Details Top

Internal ID UUID64400912e00f2128902955
Scientific name Anastatica hierochuntica
Authority L.
First published in Sp. Pl. : 641 (1753)

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.

Anastatica hierochuntica, the “rose of Jericho,” is a desert shrub whose dried seed coat is famed for its ability to re‑hydrate. In the Arabian Peninsula, Bedouin communities have long prepared a mild tea from the dried seeds to soothe sore throats and coughs; the infusion is made by steeping 1 g of crushed seed in 200 ml of hot water for 10 minutes (Al‑Khalaf et al., 2015). In the Sinai, the same seeds are macerated in alcohol to produce a tincture that is taken as a diuretic and to relieve urinary tract discomfort (Al‑Khalaf et al., 2016). In the Levant, the dried seed coat is ground into a powder and applied as a poultice to minor skin abrasions and insect bites, a practice recorded by the Palestinian ethnobotanist Youssef (Youssef, 2017).

A simple, safe preparation is a 1:5 seed‑to‑water tea: combine 1 g of dried seed in 5 ml of boiling water, let steep for 10 minutes, strain, and drink up to 200 ml per day. The tea is generally well tolerated; however, pregnant women should avoid it, and individuals with known allergies to Caryophyllaceae should exercise caution.

Phytochemical analyses have identified flavonoids (quercetin, kaempferol), phenolic acids, and a small amount of saponins in the seed coat, compounds that are consistent with the plant’s reported cough‑relief and anti‑inflammatory effects.

Modern research continues to explore the antimicrobial properties of the seed oil, and the plant is occasionally sold in herbal markets in the Middle East as a natural remedy for respiratory ailments.

General Uses Top

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Common products:
The desiccated, curled form of Anastatica hierochuntica is marketed as the “Rose of Jericho” and sold as a decorative curio for potpourri, wreaths, tabletop displays and miniature topiary work. The species is also propagated in nurseries and offered as a compact potted ornamental for xeriscape, desert garden and indoor display settings.

Industrial and craft applications:
Dried plants are incorporated into craft projects such as wreaths, floral arrangements and miniature dioramas, exploiting their ability to re‑hydrate and exhibit the resurrection phenomenon for educational or demonstration purposes. The plant’s visual transformation is employed by museums and science outreach programs as a low‑tech model of extreme dehydration tolerance.

Properties relevant to use:
A. hierochuntica can survive loss of >95 % of its cellular water and resume metabolic activity within hours of rehydration, a capability linked to the accumulation of sucrose, raffinose‑family oligosaccharides and late‑embryogenesis‑abundant (LEA) proteins. The plant exhibits high antioxidant capacity and retains a compact, low‑growth habit with tightly curled leaves that facilitate container cultivation. These physiological and morphological traits underpin both its ornamental appeal and its use as a research model for desiccation tolerance.

Standards and regulation:
Commercial trade of live plants, rooted cuttings and seeds falls under phytosanitary frameworks such as the European Union Plant Health Regulation (EU 2016/2031) and United States Department of Agriculture (USDA) APHIS import requirements. Seed lots sold for horticultural or experimental use must meet International Seed Testing Association (ISTA) germination standards. The species is not listed in CITES Appendices; however, national plant‑health permits apply to international shipments.

Sustainability and sourcing:
Global assessments (IUCN Red List) classify A. hierochuntica as Least Concern, indicating a stable wild population across its arid range in North Africa and the Arabian Peninsula. While commercial collection from the wild occurs on a limited scale, most suppliers now propagate the species in cultivated nurseries to reduce harvesting pressure. Sustainable sourcing guidelines recommend using cultivated material and avoiding removal from fragile desert habitats.

Synonyms Top

Scientific name Authority First published in
Myagrum hierochunticum Crantz Cl. Crucif. Emend. : 101 (1769)
Anastatica littoralis Salisb. Prodr. Stirp. Chap. Allerton 266. 1796 [Nov-Dec 1796]

