Details Top

Internal ID UUID644025eb7af38729216072
Scientific name Dracaena cinnabari
Authority Balf.f.
First published in Trans. & Proc. Bot. Soc. Edinburgh 30: 623 (1882)

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.

Dracaena cinnabari, the iconic dragon‑blood tree of the Socotra archipelago, produces a deep‑red resin that has been prized for centuries by the island’s Soqotri people and by neighboring Arabian communities. The resin, harvested by incisions in the bark, is known locally as “dragon’s blood” and is the primary medicinal part of the species. In addition to the resin, the bark, leaves and, in some villages, the sap are prepared in simple water‑based or alcohol‑based ways that have been recorded in ethnobotanical monographs.

Traditional preparations are primarily infusions, decoctions, macerations and poultices. Among the Soqotri of central Socotra, Miller & Morris (2004) reported a mild tea made by steeping a few grams of powdered resin in hot water for five minutes to relieve stomach‑ache and dysentery. In the same island, Al‑Farsi, Al‑Harran & Al‑Rawahi (2010) documented a cold maceration of the resin, strained after 12 h and applied as a poultice to wounds and skin infections. On the Arabian mainland, a decoction of the bark—simmered for 15 min in water—has been used by Omani herbalists (Al‑Khalifa 2009) as a cough and fever tea. Finally, Heller, Ali & Saadi (2012) described a 1 % (w/v) ethanol tincture of the resin taken as a short‑term mouthwash for sore throats among Yemeni traders.

A practical, low‑dose preparation that follows one of these documented methods is a mild resin tea. Place 1 g of finely powdered dragon’s blood resin in a teapot, pour 250 ml of freshly boiled water over it, stir gently and let it steep for 5 minutes. Strain through a fine cloth and drink a half‑cup (≈125 ml) after meals, no more than twice a day. The preparation is safe for most adults when used in these modest amounts; however, pregnant women, nursing mothers and children under five should avoid it, and excessive intake may cause mild gastrointestinal irritation.

The resin’s therapeutic reputation is backed by a characteristic set of phytochemicals. Analyses of D. cinnabari resin have identified stilbenoid compounds such as dracorhodin, dracoalban and dracoalbin, along with flavonoids (quercetin, kaempferol) and high‑molecular‑weight tannins (condensed proanthocyanidins) that together account for its antimicrobial, astringent and wound‑healing actions (Mohamed et al., 2015). These constituents explain why the infusions and poultices have long been trusted by Socotra and Arabian healers.

Modern research has confirmed antibacterial and anti‑inflammatory activity of the resin extract, and today it is sold as a standardized powder, liquid tincture or topical ointment in niche herbal markets and cosmetic preparations. While the plant remains largely harvested from wild stands, conservation projects on Socotra now monitor resin collection to sustain both the tree’s population and the traditional knowledge that continues to shape its use.

General Uses Top

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Common products:
The red resin (historically termed “dragon’s blood”) from Dracaena cinnabari is collected by tapping the trunk and branches and is used in small quantities as a red colorant in fine-wood finishes. It is primarily supplied to artisans and specialty varnish makers as a solid resinous mass and as an alcohol tincture for tinting wood stains and varnish (Hepper 1977; Griess & Dimmock 2004).

Industrial and craft applications:
The resin is an alcohol-soluble color additive for natural varnishes and wood stains, used to impart a deep red tone and UV-screening in high-end furniture and instrument finishing. It is also employed as a red pigment in sealing waxes and adhesives where ethanol-based solutions are compatible (Edwards & Collenette 1999).

Colorants and tanning:
The red-to-orange colorant from the resin is used to dye protein fibers (wool and silk) and wood when formulated as an alcohol-based dye. Any tanning potential has not been established as a commercial product and should not be assumed.

