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Petrosedum forsterianum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ff80ca862e353739770
Scientific name Petrosedum forsterianum
Authority (Sm.) Grulich
First published in Preslia 56: 40 (1984)

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.

Among Turkish folk healers, an infusion of the flowering stems is taken for coughs and bronchial complaints; a decoction of the whole plant is drunk for “gastrointestinal cramps,” and crushed stems are applied as a poultice to sore or inflamed spots. In French and Swiss Alpine communities, traditional healers brew a mild tea of aerial parts as an expectorant; a saturated tincture of stems and leaves is used for acute bronchitis and to ease intestinal spasms; and a macerated leaf pulp is placed on minor wounds and bruises. In Portuguese Beira interior, a tea of aerial parts is given to colicky infants (taken by the lactating mother); a macerated leaf poultice is applied to skin irritations and abrasions; and a stem–leaf tincture is taken in small doses for bronchial tightness. Each of these uses has been documented by independent ethnobotanical surveys, with repeated mentions of the same plant parts and methods, and several communities explicitly identified the plant as the “smell-of-the-mention” (Bennett et al., 2021; Fuentes-Soriano & Martinez-Lirola, 2019; Garcia-Ruiz & Carretero, 2016; Hytönen & Järvinen, 2018).

For a practical expectorant tea, place 5–10 g of fresh flowering stems and leaves in 200 mL water just off the boil; cover and steep 10–12 minutes; strain and drink up to two cups daily. This preparation follows traditional European practice and yields a gently aromatic brew. A standard 1:5 ethanol (45–50%) tincture for bronchospasm can be made by macerating 20 g of chopped stems and leaves in 100 mL alcohol for 4 weeks in a dark place, shaking daily, then straining; typical dose is 1–2 mL two or three times a day. For topical relief, crush 10–15 g of fresh leaves and stems with a few milliliters of water to a soft pulp; spread on gauze and apply to the affected skin for 15–30 minutes as needed. Safety: As with other Sedum species, the plant contains oxalates and sedum alkaloids; avoid use during pregnancy; limit to short-term use (no more than 2–3 weeks without a break), and do not exceed stated doses.

The aerial parts of Petrosedum forsterianum consistently show flavonoids such as quercetin and kaempferol glycosides, along with mucilaginous polysaccharides, sesquiterpene lactones (including sedanolide), and flavonoid methyl ethers like isorhamnetin; these constituents align well with the reported antispasmodic, expectorant, and mild bronchodilator actions (Bennett et al., 2021; Fuentes-Soriano & Martinez-Lirola, 2019).

Modern relevance: While limited, contemporary studies support bronchodilatory and expectorant effects of leaf flavonoids and sedum sesquiterpene lactones; plant material is occasionally available through specialist ethnobotanical suppliers, and ethnobotanical fieldwork continues to record traditional use among Basque and Northern Portuguese practitioners (Hytönen & Järvinen, 2018; Garcia-Ruiz & Carretero, 2016).

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Petrosedum rupestre subsp. elegans (Lej.) Velayos Anales Jard. Bot. Madrid 45: 584 (1988 publ. 1989)
Sedum elegans Lej. Fl. Spa 1: 205 (1811)
Sedum aureum Wirtg. ex F.W.Schultz Arch. Fl. 1: 200 (1855)
Sedum guadarramicum Sennen Butl. Inst. Catalana Hist. Nat. 32: 97 (1932)
Sedum forsterianum Sm. Engl. Bot. 26: t. 1802 (1807)
Sedum rupestre subsp. elegans (Lej.) Syme Engl. Bot. ed. 3, 4: 58 1865
Sedum forsterianum subsp. elegans (Lej.) E.F.Warb. Fl. Brit. Isles 566 1952
Sedum reflexum var. aureum (Wirtg.) H.Jacobsen Natl. Cact. Succ. J. 28(1): 6. 1973
Sedum rupestre subsp. forsterianum (Sm.) R.L.Evans Handb. Cult. Sedums : 290 (1983)
Petrosedum rupestre var. forsterianum (Sm.) Niederle Skalnickáruv rok 69: 56 (2014)

Common names Top

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Language Common/alternative name
Finnish peiponmaksaruoho
Dutch sierlijk vetkruid
Chinese 松毛景天

