| ID | 6610 |
| Metal | Os |
| Oxidation state | 2 |
| Charge | 1 |
| Donor atoms | {"N": 4} |
| Abbreviation | 10 |
| SMILES | CN(C)c1ccc(/N=N/c2ccccn2)cc1.Cc1ccc(C(C)C)cc1.Cc1ccc(C(C)C)cc1.[I-] |
| Cell line | IC₅₀ dark (µM) | IC₅₀ light (µM) | DOI | Year |
| A2780 | 0.15 | — | 10.1021/acs.jmedchem.8b00958 | 2018 |
| A2780cisR | 0.15 | — | 10.1021/acs.jmedchem.8b00958 | 2018 |
| HCT-116 | 0.26 | — | 10.1021/acs.jmedchem.8b00958 | 2018 |
| HCT-116Ox | 0.96 | — | 10.1021/acs.jmedchem.8b00958 | 2018 |
| A549 | 1.1 | — | 10.1021/acs.jmedchem.8b00958 | 2018 |
| HOF | 2.3 | — | 10.1021/acs.jmedchem.8b00958 | 2018 |
| MRC-5 | 4.5 | — | 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.