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Shenyang Pharma Univ. CDK9 compound LB-1: sourced facts only. name: "Moreover, compared with AZD5438, LB-1 demonstrated highly selective CDK9 inhibitory activity, with an IC50 value of 9.22 nM." [PMID:40162202]; target: "Moreover, compared with AZD5438, LB-1 demonstrated highly selective CDK9 inhibitory activity, with an IC50 value of 9.22 nM." [PMID:40162202]; developer: "Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, School of Pharmaceutical Engineering, Shenyang Pharmaceutical University Shenyang 110016 China [email protected]." [PMID:40162202]; stage: "Compound LB-1 exhibited potent CDK9 inhibition and induced apoptosis in the HCT116 cell line." [PMID:40162202]
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