NCBI Taxonomy: 9971

Pholidota (ncbi_taxid: 9971)

found 61 associated metabolites at order taxonomy rank level.

Ancestor: Laurasiatheria

Child Taxonomies: Manidae

Resveratrol

(E)-5-(2-(4-hydroxyphenyl)ethenyl)-1,3-benzenediol(E)-5-(2-(4-hydroxyphenyl)ethenyl)-1,3-benzenediol

C14H12O3 (228.0786402)


Resveratrol is a stilbenol that is stilbene in which the phenyl groups are substituted at positions 3, 5, and 4 by hydroxy groups. It has a role as a phytoalexin, an antioxidant, a glioma-associated oncogene inhibitor and a geroprotector. It is a stilbenol, a polyphenol and a member of resorcinols. Resveratrol (3,5,4-trihydroxystilbene) is a polyphenolic phytoalexin. It is a stilbenoid, a derivate of stilbene, and is produced in plants with the help of the enzyme stilbene synthase. It exists as cis-(Z) and trans-(E) isomers. The trans- form can undergo isomerisation to the cis- form when heated or exposed to ultraviolet irradiation. In a 2004 issue of Science, Dr. Sinclair of Harvard University said resveratrol is not an easy molecule to protect from oxidation. It has been claimed that it is readily degraded by exposure to light, heat, and oxygen. However, studies find that Trans-resveratrol undergoes negligible oxidation in normal atmosphere at room temperature. Resveratrol is a plant polyphenol found in high concentrations in red grapes that has been proposed as a treatment for hyperlipidemia and to prevent fatty liver, diabetes, atherosclerosis and aging. Resveratrol use has not been associated with serum enzyme elevations or with clinically apparent liver injury. Resveratrol is a natural product found in Vitis rotundifolia, Vitis amurensis, and other organisms with data available. Resveratrol is a phytoalexin derived from grapes and other food products with antioxidant and potential chemopreventive activities. Resveratrol induces phase II drug-metabolizing enzymes (anti-initiation activity); mediates anti-inflammatory effects and inhibits cyclooxygenase and hydroperoxidase functions (anti-promotion activity); and induces promyelocytic leukemia cell differentiation (anti-progression activity), thereby exhibiting activities in three major steps of carcinogenesis. This agent may inhibit TNF-induced activation of NF-kappaB in a dose- and time-dependent manner. (NCI05) Resveratrol is a metabolite found in or produced by Saccharomyces cerevisiae. A stilbene and non-flavonoid polyphenol produced by various plants including grapes and blueberries. It has anti-oxidant, anti-inflammatory, cardioprotective, anti-mutagenic, and anti-carcinogenic properties. It also inhibits platelet aggregation and the activity of several DNA HELICASES in vitro. Resveratrol is a polyphenolic phytoalexin. It is also classified as a stilbenoid, a derivate of stilbene, and is produced in plants with the help of the enzyme stilbene synthase. The levels of resveratrol found in food vary greatly. Red wine contains between 0.2 and 5.8 mg/L depending on the grape variety, while white wine has much less. The reason for this difference is that red wine is fermented with grape skins, allowing the wine to absorb the resveratrol, whereas white wine is fermented after the skin has been removed. Resveratrol is also sold as a nutritional supplement. A number of beneficial health effects, such as anti-cancer, antiviral, neuroprotective, anti-aging, anti-inflammatory, and life-prolonging effects have been reported for resveratrol. The fact that resveratrol is found in the skin of red grapes and as a constituent of red wine may explain the "French paradox". This paradox is based on the observation that the incidence of coronary heart disease is relatively low in southern France despite high dietary intake of saturated fats. Resveratrol is thought to achieve these cardioprotective effects by a number of different routes: (1) inhibition of vascular cell adhesion molecule expression; (2) inhibition of vascular smooth muscle cell proliferation; (3) stimulation of endothelial nitric oxide synthase (eNOS) activity; (4) inhibition of platelet aggregation; and (5) inhibition of LDL peroxidation (PMID: 17875315, 14676260, 9678525). Resveratrol is a biomarker for the consumption of grapes and raisins. A stilbenol that is stilbene in which the phenyl groups are substituted at positions 3, 5, and 4 by hydroxy groups. COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials D006401 - Hematologic Agents > D010975 - Platelet Aggregation Inhibitors C1892 - Chemopreventive Agent > C54630 - Phase II Enzymes Inducer D020011 - Protective Agents > D000975 - Antioxidants C26170 - Protective Agent > C275 - Antioxidant D004791 - Enzyme Inhibitors Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9638; ORIGINAL_PRECURSOR_SCAN_NO 9635 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9646; ORIGINAL_PRECURSOR_SCAN_NO 9641 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4381; ORIGINAL_PRECURSOR_SCAN_NO 4379 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9607; ORIGINAL_PRECURSOR_SCAN_NO 9606 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9642; ORIGINAL_PRECURSOR_SCAN_NO 9638 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4383; ORIGINAL_PRECURSOR_SCAN_NO 4379 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4396; ORIGINAL_PRECURSOR_SCAN_NO 4394 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4381; ORIGINAL_PRECURSOR_SCAN_NO 4376 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9641; ORIGINAL_PRECURSOR_SCAN_NO 9638 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4375; ORIGINAL_PRECURSOR_SCAN_NO 4373 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9614; ORIGINAL_PRECURSOR_SCAN_NO 9611 CONFIDENCE standard compound; INTERNAL_ID 1110; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4398; ORIGINAL_PRECURSOR_SCAN_NO 4397 IPB_RECORD: 1781; CONFIDENCE confident structure IPB_RECORD: 321; CONFIDENCE confident structure Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7].