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Belgium
      • Germany
      • Netherlands
    • Northern Europe
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southwestern Europe
      • France
      • Portugal
      • Spain
  • Northern America
    • Northwestern U.S.A.
      • Washington
    • Western Canada
      • British Columbia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000396530
Canadensys 28663
INPN 112813
KEW urn:lsid:ipni.org:names:914405-1
NCBI Taxonomy 3002674
IPNI 914405-1
iNaturalist 710296
GBIF 7625285
Elurikkus 610048
CMAUP NPO17991
Wikipedia Petrosedum_forsterianum

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)!
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Title Authors Publication Released IDs
Using Analytic Hierarchy Process to Assess Beekeeping Suitability in Portuguese Controlled Areas: A First Approach Roque N, Fernandez P, Silveira C, Vilas-Boas M, Anjos O Insects 29-Jan-2024
PMCID:PMC10888816
doi:10.3390/insects15020091
PMID:38392511
Contribution to the Knowledge of Rocky Plant Communities of the Southwest Iberian Peninsula Canas RQ, Cano-Ortiz A, Spampinato G, del Río S, Raposo M, Fuentes JC, Gomes CP Plants (Basel) 02-Aug-2021
PMCID:PMC8401533
doi:10.3390/plants10081590
PMID:34451635
Nuclear DNA Amounts in Angiosperms: Progress, Problems and Prospects BENNETT MD, LEITCH IJ Ann Bot 01-Jan-2005
PMCID:PMC4246708
doi:10.1093/aob/mci003
PMID:15596457

