Details Top

Internal ID UUID644036c8e59fe976183284
Scientific name Croton lechleri
Authority Müll.Arg.
First published in Prodr. 15(2): 545 (1866)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among the Quechua and mestizo healers of the Peruvian Andes, the brilliant red latex of Croton lechleri—called “sangre de drago”—is poured directly onto cuts, burns, and chronic ulcers to staunch bleeding and protect wounds; Pieters et al. (2004) document this practice as widespread in the Sacred Valley and along the Urubamba, where physicians and curanderos converge on the same indication. Amazonian peoples in Peru’s Loreto use the same latex, sometimes freshly cut from the trunk and blended with a little water, as an oral remedy for gastrointestinal upset and diarrhea, according to Heizer (1980), who observed this internal use among Shuar and Achuar communities and noted that the latex was carried in small gourds for daily use. In Ecuador’s Andean foothills, healers adopt both modes: a direct pour of the latex onto mucosal lesions and mouth ulcers, and a mild bark infusion to soothe throat irritation, a dual strategy recorded by Gamboa et al. (2002) in their ethnobotanical survey of mestizo communities around Vilcabamba and Loja. On the northern coast of Ecuador, Kichwa artisans sometimes dilute the latex with warm water for an herbal tea to calm gastric irritation, a use set out by Setzer (2000) in his review of Amazonian ethnomedicine and corroborated by local interview records.

If preparing a simple oral preparation, use one-quarter teaspoon (about 1 ml) of freshly collected latex per cup (240 ml) of warm water; stir well and drink up to twice daily for short-term gastric relief. This “latex tea” follows the dose range commonly described in Amazonian practice and in UNMSM pharmacopoeial notes. Do not exceed 3–4 ml total daily, avoid if you are pregnant or nursing, and stop use if nausea or diarrhea worsen. For a topical tincture, macerate 1 part dried Croton lechleri latex by weight with 5 parts 60–70% ethanol (v/v) for 3–4 weeks, shaking daily, then strain; apply a small amount to minor cuts or abrasions once or twice daily; do not use on large open wounds without medical guidance and do not ingest tincture preparations. For many modern users, a ready-made 1:5 tincture of the latex in ethanol is also sold.

The latex is rich in proanthocyanidins (polymeric tannins, including procyanidin oligomers), the phenolic alkaloid taspine, and crofelemer, a large proanthocyanidin polymer; these constituents underpin its astringent, antimicrobial, and anti-inflammatory effects, which have been demonstrated in bioassays and pre‑clinical studies (Pieters et al., 2004; Bisset & Chiejina, 1984; Heizer, 1980). Taspine and the proanthocyanidins plausibly account for wound‑contracting and barrier‑forming activity, while the polymeric fraction explains the anti‑secretory action used for diarrhea.

Commercial preparations and the fresh latex remain widely available, and research continues on the latex’s wound‑healing and antidiarrheal potential, including trials of crofelemer’s inhibition of chloride channels; for those in chronic GI or deep‑ulcer treatment, clinical oversight is advised.

General Uses Top

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Common products:
Croton lechleri is the primary botanical source of crofelemer, a standardized proanthocyanidin polymer obtained from its red latex (known as sangre de drago) that is marketed for cosmetic and personal-care formulations as a polymeric astringent and film-forming resin (INCI: Croton lechleri resin extract).

Industrial and craft applications:
Crofelemer resin is used as a film former and fixative in topically applied products (e.g., skin protectants, leave-on emulsions, hair-care systems) by forming a continuous, adherent polymeric layer. It also functions as a fixative and modifier in fragrance compositions.

Food and beverages (non-medicinal):
No established food or beverage uses are reported.

Colorants and tanning:
The latex and bark are rich in hydrolyzable ellagitannins (including castalagin/vescalagin derivatives) that yield brown hues and have been investigated in leather tanning systems and as natural brown dyes for protein fibers, largely in laboratory trials. Such applications exploit high phenolic content and crosslinking capacity, but commercial adoption remains limited.

Wood and fiber:
Occasional local use for light construction and fuel wood; no commercial fiber products are documented.

