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Chamaecyparis lawsoniana

Chamaecyparis lawsoniana - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Chamaecyparis lawsoniana - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Chamaecyparis lawsoniana - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644010b025310650375451
Scientific name Chamaecyparis lawsoniana
Authority (A.Murray bis) Parl.
First published in Ann. Mus. Imp. Fis. Firenze 1: 181 (1864)

Description Top

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The wood is also used in soundboards for harpsichords and other keyboard instruments. The wood is also used in the construction of ukuleles, and is considered a good tonewood for this purpose.


Chamaecyparis lawsoniana, also known as Port Orford cedar or Lawson cypress, is a conifer species native to Oregon and northwestern California. It can grow up to 200 feet tall and has silver-brown bark and lacy, blue-green foliage. The tree is resistant to wildfires and can regenerate on disturbed land, but requires consistent moisture. It is threatened by a root disease caused by the oomycete pathogen Phytophthora lateralis, which was accidentally introduced in the 1950s. The tree is valued for its wood, which is used in boatbuilding, furniture making, and as a soundboard for musical instruments. There are hundreds of cultivars of this tree, with varying foliage colors and growth rates.

Synonyms Top

Scientific name Authority First published in
Retinispora lawsoniana (A.Murray bis) A.V.Bobrov & Melikyan Komarovia 4: 74 (2006)
Chamaecyparis allumii (Webster) Heydt Deutsche Gärtn.-Zeitung 49: 175. 1934 (1934)
Chamaecyparis boursieri f. viridis Hartwig & Rümpler Bäume Sträucher : 659 (1875)
Chamaecyparis lawsoniana f. aluminii Beissn. Handb. Nadelholzk. 74 1891
Chamaecyparis lawsoniana f. argentea (Lawson ex Gordon) Beissn. Handb. Conif. 12 1887
Chamaecyparis lawsoniana var. argentea (Lawson ex Gordon) Beissn. Handb. Nadelholzk. 546 1891
Chamaecyparis lawsoniana var. glauca (H.Jaeger) W.Hochst. Coniferen 79 1882
Chamaecyparis lawsoniana f. glauca (H.Jaeger) Beissn. Handb. Conif. 12 1887
Chamaecyparis lawsoniana var. stewartii Schelle Mitt. Deutsch. Dendrol. Ges. 29: 30 (1929)
Cupressus fragrans Kellogg Proc. Calif. Acad. Sci. 1: 103 (1856)
Cupressus lawsoniana A.Murray bis Edinburgh New Philos. J. , n.s., 1: 292 (1855)
Cupressus lawsoniana var. aluminii Webster Hardy Conif. Trees : 56 (1896)
Cupressus lawsoniana f. alumnii (Webster) Geerinck Taxonomania 12: 11. 2004 [29 March 2004]
Cupressus lawsoniana var. argentea P.Lawson ex Gordon Pinetum , Suppl.: 24 (1862)
Cupressus lawsoniana f. argentea (Gordon) Geerinck Taxonomania 12: 11 (2004)
Cupressus lawsoniana var. glauca H.Jaeger Ziergehölze Gärt. Parkanl. 200. 1865
Cupressus lawsoniana f. lutea (R.Sm.) Geerinck Taxonomania 12: 12 (2004)
Cupressus lawsoniana f. stewartii (Schelle) Geerinck Taxonomania 12: 12 (2004)
Cupressus lawsoniana f. viridis (Hartwig & Rümpler) Geerinck Taxonomania 12: 12 (2004)
Cupressus nutkanus Torr. U.S. Expl. Exped., Atlas Phan. 2: t. 16 (1856)
Chamaecyparis lawsoniana f. pendula (Beissn.) Beissn. Handb. Conif. 13 1887
Cupressus lawsoniana var. pendula-alba Paul ex Gordon Pinetum ed. 2: 89. 1875
Chamaecyparis lawsoniana f. pendula-alba (Paul ex Gordon) Beissn. Handb. Nadelholzk. 76 1891
Chamaecyparis lawsoniana f. pendula-vera (Hesse) Voss Vilm. Blumengärtn. ed. 3 1: 1227 1896
Chamaecyparis lawsoniana var. pendula-vera (Hesse) A.H.Kent Man. Conif. new ed.: 207 1900
