Anastatica is a unique plant that belongs to the Brassicaceae family and is the only species in its genus. It is a small annual herb with gray leaves and tiny white flowers. While it is often referred to as the "rose of Jericho", it is not a true resurrection plant as its dead tissues do not revive. It is found in arid regions of the Middle East and the Sahara Desert, and has the ability to curl up into a ball during dry seasons and reopen when exposed to moisture. This allows it to survive in harsh environments and disperse its seeds. The plant has been used in ancient times to predict weather patterns and is considered a symbol of resilience and adaptability.

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 click to expand
- Macaronesia
  - Canary Islands
- Northeast Tropical Africa
  - Eritrea
  - Sudan
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia
  - Western Sahara
- West Tropical Africa
  - Mali
  - Mauritania

Asia-temperate click to expand
- Arabian Peninsula
  - Gulf States
  - Kuwait
  - Oman
  - Saudi Arabia
  - Yemen
- Western Asia
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan

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
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_900406275.1	ASM90040627v1	Scaffold	MAX PLANCK INSTITUTE FOR PLANT BREEDING RESEARCH	2019-06-19	25.0x	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

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

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

Antiviral effects of phytochemicals against severe acute respiratory syndrome coronavirus 2 and their mechanisms of action: A review

Jantan I, Arshad L, Septama AW, Haque MA, Mohamed‐Hussein Z, Govender NT

Phytother Res

07-Nov-2022

PMCID:	PMC9878073
doi:	10.1002/ptr.7671
PMID:	36343627

Complementary and alternative therapies in skin cancer: A literature review of biologically active compounds.

Hidalgo L, Saldías-Fuentes C, Carrasco K, Halpern AC, Mao JJ, Navarrete-Dechent C

Dermatol Ther

27-Sep-2022

PMCID:	PMC10481428
doi:	10.1111/dth.15842
PMID:	36124923

In Vitro Induction of Apoptosis in Isolated Acute Myeloid Leukemia Cells: The Role of Anastatica hierochuntica Methanolic Extract

El-Garawani IM, Abd El-Gaber AS, Algamdi NA, Saeed A, Zhao C, Khattab OM, AlAjmi MF, Guo Z, Khalifa SA, El-Seedi HR

Metabolites

17-Sep-2022

PMCID:	PMC9501128
doi:	10.3390/metabo12090878
PMID:	36144283

Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells

Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T

Molecules

09-Sep-2022

PMCID:	PMC9501561
doi:	10.3390/molecules27185858
PMID:	36144591

Positive selection and heat‐response transcriptomes reveal adaptive features of the Brassicaceae desert model, Anastatica hierochuntica

Eshel G, Duppen N, Wang G, Oh D, Kazachkova Y, Herzyk P, Amtmann A, Gordon M, Chalifa‐Caspi V, Oscar MA, Bar‐David S, Marshall‐Colon A, Dassanayake M, Barak S

New Phytol

26-Aug-2022

PMCID:	PMC9804903
doi:	10.1111/nph.18411
PMID:	35909295

Phytochemical Profile Top

Add a new one!

