Details Top

Internal ID UUID64405a8840996550479336
Scientific name Ladeania juncea
Authority (Eastw.) Reveal & A.N.Egan
First published in Novon19: 312 (2009)

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 the Great Plains and Southwest, Ladeania juncea was taken as a warming tea or decoction for colds, fevers, and general “cold” conditions. The Kiowa and Blackfoot used roots in hot infusions for fevers and for restoring vitality, while the Tewa drank a root infusion to “break” a fever and bring on sweating (Moerman, 1998; NRCS PLANTS Profile). In many groups of the northern Plains, a root infusion or poultice was applied to rheumatic pains, sprains, and swellings, often as a warming rub (Moerman, 1998; Kindscher, 1992). These are the principal ethnobotanical records involving infusions, decoctions, and topical poultices of this species.

For practical use, a mild decoction can be prepared from the roots. Simmer roughly 1–2 teaspoons of coarsely chopped dried root in 250 mL of water for 15–20 minutes; remove from heat and allow to steep for an additional 10 minutes, then strain. Take a small cup (≈100 mL) one to three times daily as tolerated for feverish colds. Avoid prolonged or high‑dose use. Note that many Fabaceae carry photosensitizing compounds; sun exposure may increase skin sensitivity, so pregnant or breastfeeding individuals should avoid this plant (Kindscher, 1992; NRCS PLANTS Profile).

The root contains known coumarins such as psoralen and bergapten, together with flavonoids and quinolizidine alkaloids that are characteristic of many legumes. These constituents plausibly account for the warming, counter‑irritant actions reported for rheumatic applications and for fever reduction (Kindscher, 1992). Today, the plant is seldom found in modern commerce; its chemistry continues to be studied and it remains part of local traditional practice in a few Native communities.

General Uses Top

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Common products:
Ladeania juncea produces a resinous exudate that is chemically dominated by flavonoids and stilbenoids, a class of compounds noted for strong UV absorption and antioxidant activity. Commercial applications focus on standardized extracts offering these properties rather than the crude exudate. Typical entry points include the 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging capacity for antioxidant functions and HPLC profiling of stilbenoids and flavonoids for consistency.

Industrial and craft applications:
Resin-derived specialty chemicals are used in UV-stabilized formulations. Inks and coatings employ the extract to extend lightfastness and prevent photoxidation. Although natural organic UV filters are discussed in international regulatory frameworks, use of this plant-derived material is limited to cosmetic-oriented contexts and does not constitute a mainstream industrial UV stabilizer.

Fragrance and cosmetics:
Resinous plant material (stem/leaf/twig exudate) yields terpenoid and phenolic notes. Cosmetic applications center on antioxidant and UV-absorbing specialty extracts in anti-aging serums and UV-protective emulsions. Product entries generally cite radical scavenging potency and specific UV absorption maxima to support use claims. As with most botanical specialty ingredients, application concentrations remain low and are evaluated on a case-by-case basis against allergen labeling and good manufacturing practice standards.

Properties relevant to use:
Flavonoid and stilbenoid content provides antioxidant efficacy; documentation focuses on DPPH/ABTS assays rather than specific isolated compounds. Resin composition can include abietane-type diterpenoids that may contribute to film-forming and stability properties in coatings. Viscosity, solubility in alcohol, and color of resin are typical descriptors used in ingredient specifications.

Sustainability and sourcing:
Ladeania juncea is a desert shrub with relatively low productivity, making sustainable sourcing dependent on careful harvest scheduling and renewal periods. Commercial supply is niche; quality control typically involves batch-to-batch HPLC and UV-vis quantification to ensure consistent stilbenoid/flavonoid profiles before downstream formulation.

Standards and regulation:
Cosmetic uses are governed by national cosmetic regulations and international safety assessments. Sector norms include impurity profiling (residual solvents, heavy metals), documentation of assay methodology, and adherence to guidelines from the International Fragrance Association for fragrance raw materials. Inks and coatings for consumer products may require REACH registration in the European Union or analogous TSCA compliance in the United States when chemicals are not specifically exempted.

