Downstream Synthetic Route Of 3685-23-2

The article 《Identification and Biological Evaluation of a Series of 1H-Benzo[de]isoquinoline-1,3(2H)-diones as Hepatitis C Virus NS5B Polymerase Inhibitors》 also mentions many details about this compound(3685-23-2)Formula: C7H13NO2, you can pay attention to it or contacet with the author([email protected]) to get more information.

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Identification and Biological Evaluation of a Series of 1H-Benzo[de]isoquinoline-1,3(2H)-diones as Hepatitis C Virus NS5B Polymerase Inhibitors, published in 2009-08-27, which mentions a compound: 3685-23-2, Name is cis-4-Aminocyclohexane carboxylic acid, Molecular C7H13NO2, Formula: C7H13NO2.

The hepatitis C virus (HCV) NS5B RNA-dependent RNA polymerase (RdRp) plays a central role in virus replication. NS5B has no functional equivalent in mammalian cells and, as a consequence, is an attractive target for inhibition. Herein, we present 1H-benzo[de]isoquinoline-1,3(2H)-diones as a new series of selective inhibitors of HCV NS5B polymerase. The HTS hit 1 shows submicromolar potency in two different HCV replicons (1b and 2b) and displays no activity on other polymerases (HIV-RT, Polio-pol, GBV-b-pol). These inhibitors act during the pre-elongation phase by binding to NS5B non-nucleoside binding site Thumb Site II as demonstrated by crystal structure of compound 1 with the ΔC55-1b and ΔC21-2b enzymes and by mutagenesis studies. SAR in this new series reveals inhibitors, such as 20, with low micromolar activity in the HCV replicon and with good activity/toxicity window in cells.

The article 《Identification and Biological Evaluation of a Series of 1H-Benzo[de]isoquinoline-1,3(2H)-diones as Hepatitis C Virus NS5B Polymerase Inhibitors》 also mentions many details about this compound(3685-23-2)Formula: C7H13NO2, you can pay attention to it or contacet with the author([email protected]) to get more information.

Reference:
Synthesis and Crystal Structure of a Chiral C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur–nitrogen–oxygen ligand derived from aminothiourea and sodium D-camphor-β-sulfonate

The effect of the change of synthetic route on the product 3685-23-2

The article 《Intramolecular, Intermolecular, and Heterogeneous Nonadiabatic Dissociative Electron Transfer to Peresters》 also mentions many details about this compound(3685-23-2)Safety of cis-4-Aminocyclohexane carboxylic acid, you can pay attention to it, because details determine success or failure

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Intramolecular, Intermolecular, and Heterogeneous Nonadiabatic Dissociative Electron Transfer to Peresters, published in 2001-10-03, which mentions a compound: 3685-23-2, Name is cis-4-Aminocyclohexane carboxylic acid, Molecular C7H13NO2, Safety of cis-4-Aminocyclohexane carboxylic acid.

The electron transfer to peresters was studied by electrochem. means in N,N-dimethylformamide. The reduction was carried out by three independent methods: (i) heterogeneously, by using glassy carbon electrodes, (ii) homogeneously, by using electrogenerated radical anions as the donors, and (iii) intramolecularly, by using purposely synthesized donor-spacer-acceptor (D-Sp-A) systems (tert-Bu 1,3-dihydro-α,α-di-Methyl-1,3-dioxo-peroxy-2H-isoindole-2-acetate and tert-Bu cis-4-Phthalimidocyclohexanepercarboxylate). Convolution anal. of the heterogeneous data led to results in excellent agreement with the dissociative electron transfer theory. The homogeneous redox catalysis data also confirmed the reduction mechanism. The cyclic voltammetries of the D-Sp-A mols. could be simulated, leading to determination of the corresponding intramol. dissociative rate constants Anal. of the results showed that, regardless of the way by which the acceptor is reduced, the investigated dissociative electron transfers are strongly nonadiabatic and, particularly, that the exptl. rates are several orders of magnitude smaller than the adiabatic limit. A possible mechanism responsible for the observed behavior is discussed.

The article 《Intramolecular, Intermolecular, and Heterogeneous Nonadiabatic Dissociative Electron Transfer to Peresters》 also mentions many details about this compound(3685-23-2)Safety of cis-4-Aminocyclohexane carboxylic acid, you can pay attention to it, because details determine success or failure

Reference:
Synthesis and Crystal Structure of a Chiral C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur–nitrogen–oxygen ligand derived from aminothiourea and sodium D-camphor-β-sulfonate