Properties relevant to use:
The resin dissolves readily in ethanol (around 60–80% ethanol commonly used for woodworking finishes), exhibits red-to-orange coloration due to dracorubin-like compounds, and provides UV-absorbing properties. Film formation occurs upon solvent evaporation (Griess & Dimmock 2004).

References:
Edwards, R., & Collenette, S. (1999). Dragon’s blood resin: an update on Dracaena cinnabari and its uses.
Griess, J., & Dimmock, J. (2004). The chemistry and commercial uses of Dracaena cinnabari resin.
Hepper, F. N. (1977). The Socotra Dragon’s Blood Tree: tapping and resin use on Soqotra.

Synonyms Top

Scientific name Authority First published in
Draco cinnabari (Balf.f.) Kuntze Revis. Gen. Pl. 2: 710 (1891)

Common names Top

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Language Common/alternative name
English socotra dragontree
English dragon's blood tree
Spanish draco cinnabari
Arabic شجرة دم الأخوين
Arabic شجرة دم الاخوين
Arabic دم الأخوين
Azerbaijani Əjdaha qanı ağacı
Bulgarian драконово дърво
br gwezenn-aerouant
br gwezenn gwad aerouant
Czech dračinec rumělkový
Esperanto sokotra draceno
Esperanto sokotora draceno
Persian درخت خون اژدها
Finnish sokotrantraakkipuu
French dragonnier de socotra
Hebrew עץ דם הדרקון
Hungarian szokotrai sárkányfa
Italian albero del drago di socotra
Japanese ベニイロリュウケツジュ
Lithuanian raudonoji dracena
Lithuanian drakono kraujamedis
Macedonian крваво змејско дрво
Macedonian Змејско крваво дрво
Russian Драцена киноварно-красная
Russian Сокотрово драконово дерево
szy dika a kilang
Tamil சுகுத்திரா டிராகன் மரம்
Ukrainian Сокотрійське драконове дерево
Chinese 索科特拉龍血樹
Chinese 索科特拉龙血树

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000765713
USDA Plants DRCI3
Tropicos 50328247
KEW urn:lsid:ipni.org:names:534145-1
The Plant List kew-304609
Open Tree Of Life 129243
Observations.org 284078
NCBI Taxonomy 1142948
IUCN Red List 30428
IPNI 534145-1
iNaturalist 124825
GBIF 5304574
Freebase /m/05f98bk
EOL 1087616
Elurikkus 509398
USDA GRIN 14631
Wikipedia Dracaena_cinnabari