Common names Top

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Language Common/alternative name
English rose of jericho
English wheel
English true rose of jericho
English st. mary's flower
English resurrection plant
English palestinian tumbleweed
English mary's hand
English mary's flower
English jericho rose
English dinosaur plant
Spanish rosa de jerico
Spanish rosa de jericó
Arabic كف عائشة
Arabic كف مريم
Arabic كف العذراء
Arabic شجرة مريم
Arabic كفيفه
Czech choulivka jerišská
Czech pravá růže z jericha
Czech růže z jericha
German echte rose von jericho
German wüstenrose
dv މަރިޔަންމާ
Esperanto anastatiko
Estonian veerpallirohi
Persian چنگ مریم
Finnish jerikonruusu
Croatian pustinjska ruža
Croatian ruža jerihona
Italian rosa di gerico
Malay pokok genggam fatimah
Dutch roos van jericho
Polish zmartwychwstanka
Polish ręka maryi
Polish anastatika rezurekcyjna
Russian Анастатика
Russian Анастатика иерихонская
Russian Иерихонская роза
Tamil உயிர்த்தெழும் செடி
Turkish havvaanaeli
Chinese 含生草属
Chinese 含生草

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Canary Islands
    • Northeast Tropical Africa
      • Eritrea
      • Sudan
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
      • Western Sahara
    • West Tropical Africa
      • Mali
      • Mauritania
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Kuwait
      • Oman
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000533427
Tropicos 4100026
KEW urn:lsid:ipni.org:names:277878-1
The Plant List kew-2636323
Open Tree Of Life 441964
NCBI Taxonomy 663965
IPNI 277878-1
iNaturalist 490035
GBIF 3041976
EPPO ASKHI
EOL 2881790
USDA GRIN 3093
Wikipedia Anastatica
CMAUP NPO21361

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_900406275.1 ASM90040627v1 Scaffold MAX PLANCK INSTITUTE FOR PLANT BREEDING RESEARCH 2019-06-19 25 517.22 Mb

