//! Sample data utilities for drug binding demo.
//!
//! Provides SMILES parsing and protein lookup functionality.

use drugbinder_shared::{
    Atom, BindingPocket, Bond, BondType, Coordinate3D, Element, Hybridization, MolecularProperties,
    Molecule, ProteinTarget,
};

use crate::DrugBinderError;

/// Convert SMILES string to Molecule.
pub fn smiles_to_molecule(smiles: &str, name: Option<String>) -> Result<Molecule, DrugBinderError> {
    // Parse SMILES
    let (atoms, bonds) = parse_smiles(smiles)?;

    // Calculate molecular weight
    let mw: f32 = atoms.iter().map(|a| element_mass(&a.element)).sum();

    // Calculate properties
    let properties = calculate_properties(&atoms, &bonds);

    Ok(Molecule {
        id: format!("mol_{}", hash_smiles(smiles)),
        name,
        smiles: smiles.to_string(),
        molecular_weight: mw,
        num_atoms: atoms.len(),
        num_bonds: bonds.len(),
        atoms,
        bonds,
        coordinates_3d: None,
        properties,
    })
}

/// Get protein by ID.
pub fn get_protein_by_id(protein_id: &str) -> Result<ProteinTarget, DrugBinderError> {
    // Look up in sample database
    let targets = get_protein_database();

    targets
        .into_iter()
        .find(|t| t.id == protein_id)
        .ok_or_else(|| DrugBinderError::InvalidProtein(format!("Unknown protein ID: {protein_id}")))
}

/// Convert sequence to protein.
#[must_use]
pub fn sequence_to_protein(sequence: &str, name: Option<String>) -> ProteinTarget {
    ProteinTarget {
        id: format!("seq_{}", hash_sequence(sequence)),
        name: name.unwrap_or_else(|| "Custom protein".to_string()),
        organism: "Unknown".to_string(),
        sequence: sequence.to_string(),
        pdb_id: None,
        pockets: vec![],
    }
}

/// Parse SMILES to atoms and bonds.
fn parse_smiles(smiles: &str) -> Result<(Vec<Atom>, Vec<Bond>), DrugBinderError> {
    let mut atoms = Vec::new();
    let mut bonds = Vec::new();
    let mut ring_atoms: std::collections::HashMap<char, usize> = std::collections::HashMap::new();
    let mut branch_stack: Vec<usize> = Vec::new();
    let mut prev_atom: Option<usize> = None;
    let mut pending_bond_type = BondType::Single;
    let mut in_aromatic = false;

    let chars: Vec<char> = smiles.chars().collect();
    let mut i = 0;

    while i < chars.len() {
        let c = chars[i];

        match c {
            // Branch handling
            '(' => {
                if let Some(atom_idx) = prev_atom {
                    branch_stack.push(atom_idx);
                }
                i += 1;
                continue;
            }
            ')' => {
                prev_atom = branch_stack.pop();
                i += 1;
                continue;
            }

            // Bond types
            '-' => {
                pending_bond_type = BondType::Single;
                i += 1;
                continue;
            }
            '=' => {
                pending_bond_type = BondType::Double;
                i += 1;
                continue;
            }
            '#' => {
                pending_bond_type = BondType::Triple;
                i += 1;
                continue;
            }
            ':' => {
                pending_bond_type = BondType::Aromatic;
                i += 1;
                continue;
            }

            // Ring closures
            '0'..='9' => {
                if let Some(atom_idx) = prev_atom {
                    if let Some(&ring_start) = ring_atoms.get(&c) {
                        // Close ring
                        bonds.push(Bond {
                            atom1: ring_start,
                            atom2: atom_idx,
                            bond_type: if in_aromatic {
                                BondType::Aromatic
                            } else {
                                BondType::Single
                            },
                            is_conjugated: in_aromatic,
                            is_in_ring: true,
                        });
                        ring_atoms.remove(&c);
                    } else {
                        // Start ring
                        ring_atoms.insert(c, atom_idx);
                    }
                }
                i += 1;
                continue;
            }

            // Skip stereochemistry and charges
            '/' | '\\' | '@' | '+' | '[' | ']' => {
                // Skip bracket contents
                if c == '[' {
                    while i < chars.len() && chars[i] != ']' {
                        i += 1;
                    }
                }
                i += 1;
                continue;
            }