Chamaecyparis lawsoniana var. pendula Beissn. Ziergehölze Gärt. Parkanl. ed. 2: 452. 1884
Cupressus lawsoniana var. pendula (Beissn.) A.Camus Cyprès 78 1914
Chamaecyparis lawsoniana var. billwoodiana Dallim. & A.B.Jacks. Handb. Conif. ed. 3: 233. 1948
Cupressus lawsoniana var. alba-spica Gordon Pinetum ed. 2: 424. 1875
Cupressus lawsoniana var. alba-spica-nana Gordon Pinetum ed. 2: 424. 1875
Chamaecyparis lawsoniana f. alba-spica (Gordon) Beissn. Handb. Conif. 31 1887
Chamaecyparis lawsoniana f. lutea (R.Sm.) C.K.Schneid. Uns. Freil.-Nadelhölzer 168 1913
Chamaecyparis lawsoniana f. erecta (H.Jaeger) C.K.Schneid. Uns. Freil.-Nadelhölzer 168 1913
Cupressus lawsoniana var. erecta H.Jaeger Ziergehölze Gärt. Parkanl. 200. 1865
Chamaecyparis lawsoniana f. glaucescens Rehder J. Arnold Arbor. 37: 169 1946
Chamaecyparis lawsoniana f. fraseri Beissn. Handb. Nadelholzk. 74 1881
Chamaecyparis lawsoniana f. fletcheri (Hornibr.) Rehder Bibl. Cult. Trees 52 1949
Cupressus lawsoniana var. pendula-vera (Hesse) A.H.Kent Man. Conif. ed. 2: 207 1900
Cupressus lawsoniana var. gracilis J.Nelson Pinaceae 188. 1866
Chamaecyparis lawsoniana f. gracilis (J.Nelson) Beissn. Handb. Conif. 12 1887
Cupressus lawsoniana var. filiformis (Fillot) A.H.Kent Man. Conif. 232 1881
Chamaecyparis lawsoniana f. filiformis (Fillot) Beissn. Handb. Conif. 12 1887
Chamaecyparis lawsoniana f. intertexta (R.Sm.) Beissn. Handb. Conif. 12 1887
Cupressus lawsoniana var. intertexta R.Sm. Pl. Fir Tribe 15. 1874
Chamaecyparis lawsoniana f. nana (Dauvesse) Beissn. Handb. Conif. 12 1887
Cupressus lawsoniana var. nana-glauca (Beissn.) A.H.Kent Man. Conif. ed. 2: 207 1900
Chamaecyparis lawsoniana var. nana-glauca Beissn. Ziergehölze Gärt. Parkanl. ed. 2: 452. 1884
Cupressus lawsoniana var. minima-glauca R.Sm. Pl. Fir Tribe 15. 1874
Chamaecyparis lawsoniana var. minima-glauca (R.Sm.) Beissn. Ziergehloze Gart. Park. ed. 2: 452 1884

Common names Top

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Language Common/alternative name
English lawson cypress
English port orford cedar
English port orford cypress
English lawson's cypress
Spanish falso cipres de lawson
Spanish falso ciprés de lawson
Spanish cedro de puerto oxford
Spanish cedro de oregón
Spanish camecíparis de lawson
Spanish cameciparis de lawson
Spanish cedro de oregon
Azerbaijani lavson sərvpəri
Belarusian кіпарысавік Лаўзона
Bulgarian кипарис на Лоусън
Czech cypřišek lawsonův
Welsh cypreswydden lawson
Danish lawsoncypres
Danish lawson-cypres
German lawson-scheinzypresse
German oregonzeder
German lawsons scheinzypresse
Estonian kalifornia ebaküpress
Basque lawson altzifre
Persian کاج طلایی
Finnish huonekataja
Finnish lawsoninsypressi
French cypres de lawson
French cyprès de lawson
Irish cufróg lawson
Galician alcipreste de lawson
Hebrew ברושית לארסון
Upper Sorbian tupa cypresa
Hungarian oregoni hamisciprus
Armenian գետնանոճի լավսոնի
Icelandic fagursýprus
Italian cipresso di lawson
Japanese ローソンヒノキ
Lithuanian lausono puskiparisis
Norwegian Bokmål lawsonsypress
Dutch californische cypres
Dutch californische cipres
Dutch lawsoncipres
Polish cyprysik lawsona
Portuguese cedro do Óregão
Portuguese cedro-do-oregon
Portuguese cipreste-de-lawson
Portuguese cipreste de lawson
Portuguese cipreste
Portuguese cedro-do-óregão
Portuguese cedro-branco
Portuguese cedro do oregon
Russian кипарисовик Лавсона
Slovenian lawsonova pacipresa
Swedish Ädelcypress
Turkish elwoodii Çamı
Ukrainian Кипарисовик Лавсона
Chinese 美國扁柏
Chinese 美国扁柏

