Euphorbia lathyris - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Euphorbia lathyris - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Euphorbia lathyris - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID64403b49934de204354721
Scientific name Euphorbia lathyris
Authority L.
First published in Sp. Pl. 1: 457. 1753 [1 May 1753]

Description Top

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of the Euphorbia lathyris plant, also known as caper spurge or paper spurge, are native to southern Europe, northwest Africa, and parts of Asia. It is a biennial plant that can grow up to 1.5 meters tall and has blue-green stems and lanceolate leaves. The flowers are small and green to yellow-green in color, and the seeds are green when young and turn brown or grey when mature. All parts of the plant are poisonous, but goats are immune to the toxin and sometimes eat it. It is considered an invasive weed in many regions and is used in folk medicine for various ailments.

Synonyms Top

Scientific name Authority First published in
Tithymalus cataputia Garsault Fig. Pl. Méd. : 593 (1764)
Tithymalus lathyris Hill Hort. Kew. : 172.3 (1768)
Galarhoeus decussatus Gray Nat. Arr. Brit. Pl. 2: 256 (1821 publ. 1822)
Galarhoeus lathyris Haw. Syn. Pl. Succ. : 143 (1812)
Keraselma lathyris (L.) Raf. Fl. Tellur. 4: 116 (1838)
Epurga lathyris Fourr. Ann. Soc. Linn. Lyon , n.s., 17: 150 (1869)
Euphorbia decussata Salisb. Prodr. Stirp. Chap. Allerton : 389 (1796)
Euphorbia lathyris var. minor Hook. & Arn. Bot. Beechey Voy. : 44 (1830)
Euphorbia spongiosa Ledeb. ex Schrank Syll. Pl. Nov. 1: 214 (1824)
Euphorbion lathyrum St.-Lag. Ann. Soc. Bot. Lyon 7: 126 (1880)

Common names Top

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Language Common/alternative name
English gopher spurge
English gopher plant
English caper spurge
English moleplant
English mole plant
Spanish targago
Spanish tartagos de judas
Spanish tártagos de judas
Spanish tartagos de la cruz
Spanish tártagos de la cruz
Spanish tartagos gordos
Spanish tartagos horadados
Spanish tartagos menudos
Spanish tartagos que matan los ratones
Spanish pildoras de judas
Spanish grano menor de reyes
Spanish cagarríos
Spanish cagarrios
Spanish tartagos
Spanish planta de las muelas
Arabic أبو قابوس
Arabic سوسب
Arabic فربيون
Arabic تيوع
Arabic يتوع
Catalan cagamuja
Czech pryšec skočcový
Welsh llaethlys caprys
German springwurzel
German spring-wolfsmilch
German kreuzblättrige wolfsmilch
Basque tartiku
French Épurge
French epurge
French euphorbe épurge
Galician herba da cuca
Galician herba rateira
gn mba'ysyvo
Croatian unakrsnolisna mlječika
Upper Sorbian Čoskač
Upper Sorbian křižna mlóčeń
Hungarian hasindító kutyatej
Italian euforbia catapuzia
Japanese ホルトソウ
lzh 續隨子
Dutch kruisbladige wolfsmelk
Dutch kruisbladwolfsmelk
Polish wilczomlecz groszkowy
Russian Молочай лекарственный
Russian Молочай масличный
Russian Молочай чиновидный
Russian Молочай чины
Serbian Царевац
Swedish korstörel
Vietnamese tục tùy
Chinese 续随子叶
Chinese 一种维管植物
Chinese 续随子
Chinese 千金子
Chinese 续随子茎中白汁
Chinese 大戟
Chinese 續隨子

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Azores
    • Northeast Tropical Africa
      • Ethiopia
    • Northern Africa
      • Morocco
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Tibet
      • Xinjiang
    • Middle Asia
      • Kirgizstan
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • Pakistan
      • West Himalaya
    • Indo-China
      • Vietnam
  • Australasia
    • Australia
      • Tasmania
    • New Zealand
      • New Zealand North
      • New Zealand South
  • Europe
    • Middle Europe
      • Belgium
      • Czechoslovakia
      • Germany
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Romania
    • Southwestern Europe
      • France
      • Portugal
      • Spain
  • Northern America
    • Eastern Canada
      • Ontario
      • Québec
    • Mexico
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest
    • North-central U.S.A.
      • Illinois
    • Northeastern U.S.A.
      • Connecticut
      • Massachusetts
      • New York
      • Ohio
      • Pennsylvania
      • West Virginia
    • Northwestern U.S.A.
      • Idaho
      • Montana
      • Oregon
      • Washington
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southeastern U.S.A.
