Info
| ID | 4831 |
| Metal | Ru |
| Oxidation state | 2 |
| Charge | 0 |
| Donor atoms | {"N": 1} |
| Abbreviation | 1bBr |
| SMILES | Cc1ccc(C(C)C)cc1.[Br-].[Br-].[c-]1n(Cc2ccccc2)c2ccccc2[n+]1Cc1ccccc1 |
TUCAN
C31Br2N2Ru/(1-22)(2-25)(3-25)(4-7)(4-23)(5-9)(5-23)(6-10)(6-29)(7-8)(8-9)(10-20)(11-13)(11-17)(12-15)(12-26)(13-24)(14-17)(14-18)(15-22)(16-21)(16-26)(18-24)(19-20)(19-30)(21-22)(23-27)(24-28)(25-26)(27-32)(28-33)(29-30)(29-32)(30-33)(31-32)(31-33)
Measurements (3)
| Cell line | IC₅₀ dark (µM) | IC₅₀ light (µM) | DOI | Year |
| HCT-116 | 24 | — | 10.1021/acs.inorgchem.8b02634 | 2018 |
| SiHa | 25 | — | 10.1021/acs.inorgchem.8b02634 | 2018 |
| NCI-H460 | 30 | — | 10.1021/acs.inorgchem.8b02634 | 2018 |
Source-assisted 2D generator
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.
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The generated SVG will appear here. The legacy ligand image above stays visible for side-by-side review.