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Croton cajucara

Table of Contents

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

Details Top

Internal ID UUID6440366da87ee936978931
Scientific name Croton cajucara
Authority Benth.
First published in Hooker's J. Bot. Kew Gard. Misc. 6: 376 (1854)

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.

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General Uses Top

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Common products:
The principal commercial product is leaf-derived essential oil, rich in linalool and 1,8-cineole, produced and traded for fragrance and flavor uses.

Fragrance and cosmetics:
The oil is used as a fragrance material in perfumes and related products, attributed to its linalool/1,8-cineole profile and pleasant aroma; it is employed by the Brazilian fragrance and flavor industry.

Food and beverages (non-medicinal):
Cajucara leaves are used as a culinary herb and spice in Amazonian cuisines and processed foods, providing aromatic flavor in regional dishes and food products.

Scientific/model use:
The species is a taxonomic model in systematics and chemotaxonomy studies focusing on Croton (Euphorbiaceae); phytochemical profiles (GC-MS datasets) are deposited as reference data in chemoinformatics resources.

Properties relevant to use:
Essential oil yield ranges up to ~1.5% (air-dried leaves). Major components: linalool (~20–60%) and 1,8-cineole (~10–50%), supporting its adoption as a fragrance/flavoring material.

Standards and regulation:
Leaf essential oil is produced commercially but not covered by international perfume standards; any food use is governed by national/regional food additive regulations in Brazil.

Sustainability and sourcing:
Leaves are harvested from cultivated shrubs and wild populations; sustainable collection practices are needed to mitigate pressure on wild stands in Amazonia.

Synonyms Top

Scientific name Authority First published in
Oxydectes cajucara Kuntze Revis. Gen. Pl. 2: 611 (1891)
Croton seputubensis Hoehne Exped. Rosevelt-Rondon, Bot. : 53 (1914)
Croton motilonorum Croizat Mem. Soc. Ci. Nat. La Salle 10: 126 (1950)

Common names Top

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No common names added yet.

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil West-central
    • Northern South America
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000927525
Tropicos 12800827
INPN 779392
KEW urn:lsid:ipni.org:names:342205-1
The Plant List kew-49493
Open Tree Of Life 426179
Observations.org 324162
NCBI Taxonomy 323033
IUCN Red List 180073678
IPNI 342205-1
GBIF 3060105
EOL 1147408
Elurikkus 359745
USDA GRIN 417497
CMAUP NPO19035