      • Maryland
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • Arizona
      • California
    • Western Canada
      • British Columbia
  • Southern America
    • Brazil
      • Brazil South
    • Northern South America
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Chile Central
      • Juan Fernández Islands
      • Uruguay
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000962968
UNII GHV7FV90K2
UNII SH84TF2577
Canadensys 5611
USDA Plants EULA4
Tropicos 12800159
Tropicos 100413128
INPN 97556
Flora of Italy 2937
KEW urn:lsid:ipni.org:names:347072-1
The Plant List kew-80521
Open Tree Of Life 907417
Observations.org 6773
NCBI Taxonomy 212925
NBN Atlas NBNSYS0000003725
Nature Serve 2.143475
IPNI 347072-1
iNaturalist 77114
GBIF 3917809
GBIF 3066965
Freebase /m/0f9s8k
EPPO EPHLA
EOL 1144553
Calflora (Californian flora) 3557
World Flora Online wfo-0001350602
USDA GRIN 70275
USDA GRIN 400532
Wikipedia Euphorbia_lathyris
CMAUP NPO520
Plantarium 15575

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_963576675.1 ddEupLath1.1 Chromosome WELLCOME SANGER INSTITUTE 2023-11-03 28.0x 0.95 Gb

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
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Characterization, antioxidant and antitumor activities of phenolic compounds from Amomum villosum Lour. Zhang M, Shuai XX, Wei Z, Dai TT, Wei CB, Li Y, He JJ, Du LQ Front Nutr 06-Feb-2024
PMCID:PMC10876855
doi:10.3389/fnut.2024.1327164
PMID:38379541
Identification of One O-Methyltransferase Gene Involved in Methylated Flavonoid Biosynthesis Related to the UV-B Irradiation Response in Euphorbia lathyris Zhao W, Huang L, Xu S, Wu J, Wang F, Li P, Li L, Tian M, Feng X, Chen Y Int J Mol Sci 08-Jan-2024
PMCID:PMC10815478
doi:10.3390/ijms25020782
PMID:38255854
Nature’s Green Potential: Anticancer Properties of Plants of the Euphorbiaceae Family Jiménez-González V, Kowalczyk T, Piekarski J, Szemraj J, Rijo P, Sitarek P Cancers (Basel) 25-Dec-2023
PMCID:PMC10778523
doi:10.3390/cancers16010114
PMID:38201542
Euphorbia factor L2 suppresses the generation of liver metastatic ascites in breast cancer via inhibiting NLRP3 inflammasome activation Jiang D, Liu X, Tan R, Zhu Y, Zhang L Int J Mol Med 04-Dec-2023
PMCID:PMC10712698
doi:10.3892/ijmm.2023.5332
PMID:38063231
Euphorbiasteroid Induces Apoptosis as Well as Autophagy through Modulating SHP-1/STAT3 Pathway in Hepatocellular Carcinoma Cells Kim NY, Sethi G, Um JY, Ahn KS Int J Mol Sci 05-Sep-2023
PMCID:PMC10531000
doi:10.3390/ijms241813713
PMID:37762016
EupDB: An integrative and comprehensive functional genomics data hub for Euphorbiaceae plants Liu J, Li Y, Li J, Chen W, Pan B, Liu A, Xu ZF, Xu W, Liu C Plant Commun 04-Sep-2023
PMCID:PMC10811364
doi:10.1016/j.xplc.2023.100683
PMID:37671605
Esculetin Alleviates Inflammation, Oxidative Stress and Apoptosis in Intestinal Ischemia/Reperfusion Injury via Targeting SIRT3/AMPK/mTOR Signaling and Regulating Autophagy Shen X, Shi H, Chen X, Han J, Liu H, Yang J, Shi Y, Ma J J Inflamm Res 23-Aug-2023
PMCID:PMC10460583
doi:10.2147/JIR.S413941
PMID:37641705
Standardization of Euphorbia tithymaloides (L.) Poit. (Root) by Conventional and DNA Barcoding Methods Patil S, Imran M, Jaquline RS, Aeri V ACS Omega 04-Aug-2023
PMCID:PMC10433337
doi:10.1021/acsomega.3c02543
PMID:37599932
Scientific connotation of the compatibility of traditional Chinese medicine from the perspective of the intestinal flora Gao Y, Wu X, Zhao N, Bai D Front Pharmacol 19-Jul-2023
PMCID:PMC10395102
doi:10.3389/fphar.2023.1152858
PMID:37538183
Seasonal variations of triterpene acid contents in Viscum album L. on typical host trees of Hyrcanian forests Soursouri A, Hosseini SM, Fattahi F Sci Rep 18-Jul-2023
