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SCR-7952: sourced facts only. name: "In biochemical assay, SCR-7952 exhibited potent inhibitory activity on MAT2A enzyme with IC50 of 21 nM, which was more potent than AG-270 (IC50, 68 nM)." [DOI:10.1158/1538-7445.am2022-5434]; target: "In biochemical assay, SCR-7952 exhibited potent inhibitory activity on MAT2A enzyme with IC50 of 21 nM, which was more potent than AG-270 (IC50, 68 nM)." [DOI:10.1158/1538-7445.am2022-5434]; developer: "1Simcere Pharmaceutical Group, Shanghai, China." [DOI:10.1158/1538-7445.am2022-5434]; stage: "In the HCT-116 MTAP-/- xenograft model, SCR-7952 demonstrated robust anti-tumor activity and achieved 72% tumor growth inhibition (TGI) at 1 mpk, QD, which was more potent than AG-270 (TGI 56% at 200 mpk, QD)." [DOI:10.1158/1538-7445.am2022-5434]
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