CI-1044
Modify Date: 2024-01-18 18:01:27
CI-1044 structure
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Common Name | CI-1044 | ||
|---|---|---|---|---|
| CAS Number | 197894-84-1 | Molecular Weight | 397.429 | |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 773.2±60.0 °C at 760 mmHg | |
| Molecular Formula | C23H19N5O2 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 421.4±32.9 °C | |
Use of CI-1044CI-1044 is an orally active PDE4 inhibitor with IC50s of 0.29, 0.08, 0.56, 0.09 μM for PDE4A5, PDE4B2, PDE4C2 and PDE4D3, respectively. |
| Name | CI-1044 |
|---|---|
| Synonym | More Synonyms |
| Description | CI-1044 is an orally active PDE4 inhibitor with IC50s of 0.29, 0.08, 0.56, 0.09 μM for PDE4A5, PDE4B2, PDE4C2 and PDE4D3, respectively. |
|---|---|
| Related Catalog | |
| Target |
PDE4A5:0.29 μM (IC50) PDE4B2:0.08 μM (IC50) PDE4C2:0.56 μM (IC50) PDE4D3:0.09 μM (IC50) |
| In Vitro | CI-1044 is an orally active PDE4 inhibitor with IC50s of 0.29, 0.08, 0.56, 0.09 μM for PDE4A5, PDE4B2, PDE4C2 and PDE4D3, respectively. CI-1044 selectively inhibits PDE4 crude extract from U937 cells with an IC50 value of 0.27±0.02 μM being threefold more potent than rolipram (IC50=0.91±0.14) and tenfold less potent than cilomilast (IC50=0.026±0.007) in the same assay. In the presence of PDE4 inhibitors, the production of TNF-α is dose dependently decreased with mean IC50 values from three separate experiments of 0.31±0.05, 0.26±0.05 and 0.11±0.01 μM, for CI-1044, cilomilast and rolipram, respectively[1]. |
| In Vivo | TNF-α production is dose-dependently inhibited by CI-1044, rolipram and cilomilast with ID50s of 0.4, 1.4 and 1.6 mg/kg respectively following single oral administration. Following repeated administration with CI-1044, the ID50 value represents 0.5 mg/kg p.o.. CI-1044 plasma levels increase proportionally with doses ranging between 0.1 and 40 mg/kg p.o. (R2=0.878). CI-1044 dose dependently inhibits the accumulation of eosinophils in Bronchoalveolar lavages (BAL) fluids with an ID50 value of 3.25 mg/kg. A single dose treatment with CI-1044 (10 mg/kg, p.o.) 24, 8, 3 or 1 h before the antigen challenge induces 6, 56, 48 and 79% inhibition in the number of eosinophils in BAL[1]. |
| Cell Assay | Blood from anesthetized rats is collected in heparin tubes, immediately distributed in 96-well microplates (250 μL/well) and incubated for 30 min at 37°C/5% CO2. Twenty-five microliters of vehicle or increasing concentrations of CI-1044, rolipram, cilomilast or solvant (saline/DMSO<0.1%) are added in wells and incubated for 30 min before the addition of LPS (100 μg/mL) or saline. Plasma is removed after a 22 to 24 h incubation at 37°C/5% CO2, transferred in another 96-well microplate and stored at ) -80°C until a TNF-α assay by ELISA[1]. |
| Animal Admin | Male rats (200 to 220 g) are used and receive either vehicle or CI-1044 orally at 0.4, 1, 4, 10 and 40 mg/kg. In the single administration experiment, all treatments are given 1 h before blood collection. In the repeated administration experiment, the treatments are given twice a day during 13 days and once on day 14, 1 h before blood sampling[1]. |
| References |
| Density | 1.4±0.1 g/cm3 |
|---|---|
| Boiling Point | 773.2±60.0 °C at 760 mmHg |
| Molecular Formula | C23H19N5O2 |
| Molecular Weight | 397.429 |
| Flash Point | 421.4±32.9 °C |
| Exact Mass | 397.153870 |
| LogP | 0.30 |
| Vapour Pressure | 0.0±2.6 mmHg at 25°C |
| Index of Refraction | 1.750 |
| Storage condition | 2-8℃ |
| 3-Pyridinecarboxamide, N-[(3R)-9-amino-3,4,6,7-tetrahydro-4-oxo-1-phenyl[1,4]diazepino[6,7,1-hi]indol-3-yl]- |
| O4T475XIIY |
| CI-1044 |
| N-[(3R)-9-amino-4-oxo-1-phenyl-3,4,6,7-tetrahydro[1,4]diazepino[6,7,1-hi]indol-3-yl]pyridine-3-carboxamide |
| N-[(3R)-9-Amino-4-oxo-1-phenyl-3,4,6,7-tetrahydro[1,4]diazepino[6,7,1-hi]indol-3-yl]nicotinamide |