Structure Info
- Chemspace ID
- CSCS17764111897 (Synthesis)
- IUPAC Name
- 2,6-dibromophenyl (3S)-2-[3-(3,4-dihydroxyphenyl)propanoyl]-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylate
- Mol formula
- C25H21Br2NO7
- Mol weight
- 607 Da
- Catalog Number(s)
- HY-158028
- Copy structure to query editor
- SMILES
- INCHI
- INCHI key
- MOL
Properties
- LogP
- 5.28
- Heavy atoms count
- 35
- Rotatable bond count
- 6
- Number of rings
- 4
- Carbon bond saturation, Fsp3
- 0.2
- Polar surface area (Å)
- 128
- Hydrogen bond acceptors count
- 6
- Hydrogen bond donors count
- 4
- Zoom the structure
- CSCS17764111897
Items Overall 2 items from 2 suppliers
Supplier | Lead time | Ships from | Purity | Pack | Price, € | Qty |
---|---|---|---|---|---|---|
MedChemExpress | TBD | United States To: | 90 | 1 mg | POA | |
Description: Names: PAN endonuclease-IN-2; Product Description: PAN endonuclease-IN-2 (compound T-31) is a PA N endonuclease inhibitor ( IC 50 : 0.15 μM) and antiviral agent with broad-spectrum anti- Influenza activity. PAN is the N-terminal PA subunit of the polymerase-RNA complex and the dependent endonuclease (CEN) active site. PAN initiates RNA replication by promoting cleavage of the RNA strand and allowing the polymerase to begin synthesizing new RNA molecules. PAN endonuclease-IN-2 targets both the influenza HA and RdRp complexes, thereby interfering with viral entry into host cells and viral replication .; Target: Influenza Virus | ||||||
MedChemExpress EU | TBD | Sweden To: | 90 | 1 mg | POA | |
Description: Names: PAN endonuclease-IN-2; Product Description: PAN endonuclease-IN-2 (compound T-31) is a PAN endonuclease inhibitor (IC50: 0.15 μM) and antiviral agent with broad-spectrum anti- Influenza activity. PAN is the N-terminal PA subunit of the polymerase-RNA complex and the dependent endonuclease (CEN) active site. PAN initiates RNA replication by promoting cleavage of the RNA strand and allowing the polymerase to begin synthesizing new RNA molecules. PAN endonuclease-IN-2 targets both the influenza HA and RdRp complexes, thereby interfering with viral entry into host cells and viral replication; Target: Influenza Virus |
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