RDR 02308
Modify Date: 2025-08-26 14:06:03
RDR 02308 structure
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Common Name | RDR 02308 | ||
|---|---|---|---|---|
| CAS Number | 4155-82-2 | Molecular Weight | 333.34 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C19H15N3O3 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of RDR 02308RDR 02308 is a TLR4-MyD88 binding inhibitor that inhibits full-length β-lactamase[1]. |
| Name | RDR 02308 |
|---|
| Description | RDR 02308 is a TLR4-MyD88 binding inhibitor that inhibits full-length β-lactamase[1]. |
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| Related Catalog | |
| In Vitro | RDR 02308 (0-10 μM; 1 h) 在 RAW264.7 细胞中抑制 LPS (HY-D1056) 介导的 IL-6 产生[1]。 Western Blot Analysis[1] Cell Line: RAW264.7 cells Concentration: 0-10 μM Incubation Time: 1 h Result: Inhibited LPS-mediated IL-6 production. |
| References |
| Molecular Formula | C19H15N3O3 |
|---|---|
| Molecular Weight | 333.34 |
| InChIKey | DCFSIJLWXJXSQC-UHFFFAOYSA-N |
| SMILES | O=[N+]([O-])c1ccc(C2=NN(c3ccccc3)C(c3ccco3)C2)cc1 |
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Name: Primary cell-based high-throughput screening assay for identification of compounds th...
Source: Johns Hopkins Ion Channel Center
Target: regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id: JHICC_RGS_Act_HTS
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Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
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Name: Single Concentration Validation of Csn-Mediated Deneddylation of Cullin-Ring Ligase U...
Source: Burnham Center for Chemical Genomics
Target: COP9 signalosome complex subunit 5 [Homo sapiens]
External Id: SBCCG-A995-CSN5-CP-Assay
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Name: Single concentration validation of Csn-Mediated Deneddylation of Cullin-Ring Ligase H...
Source: Burnham Center for Chemical Genomics
Target: 72 kDa type IV collagenase isoform a preproprotein [Homo sapiens]
External Id: SBCCG-A996-CSN5-MMP2-CP-Assay
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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Name: HCS to Identify Inhibitors of Dynein Mediated Cargo Transport on Microtubules: Confir...
Source: University of Pittsburgh Molecular Library Screening Center
Target: N/A
External Id: HCS to Identify Inhibitors of Dynein Mediated Cargo Transport on Microtubules: Confirmation Assay, R21NS057026
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Name: High throughput fluorescence intensity-based biochemical assay to screen for small mo...
Source: University of Pittsburgh Molecular Library Screening Center
Target: furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id: MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
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Name: Single concentration validation of Csn-Mediated Deneddylation of Cullin-Ring Ligase U...
Source: Burnham Center for Chemical Genomics
Target: TPA: prothrombin [Bos taurus]
External Id: SBCCG-A997-CSN5-thrombin-CP-Assay
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