Description
H-151 is a STING antagonist.
Product Unit Size | Cost | Quantity | Stock |
---|
H-151 is a STING antagonist.
Cas No. | 941987-60-6 |
---|---|
Purity | ≥99% |
Formula | C17H17N3O |
Formula Wt. | 279.34 |
Chemical Name | 1-(4-Ethylphenyl)-3-(1H-indol-3-yl) urea |
IUPAC Name | 1-(4-ethylphenyl)-3-(1H-indol-3-yl)urea |
Synonym | H151; N-(4-ethylphenyl)-N'-1H-indol-3-yl-urea |
Appearance | Pale yellow to white solid |
Store Temp | -20°C |
---|---|
Ship Temp | Ambient |
Info Sheet |
---|
Zeng H, Gao Y, Yu W, et al. Pharmacological inhibition of STING/TBK1 signaling attenuates myeloid fibroblast activation and macrophage to myofibroblast transition in renal fibrosis. Front Pharmacol. 2022 Jul 18;13:940716. PMID: 35924048
Sun C, Wu G, Zhang Z, et al. Protein tyrosine phosphatase receptor type D regulates neuropathic pain after nerve injury via the STING-IFN-I pathway. Front Mol Neurosci. 2022 Apr 14;15:859166. PMID: 35493326
Hu S, Gao Y, Gao R, et al. The selective STING inhibitor H-151 preserves myocardial function and ameliorates cardiac fibrosis in murine myocardial infarction. Int Immunopharmacol. 2022 Jun;107:108658. PMID: 35278833
Benzyl taxol analog; potential microtubule depo...
Lincosamide; peptidyl transferase inhibitor, pr...
Triterpene aglycone found in Radix Astragali; t...
Found in Cladosporium; PKC inhibitor.
Taxane found in species of Taxus; potential mic...
Pyridine; PDE3 inhibitor.
p110δ PI3K inhibitor.
BK K+ channel and L-type Ca2+ channel blocker.<...
Thienylbutyl ITC analog.
Benzophenanthridine alkaloid, sanguinarine meta...
Endogenous peptide hormone inolved in gastric e...
Impurity of omeprazole
CDK inhibitor, L-type Ca2+ channel blocker.
ROCK inhibitor.
Histamine H2 inverse agonist.
Isoquinoline alkaloid found in a variety of pla...
Labdane diterpene found in Andrographis.
PI3K and mTOR inhibitor.
Antimicrobial peptide found in bee and wasp ven...