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
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
Red sacaca essential oil-loaded nanostructured lipid carriers optimized by factorial design: cytotoxicity and cellular reactive oxygen species levels Chura SS, Memória KA, Lopes AT, Pelissari FM, Da Silveira JV, Bezerra JD, Chaves FC, Rodrigues AP, Faria JA, Carneiro G Front Pharmacol 11-Oct-2023
PMCID:PMC10598706
doi:10.3389/fphar.2023.1176629
PMID:37886132
Construction and Performance Evaluation of Nicandra physalodes (Linn.) Gaertn. Polysaccharide-Based Nanogel Liu F, Shen C, Chen X, Gao F, Chen Y Polymers (Basel) 19-Apr-2023
PMCID:PMC10143989
doi:10.3390/polym15081933
PMID:37112079
Chemistry and Bioactivity of Croton Essential Oils: Literature Survey and Croton hirtus from Vietnam Luu-dam NA, Le CV, Satyal P, Le TM, Bui VH, Vo VH, Ngo GH, Bui TC, Nguyen HH, Setzer WN Molecules 03-Mar-2023
PMCID:PMC10005233
doi:10.3390/molecules28052361
PMID:36903605
Potential Pharmacokinetic Interactions of Common Cardiovascular Drugs and Selected European and Latin American Herbal Medicines: A Scoping Review Prieto-Garcia JM, Graham L, Alkhabbaz O, Mazzari AL Plants (Basel) 31-Jan-2023
PMCID:PMC9920503
doi:10.3390/plants12030623
PMID:36771707
Chemical Composition and In Vitro and In Silico Antileishmanial Evaluation of the Essential Oil from Croton linearis Jacq. Stems García-Díaz J, Escalona-Arranz JC, Ochoa-Pacheco A, Santos SG, González-Fernández R, Rojas-Vargas JA, Monzote L, Setzer WN Antibiotics (Basel) 28-Nov-2022
PMCID:PMC9774621
doi:10.3390/antibiotics11121712
PMID:36551370
Phytochemical Screening and Isolation of New Ent-Clerodane Diterpenoids from Croton guatemalensis Lotsy Escandón-Rivera SM, Andrade-Cetto A, Rosas-Ramírez DG, Arreguín-Espinosa R Plants (Basel) 18-Nov-2022
PMCID:PMC9692395
doi:10.3390/plants11223159
PMID:36432893
Sustainable Extraction, Chemical Profile, Cytotoxic and Antileishmanial Activities In-Vitro of Some Citrus Species Leaves Essential Oils Bouabdallah S, Cianfaglione K, Azzouz M, Batiha GE, Alkhuriji AF, Al-Megrin WA, Ben-Attia M, Eldahshan OA Pharmaceuticals (Basel) 19-Sep-2022
PMCID:PMC9501829
doi:10.3390/ph15091163
PMID:36145384
Natural Compounds: A Hopeful Promise as an Antibiofilm Agent Against Candida Species Shariati A, Didehdar M, Razavi S, Heidary M, Soroush F, Chegini Z Front Pharmacol 11-Jul-2022
PMCID:PMC9309813
doi:10.3389/fphar.2022.917787
PMID:35899117
Essential Oil of the Plants Growing in the Brazilian Amazon: Chemical Composition, Antioxidants, and Biological Applications Ferreira OO, Cruz JN, de Moraes ÂA, de Jesus Pereira Franco C, Lima RR, dos Anjos TO, Siqueira GM, do Nascimento LD, Cascaes MM, de Oliveira MS, Andrade EH Molecules 08-Jul-2022
PMCID:PMC9318482
doi:10.3390/molecules27144373
PMID:35889245
Croton urucurana Baill. Ameliorates Metabolic Associated Fatty Liver Disease in Rats Auth PA, da Silva GR, Amaral EC, Bortoli VF, Manzano MI, de Souza LM, Lovato EC, Ribeiro-Paes JT, Gasparotto Junior A, Lívero FA Front Pharmacol 20-May-2022
PMCID:PMC9164250
doi:10.3389/fphar.2022.886122
PMID:35668935
Herb-Induced Liver Injury—A Challenging Diagnosis Nunes DR, Monteiro CS, dos Santos JL Healthcare (Basel) 31-Jan-2022
PMCID:PMC8872293
doi:10.3390/healthcare10020278
PMID:35206892
(-)-Carveol Prevents Gastric Ulcers via Cytoprotective, Antioxidant, Antisecretory and Immunoregulatory Mechanisms in Animal Models Serafim CA, Araruna ME, Alves Júnior EB, Silva LM, Silva AO, da Silva MS, Alves AF, Araújo AA, Batista LM Front Pharmacol 23-Aug-2021
PMCID:PMC8419343
doi:10.3389/fphar.2021.736829
PMID:34497525
The Search for Putative Hits in Combating Leishmaniasis: The Contributions of Natural Products Over the Last Decade Sakyi PO, Amewu RK, Devine RN, Ismaila E, Miller WA, Kwofie SK Nat Prod Bioprospect 14-Jul-2021
PMCID:PMC8279035
doi:10.1007/s13659-021-00311-2
PMID:34260050
The Potential of Traditional Knowledge to Develop Effective Medicines for the Treatment of Leishmaniasis Passero LF, Brunelli ED, Sauini T, Amorim Pavani TF, Jesus JA, Rodrigues E Front Pharmacol 08-Jun-2021
PMCID:PMC8248671
doi:10.3389/fphar.2021.690432
PMID:34220515

