We present results from a global three-dimensional chemical model for the troposphere, named Chemical AGCM for Study of Atmospheric Environment and Radiative Forcing (CHASER). This model has been developed to simulate the tropospheric photochemistry involving the O3-HOx-NOx-CH4-CO photochemical system and oxidation of nonmethane hydrocarbons (NMHCs), based on an atmospheric general circulation model (AGCM). In this paper, we present results from a climatological run of the model, and evaluate them with observational data. The simulation was conducted at the model horizontal resolution of T21 (5.6¿ ¿ 5.6¿) with 32 vertical layers from the surface to about 40 km altitude. The model reproduces well the observed vertical profiles of CO and NMHCs as ethane, propane, and acetone in almost all cases. The simulated seasonal cycle of surface CO in the biomass-burning region (South America) shows a good agreement with observation. In the case of nitric oxide (NO), the model generally reproduces the observed vertical profiles well, though it appears to somewhat underestimate NO in the upper troposphere in the low latitudes. Although the model overestimates nitric acid (HNO3) in some cases like other model studies, the calculated HNO3 is generally within the range of observations. Peroxyacetyl nitrate (PAN) appears to be generally simulated well, but overestimated by the model in some remote regions. In the simulation of O3, the vertical profiles and seasonal variations observed in polluted and remote sites are well reproduced. The ozone distributions calculated in the biomass-burning-related regions as South America, Africa, and the South Atlantic show good agreements with observations. However, in the midlatitudes, the model tends to overestimate O3 in the upper troposphere in winter-springtime, maybe indicating the need of improving the model's horizontal resolution. The model calculates a net chemical ozone production of 397 TgO3/yr in the global troposphere (4895 TgO3/yr production and 4498 TgO3/yr destruction). The estimated net O3 flux from the stratosphere is 593 TgO3/yr, well within the range suggested by recent studies. The calculated global OH concentration leads to a global mean CH4 lifetime of 7.9 years in this simulation.