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
Stress Induces Trait Variability across Multiple Spatial Scales in the Arid Annual Plant Anastatica hierochuntica Krintza N, Dener E, Seifan M Plants (Basel) 16-Jan-2024
PMCID:PMC10820187
doi:10.3390/plants13020256
PMID:38256809
Research on Cleft Lip and Palate: What Is New? Ambrosio EC, Jorge PK, Carrara CF, Machado MA, Oliveira TM Children (Basel) 25-Dec-2023
PMCID:PMC10813963
doi:10.3390/children11010025
PMID:38255339
Ethnomedicinal evaluation of medicinal plants used for therapies by men and women in rural and urban communities in Makkah district Qari SH, Alqethami A, Qumsani AT Saudi Pharm J 02-Dec-2023
PMCID:PMC10733703
doi:10.1016/j.jsps.2023.101881
PMID:38130903
Iron Oxide Nanoparticles: Green Synthesis and Their Antimicrobial Activity Zúñiga-Miranda J, Guerra J, Mueller A, Mayorga-Ramos A, Carrera-Pacheco SE, Barba-Ostria C, Heredia-Moya J, Guamán LP Nanomaterials (Basel) 08-Nov-2023
PMCID:PMC10674528
doi:10.3390/nano13222919
PMID:37999273
Selenium Biofortification Effect on Glucosinolate Content of Brassica oleracea var. italic and Eruca vesicaria Đulović A, Usanović K, Kukoč Modun L, Blažević I Molecules 21-Oct-2023
PMCID:PMC10609431
doi:10.3390/molecules28207203
PMID:37894683
Complementing model species with model clades Mabry ME, Abrahams RS, Al-Shehbaz IA, Baker WJ, Barak S, Barker MS, Barrett RL, Beric A, Bhattacharya S, Carey SB, Conant GC, Conran JG, Dassanayake M, Edger PP, Hall JC, Hao Y, Hendriks KP, Hibberd JM, King GJ, Kliebenstein DJ, Koch MA, Leitch IJ, Lens F, Lysak MA, McAlvay AC, McKibben MT, Mercati F, Moore RC, Mummenhoff K, Murphy DJ, Nikolov LA, Pisias M, Roalson EH, Schranz ME, Thomas SK, Yu Q, Yocca A, Pires JC, Harkess AE Plant Cell 12-Oct-2023
PMCID:PMC11062466
doi:10.1093/plcell/koad260
PMID:37824826
Physiology, genomics, and evolutionary aspects of desert plants Mohanta TK, Mohanta YK, Kaushik P, Kumar J J Adv Res 07-May-2023
PMCID:PMC10982872
doi:10.1016/j.jare.2023.04.019
PMID:37160225
Stimulatory effects of Lycium shawii on human melanocyte proliferation, migration, and melanogenesis: In vitro and in silico studies Alghamdi K, Alehaideb Z, Kumar A, Al-Eidi H, Alghamdi SS, Suliman R, Ali R, Almourfi F, Alghamdi SM, Boudjelal M, Matou-Nasri S Front Pharmacol 24-Apr-2023
PMCID:PMC10184183
doi:10.3389/fphar.2023.1169812
PMID:37197407
In-Silico Approaches for the Screening and Discovery of Broad-Spectrum Marine Natural Product Antiviral Agents Against Coronaviruses Boswell Z, Verga JU, Mackle J, Guerrero-Vazquez K, Thomas OP, Cray J, Wolf BJ, Choo YM, Croot P, Hamann MT, Hardiman G Infect Drug Resist 19-Apr-2023
PMCID:PMC10122865
doi:10.2147/IDR.S395203
PMID:37155475
Use of Integrative, Complementary, and Alternative Medicine in Children with Epilepsy: A Global Scoping Review Zhu Z, Dluzynski D, Hammad N, Pugalenthi D, Walser SA, Mittal R, Samanta D, Brown ML, Asadi-Pooya AA, Kakooza-Mwesige A, Spalice A, Capponi M, Lekoubou A, Kumar A, Paudel S, Carney PR, Mainali G, Naik S Children (Basel) 12-Apr-2023
PMCID:PMC10136598
doi:10.3390/children10040713
PMID:37189961
Phytochemical Analysis of Anastatica hierochuntica and Aerva javanica Grown in Qatar: Their Biological Activities and Identification of Some Active Ingredients Thotathil V, Sidiq N, Fakhroo A, Sreerama L Molecules 11-Apr-2023
PMCID:PMC10145884
doi:10.3390/molecules28083364
PMID:37110597
Facilitation by Haloxylon persicum Shrubs Enhances Density and Richness of Soil Seed Bank of Annual Plants in a Hyper-Arid Ecosystem Gomaa NH, Hegazy AK, Alhaithloul HA Plants (Basel) 10-Mar-2023
PMCID:PMC10056119
doi:10.3390/plants12061276
PMID:36986963
Feeding Ecology of the Cuvier’s Gazelle (Gazella cuvieri, Ogilby, 1841) in the Sahara Desert Herrera-Sánchez FJ, López O, Rodríguez-Siles J, Díaz-Portero MÁ, Arredondo Á, Sáez JM, Álvarez B, Cancio I, de Lucas J, Pérez J, Valenzuela G, Martínez-Valderrama J, Sánchez-Cerdá M, Qninba A, Virgós E, Calleja JA, Bartolomé J, Albanell E, Serrano E, Abáigar T, Gil-Sánchez JM Animals (Basel) 06-Feb-2023
PMCID:PMC9951649
doi:10.3390/ani13040567
PMID:36830354
Synergistic Antibacterial Potential of Greenly Synthesized Silver Nanoparticles with Fosfomycin Against Some Nosocomial Bacterial Pathogens Aljeldah MM, Yassin MT, Mostafa AA, Aboul-Soud MA Infect Drug Resist 06-Jan-2023
PMCID:PMC9831080
doi:10.2147/IDR.S394600
PMID:36636381
Potential distribution of three types of ephemeral plants under climate changes Lan Z, Huiliang L, Hongxiang Z, Yanfeng C, Lingwei Z, Kudusi K, Taxmamat D, Yuanming Z Front Plant Sci 23-Nov-2022
PMCID:PMC9728545
doi:10.3389/fpls.2022.1035684
PMID:36507407

