Others - BioCrick

Cat.No. Product Name Information/Activity

BCC6245 Pam3CSK4 Pam3CSK4 is a toll-like receptor 1/2 (TLR1/2) agonist with an EC50 of 0.47 ng/mL for human TLR1/2. Pam3CSK4 chemical structure

BCC6138 Poly(I:C) 24939-03-5 Poly(I:C) chemical structure

BCC5603 C34 TLR4-IN-C34 is an orally active TLR4 inhibitor and reduces systemic inflammation in models of endotoxemia and necrotizing enterocolitis. C34 chemical structure

BCC6320 CU CPT 22 CU-CPT22 is a potent protein complex of toll-like receptor 1 and 2 (TLR1/2) inhibitor, and competes with the synthetic triacylated lipoprotein (Pam3CSK4) binding to TLR1/2 with a Ki of 0.41 µM. CU-CPT22 blocks Pam3CSK4-induced TLR1/2 activation with an IC50 of 0.58 µM. CU CPT 22 chemical structure

BCC6319 CU CPT 4a 1279713-77-7 CU CPT 4a chemical structure

BCC5560 Hydroxychloroquine Sulfate Hydroxychloroquine sulfate (HCQ sulfate) is a synthetic antimalarial drug which can also inhibit Toll-like receptor 7/9 (TLR7/9) signaling. Hydroxychloroquine Sulfate chemical structure

Hydroxychloroquine Sulfate chemical structure

BCC5203 VGX-1027 VGX-1027(GIT27) is an isoxazole compound that exhibits various immunomodulatory properties; reduce the secretion of IL-1beta, TNF-alpha and IL-10 from purified murine macrophages. VGX-1027 chemical structure

BCC7161 2-Chloro-N6-cyclopentyladenosine Potent, selective A<sub>1</sub> agonist

2-Chloro-N6-cyclopentyladenosine chemical structure

BCC7160 N6-Cyclopentyladenosine N6-Cyclopentyladenosine (CPA) is a selective Adenosine A1 receptor agonist, with Ki values of 2.3 nM, 790 nM and 43 nM for human A1, A2A and A3 receptors, respectively. N6-Cyclopentyladenosine chemical structure

N6-Cyclopentyladenosine chemical structure

BCC7716 (±)-5'-Chloro-5'-deoxy-ENBA Highly selective A<sub>1</sub> agonist (±)-5'-Chloro-5'-deoxy-ENBA chemical structure

Others Products Targets

Products for Others - Page 23