Crystallography Open Database
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Result: there are 22 entries in the selection
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Searching journal of publication like 'MedChemComm' volume of publication is 3
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 7112578 | CIF | C29 H32 Cr O5 | P 1 21/c 1 | 9.8549; 15.641; 16.5024 90; 100.507; 90 | 2501 | Saiai, Aroonchai; Bielig, Harald; Velder, Janna; Neudörfl, Jörg-Martin; Menning, Maureen; Kufer, Thomas A.; Schmalz, Hans-Günther Hydrophenalene‒Cr(CO)3 complexes as anti-inflammatory agents based on specific inhibition of NOD2 signalling: a SAR study MedChemComm, 2012, 3, 1377 |
| 7112579 | CIF | C29 H31 Cr F O5 | P -1 | 7.9722; 12.8619; 13.5661 68.848; 81.683; 81.459 | 1276.66 | Saiai, Aroonchai; Bielig, Harald; Velder, Janna; Neudörfl, Jörg-Martin; Menning, Maureen; Kufer, Thomas A.; Schmalz, Hans-Günther Hydrophenalene‒Cr(CO)3 complexes as anti-inflammatory agents based on specific inhibition of NOD2 signalling: a SAR study MedChemComm, 2012, 3, 1377 |
| 7112580 | CIF | C30 H34 Cr O5 | P -1 | 8.9498; 11.2208; 13.8926 90.023; 106.008; 104.171 | 1296.78 | Saiai, Aroonchai; Bielig, Harald; Velder, Janna; Neudörfl, Jörg-Martin; Menning, Maureen; Kufer, Thomas A.; Schmalz, Hans-Günther Hydrophenalene‒Cr(CO)3 complexes as anti-inflammatory agents based on specific inhibition of NOD2 signalling: a SAR study MedChemComm, 2012, 3, 1377 |
| 7112581 | CIF | C30 H31 Cr F3 O5 | F d d 2 | 32.4358; 34.6; 9.8268 90; 90; 90 | 11028.4 | Saiai, Aroonchai; Bielig, Harald; Velder, Janna; Neudörfl, Jörg-Martin; Menning, Maureen; Kufer, Thomas A.; Schmalz, Hans-Günther Hydrophenalene‒Cr(CO)3 complexes as anti-inflammatory agents based on specific inhibition of NOD2 signalling: a SAR study MedChemComm, 2012, 3, 1377 |
| 7112582 | CIF | C19 H11 Br Cl2 N2 O4 S | P -1 | 9.2497; 10.8904; 11.0733 84.708; 73.497; 69.745 | 1003.34 | Ali, Sher; Saeed, Aamer; Abbas, Naeem; Shahid, Mohammad; Bolte, Michael; Iqbal, Jamshed Design, synthesis and molecular modelling of novel methyl[4-oxo-2-(aroylimino)-3-(substituted phenyl)thiazolidin-5-ylidene]acetates as potent and selective aldose reductase inhibitors MedChemComm, 2012, 3, 1428 |
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