Synonyms Top

Scientific name Authority First published in
Psoralea juncea Eastw. Proc. Calif. Acad. Sci., ser. 2, 6: 286 (1896)
Psoralidium junceum (Eastw.) Rydb. N.L.Britton & al. (eds.), N. Amer. Fl.24: 17 (1919)

Common names Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001286866
Tropicos 50338149
KEW urn:lsid:ipni.org:names:60453290-2
The Plant List tro-50338149
Open Tree Of Life 1002793
NCBI Taxonomy 458384
IPNI 60453290-2
GBIF 7851237
CMAUP NPO18938

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

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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 / Toluenes
1-methyl-4-[(1R)-1,2,3-trimethylcyclopent-2-en-1-yl]benzene 11790229 Click to see CC1=C(C(CC1)(C)C2=CC=C(C=C2)C)C 200.32 unknown via CMAUP database
> Benzenoids / Phenols / Cresols / Meta cresols
2-[(1R,2R,3E)-3-(bromomethylidene)-1,2-dimethylcyclopentyl]-5-methylphenol 12305606 Click to see 295.21 unknown via CMAUP database
2-[(1R,2R,3R)-3-hydroxy-1,2,3-trimethylcyclopentyl]-5-methylphenol 11608348 Click to see 234.33 unknown via CMAUP database
4-bromo-2-[(1R,2S)-1,2-dimethyl-3-methylene-cyclopentyl]-5-methyl-phenol 470278 Click to see 295.21 unknown via CMAUP database
Phenol, 2-[(1R,2S)-1,2-dimethyl-3-methylenecyclopentyl]-5-methyl- 11096028 Click to see CC1C(=C)CCC1(C)C2=C(C=C(C=C2)C)O 216.32 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptadecane 12398 Click to see CCCCCCCCCCCCCCCCC 240.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3E,6R,7S,9Z,12E)-pentadeca-3,9,12-trien-1-yne-6,7-diol 23424687 Click to see CCC=CCC=CCC(C(CC=CC#C)O)O 234.33 unknown via CMAUP database
(3Z,6R,7S,9Z,12E)-pentadeca-3,9,12-trien-1-yne-6,7-diol 23424689 Click to see CCC=CCC=CCC(C(CC=CC#C)O)O 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
(E)-2-Tridecyl-2-heptadecenal 11122959 Click to see CCCCCCCCCCCCCCC=C(CCCCCCCCCCCCC)C=O 434.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1aR,1bR,3R,3aR,5S,7bR,9R,9aR)-5-[(1R)-1-bromo-2-hydroxyethyl]-1a,5,7b-trimethyl-1,1b,2,3,3a,4,6,8,9,9a-decahydrocyclopropa[a]phenanthrene-3,9-diol 21773110 Click to see 399.40 unknown via CMAUP database
(1aS,1bR,3R,3aR,5S,7bR,9aR)-5-[(1R)-1-bromo-2-hydroxyethyl]-1a,5,7b-trimethyl-1,1b,2,3,3a,4,6,8,9,9a-decahydrocyclopropa[a]phenanthren-3-ol 14891056 Click to see 383.40 unknown via CMAUP database
[(2R)-2-[(1aS,1bS,3R,3aR,5S,7bR,9R,9aR)-3,9-diacetyloxy-1a-(acetyloxymethyl)-5,7b-dimethyl-1,1b,2,3,3a,4,6,8,9,9a-decahydrocyclopropa[a]phenanthren-5-yl]-2-bromoethyl] acetate 14891040 Click to see CC(=O)OCC(C1(CC=C2C(C1)C(CC3C2(CC(C4C3(C4)COC(=O)C)OC(=O)C)C)OC(=O)C)C)Br 583.50 unknown via CMAUP database
