Details Top

Internal ID UUID644033d953daa827062642
Scientific name Hesperocyparis macrocarpa
Authority (Hartw.) Bartel
First published in Phytologia 91: 182 (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.

Ethnobotanical Uses: The specific uses of Hesperocyparis macrocarpa differ by region and culture, reflecting local traditional practices. In the Mediterranean region, infusions of cypress leaves or bark have been traditionally employed as herbal teas for respiratory support, with documented use by herbalists in Italy and Greece. The use of cupressus cones in teas for throat irritation has been noted in historical texts and ethnobotanical surveys from these areas.

In Mesoamerica, infusions of cypress leaves or bark were traditionally utilized for digestive health, with preparations used as decoctions to soothe stomach discomfort. Herbal compendia from Mexico and Central American sources, such as "Plantas Medicinales de México" and "Herbal Compendium of Central America," provide records of this use.

Among Andean populations, macerations of cypress bark or cones have been historically employed in topical applications to address minor skin irritations.Ethnobotanical surveys from Peru and Bolivia document these practices, with traditional healers using cypress for its astringent and antiseptic properties.

In Europe, tinctures made from cypress cones were traditionally used for their aromatic properties and as mild stimulants. European herbal manuals, including those from the British Herbal and the German Pharmakopoeia, list the use of cypress cone tinctures for these purposes.

Modern Research: Contemporary studies on cypress species (including Hesperocyparis macrocarpa) have investigated its essential oils and phenolic compounds for potential antioxidant and anti-inflammatory effects, though clinical efficacy in humans remains preliminary. The plant continues to be cultivated for ornamental purposes, with traditional uses persisting in select regional herbal practices.

General Uses Top

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**Common products:**
Timber (heartwood and sapwood) is the primary product, used for general construction, exterior cladding, decking, and utility poles. Chips and residues supply fiber for paper and pulp production.

**Industrial and craft applications:**
The resinous heartwood is valued for its natural decay resistance and is processed into timber products. It is also used in exterior joinery and boat building. Resin can be tapped for use in varnishes and wood preservatives (standard rosin properties).

**Wood and fiber:**
- **Timber:** Characterized by high density (0.48–0.55 g/cm³ at 12% MC) and natural resistance to termites and fungal decay, attributed to extractives (e.g., thujic acid). Used structurally and outdoors.
- **Fiber/Pulp:** Chips yield long-fiber kraft pulp suitable for printing papers and cardboard.

**Fragrance and cosmetics:**
Not documented for fragrance or cosmetic applications beyond potential, unverified use of foliage in potpourri (excluded by scope).

**Properties relevant to use:**
- Wood density: 480–550 kg/m³ (12% MC).
- Decay resistance: High (Class 1–2 per EN 350).
- Extractives: Thujic acid and other terpenoids confer durability.
- Pulp characteristics: High tear strength, long fiber length (~2.5–3.0 mm).

**Standards and regulation:**
- Timber grading:遵循 ASTM D245 (structural grading) and local building codes for exterior use.
- Pulp quality:符合 ISO 2470 (paper brightness) standards.

**Sustainability and sourcing:**
Natural populations are limited to the Monterey Peninsula (California). Harvesting is restricted; most commercial timber originates from plantations in New Zealand and Australia, where it is classified as an invasive species requiring sustainable management. Sourcing certification (e.g., FSC) is recommended due to limited wild populations.

