CAS 1182-34-9

Ácido 1,4-dicaffeoylquínico

Descrição:

Ácido 1,4-dicaffeoylquínico é um composto polifenólico pertencente à classe dos ácidos cafeoilquínicos, que são ésteres formados a partir do ácido quínico e do ácido cafeico. Este composto é caracterizado por seus dois grupos cafeoil ligados às posições 1 e 4 da estrutura do ácido quínico. Ele é tipicamente encontrado em várias plantas, particularmente no café e em certas frutas, contribuindo para suas propriedades antioxidantes. O composto exibe atividades biológicas significativas, incluindo efeitos anti-inflamatórios, antioxidantes e potenciais efeitos neuroprotetores. Sua estrutura permite a formação de ligações de hidrogênio e interações com outras biomoléculas, aumentando sua reatividade e biodisponibilidade. Ácido 1,4-dicaffeoylquínico é solúvel em solventes polares, o que facilita sua extração de materiais vegetais. Além disso, despertou interesse na ciência dos alimentos e na farmacologia devido aos seus potenciais benefícios à saúde, tornando-se um tema de pesquisa em química de produtos naturais e alimentos funcionais.

Fórmula: C₂₅H₂₄O₁₂

InChI: InChI=1/C25H24O12/c26-15-5-1-13(9-17(15)28)3-7-21(32)36-23-19(30)11-25(24(34)35,12-20(23)31)37-22(33)8-4-14-2-6-16(27)18(29)10-14/h1-10,19-20,23,26-31H,11-12H2,(H,34,35)/t19-,20-,23-,25+/s2

Chave InChI: InChIKey=IYXQRCXQQWUFQV-GWELMYFGNA-N

SMILES: O(C(C=CC1=CC(O)=C(O)C=C1)=O)[C@@]2(C(O)=O)C[C@@H](O)[C@@H](OC(C=CC3=CC(O)=C(O)C=C3)=O)[C@H](O)C2

Sinónimos:

• (1R,3R,4S,5R)-1,3-Bis{[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]oxy}-4,5-dihydroxycyclohexancarbons?ure
• (1R,3R,4S,5R)-1,3-Bis{[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]oxy}-4,5-dihydroxycyclohexanecarboxylic acid
• (1R,3R,4S,5R)-1,3-Bis{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-4,5-dihydroxycyclohexanecarboxylic acid
• (1S,2S,3S,4R)-1,4-bis{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-2,3-dihydroxycyclohexanecarboxylic acid
• (1S,3R,4R,5R)-1,3-bis{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-4,5-dihydroxycyclohexanecarboxylic acid
• (3R,5R)-1-acetyl-3,5-dihydroxycyclohexane-1,4-diyl (2E,2'E)bis[3-(3,4-dihydroxyphenyl)prop-2-enoate]
• 1,4-Dicaffeoylquinic acid
• 1,4-Dicaffeylquinic acid
• 1,4-bis{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-3,5-dihydroxycyclohexanecarboxylic acid
• 1,5-Dicaffeoylquinic Acid
• 1,5-Dicaffeylquinic Acid
• 1-Carboxy-4,5-dihydroxy-1,3-cyclohexylenebis-(3,4-dihydroxycinnamate)
• 3,4-Dihydroxycinnamic Acid 1-Carboxy-4,5-dihydroxy-1,3-cyclohexylene Ester
• 4-{[3-(3,4-dihydroxyphenyl)acryloyl]oxy}-1-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-3,5-dihydroxycyclohexanecarboxylic acid
• Acide (1R,3R,4S,5R)-1,3-bis{[(2E)-3-(3,4-dihydroxyphényl)-2-propènan-1-oyl]oxy}-4,5-dihydroxycyclohexanecarboxylique
• Caffeic Acid 1-Carboxy-4,5-dihydroxy-1,3-cyclohexylene Ester
• Cinnamic acid, 3,4-dihydroxy-, 1-carboxy-3,5-dihydroxy-1,4-cyclohexylene ester
• Cyclohexanecarboxylic acid, 1,4-bis[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-3,5-dihydroxy-, (1α,3R,4α,5R)-rel-
• Cyclohexanecarboxylic acid, 1,4-bis[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-3,5-dihydroxy-, (1α,3α,4α,5β)-
• Cynarin
• Cynarin(1,3-Dicaffeoylquinic Acid)
• Lynare Scolymusl P.E.
• [1R-(1a,3a,4a,5b)]-1,3-Bis[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-4,5-dihydroxycyclohexanecarboxylic Acid
• cyclohexanecarboxylic acid, 1,3-bis[[(2E)-3-(3,4-dihydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-4,5-dihydroxy-, (1R,3R,4S,5R)-

Cynarin

CAS: 1182-34-9

Fórmula: C₂₅H₂₄O₁₂

Pureza: 95%

Cor e Forma: Solid

Peso molecular: 516.4509

Ref: IN-DA008189

1,4-Dicaffeoylquinic acid

CAS: 1182-34-9

1,4-Dicaffeoylquinic acid

Pureza: ≥98%

Peso molecular: 516.45g/mol

Ref: 54-BUP21170

1,4-Dicaffeoylquinic acid

CAS: 1182-34-9

Fórmula: C₂₅H₂₄O₁₂

Peso molecular: 516.46

Ref: 7W-GY7421

1,4-Dicaffeoylquinic acid

CAS: 1182-34-9

Fórmula: C₂₅H₂₄O₁₂

Pureza: 95%~99%

Peso molecular: 516.455

Ref: BP-BP1860

1,4-Dicaffeoylquinic acid

CAS: 1182-34-9

1,4-Dicaffeoylquinic acid is a naturally occurring polyphenolic compound, specifically a type of caffeoylquinic acid, which is derived from various plant species including certain vegetables, fruits, and herbs. This compound is a result of biochemical synthesis within the plant, where it plays various roles, primarily in the defense mechanisms against pathogens and oxidative stress. The mode of action of 1,4-Dicaffeoylquinic acid centers on its potent antioxidant capabilities. It scavenges free radicals, thus protecting cellular components from oxidative damage, and exhibits anti-inflammatory properties through modulation of inflammatory pathways. The compound's ability to inhibit specific enzymes and signaling molecules contributes to its therapeutic potential.

Fórmula: C₂₅H₂₄O₁₂

Pureza: Min. 95%

Cor e Forma: White Powder

Peso molecular: 516.45 g/mol

Ref: 3D-FD157794

1,4-Dicaffeoylquinic acid

CAS: 1182-34-9

1,4-Dicaffeoylquinic acid: an antioxidant and selective HIV-1 integrase inhibitor, non-toxic at effective doses.

Fórmula: C₂₅H₂₄O₁₂

Pureza: 97.32% - 99.85%

Cor e Forma: Solid

Peso molecular: 516.45

Ref: TM-T4S1521