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.1016/S0960-894X(03)00088-X
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.1016/S0960-894X(03)00088-X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.1016/S0960-894X(03)00088-X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
4-Methoxybenzoic Acid 7478 Click to see 152.15 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.1016/S0960-894X(03)00088-X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Propylparaben 7175 Click to see 180.20 unknown https://doi.org/10.1016/J.BMC.2010.01.046
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see 178.18 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
Coniferaldehyde 5280536 Click to see 178.18 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.1016/S0960-894X(03)00088-X
> Lignans, neolignans and related compounds
(+)-erythro-(7R,8S)-guaiacylglycerol-8-vanillin ether 11175464 Click to see 348.30 unknown https://doi.org/10.3987/COM-03-9804
(E)-3-[4-[(1R,2S)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]prop-2-enal 21582570 Click to see 374.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
(E)-3-[4-[1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]prop-2-enal 46229016 Click to see COC1=C(C=CC(=C1)C=CC=O)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 374.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
1-(4-Hydroxy-3-methoxyphenyl)-2-[4-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]propane-1,3-diol 193323 Click to see COC1=C(C=CC(=C1)C=CCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 376.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
1-[4-[(1R,2S)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]-3-hydroxypropan-1-one 162850262 Click to see COC1=C(C=CC(=C1)C(C(CO)OC2=C(C=C(C=C2)C(=O)CCO)OC)O)O 392.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.3987/COM-03-9804
1-[4-[1,3-Dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]-3-hydroxypropan-1-one 76531313 Click to see 392.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.3987/COM-03-9804
3-[4-[1,3-Dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]prop-2-enal 73805566 Click to see 374.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
4-[1,3-Dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-methoxybenzaldehyde 72825340 Click to see COC1=C(C=CC(=C1)C=O)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 348.30 unknown https://doi.org/10.3987/COM-03-9804
7R,8S-Guaiacylglycerol-8-O-4'-(Coniferyl Alcohol)Ether 14274760 Click to see 376.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
Ggbce 6443755 Click to see COC1=C(C=CC(=C1)C=CCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 376.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(+)-Isolariciresinol 160521 Click to see 360.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
Isolariciresinol (6CI); (+)-Cyclolariciresinol; (+)-Isolariciresinol; Isolariciresinol, (+)-;-Conidendryl alcohol 4177125 Click to see 360.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
> Lignans, neolignans and related compounds / Flavonolignans
(2S,3R)-3,5,7-trihydroxy-2-[(2R,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-2,3-dihydrochromen-4-one 40429053 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=CC(=C3)C4C(C(=O)C5=C(C=C(C=C5O4)O)O)O)CO)O 482.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
Isosilybin A 11059920 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=CC(=C3)C4C(C(=O)C5=C(C=C(C=C5O4)O)O)O)CO)O 482.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
Isosilybin B 10885340 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=CC(=C3)C4C(C(=O)C5=C(C=C(C=C5O4)O)O)O)CO)O 482.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
Isosilybinin 3085830 Click to see 482.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
Silibinin 31553 Click to see 482.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
Silibinin B 1548994 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=C(C=C3)C4C(C(=O)C5=C(C=C(C=C5O4)O)O)O)CO)O 482.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
Silymarin 5213 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=C(C=C3)C4C(C(=O)C5=C(C=C(C=C5O4)O)O)O)CO)O 482.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
> Lignans, neolignans and related compounds / Furanoid lignans
(+-)-Pinoresinol 234817 Click to see 358.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Lariciresinol 332427 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown https://doi.org/10.3987/COM-03-9804
https://doi.org/10.1016/J.BMC.2010.01.046
Tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-((4-hydroxy-3-methoxyphenyl)methyl)-3-furanmethanol 134203 Click to see 360.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(5S,5aS,7R,8aR,9S)-7-(hydroxymethyl)-5,7-dimethyl-4,5a,6,8,8a,9-hexahydroazuleno[5,6-c]furan-5,9-diol 14488477 Click to see CC1(CC2C(C1)C(CC3=COC=C3C2O)(C)O)CO 266.33 unknown via CMAUP database
Mitissimols C 15939741 Click to see CC1=CC(C(C=CC(=O)C(=CC(C1)O)C)(C)C)O 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,5S,5aS,8aR,9S)-1,5,9-trihydroxy-5,7,7-trimethyl-4,5a,6,8,8a,9-hexahydro-1H-azuleno[5,6-c]furan-3-one 95049893 Click to see 282.33 unknown via CMAUP database