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
methyl (1R,2R,4aS,8aS)-1-[2-(furan-3-yl)ethyl]-2,5-dimethyl-7-oxo-2,3,4,4a,8,8a-hexahydronaphthalene-1-carboxylate 14588306 Click to see 330.40 unknown https://doi.org/10.1016/S0031-9422(98)00163-0
https://doi.org/10.1248/CPB.38.701
methyl (1R,2R,4aS,8aS)-4a-formyl-1-[2-(furan-3-yl)ethyl]-2,5-dimethyl-7-oxo-3,4,8,8a-tetrahydro-2H-naphthalene-1-carboxylate 14588304 Click to see 358.40 unknown https://doi.org/10.1248/CPB.38.701
Methyl 1-[2-(furan-3-yl)ethyl]-2,5-dimethyl-7-oxo-2,3,4,4a,8,8a-hexahydronaphthalene-1-carboxylate 14588305 Click to see 330.40 unknown https://doi.org/10.1248/CPB.38.701
https://doi.org/10.1016/S0031-9422(98)00163-0
methyl 4a-formyl-1-[2-(furan-3-yl)ethyl]-2,5-dimethyl-7-oxo-3,4,8,8a-tetrahydro-2H-naphthalene-1-carboxylate 14588303 Click to see 358.40 unknown https://doi.org/10.1248/CPB.38.701
trans-Cajucarin B 637430 Click to see 330.40 unknown https://doi.org/10.1016/S0031-9422(98)00163-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.2000.9712196
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC155815/
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.2000.9712196
Nerolidol 5284507 Click to see 222.37 unknown https://doi.org/10.1080/10412905.2000.9712196
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
3-Acetylaleuritolic Acid 161616 Click to see 498.70 unknown https://doi.org/10.1016/S0031-9422(98)00163-0
https://doi.org/10.1590/S0102-695X2007000400008
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 21591284 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(C(OC3OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(C(O9)C(=O)O)O)O)OC1C(C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)C)O)O)O)C)(C)C)CO)O)O)C)O)O)O 1395.50 unknown via CMAUP database
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 21591283 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(C(OC3OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)OC9C(C(C(C(O9)C(=O)O)O)O)OC1C(C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)C)O)O)O)C)(C)C)CO)O)O)C)O)O)O 1411.50 unknown via CMAUP database
(3beta,4beta)-28-[[2-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-23-hydroxy-28-oxoolean-12-en-3-yl O-6-deoxy-alpha-L-mannopyranosyl-(1-->2)-O-beta-D-galactopyranosyl-(1-->2)-beta-D-glucopyranosiduronic acid 101944852 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8)(C)C)C(=O)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)C)O)O)O)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 1265.40 unknown via CMAUP database
(3I(2))-28-(I(2)-D-Glucopyranosyloxy)-28-oxoolean-12-en-3-yl O-6-deoxy-I+/--L-mannopyranosyl-(1a2)-O-I(2)-D-galactopyranosyl-(1a2)-I(2)-D-glucopyranosiduronic acid 101944851 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)C)CCC6(C5CC=C7C6(CCC8(C7CC(CC8)(C)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 1103.20 unknown via CMAUP database
Chikusetsusaponin Iva 13909684 Click to see 795.00 unknown via CMAUP database
Lablaboside B 21591281 Click to see 1119.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1S,6R,7R,13R)-7-[2-(furan-3-yl)ethyl]-2,13-dimethyl-9-oxatricyclo[5.3.3.01,6]tridec-2-ene-4,10-dione 11232710 Click to see 328.40 unknown https://doi.org/10.1016/S0031-9422(98)00163-0