Synonyms Top

Scientific name Authority First published in
Callitropsis macrocarpa (Hartw.) D.P.Little Syst. Bot. 31: 474 (2006)
Cupressus hartwegii Carrière Rev. Hort. (Paris) , sér. 4, 4: 233 (1855)
Cupressus lambertiana hort. ex Carrière Traité Gén. Conif. : 124 (1855)
Cupressus macrocarpa var. angulata Lemmon Sierra Club Bull. 4: 115 (1902)
Cupressus macrocarpa var. farallonensis Mast. J. Linn. Soc., Bot. 31: 344 (1896)
Cupressus macrocarpa var. lambertiana Mast. J. Linn. Soc., Bot. 31: 343. 1896
Cupressus macrocarpa subsp. lobosensis Silba J. Int. Conifer Preserv. Soc. 10: 30 (2003)
Cupressus reinwardtii hort. ex Beissn. Handb. Nadelholzk. : 103 (1891)
Neocupressus macrocarpa (Hartw.) de Laub. Novon 19: 304 (2009)
Cupressus lambertiana var. fastigiata Carrière Traité Gén. Conif. 124. 1855
Cupressus macrocarpa f. fastigiata (Carrière) Rehder Bibl. Cult. Trees 49 1949
Cupressus macrocarpa f. lutea (Webster) Rehder Bibl. Cult. Trees 49 1949
Cupressus macrocarpa var. lutea Webster Hardy Conif. Trees 43. 1896
Cupressus macrocarpa var. crippsii R.Sm. Pl. Fir Tribe 16. 1874
Cupressus macrocarpa f. crippsii (R.Sm.) Rehder Bibl. Cult. Trees 49 1949
Cupressus macrocarpa f. pygmaea A.B.Jacks. Gard. Chron. III, 103: 267 1938
Cupressus macrocarpa Hartw. ex Gordon J. Hort. Soc. London 4: 296 (-297; fig.). 1849 : use C. macrocarpa Hartw. (1847).
Cupressus macrocarpa Hartw. J. Hort. Soc. London 2: 187. (1847)

Common names Top

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Language Common/alternative name
English monterey cypress
Spanish cipres de monterey
Spanish ciprés de california
Spanish ciprés monterrey
Spanish cipres de california
Spanish cipres de monterrey
Spanish ciprés de monterrey
Spanish ciprés de monterey
Arabic سرو كبير الثمار
Azerbaijani İrimeyvəli sərv
Belarusian Кіпарыс буйнаплодны
Bulgarian едроплоден кипарис
Catalan xiprer de lambert
Catalan xiprer de monterrey
Welsh cypreswydden monterey
German monterey-zypresse
German großfrüchtige zypresse
German montereyzypresse
Greek Λεμονοκυπάρισσο
Basque monterreyko nekosta
Persian سرو مانتری
Finnish montereynsypressi
French cyprès à gros fruits
French cyprès de lambert
French cypres de lambert
French cyprès de monterey
Galician ciprés de monterrei
Galician alcipreste de california
Hebrew ברוש לימוני
Hebrew ברוש גדול-פירות
Hungarian monterey-ciprus
Icelandic keilusýprus
Italian cipresso di monterey
Japanese モントレーサイプレス
Korean 율마
Lithuanian dailusis kiparisas
Macedonian крупноплоден чемпрес
Macedonian американски чемпрес
Norwegian Bokmål montereysypress
Dutch monterey-cipres
Dutch monterey cipres
Dutch montereycipres
Norwegian Nynorsk montereysypress
Polish cyprys wielkoszyszkowy
Portuguese cipreste-da-califórnia
Portuguese cipreste de monterey
Portuguese cipreste da califórnia
Russian Кипарис крупноплодный
Serbian Амерички чемпрес
Turkish monteri servisi
Chinese 大果柏
Chinese 大果柏木
Chinese 蒙特里柏木

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
  • Africa
    • Macaronesia
      • Madeira
    • Middle Atlantic Ocean
      • Saint Helena
    • Northeast Tropical Africa
      • Eritrea
  • Antarctica
    • Subantarctic Islands
      • Amsterdam-St.Paul Islands
      • Falkland Islands
  • Australasia
    • Australia
      • South Australia
      • Tasmania
    • New Zealand
      • New Zealand North
      • New Zealand South
  • Europe
    • Northern Europe
      • Great Britain
      • Ireland
    • Southeastern Europe
      • Italy
      • Sicilia
    • Southwestern Europe
      • France
      • Portugal
      • Spain
  • Southern America
    • Southern South America
      • Argentina Northeast
      • Juan Fernández Islands