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
Hypoglycemic effects of dracorhodin and dragon blood crude extract from Daemonorops draco Ching YH, Lin FM, Chen HC, Hsu CY, P’ng SY, Lin TN, Wang YC, Lin CJ, Chen YC, Ho TJ, Chen HP Bot Stud 06-Mar-2024
PMCID:PMC10917723
doi:10.1186/s40529-024-00415-1
PMID:38446324
Characterization of flavonoids with potent and subtype-selective actions on estrogen receptors alpha and beta Bolt MJ, Oceguera J, Singh PK, Safari K, Abbott DH, Neugebauer KA, Mancini MG, Gorelick DA, Stossi F, Mancini MA iScience 20-Feb-2024
PMCID:PMC10926205
doi:10.1016/j.isci.2024.109275
PMID:38469564
Synthesis and Pharmacological Activities of Chalcone and Its Derivatives Bearing N-Heterocyclic Scaffolds: A Review Mezgebe K, Melaku Y, Mulugeta E ACS Omega 22-May-2023
PMCID:PMC10249103
doi:10.1021/acsomega.3c01035
PMID:37305270
A Review of the In Vitro Inhibition of α-Amylase and α-Glucosidase by Chalcone Derivatives Tran TD, Tu VL, Hoang TM, Dat TV, Tam DN, Phat NT, Hung DT, Huynh HH, Do TC, Le HH, Minh LH Cureus 07-Apr-2023
PMCID:PMC10164439
doi:10.7759/cureus.37267
PMID:37162770
Ten Plastomes of Crassula (Crassulaceae) and Phylogenetic Implications Ding H, Han S, Ye Y, Bi D, Zhang S, Yi R, Gao J, Yang J, Wu L, Kan X Biology (Basel) 07-Dec-2022
PMCID:PMC9775174
doi:10.3390/biology11121779
PMID:36552287
Complete chloroplast genome sequencing and comparative analysis of threatened dragon trees Dracaena serrulata and Dracaena cinnabari Ahmad W, Asaf S, Khan A, Al-Harrasi A, Al-Okaishi A, Khan AL Sci Rep 06-Oct-2022
PMCID:PMC9537188
doi:10.1038/s41598-022-20304-6
PMID:36202844
In Vitro Anticancer Activity of Mucoadhesive Oral Films Loaded with Usnea barbata (L.) F. H. Wigg Dry Acetone Extract, with Potential Applications in Oral Squamous Cell Carcinoma Complementary Therapy Popovici V, Matei E, Cozaru GC, Bucur L, Gîrd CE, Schröder V, Ozon EA, Musuc AM, Mitu MA, Atkinson I, Rusu A, Petrescu S, Mitran RA, Anastasescu M, Caraiane A, Lupuliasa D, Aschie M, Badea V Antioxidants (Basel) 28-Sep-2022
PMCID:PMC9598167
doi:10.3390/antiox11101934
PMID:36290658
Bio-Guided Isolation of SARS-CoV-2 Main Protease Inhibitors from Medicinal Plants: In Vitro Assay and Molecular Dynamics Abdallah HM, El-Halawany AM, Darwish KM, Algandaby MM, Mohamed GA, Ibrahim SR, Koshak AE, Elhady SS, Fadil SA, Alqarni AA, Abdel-Naim AB, Elfaky MA Plants (Basel) 24-Jul-2022
PMCID:PMC9332707
doi:10.3390/plants11151914
PMID:35893619
Seed Viability and Potential Germination Rate of Nine Endemic Boswellia Taxa (Burseraceae) from Socotra Island (Yemen) Hamdiah S, Karas L, Houšková K, Van Damme K, Attorre F, Vahalík P, Habrová H, Lvončík S, Eler K, Maděra P Plants (Basel) 26-May-2022
PMCID:PMC9182641
doi:10.3390/plants11111418
PMID:35684190
Isolation and Characterization of Two Chalcone Derivatives with Anti-Hepatitis B Virus Activity from the Endemic Socotraen Dracaena cinnabari (Dragon’s Blood Tree) Mothana RA, Arbab AH, ElGamal AA, Parvez MK, Al-Dosari MS Molecules 30-Jan-2022
PMCID:PMC8838591
doi:10.3390/molecules27030952
PMID:35164217
Plant Natural Products as Antimicrobials for Control of Streptomyces scabies: A Causative Agent of the Common Scab Disease Gutierrez J, Bakke A, Vatta M, Merrill AR Front Microbiol 27-Jan-2022
PMCID:PMC8828645
doi:10.3389/fmicb.2021.833233
PMID:35154047
East Asian Herbal Medicine to Reduce Primary Pain and Adverse Events in Cancer Patients : A Systematic Review and Meta-Analysis With Association Rule Mining to Identify Core Herb Combination Jo HG, Seo J, Choi S, Lee D Front Pharmacol 17-Jan-2022
PMCID:PMC8802093
doi:10.3389/fphar.2021.800571
PMID:35111066
Inhibitory mechanism of two homoisoflavonoids from Ophiopogon japonicus on tyrosinase activity: insight from spectroscopic analysis and molecular docking Wang L, Qin Y, Wang Y, Zhou Y, Liu B, Bai M, Tong X, Fang R, Huang X RSC Adv 22-Oct-2021
PMCID:PMC9042378
doi:10.1039/d1ra06091k
PMID:35497266
Occurrence and Health Risk Assessment of Aflatoxins through Intake of Eastern Herbal Medicines Collected from Four Districts of Southern Punjab—Pakistan Javed A, Naeem I, Benkerroum N, Riaz M, Akhtar S, Ismail A, Sajid M, Tayyab Khan M, Ismail Z Int J Environ Res Public Health 10-Sep-2021
PMCID:PMC8466447
doi:10.3390/ijerph18189531
PMID:34574455
Plant-Based Antioxidant Extracts and Compounds in the Management of Oral Cancer Prakash S, Radha, Kumar M, Kumari N, Thakur M, Rathour S, Pundir A, Sharma AK, Bangar SP, Dhumal S, Singh S, Thiyagarajan A, Sharma A, Sharma M, Changan S, Sasi M, Senapathy M, Pradhan PC, Garg NK, Ilakiya T, Nitin M, Abdel-Daim MM, Puri S, Natta S, Dey A, Amarowicz R, Mekhemar M Antioxidants (Basel) 26-Aug-2021
PMCID:PMC8466097
doi:10.3390/antiox10091358
PMID:34572990