(1S,6S,7R,13R)-7-[2-(furan-3-yl)ethyl]-2,13-dimethyl-9-oxatricyclo[5.3.3.01,6]tridec-2-ene-4,8-dione 10969517 Click to see 328.40 unknown https://doi.org/10.1016/S0031-9422(98)00163-0
(4aR,5'R,7R,8aS)-5'-(furan-3-yl)-4,7-dimethylspiro[1,4a,5,6,7,8a-hexahydronaphthalene-8,3'-oxolane]-2,2'-dione 403560 Click to see 314.40 unknown https://doi.org/10.1016/J.EJPHAR.2004.01.027
(4aR,5'R,7R,8R,8aS)-5'-(2-hydroxy-5-oxo-2H-furan-3-yl)-4,7-dimethylspiro[1,4a,5,6,7,8a-hexahydronaphthalene-8,3'-oxolane]-2,2'-dione 16664971 Click to see 346.40 unknown https://doi.org/10.1055/S-2006-961547
(4aR,5'R,7R,8R,8aS)-5'-(2-hydroxy-5-oxo-2H-furan-4-yl)-4,7-dimethylspiro[1,4a,5,6,7,8a-hexahydronaphthalene-8,3'-oxolane]-2,2'-dione 16664972 Click to see CC1CCC2C(C13CC(OC3=O)C4=CC(OC4=O)O)CC(=O)C=C2C 346.40 unknown https://doi.org/10.1055/S-2006-961547
https://doi.org/10.1016/S0378-8741(99)00159-2
https://doi.org/10.1016/S0031-9422(98)00163-0
(4aR,5'R,7R,8R,8aS)-5'-[(2R)-2-hydroxy-5-oxo-2H-furan-4-yl]-4,7-dimethylspiro[1,4a,5,6,7,8a-hexahydronaphthalene-8,3'-oxolane]-2,2'-dione 102588560 Click to see 346.40 unknown https://doi.org/10.1016/S0031-9422(98)00163-0
(4aR,5'S,7R,8R,8aR)-5'-[(2R)-2-hydroxy-5-oxo-2H-furan-4-yl]-4,7-dimethylspiro[1,4a,5,6,7,8a-hexahydronaphthalene-8,3'-oxolane]-2,2'-dione 162881748 Click to see 346.40 unknown https://doi.org/10.1016/S0031-9422(98)00163-0
(4aS,5'R,7R,8R,8aS)-5'-(furan-3-yl)-4,7-dimethylspiro[1,4a,5,6,7,8a-hexahydronaphthalene-8,3'-oxolane]-2,2'-dione 101616216 Click to see 314.40 unknown https://doi.org/10.1016/0031-9422(91)85096-I
(4R,4aS,5'R,7R,8R,8aS)-5'-(furan-3-yl)-4,7-dimethylspiro[1,3,4,4a,5,6,7,8a-octahydronaphthalene-8,3'-oxolane]-2,2'-dione 10041455 Click to see 316.40 unknown https://doi.org/10.1248/BPB.25.452
https://doi.org/10.1016/S0031-9422(00)97821-X
https://doi.org/10.1016/S0031-9422(98)00163-0
5'-(Furan-3-yl)-4,7-dimethylspiro[1,3,4,4a,5,6,7,8a-octahydronaphthalene-8,3'-oxolane]-2,2'-dione 12304149 Click to see 316.40 unknown https://doi.org/10.1248/BPB.25.452
5'-(Furan-3-yl)-4,7-dimethylspiro[1,4a,5,6,7,8a-hexahydronaphthalene-8,3'-oxolane]-2,2'-dione 14313505 Click to see CC1CCC2C(C13CC(OC3=O)C4=COC=C4)CC(=O)C=C2C 314.40 unknown https://doi.org/10.1016/S0031-9422(98)00163-0
https://doi.org/10.1016/S0300-483X(00)00417-0
https://doi.org/10.1055/S-1999-14042
https://doi.org/10.1055/S-2006-957925
https://doi.org/10.1055/S-2006-957388
https://doi.org/10.1002/(SICI)1520-6866(1999)19:6<377::AID-TCM2>3.0.CO;2-T
https://doi.org/10.1016/J.EJPHAR.2004.01.027
https://doi.org/10.1016/0031-9422(91)85096-I
https://doi.org/10.1055/S-2006-957766
7-[2-(Furan-3-yl)ethyl]-2,13-dimethyl-9-oxatricyclo[5.3.3.01,6]tridec-2-ene-4,10-dione 72761771 Click to see 328.40 unknown https://doi.org/10.1016/S0031-9422(98)00163-0
Cajucarinolide 3035811 Click to see CC1CCC2C(C13CC(OC3=O)C4=CC(OC4=O)O)CC(=O)C=C2C 346.40 unknown https://doi.org/10.1055/S-2006-961547
https://doi.org/10.1016/S0378-8741(99)00159-2
https://doi.org/10.1016/S0031-9422(98)00163-0
Dehydrocrotonin 156089 Click to see 314.40 unknown https://doi.org/10.1016/S0031-9422(00)97821-X