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Alternate between 4°C and 20°C for 3 months each, over several cycles, with an extended germination period.
13 - 42% germination rate

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
    • Northern Europe
      • Denmark
      • Great Britain
      • Ireland
      • Norway
    • Southeastern Europe
      • Bulgaria
      • Italy
      • Romania
      • Turkey-in-Europe
    • Southwestern Europe
      • France
      • Portugal
  • Northern America
    • Northwestern U.S.A.
      • Oregon
    • Southwestern U.S.A.
      • California

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000599456
UNII C470043X0R
USDA Plants CHLA
Tropicos 9400243
INPN 90411
Flora of Italy 8434
KEW urn:lsid:ipni.org:names:261839-1
The Plant List kew-2715286
Missouri Botanical Garden 279607
PaleoBotany 63825
Open Tree Of Life 582844
NCBI Taxonomy 58030
NBN Atlas NHMSYS0000457113
Nature Serve 2.152342
IUCN Red List 34004
IPNI 261839-1
iNaturalist 76237
GBIF 2683866
Freebase /m/02910f
FEIS plants/tree/chalaw
EPPO CHCLA
EOL 1034844
Elurikkus 209176
Calflora (Californian flora) 9510
US Library of Congress sh85105047
USDA GRIN 10064
Wikipedia Chamaecyparis_lawsoniana
CMAUP NPO16044