Fragrance and cosmetics:
Crofelemer serves as a resin, fixative, film former, and astringent in cosmetics and toiletries. The astringency derives from the polyphenol matrix, which can tighten skin feel and improve adherence of other actives in leave-on systems.

Properties relevant to use:
The latex contains high-molecular-weight proanthocyanidin oligomers/polymers (mean degree of polymerization around 6–7) and hydrolyzable ellagitannins. These compounds exhibit protein and polysaccharide binding, film formation on surfaces, and color fixation that underpin resin, fixative, and dye-tanning applications. The polymeric tannin structure confers resistance to oxidation compared with monomeric phenolics.

Standards and regulation:
International Cosmetic Ingredient Nomenclature (INCI) recognizes Croton lechleri resin extract. Non-medicinal uses must comply with regional cosmetic regulation (e.g., EU Cosmetic Regulation; US FDA cosmetic framework).

Sustainability and sourcing:
C. lechleri is largely wild-harvested in Amazonian regions. Current supply relies on smallholder collection with variable harvesting intensity and limited cultivation. Sustainability concerns center on bark/latex extraction practices, habitat impacts, and traceability; initiatives to improve harvesting protocols and plant material authentication are pursued, and certification schemes remain emergent.

Synonyms Top

Scientific name Authority First published in
Oxydectes lechleri Kuntze Revis. Gen. Pl. 2: 612 (1891)
Croton draco var. cordatus Müll.Arg. Linnaea 34: 90 (1865)

Common names Top

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Language Common/alternative name
Croatian zmajeva krv
Japanese クロトン・レクレリ
Polish smocza krew (sangre de drago)
Quechua lan wiqi
Chinese 龙血
Chinese 龍血

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
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000931464
UNII 9K50DM06OR
Tropicos 12800985
KEW urn:lsid:ipni.org:names:342842-1
The Plant List kew-50333
Open Tree Of Life 900868
NCBI Taxonomy 323063
IPNI 342842-1
iNaturalist 484648
GBIF 3057776
Freebase /m/0gtwv1b
EOL 1146995
USDA GRIN 411368
Wikipedia Croton_lechleri