            _ => {}
        }

        // Try to parse element
        let (element, is_aromatic_elem, chars_consumed) = parse_element(&chars, i);

        if let Some(elem) = element {
            let atom_idx = atoms.len();

            // Determine aromaticity
            let is_aromatic_atom = is_aromatic_elem;
            if is_aromatic_atom {
                in_aromatic = true;
            }

            atoms.push(Atom {
                index: atom_idx,
                element: elem,
                formal_charge: 0,
                num_hydrogens: implicit_h_count(&elem, is_aromatic_atom),
                is_aromatic: is_aromatic_atom,
                hybridization: if is_aromatic_atom {
                    Hybridization::Sp2
                } else {
                    Hybridization::Sp3
                },
            });

            // Add bond to previous atom
            if let Some(prev_idx) = prev_atom {
                let bond_type =
                    if is_aromatic_atom && atoms.get(prev_idx).is_some_and(|a| a.is_aromatic) {
                        BondType::Aromatic
                    } else {
                        pending_bond_type
                    };

                bonds.push(Bond {
                    atom1: prev_idx,
                    atom2: atom_idx,
                    bond_type,
                    is_conjugated: bond_type == BondType::Aromatic || bond_type == BondType::Double,
                    is_in_ring: false, // Updated later for ring bonds
                });
            }

            prev_atom = Some(atom_idx);
            pending_bond_type = BondType::Single;
            i += chars_consumed;
        } else {
            i += 1;
        }
    }

    if atoms.is_empty() {
        return Err(DrugBinderError::InvalidMolecule(format!(
            "Could not parse SMILES: {smiles}"
        )));
    }

    Ok((atoms, bonds))
}

/// Parse element from character stream.
fn parse_element(chars: &[char], start: usize) -> (Option<Element>, bool, usize) {
    if start >= chars.len() {
        return (None, false, 0);
    }

    let c = chars[start];

    // Check for two-letter elements
    if start + 1 < chars.len() {
        let next = chars[start + 1];
        if next.is_lowercase() {
            let elem_str: String = vec![c, next].into_iter().collect();
            let elem = match elem_str.as_str() {
                "Cl" => Some(Element::Cl),
                "Br" => Some(Element::Br),
                "Na" => Some(Element::Na),
                "Mg" => Some(Element::Mg),
                "Ca" => Some(Element::Ca),
                "Fe" => Some(Element::Fe),
                "Zn" => Some(Element::Zn),
                "Cu" => Some(Element::Cu),
                _ => None,
            };
            if elem.is_some() {
                return (elem, false, 2);
            }
        }
    }

    // Single letter elements
    match c {
        'C' => (Some(Element::C), false, 1),
        'N' => (Some(Element::N), false, 1),
        'O' => (Some(Element::O), false, 1),
        'S' => (Some(Element::S), false, 1),
        'P' => (Some(Element::P), false, 1),
        'F' => (Some(Element::F), false, 1),
        'I' => (Some(Element::I), false, 1),
        'H' => (Some(Element::H), false, 1),
        // Aromatic atoms (lowercase)
        'c' => (Some(Element::C), true, 1),
        'n' => (Some(Element::N), true, 1),
        'o' => (Some(Element::O), true, 1),
        's' => (Some(Element::S), true, 1),
        _ => (None, false, 1),
    }
}

/// Calculate implicit hydrogen count.
fn implicit_h_count(element: &Element, is_aromatic: bool) -> u8 {
    let valence: u8 = match element {
        Element::C => 4,
        Element::N => 3,
        Element::O => 2,
        Element::S => 2,
        Element::P => 3,
        Element::F | Element::Cl | Element::Br | Element::I => 1,
        _ => 0,
    };

    // Aromatic atoms typically have one less H
    if is_aromatic {
        valence.saturating_sub(1)
    } else {
        valence
    }
}

/// Calculate molecular properties.
fn calculate_properties(atoms: &[Atom], bonds: &[Bond]) -> MolecularProperties {
    // Count HBD (NH, OH)
    let hbd: u8 = atoms
        .iter()
        .filter(|a| matches!(a.element, Element::N | Element::O) && a.num_hydrogens > 0)
        .count() as u8;

    // Count HBA (N, O)
    let hba: u8 = atoms
        .iter()
        .filter(|a| matches!(a.element, Element::N | Element::O))
        .count() as u8;