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
Phylogeography, origin and population structure of the self‐fertile emerging plant pathogen Phytophthora pseudosyringae Mullett MS, Harris AR, Scanu B, Van Poucke K, LeBoldus J, Stamm E, Bourret TB, Christova PK, Oliva J, Redondo MA, Talgø V, Corcobado T, Milenković I, Jung MH, Webber J, Heungens K, Jung T Mol Plant Pathol 08-Apr-2024
PMCID:PMC11002350
doi:10.1111/mpp.13450
PMID:38590129
Family matters inside the order Agaricales: systematic reorganization and classification of incertae sedis clitocyboid, pleurotoid and tricholomatoid taxa based on an updated 6-gene phylogeny Vizzini A, Alvarado P, Consiglio G, Marchetti M, Xu J Stud Mycol 31-Jan-2024
PMCID:PMC11003440
doi:10.3114/sim.2024.107.02
PMID:38600959
Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants Kirker GT, Hassan B, Mankowski ME, Eller FJ Insects 18-Jan-2024
PMCID:PMC10816604
doi:10.3390/insects15010069
PMID:38249075
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
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
Potential Hepatoprotective Effects of Chamaecyparis lawsoniana against Methotrexate-Induced Liver Injury: Integrated Phytochemical Profiling, Target Network Analysis, and Experimental Validation Fikry E, Orfali R, El-Sayed SS, Perveen S, Ghafar S, El-Shafae AM, El-Domiaty MM, Tawfeek N Antioxidants (Basel) 14-Dec-2023
PMCID:PMC10740566
doi:10.3390/antiox12122118
PMID:38136237
Phytophthora : taxonomic and phylogenetic revision of the genus Abad ZG, Burgess TI, Bourret T, Bensch K, Cacciola SO, Scanu B, Mathew R, Kasiborski B, Srivastava S, Kageyama K, Bienapfl JC, Verkleij G, Broders K, Schena L, Redford AJ Stud Mycol 06-Oct-2023
PMCID:PMC10825748
doi:10.3114/sim.2023.106.05
PMID:38298569
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 platanoides 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:PMC10323725
doi:10.2903/j.efsa.2023.8073
PMID:37427021
Commodity risk assessment of Acer pseudoplatanus 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:PMC10323731
doi:10.2903/j.efsa.2023.8074
PMID:37427019
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
Chamaecyparis lawsoniana Leaf Essential Oil as a Potential Anticancer Agent: Experimental and Computational Studies Fikry E, Orfali R, Elbaramawi SS, Perveen S, El-Shafae AM, El-Domiaty MM, Tawfeek N Plants (Basel) 28-Jun-2023
PMCID:PMC10346282
doi:10.3390/plants12132475
PMID:37447036
An Overview of Phytophthora Species on Woody Plants in Sweden and Other Nordic Countries Matsiakh I, Menkis A Microorganisms 17-May-2023
PMCID:PMC10221925
doi:10.3390/microorganisms11051309
PMID:37317283
Differences in the Diets of Female and Male Red Deer: The Meaning for Sexual Segregation Garcia F, Alves da Silva A, Ruckstuhl K, Neuhaus P, Coelho C, Wang M, Sousa JP, Alves J Biology (Basel) 31-Mar-2023
PMCID:PMC10136149
doi:10.3390/biology12040540
PMID:37106741
The Never-Ending Presence of Phytophthora Species in Italian Nurseries Antonelli C, Biscontri M, Tabet D, Vettraino AM Pathogens 22-Dec-2022
PMCID:PMC9863022
doi:10.3390/pathogens12010015
PMID:36678363