PMCID:PMC10354082
doi:10.1038/s41598-023-38649-x
PMID:37463985
Hydroxylases involved in terpenoid biosynthesis: a review Zhang Z, Wu QY, Ge Y, Huang ZY, Hong R, Li A, Xu JH, Yu HL Bioresour Bioprocess 13-Jul-2023
PMCID:PMC10992849
doi:10.1186/s40643-023-00656-1
Phytochemical Analysis, Antioxidant Activities In Vitro and In Vivo, and Theoretical Calculation of Different Extracts of Euphorbia fischeriana Sun Y, Feng JX, Wei ZB, Sun H, Li L, Zhu JY, Xia GQ, Zang H Molecules 02-Jul-2023
PMCID:PMC10343448
doi:10.3390/molecules28135172
PMID:37446834
Plastid DNA Barcoding and RtActin cDNA Fragment Isolation of Reutealis Trisperma: A Promising Bioresource for Biodiesel Production Jadid N, Rosidah NL, Ramadani MR, Prasetyowati I, Sa’adah NN, Widodo AF, Oktafitria D Bioinform Biol Insights 20-Jun-2023
PMCID:PMC10286179
doi:10.1177/11779322231182768
PMID:37360051
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191

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 / Biphenols
Euphorbetin 5317297 Click to see C1=CC(=O)OC2=C1C(=C(C(=C2)O)O)C3=C(C(=CC4=C3C=CC(=O)O4)O)O 354.30 unknown via CMAUP database
Isoeuphorbetin 71438018 Click to see C1=CC(=O)OC2=C(C(=C(C=C21)O)O)C3=C(C(=CC4=C3C=CC(=O)O4)O)O 354.30 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols / Catecholamines and derivatives
2-(3,4-Dihydroxyphenyl-d3)ethylamine 11993858 Click to see C1=CC(=C(C=C1CCN)O)O 156.20 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown https://doi.org/10.1002/JPS.2600561041
https://doi.org/10.1016/S0031-9422(00)89911-2
Heptacosane 11636 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC 380.70 unknown https://doi.org/10.1002/JPS.2600561041
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1002/JPS.2600561041
Tritriacontane 12411 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 464.90 unknown https://doi.org/10.1002/JPS.2600561041
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Tricos-10-enoic acid 53921228 Click to see CCCCCCCCCCCCC=CCCCCCCCCC(=O)O 352.60 unknown https://doi.org/10.1055/S-2007-969693
https://doi.org/10.1021/NP980294Q
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1,11-Diacetyloxy-13-benzoyloxy-3,6,6,14-tetramethyl-10-methylidene-2-oxo-9-tricyclo[10.3.0.05,7]pentadec-3-enyl) benzoate 75111171 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=C)C(CC4C(C4(C)C)C=C(C2=O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C 642.70 unknown https://doi.org/10.1016/J.BMC.2009.04.041
(1',11'-Diacetyloxy-3',6',6',14'-tetramethyl-2'-oxospiro[oxirane-2,10'-tricyclo[10.3.0.05,7]pentadec-3-ene]-13'-yl) 2-phenylacetate 72763974 Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C 552.70 unknown https://doi.org/10.1016/J.BMC.2009.04.041
(1'R,2R,3'E,5'R,7'S,11'S,12'R,13'S,14'S)-1',11',13'-trihydroxy-3',6',6',14'-tetramethylspiro[oxirane-2,10'-tricyclo[10.3.0.05,7]pentadec-3-ene]-2'-one 15225985 Click to see CC1CC2(C(C1O)C(C3(CCC4C(C4(C)C)C=C(C2=O)C)CO3)O)O 350.40 unknown via CMAUP database
(1'R,3'E,11'R,13'S,14'S)-1',11',13'-trihydroxy-3',6',6',14'-tetramethylspiro[oxirane-2,10'-tricyclo[10.3.0.05,7]pentadec-3-ene]-2'-one 101136463 Click to see CC1CC2(C(C1O)C(C3(CCC4C(C4(C)C)C=C(C2=O)C)CO3)O)O 350.40 unknown via CMAUP database
(11-Acetyloxy-13-benzoyloxy-1-hydroxy-3,6,6,14-tetramethyl-10-methylidene-2-oxo-9-tricyclo[10.3.0.05,7]pentadec-3-enyl) benzoate 163043671 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=C)C(CC4C(C4(C)C)C=C(C2=O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O 600.70 unknown https://doi.org/10.1021/OL050206A
(1R,3E,11S,13S,14S)-1,11,13-trihydroxy-3,6,6,14-tetramethyl-10-methylidenetricyclo[10.3.0.05,7]pentadec-3-en-2-one 118701516 Click to see CC1CC2(C(C1O)C(C(=C)CCC3C(C3(C)C)C=C(C2=O)C)O)O 334.40 unknown via CMAUP database