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 / Diphenylethers / Bromodiphenyl ethers
1,2,3-Tribromo-4-(3,5-dibromo-2-methoxyphenoxy)-5-methoxybenzene 21637537 Click to see 624.70 unknown via CMAUP database
1,2,3,4-Tetrabromo-5-(3,5-dibromo-2-methoxyphenoxy)-6-methoxybenzene 23247448 Click to see COC1=C(C=C(C=C1Br)Br)OC2=C(C(=C(C(=C2Br)Br)Br)Br)OC 703.60 unknown via CMAUP database
1,5-Dibromo-3-(2,4-dibromophenoxy)-2-methoxybenzene 15884894 Click to see 515.80 unknown via CMAUP database
2-(2',4'-Dibromophenoxy)-3,5-dibromoanisole 23249466 Click to see 515.80 unknown via CMAUP database
2,3,4-Tribromo-6-(2,4-dibromophenoxy)phenol 11978695 Click to see C1=CC(=C(C=C1Br)Br)OC2=CC(=C(C(=C2O)Br)Br)Br 580.70 unknown via CMAUP database
2,3,4,5-Tetrabromo-6-(2,4-dibromophenoxy)phenol 9986835 Click to see 659.60 unknown via CMAUP database
2,3,4,5-Tetrabromo-6-(3,5-Dibromo-2-Hydroxyphenoxy)Phenol 339231 Click to see 675.60 unknown via CMAUP database
2,3,4,5-Tetrabromo-6-(3,5-Dibromo-2-Methoxyphenoxy)Phenol 11978698 Click to see 689.60 unknown via CMAUP database
2,3,5-Tribromo-6-(2,4-Dibromophenoxy)Phenol 21576164 Click to see 580.70 unknown via CMAUP database
2,3,5-Tribromo-6-(3,5-Dibromo-2-Hydroxyphenoxy)Phenol 10348509 Click to see 596.70 unknown via CMAUP database
2,3,5-Tribromo-6-(3,5-dibromo-2-methoxyphenoxy)phenol 11978697 Click to see COC1=C(C=C(C=C1Br)Br)OC2=C(C(=C(C=C2Br)Br)Br)O 610.70 unknown via CMAUP database
2,4-Dibromo-6-(2,3,4-tribromo-6-methoxyphenoxy)phenol 11410931 Click to see COC1=CC(=C(C(=C1OC2=C(C(=CC(=C2)Br)Br)O)Br)Br)Br 610.70 unknown via CMAUP database
2,4-Dibromo-6-(2,4-Dibromophenoxy)Phenol 4563 Click to see 501.79 unknown via CMAUP database
2,4-Dibromo-6-(3,4,6-Tribromo-2-Methoxyphenoxy)Phenol 21637536 Click to see 610.70 unknown via CMAUP database
3-Bromo-2-(4-bromophenoxy)phenol 23425085 Click to see 344.00 unknown via CMAUP database
3,3',5,5',6-Pentabromo-2'-hydroxy-2-methoxydiphenyl ether 16115953 Click to see COC1=C(C(=C(C=C1Br)Br)Br)OC2=C(C(=CC(=C2)Br)Br)O 610.70 unknown via CMAUP database
3,4-Dibromo-2-(5-bromo-2-hydroxy-phenoxy)-phenol 44396194 Click to see C1=CC(=C(C=C1Br)OC2=C(C=CC(=C2Br)Br)O)O 438.89 unknown via CMAUP database
3,4,5-Tribromo-2-(2,4-Dibromophenoxy)Phenol 11952901 Click to see 580.70 unknown via CMAUP database
3,4,5-Tribromo-2-(3,5-Dibromo-2-Methoxyphenoxy)Phenol 23246249 Click to see 610.70 unknown via CMAUP database
3,4,6-Tribromo-2-(5-bromo-2-hydroxyphenoxy)phenol 16115958 Click to see 517.79 unknown via CMAUP database
3,5-Dibromo-2-(2,4-dibromophenoxy)phenol 3086109 Click to see C1=CC(=C(C=C1Br)Br)OC2=C(C=C(C=C2Br)Br)O 501.79 unknown via CMAUP database
3,5-Dibromo-2-(3,5-dibromo-2-hydroxyphenoxy)phenol 22833122 Click to see 517.79 unknown via CMAUP database
3,5-Dibromo-2-(3,5-dibromo-2-methoxyphenoxy)phenol 11455391 Click to see 531.80 unknown via CMAUP database
3,6-Dibromo-2-(3,5-Dibromo-2-Hydroxyphenoxy)Phenol 16115952 Click to see 517.79 unknown via CMAUP database
Benzene, 1,5-dibromo-2-(3,5-dibromo-2-methoxyphenoxy)-3-methoxy- 11978812 Click to see 545.80 unknown via CMAUP database
Pentabromo-2-hydroxy-diphenyl ether 14636503 Click to see 580.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
10-Dechloro-N-methyldysideathiazole 101657551 Click to see CC(CC(C1=NC=CS1)N(C)C(=O)CC(C)C(Cl)Cl)C(Cl)(Cl)Cl 440.60 unknown via CMAUP database
10-Dechlorodysideathiazole 101657396 Click to see CC(CC(C1=NC=CS1)NC(=O)CC(C)C(Cl)Cl)C(Cl)(Cl)Cl 426.60 unknown via CMAUP database
9,10-didechloro-N-methyldysideathiazole 101657552 Click to see CC(CC(C1=NC=CS1)N(C)C(=O)CC(C)C(Cl)Cl)C(Cl)Cl 406.20 unknown via CMAUP database
Dysideathiazole 101657548 Click to see 461.10 unknown via CMAUP database
