Instructions to use HauserGroup/ApeTokenizer-SMILES with libraries, inference providers, notebooks, and local apps. Follow these links to get started.
- Libraries
- Transformers
How to use HauserGroup/ApeTokenizer-SMILES with Transformers:
# Load model directly from transformers import AutoModel model = AutoModel.from_pretrained("HauserGroup/ApeTokenizer-SMILES", dtype="auto") - Notebooks
- Google Colab
- Kaggle
| { | |
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| "#N)": 643, | |
| "%10": 81, | |
| "%11": 91, | |
| "%12": 92, | |
| "%13": 93, | |
| "%14": 94, | |
| "%15": 95, | |
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| "CN2": 479, | |
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| "CO": 294, | |
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| "C[C@@H](": 502, | |
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| "C[C@@H](N": 877, | |
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| "C[C@@H](O)": 626, | |
| "C[C@@H]1": 482, | |
| "C[C@@H]1CC": 924, | |
| "C[C@@H]1CN(": 1193, | |
| "C[C@@H]2": 579, | |
| "C[C@@H]3": 700, | |
| "C[C@@H]4": 1029, | |
| "C[C@@]1": 963, | |
| "C[C@@]2": 1273, | |
| "C[C@H]": 335, | |
| "C[C@H](": 473, | |
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| "C[C@H]2": 550, | |
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| "C[C@]1": 851, | |
| "C[C@]12CC": 1341, | |
| "Cc1": 378, | |
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| "F)cc(": 1177, | |
| "F)cc1": 423, | |
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| "F)cc2": 568, | |
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| "N(C)C)": 937, | |
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| "N)": 311, | |
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| "N)cc1": 1301, | |
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| "N1": 427, | |
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| "N3": 1170, | |
| "N4": 1068, | |
| "N=C(": 558, | |
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| "NC": 984, | |
| "NC(": 1160, | |
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| "NC(C)": 894, | |
| "NCC": 633, | |
| "NCc1cc": 1216, | |
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| "[11CH3]": 60, | |
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| "[11c]": 112, | |
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| "[123Te]": 155, | |
| "[124I-]": 265, | |
| "[124I]": 113, | |
| "[125I-]": 143, | |
| "[125I]": 57, | |
| "[127I]": 244, | |
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| "[131Cs]": 222, | |
| "[131I-]": 269, | |
| "[131I]": 68, | |
| "[133Xe]": 263, | |
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| "[13CH]": 219, | |
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| "[13cH]": 164, | |
| "[13c]": 163, | |
| "[14C@@H]": 259, | |
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| "[14CH]": 154, | |
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| "[18F-]": 239, | |
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| "[18OH]": 205, | |
| "[18O]": 258, | |
| "[19F]": 122, | |
| "[211At]": 231, | |
| "[223Ra]": 162, | |
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| "[32PH]": 210, | |
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| "[35S]": 151, | |
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| "[45Ca+2]": 148, | |
| "[47Ca+2]": 166, | |
| "[68Ga+3]": 220, | |
| "[73Se]": 200, | |
| "[75Se]": 267, | |
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| "[82Rb]": 226, | |
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| "[89Sr+2]": 260, | |
| "[Ag+]": 159, | |
| "[Ag-4]": 268, | |
| "[Ag]": 123, | |
| "[Al+3]": 184, | |
| "[Al]": 186, | |
| "[Ar]": 214, | |
| "[As+]": 158, | |
| "[As-]": 241, | |
| "[AsH3]": 257, | |
| "[AsH]": 227, | |
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| "[At]": 235, | |
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| "[BH3-]": 111, | |
| "[B]": 139, | |
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| "[Be+2]": 202, | |
| "[Bi+3]": 141, | |
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| "[C@@H](": 365, | |
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| "[C@@H]12": 951, | |
| "[C@@H]1CC": 609, | |
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| "[C@@H]3": 477, | |
| "[C@@H]3CC": 713, | |
| "[C@@H]4": 613, | |
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| "[CH3]": 187, | |
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| "[Ca+2]": 89, | |
| "[CaH2]": 233, | |
| "[Ca]": 193, | |
| "[Cl+2]": 199, | |
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| "[F-]": 84, | |
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| "[H-]": 230, | |
| "[He]": 86, | |
| "[I+2]": 249, | |
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| "[I+]": 129, | |
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| "[K]": 254, | |
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| "[LiH]": 192, | |
| "[Li]": 223, | |
| "[Mg+2]": 61, | |
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| "[MgH2]": 195, | |
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| "[N-]": 34, | |
| "[N@+]": 75, | |
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| "[N@]": 72, | |
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| "[NH-]": 107, | |
| "[NH2+]": 177, | |
| "[NH3+]": 238, | |
| "[NH4+]": 211, | |
| "[NH]": 136, | |
| "[N]": 197, | |
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| "[NaH]": 183, | |
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| "[O+]": 116, | |
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| "[O-]": 28, | |
| "[O-])": 528, | |
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| "[OH-]": 130, | |
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| "[P@+]": 137, | |
| "[P@@+]": 196, | |
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| "[PH2+]": 247, | |
| "[PH2]": 168, | |
| "[PH]": 109, | |
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| "[Rb+]": 171, | |
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| "[S+]([O-])": 1300, | |
| "[S-2]": 144, | |
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| "[SH]": 126, | |
| "[S]": 142, | |
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| "[Si@]": 232, | |
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| "[SiH3-]": 181, | |
| "[SiH4]": 218, | |
| "[SiH]": 78, | |
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| "[TeH2]": 198, | |
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| "[Te]": 63, | |
| "[Xe]": 261, | |
| "[Yb]": 173, | |
| "[Zn+2]": 124, | |
| "[Zn+]": 176, | |
| "[Zn-2]": 212, | |
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| "c(C(F)": 625, | |
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| } |