(1R,3E,5S,7S,11R,12R,13S,14S)-1,11,13-trihydroxy-3,6,6,14-tetramethyl-10-methylidenetricyclo[10.3.0.05,7]pentadec-3-en-2-one 24721223 Click to see CC1CC2(C(C1O)C(C(=C)CCC3C(C3(C)C)C=C(C2=O)C)O)O 334.40 unknown via CMAUP database
(1R,3Z,5R,7S,11S,12R,13S,14S)-1,11,13-trihydroxy-3,6,6,14-tetramethyl-10-methylidenetricyclo[10.3.0.05,7]pentadec-3-en-2-one 102004529 Click to see CC1CC2(C(C1O)C(C(=C)CCC3C(C3(C)C)C=C(C2=O)C)O)O 334.40 unknown via CMAUP database
(1R,5S,7R,12S)-1,11,13-trihydroxy-3,6,6,14-tetramethyl-10-methylidenetricyclo[10.3.0.05,7]pentadec-3-en-2-one 138115035 Click to see CC1CC2(C(C1O)C(C(=C)CCC3C(C3(C)C)C=C(C2=O)C)O)O 334.40 unknown https://doi.org/10.1002/PCA.592
[(1'R,2R,3'E,5'R,7'S,11'R,12'R,13'S,14'S)-1',11'-diacetyloxy-3',6',6',14'-tetramethyl-2'-oxospiro[oxirane-2,10'-tricyclo[10.3.0.05,7]pentadec-3-ene]-13'-yl] 2-phenylacetate 10626539 Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C 552.70 unknown via CMAUP database
[(1'R,2R,3'E,5'S,7'S,11'R,12'R,13'S,14'S)-1',11'-diacetyloxy-3',6',6',14'-tetramethyl-2'-oxospiro[oxirane-2,10'-tricyclo[10.3.0.05,7]pentadec-3-ene]-13'-yl] 2-phenylacetate 100933326 Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C 552.70 unknown via CMAUP database
[(1R,2S,4R,7S,9R,10E,13R,15S,16S)-16-hydroxy-4,8,8,11,15-pentamethyl-12-oxo-3-oxatetracyclo[11.3.0.02,4.07,9]hexadec-10-en-13-yl] (E)-3-phenylprop-2-enoate 101316978 Click to see CC1CC2(C(C1O)C3C(O3)(CCC4C(C4(C)C)C=C(C2=O)C)C)OC(=O)C=CC5=CC=CC=C5 464.60 unknown https://doi.org/10.1055/S-2007-969693
[(1R,3E,5R,7S,10E,12S,13S,14S)-1-acetyloxy-10-(acetyloxymethyl)-3,6,6,14-tetramethyl-2-oxo-13-tricyclo[10.3.0.05,7]pentadeca-3,10-dienyl] (E)-3-phenylprop-2-enoate 44241674 Click to see CC1CC2(C(C1OC(=O)C=CC3=CC=CC=C3)C=C(CCC4C(C4(C)C)C=C(C2=O)C)COC(=O)C)OC(=O)C 548.70 unknown via CMAUP database
[(1R,3E,5R,7S,10Z,12S,13S,14S)-1-acetyloxy-10-(hydroxymethyl)-3,6,6,14-tetramethyl-2-oxo-13-tricyclo[10.3.0.05,7]pentadeca-3,10-dienyl] hexanoate 11754671 Click to see CCCCCC(=O)OC1C(CC2(C1C=C(CCC3C(C3(C)C)C=C(C2=O)C)CO)OC(=O)C)C 474.60 unknown https://doi.org/10.1021/NP0203537
[(1R,3E,5R,7S,9E,11R,12R,13S,14S)-1,11-diacetyloxy-10-(acetyloxymethyl)-3,6,6,14-tetramethyl-2-oxo-13-tricyclo[10.3.0.05,7]pentadeca-3,9-dienyl] benzoate 44241675 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=CCC4C(C4(C)C)C=C(C2=O)C)COC(=O)C)OC(=O)C)OC(=O)C 580.70 unknown via CMAUP database
[(1R,3E,5R,7S,9E,11S,12R,13S,14S)-1,11-diacetyloxy-10-(acetyloxymethyl)-3,6,6,14-tetramethyl-2-oxo-13-tricyclo[10.3.0.05,7]pentadeca-3,9-dienyl] benzoate 163074041 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=CCC4C(C4(C)C)C=C(C2=O)C)COC(=O)C)OC(=O)C)OC(=O)C 580.70 unknown https://doi.org/10.1016/S0031-9422(00)80486-0
[(1R,3E,5R,7S,9S,11R,12R,13S,14S)-1,11-diacetyloxy-13-benzoyloxy-3,6,6,14-tetramethyl-10-methylidene-2-oxo-9-tricyclo[10.3.0.05,7]pentadec-3-enyl] benzoate 45270942 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=C)C(CC4C(C4(C)C)C=C(C2=O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C 642.70 unknown https://doi.org/10.1016/J.BMC.2009.04.041
[(1R,3E,5S,7S,11R,12R,13S,14S)-1,11-diacetyloxy-3,6,6,14-tetramethyl-10-methylidene-2-oxo-13-tricyclo[10.3.0.05,7]pentadec-3-enyl] pyridine-3-carboxylate 100933329 Click to see CC1CC2(C(C1OC(=O)C3=CN=CC=C3)C(C(=C)CCC4C(C4(C)C)C=C(C2=O)C)OC(=O)C)OC(=O)C 523.60 unknown via CMAUP database
[(1R,3Z,5R,7R,11R,12R,13S,14S)-1,11-diacetyloxy-3,6,6,14-tetramethyl-10-methylidene-2-oxo-13-tricyclo[10.3.0.05,7]pentadec-3-enyl] benzoate 90656910 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=C)CCC4C(C4(C)C)C=C(C2=O)C)OC(=O)C)OC(=O)C 522.60 unknown via CMAUP database
