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Polyporic acid is a triterpenoid compound derived from the Polyporus umbellatus mushroom, which is commonly found in East Asia. It exhibits various biological activities, including anti-inflammatory, antitumor, and immunomodulatory effects. The chemical structure of polyporic acid consists of a pentacyclic triterpene with a carboxylic acid group, and it is known for its ability to modulate the immune system, particularly by enhancing the activity of natural killer cells and cytotoxic T lymphocytes. This makes it a subject of interest in the field of immunotherapy and cancer research.

548-59-4

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548-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 548-59-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 548-59:
(5*5)+(4*4)+(3*8)+(2*5)+(1*9)=84
84 % 10 = 4
So 548-59-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H12O4/c19-15-13(11-7-3-1-4-8-11)16(20)18(22)14(17(15)21)12-9-5-2-6-10-12/h1-10,19,22H

548-59-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dihydroxy-3,6-diphenylcyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2,5-dihydroxy-3,6-diphenylbenzoquinone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:548-59-4 SDS

548-59-4Relevant academic research and scientific papers

Synthesis of a focused chemical library based on derivatives of embelin, a natural product with proapoptotic and anticancer properties

Viault, Guillaume,Gree, Danielle,Das, Saibal,Yadav, Jhillu Singh,Gree, Rene

experimental part, p. 1233 - 1241 (2011/04/17)

The synthesis of new derivatives of embelin, a natural inhibitor of X-linked inhibitor of apoptosis protein (XIAP) is described. The design of these new molecules involved introduction of aromatic groups directly linked to the benzoquinone core. To allow a large flexibility in the nature and the length of the added chain, the strategy involves first aSuzuki-Miyaura reaction with functionalized aromatics, yielding a first generation of molecules. Then, by appropriate use of the functional groups, a second generation of representative embelin derivatives was prepared.

Synthesis of Grevillins, Novel Pyrandione Pigments of Fungi. Biogenetic Interrelationships between Grevillins, Pulvinic Acids, Terphenylquinones and Xylerythrins

Pattenden, Gerald,Pegg, Neil A.,Kenyon, Ronald W.

, p. 2363 - 2372 (2007/10/02)

A synthesis of the grevillin group of pyrandione pigments, e.g. 3, 23 and 24 present in fungi is described.The synthesis, which is based on a biogenetic model, uses bis-benzylacyloins 9 and their corresponding oxalate derivatives as key intermediates (Scheme 3).Treatment of the grevillins 25a-c with sodium ethoxide in ethanol effects their quantitative isomerisation into the corresponding terphenylquinone pigments 4a-c.Perkin-type condensations between the terphenylquinones 4 and arylacetic acids in the presence of sodium acetate-acetic anhydride then produces the xylerythrin pigments 29a-e, whereas rearrangements of 4 in the presence of dimethyl sulphoxide leads to pulvinic acid derivative, e.g. 31, 32 and 5.These synthetic studies interrelate the biosynthetic origins of the pigment types 3, 4, 5 and 8 together with the related pulvinones 6 and furanone 7 fungal pigments.

SYNTHESIS OF GREVILLINS AND THEIR BIOGENETIC INTERRELATIONSHIP WITH TERPHENYLQUINONES, XYLERYTHRINS AND PULVINIC ACIDS

Pattenden, Gerald,Pegg, Neil A.,Kenyon, Ronald W.

, p. 4749 - 4752 (2007/10/02)

A synthesis of the grevillin group , of pigments present in fungi, using benzylacyloins, viz (9), as key intermediates is described, and the biogenetic interrelationships between them and the terphenylquinone, xylerythrin and pulvinic acid families of natural colouring matter, are exemplified with the in vitro conversions (16)-(17), (17)-(20) and (17)-(22).

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