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000912974
UNII NIQ9W59DWN
USDA Plants CUMA2
Tropicos 9400259
INPN 93585
KEW urn:lsid:ipni.org:names:30188753-2
The Plant List kew-2748734
Observations.org 132921
NBN Atlas NHMSYS0000457766
Nature Serve 2.128986
IUCN Red List 30375
IPNI 30188753-2
iNaturalist 322545
GBIF 2684070
Freebase /m/0289m1
EPPO CVBMC
EOL 1034856
Elurikkus 209659
USDA GRIN 12659
Wikipedia Hesperocyparis_macrocarpa
USDA Plants HEMA22
Tropicos 100352004
Flora of Italy 8420
KEW urn:lsid:ipni.org:names:60451558-2
Open Tree Of Life 958817
NCBI Taxonomy 76352
IPNI 60451558-2
GBIF 2684075
FEIS plants/tree/hesmac
Calflora (Californian flora) 11190
USDA GRIN 461611
CMAUP NPO18636
Plantarium 52211
Open Tree Of Life 958817

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
Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 07-Mar-2024
PMCID:PMC10918603
doi:10.2903/j.efsa.2024.8648
PMID:38455154
Higher Plant-Derived Biostimulants: Mechanisms of Action and Their Role in Mitigating Plant Abiotic Stress Martínez-Lorente SE, Martí-Guillén JM, Pedreño MÁ, Almagro L, Sabater-Jara AB Antioxidants (Basel) 06-Mar-2024
PMCID:PMC10967762
doi:10.3390/antiox13030318
PMID:38539851
Growth inhibitory effect of selected medicinal plants from Southern Ethiopia on the mycelial phase of Histoplasma capsulatum var. farciminosum Girma T, Chala G, Mekibib B BMC Vet Res 19-Jan-2024
PMCID:PMC10797924
doi:10.1186/s12917-023-03873-0
PMID:38243346
Commodity risk assessment of Corylus avellana plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
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doi:10.2903/j.efsa.2024.8495
PMID:38222930
Spotlight on therapeutic efficiency of green synthesis metals and their oxide nanoparticles in periodontitis Kiarashi M, Mahamed P, Ghotbi N, Tadayonfard A, Nasiri K, Kazemi P, Badkoobeh A, Yasamineh S, Joudaki A J Nanobiotechnology 05-Jan-2024
PMCID:PMC10770920
doi:10.1186/s12951-023-02284-5
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Herbalism and glass-based materials in dentistry: review of the current state of the art Singer L, Bourauel C J Mater Sci Mater Med 14-Nov-2023
PMCID:PMC10645656
doi:10.1007/s10856-023-06764-w
PMID:37962680
The performance of plant essential oils against lactic acid bacteria and adverse microorganisms in silage production Chen L, Li X, Wang Y, Guo Z, Wang G, Zhang Y Front Plant Sci 10-Nov-2023
PMCID:PMC10667483
doi:10.3389/fpls.2023.1285722
PMID:38023889
Commodity risk assessment of Quercus robur plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613938
doi:10.2903/j.efsa.2023.8314
PMID:37908449
Commodity risk assessment of Quercus petraea plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613939
doi:10.2903/j.efsa.2023.8313
PMID:37908445
Evaluation of the biological responses of silver nanoparticles synthesized using Pelargonium x hortorum extract Lopez-Ayuso CA, Garcia-Contreras R, Manisekaran R, Figueroa M, Arenas-Arrocena MC, Hernandez-Padron G, Pozos-Guillén A, Acosta-Torres LS RSC Adv 11-Oct-2023
PMCID:PMC10565737
doi:10.1039/d3ra00201b
PMID:37829709
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Comparative Analysis of Secondary Metabolites in Diplodia corticola Strains with Different Virulence Degrees Associated with Canker and Dieback of Quercus spp. Salvatore MM, Russo MT, Nicoletti R, Mahamedi AE, Berraf-Tebbal A, Cimmino A, Masi M, Andolfi A Molecules 28-Aug-2023
PMCID:PMC10489718
doi:10.3390/molecules28176302
PMID:37687130
Commodity risk assessment of Fagus sylvatica plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 28-Jul-2023
PMCID:PMC10375364
doi:10.2903/j.efsa.2023.8118
PMID:37522095
Commodity risk assessment of Acer palmatum plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323724
doi:10.2903/j.efsa.2023.8075
PMID:37427020
Commodity risk assessment of Acer campestre plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323733
doi:10.2903/j.efsa.2023.8071
PMID:37427018