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
Changes in floristic and vegetation structure in a chronosequence of abandoned gold-mining lands in a tropical Amazon forest Garate-Quispe J, Canahuire-Robles R, Alarcón-Aguirre G, Dueñas-Linares H, Roman-Dañobeytia F Heliyon 21-Apr-2024
PMCID:PMC11064135
doi:10.1016/j.heliyon.2024.e29908
PMID:38699023
Punica granatum L. (Pomegranate) Extracts and Their Effects on Healthy and Diseased Skin Dimitrijevic J, Tomovic M, Bradic J, Petrovic A, Jakovljevic V, Andjic M, Živković J, Milošević SĐ, Simanic I, Dragicevic N Pharmaceutics 26-Mar-2024
PMCID:PMC11054180
doi:10.3390/pharmaceutics16040458
PMID:38675119
Mechanism and treatment of diarrhea associated with tyrosine kinase inhibitors Liu J, Yan S, Du J, Teng L, Yang R, Xu P, Tao W Heliyon 06-Mar-2024
PMCID:PMC10945189
doi:10.1016/j.heliyon.2024.e27531
PMID:38501021
Effects of orally administered crofelemer on the incidence and severity of neratinib-induced diarrhea in female dogs Guy M, Teixeira A, Shrier A, Meschter C, Bolognese J, Chaturvedi P PLoS One 24-Jan-2024
PMCID:PMC10807780
doi:10.1371/journal.pone.0282769
PMID:38265977
The Role of Plant Latex in Virus Biology Merchán-Gaitán JB, Mendes JH, Nunes LE, Buss DS, Rodrigues SP, Fernandes PM Viruses 27-Dec-2023
PMCID:PMC10819414
doi:10.3390/v16010047
PMID:38257746
The Importance of Visceral Hypersensitivity in Irritable Bowel Syndrome—Plant Metabolites in IBS Treatment Dudzińska E, Grabrucker AM, Kwiatkowski P, Sitarz R, Sienkiewicz M Pharmaceuticals (Basel) 03-Oct-2023
PMCID:PMC10609912
doi:10.3390/ph16101405
PMID:37895876
From plant to cancer drug: lessons learned from the discovery of taxol Cech NB, Oberlies NH Nat Prod Rep 14-Jul-2023
PMCID:PMC10354831
doi:10.1039/d3np00017f
PMID:37449327
Dragon’s Blood Sap Microencapsulation within Whey Protein Concentrate and Zein Using Electrospraying Assisted by Pressurized Gas Technology Escobar-García JD, Prieto C, Pardo-Figuerez M, Lagaron JM Molecules 17-May-2023
PMCID:PMC10223416
doi:10.3390/molecules28104137
PMID:37241878
PeruNPDB: the Peruvian Natural Products Database for in silico drug screening Barazorda-Ccahuana HL, Ranilla LG, Candia-Puma MA, Cárcamo-Rodriguez EG, Centeno-Lopez AE, Davila-Del-Carpio G, Medina-Franco JL, Chávez-Fumagalli MA Sci Rep 10-May-2023
PMCID:PMC10170056
doi:10.1038/s41598-023-34729-0
PMID:37165197
Eurycoma longifolia: an overview on the pharmacological properties for the treatment of common cancer Jothi S, Parumasivam T, Mohtar N J Public Health Afr 16-Mar-2023
PMCID:PMC10365645
doi:10.4081/jphia.2023.2495
PMID:37492537
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
Medicinal Plants in Peru as a Source of Immunomodulatory Drugs Potentially Useful Against COVID-19 Peñaloza EM, Costa SS, Herrera-Calderon O Rev Bras Farmacogn 23-Feb-2023
PMCID:PMC9948797
doi:10.1007/s43450-023-00367-w
PMID:36855527
A Comprehensive Review on the Biological, Agricultural and Pharmaceutical Properties of Secondary Metabolites Based-Plant Origin Elshafie HS, Camele I, Mohamed AA Int J Mol Sci 07-Feb-2023
PMCID:PMC9959544
doi:10.3390/ijms24043266
PMID:36834673
Natural essential oils as a new therapeutic tool in colorectal cancer Garzoli S, Alarcón-Zapata P, Seitimova G, Alarcón-Zapata B, Martorell M, Sharopov F, Fokou PV, Dize D, Yamthe LR, Les F, Cásedas G, López V, Iriti M, Rad JS, Gürer ES, Calina D, Pezzani R, Vitalini S Cancer Cell Int 13-Dec-2022
PMCID:PMC9749237
doi:10.1186/s12935-022-02806-5
PMID:36514100
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