    // Calculate LogP (Wildman-Crippen method, simplified)
    let mut log_p = 0.0_f32;
    for atom in atoms {
        log_p += match atom.element {
            Element::C => {
                if atom.is_aromatic {
                    0.29
                } else {
                    0.50
                }
            }
            Element::N => {
                if atom.num_hydrogens > 0 {
                    -1.03
                } else {
                    -0.57
                }
            }
            Element::O => {
                if atom.num_hydrogens > 0 {
                    -0.47
                } else {
                    -0.11
                }
            }
            Element::S => 0.37,
            Element::F => 0.37,
            Element::Cl => 0.71,
            Element::Br => 0.86,
            Element::I => 1.15,
            Element::H => 0.12,
            _ => 0.0,
        };
    }

    // Count rotatable bonds
    let rotatable_bonds: u8 = bonds
        .iter()
        .filter(|b| b.bond_type == BondType::Single && !b.is_in_ring)
        .count() as u8;

    // Count rings (estimate from ring bonds)
    let ring_bond_count = bonds.iter().filter(|b| b.is_in_ring).count();
    let num_rings = (ring_bond_count / 5).max(1) as u8;

    // Count aromatic rings
    let aromatic_atoms = atoms.iter().filter(|a| a.is_aromatic).count();
    let num_aromatic_rings = (aromatic_atoms / 5) as u8;

    // Calculate TPSA
    let tpsa: f32 = atoms
        .iter()
        .map(|a| match a.element {
            Element::N => {
                if a.num_hydrogens > 0 {
                    26.0
                } else {
                    12.0
                }
            }
            Element::O => {
                if a.num_hydrogens > 0 {
                    20.0
                } else {
                    9.2
                }
            }
            Element::S => 25.0,
            _ => 0.0,
        })
        .sum();

    // Calculate MW
    let mw: f32 = atoms.iter().map(|a| element_mass(&a.element)).sum();

    // Check Lipinski
    let lipinski_pass = mw <= 500.0 && log_p <= 5.0 && hbd <= 5 && hba <= 10;

    // Calculate QED
    let qed = calculate_qed(mw, log_p, hbd, hba, tpsa, rotatable_bonds);

    MolecularProperties {
        log_p,
        hbd,
        hba,
        tpsa,
        rotatable_bonds,
        num_rings,
        num_aromatic_rings,
        lipinski_pass,
        qed,
    }
}

fn calculate_qed(mw: f32, log_p: f32, hbd: u8, hba: u8, tpsa: f32, rotatable_bonds: u8) -> f32 {
    let gaussian =
        |x: f32, mean: f32, std: f32| -> f32 { (-0.5 * ((x - mean) / std).powi(2)).exp() };

    let mw_score = gaussian(mw, 350.0, 100.0);
    let logp_score = gaussian(log_p, 2.5, 1.5);
    let hbd_score = gaussian(f32::from(hbd), 1.0, 2.0);
    let hba_score = gaussian(f32::from(hba), 4.0, 3.0);
    let tpsa_score = gaussian(tpsa, 70.0, 30.0);
    let rotb_score = gaussian(f32::from(rotatable_bonds), 3.0, 3.0);

    (mw_score * logp_score * hbd_score * hba_score * tpsa_score * rotb_score).powf(1.0 / 6.0)
}

fn element_mass(element: &Element) -> f32 {
    match element {
        Element::H => 1.008,
        Element::C => 12.011,
        Element::N => 14.007,
        Element::O => 15.999,
        Element::F => 18.998,
        Element::P => 30.974,
        Element::S => 32.065,
        Element::Cl => 35.453,
        Element::Br => 79.904,
        Element::I => 126.90,
        Element::Na => 22.990,
        Element::Mg => 24.305,
        Element::K => 39.098,
        Element::Ca => 40.078,
        Element::Fe => 55.845,
        Element::Zn => 65.38,
        Element::Cu => 63.546,
        Element::Other => 12.0,
    }
}

fn hash_smiles(smiles: &str) -> u32 {
    smiles.bytes().fold(0u32, |acc, b| {
        acc.wrapping_mul(31).wrapping_add(u32::from(b))
    })
}

fn hash_sequence(sequence: &str) -> u32 {
    sequence.bytes().fold(0u32, |acc, b| {
        acc.wrapping_mul(37).wrapping_add(u32::from(b))
    })
}