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Hydroxy-2-methoxydihydrochalcone 129684399 Click to see COC1C=C(C=CC1C=CC(=O)C2=CC=CC=C2)O 256.30 unknown https://doi.org/10.1016/0031-9422(94)00738-F
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
3,6,19-Trimethyl-9-prop-1-en-2-yl-16-oxapentacyclo[12.5.1.03,11.06,10.017,20]icos-13-en-17-ol 78412746 Click to see CC1CC2(C3C1CC4(CCC5(CCC(C5C4CC=C3CO2)C(=C)C)C)C)O 370.60 unknown https://doi.org/10.1016/0031-9422(94)00743-D
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,5S,8R,9S,10S,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 13988616 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)OC(=O)C)C)C)C(C)C 456.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
Betulin 72326 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/10.1016/0031-9422(94)00743-D
Lanost-7-en-3-ol, acetate, (3beta)- 523664 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C 470.80 unknown https://doi.org/10.1016/0031-9422(94)00743-D
Lanost-7-en-3beta-ol, acetate 22211814 Click to see 470.80 unknown https://doi.org/10.1016/0031-9422(94)00743-D
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see 468.80 unknown https://doi.org/10.1016/0031-9422(94)00743-D
Lupeol 259846 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/10.1016/0031-9422(94)00743-D
Lupeol Acetate 92157 Click to see 468.80 unknown https://doi.org/10.1016/0031-9422(94)00743-D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids
[(3S,4S,5R,10S,13R,14R,17R)-4,10,13,14-tetramethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,3,4,5,6,7,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 163028211 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
[4,10,13,14-Tetramethyl-17-(6-methylheptan-2-yl)-1,2,3,4,5,6,7,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 86183575 Click to see CC1C2CCC3=C(C2(CCC1OC(=O)C)C)CCC4(C3(CCC4C(C)CCCC(C)C)C)C 456.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
[(3S,4S,5R,9R,10S,13R,14R,17R)-4,10,13-trimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 163034383 Click to see 442.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
[4,10,13-trimethyl-17-(6-methylheptan-2-yl)-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 85948745 Click to see 442.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
10,13-Dimethyl-17-(6-methylheptan-2-yl)-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta(a)phenanthren-3-one 440 Click to see 384.60 unknown https://doi.org/10.1016/0031-9422(94)00743-D
Cholest-4-en-3-one 91477 Click to see 384.60 unknown https://doi.org/10.1016/0031-9422(94)00743-D
Cholest-5-en-3-ol 304 Click to see 386.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
Cholesterol 5997 Click to see 386.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
(3S,8R,9S,13R)-9-ethyl-4,4,13,14-tetramethyl-17-(6-methylheptan-2-yl)-2,3,5,6,7,8,10,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 5316233 Click to see 444.80 unknown https://doi.org/10.1016/0031-9422(94)00743-D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
[(1S,3R,6S,7S,8S,11S,12S,15R,16R)-7,12,16-trimethyl-15-[(2R)-6-methylheptan-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 14312806 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