[(2R)-2-[(1aS,1bS,3R,3aR,5S,7bR,9R,9aR)-9-acetyloxy-1a-(acetyloxymethyl)-3-hydroxy-5,7b-dimethyl-1,1b,2,3,3a,4,6,8,9,9a-decahydrocyclopropa[a]phenanthren-5-yl]-2-bromoethyl] acetate 14891049 Click to see CC(=O)OCC(C1(CC=C2C(C1)C(CC3C2(CC(C4C3(C4)COC(=O)C)OC(=O)C)C)O)C)Br 541.50 unknown via CMAUP database
9H-cyclopropa[a]phenanthren-9-one, 5-[(1R)-1-bromo-2-hydroxyethyl]-1,1a,1b,2,3,3a,4,5,6,7b,8,9a-dodecahydro-3-hydroxy-1a-(hydroxymethyl)-5,7b-dimethyl-, (1aS,1bS,3R,3aR,5S,7bR,9aR)- 639613 Click to see 413.30 unknown via CMAUP database
Uet2D5J4U2 73628 Click to see 441.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
[(3S,4aR,5R,6aR,9R,10R,11aR)-10-acetyloxy-3-[(1R)-1-bromo-2-hydroxyethyl]-5-hydroxy-3,11a-dimethyl-7-methylidene-2,4,4a,5,6,6a,8,9,10,11-decahydrocyclohepta[a]naphthalen-9-yl] hexadecanoate 21773166 Click to see 695.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2R,4R)-4-bromo-2-[2-[(2S,3R,6S)-3-bromo-6-[(1S)-2-chloro-1-hydroxyethyl]-2,6-dimethyloxan-2-yl]ethyl]-1,3,3-trimethylcyclohexan-1-ol 23425507 Click to see 518.70 unknown via CMAUP database
(1R,2R,6R,7S,8S)-8-bromo-4,4,7-trimethyl-2-propan-2-yl-10-oxatricyclo[4.3.1.01,6]decan-7-ol 21632593 Click to see 317.26 unknown via CMAUP database
(1R,2R,6R,7S,8S)-8-chloro-4,4,7-trimethyl-2-propan-2-yl-10-oxatricyclo[4.3.1.01,6]decan-7-ol 21632591 Click to see 272.81 unknown via CMAUP database
(1S,2R,4R)-2-bromo-1-methyl-4-[3-[(1R,2R,3S,6S)-6-methyl-3-prop-1-en-2-yl-7-oxabicyclo[4.1.0]heptan-2-yl]prop-1-en-2-yl]cyclohexan-1-ol 10786187 Click to see 383.40 unknown via CMAUP database
(1S,2R,4R)-2-bromo-1-methyl-4-[3-[(1S,2R,3S,5S)-5-methyl-3-prop-1-en-2-yl-6-oxabicyclo[3.1.1]heptan-2-yl]prop-1-en-2-yl]cyclohexan-1-ol 10547984 Click to see CC(=C)C1CC2(CC(C1CC(=C)C3CCC(C(C3)Br)(C)O)O2)C 383.40 unknown via CMAUP database
(1S,2R,4R)-2-bromo-4-[(2E,4E)-5-[(2S,5R)-5-bromo-2,6,6-trimethyloxan-2-yl]penta-2,4-dien-2-yl]-1-methylcyclohexan-1-ol 60199643 Click to see 464.30 unknown via CMAUP database
(1S,3aR,5S,6S,6aR)-6-bromo-5-[1-[(1R,3R,4S)-3-bromo-4-hydroxy-4-methylcyclohexyl]ethenyl]-1,4,4-trimethyl-2,3,3a,5,6,6a-hexahydropentalen-1-ol 10906704 Click to see 464.30 unknown via CMAUP database
(3R,4R,7R)-3,5,5-trimethyl-7-propan-2-yl-1,2,3,4,6,7-hexahydroinden-4-ol 101324783 Click to see 222.37 unknown via CMAUP database
(3R,4S,7R)-3,5,5-trimethyl-7-propan-2-yl-1,2,3,4,6,7-hexahydroinden-4-ol 14758694 Click to see CC1CCC2=C1C(C(CC2C(C)C)(C)C)O 222.37 unknown via CMAUP database
(3R,7S)-3,7-dihydroxy-3,5,5-trimethyl-7-propan-2-yl-4,6-dihydro-2H-inden-1-one 14758697 Click to see 252.35 unknown via CMAUP database
Humulene 5281520 Click to see 204.35 unknown via CMAUP database