   
   

Resveratrol

3,4,5-Trihydroxystilbene

C14H12O3 (228.0786402)


COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials D006401 - Hematologic Agents > D010975 - Platelet Aggregation Inhibitors C1892 - Chemopreventive Agent > C54630 - Phase II Enzymes Inducer D020011 - Protective Agents > D000975 - Antioxidants CONFIDENCE standard compound; EAWAG_UCHEM_ID 3241 C26170 - Protective Agent > C275 - Antioxidant D004791 - Enzyme Inhibitors Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7].

   

2-methoxy-9,10-dihydrophenanthrene-4,5-diol

2-methoxy-9,10-dihydrophenanthrene-4,5-diol

C15H14O3 (242.0942894)


   

7-Methoxy-9,10-dihydrophenanthrene-3,5-diol

7-Methoxy-9,10-dihydrophenanthrene-3,5-diol

C15H14O3 (242.0942894)


   

Dotriacontanol

Dotriacontan-1-ol

C32H66O (466.5113386)


   

9,10-dihydrophenanthrene-2,4,7-triol

2,4,7-Trihydroxy-9,10-dihydrophenanthrene

C14H12O3 (228.0786402)


2,4,7-Trihydroxy-9,10-dihydrophenanthrene is a natural product found in Dendrobium moniliforme and Pholidota chinensis with data available.

   

Resveratrol

trans-resveratrol

C14H12O3 (228.0786402)


Resveratrol, also known as 3,4,5-trihydroxystilbene or trans-resveratrol, is a member of the class of compounds known as stilbenes. Stilbenes are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids. Thus, resveratrol is considered to be an aromatic polyketide lipid molecule. Resveratrol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Resveratrol is a bitter tasting compound and can be found in a number of food items such as broccoli, yellow wax bean, bilberry, and turnip, which makes resveratrol a potential biomarker for the consumption of these food products. Resveratrol can be found primarily in urine, as well as throughout most human tissues. Resveratrol exists in all eukaryotes, ranging from yeast to humans. Resveratrol (3,5,4′-trihydroxy-trans-stilbene) is a stilbenoid, a type of natural phenol, and a phytoalexin produced by several plants in response to injury or, when the plant is under attack by pathogens such as bacteria or fungi. Sources of resveratrol in food include the skin of grapes, blueberries, raspberries, mulberries . Resveratrol suppresses NF-kappaB (NF-kappaB) activation in HSV infected cells. Reports have indicated that HSV activates NF-kappaB during productive infection and this may be an essential aspect of its replication scheme [PMID: 9705914] (DrugBank). relative retention time with respect to 9-anthracene Carboxylic Acid is 0.738 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.740 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.730 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.733 Acquisition and generation of the data is financially supported by the Max-Planck-Society COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials D006401 - Hematologic Agents > D010975 - Platelet Aggregation Inhibitors C1892 - Chemopreventive Agent > C54630 - Phase II Enzymes Inducer D020011 - Protective Agents > D000975 - Antioxidants C26170 - Protective Agent > C275 - Antioxidant D004791 - Enzyme Inhibitors Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS IPB_RECORD: 2101; CONFIDENCE confident structure IPB_RECORD: 2901; CONFIDENCE confident structure Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7]. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7].