[(1R,5R,7S,11R,12R,13S,14S)-1,11-diacetyloxy-3,6,6,14-tetramethyl-10-methylidene-2-oxo-13-tricyclo[10.3.0.05,7]pentadec-3-enyl] benzoate 85364164 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=C)CCC4C(C4(C)C)C=C(C2=O)C)OC(=O)C)OC(=O)C 522.60 unknown via CMAUP database
[(1S,2S,4S,7R,9R,10Z,13R,15S,16S)-16-hydroxy-4,8,8,11,15-pentamethyl-12-oxo-3-oxatetracyclo[11.3.0.02,4.07,9]hexadec-10-en-13-yl] (E)-3-phenylprop-2-enoate 163073905 Click to see CC1CC2(C(C1O)C3C(O3)(CCC4C(C4(C)C)C=C(C2=O)C)C)OC(=O)C=CC5=CC=CC=C5 464.60 unknown https://doi.org/10.1021/NP980294Q
[(1S,3E,5S,7R,9S,11S,12S,13R,14R)-11-acetyloxy-13-benzoyloxy-1-hydroxy-3,6,6,14-tetramethyl-10-methylidene-2-oxo-9-tricyclo[10.3.0.05,7]pentadec-3-enyl] benzoate 163043679 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=C)C(CC4C(C4(C)C)C=C(C2=O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O 600.70 unknown https://doi.org/10.1021/OL050206A
[(1S,4R,7S,9R,13R)-16-hydroxy-11-(hydroxymethyl)-4,8,8,15-tetramethyl-12-oxo-3-oxatetracyclo[11.3.0.02,4.07,9]hexadec-10-en-13-yl] 3-phenylprop-2-enoate 129316723 Click to see CC1CC2(C(C1O)C3C(O3)(CCC4C(C4(C)C)C=C(C2=O)CO)C)OC(=O)C=CC5=CC=CC=C5 480.60 unknown https://doi.org/10.1055/S-2007-969693
[(3'Z)-1',11'-diacetyloxy-3',6',6',14'-tetramethyl-2'-oxospiro[oxirane-2,10'-tricyclo[10.3.0.05,7]pentadec-3-ene]-13'-yl] 2-phenylacetate 45934366 Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C 552.70 unknown via CMAUP database
[(3E)-1,11-diacetyloxy-3,6,6,14-tetramethyl-10-methylidene-2-oxo-13-tricyclo[10.3.0.05,7]pentadec-3-enyl] benzoate 9936579 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=C)CCC4C(C4(C)C)C=C(C2=O)C)OC(=O)C)OC(=O)C 522.60 unknown via CMAUP database
[1-Acetyloxy-10-(hydroxymethyl)-3,6,6,14-tetramethyl-2-oxo-13-tricyclo[10.3.0.05,7]pentadeca-3,10-dienyl] hexanoate 73086732 Click to see CCCCCC(=O)OC1C(CC2(C1C=C(CCC3C(C3(C)C)C=C(C2=O)C)CO)OC(=O)C)C 474.60 unknown https://doi.org/10.1021/NP0203537
6,17-Epoxylathyrol 133561659 Click to see CC1CC2(C(C1O)C(C3(CCC4C(C4(C)C)C=C(C2=O)C)CO3)O)O 350.40 unknown https://doi.org/10.1002/PCA.592
CID 101306826 101306826 Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C 552.70 unknown via CMAUP database
CID 5281376 5281376 Click to see CC1CC2(C(C1O)C(C(=C)CCC3C(C3(C)C)C=C(C2=O)C)O)O 334.40 unknown https://doi.org/10.1002/PCA.592
CID 6443057 6443057 Click to see CC1CC2(C(C1O)C(C(=C)CCC3C(C3(C)C)C=C(C2=O)C)O)O 334.40 unknown via CMAUP database
CID 74962707 74962707 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=CCC4C(C4(C)C)C=C(C2=O)C)COC(=O)C)OC(=O)C)OC(=O)C 580.70 unknown https://doi.org/10.1016/S0031-9422(00)80486-0
https://doi.org/10.1016/J.BMC.2009.04.041
Diacetyl benzoyl lathyrol 10577938 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=C)CCC4C(C4(C)C)C=C(C2=O)C)OC(=O)C)OC(=O)C 522.60 unknown https://doi.org/10.1007/BF02154248
https://doi.org/10.1016/J.BMC.2009.04.041
Epoxylathyrol 56841080 Click to see CC1CC2(C(C1O)C(C3(CCC4C(C4(C)C)C=C(C2=O)C)CO3)O)O 350.40 unknown via CMAUP database
Euphorbia factor L1 11238221 Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C 552.70 unknown https://doi.org/10.1016/J.BMC.2009.04.041
Euphorbia factor L3 78384799 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=C)CCC4C(C4(C)C)C=C(C2=O)C)OC(=O)C)OC(=O)C 522.60 unknown https://doi.org/10.1007/BF02154248
https://doi.org/10.1016/J.BMC.2009.04.041
Euphorbia factor L7b 156599174 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=CCC4C(C4(C)C)C=C(C2=O)C)COC(=O)C)OC(=O)C)OC(=O)C 580.70 unknown https://doi.org/10.1016/J.BMC.2009.04.041
Euphorbia factor L8 10697375 Click to see CC1CC2(C(C1OC(=O)C3=CN=CC=C3)C(C(=C)CCC4C(C4(C)C)C=C(C2=O)C)OC(=O)C)OC(=O)C 523.60 unknown via CMAUP database