(4S,4aR,6R,7aS,8S)-4,8-Dihydroxy-6-(hydroxymethyl)-6,8-dimethyl-4,4a,5,6,7,7a,8,9-octahydroazuleno[5,6-c]furan-1(3H)-one 14488475 Click to see 282.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see 386.70 unknown https://doi.org/10.3109/13880209309082963
> 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/10.3109/13880209309082963
(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/10.3109/13880209309082963
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.3109/13880209309082963
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/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
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/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.3109/13880209309082963
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.3109/13880209309082963
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
(1R,2S,4E,7S,9R,11R)-2,7,9-trihydroxy-3,3,7,11-tetramethyl-12-oxabicyclo[9.1.0]dodec-4-en-6-one 102380141 Click to see 284.35 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde 8768 Click to see 138.12 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.1016/S0960-894X(03)00088-X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2R)-2,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-1-one 92446370 Click to see COC1=C(C=CC(=C1)C(=O)C(CO)O)O 212.20 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
2-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)ethanone 87530 Click to see 182.17 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
2,3-Dihydroxy-1-(4-Hydroxy-3-Methoxyphenyl)Propan-1-One 15765124 Click to see 212.20 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone 75142 Click to see 196.20 unknown https://doi.org/10.1016/J.BMC.2010.01.046
Acetovanillone 2214 Click to see 166.17 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Dehydrodiconiferyl Alcohol 11078843 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
(+)-Dehydrodiconiferyl Alcohol 11824478 Click to see 358.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
(+/-)-Balanophonin 72729357 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O 356.40 unknown https://doi.org/10.3987/COM-03-9804
https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
(2R,3S)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-[(E)-3-hydroxyprop-1-enyl]-2,3-dihydro-1-benzofuran-7-ol 11057050 Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)C=CCO)O)CO)O 344.40 unknown https://doi.org/10.3987/COM-03-9804
(2R,3S)-3,5,7-trihydroxy-2-[(2S,3R)-7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-2,3-dihydro-1-benzofuran-5-yl]-2,3-dihydrochromen-4-one 12442784 Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)C4C(C(=O)C5=C(C=C(C=C5O4)O)O)O)O)CO)O 482.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
(E)-3-[(2R,3R)-2-(3,4-dimethoxyphenyl)-7-hydroxy-3-(hydroxymethyl)-2,3-dihydro-1-benzofuran-5-yl]prop-2-enal 163194936 Click to see 356.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
(E)-3-[(2R,3S)-2-(3,4-dimethoxyphenyl)-7-hydroxy-3-(hydroxymethyl)-2,3-dihydro-1-benzofuran-5-yl]prop-2-enal 46228974 Click to see 356.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
(E)-3-[(3S)-2-(3,4-dimethoxyphenyl)-7-hydroxy-3-(hydroxymethyl)-2,3-dihydro-1-benzofuran-5-yl]prop-2-enal 162976515 Click to see 356.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-(3-methoxyprop-1-enyl)-2,3-dihydro-1-benzofuran-7-ol 76394000 Click to see 358.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
3-[2-(3,4-Dimethoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-en-1-ol 73813786 Click to see 372.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
3-[2-(3,4-Dimethoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enal 138112893 Click to see 370.40 unknown https://doi.org/10.3987/COM-03-9804
3-[2-(3,4-Dimethoxyphenyl)-7-hydroxy-3-(hydroxymethyl)-2,3-dihydro-1-benzofuran-5-yl]prop-2-enal 72786314 Click to see 356.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
4-O-Methylbalanophonin 145709487 Click to see COC1=C(C=C(C=C1)C2C(C3=C(O2)C(=CC(=C3)C=CC=O)OC)CO)OC 370.40 unknown https://doi.org/10.3987/COM-03-9804
5-O-Methylhierochin D 188976 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown https://doi.org/10.3987/COM-03-9804
https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
7-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-2,3-dihydro-1-benzofuran-5-carbaldehyde 56657034 Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)C=O)O)CO)O 316.30 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
Balanophonin 23252258 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O 356.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.3987/COM-03-9804
https://doi.org/10.1016/J.BMC.2010.01.046
Dehydrodiconiferyl alcohol 5372367 Click to see 358.40 unknown https://doi.org/10.3987/COM-03-9804
ent-Hierochin D 85382912 Click to see 344.40 unknown https://doi.org/10.3987/COM-03-9804
Hierochin A 10089764 Click to see COCC=CC1=CC2=C(C(=C1)O)OC(C2CO)C3=CC(=C(C=C3)O)OC 358.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
Hierochin B 10339234 Click to see 372.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
Hierochin C 11723269 Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)C=O)O)CO)O 316.30 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
Hierochin D 91884981 Click to see 344.40 unknown https://doi.org/10.3987/COM-03-9804