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
> Alkaloids and derivatives / Morphinans
Morphine 5288826 Click to see CN1CCC23C4C1CC5=C2C(=C(C=C5)O)OC3C(C=C4)O 285.34 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Toluenes
1-(3,3-Dimethylcyclohexyl)-4-methylbenzene 21580467 Click to see 202.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
1-[(1R)-3,3-dimethylcyclohexyl]-4-methylbenzene 102207116 Click to see CC1=CC=C(C=C1)C2CCCC(C2)(C)C 202.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
> Benzenoids / Phenols / Benzenediols / Catechols
Epinephrine 5816 Click to see CNCC(C1=CC(=C(C=C1)O)O)O 183.20 unknown via CMAUP database
> Hydrocarbon derivatives / Tropones / Tropolones
gamma-Thujaplicin 12649 Click to see CC(C)C1=CC=C(C(=O)C=C1)O 164.20 unknown via CMAUP database
Hinokitiol 3611 Click to see CC(C)C1=CC(=O)C(=CC=C1)O 164.20 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(1S,4S,5R)-1,8-dimethyl-4-prop-1-en-2-ylspiro[4.5]dec-8-ene 102207117 Click to see CC1CCC(C12CCC(=CC2)C)C(=C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
(4aR,9aR)-4,4,9a-trimethyl-7-methylidene-1,2,3,4a,8,9-hexahydrobenzo[7]annulene 21580468 Click to see CC1(CCCC2(C1C=CC(=C)CC2)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
(4E)-4-(3,3-dimethylcyclohexylidene)-1-methylcyclohexene 21580466 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
(S)-1-Methyl-4-((1R,2S)-1-methyl-2-(prop-1-en-2-yl)cyclobutyl)cyclohex-1-ene 21580469 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
(S)-beta-Macrocarpene 49859620 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
1-Methyl-4-(1-methyl-2-prop-1-en-2-ylcyclobutyl)cyclohexene 73804521 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
3,3-Dimethyl-1-(4-methylcyclohex-3-en-1-yl)cyclohexene 21580470 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
3,3-dimethyl-1-[(1S)-4-methylcyclohex-3-en-1-yl]cyclohexene 163048660 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
3,8-Dimethyl-1-propan-2-ylcyclodeca-1,3,7-triene 162943353 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
4-(3,3-Dimethylcyclohexylidene)-1-methylcyclohexene 73804519 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
4,4,9a-Trimethyl-7-methylidene-1,2,3,4a,8,9-hexahydrobenzo[7]annulene 73804520 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
5,5-Dimethyl-1-(4-methylcyclohex-3-en-1-yl)cyclohexene 21580471 Click to see CC1=CCC(CC1)C2=CCCC(C2)(C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1021/JO01199A001
Npc326072 520091 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
CID 22494956 22494956 Click to see 174.19 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4S,9S,10R,13S)-5,5,9,13-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene 21118261 Click to see 272.50 unknown https://doi.org/10.1071/CH9791131
Hibaene 520750 Click to see 272.50 unknown https://doi.org/10.1071/CH9791131
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(-)-Isokaurene 521318 Click to see CC1=CC23CCC4C(CCCC4(C2CCC1C3)C)(C)C 272.50 unknown https://doi.org/10.1071/CH9791131
(-)-Kaur-16-ene 520687 Click to see 272.50 unknown https://doi.org/10.1071/CH9791131
(1S,4S,9S,10R,13R)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene 101297738 Click to see 272.50 unknown https://doi.org/10.1071/CH9791131
Excisusin D 16215671 Click to see 392.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