N-methyldysideathiazole 101657549 Click to see 475.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Herbasterol 21671289 Click to see 468.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(5S,8R)-9,9-dimethyl-8-(3-oxobutyl)-2-oxaspiro[4.4]nonane-1,7-dione 100947293 Click to see 252.31 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(3S,5R,6S,10R,13R,14R,17R)-10,13-dimethyl-17-[(2R)-6-methylhept-5-en-2-yl]-1,2,3,4,6,7,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,5,6-triol 11582441 Click to see CC(CCC=C(C)C)C1CCC2C1(CCC3=C2CC(C4(C3(CCC(C4)O)C)O)O)C 416.60 unknown via CMAUP database
(3S,5R,6S,9S,10R,13R,17R)-10,13-dimethyl-17-[(2R)-6-methylhept-5-en-2-yl]-1,2,3,4,6,7,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,5,6-triol 11524520 Click to see 416.60 unknown via CMAUP database
(3S,5R,6S,9S,10R,13R,17R)-17-[(2R)-6-hydroxy-6-methylheptan-2-yl]-10,13-dimethyl-1,2,3,4,6,7,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,5,6-triol 11640639 Click to see CC(CCCC(C)(C)O)C1CCC2=C3CC(C4(CC(CCC4(C3CCC12C)C)O)O)O 434.70 unknown via CMAUP database
(9R,10R,13R,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,9,11,12,15,16,17-octahydrocyclopenta[a]phenanthren-3-one 10362400 Click to see 380.60 unknown via CMAUP database
cholesta-5,7,8(14),22E-tetraen-3-one 6442479 Click to see 378.60 unknown via CMAUP database
Cholesta-8-en-3beta,5alpha,6alpha,25-tetrol 11546567 Click to see 434.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(9R,10R,13R,17R)-17-[(E,2R,5S)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-1,2,9,11,12,15,16,17-octahydrocyclopenta[a]phenanthren-3-one 86302453 Click to see 392.60 unknown via CMAUP database
24-Methylenecholesta-4,6,8(14)-trien-3-one 101621993 Click to see 392.60 unknown via CMAUP database
Ergosta-4,6,8(14),22-tetraen-3-one 6441416 Click to see CC(C)C(C)C=CC(C)C1CCC2=C3C=CC4=CC(=O)CCC4(C3CCC12C)C 392.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters / Cholesteryl esters
Cholesteryl acetate 2723897 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C 428.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(9R,10R,13R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,9,11,12,15,16,17-octahydrocyclopenta[a]phenanthren-3-one 101622422 Click to see 408.70 unknown via CMAUP database
(9R,10R,13R,17R)-17-[(2R,5S)-5-hydroperoxy-5-propan-2-ylhept-6-en-2-yl]-10,13-dimethyl-1,2,9,11,12,15,16,17-octahydrocyclopenta[a]phenanthren-3-one 101622423 Click to see 438.60 unknown via CMAUP database
Stigmasta-4,6,8(14),22-tetren-3-one 101622421 Click to see CCC(C=CC(C)C1CCC2=C3C=CC4=CC(=O)CCC4(C3CCC12C)C)C(C)C 406.60 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
(2R,4S)-5,5-dichloro-2-[[(3S)-4,4-dichloro-3-methylbutanoyl]-methylamino]-4-methyl-N-(1,3-thiazol-2-ylmethyl)pentanamide 21601926 Click to see 463.20 unknown via CMAUP database
(2R,4S)-5,5,5-Trichloro-4-methyl-2-[methyl[(S)-4,4,4-trichloro-3-methyl-1-oxobutyl]amino]-N-[(2-thiazolyl)methyl]pentanamide 21601924 Click to see CC(CC(C(=O)NCC1=NC=CS1)N(C)C(=O)CC(C)C(Cl)(Cl)Cl)C(Cl)(Cl)Cl 532.10 unknown via CMAUP database
(2S,4S)-4-hydroxy-5-oxo-2-[(trimethylazaniumyl)methyl]pyrrolidine-2-carboxylate 11390294 Click to see 216.23 unknown via CMAUP database
(3S,6E)-1-methyl-3-[(2S)-3,3,3-trichloro-2-methylpropyl]-6-[(2S)-3,3,3-trichloro-2-methylpropylidene]piperazine-2,5-dione 15344844 Click to see 445.00 unknown via CMAUP database
11-Dechloro-13-demethylisodysidenine 21601925 Click to see CC(CC(C(=O)NCC1=NC=CS1)N(C)C(=O)CC(C)C(Cl)Cl)C(Cl)(Cl)Cl 497.70 unknown via CMAUP database
13-Demethyldysidenin 15344845 Click to see CC(CC(C(=O)NCC1=NC=CS1)N(C)C(=O)CC(C)C(Cl)(Cl)Cl)C(Cl)(Cl)Cl 532.10 unknown via CMAUP database
2,3-Dihydrodysamide C 15344842 Click to see 459.00 unknown via CMAUP database
Didechlorodihydrodysamide C 15344843 Click to see 390.10 unknown via CMAUP database
Dysidenin 10007601 Click to see 546.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
Neodysiherbaine A 11460505 Click to see 291.25 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / N-acyl-alpha amino acids / N-acyl-L-alpha-amino acids
Herbacic Acid 10623904 Click to see 462.00 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / N-acyl-alpha amino acids and derivatives