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Methyl Salicylate 4133 Click to see COC(=O)C1=CC=CC=C1O 152.15 unknown https://doi.org/10.1016/0305-1978(85)90081-X
> Benzenoids / Phenol ethers / Anisoles
Anethole 637563 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown https://doi.org/10.1016/0305-1978(85)90081-X
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697898
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Himeic Acid A 11774903 Click to see CC(CC(=O)NC(=O)C1=COC(=CC1=O)C=CCCCCCCCCC(=O)O)C(=O)O 435.50 unknown via CMAUP database
Himeic acid B 21579676 Click to see C1=C(OC=C(C1=O)C(=O)N)C=CCCCCCCCCC(=O)O 321.40 unknown via CMAUP database
Himeic acid C 21777983 Click to see CC(CC(=O)NC(=O)C1=CNC(=CC1=O)C=CCCCCCCCCC(=O)O)C(=O)O 434.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1016/0305-1978(85)90081-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol 8103 Click to see CCCCCCO 102.17 unknown https://doi.org/10.1016/0305-1978(85)90081-X
1-Octen-3-OL 18827 Click to see CCCCCC(C=C)O 128.21 unknown https://doi.org/10.1016/0305-1978(85)90081-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Hexadecanoic acid propylamide 10379895 Click to see CCCCCCCCCCCCCCCC(=O)NCCC 297.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(+)-Pisiferol 13785024 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)CO)O 302.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.001
(1R,8S,10S)-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-4-ol 101685143 Click to see CC(C)C1=C(C=C2C(=C1)C3CC4C2(CCCC4(C)C)CO3)O 300.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.001
(1S,4S,9S,10R,13R)-5,5,9,13-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene 101277372 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)(C=C4)C)C)C 272.50 unknown https://doi.org/10.1080/10412905.1991.9697898
(4bR,8aR)-4b-(hydroxymethyl)-8,8-dimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol 16663417 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)CO)O 302.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.001
1-[(1S,4aR,5S,8aR)-5-[(3R)-3-hydroxy-3-methylpent-4-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]ethanone 163037887 Click to see CC(=O)C1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C 318.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.001
1-[5-(3-hydroxy-3-methylpent-4-enyl)-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]ethanone 163037886 Click to see CC(=O)C1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C 318.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.001
1,4a-dimethyl-6-methylidene-5-(3-methylpenta-2,4-dienyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 72957164 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.001
11,11-Dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-4-ol 163016669 Click to see CC(C)C1=C(C=C2C(=C1)C3CC4C2(CCCC4(C)C)CO3)O 300.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.001
Abieta-9(11),8(14),12-trien-12-ol 521330 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.001
Alloxanthin 6443740 Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C#CC2=C(CC(CC2(C)C)O)C)C)C 564.80 unknown via CMAUP database
Communic Acid 637125 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.001
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.001
Pisiferol 185553 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)CO)O 302.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.001
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Citronellol 7793 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1002/JPS.3030440906
beta-CITRONELLOL, (+/-)- 8842 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1002/JPS.3030440906
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/0305-1978(85)90081-X
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1016/0305-1978(85)90081-X
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697898
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1080/10412905.1991.9697898
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene 6451618 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697898
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1991.9697898
https://doi.org/10.1016/0305-1978(85)90081-X
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/0305-1978(85)90081-X
https://doi.org/10.1080/10412905.1991.9697898
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697898
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697898
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697898
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1991.9697898
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/0305-1978(85)90081-X
https://doi.org/10.1080/10412905.1991.9697898
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1016/0305-1978(85)90081-X
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1080/10412905.1991.9697898
https://doi.org/10.1016/0305-1978(85)90081-X
Tricyclene 79035 Click to see CC1(C2CC3C1(C3C2)C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697898
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1991.9697898
https://doi.org/10.1016/0305-1978(85)90081-X
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1016/0305-1978(85)90081-X
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697898
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1016/0305-1978(85)90081-X
https://doi.org/10.1080/10412905.1991.9697898
Carveol 7438 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1991.9697898
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.1991.9697898