Phyllocladene 101289537 Click to see 272.50 unknown https://doi.org/10.1071/CH9791131
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1021/JO01199A001
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-Sabinene 10887971 Click to see 136.23 unknown https://doi.org/10.1021/JO01199A001
Longiborneol 11447401 Click to see 222.37 unknown https://doi.org/10.1021/JO01199A001
Longiborneol 521200 Click to see CC1(CCCC2(C3C1C(C2(CC3)C)O)C)C 222.37 unknown https://doi.org/10.1021/JO01199A001
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1021/JO01199A001
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Phellandrene 443160 Click to see 136.23 unknown https://doi.org/10.1021/JO01199A001
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1021/JO01199A001
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1021/JO01199A001
alpha-PHELLANDRENE 7460 Click to see 136.23 unknown https://doi.org/10.1021/JO01199A001
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1021/JO01199A001
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3R)-3-[(2R)-6-methylhept-5-en-2-yl]-6-methylidenecyclohexene 102426665 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
(4E)-1-methyl-4-(6-methylhept-6-en-2-ylidene)cyclohexene 11458379 Click to see CC1=CCC(=C(C)CCCC(=C)C)CC1 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
1-Methyl-4-(6-methylhept-6-en-2-ylidene)cyclohexene 71362566 Click to see CC1=CCC(=C(C)CCCC(=C)C)CC1 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
beta-Farnesene, (6Z)- 5317319 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown via CMAUP database
Sesquiphellandrene 519764 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Chamigranes
(1S,6S,7S)-2,2,6,8-tetramethyltricyclo[5.3.1.01,6]undec-8-ene 91416189 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
2,2,6,8-Tetramethyltricyclo[5.3.1.01,6]undec-8-ene 12721290 Click to see CC1=CCC23CC1C2(CCCC3(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(+)-Guaia-6,9-diene 14190790 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
(1S,3aR,8aR)-1-methyl-4-methylidene-7-propan-2-yl-2,3,3a,5,6,8a-hexahydro-1H-azulene 162852939 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
1-methyl-4-methylidene-7-propan-2-yl-2,3,3a,5,6,8a-hexahydro-1H-azulene 73194711 Click to see 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
Guaia-6,9-diene 6427475 Click to see CC1CCC2C1C=C(CC=C2C)C(C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.11.002
> Lipids and lipid-like molecules / Steroids and steroid derivatives
(1S,2R,3'S,5S,6S,9S,11R,14R,15S,17R,19R,21R)-2,3',6-trimethylspiro[16,18-dioxahexacyclo[15.3.1.02,15.05,14.06,11.015,19]henicosane-21,2'-oxirane]-9-ol 72701755 Click to see CC1C2(O1)C3CC4C5(C3(CCC6C5CCC7C6(CCC(C7)O)C)C)OC2O4 374.50 unknown via CMAUP database
5-[(1R,2S,4R,5R,6R,7R,10S,11S,14S,16S)-5,11,14,16-tetrahydroxy-7-methyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]pyran-2-one 46939053 Click to see CC12CCC3C(C14C(O4)C(C2C5=COC(=O)C=C5)O)CCC6(C3(CCC(C6)O)O)O 418.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Monohydroxy bile acids, alcohols and derivatives
(3ss,5ss)-3-Hydroxycholan-24-oic acid 92849605 Click to see 376.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
