3, 4, 5-Tricaffeoylquinic acid Catalog No.:M16772-C Chemical Name: (3S)-4-amino-3-[[(2S)-5-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-1-[(2S)-2-[[(2S)-5-amino-2-[[(2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-4-amino-2-[[(2S)-2-[[(2S

Name: 3, 4, 5-Tricaffeoylquinic acid Catalog No.:M16772-C Chemical Name: (3S)-4-amino-3-[[(2S)-5-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-1-[(2S)-2-[[(2S)-5-amino-2-[[(2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-4-amino-2-[[(2S)-2-[[(2S
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Description

Chemical Name: (3S)-4-amino-3-[[(2S)-5-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-1-[(2S)-2-[[(2S)-5-amino-2-[[(2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-4-amino-2-[[(2S)-2-[[(2S

[O-]C(=O)CCNC1=CC(=NC(=N1)C1=CC=CC=N1)N1CCC2=CC=CC=C2CC1

(2011) Blood

COX1 levels are increased by ~60%

IQ-3 exhibits IC50 of 2

3, 4, 5-Tricaffeoylquinic acid Catalog No.:M16772-C Chemical Name: (3S)-4-amino-3-[[(2S)-5-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-1-[(2S)-2-[[(2S)-5-amino-2-[[(2S)-1-[(2S)-2-[[(2S)-2-[[(2S)-4-amino-2-[[(2S)-2-[[(2S3,4,5 Tricaffeoylquinic acid (3,4,5 triCQA) inhibits tumor necrosis factor stimulated production of inflammatory mediators in keratinocytes via suppression of Akt and NF B pathways. 3,4,5 Tricaffeoylquinic acid induces cell cycle arrest at G0 G1, actin cytoskeleton organization, chromatin remodeling, neuronal differentiation, and bone morphogenetic protein signaling in human neural stem cells. 3,4,5 Tricaffeoylquinic acid has the potential for the

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