   

3-[2-(3-hydroxyphenyl)ethyl]-5-methoxyphenol

NCGC00385266-01!3-[2-(3-hydroxyphenyl)ethyl]-5-methoxyphenol

C15H16O3 (244.1099386)


   

7-methoxy-9,10-dihydrophenanthrene-2,5-diol

NCGC00385352-01!7-methoxy-9,10-dihydrophenanthrene-2,5-diol

C15H14O3 (242.0942894)


   

4-methoxy-9,10-dihydrophenanthrene-2,7-diol

4-methoxy-9,10-dihydrophenanthrene-2,7-diol

C15H14O3 (242.0942894)


   

FOH 32:0

Dotriacontan-1-ol

C32H66O (466.5113386)


   

Phoyunbene B

Phoyunbene B

C17H18O5 (302.1154178)


A stilbenoid that is trans-stilbene substituted by hydroxy groups at positions 3 and 4 and methoxy groups at positions 2, 3 and 5. Isolated from Pholidota yunnanensis, it exhibits inhibitory effects on production of nitric oxide.

   

Phoyunbene C

Phoyunbene C

C16H16O4 (272.1048536)


A stilbenoid that is trans-stilbene substituted by hydroxy groups at positions 3 and 3 and methoxy groups at positions 2 and 5. Isolated from Pholidota yunnanensis, it exhibits inhibitory activity on nitric oxide production.

   

Phoyunbene D

Phoyunbene D

C17H18O4 (286.1205028)


A stilbenoid that is trans-stilbene substituted by a hydroxy group at position 3 and methoxy groups at positions 2, 3 and 5. Isolated from Pholidota yunnanensis, it exhibits inhibitory effects on production of nitric oxide.

   

Phoyunbene A

Phoyunbene A

C17H18O5 (302.1154178)


A stilbenoid that is trans-stilbene substituted by hydroxy groups at positions 3 and 3 and methoxy groups at positions 2, 4 and 5. Isolated from Pholidota yunnanensis, it exhibits inhibitory effects on production of nitric oxide.

   

Dotriacontan-1-ol

Dotriacontan-1-ol

C32H66O (466.5113386)


An ultra-long-chain primary fatty alcohol that is dotriacontane in which a hydrogen attached to one of the terminal carbons is replaced by a hydroxy group.

   

8-[(5-hydroxy-7-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

8-[(5-hydroxy-7-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H26O6 (482.17292960000003)


   

2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),11(15),12-hexaene-6,13-diol

2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),11(15),12-hexaene-6,13-diol

C15H12O3 (240.0786402)


   

3-[2-(3-hydroxyphenyl)ethenyl]-5-methoxyphenol

3-[2-(3-hydroxyphenyl)ethenyl]-5-methoxyphenol

C15H14O3 (242.0942894)


   

8-{4-hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl}-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

8-{4-hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl}-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H28O6 (484.1885788)


   

3-[2-(3-hydroxy-5-methoxyphenyl)ethenyl]-2,6-dimethoxyphenol

3-[2-(3-hydroxy-5-methoxyphenyl)ethenyl]-2,6-dimethoxyphenol

C17H18O5 (302.1154178)


   

4,4'-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-2,2',7,7'-tetrol

4,4'-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-2,2',7,7'-tetrol

C30H26O6 (482.17292960000003)


   

3-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-5-methoxyphenol

3-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-5-methoxyphenol

C16H18O4 (274.1205028)


   

