CAS 2219320-08-6

Formel: C29H29F3N2

InChl: InChI=1S/C29H29F3N2/c30-22-8-4-20(5-9-22)25(21-6-10-23(31)11-7-21)2-1-15-33-18-19-3-13-28-26(16-19)27-17-24(32)12-14-29(27)34-28/h4-12,14,17,19,25,33-34H,1-3,13,15-16,18H2

InChI Key: OCZIMUMAPGQEBH-UHFFFAOYSA-N

SMILES: C1CC2=C(CC1CNCCCC(C3=CC=C(C=C3)F)C4=CC=C(C=C4)F)C5=C(N2)C=CC(=C5)F

N-((6-Fluoro-2,3,4,9-tetrahydro-1H-carbazol-3-yl)methyl)-4,4-bis(4-fluorophenyl)butan-1-amine

CAS: 2219320-08-6

N-((6-Fluoro-2,3,4,9-tetrahydro-1H-carbazol-3-yl)methyl)-4,4-bis(4-fluorophenyl)butan-1-amine

Formel: C₂₉H₂₉F₃N₂

Reinheit: ≥98%

Molekulargewicht: 462.56

Ref: 54-PC1005768

MSC1094308

CAS: 2219320-08-6

MSC1094308 is a reversible, non-ATP-competitive inhibitor targeting type II AAA ATPase (VCP/p97) and type I AAA ATPase (VPS4B) and affects protein degradation.

Formel: C₂₉H₂₉F₃N₂

Farbe und Form: Solid

Molekulargewicht: 462.5492

Ref: TM-T12114

MSC1094308

CAS: 2219320-08-6

Formel: C₂₉H₂₉F₃N₂

Reinheit: 98%

Molekulargewicht: 462.5492

Ref: IN-DA01V4MZ

MSC1094308

CAS: 2219320-08-6

MSC1094308 is a molecule that inhibits the replication of viral DNA. It has been shown to be active against a broad range of viruses, including HIV, poliovirus, herpes simplex virus type 1 and influenza A virus. MSC1094308 also exhibits anti-cancer and anti-inflammatory properties, which may be due to its ability to induce autophagy. The mechanism of action for this drug is not yet known.

Formel: C₂₉H₂₉F₃N₂

Reinheit: Min. 95%

Molekulargewicht: 462.5 g/mol

Ref: 3D-UND32008