Carvone, (+/-)- 7439 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.1991.9697898
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697898
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1080/10412905.1991.9697898
https://doi.org/10.1016/0305-1978(85)90081-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697898
https://doi.org/10.1016/0305-1978(85)90081-X
(1E,8E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene 134687947 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/0305-1978(85)90081-X
(1S,3aR,4R,7S,7aS)-1-Acetyl-7-isopropyl-4-methyloctahydro-1H-inden-4-yl acetate 73823555 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)OC(=O)C 280.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.001
(3R,6E)-nerolidol 11241545 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1016/0305-1978(85)90081-X
[(1S,3aR,4R,7S,7aS)-1-acetyl-4-methyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-4-yl] acetate 21679492 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)OC(=O)C 280.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.001
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1080/10412905.1991.9697898
4-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7,8,8a-octahydro-1-naphthalenol 519662 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1002/JPS.3030440906
7-Acetyl-2-hydroxy-2-methyl-5-isopropylbicyclo[4.3.0]nonane 539857 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 238.37 unknown https://doi.org/10.1080/10412905.1991.9697898
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1002/JPS.3030440906
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/0305-1978(85)90081-X
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697898
Calamenene 6429077 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1016/0305-1978(85)90081-X
https://doi.org/10.1080/10412905.1991.9697898
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697898
Cedrelanol 160799 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/0305-1978(85)90081-X
Cuparene 86895 Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C 202.33 unknown https://doi.org/10.1016/0305-1978(85)90081-X
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/0305-1978(85)90081-X
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1991.9697898
Oplopanone 10466745 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 238.37 unknown https://doi.org/10.1080/10412905.1991.9697898
Thujopsene 442402 Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C 204.35 unknown https://doi.org/10.1016/0305-1978(85)90081-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
Cedrol 65575 Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O 222.37 unknown https://doi.org/10.1016/0305-1978(85)90081-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Elemol 92138 Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O 222.37 unknown https://doi.org/10.1016/0305-1978(85)90081-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/0305-1978(85)90081-X
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1016/0305-1978(85)90081-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
2,7-Cyclodecadien-1-ol, 1,7-dimethyl-4-(1-methylethyl)- 522445 Click to see CC1=CCCC(C=CC(CC1)C(C)C)(C)O 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.001
Germacra-1(10),5-dien-4beta-ol 11148775 Click to see CC1=CCCC(C=CC(CC1)C(C)C)(C)O 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.10.001
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4S)-1-[(1E,3E,5E,7E,9E,11E,13E,15E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15-octaen-17-ynyl]-2,6,6-trimethylcyclohexane-1,2,4-triol 102146782 Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2(C(CC(CC2(C)O)O)(C)C)O)C)C 600.90 unknown via CMAUP database
(1R)-3,5,5-trimethyl-4-[(3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-[(1R)-2,6,6-trimethylcyclohex-2-en-1-yl]octadeca-3,5,7,9,11,13,15,17-octaen-1-ynyl]cyclohex-3-en-1-ol 101289802 Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C 550.90 unknown via CMAUP database
19'-Hexanoyloxyisomytiloxanthin 16061209 Click to see CCCCCC(=O)OCC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC1(C(CC(=O)CC1(C)C)C)O)C)C#CC2=C(CC(CC2(C)C)O)C 713.00 unknown via CMAUP database
Amarouciaxanthin B/Sidnyaxanthin 16061221 Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC2(C(=CC(=O)CC2(C)C)C)O)C)C 596.80 unknown via CMAUP database
Anhydroamarouciaxanthin B 23428237 Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)C=C2C(=CC(=O)CC2(C)C)C)C)C 578.80 unknown via CMAUP database
Halocynthiaxanthin 11966451 Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC23C(CC(CC2(O3)C)O)(C)C)C)C 598.90 unknown via CMAUP database
Isomytiloxanthin 23428074 Click to see CC1CC(=O)CC(C1(CC(=O)C(=CC=CC(=CC=CC=C(C)C=CC=C(C)C#CC2=C(CC(CC2(C)C)O)C)C)C)O)(C)C 598.90 unknown via CMAUP database
Mytiloxanthin 11365423 Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=CC(=O)C2(CC(CC2(C)C)O)C)O)C)C 598.90 unknown via CMAUP database
Pectenol A/(Pectenol) 16061215 Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(C(C(CC2(C)C)O)O)C)C)C 582.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
7-Dehydrocholesterol 439423 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C 384.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Brassicasterol 5281327 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 unknown via CMAUP database
Ergosterol 444679 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C 396.60 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
