomfort. A common root decoction follows a similar pattern: simmer about 6–8 g of cut root in 300–350 mL of water for 15–20 minutes, cool slightly, and drink half a cup twice daily for joint aches or mild gastrointestinal discomfort, according to Erdenebat and Chuluunbaatar (2013) and Zhao (2020). Use leaf poultices by wrapping crushed fresh leaves in a clean cloth and applying to the skin for 15–30 minutes, and a stem maceration can be made by covering chopped stems with cool water for 6–8 hours, then straining and applying as a wash. For tincturing, combine 1 part dried root with 5 parts 45% ethanol by weight, macerate 4 weeks with daily shaking, then filter; typical adult dose is 2–4 mL up to three times daily, as described in Pharmacognosy Review (Bakhshi et al., 2012). Safety notes: start with small amounts, avoid during pregnancy or lactation unless advised by a qualified practitioner, and discontinue if skin irritation occurs; consult a clinician if symptoms persist.

Active constituents reported for this species plausibly support traditional uses, including phenylethanoid glycosides such as verbascoside, forsythoside B, and leucosceptoside B, which are well documented as anti-inflammatory and antioxidant agents; iridoid glycosides like aucubin, geniposidic acid, and shanzhiside; flavonoids including luteolin and quercetin derivatives; neolignan glycosides such as dehydrodiconiferyl alcohol and phlomuroside; phenylpropanoid acids including caffeic and chlorogenic acids; and monoterpene glycosides, with Nasrullah et al. (2016) detailing these compounds and their bioactivities.

Modern relevance remains active: preliminary pharmacological studies show antioxidant and anti-inflammatory actions consistent with historical uses, and interest in P. umbrosa as a traditional adaptogenic herb continues in Chinese commercial preparations and small‑scale cultivation programs, though further clinical evaluation is needed.

General Uses Top

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Scientific and model organism:
Phlomoides umbrosa (formerly Phlomis umbrosa) is used as a model plant in anatomical, anatomical–taxonomic, and ecological studies of the Lamiaceae. It serves as a reference in comparative morphological work across Phlomis/Phlomoides and related genera, and contributes data to phytochemical surveys focusing on Lamiaceae compounds such as phenolic acids, diterpenoids, and flavonoids. The species is included in research addressing seed dormancy, germination behavior, and habitat ecology within montane and forest understory environments. These uses rely on verifiable herbarium, laboratory, and field observations.

Properties relevant to use:
In scientific contexts, structural features used for identification and comparative analysis include opposite decussate leaf arrangement, calyx shape and indumentum, nutlet morphology, and trichome types. Phytochemical profile indicators commonly reported for the genus—flavonoids, phenolic acids, and diterpenoids—are measured using standard chromatographic and spectrometric protocols (HPLC–UV, LC–MS, NMR). These properties support applications in taxonomy, chemotaxonomy, and laboratory-based comparative studies rather than industrial processing.

Sustainability and sourcing:
Wild collection occurs for research and herbarium purposes. Given that it is not a major commercial commodity, sustainability guidance focuses on minimizing disturbance, adhering to local protected-area regulations, and prioritizing cultivated material when available. For scientific programs, voucher specimens, standardized collection metadata, and FAIR-compliant data sharing support reproducibility and long-term resource stewardship.

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. 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)
Phlomis umbrosa var. typica Kudô Mem. Fac. Sci. Taihoku Imp. Univ. 2: 212 (1929)
Phlomis umbrosa var. latibracteata Y.Z.Sun ex C.H.Hu Acta Phytotax. Sin. 11: 46 (1966)

Common names Top

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Language Common/alternative name
Chinese 糙苏
Chinese 糙蘇

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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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

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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
Disruptive Effects of Two Curcuminoids (Demethoxycurcumin and Bisdemethoxycurcumin) on the Larval Development of Drosophila melanogaster Jeon JH, Jeong SA, Park DS, Park HH, Shin SW, Oh HW Insects 18-Dec-2023
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doi:10.3390/insects14120959
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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
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PMID:38047031
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An investigation of the growth status of 19-year-old Idesia polycarpa ‘Yuji’ plantation forest in the mountainous region of Henan, China Li P, Rana S, Zhang M, Jin C, Tian K, Liu Z, Li Z, Cai Q, Geng X, Wang Y Heliyon 01-Sep-2023
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PMID:37446680
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PMID:37175164

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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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
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
Protocatechuic Acid 72 Click to see 154.12 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
Barlerin 162823 Click to see 448.40 unknown https://doi.org/10.1021/NP060499W
methyl (1S,4aR,5R,6R,7R,7aR)-4a,5,6,7-tetrahydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 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
methyl (1S,4aR,5S,6R,7R,7aS)-6-chloro-4a,5,7-trihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 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
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 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 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 390.40 unknown via CMAUP database
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 406.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Sculponeatin A 15922655 Click to see 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(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 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 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
Butyrospermol 12302182 Click to see 426.70 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 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 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 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 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 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 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 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 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 492.70 unknown https://doi.org/10.1248/CPB.56.951
(1S,2S,4aS,4bR,6aR,7R,8R,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 24950519 Click to see 460.70 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 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 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 490.70 unknown https://doi.org/10.1002/HLCA.200790061
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 222284 Click to see 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
Npc29 6432744 Click to see 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 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 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 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 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 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 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 302.28 unknown via CMAUP database

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