/// Get protein database.
fn get_protein_database() -> Vec<ProteinTarget> {
    vec![
        // Carbonic anhydrase 2
        ProteinTarget {
            id: "P00918".to_string(),
            name: "Carbonic anhydrase 2".to_string(),
            organism: "Homo sapiens".to_string(),
            sequence: "MSHHWGYGKHNGPEHWHKDFPIAKGERQSPVDIDTHTAKYDPSLKPLSVSYDQATSLRILNNGHAFNVEFDDSQDKAVLKGGPLDGTYRLIQFHFHWGSLDGQGSEHTVDKKKYAAELHLVHWNTKYGDFGKAVQQPDGLAVLGIFLKVGSAKPGLQKVVDVLDSIKTKGKSADFTNFDPRGLLPESLDYWTYPGSLTTPPLLECVTWIVLKEPISVSSEQVLKFRKLNFNGEGEPEELMVDNWRPAQPLKNRQIKASFK".to_string(),
            pdb_id: Some("1CA2".to_string()),
            pockets: vec![
                BindingPocket {
                    id: 0,
                    name: "Active site".to_string(),
                    residues: vec![91, 92, 94, 96, 119, 143, 198, 199, 200],
                    center: Coordinate3D { x: 12.5, y: 8.3, z: 15.2 },
                    volume: 350.0,
                    druggability: 0.85,
                },
            ],
        },
        // EGFR
        ProteinTarget {
            id: "P00533".to_string(),
            name: "Epidermal growth factor receptor".to_string(),
            organism: "Homo sapiens".to_string(),
            sequence: "MRPSGTAGAALLALLAALCPASRALEEKKVCQGTSNKLTQLGTFEDHFLSLQRMFNNCEVVLGNLEITYVQRNYDLSFLKTIQEVAGYVLIALNTVERIPLENLQIIRGNMYYENSYALAVLSNYDANKTGLKELPMRNLQEILHGAVRFSNNPALCNVESIQWRDIVSSDFLSNMSMDFQNHLGSCQKCDPSCPNGSCWGAGEENCQKLTKIICAQQCSGRCRGKSPSDCCHNQCAAGCTGPRESDCLVCRKFRDEATCKDTCPPLMLYNPTTYQMDVNPEGKYSFGATCVKKCPRNYVVTDHGSCVRACGADSYEMEEDGVRKCKKCEGPCRKVCNGIGIGEFKDSLSINATNIKHFKNCTSISGDLHILPVAFRGDSFTHTPPLDPQELDILKTVKEITGFLLIQAWPENRTDLHAFENLEIIRGRTKQHGQFSLAVVSLNITSLGLRSLKEISDGDVIISGNKNLCYANTINWKKLFGTSGQKTKIISNRGENSCKATGQVCHALCSPEGCWGPEPRDCVSCRNVSRGRECVDKCNLLEGEPREFVENSECIQCHPECLPQAMNITCTGRGPDNCIQCAHYIDGPHCVKTCPAGVMGENNTLVWKYADAGHVCHLCHPNCTYGCTGPGLEGCPTNGPKIPS".to_string(),
            pdb_id: Some("1M17".to_string()),
            pockets: vec![
                BindingPocket {
                    id: 0,
                    name: "ATP binding site".to_string(),
                    residues: vec![718, 719, 721, 726, 745, 790, 791, 792, 793, 854, 855],
                    center: Coordinate3D { x: 25.0, y: 18.5, z: 42.0 },
                    volume: 480.0,
                    druggability: 0.92,
                },
            ],
        },
        // COX-2
        ProteinTarget {
            id: "P35354".to_string(),
            name: "Prostaglandin G/H synthase 2 (COX-2)".to_string(),
            organism: "Homo sapiens".to_string(),
            sequence: "MLARALLLCAVLALSHTANPCCSHPCQNRGVCMSVGFDQYKCDCTRTGFYGENCSTPEFLTRIKLFLKPTPNTVHYILTHFKGFWNVVNNIPFLRNAIMSYVLTSRSHLIDSPPTYNADY".to_string(),
            pdb_id: Some("5KIR".to_string()),
