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requirements.txt

@@ -1,107 +1,5 @@
-import gradio as gr
-from rdkit import Chem
-from rdkit.Chem import Descriptors, Draw
-import cirpy
-
-
-def _mol_from_smiles(smiles: str):
-    mol = Chem.MolFromSmiles(smiles)
-    if mol is None:
-        raise gr.Error("Invalid SMILES string.")
-    return mol
-
-
-def smiles_to_canonical(smiles: str) -> str:
-    mol = _mol_from_smiles(smiles)
-    return Chem.MolToSmiles(mol)
-
-
-def molecular_weight(smiles: str) -> float:
-    mol = _mol_from_smiles(smiles)
-    return float(Descriptors.MolWt(mol))
-
-
-def logp(smiles: str) -> float:
-    mol = _mol_from_smiles(smiles)
-    return float(Descriptors.MolLogP(mol))
-
-
-def tpsa(smiles: str) -> float:
-    mol = _mol_from_smiles(smiles)
-    return float(Descriptors.TPSA(mol))
-
-
-def mol_image(smiles: str):
-    mol = _mol_from_smiles(smiles)
-    return Draw.MolToImage(mol)
-
-
-def name_to_smiles(name: str) -> str:
-    """Convert chemical name to SMILES using Chemical Identifier Resolver (CIR)"""
-    try:
-        smiles = cirpy.resolve(name, 'smiles')
-        if smiles is None:
-            raise gr.Error(f"Could not find SMILES for chemical name: {name}")
-        return smiles
-    except Exception as e:
-        raise gr.Error(f"Error converting name to SMILES: {str(e)}")
-
-
-smiles_interface = gr.Interface(
-    fn=smiles_to_canonical,
-    inputs=gr.Textbox(label="SMILES"),
-    outputs=gr.Textbox(label="Canonical SMILES"),
-    api_name="smiles_to_mol",
-    description="Convert an input SMILES string to its canonical form.",
-)
-
-name_interface = gr.Interface(
-    fn=name_to_smiles,
-    inputs=gr.Textbox(label="Chemical Name", placeholder="e.g., aspirin, caffeine, benzene"),
-    outputs=gr.Textbox(label="SMILES"),
-    api_name="name_to_smiles",
-    description="Convert a chemical name to SMILES notation.",
-    examples=[["aspirin"], ["caffeine"], ["benzene"], ["ethanol"]],
-)
-
-mw_interface = gr.Interface(
-    fn=molecular_weight,
-    inputs=gr.Textbox(label="SMILES"),
-    outputs=gr.Number(label="Molecular Weight (g/mol)"),
-    api_name="molecular_weight",
-    description="Compute the molecular weight from a SMILES string.",
-)
-
-logp_interface = gr.Interface(
-    fn=logp,
-    inputs=gr.Textbox(label="SMILES"),
-    outputs=gr.Number(label="logP"),
-    api_name="logp",
-    description="Calculate the octanol/water partition coefficient (logP).",
-)
-
-tpsa_interface = gr.Interface(
-    fn=tpsa,
-    inputs=gr.Textbox(label="SMILES"),
-    outputs=gr.Number(label="TPSA"),
-    api_name="tpsa",
-    description="Calculate the topological polar surface area (TPSA).",
-)
-
-
-demo = gr.TabbedInterface(
-    [name_interface, smiles_interface, mw_interface, logp_interface, tpsa_interface],
-    [
-        "Name to SMILES",
-        "SMILES to Canonical",
-        "Molecular Weight",
-        "LogP",
-        "TPSA",
-    ],
-    title="RDKit API",
-    css=".gradio-container {max-width: 800px; margin: auto;}",
-)
-
-
-if __name__ == "__main__":
-    demo.queue().launch(server_name="0.0.0.0", server_port=7860)
+# RDKit dependencies
+rdkit
+gradio==4.44.1
+huggingface_hub==0.19.4
+cirpy