Info
| ID | 460 |
| Metal | Ru |
| Oxidation state | 2 |
| Charge | 1 |
| Donor atoms | {"N": 1} |
| Abbreviation | 1l |
| SMILES | Brc1ccc(SCCn2[c-][n+](Cc3ccccc3)cc2)cc1.Cc1ccc(C(C)C)cc1.[Cl-] |
TUCAN
C28BrClN2RuS/(1-20)(2-19)(3-20)(4-6)(4-19)(5-12)(5-13)(6-17)(7-16)(7-19)(8-9)(8-28)(9-27)(10-11)(10-27)(11-28)(12-18)(13-15)(14-15)(14-18)(16-17)(17-20)(18-23)(21-22)(21-30)(22-29)(23-29)(24-26)(24-30)(25-29)(25-30)(26-31)(27-31)(28-33)
Measurements (3)
| Cell line | IC₅₀ dark (µM) | IC₅₀ light (µM) | DOI | Year |
| HCT-116 | 9.8 | — | 10.1039/C9DT04825A | 2020 |
| PC-3 | 10 | — | 10.1039/C9DT04825A | 2020 |
| MCF-7 | 13 | — | 10.1039/C9DT04825A | 2020 |
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.
Loading source metadata…
The generated SVG will appear here. The legacy ligand image above stays visible for side-by-side review.