| ID | 6612 |
| Metal | Os |
| Oxidation state | 2 |
| Charge | 1 |
| Donor atoms | {"N": 4} |
| Abbreviation | 12 |
| SMILES | CN(C)c1ccc(/N=N/c2ccccn2)cc1.Cc1ccc(C(C)C)cc1.[I-].c1ccc(-c2ccccc2)cc1 |
| Cell line | IC₅₀ dark (µM) | IC₅₀ light (µM) | DOI | Year |
| A2780cisR | 0.11 | — | 10.1021/acs.jmedchem.8b00958 | 2018 |
| A2780 | 0.14 | — | 10.1021/acs.jmedchem.8b00958 | 2018 |
| A549 | 0.27 | — | 10.1021/acs.jmedchem.8b00958 | 2018 |
| HCT-116Ox | 0.33 | — | 10.1021/acs.jmedchem.8b00958 | 2018 |
| HOF | 0.35 | — | 10.1021/acs.jmedchem.8b00958 | 2018 |
| MRC-5 | 0.42 | — | 10.1021/acs.jmedchem.8b00958 | 2018 |
| HCT-116 | 0.82 | — | 10.1021/acs.jmedchem.8b00958 | 2018 |
Builds the drawing from source ligand graphs and explicit donor metadata, then uses Metal2D only for layout. Publication output uses black bonds without arrows or colour highlighting; validated octahedral enantiomers are encoded directly with solid and hashed wedge bonds.