CAS 25465-77-4
:Purpurin 18
Description:
Purpurin 18, with the CAS number 25465-77-4, is an organic compound that belongs to the class of anthraquinone dyes. It is characterized by its vibrant red color, which is attributed to its conjugated double bond system that allows for effective light absorption. Purpurin 18 is soluble in organic solvents but has limited solubility in water, making it useful in various applications, including textiles and inks. The compound exhibits strong dyeing properties and is often used in the production of colorants due to its stability and resistance to fading. Additionally, Purpurin 18 has been studied for its potential applications in biological systems, including its use as a photosensitizer in photodynamic therapy. Its chemical structure features multiple hydroxyl groups, contributing to its reactivity and interaction with other substances. Overall, Purpurin 18 is notable for its aesthetic appeal and functional properties in both industrial and research contexts.
Formula:C33H32N4O5
InChI:InChI=1/C33H32N4O5/c1-7-18-14(3)21-11-23-16(5)20(9-10-27(38)39)30(36-23)29-31-28(32(40)42-33(29)41)17(6)24(37-31)13-26-19(8-2)15(4)22(35-26)12-25(18)34-21/h7,11-13,16,20,34,37H,1,8-10H2,2-6H3,(H,38,39)/b21-11-,22-12-,23-11-,24-13-,25-12-,26-13-,30-29+/t16-,20-/m0/s1
Synonyms:- (17S-trans)-18-(2-Carboxyethyl)-12-ethenyl-7-ethyl-17,18-dihydro-3,8,13,17-tetramethyl-21H,23H-porphine-2,20-dicarboxylic acid cyclic 2,20-anhydride
- 3-[(10Z,14Z,20Z,22S,23S)-17-ethenyl-12-ethyl-13,18,22,27-tetramethyl-3,5-dioxo-4-oxa-8,24,25,26-tetraazahexacyclo[19.2.1.16,9.111,14.116,19.02,7]heptacosa-1(24),2(7),6(27),8,10,12,14,16,18,20-decaen-23-yl]propanoic acid (non-preferred name)
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Found 8 products.
Purpurin 18
CAS:Purpurin 18 is an interesting dihydroporphyrin for generating photosensitizers. It has antioxidant activityFormula:C33H32N4O5Purity:95%Color and Shape:SolidMolecular weight:564.63Purpurin 18
CAS:Purpurin 18 is a choroidal neovascularization inhibitor that binds to ABCG2, an efflux pump protein in the blood-brain barrier. This binding prevents efflux of the drug, which leads to inhibition of ABCG2-mediated transport of hydrophobic drugs and xenobiotics out of cells. Purpurin 18 has been shown to inhibit tumor growth in vivo by a mechanism that may involve inhibition of vascular endothelial growth factor (VEGF) production. Purpurin 18 also has anti-inflammatory properties and can be used for the treatment of alopecia areata. The anti-inflammatory effects are probably caused by inhibition of prostaglandin synthesis and induction of apoptosis in activated T cells. The uptake of purpurin 18 into cells is mediated by an acidic environment as well as its hydroxyl group, which provides it with a hydrophobic effect. Purpurin 18 also disrupts mitochondrial membrane potential, leading to cell death.Formula:C33H32N4O5Purity:Min. 95%Molecular weight:564.63 g/mol