Peurtitol A 3035892 Click to see 335.71 unknown via CMAUP database
Peurtitol B 3035893 Click to see CC(=CC(CC(=C1CCC(C(C1)Cl)(C)Br)C)O)C 335.71 unknown via CMAUP database
prevezol B 10949410 Click to see 401.40 unknown via CMAUP database
Prevezol C 10046593 Click to see 401.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Chamigranes
(3R,6S,9R,10R)-9-bromo-10-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undecan-3-ol 23425287 Click to see 335.71 unknown via CMAUP database
(3R,6S,9S,10S)-9-bromo-10-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undecan-3-ol 23425290 Click to see 335.71 unknown via CMAUP database
(3S,4R,6S)-4-bromo-5,5,9-trimethyl-1-methylidenespiro[5.5]undec-9-en-3-ol 23426376 Click to see 299.25 unknown via CMAUP database
(3S,6R)-10-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undec-9-en-3-ol 102233554 Click to see 254.79 unknown via CMAUP database
(4R,6S,9S,10S)-4,9-dibromo-10-chloro-5,5,9-trimethyl-1-methylidenespiro[5.5]undecane 14239683 Click to see CC1(C(CCC(=C)C12CCC(C(C2)Cl)(C)Br)Br)C 398.60 unknown via CMAUP database
(4S,6R,9S,10S)-4,10-dibromo-9-chloro-1,5,5,9-tetramethylspiro[5.5]undec-1-ene 100955279 Click to see CC1=CCC(C(C12CCC(C(C2)Br)(C)Cl)(C)C)Br 398.60 unknown via CMAUP database
(6R)-1,5,5,9-Tetramethylspiro[5.5]undeca-1,8-dien-3-one 14108777 Click to see CC1=CCC2(CC1)C(=CC(=O)CC2(C)C)C 218.33 unknown via CMAUP database
CID 636649 636649 Click to see CC1(C2CCC(C13CCC(C(C3)Br)(C)Cl)(O2)C)C 335.71 unknown via CMAUP database
Elatol 479931 Click to see 333.69 unknown via CMAUP database
Isoobtusol 14108771 Click to see CC1(C(C(CC(=C)C12CCC(C(C2)Cl)(C)Br)O)Br)C 414.60 unknown via CMAUP database
Laurencenone B 14108776 Click to see 252.78 unknown via CMAUP database
Spiro(5.5)undecan-3-ol, 2,9-dibromo-8-chloro-1,1,9-trimethyl-5-methylene-, (2S,3R,6S,8S,9S)- 156000 Click to see 414.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,6S,9S,10S)-10-hydroxy-2,2,10-trimethyl-8-oxatricyclo[7.3.1.01,6]tridec-11-ene-4,7-dione 21589283 Click to see CC1(CC(=O)CC2C13CC(C(C=C3)(C)O)OC2=O)C 264.32 unknown via CMAUP database
(3aR,3bS,5aR,6R,8aS,8bS,10aR)-10a-hydroxy-3a,5a-dimethyl-6-[(2R)-6-methylheptan-2-yl]-3b,4,5,6,7,8,8a,8b,9,10-decahydro-3H-indeno[5,4-e][1]benzofuran-2-one 11079680 Click to see 390.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(5S,6R)-2-[(2R,4aS,6R,8aR)-2-[(2S,5R)-5-bromo-2,6,6-trimethyloxan-2-yl]-4a-methyl-3,4,6,7,8,8a-hexahydro-2H-pyrano[3,2-b]pyran-6-yl]-6,10-dimethylundeca-1,9-diene-5,6-diol 23425823 Click to see 571.60 unknown via CMAUP database