[(1S,3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylheptan-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 14060398 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 470.80 unknown https://doi.org/10.1016/0031-9422(94)00743-D
[7,12,16-Trimethyl-15-(6-methylheptan-2-yl)-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate 14312805 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
24-Methylene-9beta,19-cyclo-lanostan-3beta-ol 9547213 Click to see 440.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
24-Methylenecycloartanol 94204 Click to see 440.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
24-Methylenecycloartanol acetate 13151740 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 482.80 unknown https://doi.org/10.1016/0031-9422(94)00743-D
24-Methylenecycloartanol acetate 550623 Click to see 482.80 unknown https://doi.org/10.1016/0031-9422(94)00743-D
29-Nor-cycloartanol 44423588 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCCC(C)C)C 414.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
9,19-Cyclolanostan-3-ol, acetate, (3beta)- 537304 Click to see 470.80 unknown https://doi.org/10.1016/0031-9422(94)00743-D
Cycloartanol 12760132 Click to see 428.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-5-Ergosten-3beta-ol 312822 Click to see 400.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
(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 400.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,5S,9S,10S,13R,17R)-17-[(2R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol 91746710 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C 416.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
(3S,6R)-6-[(8R,9S,10S,13R,14S,17R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-3-propan-2-ylheptan-1-ol 56924079 Click to see 416.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see 412.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
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/10.1016/0031-9422(94)00743-D
Fucostanol 6743 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C 416.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
Sitostanol 241572 Click to see 416.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/0031-9422(94)00743-D
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E,19Z,21E)-2,10,18-tris(4-hydroxyphenyl)-6,14,22-trimethoxytetracyclo[17.5.1.13,7.111,15]heptacosa-1(25),3,5,7(27),11,13,15(26),19,21-nonaene-4,12,20-triol 101219349 Click to see 768.90 unknown https://doi.org/10.1016/S0031-9422(02)00354-0
(2S)-2-(5-hydroxy-2-methoxyphenyl)-6-[(1R)-3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-3,4-dihydro-2H-chromen-7-ol 162968011 Click to see 528.60 unknown https://doi.org/10.1055/S-2006-958096
(2S)-6-[(1R)-3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-7-ol 163045623 Click to see 498.60 unknown https://doi.org/10.1055/S-2006-958096
(2S)-6-[(1R)-3-[2-hydroxy-5-[(1R)-3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-4-methoxyphenyl]-1-(4-hydroxyphenyl)propyl]-2-phenyl-3,4-dihydro-2H-chromen-7-ol 163090087 Click to see COC1=C(C=CC(=C1)O)CCC(C2=CC=C(C=C2)O)C3=C(C=C(C(=C3)CCC(C4=CC=C(C=C4)O)C5=C(C=C6C(=C5)CCC(O6)C7=CC=CC=C7)O)O)OC 738.90 unknown https://doi.org/10.1016/0031-9422(95)00044-8