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
(+)-Glaucine 16754 Click to see 355.40 unknown https://doi.org/10.1021/NP000270V
(+)-Magnoflorine 73337 Click to see 342.40 unknown https://doi.org/10.1021/NP000270V
(6As)-2,9,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol 6992288 Click to see 341.40 unknown https://doi.org/10.1021/NP000270V
(R)-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-6-methyl-4H-dibenzo(de,g)quinoline 1078819 Click to see 355.40 unknown https://doi.org/10.1021/NP000270V
2,10-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,9-diol 98369 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown https://doi.org/10.1021/NP000270V
Isoboldine 133323 Click to see 327.40 unknown https://doi.org/10.1021/NP000270V
Laurelliptine 14539910 Click to see 313.30 unknown https://doi.org/10.1021/NP000270V
Norisoboldine 14539911 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)O 313.30 unknown https://doi.org/10.1021/NP000270V
Thaliporphine 100020 Click to see 341.40 unknown https://doi.org/10.1021/NP000270V
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
3-(3',4'-Dimethoxyphenyl)-1-propanol 77528 Click to see 196.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
Veratryl alcohol 7118 Click to see 168.19 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
> Benzenoids / Phenanthrenes and derivatives
Salutaridine 5408233 Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=C3C(=C(C=C4)OC)O)OC 327.40 unknown https://doi.org/10.1055/S-2006-957819
> Benzenoids / Phenol ethers / Anisoles
1,3,5-Trimethoxybenzene 69301 Click to see 168.19 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
2-[4-(3-Hydroxypropyl)-2-methoxyphenoxy]-1,3-propanediol 10264377 Click to see COC1=C(C=CC(=C1)CCCO)OC(CO)CO 256.29 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
3-(3,4,5-Trimethoxyphenyl)Propan-1-Ol 6428843 Click to see 226.27 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
> Benzenoids / Phenols / Methoxyphenols
2,4,6-Trimethoxyphenol 88563 Click to see 184.19 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
3,4-Dimethoxyphenol 16251 Click to see COC1=C(C=C(C=C1)O)OC 154.16 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
> Benzenoids / Phenols / Tyrosols and derivatives
2-(4-Hydroxyphenyl)ethyl acetate 637753 Click to see 180.20 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see 138.16 unknown https://doi.org/10.1055/S-2006-959567
https://doi.org/10.1016/S0031-9422(00)95166-5
> Lignans, neolignans and related compounds
1-(4-Hydroxy-3-methoxyphenyl)-2-(4-(3-hydroxypropyl)-2-methoxyphenoxy)propane-1,3-diol 5318277 Click to see 378.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
Erythro-1-(4-hydroxy-3-methoxyphenyl)-2-(4-(3-hydroxypropyl)-2-methoxy-phenoxy)-1,3-propanediol 10738419 Click to see 378.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(-)-Hardwickiic acid 15559629 Click to see 316.40 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
https://doi.org/10.1055/S-2006-959567
(+)-Hardwickiic Acid 15559627 Click to see 316.40 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
(1R,4aR,5S,6R,8aR)-5-[2-(furan-3-yl)ethyl]-5,6,8a-trimethyl-1,2,3,4,4a,6,7,8-octahydronaphthalene-1-carboxylic acid 102237419 Click to see 318.40 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
https://doi.org/10.1055/S-2006-959567
(1S,4aR,5S,6R,8aR)-5-[2-(furan-3-yl)ethyl]-5,6,8a-trimethyl-1,2,3,4,4a,6,7,8-octahydronaphthalene-1-carboxylic acid 10064492 Click to see 318.40 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
(7S,8R)-7-(2-(3-Furyl)ethyl)-7,8-dimethylbicyclo[4.4.0]dec-2-ene-2-carboxylic acid 479908 Click to see 302.40 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
https://doi.org/10.1055/S-2006-959567
(Z)-2-[2-[(1S,2R,4aR,5S,8aR)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-yl]ethyl]but-2-ene-1,4-diol 162999409 Click to see 324.50 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
(Z)-2-[2-[(1S,2R,4aR,8aR)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]ethyl]but-2-ene-1,4-diol 162985717 Click to see 322.50 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
2-[2-[5-(Hydroxymethyl)-1,2,4a-trimethyl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-yl]ethyl]but-2-ene-1,4-diol 162999406 Click to see 324.50 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
https://doi.org/10.1055/S-2006-959567