Euphorbiasteroid 15940183 Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C 552.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
(1aR,2S,5R,5aR,6S,8aS,9R,10aR)-1a,2,5,5a,6,9,10,10a-Octahydro-5,5a,6-trihydroxy-4-(hydroxymethyl)-1,1,7,9-tetramethyl-1H-2,8a-methanocyclopenta[a]cyclopropa[e]cyclodecen-11-one 9975051 Click to see CC1CC2C(C2(C)C)C3C=C(C(C4(C1(C3=O)C=C(C4O)C)O)O)CO 348.40 unknown via CMAUP database
(1S,5R,9S,10R,12S)-4,5,6-trihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyltetracyclo[7.5.1.01,5.010,12]pentadeca-2,7-dien-15-one 137795436 Click to see CC1CC2C(C2(C)C)C3C=C(C(C4(C1(C3=O)C=C(C4O)C)O)O)CO 348.40 unknown https://doi.org/10.1002/PCA.592
https://doi.org/10.1021/NP980218N
(4S,5R,6R,14R)-4,5,6-trihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyltetracyclo[7.5.1.01,5.010,12]pentadeca-2,7-dien-15-one 92043390 Click to see CC1CC2C(C2(C)C)C3C=C(C(C4(C1(C3=O)C=C(C4O)C)O)O)CO 348.40 unknown via CMAUP database
[(1S,2R,6S,10S,11R,13S,14R)-14-acetyloxy-1-hydroxy-8-(hydroxymethyl)-4,12,12,15-tetramethyl-5-oxo-13-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] (2Z,4E,6E)-deca-2,4,6-trienoate 6325171 Click to see CCCC=CC=CC=CC(=O)OC12C(C1(C)C)C3C=C(CC4C(C3(C(C2OC(=O)C)C)O)C=C(C4=O)C)CO 538.70 unknown via CMAUP database
[(1S,4S,5R,6R,9S,14R)-4,5,6-trihydroxy-3,11,11,14-tetramethyl-15-oxo-7-tetracyclo[7.5.1.01,5.010,12]pentadeca-2,7-dienyl]methyl hexadecanoate 5318035 Click to see CCCCCCCCCCCCCCCC(=O)OCC1=CC2C3C(C3(C)C)CC(C4(C2=O)C=C(C(C4(C1O)O)O)C)C 586.80 unknown via CMAUP database
5,5a-Dihydroxy-4-(hydroxymethyl)-1,1,7,9-tetramethyl-11-oxo-1a,2,5,5a,6,9,10,10a-octahydro-1H-2,8a-methanocyclopenta[a]cyclopropa[e][10]annulen-6-yl hexadecanoate 162684 Click to see CCCCCCCCCCCCCCCC(=O)OC1C(=CC23C1(C(C(=CC(C2=O)C4C(C4(C)C)CC3C)CO)O)O)C 586.80 unknown https://doi.org/10.1021/NP980294Q
CID 3719 3719 Click to see CC1CC2C(C2(C)C)C3C=C(C(C4(C1(C3=O)C=C(C4O)C)O)O)CO 348.40 unknown https://doi.org/10.1002/PCA.592
https://doi.org/10.1021/NP980218N
CID 463008 463008 Click to see CC1CC2C(C2(C)C)C3C=C(C(C4(C1(C3=O)C=C(C4O)C)O)O)CO 348.40 unknown via CMAUP database
Ingenol 442042 Click to see CC1CC2C(C2(C)C)C3C=C(C(C4(C1(C3=O)C=C(C4O)C)O)O)CO 348.40 unknown https://doi.org/10.1021/NP980218N
Ingenol 3-palmitate 56841025 Click to see CCCCCCCCCCCCCCCC(=O)OC1C(=CC23C1(C(C(=CC(C2=O)C4C(C4(C)C)CC3C)CO)O)O)C 586.80 unknown https://doi.org/10.1021/NP980294Q
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
17beta(H),21beta(H)-HOP-22(29)-EN-3-ONE 15560618 Click to see CC(=C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C 424.70 unknown https://doi.org/10.1016/0168-9452(91)90045-A
hopenol B 10093995 Click to see CC(=C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(95)00075-I
https://doi.org/10.1016/0168-9452(91)90045-A
Hopenone I 21603525 Click to see CC(C)C1=C2CCC3(C(C2(CC1)C)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C 424.70 unknown https://doi.org/10.1016/0168-9452(91)90045-A
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(E)-3-[(1S,3R)-3-[(2S)-3-[(R)-acetyloxy-[(3R)-3-methyl-5-oxocyclopenten-1-yl]methyl]-2-benzoyloxybut-3-enyl]-2,2-dimethylcyclopropyl]-2-methylprop-2-enoic acid 163048305 Click to see CC1CC(=O)C(=C1)C(C(=C)C(CC2C(C2(C)C)C=C(C)C(=O)O)OC(=O)C3=CC=CC=C3)OC(=O)C 494.60 unknown https://doi.org/10.1021/OL050206A
3-[3-[3-[Acetyloxy-(3-methyl-5-oxocyclopenten-1-yl)methyl]-2-benzoyloxybut-3-enyl]-2,2-dimethylcyclopropyl]-2-methylprop-2-enoic acid 75631978 Click to see CC1CC(=O)C(=C1)C(C(=C)C(CC2C(C2(C)C)C=C(C)C(=O)O)OC(=O)C3=CC=CC=C3)OC(=O)C 494.60 unknown https://doi.org/10.1021/OL050206A