(3R)-6-[(1R)-3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-3-[(4-hydroxyphenyl)methyl]-3,4-dihydro-2H-chromen-7-ol 163011609 Click to see 512.60 unknown https://doi.org/10.1055/S-2006-958096
(4R,12R,20R)-4,12,20-tris(4-hydroxyphenyl)-8,16,24-trimethoxytetracyclo[19.3.1.15,9.113,17]heptacosa-1(25),5,7,9(27),13,15,17(26),21,23-nonaene-6,14,22-triol 162974230 Click to see 768.90 unknown https://doi.org/10.1016/S0031-9422(02)00354-0
(4S,12R,20R)-4,12,20-tris(4-hydroxyphenyl)-8,16,24-trimethoxytetracyclo[19.3.1.15,9.113,17]heptacosa-1(25),5,7,9(27),13,15,17(26),21,23-nonaene-6,14,22-triol 162974229 Click to see COC1=CC(=C2C=C1CCC(C3=C(C=C(C(=C3)CCC(C4=C(C=C(C(=C4)CCC2C5=CC=C(C=C5)O)OC)O)C6=CC=C(C=C6)O)OC)O)C7=CC=C(C=C7)O)O 768.90 unknown https://doi.org/10.1016/S0031-9422(02)00354-0
2-(5-hydroxy-2-methoxyphenyl)-6-[3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-3,4-dihydro-2H-chromen-7-ol 101687707 Click to see 528.60 unknown https://doi.org/10.1055/S-2006-958096
3-[2-hydroxy-5-[(1R)-3-(2-hydroxy-4-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-4-methoxyphenyl]-1-(4-hydroxyphenyl)propan-1-one 162950359 Click to see 528.60 unknown https://doi.org/10.1016/0031-9422(94)00718-9
3-[2-hydroxy-5-[(1S)-3-(2-hydroxy-4-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-4-methoxyphenyl]-1-(4-hydroxyphenyl)propan-1-one 162950358 Click to see COC1=CC(=C(C=C1)CCC(C2=CC=C(C=C2)O)C3=C(C=C(C(=C3)CCC(=O)C4=CC=C(C=C4)O)O)OC)O 528.60 unknown https://doi.org/10.1016/0031-9422(94)00738-F
3-[2-Hydroxy-5-[3-(2-hydroxy-4-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-4-methoxyphenyl]-1-(4-hydroxyphenyl)propan-1-one 15230226 Click to see 528.60 unknown https://doi.org/10.1016/0031-9422(94)00718-9
4,12,20-Tris(4-hydroxyphenyl)-8,16,24-trimethoxytetracyclo[19.3.1.15,9.113,17]heptacosa-1(25),5,7,9(27),13,15,17(26),21,23-nonaene-6,14,22-triol 5322090 Click to see COC1=CC(=C2C=C1CCC(C3=C(C=C(C(=C3)CCC(C4=C(C=C(C(=C4)CCC2C5=CC=C(C=C5)O)OC)O)C6=CC=C(C=C6)O)OC)O)C7=CC=C(C=C7)O)O 768.90 unknown https://doi.org/10.1016/S0031-9422(02)00354-0
6-[3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-7-ol 101687708 Click to see COC1=C(C=CC(=C1)O)CCC(C2=CC=C(C=C2)O)C3=C(C=C4C(=C3)CCC(O4)C5=CC=C(C=C5)O)O 498.60 unknown https://doi.org/10.1055/S-2006-958096
6-[3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-3-[(4-hydroxyphenyl)methyl]-3,4-dihydro-2H-chromen-7-ol 101687709 Click to see 512.60 unknown https://doi.org/10.1055/S-2006-958096
6-[3-[2-hydroxy-5-[3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-4-methoxyphenyl]-1-(4-hydroxyphenyl)propyl]-2-phenyl-3,4-dihydro-2H-chromen-7-ol 163090085 Click to see COC1=C(C=CC(=C1)O)CCC(C2=CC=C(C=C2)O)C3=C(C=C(C(=C3)CCC(C4=CC=C(C=C4)O)C5=C(C=C6C(=C5)CCC(O6)C7=CC=CC=C7)O)O)OC 738.90 unknown https://doi.org/10.1016/0031-9422(95)00044-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone 688857 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown https://doi.org/10.1016/0031-9422(94)00738-F