6,13-dihydroxy-5-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

6,13-dihydroxy-5-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

C16H12O5 (284.0684702)


   

3-[2-(2,3-dimethoxyphenyl)ethenyl]-5-methoxyphenol

3-[2-(2,3-dimethoxyphenyl)ethenyl]-5-methoxyphenol

C17H18O4 (286.1205028)


   

5-[2-(3-hydroxyphenyl)ethyl]-7-methoxy-2h-1,3-benzodioxol-4-ol

5-[2-(3-hydroxyphenyl)ethyl]-7-methoxy-2h-1,3-benzodioxol-4-ol

C16H16O5 (288.0997686)


   

3-[(1e)-2-(3-hydroxy-5-methoxyphenyl)ethenyl]benzene-1,2-diol

3-[(1e)-2-(3-hydroxy-5-methoxyphenyl)ethenyl]benzene-1,2-diol

C15H14O4 (258.0892044)


   

2',3-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-4,4',7,7'-tetrol

2',3-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-4,4',7,7'-tetrol

C30H26O6 (482.17292960000003)


   

7-{4-hydroxy-2-[2-(4-hydroxyphenyl)ethyl]-6-methoxyphenoxy}-2-methoxy-9,10-dihydrophenanthren-4-ol

7-{4-hydroxy-2-[2-(4-hydroxyphenyl)ethyl]-6-methoxyphenoxy}-2-methoxy-9,10-dihydrophenanthren-4-ol

C30H28O6 (484.1885788)


   

7-{4-hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenoxy}-2-methoxy-9,10-dihydrophenanthren-4-ol

7-{4-hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenoxy}-2-methoxy-9,10-dihydrophenanthren-4-ol

C30H28O6 (484.1885788)


   

3,7'-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-2',4,5',7-tetrol

3,7'-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-2',4,5',7-tetrol

C30H26O6 (482.17292960000003)


   

5-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4(16),5,7,11(15),12-hexaene-6,13-diol

5-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4(16),5,7,11(15),12-hexaene-6,13-diol

C16H14O4 (270.0892044)


   

8-[(7-hydroxy-4-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

8-[(7-hydroxy-4-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H26O6 (482.17292960000003)


   

8-{2-hydroxy-6-[2-(3-hydroxyphenyl)ethenyl]-4-methoxyphenyl}-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

8-{2-hydroxy-6-[2-(3-hydroxyphenyl)ethenyl]-4-methoxyphenyl}-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H26O6 (482.17292960000003)


   

13-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),11(15),12-hexaen-6-ol

13-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(14),4,6,8(16),11(15),12-hexaen-6-ol

C16H14O3 (254.0942894)


   

(2s,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(3-hydroxy-5-methoxyphenyl)-10-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-7-ol

(2s,3s)-2-(4-hydroxy-3-methoxyphenyl)-3-(3-hydroxy-5-methoxyphenyl)-10-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-7-ol

C31H28O7 (512.1834938)


   

3-{4-hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl}-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

3-{4-hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl}-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H28O6 (484.1885788)


   

4,4'-dimethoxy-9h,9'h,10h,10'h-[1,1'-biphenanthrene]-2,2',7,7'-tetrol

4,4'-dimethoxy-9h,9'h,10h,10'h-[1,1'-biphenanthrene]-2,2',7,7'-tetrol

C30H26O6 (482.17292960000003)


   

8-[(7-hydroxy-5-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

8-[(7-hydroxy-5-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H26O6 (482.17292960000003)


   

3-[2-(3-hydroxy-5-methoxyphenyl)ethenyl]benzene-1,2-diol

3-[2-(3-hydroxy-5-methoxyphenyl)ethenyl]benzene-1,2-diol

C15H14O4 (258.0892044)


   

3,3'-dimethoxy-9,10-dihydro-[1,1'-biphenanthrene]-4,4',7,7'-tetrol

3,3'-dimethoxy-9,10-dihydro-[1,1'-biphenanthrene]-4,4',7,7'-tetrol

C30H24O6 (480.1572804)


   

3-[(1e)-2-(3-hydroxyphenyl)ethenyl]-5-methoxyphenol

3-[(1e)-2-(3-hydroxyphenyl)ethenyl]-5-methoxyphenol

C15H14O3 (242.0942894)