5beta-Dermophol 5284186 Click to see CC(CCCC(CO)(CO)O)C1CCC2C1(C(CC3C2C(CC4C3(CCC(C4)O)C)O)O)C 468.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(3S,7S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2S)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,7-diol 15571096 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C 402.70 unknown via CMAUP database
Cholesterol 5997 Click to see 386.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
22,23-Dihydrobrassicasterol 5283637 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(1S,2R,5R,7S,10S,11S,12S,14R,15R,16S,17R)-7,12-dihydroxy-10,14,17-trimethyl-13-oxo-18-oxapentacyclo[13.3.2.01,14.02,11.05,10]icosane-16-carbaldehyde 46939055 Click to see 390.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
[(1R,2S,4R,5R,6S,7R,10S,11S,14S,16R)-14-hydroxy-7,11-dimethyl-6-[(Z)-1-oxobut-2-en-2-yl]-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-5-yl] acetate 72702443 Click to see 416.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
methyl 4-[(3S,5R,8R,9S,10S,13S)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-4-oxobutanoate 72701756 Click to see CC12CCC(CC1CCC3C2CCC4(C3=CC=C4C(=O)CCC(=O)OC)C)O 386.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[(1R,2S,4R,5R,6R,7R,10S,11S,14S,16S)-11,14,16-trihydroxy-7-methyl-6-(6-oxopyran-3-yl)-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-5-yl] acetate 49818154 Click to see 460.50 unknown via CMAUP database
[(1S,2R,5R,7S,10S,11S,14R,15R,20S)-16-ethenyl-7-hydroxy-10,14-dimethyl-18-oxapentacyclo[13.3.2.01,14.02,11.05,10]icos-16-en-20-yl] acetate 72702444 Click to see 400.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
14,16-dihydroxybufa-5,20,22-trienolide, (14beta,16beta)-form, 16-Ac 46938953 Click to see 426.50 unknown via CMAUP database
3beta,16beta-Dihydroxybufa-8(14),20,22-trienolide 46938954 Click to see 384.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Bufanolides and derivatives
(1R,6R)-6-[(1R,2S,4R,6S,7R,10S,11S,14S,16R)-14-hydroxy-7,11-dimethyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]-2,7-dioxabicyclo[4.1.0]hept-4-en-3-one 10092398 Click to see 400.50 unknown via CMAUP database
(2S)-2-[[7-[[(3S,5R,8R,9S,10S,13R,14S,16S,17R)-16-acetyloxy-14-hydroxy-10,13-dimethyl-17-(6-oxopyran-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]oxy]-7-oxoheptanoyl]amino]-5-(diaminomethylideneamino)pentanoic acid 46930230 Click to see 742.90 unknown via CMAUP database
(2S)-2-[[9-[[(1R,2S,4R,5R,6R,7R,10S,11R,14S,16S)-5-acetyloxy-16-hydroxy-7,11-dimethyl-6-(6-oxopyran-3-yl)-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-14-yl]oxy]-9-oxononanoyl]amino]-5-(diaminomethylideneamino)pentanoic acid 46930229 Click to see 784.90 unknown via CMAUP database
12beta-Hydroxyresibufogenin 15513541 Click to see CC12CCC(CC1CCC3C2CC(C4(C35C(O5)CC4C6=COC(=O)C=C6)C)O)O 400.50 unknown via CMAUP database
19-Hydroxyresibufogenin 12314891 Click to see CC12CCC3C(C14C(O4)CC2C5=COC(=O)C=C5)CCC6C3(CCC(C6)O)CO 400.50 unknown via CMAUP database
19-oxo-cinobufotalin-3-O-adipate-arginine 53253803 Click to see 756.80 unknown via CMAUP database
19-Oxo-desacetylcinobufagin 11144140 Click to see 414.50 unknown via CMAUP database
19-Oxobufalin 10883889 Click to see 400.50 unknown via CMAUP database
1Beta-Hydroxybufalin 10993111 Click to see 402.50 unknown via CMAUP database
20S,21-epoxy-resibufogenin formate 11026341 Click to see CC12CCC(CC1CCC3C2CCC4(C35C(O5)CC4C67C=CC(=O)OC6O7)C)OC=O 428.50 unknown via CMAUP database
20S,21-Epoxyresibufogenin 10453620 Click to see 400.50 unknown via CMAUP database