            pockets: vec![
                BindingPocket {
                    id: 0,
                    name: "Cyclooxygenase active site".to_string(),
                    residues: vec![83, 89, 90, 120, 355, 523, 530],
                    center: Coordinate3D { x: 30.0, y: 25.0, z: 35.0 },
                    volume: 420.0,
                    druggability: 0.88,
                },
            ],
        },
        // ACE2
        ProteinTarget {
            id: "Q9BYF1".to_string(),
            name: "Angiotensin-converting enzyme 2 (ACE2)".to_string(),
            organism: "Homo sapiens".to_string(),
            sequence: "MSSSSWLLLSLVAVTAAQSTIEEQAKTFLDKFNHEAEDLFYQSSLASWNYNTNITEENVQNMNNAGDKWSAFLKEQSTLAQMYPLQEIQNLTVKLQLQALQQNGSSVLSEDKSKRLNTILNTMSTIYSTGKVCNPDNPQECLLLEPGLNEIMANSLDYNERLWAWESWRSEVGKQLRPLYEEYVVLKNEMARANHYEDYGDYWRGDYEVNGVDGYDYSRGQLIEDVEHTFEEIKPLYEHLHAYVRAKLMNAYPSYISPIGCLPAHLLGDMWGRFWTNLYSLTVPFGQKPNIDVTDAMVDQAWDAQRIFKEAEKFFVSVGLPNMTQGFWENSMLTDPGNVQKAVCHPTAWDLGKGDFRILMCTKVTMDDFLTAHHEMGHIQYDMAYAAQPFLLRNGANEGFHEAVGEIMSLSAATPKHLKSIGLLSPDFQEDNETEINFLLKQALTIVGTLPFTYMLEKWRWMVFKGEIPKDQWMKKWWEMKREIVGVVEPVPHDETYCDPASLFHVSNDYSFIRYYTRTLYQFQFQEALCQAAKHEGPLHKCDISNSTEAGQKLFNMLRLGKSEPWTLALENVVGAKNMNVRPLLNYFEPLFTWLKDQNKNSFVGWSTDWSPYADQSIKVRISLKSALGDKAYEWNDNEMYLFRSSVAYAMRQYFLKVKNQMILFGEEDVRVANLKPRISFNFFVTAPKNVSDIIPRTEVEKAIRMSRSRINDAFRLNDNSLEFLGIQPTLGPPNQPPVSIWLIVFGVVMGVIVVGIVILIFTGIRDRKKKNKARSGENPYASIDISKGENNPGFQNTDDVQTSF".to_string(),
            pdb_id: Some("6M0J".to_string()),
            pockets: vec![
                BindingPocket {
                    id: 0,
                    name: "Peptidase active site".to_string(),
                    residues: vec![273, 345, 371, 374, 378, 384, 394, 402, 417],
                    center: Coordinate3D { x: 40.0, y: 32.0, z: 28.0 },
                    volume: 520.0,
                    druggability: 0.82,
                },
            ],
        },
        // HIV protease
        ProteinTarget {
            id: "P04585".to_string(),
            name: "HIV-1 protease".to_string(),
            organism: "Human immunodeficiency virus 1".to_string(),
            sequence: "PQITLWQRPLVTIKIGGQLKEALLDTGADDTVLEEMNLPGRWKPKMIGGIGGFIKVRQYDQILIEICGHKAIGTVLVGPTPVNIIGRNLLTQIGCTLNF".to_string(),
            pdb_id: Some("1HVR".to_string()),
            pockets: vec![
                BindingPocket {
                    id: 0,
                    name: "Active site".to_string(),
                    residues: vec![23, 25, 27, 28, 29, 30, 32, 47, 48, 49, 50, 76, 80, 81, 82, 84],
                    center: Coordinate3D { x: 18.0, y: 12.0, z: 22.0 },
                    volume: 380.0,
                    druggability: 0.95,
                },
            ],
        },
    ]
}