   

8-{2-hydroxy-6-[(1e)-2-(3-hydroxyphenyl)ethenyl]-4-methoxyphenyl}-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

8-{2-hydroxy-6-[(1e)-2-(3-hydroxyphenyl)ethenyl]-4-methoxyphenyl}-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H26O6 (482.17292960000003)


   

13-methoxy-3-oxo-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-6-yl acetate

13-methoxy-3-oxo-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-6-yl acetate

C18H14O5 (310.0841194)


   

8-[(5-hydroxy-7-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

8-[(5-hydroxy-7-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H26O6 (482.17292960000003)


   

13-methoxy-2,15,17-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaen-6-ol

13-methoxy-2,15,17-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaen-6-ol

C16H14O5 (286.0841194)


   

3-[2-(3-hydroxy-2-methoxyphenyl)ethenyl]-5-methoxyphenol

3-[2-(3-hydroxy-2-methoxyphenyl)ethenyl]-5-methoxyphenol

C16H16O4 (272.1048536)


   

3-{2-hydroxy-4-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl}-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

3-{2-hydroxy-4-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl}-7-methoxy-9,10-dihydrophenanthrene-2,5-diol

C30H28O6 (484.1885788)


   

3,4-dimethoxy-9,10-dihydrophenanthrene-2,7-diol

3,4-dimethoxy-9,10-dihydrophenanthrene-2,7-diol

C16H16O4 (272.1048536)


   

2-(4-hydroxy-3-methoxyphenyl)-3-(3-hydroxy-5-methoxyphenyl)-10-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-7-ol

2-(4-hydroxy-3-methoxyphenyl)-3-(3-hydroxy-5-methoxyphenyl)-10-methoxy-2h,3h,4h,5h-phenanthro[2,1-b]furan-7-ol

C31H28O7 (512.1834938)


   

5-[2-(2h-1,3-benzodioxol-5-yl)ethyl]-7-methoxy-2h-1,3-benzodioxol-4-ol

5-[2-(2h-1,3-benzodioxol-5-yl)ethyl]-7-methoxy-2h-1,3-benzodioxol-4-ol

C17H16O6 (316.0946836)


   

4,5'-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-2,2',7,7'-tetrol

4,5'-dimethoxy-9h,9'h,10h,10'h-[1,3'-biphenanthrene]-2,2',7,7'-tetrol

C30H26O6 (482.17292960000003)


   

6-hydroxy-13-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

6-hydroxy-13-methoxy-2-oxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

C16H12O4 (268.0735552)


   

1-[(7-hydroxy-4-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-4-methoxy-9,10-dihydrophenanthrene-2,7-diol

1-[(7-hydroxy-4-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-4-methoxy-9,10-dihydrophenanthrene-2,7-diol

C30H26O6 (482.17292960000003)


   

3-[(1z)-2-(3-hydroxyphenyl)ethenyl]-5-methoxyphenol

3-[(1z)-2-(3-hydroxyphenyl)ethenyl]-5-methoxyphenol

C15H14O3 (242.0942894)


   

3-[2-(4-hydroxyphenyl)ethyl]-5-methoxyphenol

3-[2-(4-hydroxyphenyl)ethyl]-5-methoxyphenol

C15H16O3 (244.1099386)


   

5-[2-(4-hydroxyphenyl)ethyl]-2-methoxyphenol

5-[2-(4-hydroxyphenyl)ethyl]-2-methoxyphenol

C15H16O3 (244.1099386)


   

2',7-dimethoxy-9h,9'h,10h,10'h-[3,3'-biphenanthrene]-2,4',5,7'-tetrol

2',7-dimethoxy-9h,9'h,10h,10'h-[3,3'-biphenanthrene]-2,4',5,7'-tetrol

C30H26O6 (482.17292960000003)


   

4-[2-(3-hydroxy-5-methoxyphenyl)ethenyl]-2,3-dimethoxyphenol

4-[2-(3-hydroxy-5-methoxyphenyl)ethenyl]-2,3-dimethoxyphenol

C17H18O5 (302.1154178)