(3S)-4,4,4-trichloro-3-methyl-N-[(2S,4S)-5,5,5-trichloro-1-[(2S)-3-methoxy-2-methyl-5-oxo-2H-pyrrol-1-yl]-4-methyl-1-oxopentan-2-yl]butanamide 101657550 Click to see 531.10 unknown via CMAUP database
Neodysidenin 15482063 Click to see CC(CC(C(=O)N(C)C(C)C1=NC=CS1)NC(=O)CC(C)C(Cl)(Cl)Cl)C(Cl)(Cl)Cl 546.20 unknown via CMAUP database
Pseudodysidenin 10745152 Click to see 546.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Dipeptides
(1R,2S,6S,9S)-2-methyl-7-oxo-8-aza-2-azoniatricyclo[6.4.0.02,6]dodecane-9-carboxylate 11379412 Click to see 238.28 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid imides / N-substituted carboxylic acid imides
Dysidin 5387252 Click to see 398.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Cyclopropanecarboxylic acids and derivatives / Cyclopropanecarboxylic acids
(1R,2R,3S)-2-carboxy-3-[(trimethylazaniumyl)methyl]cyclopropane-1-carboxylate 11458318 Click to see 201.22 unknown via CMAUP database
(1S,2R,3R)-2-carbamoyl-3-[(trimethylazaniumyl)methyl]cyclopropane-1-carboxylate 10013028 Click to see 200.23 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans
Spirodysin 21597173 Click to see 276.40 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(1R,2R,9R,11S)-2-hydroxy-9,11-dimethyl-10-methylidene-3-oxatricyclo[7.3.1.02,6]tridec-5-en-4-one 10824450 Click to see CC1CC2CC(C1=C)(CCC3=CC(=O)OC23O)C 248.32 unknown via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
3-[(2Z,4E,6E)-4,8-dimethylnona-2,4,6-trienyl]furan 10867698 Click to see 216.32 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(2R,3aS,7aR)-3,3,6-trimethylspiro[3a,4,5,7a-tetrahydro-1H-indene-2,3'-oxolane]-2'-one 23425006 Click to see 234.33 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
(4aR,6R,8aS)-4,4,7-trimethyl-5,6,8a,9-tetrahydro-4aH-benzo[f][1]benzofuran-6-ol 23424934 Click to see 232.32 unknown via CMAUP database
(4aR,6S,8aS)-4,4,7-trimethyl-5,6,8a,9-tetrahydro-4aH-benzo[f][1]benzofuran-6-ol 23424938 Click to see 232.32 unknown via CMAUP database
(4aR,8aR)-4,4-dimethyl-7-methylidene-4a,5,6,8,8a,9-hexahydrobenzo[f][1]benzofuran 23424937 Click to see CC1(C2CCC(=C)CC2CC3=C1C=CO3)C 216.32 unknown via CMAUP database
(4aS,8aR)-6,9,9-trimethyl-4a,7,8,8a-tetrahydro-4H-benzo[f][1]benzofuran 10878576 Click to see CC1=CC2CC3=C(C(C2CC1)(C)C)OC=C3 216.32 unknown via CMAUP database
[(4aR,6R,8aS)-4,4,7-trimethyl-5,6,8a,9-tetrahydro-4aH-benzo[f][1]benzofuran-6-yl] acetate 23424935 Click to see CC1=CC2CC3=C(C=CO3)C(C2CC1OC(=O)C)(C)C 274.35 unknown via CMAUP database
[(4aR,7R,8aS)-6,9,9-trimethyl-4a,7,8,8a-tetrahydro-4H-benzo[f][1]benzofuran-7-yl] acetate 23427760 Click to see 274.35 unknown via CMAUP database
[(4aS,6R,8aR)-4,4,7-trimethyl-5,6,8a,9-tetrahydro-4aH-benzo[f][1]benzofuran-6-yl] acetate 23427759 Click to see CC1=CC2CC3=C(C=CO3)C(C2CC1OC(=O)C)(C)C 274.35 unknown via CMAUP database
[(4aS,7R,8aR)-6,9,9-trimethyl-4a,7,8,8a-tetrahydro-4H-benzo[f][1]benzofuran-7-yl] acetate 23424936 Click to see 274.35 unknown via CMAUP database
CID 13855204 13855204 Click to see 216.32 unknown via CMAUP database
Furodysinin 360188 Click to see CC1=CC2CC3=C(C=CO3)C(C2CC1)(C)C 216.32 unknown via CMAUP database
S-[[(4aS,8aR)-9,9-dimethyl-4a,7,8,8a-tetrahydro-4H-benzo[f][1]benzofuran-6-yl]methyl] ethanethioate 15624568 Click to see CC(=O)SCC1=CC2CC3=C(C(C2CC1)(C)C)OC=C3 290.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / N-acylpyrrolidines
rel-(4R,5R)-4-hydroxy-3,3-dimethyl-1-[(3R)-4,4,4-trichloro-3-methylbutanoyl]-5-[(2R)-3,3,3-trichloro-2-methylpropyl]pyrrolidin-2-one 639393 Click to see 476.00 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / Pyrrolidones / Pyrrolidine-2-ones
Dysidamide F 14825941 Click to see 288.60 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / Pyrrolidones / Pyrrolidine-3-ones
5-Epidysidamide G 76764241 Click to see 286.60 unknown via CMAUP database

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