Urolithin A 8-Methyl Ether
Modify Date: 2025-08-25 13:09:30
Urolithin A 8-Methyl Ether structure
|
Common Name | Urolithin A 8-Methyl Ether | ||
|---|---|---|---|---|
| CAS Number | 35233-17-1 | Molecular Weight | 242.22700 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C14H10O4 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
| Name | 8-O-methylurolithin A |
|---|---|
| Synonym | More Synonyms |
| Molecular Formula | C14H10O4 |
|---|---|
| Molecular Weight | 242.22700 |
| Exact Mass | 242.05800 |
| PSA | 59.67000 |
| LogP | 2.66040 |
| InChIKey | IGJLBTGXYKPECW-UHFFFAOYSA-N |
| SMILES | COc1ccc2c(c1)c(=O)oc1cc(O)ccc12 |
| Precursor 0 | |
|---|---|
| DownStream 1 | |
CAS#:1143-70-0|
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
|
|
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
|
|
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
|
|
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
|
|
Name: uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
Source: Burnham Center for Chemical Genomics
Target: N/A
External Id: BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
|
|
Name: A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
Source: ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id: HMS979
|
|
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.
|
|
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
|
|
Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
|
|
Name: Dicer-mediated maturation of pre-microRNA
Source: Center for Chemical Genomics, University of Michigan
Target: N/A
External Id: TargetID_659_CEMA
|
Total 121, Current Page 1 of 13
1
2
3
4
5
| 3-hydroxy-8-methoxy-6H-dibenzo[b,d]pyran-6-one |
| 8-O-METHYL-UROLITHIN A |
| 3-hydroxy-8-methoxybenzo[c]chromen-6-one |
| 3-hydroxy-8-methoxy-dibenzo[b,d]pyran-6-one |
| 3-hydroxy-8-methoxy-benzo[c]chromen-6-one |
| Urolithin A 8-Methyl Ether |
| 8-O-methylurolithin |