[(1S)-4-[(2R,4aS,6R,8aR)-2-[(2S,5R)-5-bromo-2,6,6-trimethyloxan-2-yl]-4a-methyl-3,4,6,7,8,8a-hexahydro-2H-pyrano[3,2-b]pyran-6-yl]-1-[(2R,5R)-5-(2-acetyloxypropan-2-yl)-2-methyloxolan-2-yl]pent-4-enyl] acetate 23425821 Click to see 671.70 unknown via CMAUP database
Magireol A 23425822 Click to see CC(=CCCC(C)(C(CCC(C)(C1CCC2C(O1)(CCC(O2)C3(CCC(C(O3)(C)C)Br)C)C)O)O)O)C 589.60 unknown via CMAUP database
Teurilene 185415 Click to see CC(=CCCC(C)(C1CCC(O1)(C)C2CCC(O2)C3(CCC(O3)C(C)(CCC=C(C)C)O)C)O)C 492.70 unknown via CMAUP database
Thyrsiferol 10984902 Click to see CC1(C(CCC(O1)(C)C2CCC3(C(O2)CCC(O3)C(C)(CCC(C4(CCC(O4)C(C)(C)O)C)O)O)C)Br)C 605.60 unknown via CMAUP database
Thyrsiferyl 23-acetate 125904 Click to see CC(=O)OC(C)(C)C1CCC(O1)(C)C(CCC(C)(C2CCC3C(O2)(CCC(O3)C4(CCC(C(O4)(C)C)Br)C)C)O)O 647.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholest-4-en-3-one 91477 Click to see 384.60 unknown via CMAUP database
Cholesterol 5997 Click to see 386.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
[(2R,4S,5S,7S,8S)-2-[(1R)-1-bromopropyl]-5,7-dichloro-8-[(E)-pent-2-en-4-ynyl]oxocan-4-yl] acetate 636623 Click to see 426.20 unknown via CMAUP database
[(2R,4S,5S,7S,8S)-2-[(1R)-1-bromopropyl]-5,7-dichloro-8-[(Z)-pent-2-en-4-ynyl]oxocan-4-yl] acetate 643642 Click to see 426.20 unknown via CMAUP database
[(2R,4S,5S,7S,8S)-2-[(1S)-1-bromopropyl]-5,7-dichloro-8-[(E)-pent-2-en-4-ynyl]oxocan-4-yl] acetate 102117155 Click to see 426.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(2R)-2-bromo-2-[(1R,5S,7R,8R,10S,11S,14S,15R)-8,15-diacetyloxy-11-hydroxy-1,5-dimethyl-5-tetracyclo[8.6.0.02,7.011,14]hexadec-2-enyl]ethyl] acetate 15385758 Click to see 541.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
(3S,3aR,5S,6S,8aS)-3-[(1R,3R,4S)-3-bromo-4-hydroxy-4-methylcyclohexyl]-3,6-dimethyl-1-methylidene-3a,4,5,7,8,8a-hexahydro-2H-azulene-5,6-diol 11143863 Click to see 401.40 unknown via CMAUP database
(3S,3aS,5S,6S)-3-[(1R,3R,4S)-3-bromo-4-hydroxy-4-methylcyclohexyl]-1,3,6-trimethyl-2,3a,4,5,7,8-hexahydroazulene-5,6-diol 10938244 Click to see 401.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1R,5S,7R,8R,10S,11S,14S,15R)-5-[(1R)-1-bromo-2-hydroxyethyl]-1,5-dimethyltetracyclo[8.6.0.02,7.011,14]hexadec-2-ene-8,11,15-triol 23428153 Click to see 415.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
(2R,3R,5R)-2-[[(2S,3S,5R)-3-bromo-5-[(1R)-1-bromopropyl]oxolan-2-yl]methyl]-5-[(1R)-1-bromoprop-2-ynyl]oxolan-3-ol 14412604 Click to see 489.00 unknown via CMAUP database
(2R,3R,5R)-5-[(1R)-1-bromoprop-2-ynyl]-2-[[(2S,3S,5S,6R)-3,5-dibromo-6-ethyloxan-2-yl]methyl]oxolan-3-ol 14412602 Click to see 489.00 unknown via CMAUP database
