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Listado de productos por fabricante AbMole
(4-2)-Abeo-16-hydroxycleroda-2,13-dien-15,16-olide-3-al
(4→2)-Abeo-16-hydroxycleroda-2,13-dien-15,16-olide-3-al is extracted from the unripe fruits of Polyalthia longifolia var. pendula.
(Ala1)-PAR-4 (1-6) (mouse)
(Ala1)-PAR-4 (1-6) (mouse)
(Arg)9
(Arg)9 (Nona-L-arginine) is a cell-penetrating peptide (CPP) made up of 9 arginine residues.
(D) PPA-1 TFA
(D) PPA-1 TFA is the first hydrolysisresistant D-peptide antagonists to target the PD-1/PD-L1 pathway. (D) PPA-1 could bind PD-L1 at an affinity of 0.51 μM in vitro.
(D) PPA-1 TFA
(D) PPA-1 TFA is the first hydrolysisresistant D-peptide antagonists to target the PD-1/PD-L1 pathway. (D) PPA-1 could bind PD-L1 at an affinity of 0.51 μM in vitro.
(D) PPA-1 TFA
(D) PPA-1 TFA is the first hydrolysisresistant D-peptide antagonists to target the PD-1/PD-L1 pathway. (D) PPA-1 could bind PD-L1 at an affinity of 0.51 μM in vitro.
(E)-3,4-Dimethoxycinnamic acid
(E)-3,4-Dimethoxycinnamic acid is a lowly active isomer of 3,4-Dimethoxycinnamic acid. 3,4-Dimethoxycinnamic acid exerts an anti-apoptotic effect on L-02 cells through a ROS-mediated signaling pathway.
(E)-Cardamonin
(E)-Cardamonin is a novel antagonist of hTRPA1 cation channel with an IC50 of 454 nM, Cardamonin alleviates inflammatory bowel disease by the inhibition of NLRP3 inflammasome activation via an AhR/Nrf2/NQO1 pathway.
(E)-Cardamonin
(E)-Cardamonin is a novel antagonist of hTRPA1 cation channel with an IC50 of 454 nM, Cardamonin alleviates inflammatory bowel disease by the inhibition of NLRP3 inflammasome activation via an AhR/Nrf2/NQO1 pathway.
(E)-Cardamonin
(E)-Cardamonin is a novel antagonist of hTRPA1 cation channel with an IC50 of 454 nM, Cardamonin alleviates inflammatory bowel disease by the inhibition of NLRP3 inflammasome activation via an AhR/Nrf2/NQO1 pathway.
(E)-Cyclooct-2-en-1-yl (4-nitrophenyl) carbonate
(E)-Cyclooct-2-en-1-yl (4-nitrophenyl) carbonate
(E)-Cyclooct-2-en-1-yl (4-nitrophenyl) carbonate
(E)-Cyclooct-2-en-1-yl (4-nitrophenyl) carbonate