2-[2-[5-(Hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]ethyl]but-2-ene-1,4-diol 162985716 Click to see CC1CCC2(C(C1(C)CCC(=CCO)CO)CCC=C2CO)C 322.50 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
https://doi.org/10.1055/S-2006-959567
5-[2-(Furan-3-yl)ethyl]-5,6,8a-trimethyl-1,2,3,4,4a,6,7,8-octahydronaphthalene-1-carboxylic acid 85108353 Click to see 318.40 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Excisanin H 10066342 Click to see CC1(CCC(C23C1CC(C45C2CCC(C4(OC3)O)C(=C)C5=O)O)O)C 348.40 unknown https://doi.org/10.1021/NP000270V
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(4R)-4-[(3S)-3-hydroxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one 45257929 Click to see 210.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
(S)-4-Hydroxy-4-((S)-3-hydroxybutyl)-3,5,5-trimethylcyclohex-2-en-1-one 25755223 Click to see 226.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
4-(3-Hydroxybutyl)-3,5,5-trimethylcyclohex-2-en-1-one 118284 Click to see 210.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
4-Hydroxy-4-(3-hydroxybut-1-en-1-yl)-3,3,5-trimethylcyclohexan-1-one 71344200 Click to see CC1CC(=O)CC(C1(C=CC(C)O)O)(C)C 226.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
9-Epiblumenol B 14135401 Click to see CC1=CC(=O)CC(C1(CCC(C)O)O)(C)C 226.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
trans-(4S,5S)-4-hydroxy-4-[(E,3R)-3-hydroxybut-1-enyl]-3,3,5-trimethylcyclohexan-1-one 162964206 Click to see 226.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (2S,4aR,6aR,10aR,10bS)-2-(furan-3-yl)-6a,10b-dimethyl-4-oxo-1,2,4a,5,6,9,10,10a-octahydrobenzo[f]isochromene-7-carboxylate 162877854 Click to see 506.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 2-(furan-3-yl)-6a,10b-dimethyl-4-oxo-1,2,4a,5,6,9,10,10a-octahydrobenzo[f]isochromene-7-carboxylate 85446210 Click to see CC12CCC3C(=O)OC(CC3(C1CCC=C2C(=O)OC4C(C(C(C(O4)CO)O)O)O)C)C5=COC=C5 506.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
methyl (1aR,3aS,4R,5R,5'S,7R,7aS,7bS)-7-acetyloxy-5'-(furan-3-yl)-5,7a-dimethyl-2'-oxospiro[2,3,3a,5,6,7-hexahydro-1aH-naphtho[1,2-b]oxirene-4,3'-oxolane]-7b-carboxylate 101926685 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC5C2(O5)C(=O)OC)C)OC(=O)C 432.50 unknown https://doi.org/10.1016/S0031-9422(00)90816-1
https://doi.org/10.1055/S-2006-959567
methyl (1aR,3aS,4R,5R,5'S,7S,7aS,7bS)-7-acetyloxy-5'-(furan-3-yl)-5,7a-dimethyl-2'-oxospiro[2,3,3a,5,6,7-hexahydro-1aH-naphtho[1,2-b]oxirene-4,3'-oxolane]-7b-carboxylate 10025796 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC5C2(O5)C(=O)OC)C)OC(=O)C 432.50 unknown https://doi.org/10.1016/S0031-9422(00)90816-1
methyl (4aS,5R,5'S,6R,8S,8aR)-8-acetyloxy-5'-(furan-3-yl)-6,8a-dimethyl-2'-oxospiro[3,4,4a,6,7,8-hexahydronaphthalene-5,3'-oxolane]-1-carboxylate 10454574 Click to see 416.50 unknown https://doi.org/10.1016/S0031-9422(00)90816-1
methyl 7-acetyloxy-5'-(furan-3-yl)-5,7a-dimethyl-2'-oxospiro[2,3,3a,5,6,7-hexahydro-1aH-naphtho[1,2-b]oxirene-4,3'-oxolane]-7b-carboxylate 85096115 Click to see 432.50 unknown https://doi.org/10.1016/S0031-9422(00)90816-1
Methyl 8-acetyloxy-5'-(furan-3-yl)-6,8a-dimethyl-2'-oxospiro[3,4,4a,6,7,8-hexahydronaphthalene-5,3'-oxolane]-1-carboxylate 85147506 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC=C2C(=O)OC)C)OC(=O)C 416.50 unknown https://doi.org/10.1016/S0031-9422(00)90816-1
https://doi.org/10.1055/S-2006-959567
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
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/10.1055/S-2006-959567
https://doi.org/10.1016/S0031-9422(00)95166-5
b-Sitostenone 579897 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
beta-Sitostenone 60123241 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
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/S0031-9422(00)95166-5
https://doi.org/10.1055/S-2006-959567
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/S0031-9422(00)95166-5
https://doi.org/10.1055/S-2006-959567
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1055/S-2006-959567
https://doi.org/10.1016/S0031-9422(00)95166-5
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
3-[2-(3,4-Dimethoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propan-1-ol 4639677 Click to see COC1=C(C=C(C=C1)C2C(C3=C(O2)C(=CC(=C3)CCCO)OC)CO)OC 374.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
3',4-O-Dimethylcedrusin 124426 Click to see 374.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
4-O-Methylcedrusin 44149614 Click to see COC1=C(C=C(C=C1)C2C(C3=C(O2)C(=CC(=C3)CCCO)O)CO)OC 360.40 unknown https://doi.org/10.1021/NP50096A013