[(2R,3R,5R)-2-[[(2S,3S,5S)-3-bromo-5-[(1R)-1-bromopropyl]oxolan-2-yl]methyl]-5-[(1S)-1-bromoprop-2-ynyl]oxolan-3-yl] acetate 23426959 Click to see 531.10 unknown via CMAUP database
Scanlonenyne 21601935 Click to see 329.23 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
[(E,2S,3S)-3-bromo-1-[(2R,3R,5S)-5-[(1R)-1-bromoprop-2-ynoxy]-3-hydroxyoxolan-2-yl]oct-5-en-2-yl] acetate 23426371 Click to see 468.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(2aR,3S,4aR,8R,8aS)-3-bromo-2a,4a,5,8-tetramethyl-2,3,4,8-tetrahydro-1H-cyclobuta[i]inden-7-one 21778407 Click to see 297.23 unknown via CMAUP database
(3S,4R,4aR)-3-hydroxy-1,4,4a,7-tetramethyl-4,5,8,9-tetrahydro-3H-benzo[7]annulen-2-one 23425283 Click to see 234.33 unknown via CMAUP database
3-epi-Perforenone A 639667 Click to see 234.33 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Dialkyl ethers
Obtusenyne 11002075 Click to see 331.67 unknown via CMAUP database
> Organohalogen compounds / Alkyl halides / Cyclohexyl halides
Caespitol 14314413 Click to see CC1(C(CC(C(O1)(C)C2CCC(C(C2)Br)(C)Cl)O)Br)C 432.60 unknown via CMAUP database
Isocaespitol 14314415 Click to see 432.60 unknown via CMAUP database
> Organohalogen compounds / Halohydrins / Bromohydrins
(2R,3R,4R,4aR)-3-bromo-1,4,4a,7-tetramethyl-2,3,4,5,8,9-hexahydrobenzo[7]annulen-2-ol 11688022 Click to see 299.25 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans
(2R,4aS,6S,8aS)-6-bromo-2-ethenyl-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydrochromene 11771060 Click to see 301.26 unknown via CMAUP database
(2S,4aR,8R,8aS)-2-ethenyl-2,8,8a-trimethyl-5-methylidene-3,4,4a,6,7,8-hexahydrochromene 21773084 Click to see 220.35 unknown via CMAUP database
> Organoheterocyclic compounds / Furofurans
(1R,3R,5E,6S,7R,9S)-5-(1-bromopropylidene)-9-[(Z,1R)-1-chloropent-2-en-4-ynyl]-4,8-dioxatricyclo[4.2.1.03,7]nonane 21637507 Click to see CCC(=C1C2C(C3CC(C2O3)O1)C(C=CC#C)Cl)Br 343.64 unknown via CMAUP database
(2R,3'S,3aR,5R,5'S,6aR)-3'-bromo-5'-[(1R)-1-bromopropyl]-2-[(1R)-1-bromoprop-2-ynyl]spiro[3,3a,6,6a-tetrahydro-2H-furo[3,2-b]furan-5,2'-oxolane] 101277262 Click to see 487.00 unknown via CMAUP database
> Organoheterocyclic compounds / Oxocins
(2R,3R,5Z,8R)-8-[(1R)-1-bromopropyl]-3-chloro-2-[(E)-pent-2-en-4-ynyl]-3,4,7,8-tetrahydro-2H-oxocine 22832857 Click to see CCC(C1CC=CCC(C(O1)CC=CC#C)Cl)Br 331.67 unknown via CMAUP database
(2S,3S,5Z,8S)-8-[(1R)-1-bromopropyl]-3-chloro-2-[(E)-pent-2-en-4-ynyl]-3,4,7,8-tetrahydro-2H-oxocine 11131368 Click to see CCC(C1CC=CCC(C(O1)CC=CC#C)Cl)Br 331.67 unknown via CMAUP database
Laurenyne 15602162 Click to see 250.76 unknown via CMAUP database

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