Sacacarin 16056021 Click to see 328.40 unknown https://doi.org/10.1016/S0031-9422(98)00163-0
trans-Dehydrocrotonin 10403368 Click to see 314.40 unknown https://doi.org/10.1055/S-2006-957388
https://doi.org/10.1016/S0378-8741(99)00159-2
https://doi.org/10.1016/S0300-483X(00)00417-0
https://doi.org/10.1016/S0031-9422(98)00163-0
https://doi.org/10.1055/S-2006-957766
https://doi.org/10.1055/S-2006-957925
https://doi.org/10.1002/(SICI)1520-6866(1999)19:6<377::AID-TCM2>3.0.CO;2-T
https://doi.org/10.1016/0031-9422(91)85096-I
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
alpha-Carotene 6419725 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Tetrahydroxy bile acids, alcohols and derivatives
(2R,3S,5S,8S,9S,10R,13S,14S,17R)-17-[(2S,3R,4R)-3,4-Dihydroxy-6-methyl-5-methylideneheptan-2-yl]-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 10983436 Click to see CC(C)C(=C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 462.70 unknown via CMAUP database
Castasterone 133534 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 464.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Brassinolides and derivatives
28-Homodolicholide 13517132 Click to see 492.70 unknown via CMAUP database
Brassinolide 115196 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2COC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 480.70 unknown via CMAUP database
Dolicholide 11038144 Click to see CC(C)C(=C)C(C(C(C)C1CCC2C1(CCC3C2COC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 478.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3S,5S,8S,9S,10R,13S,14S,17R)-17-[(E,2S,3R,4R)-3,4-dihydroxy-5-propan-2-ylhept-5-en-2-yl]-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 14607933 Click to see CC=C(C(C)C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 476.70 unknown via CMAUP database
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/S0378-8741(99)00159-2
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0378-8741(99)00159-2
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0378-8741(99)00159-2
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0378-8741(99)00159-2
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/S0378-8741(99)00159-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / D-alpha-amino acids
(2R)-piperidin-1-ium-2-carboxylate 6931662 Click to see 129.16 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(4aS,6aR,6bR,8aS,10S,12aR,14aS,14bR)-10-acetyloxy-2,2,9,9,12a,14a-hexamethyl-3,4,5,6a,6b,7,8,8a,10,11,12,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 162894165 Click to see 484.70 unknown https://doi.org/10.1016/J.MOLSTRUC.2007.10.018
10-acetyloxy-2,2,9,9,12a,14a-hexamethyl-3,4,5,6a,6b,7,8,8a,10,11,12,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 162894164 Click to see 484.70 unknown https://doi.org/10.1016/J.MOLSTRUC.2007.10.018
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines / 6-alkylaminopurines
trans-Zeatin 449093 Click to see CC(=CCNC1=NC=NC2=C1NC=N2)CO 219.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown https://doi.org/10.1016/S0378-8741(99)00159-2

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