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(3S,4aR,6aR,6aS,8aR,12aR,14aS,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol 11876268 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)89911-2
(4aR,6aR,6aS,8aR,12aR,14aS,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-2,4a,5,6,8,9,10,12,12a,13,14,14a-dodecahydro-1H-picen-3-one 11877465 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)89911-2
(4aR,6aR,6aS,8aR,12aS,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-2,4a,5,6,8,9,10,12,12a,13,14,14a-dodecahydro-1H-picen-3-one 392170 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1016/0168-9452(91)90045-A
4,4,6a,8a,11,11,12b,14b-Octamethyl-1,4,4a,5,6,6a,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-octadecahydro-3(2H)-picenone 500344 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(00)89911-2
Epitaraxerol 344467 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)89911-2
Taraxerone 92785 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1016/0168-9452(91)90045-A
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9R,11aR,11bS,13aS,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 162996338 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1007/BF02674142
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-9-ol 51340201 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 11870460 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(00)89911-2
(3S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 102004740 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(95)00075-I
(3S,5R,10R,13S,14S)-17-[(1R)-1,5-dimethylhex-4-enyl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 472759 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(95)00075-I
14a-(hydroxymethyl)-4,4a,6a,6b,8a,11,11-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 163019736 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)CO)C 442.70 unknown https://doi.org/10.1055/S-2007-969693
24-Methylene-24-dihydrolanosterol acetate 523636 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C 482.80 unknown https://doi.org/10.1016/0031-9422(95)00075-I
Euphol 441678 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1055901/
Lanosterol 246983 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(95)00075-I
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1055901/
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1007/BF02674142
Lup-20(29)-ene-3beta,28-diol 221023 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(00)89911-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives
(3R,3aR,5aS,5bR,7aR,11aR,11bR)-3a,5a,5b,8,8,11a-hexamethyl-3-propan-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13-dodecahydro-1H-cyclopenta[a]chrysen-9-one 101277259 Click to see CC(C)C1CCC2=C3CCC4C5(CCC(=O)C(C5CCC4(C3(CCC12C)C)C)(C)C)C 424.70 unknown https://doi.org/10.1016/0168-9452(91)90045-A
Hancockinol 14757777 Click to see CC(C)C1CCC2(C1C3(CCC4(C5CCC(C(C5=CCC4C3(CC2)C)(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0168-9452(91)90045-A
Simiarenone 10410123 Click to see CC(C)C1CCC2C1(CCC3(C2(CCC4(C3CC=C5C4CCC(=O)C5(C)C)C)C)C)C 424.70 unknown https://doi.org/10.1016/0168-9452(91)90045-A
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown https://doi.org/10.1016/0168-9452(91)90045-A
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 145925700 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1055901/
https://doi.org/10.1016/0031-9422(95)00075-I
7,7,12,16-Tetramethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.01,3.03,8.012,16]octadec-8-en-6-ol 162820419 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CC=C5C3(C4)CCC(C5(C)C)O)C)C 438.70 unknown https://doi.org/10.1016/0031-9422(95)00075-I
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1055901/