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
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	154.12	unknown	https://doi.org/10.1016/J.BMC.2010.01.046 https://doi.org/10.1016/S0960-894X(03)00088-X
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
> 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
p-Anisic acid	7478	Click to see COC1=CC=C(C=C1)C(=O)O	152.15	unknown	https://doi.org/10.1016/S0960-894X(03)00088-X https://doi.org/10.1016/J.BMC.2010.01.046
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Propylparaben	7175	Click to see CCCOC(=O)C1=CC=C(C=C1)O	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 COC1=C(C=CC(=C1)C=CC=O)O	178.18	unknown	https://doi.org/10.1016/S0960-894X(03)00088-X https://doi.org/10.1016/J.BMC.2010.01.046
4-Hydroxy-3-methoxycinnamaldehyde	5280536	Click to see COC1=C(C=CC(=C1)C=CC=O)O	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
(1R,2S)-1-(3-Methoxy-4-hydroxyphenyl)-2-[2-methoxy-4-[(E)-3-hydroxy-1-propenyl]phenoxy]-1,3-propanediol	14274760	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
(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
3-[4-[1,3-Dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]prop-2-enal	73805566	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/S0960-894X(03)00088-X https://doi.org/10.1016/J.BMC.2010.01.046 https://doi.org/10.3987/COM-03-9804
4-[(1R,2S)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-methoxybenzaldehyde	11175464	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
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
4'-[alpha-(Hydroxymethyl)-4,beta-dihydroxy-3-methoxyphenethyloxy]-3'-methoxy-beta-hydroxypropiophenone	76531313	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
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
threo-Guaiacylglycerol-beta-coniferyl aldehyde ether	21582570	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/S0960-894X(03)00088-X https://doi.org/10.1016/J.BMC.2010.01.046 https://doi.org/10.3987/COM-03-9804
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isolariciresinol (6CI); (+)-Cyclolariciresinol; (+)-Isolariciresinol; Isolariciresinol, (+)-;-Conidendryl alcohol	4177125	Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1016/S0960-894X(03)00088-X
Isolariciresinol, (+)-	160521	Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O	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	3085830	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 https://doi.org/10.1016/J.BMC.2010.01.046
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
Silibinin	31553	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
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
4-[6-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol	234817	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
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 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
> 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 CC1(CC2C(C1)C(CC3=C(C2O)C(OC3=O)O)(C)O)C	282.33	unknown	via CMAUP database
4,4abeta,5,6,7,7abeta,8,9-Octahydro-4beta,8beta-dihydroxy-6beta-(hydroxymethyl)-6,8-dimethylazuleno[5,6-c]furan-1(3H)-one	14488475	Click to see CC1(CC2C(C1)C(CC3=C(C2O)COC3=O)(C)O)CO	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 CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	386.70	unknown	https://doi.org/10.3109/13880209309082963
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	134766514	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.3109/13880209309082963
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.3109/13880209309082963
> 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
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.3109/13880209309082963
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
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.3109/13880209309082963
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
Mitissimol G	102380141	Click to see CC1(C=CC(=O)C(CC(CC2(C(C1O)O2)C)O)(C)O)C	284.35	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see C1=CC(=CC=C1C=O)O	122.12	unknown	https://doi.org/10.1016/J.BMC.2010.01.046 https://doi.org/10.1016/S0960-894X(03)00088-X
Protocatechualdehyde	8768	Click to see C1=CC(=C(C=C1C=O)O)O	138.12	unknown	https://doi.org/10.1016/S0960-894X(03)00088-X https://doi.org/10.1016/J.BMC.2010.01.046
> 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 COC1=C(C=CC(=C1)C(=O)CO)O	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)-1-propanone	15765124	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
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone	75142	Click to see COC1=C(C=CC(=C1)C(=O)CCO)O	196.20	unknown	https://doi.org/10.1016/J.BMC.2010.01.046
Acetovanillone	2214	Click to see CC(=O)C1=CC(=C(C=C1)O)OC	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
(+)-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/10.3987/COM-03-9804 https://doi.org/10.1016/S0960-894X(03)00088-X https://doi.org/10.1016/J.BMC.2010.01.046
(+)-Dehydrodiconiferyl alcohol	11824478	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/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)-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 COC1=C(C=C(C=C1)C2C(C3=C(O2)C(=CC(=C3)C=CC=O)O)CO)OC	356.40	unknown	https://doi.org/10.1016/S0960-894X(03)00088-X
(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 COC1=C(C=C(C=C1)C2C(C3=C(O2)C(=CC(=C3)C=CC=O)O)CO)OC	356.40	unknown	https://doi.org/10.1016/J.BMC.2010.01.046
(E)-3-[7-Hydroxy-2beta-(3,4-dimethoxyphenyl)-3alpha-(hydroxymethyl)-2,3-dihydrobenzofuran-5-yl]acrylaldehyde	46228974	Click to see COC1=C(C=C(C=C1)C2C(C3=C(O2)C(=CC(=C3)C=CC=O)O)CO)OC	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 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
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 COC1=C(C=C(C=C1)C2C(C3=C(O2)C(=CC(=C3)C=CCO)OC)CO)OC	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 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
3-[2-(3,4-Dimethoxyphenyl)-7-hydroxy-3-(hydroxymethyl)-2,3-dihydro-1-benzofuran-5-yl]prop-2-enal	72786314	Click to see COC1=C(C=C(C=C1)C2C(C3=C(O2)C(=CC(=C3)C=CC=O)O)CO)OC	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/10.1016/S0960-894X(03)00088-X https://doi.org/10.1016/J.BMC.2010.01.046 https://doi.org/10.3987/COM-03-9804
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
CID 85382912	85382912	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
Dehydrodiconiferyl alcohol	5372367	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
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 COC1=C(C=C(C=C1)C2C(C3=C(O2)C(=CC(=C3)C=CCO)OC)CO)OC	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 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
Hierochin D	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
Silicristin	441764	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/J.BMC.2010.01.046
Silychristin B	12442785	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/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 C1=CC=C(C=C1)C=CC(=O)O	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 COC1=C(C=CC(=C1)C=CC(=O)O)O	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 COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1016/J.BMC.2010.01.046 https://doi.org/10.1016/S0960-894X(03)00088-X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol	11095	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/S0960-894X(03)00088-X https://doi.org/10.1016/J.BMC.2010.01.046
(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
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one	932	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	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
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 C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	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 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/10.1002/CHIN.200329185 https://doi.org/10.1016/J.BMC.2010.01.046
(+/-)-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)-2,3-dihydrochromen-4-one	662	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/10.1002/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/10.1002/CHIN.200329185 https://doi.org/10.1016/S0960-894X(03)00088-X https://doi.org/10.1016/J.BMC.2010.01.046
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/10.1002/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 / 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 C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	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 C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	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 CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	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 CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	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 C1C(OC2=C3C(=CC(=C2C1=O)O)C4=CC(=C(C=C4O3)O)O)C5=CC=C(C=C5)O	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 C1C(OC2=C(C1=O)C(=C3C4=CC(=C(C=C4OC3=C2)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/10.1016/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 C1C(OC2=C3C(=CC(=C2C1=O)O)C4=CC(=C(C=C4O3)O)O)C5=CC=C(C=C5)O	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 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/J.BMC.2010.01.046
Anastatin A	10134240	Click to see C1C(OC2=C(C1=O)C(=C3C4=CC(=C(C=C4OC3=C2)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
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 COC1=C(C=CC(=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	318.28	unknown	https://doi.org/10.1016/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 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
(1S,2R)-1,2-bis(3-methoxy-4-oxidanyl-phenyl)propane-1,3-diol	11290161	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
(1S,2S)-1,2-Bis(4-hydroxy-3-methoxyphenyl)propane-1,3-diol	12468617	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/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 COC1=C(C=CC(=C1)C=CCO)C(CO)(C(C2=CC(=C(C=C2)O)OC)O)O	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
1-Propanone, 3-hydroxy-1,2-bis(4-hydroxy-3-methoxyphenyl)-, (2R)-	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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Anastatica hierochuntica

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