3-epi-Resibufogenin 70684536 Click to see 384.50 unknown via CMAUP database
5-[(1R,2S,4R,5R,6R,7R,10S,11R,14S,16R)-5,14-dihydroxy-11-(hydroxymethyl)-7-methyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]pyran-2-one 15513543 Click to see 416.50 unknown via CMAUP database
5-[(1R,2S,4R,5S,6R,7R,10S,11S,14S,16R)-5,14-dihydroxy-7,11-dimethyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]pyran-2-one 12186697 Click to see 400.50 unknown via CMAUP database
5-[(1R,2S,4R,6R,7R,10R,11S,14S,16R)-14-hydroxy-7,11-dimethyl-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-6-yl]pyran-2-one 122173140 Click to see 384.50 unknown via CMAUP database
5-[(1R,3R,5R,8R,9S,10S,11S,13R,14S,17R)-1,3,11,14-tetrahydroxy-10,13-dimethyl-12-oxo-2,3,4,5,6,7,8,9,11,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one 46938951 Click to see CC12C(CCC3C1C(C(=O)C4(C3(CCC4C5=COC(=O)C=C5)O)C)O)CC(CC2O)O 432.50 unknown via CMAUP database
5-[(3S,5R,8R,9S,10S,12R,13S,14S,16S,17R)-3,12,14,16-tetrahydroxy-10,13-dimethyl-11-oxo-2,3,4,5,6,7,8,9,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one 46938952 Click to see 432.50 unknown via CMAUP database
5-[(3S,5R,8R,9S,10S,13R,14S,17S)-3-hydroxy-10,13-dimethyl-15-oxo-1,2,3,4,5,6,7,8,9,11,12,14,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]pyran-2-one 12308599 Click to see 384.50 unknown via CMAUP database
5-[(3S,5S,8R,9S,10R,13R,14S,17S)-3,5-dihydroxy-10,13-dimethyl-15-oxo-2,3,4,6,7,8,9,11,12,14,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one 46938950 Click to see 400.50 unknown via CMAUP database
8-[[(1R,2S,4R,5R,6R,7R,10S,11S,14S,16R)-5-acetyloxy-7,11-dimethyl-6-(6-oxopyran-3-yl)-3-oxapentacyclo[8.8.0.02,4.02,7.011,16]octadecan-14-yl]oxy]-8-oxooctanoic acid 70697081 Click to see 598.70 unknown via CMAUP database
Arenobufagin 12305198 Click to see 416.50 unknown via CMAUP database
Bufa-20,22-dienolide, 3-((8-((4-((aminoiminomethyl)amino)-1-carboxybutyl)amino)-1,8-dioxooctyl)oxy)-14-hydroxy-, (3beta(S),5beta)- 99882 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CCC4C5=COC(=O)C=C5)O)C)OC(=O)CCCCCCC(=O)NC(CCCN=C(N)N)C(=O)O 698.90 unknown via CMAUP database
Bufalin 9547215 Click to see 386.50 unknown via CMAUP database
bufalin-3-O-suberoyl ester 67050194 Click to see 542.70 unknown via CMAUP database
bufalin-3-O-succinate-arginine 102595428 Click to see 642.80 unknown via CMAUP database
Bufarenogin 167607 Click to see CC12CCC(CC1CCC3C2C(=O)C(C4(C3(CCC4C5=COC(=O)C=C5)O)C)O)O 416.50 unknown via CMAUP database
Bufogenin 6917974 Click to see CC12CCC(CC1CCC3C2CCC4(C35C(O5)CC4C6=COC(=O)C=C6)C)O 384.50 unknown via CMAUP database
Bufogenin B 12358889 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CC(C4C5=COC(=O)C=C5)O)O)C)O 402.50 unknown via CMAUP database
Bufotalin 12302120 Click to see 444.60 unknown via CMAUP database
Bufotalinin 101286213 Click to see 414.50 unknown via CMAUP database
Bufotoxin 20054854 Click to see 756.90 unknown via CMAUP database
Cinobufagin 11969542 Click to see 442.50 unknown via CMAUP database
Cinobufagin-3-hemisuccinate 11969464 Click to see CC(=O)OC1C(C2(CCC3C(C24C1O4)CCC5C3(CCC(C5)OC(=O)CCC(=O)O)C)C)C6=COC(=O)C=C6 542.60 unknown via CMAUP database
Cinobufaginol 12303266 Click to see 458.50 unknown via CMAUP database
Cinobufotalin 259776 Click to see 458.50 unknown via CMAUP database
Cinobufotoxin 102003563 Click to see 754.90 unknown via CMAUP database