Cycloartenol 92110 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1055901/
https://doi.org/10.1016/0031-9422(95)00075-I
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0168-9452(91)90045-A
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0168-9452(91)90045-A
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)89911-2
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0168-9452(91)90045-A
https://doi.org/10.1016/S0031-9422(00)89911-2
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0168-9452(91)90045-A
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Fucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0168-9452(91)90045-A
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0168-9452(91)90045-A
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
Levodopa 6047 Click to see C1=CC(=C(C=C1CC(C(=O)O)N)O)O 197.19 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
(1,11-Diacetyloxy-13-benzoyloxy-3,14-dimethyl-10-methylidene-9-tricyclo[10.3.0.05,7]pentadec-3-enyl) pyridine-3-carboxylate 162980594 Click to see CC1CC2(CC(=CC3CC3CC(C(=C)C(C2C1OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C5=CN=CC=C5)C)OC(=O)C 601.70 unknown https://doi.org/10.1016/0031-9422(90)85062-K
[(1S,3E,5S,7S,9S,11R,12R,13S,14S)-1,11-diacetyloxy-13-benzoyloxy-3,14-dimethyl-10-methylidene-9-tricyclo[10.3.0.05,7]pentadec-3-enyl] pyridine-3-carboxylate 163187846 Click to see CC1CC2(CC(=CC3CC3CC(C(=C)C(C2C1OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C5=CN=CC=C5)C)OC(=O)C 601.70 unknown https://doi.org/10.1016/0031-9422(90)85062-K
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(3E)-3-hexa-2,4-diynylidenespiro[4.4]non-1-ene-4,9-dione 5318038 Click to see CC#CC#CC=C1C=CC2(C1=O)CCCC2=O 224.25 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
[(8bS)-4,8b-dimethyl-3-(methylcarbamoyl)-2,3a-dihydro-1H-pyrrolo[2,3-b]indol-7-yl] N-methylcarbamate 3083935 Click to see CC12CCN(C1N(C3=C2C=C(C=C3)OC(=O)NC)C)C(=O)NC 318.37 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(S)-Laudanine 821396 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)OC)OC 343.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
[(1R,3E,5R,7S,11Z,13S,14S,15S)-1-acetyloxy-11-(acetyloxymethyl)-3,6,6,15-tetramethyl-2-oxo-14-tricyclo[11.3.0.05,7]hexadeca-3,11-dienyl] (E)-3-phenylprop-2-enoate 163186698 Click to see CC1CC2(C(C1OC(=O)C=CC3=CC=CC=C3)C=C(CCCC4C(C4(C)C)C=C(C2=O)C)COC(=O)C)OC(=O)C 562.70 unknown https://doi.org/10.1016/S0031-9422(00)80486-0
[1-Acetyloxy-11-(acetyloxymethyl)-3,6,6,15-tetramethyl-2-oxo-14-tricyclo[11.3.0.05,7]hexadeca-3,11-dienyl] 3-phenylprop-2-enoate 162854362 Click to see CC1CC2(C(C1OC(=O)C=CC3=CC=CC=C3)C=C(CCCC4C(C4(C)C)C=C(C2=O)C)COC(=O)C)OC(=O)C 562.70 unknown https://doi.org/10.1016/S0031-9422(00)80486-0
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Daphnetin-8-glucoside 5316301 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
Esculin hydrate 16211025 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O.O 358.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 4-hydroxycoumarins
4,8-Dihydroxy-2H-chromen-2-one 54719604 Click to see C1=CC2=C(C(=C1)O)OC(=O)C=C2O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1271/BBB.67.631
https://doi.org/10.1021/NP0203537
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Daphnetin 5280569 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Kaempferol 3-glucuronide 5318759 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O 462.40 unknown https://doi.org/10.1515/ZNB-1969-0323
Kaempferol-3-O-glucuronoside 14185731 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O 462.40 unknown https://doi.org/10.1515/ZNB-1969-0323

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