Crystallography Open Database

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7117325 CIFC30 H30 Br Cl N2 O3P -17.799; 13.077; 14.674
102.019; 102.584; 105.196
1352.4Kalia, Dimpy; K. S., Anil Kumar; Meena, Gajanand; Sethi, Kashmir Prasad; Sharma, Rohit; Trivedi, Priyanka; Khan, Shaheb Raj; Verma, Ajay Singh; Singh, Shyam; Sharma, Sandeep; Roy, Kuldeep K.; Kant, Ruchir; Krishnan, Manju Yasodha; Singh, Bhupendra N.; Sinha, Sudhir; Chaturvedi, Vinita; Saxena, Anil K.; Dikshit, Dinesh K.
Synthesis and anti-tubercular activity of conformationally-constrained and bisquinoline analogs of TMC207
Med. Chem. Commun., 2015, 6, 1554
7117326 CIFC31 H33 Cl N2 O4P -110.198; 12.405; 12.423
79.72; 70.82; 72.77
1412Kalia, Dimpy; K. S., Anil Kumar; Meena, Gajanand; Sethi, Kashmir Prasad; Sharma, Rohit; Trivedi, Priyanka; Khan, Shaheb Raj; Verma, Ajay Singh; Singh, Shyam; Sharma, Sandeep; Roy, Kuldeep K.; Kant, Ruchir; Krishnan, Manju Yasodha; Singh, Bhupendra N.; Sinha, Sudhir; Chaturvedi, Vinita; Saxena, Anil K.; Dikshit, Dinesh K.
Synthesis and anti-tubercular activity of conformationally-constrained and bisquinoline analogs of TMC207
Med. Chem. Commun., 2015, 6, 1554
7117550 CIFC15 H25 N2 O3 P S2C 1 2/c 124.2051; 8.9799; 17.2946
90; 101.412; 90
3684.82Alexander, Benjamin E.; Coles, Simon J.; Fox, Bridget C.; Khan, Tahmina F.; Maliszewski, Joseph; Perry, Alexis; Pitak, Mateusz B.; Whiteman, Matthew; Wood, Mark E.
Investigating the generation of hydrogen sulfide from the phosphonamidodithioate slow-release donor GYY4137
Med. Chem. Commun., 2015, 6, 1649
7117770 CIFC22 H16 Cl N2 OP 1 21/c 113.5275; 7.5746; 18.3908
90; 111.098; 90
1758.1Kalalbandi, Veerendra Kumar A.; Seetharamappa, J.
1-[(2E)-3-Phenylprop-2-enoyl]-1H-benzimidazoles as anticancer agents: synthesis, crystal structure analysis and binding studies of the most potent anticancer molecule with serum albumin
Med. Chem. Commun., 2015, 6, 1942
7117864 CIFC23 H23 F N4 O5P 1 21/c 17.8954; 24.3573; 12.7445
90; 94.249; 90
2444.2Sha, Shao; Han, Hong-Wei; Gao, Fei; Liu, Tian-Bao; Li, Zhen; Xu, Chi; Zhong, Wei-Qing; Zhu, Hai-Liang
Discovery of fluoroquinolone derivatives as potent, selective inhibitors of PI3Kγ
Med. Chem. Commun., 2015, 6, 2029

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