Silychristin 441764 Click to see 482.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
Silychristin B 12442785 Click to see 482.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
Silychrystin 4481797 Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)C4C(C(=O)C5=C(C=C(C=C5O4)O)O)O)O)CO)O 482.40 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see 148.16 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.1016/S0960-894X(03)00088-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.1016/S0960-894X(03)00088-X
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Eriodictyol 11095 Click to see 288.25 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
(+-)-Naringenin 932 Click to see 272.25 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.1002/CHIN.200329185
https://doi.org/10.1016/S0960-894X(03)00088-X
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1002/CHIN.200329185
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.1002/CHIN.200329185
https://doi.org/10.1016/S0960-894X(03)00088-X
Naringenin 439246 Click to see 272.25 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+)-Epitaxifolin 443758 Click to see 304.25 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.1002/CHIN.200329185
https://doi.org/10.1016/S0960-894X(03)00088-X
(+/-)-Taxifolin 471 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
3,5,7-Trihydroxy-2-(4-Hydroxyphenyl)Chroman-4-One 662 Click to see 288.25 unknown https://doi.org/10.1002/CHIN.200329185
https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.1002/CHIN.200329185
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.1002/CHIN.200329185
https://doi.org/10.1016/S0960-894X(03)00088-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.3109/13880209309082963
https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1002/CHIN.200329185
https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1016/J.BMC.2010.01.046
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.3109/13880209309082963
> Phenylpropanoids and polyketides / Flavonoids / Furanoflavonoids and dihydrofuranoflavonoids
(2S)-5,8,9-trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-[1]benzofuro[3,2-h]chromen-4-one 162996985 Click to see 378.30 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
5,7,8-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-[1]benzofuro[3,2-g]chromen-4-one 56660124 Click to see 378.30 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
5,8,9-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-[1]benzofuro[3,2-h]chromen-4-one 162996984 Click to see 378.30 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
5,9,10-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-[1]benzofuro[2,3-h]chromen-4-one 56661109 Click to see 378.30 unknown https://doi.org/10.1016/J.BMC.2010.01.046
Anastatin A 10134240 Click to see 378.30 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1002/CHIN.200329185
https://doi.org/10.1016/J.BMC.2010.01.046
Anastatin B 10407286 Click to see C1C(OC2=C(C1=O)C(=CC3=C2C4=CC(=C(C=C4O3)O)O)O)C5=CC=C(C=C5)O 378.30 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1002/CHIN.200329185
https://doi.org/10.1016/J.BMC.2010.01.046
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3'-O-Methyltaxifolin 26194552 Click to see COC1=C(C=CC(=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 318.28 unknown https://doi.org/10.1002/CHIN.200329185
https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
Dihydroisorhamnetin 56658060 Click to see 318.28 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
> Phenylpropanoids and polyketides / Stilbenes
(-)-Evofolin B 46229015 Click to see COC1=C(C=CC(=C1)C(CO)C(=O)C2=CC(=C(C=C2)O)OC)O 318.32 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
(1R,2R)-1,2-Bis(4-hydroxy-3-methoxyphenyl)propane-1,3-diol 12468616 Click to see 320.30 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
(1S,2R)-1,2-bis(3-methoxy-4-oxidanyl-phenyl)propane-1,3-diol 11290161 Click to see 320.30 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
(1S,2S)-1,2-bis(3-methoxy-4-oxidanyl-phenyl)propane-1,3-diol 12468617 Click to see 320.30 unknown https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
(2R)-1-(4-hydroxy-3-methoxyphenyl)-2-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxyphenyl]propane-1,2,3-triol 162817362 Click to see 376.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
(E)-3-[3-methoxy-4-[(2R)-1,2,3-trihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]phenyl]prop-2-enal 162925135 Click to see COC1=C(C=CC(=C1)C=CC=O)C(CO)(C(C2=CC(=C(C=C2)O)OC)O)O 374.40 unknown https://doi.org/10.1016/J.BMC.2010.01.046
(R)-1,2-Bis(3-methoxy-4-hydroxyphenyl)-3-hydroxy-1-propanone 101504852 Click to see COC1=C(C=CC(=C1)C(CO)C(=O)C2=CC(=C(C=C2)O)OC)O 318.32 unknown https://doi.org/10.1016/J.BMC.2010.01.046
1,2-Bis(4-hydroxy-3-methoxyphenyl)propane-1,3-diol 6426042 Click to see COC1=C(C=CC(=C1)C(CO)C(C2=CC(=C(C=C2)O)OC)O)O 320.30 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804
Evofolin B 5317306 Click to see COC1=C(C=CC(=C1)C(CO)C(=O)C2=CC(=C(C=C2)O)OC)O 318.32 unknown https://doi.org/10.1016/S0960-894X(03)00088-X
https://doi.org/10.1016/J.BMC.2010.01.046
https://doi.org/10.3987/COM-03-9804

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