TLR8 agonist 2 hydrochloride
Modify Date: 2024-10-12 10:01:54
TLR8 agonist 2 hydrochloride structure
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Common Name | TLR8 agonist 2 hydrochloride | ||
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| CAS Number | 2412937-65-4 | Molecular Weight | N/A | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C16H22N8.xHCl | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of TLR8 agonist 2 hydrochlorideTLR8 agonist 2 hydrochloride is a potent and selective TLR8 agonist with an EC50 of 3 nM for human TLR8. TLR8 agonist 2 hydrochloride shows less active against human TLR7 (EC50 of 33.33 μM)[1]. |
| Name | TLR8 agonist 2 hydrochloride |
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| Description | TLR8 agonist 2 hydrochloride is a potent and selective TLR8 agonist with an EC50 of 3 nM for human TLR8. TLR8 agonist 2 hydrochloride shows less active against human TLR7 (EC50 of 33.33 μM)[1]. |
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| Related Catalog | |
| Target |
TLR8:3 nM (EC50) TLR7:33.33 μM (EC50) |
| In Vitro | TLR8 agonist 2 (Example 1) increases the levels of TNF-α, IL-12p40, IFN-γ, and IFN-α with EC50 values 105 nM, 26 nM, 29 nM, and 2800 nM, respectively, in human peripheral blood mononuclear cells (hPBMC)[1]. |
| In Vivo | The pharmacokinetic related parameters of TLR8 agonist 2 (Example 1) in mice administered with the intravenous administration of 1 mg/kg and the oral administration of 5 mg/kg are detected. The T1/2 of TLR8 agonist 2 are 0.25 h (1 mg/kg i.v.) and 0.5 h (5 mg/kg p.o.), the AUClast are 450 ng/mL*hr (i.v.) and 624 ng/mL*hr (p.o.). And for oral administration, the bioavailability (%F) is 27.7%[1] |
| References |
| Molecular Formula | C16H22N8.xHCl |
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