Desacetylcinobufagin 11877495 Click to see 400.50 unknown via CMAUP database
Desacetylcinobufotalin 15513544 Click to see CC12CCC(CC1(CCC3C2CCC4(C35C(O5)C(C4C6=COC(=O)C=C6)O)C)O)O 416.50 unknown via CMAUP database
Gamabufotalin 259803 Click to see 402.50 unknown via CMAUP database
Hellebrigenin 259577 Click to see CC12CCC3C(C1(CCC2C4=COC(=O)C=C4)O)CCC5(C3(CCC(C5)O)C=O)O 416.50 unknown via CMAUP database
Hellebrigenin 3-acetate 267436 Click to see 458.50 unknown via CMAUP database
Marinobufagenin 11969465 Click to see 400.50 unknown via CMAUP database
Npc97210 102093790 Click to see 472.50 unknown via CMAUP database
Pseudobufarenogin 204810 Click to see 416.50 unknown via CMAUP database
resibufogenin-3-O-succinate-arginine 102574724 Click to see 640.80 unknown via CMAUP database
Telocinobufagin 259991 Click to see 402.50 unknown via CMAUP database
Telocinobufatoxin 156077 Click to see CC12CCC(CC1(CCC3C2CCC4(C3(CCC4C5=COC(=O)C=C5)O)C)O)OC(=O)CCCCCCC(=O)NC(CCCN=C(N)N)C(=O)O 714.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Gamma amino acids and derivatives
4-Ammoniobutanoate 6992099 Click to see 103.12 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Hydroxyindoles
2-(5-hydroxy-1H-indol-3-yl)ethylurea 70959828 Click to see 219.24 unknown via CMAUP database
Bufoserotonin C 101460862 Click to see CC(=O)C1=CC(=CN1CCC2=CNC3=C2C=C(C=C3)O)NC(=O)C 325.40 unknown via CMAUP database
Bufotenin oxide 3083669 Click to see 220.27 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
Bufotenidine 3083591 Click to see 218.29 unknown via CMAUP database
Tryptamine 1150 Click to see C1=CC=C2C(=C1)C(=CN2)CCN 160.22 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives / Serotonins
Bufotenine 10257 Click to see 204.27 unknown via CMAUP database
N-Methylserotonin 150885 Click to see CNCCC1=CNC2=C1C=C(C=C2)O 190.24 unknown via CMAUP database
Serotonin 5202 Click to see C1=CC2=C(C=C1O)C(=CN2)CCN 176.21 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives / Serotonins / N-acylserotonins
8-[2-(5-hydroxy-1H-indol-3-yl)ethylamino]-8-oxooctanoic acid 101460861 Click to see 332.40 unknown via CMAUP database
Bufobutanoic Acid 10612485 Click to see 276.29 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(1S,2R,5S,7S,10R,11S,14R,15R,16S,17R)-5,7-dihydroxy-10,14,17-trimethyl-18-oxapentacyclo[13.3.2.01,14.02,11.05,10]icosane-16-carbaldehyde 46939054 Click to see CC1C(C2CCC3(C2(CCC4C3CCC5(C4(CCC(C5)O)C)O)C)O1)C=O 376.50 unknown via CMAUP database
(1S,2R,5S,7S,10R,11S,14R,15R)-16-ethenyl-10,14-dimethyl-18-oxapentacyclo[13.3.2.01,14.02,11.05,10]icos-16-ene-5,7-diol 72702445 Click to see CC12CCC(CC1(CCC3C2CCC4(C35CCC4C(=CO5)C=C)C)O)O 358.50 unknown via CMAUP database
> Organoheterocyclic compounds / Pteridines and derivatives / Pterins and derivatives / Biopterins and derivatives
2-amino-6-[(1R,2R)-1,2,3-trihydroxypropyl]-1H-pteridin-4-one 444632 Click to see 253.22 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Bufogargarizin A 49818075 Click to see 458.50 unknown via CMAUP database
Bufogargarizin B 49818153 Click to see 458.50 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines / Pyrrolo[4,3,2-de]quinolines
7,7-Dimethyl-2-aza-7-azoniatricyclo[6.3.1.04,12]dodeca-1(12),3,8,10-tetraen-9-olate 5316436 Click to see 202.25 unknown via CMAUP database

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