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3-(3,4,5-Trimethoxyphenyl)-2-propen-1-ol 73924 Click to see COC1=CC(=CC(=C1OC)OC)C=CCO 224.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
3,4,5-Trimethoxycinnamyl alcohol 6436306 Click to see COC1=CC(=CC(=C1OC)OC)C=CCO 224.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-[(Dimethylamino)methyl]-5,12-dimethoxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione 162998515 Click to see 355.30 unknown https://doi.org/10.1016/S0031-9422(00)95166-5
Taspine 215159 Click to see 369.40 unknown https://doi.org/10.1055/S-2003-43208
https://doi.org/10.1016/S0031-9422(00)95166-5
https://doi.org/10.1016/S0944-7113(11)80043-7
https://doi.org/10.1021/NP000270V
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
https://doi.org/10.1002/JPS.2600680145
https://doi.org/10.1055/S-2006-961907
https://doi.org/10.1021/NP50096A013
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(+)-Catechin-(4alpha->8)-(-)-epigallocatechin 11699925 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(91)85063-6
(2R,2'R,3S,3'R,4S)-2'-(3,4-Dihydroxyphenyl)-3,3',4,4'-tetrahydro-2-(3,4,5-trihydroxyphenyl)(4,8'-bi-2H-1-benzopyran)-3,3',5,5',7,7'-hexol 11527214 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(91)85063-6
(2R,3S,4R)-2-(3,4,5-trihydroxyphenyl)-4-[(2R,3R)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-8-yl]-8-[(2R,3S,4S)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 101607491 Click to see 914.80 unknown https://doi.org/10.1016/0031-9422(91)85063-6
(2R,3S,4R)-8-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-4-[(2R,3S)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-8-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 101607236 Click to see 898.80 unknown https://doi.org/10.1016/0031-9422(91)85063-6
(2S,3S)-2-(3,4,5-trihydroxyphenyl)-6-[(2R,3S,4R)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 163011745 Click to see 610.50 unknown https://doi.org/10.1016/0031-9422(91)85063-6
2-(3,4,5-trihydroxyphenyl)-6-[3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 14890506 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(91)85063-6
2-(3,4,5-trihydroxyphenyl)-8-[3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-4-[3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-8-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 5152777 Click to see 914.80 unknown https://doi.org/10.1016/0031-9422(91)85063-6
8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-4-[3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-8-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 162919238 Click to see 898.80 unknown https://doi.org/10.1016/0031-9422(91)85063-6
Epicatechin-(4beta->8)-gallocatechin 14284599 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(91)85063-6
Epigallocatechin-(4beta->8)-catechin 13831061 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(91)85063-6
Proanthocyanidin B2 5320711 Click to see 578.50 unknown https://doi.org/10.1055/S-2003-43208
Procyanidin B 130556 Click to see 578.50 unknown https://doi.org/10.1016/0031-9422(91)85063-6
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(91)85063-6
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1055/S-2003-43208
Procyanidin B4 147299 Click to see 578.50 unknown https://doi.org/10.1016/0031-9422(91)85063-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
https://doi.org/10.1016/0031-9422(91)85063-6
Catechin 9064 Click to see 290.27 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
https://doi.org/10.1055/S-2006-959567
https://doi.org/10.1055/S-2003-43208
https://doi.org/10.1016/0031-9422(91)85063-6
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1055/S-2006-959567
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
https://doi.org/10.1055/S-2003-43208
https://doi.org/10.1016/0031-9422(91)85063-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
https://doi.org/10.1055/S-2006-959567
https://doi.org/10.1055/S-2003-43208
https://doi.org/10.1016/0031-9422(91)85063-6
Flavan-3,3',4',5,5',7-hexol 1249 Click to see 306.27 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
https://doi.org/10.1016/0031-9422(91)85063-6
Gallocatechin 65084 Click to see 306.27 unknown https://doi.org/10.1055/S-2006-959567
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245398/
https://doi.org/10.1016/0031-9422(91)85063-6

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