#[cfg(test)]
mod tests {
    use super::*;

    #[test]
    fn test_smiles_to_molecule() {
        let mol = smiles_to_molecule("CCO", Some("Ethanol".to_string()));
        assert!(mol.is_ok());

        let molecule = mol.unwrap();
        assert_eq!(molecule.name, Some("Ethanol".to_string()));
        assert!(molecule.atoms.len() >= 2); // At least C and O
    }

    #[test]
    fn test_smiles_benzene() {
        let mol = smiles_to_molecule("c1ccccc1", None);
        assert!(mol.is_ok());

        let molecule = mol.unwrap();
        assert!(molecule.atoms.iter().any(|a| a.is_aromatic));
    }

    #[test]
    fn test_smiles_aspirin() {
        let mol = smiles_to_molecule("CC(=O)OC1=CC=CC=C1C(=O)O", Some("Aspirin".to_string()));
        assert!(mol.is_ok());

        let molecule = mol.unwrap();
        assert!(molecule.molecular_weight > 150.0);
        assert!(molecule.molecular_weight < 200.0);
    }

    #[test]
    fn test_get_protein_by_id() {
        let result = get_protein_by_id("P00918");
        assert!(result.is_ok());

        let protein = result.unwrap();
        assert_eq!(protein.name, "Carbonic anhydrase 2");
        assert!(!protein.pockets.is_empty());
    }

    #[test]
    fn test_get_unknown_protein() {
        let result = get_protein_by_id("UNKNOWN123");
        assert!(result.is_err());
    }

    #[test]
    fn test_sequence_to_protein() {
        let protein = sequence_to_protein("MKLAVLKLAGLLAGLLAL", Some("Test protein".to_string()));
        assert_eq!(protein.name, "Test protein");
        assert_eq!(protein.sequence.len(), 18);
    }

    #[test]
    fn test_parse_smiles_with_branches() {
        let mol = smiles_to_molecule("CC(C)C", None); // Isobutane
        assert!(mol.is_ok());

        let molecule = mol.unwrap();
        assert!(molecule.atoms.len() >= 4);
    }

    #[test]
    fn test_parse_smiles_with_ring() {
        let mol = smiles_to_molecule("C1CCCCC1", None); // Cyclohexane
        assert!(mol.is_ok());

        let molecule = mol.unwrap();
        // Should have ring closure bond
        assert!(molecule.bonds.iter().any(|b| b.is_in_ring));
    }

    #[test]
    fn test_molecular_properties() {
        let mol = smiles_to_molecule("c1ccc(O)cc1", None).unwrap(); // Phenol
        assert!(mol.properties.hbd >= 1); // OH is HBD
        assert!(mol.properties.hba >= 1); // O is HBA
        assert!(mol.properties.num_aromatic_rings >= 1);
    }

    #[test]
    fn test_lipinski_check() {
        // Small drug-like molecule
        let mol = smiles_to_molecule("CCO", None).unwrap();
        assert!(mol.properties.lipinski_pass);
    }

    #[test]
    fn test_element_mass_lookup() {
        assert!((element_mass(&Element::C) - 12.011).abs() < 0.01);
        assert!((element_mass(&Element::O) - 15.999).abs() < 0.01);
        assert!((element_mass(&Element::N) - 14.007).abs() < 0.01);
    }

    #[test]
    fn test_protein_database() {
        let proteins = get_protein_database();
        assert!(proteins.len() >= 5);

        // Check for key proteins
        assert!(proteins.iter().any(|p| p.id == "P00918")); // CA2
        assert!(proteins.iter().any(|p| p.id == "P00533")); // EGFR
        assert!(proteins.iter().any(|p| p.id == "P04585")); // HIV protease
    }

    #[test]
    fn test_qed_calculation() {
        // Drug-like molecule (aspirin)
        let mol = smiles_to_molecule("CC(=O)OC1=CC=CC=C1C(=O)O", None).unwrap();
        assert!(mol.properties.qed > 0.3);
        assert!(mol.properties.qed < 1.0);
    }

    #[test]
    fn test_halogen_parsing() {
        let mol = smiles_to_molecule("CCCl", None); // Chloroethane
        assert!(mol.is_ok());

        let molecule = mol.unwrap();
        assert!(molecule.atoms.iter().any(|a| a.element == Element::Cl));
    }

    #[test]
    fn test_double_bond() {
        let mol = smiles_to_molecule("C=C", None); // Ethene
        assert!(mol.is_ok());

        let molecule = mol.unwrap();
        assert!(
            molecule
                .bonds
                .iter()
                .any(|b| b.bond_type == BondType::Double)
        );
    }

    #[test]
    fn test_triple_bond() {
        let mol = smiles_to_molecule("C#N", None); // HCN
        assert!(mol.is_ok());

        let molecule = mol.unwrap();
        assert!(
            molecule
                .bonds
                .iter()
                .any(|b| b.bond_type == BondType::Triple)
        );
    }
}