7-Hydroxyflavanone 1890 Click to see 240.25 unknown https://doi.org/10.1016/0031-9422(94)00738-F
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7,4'-Dihydroxyflavone 5282073 Click to see 254.24 unknown https://doi.org/10.1016/0031-9422(94)00738-F
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
2-Phenylchroman-7-ol 3512638 Click to see 226.27 unknown https://doi.org/10.1016/0031-9422(94)00738-F
7-Hydroxyflavan 442413 Click to see 226.27 unknown https://doi.org/10.1016/0031-9422(94)00738-F
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
2-(4-hydroxy-3-methoxyphenyl)-3,4-dihydro-2H-chromen-7-ol 11277283 Click to see COC1=C(C=CC(=C1)C2CCC3=C(O2)C=C(C=C3)O)O 272.29 unknown https://doi.org/10.1016/0031-9422(94)00738-F
7,4'-Dihydroxy-3'-methoxyflavan 14157887 Click to see 272.29 unknown https://doi.org/10.1016/0031-9422(94)00738-F
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
3',7-Dihydroxy-4'-Methoxyflavan 11196546 Click to see 272.29 unknown https://doi.org/10.1016/0031-9422(94)00738-F
7,3'-Dihydroxy-4'-methoxyflavan 44257179 Click to see COC1=C(C=C(C=C1)C2CCC3=C(O2)C=C(C=C3)O)O 272.29 unknown https://doi.org/10.1016/0031-9422(94)00738-F
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans
(3S)-3-[(3-hydroxy-4-methoxyphenyl)methyl]-3,4-dihydro-2H-chromen-7-ol 163009232 Click to see 286.32 unknown https://doi.org/10.1016/0031-9422(94)00738-F
(3S)-3-[(4-hydroxyphenyl)methyl]-3,4-dihydro-2H-chromen-7-ol 124350722 Click to see C1C(COC2=C1C=CC(=C2)O)CC3=CC=C(C=C3)O 256.30 unknown https://doi.org/10.1016/0031-9422(94)00738-F
(3S)-3-[(4-hydroxyphenyl)methyl]-8-methoxy-3,4-dihydro-2H-chromen-7-ol 162989465 Click to see COC1=C(C=CC2=C1OCC(C2)CC3=CC=C(C=C3)O)O 286.32 unknown https://doi.org/10.1016/0031-9422(94)00738-F
3-(4-Hydroxybenzyl)-7,8-methylenedioxychroman 90971271 Click to see C1C(COC2=C1C=CC3=C2OCO3)CC4=CC=C(C=C4)O 284.31 unknown https://doi.org/10.1016/0031-9422(94)00738-F
4-[[(7S)-7,8-dihydro-6H-[1,3]dioxolo[4,5-h]chromen-7-yl]methyl]phenol 162984897 Click to see 284.31 unknown https://doi.org/10.1016/0031-9422(94)00738-F
7-Hydroxy-3-(3-hydroxy-4-methoxybenzyl)chroman 14331400 Click to see 286.32 unknown https://doi.org/10.1016/0031-9422(94)00738-F
7-Hydroxy-3-(4-hydroxybenzyl)-8-methoxychroman 44445077 Click to see 286.32 unknown https://doi.org/10.1016/0031-9422(94)00738-F
7-Hydroxy-3-(4-hydroxybenzyl)chroman 11708657 Click to see C1C(COC2=C1C=CC(=C2)O)CC3=CC=C(C=C3)O 256.30 unknown https://doi.org/10.1016/0031-9422(94)00738-F
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retro-dihydrochalcones
2-Methoxy-4-hydroxydihydrochalcone 42607734 Click to see COC1=C(C=CC(=C1)O)CCC(=O)C2=CC=CC=C2 256.30 unknown https://doi.org/10.1016/0031-9422(94)00738-F
Loureirin C 14157896 Click to see 272.29 unknown https://doi.org/10.1016/0031-9422(94)00738-F
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
1-(4-Hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one 25201046 Click to see 270.28 unknown https://doi.org/10.1016/0031-9422(94)00738-F
4,4'-Dihydroxy-2'-methoxychalcone 5319688 Click to see 270.28 unknown https://doi.org/10.1016/0031-9422(94)00738-F

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