(Q6634710)

English

pallidol

chemical compound

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type of chemical entity

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subclass of

chemical compound

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chemical structure

Pallidol.svg
229 × 165; 9 KB

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mass

454.141638 dalton

1 reference

language of work or name

Pallidol (English)

8 October 2016

(4bS,5R,9bS,10R)-5,10-bis(4-hydroxyphenyl)-4b,5,9b,10-tetrahydroindeno[2,1-a]indene-1,3,6,8-tetrol

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

5beta,10beta-Bis(4-hydroxyphenyl)-4bbeta,5,9bbeta,10-tetrahydroindeno[2,1-a]indene-1,3,6,8-tetraol

1 reference

based on heuristic

inferred from InChI

chemical formula

C₂₈H₂₂O₆

1 reference

language of work or name

Pallidol (English)

8 October 2016

C1=CC(=CC=C1C2C3C(C(C4=C(C=C(C=C34)O)O)C5=CC=C(C=C5)O)C6=CC(=CC(=C26)O)O)O

1 reference

language of work or name

Pallidol (English)

8 October 2016

C1=CC(=CC=C1[C@H]2[C@H]3[C@H]([C@@H](C4=C(C=C(C=C34)O)O)C5=CC=C(C=C5)O)C6=CC(=CC(=C26)O)O)O

1 reference

language of work or name

Pallidol (English)

8 October 2016

1 reference

Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis

Cyphostemma crotalarioides

5 references

stated in

Antifungal activity of resveratrol oligomers fromCyphostemma crotalarioides

stated in

Cyphostemmins A-B, two new antifungal oligostilbenes from Cyphostemma crotalarioides (Vitaceae)

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Cyphostemmins A-B, two new antifungal oligostilbenes from Cyphostemma crotalarioides (Vitaceae)

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Cis ε-viniferin: A New Antifungal Resveratrol Dehydrodimer from Cyphostemma crotalarioides Roots

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Cyphostemmins A-B, two new antifungal oligostilbenes from Cyphostemma crotalarioides (Vitaceae)

Caragana brevifolia

1 reference

stated in

Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis

Caragana korshinskii

1 reference

stated in

Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis

Caragana leucophloea

1 reference

stated in

Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis

Caragana sinica

5 references

stated in

Three Stilbene Tetramers from the Roots of Caragana sinica

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Determination of hypaphorine and oligomeric stilbenes in the root of Caragana sinica by capillary electrophoresis with electrochemical detection

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Five novel oligostilbenes from the roots of Caragana sinica

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Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis

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Antioxidative oligostilbenes from Caragana sinica

Caragana stenophylla

1 reference

stated in

Identification and determination of oligomeric stilbenes in the roots of Caragana species by capillary electrophoresis

Cyperus longus

2 references

stated in

Structures and Radical Scavenging Activities of Novel Norstilbene Dimer, Longusone A, and New Stilbene Dimers, Longusols A, B, and C, from Egyptian Herbal Medicine Cyperus longus

stated in

Structures of novel norstilbene dimer, longusone A, and three new stilbene dimers, longusols A, B, and C, with antiallergic and radical scavenging activities from Egyptian natural medicine Cyperus longus.

Mallotus pallidus

1 reference

stated in

Phloroglucinol derivatives from Mallotus pallidus

Parthenocissus tricuspidata

3 references

stated in

A resveratrol dimer from Parthenocissus tricuspidata

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A resveratrol dimer from Parthenocissus tricuspidata

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Two new antioxidant stilbene dimers, parthenostilbenins A and B from Parthenocissus tricuspidata

Sophora alopecuroides

2 references

stated in

Occurrence of prenylated flavonoids and oligostilbenes and its significance for chemotaxonomy of genus Sophora (Leguminosae)

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Chemical constituents isolated from the Mongolian medicinal plant Sophora alopecuroides L. and their inhibitory effects on LPS-induced nitric oxide production in RAW 264.7 macrophages

Sophora leachiana

3 references

stated in

Occurrence of prenylated flavonoids and oligostilbenes and its significance for chemotaxonomy of genus Sophora (Leguminosae)

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Two Novel Resveratrol Trimers, Leachianols A and B, from Sophora leachiana.

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Two Novel Resveratrol Trimers, Leachianols A and B, from Sophora leachiana.

Carex

1 reference

stated in

Resveratrol oligomers isolated from Carex species inhibit growth of human colon tumorigenic cells mediated by cell cycle arrest.

Carex folliculata

1 reference

stated in

Identification and bioactivities of resveratrol oligomers and flavonoids from Carex folliculata seeds

Carex unciniiformis

1 reference

stated in

Nepalensinols D-G, new resveratrol oligomers from Kobresia nepalensis (Cyperaceae) as potent inhibitors of DNA topoisomerase II.

Cissus repanda

1 reference

stated in

Pallidol, a resveratrol dimer from Cissus pallida

Rheum

1 reference

stated in

New resveratrol oligomer derivatives from the roots of Rheum lhasaense

Vitis vinifera

4 references

stated in

Two new stilbene dimer glucosides from grape (Vitis vinifera) cell cultures.

stated in

First symmetrical bicyclo[6.6.0]tetradecane resveratrol tetramer from stalks of vitis vinifera (Vitaceae)

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Resveratrol and its oligomers from wine grapes are selective (1)O2 quenchers: mechanistic implication by high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry and theoretical calculation

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Direct liquid chromatographic analysis of resveratrol derivatives and flavanonols in wines with absorbance and fluorescence detection

Cissus petiolata

1 reference

stated in

Pallidol, a resveratrol dimer from Cissus pallida

Identifiers

InChI

InChI=1S/C28H22O6/c29-15-5-1-13(2-6-15)23-25-19(9-17(31)11-21(25)33)28-24(14-3-7-16(30)8-4-14)26-20(27(23)28)10-18(32)12-22(26)34/h1-12,23-24,27-34H/t23-,24-,27+,28+/m1/s1

1 reference

language of work or name

Pallidol (English)

8 October 2016

YNVJOQCPHWKWSO-ZBVBGGFBSA-N

2 references

language of work or name

Pallidol (English)

8 October 2016

ChEBI release 2020-09-01

CAS Registry Number

105037-88-5

1 reference

imported from Wikimedia project

1 reference

language of work or name

English

title

(4bR,5R,9bR,10R)-5,10-Bis(4-hydroxyphenyl)-4b,5,9b,10-tetrahydroindeno[2,1-a]indene-1,3,6,8-tetrol (English)

8 October 2016

1 reference

language of work or name

English

title

Pallidol (English)

retrieved

8 October 2016

Reaxys registry number

7152851

1 reference

language of work or name

pallidol (English)

8 October 2016

mapping relation type

1 reference

language of work or name

pallidol (English)

8 October 2016

1 reference

language of work or name

PALLIDOL (English)

8 October 2016

1 reference

inferred from InChIKey

1 reference

0 references

DSSTOX compound identifier

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1 reference

28 October 2013

Microsoft Academic ID

2777049390

0 references

Sitelinks

Wikipedia(6 entries)

azbwiki پالیدول
enwiki Pallidol
eswiki Pallidol
fawiki پالیدول
shwiki Palidol
srwiki Palidol

(Q6634710)

pallidol

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Wikipedia(6 entries)

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