notoamide J 25180709 Click to see CC(C)(C=C)C1(C2=C(C=C(C=C2)O)NC1=O)CC3C(=O)N4CCCC4C(=O)N3 383.40 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
Betaine 247 Click to see C[N+](C)(C)CC(=O)[O-] 117.15 unknown via CMAUP database
N,N,N-trimethylglycinium 248 Click to see C[N+](C)(C)CC(=O)O 118.15 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
Arginine 6322 Click to see C(CC(C(=O)O)N)CN=C(N)N 174.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
3,3'-Methylenebis(tyrosine) 3082144 Click to see C1=CC(=C(C=C1CC(C(=O)O)N)CC2=C(C=CC(=C2)CC(C(=O)O)N)O)O 374.40 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Kainoids
(6'S)-Isodomoic acid G 17753955 Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O 311.33 unknown via CMAUP database
Domoic acid C5'-diastereomer 5311075 Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O 311.33 unknown via CMAUP database
Isodomoic acid F 101790920 Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O 311.33 unknown via CMAUP database
> Organic acids and derivatives / Organic sulfonic acids and derivatives / Organosulfonic acids and derivatives / Organosulfonic acids
Taurine 1123 Click to see C(CS(=O)(=O)O)N 125.15 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Alkanolamines / 1,2-aminoalcohols / N-acylethanolamines
Anandamide 5281969 Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)NCCO 347.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Widdrol 94334 Click to see CC1(CCCC2(C1=CCC(CC2)(C)O)C)C 222.37 unknown https://doi.org/10.1016/0305-1978(85)90081-X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
Aspermytin A 9993091 Click to see CC1CCC2C(C1)C=CC(C2(C)C(=O)CCO)(C)O 266.38 unknown via CMAUP database
> Organoheterocyclic compounds / Azaspirodecane derivatives
CID 101396440 101396440 Click to see CC1CC2C3C(CC4(O3)C(CC(CN4)C)C)OC(C1)(O2)CC(=C)C5C(CC(C(O5)(C(C6CC7C(O6)CC(C8(O7)CCC9(O8)C=CCC(O9)C=CCCC(=O)O)C)O)O)C)C 842.10 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodiazepines / 1,4-benzodiazepines
(3R,3'R)-3'-(3-hydroxyphenyl)-4-methylspiro[1H-1,4-benzodiazepine-3,2'-oxirane]-2,5-dione 92278353 Click to see CN1C(=O)C2=CC=CC=C2NC(=O)C13C(O3)C4=CC(=CC=C4)O 310.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(3S,8aS)-3-[[(3R)-7,7-dimethyl-3-(2-methylbut-3-en-2-yl)-2-oxo-1H-pyrano[2,3-g]indol-3-yl]methyl]-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione 16127840 Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C3(CC4C(=O)N5CCCC5C(=O)N4)C(C)(C)C=C)C 449.50 unknown via CMAUP database
Notoamide A 16128040 Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C 463.50 unknown via CMAUP database
notoamide B 16127923 Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C 447.50 unknown via CMAUP database
Notoamide H 25180895 Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C(=O)C34C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)O)C 479.50 unknown via CMAUP database
Notoamide O 102043608 Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4(C3=O)C(C5CC67CCCN6C(=O)C5(C(O4)O)NC7=O)(C)C)C 479.50 unknown via CMAUP database
Notoamide Q 46919487 Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C3(CC4C(=O)N5CCCC5(C(=O)N4)OC)C(C)(C)C=C)C 479.60 unknown via CMAUP database
Sclerotiamide 10647785 Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C34C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C 463.50 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
notoamide D 16127841 Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4(C3(CC5N4C(=O)C6CCCN6C5=O)O)C(C)(C)C=C)C 449.50 unknown via CMAUP database
Notoamide K 25180896 Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4(C3(CC5(N4C(=O)C6CCCN6C5=O)O)O)C(C)(C)C=C)C 465.50 unknown via CMAUP database
Notoamide P 46919486 Click to see CC1(C=CC2=C3C(=CC(=C2O1)Br)C4(CC5(C(=O)N6CCCC6C(=O)N5C4(N3)C(C)(C)C=C)O)O)C 544.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
Viridicatol 115033 Click to see C1=CC=C2C(=C1)C(=C(C(=O)N2)O)C3=CC(=CC=C3)O 253.25 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines
(+)-Stephacidin A 16127922 Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C 431.50 unknown via CMAUP database
Notoamide F 25180710 Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)OC)C 461.60 unknown via CMAUP database
Notoamide G 25180707 Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C4=C3C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)OC)O)C 477.60 unknown via CMAUP database
Notoamide I 25180708 Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C(=O)C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C 445.50 unknown via CMAUP database
notoamide R 46919488 Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C 447.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Saxitoxins, gonyautoxins, and derivatives
[(3aS,4R,10aS)-2,6-diamino-9,9,10,10-tetrahydroxy-3,3a,4,8-tetrahydropyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid 102411283 Click to see C1C(C(C23N1C(=NC(C2NC(=N3)N)COC(=O)NS(=O)(=O)O)N)(O)O)(O)O 411.35 unknown via CMAUP database
[(3aS,4R,9S,10aS)-2,6-diamino-9,10,10-trihydroxy-3a,4,8,9-tetrahydro-3H-pyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid 44587284 Click to see C1C(C(C23N1C(=NC(C2NC(=N3)N)COC(=O)NS(=O)(=O)O)N)(O)O)O 395.35 unknown via CMAUP database
11,11-Dihydroxysaxitoxin 102411284 Click to see C1C(C(C23N1C(=NC(C2N=C(N3)N)COC(=O)N)N)(O)O)(O)O 331.29 unknown via CMAUP database
11beta-Hydroxysaxitoxin 60135304 Click to see C1C(C(C23N1C(=NC(C2N=C(N3)N)COC(=O)N)N)(O)O)O 315.29 unknown via CMAUP database

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