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Home CSCS17764111897

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

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

SDS

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Items Overall 2 items from 2 suppliers

SupplierLead timeShips fromPurityPackPrice, $Qty
MedChemExpressTBDUnited States
To:
901 mgPOA
Go to cartEnquire
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 EUTBDSweden
To:
901 mgPOA
Go to cartEnquire
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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