Identifying drug-target interactions (DTIs) is an important step for drug discovery and drug repositioning. To reduce heavily experiment cost, booming machine learning has been applied to this field and developed many computational methods, especially binary classification methods. However, there is still much room for improvement in the performance of current methods. Multi-label learning can reduce difficulties faced by binary classification learning with high predictive performance, and has not been explored extensively. The key challenge it faces is the exponential-sized output space, and considering label correlations can help it. Thus, we facilitate the multi-label classification by introducing community detection methods for DTIs prediction, named DTI-MLCD. On the other hand, we updated the gold standard data set proposed in 2008 and still in use today. The proposed DTI-MLCD is performed on the gold standard data set before and after the update, and shows the superiority than other classical machine learning methods and other benchmark proposed methods, which confirms the efficiency of it. The data and code for this study can be found at https://github.com/a96123155/DTI-MLCD.[8-41], drug-target pairs and interactions are treated as samples and labels, respectively. It describes the drug-target pair by encoding drugs and targets as the feature vector, then, predicts DTIs by building a binary classifier. In addition to the binary classification methods, there are network inference methods [42][43][44][45][46][47][48][49][50][51][52][53][54][55], matrix factorization methods [56-63], kernel-based methods [64-68], restricted Boltzmann machine method [69], collaborative filtering method [70], clustering method [71], label propagation method [72], etc.It is worth noting that many of these other methods can be attributed to the binary classification method in a sense. For example, the network inference method regards the DTIs prediction problem as the bipartite network inference problem, and infers missing edges to achieve DTIs prediction. If the missing edges are regarded as negative samples and the existing edges are regarded as positive samples, it is converted into a binary classification problem.For the binary classification method, it requires the participation of positive and negative samples, so unknown DTIs are often treated as negative samples. This negative sample construction strategy will not only introduce noise but also cause data imbalance as a large number of negative samples. Besides, it is also faced with excessive computational load and overfitting due to the redundant feature space and extremely high feature dimensions. For example, 10 drugs and 10 targets will be combined into 10 × 10 = 100 samples, and the same drug or target in different samples has the same feature vector, that is, the feature vector of each drug or target will appear 10 times in the feature space of 100 samples. To reduce the above difficulties, the application of multi-label learning to DTI prediction problems is worth ...