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. 2020 May 12;43(5):419–430. doi: 10.14348/molcells.2020.0054

Table 2.

The candidate drugs/agents of antifibrotic activity

Action Drug/agent Reference
Sphingosine kinase inhibitor PF543 (SphK inhibitor) (Gonzalez-Fernandez et al., 2017)
SKI-II (SphK inhibitor, non-selective) (Yang et al., 2013)
N,N-dimethylsphingosine (DMS, SphK inhibitor) (Brunati et al., 2008; Wang et al., 2017b; Xiu et al., 2015)
S1P receptor agonist/antagonist FTY720 (S1PR1 and S1PR3 agonist) (Brunati et al., 2008; King et al., 2017; Kong et al., 2014)
VPC23019 (S1PR1 and S1PR3 antagonist) (Brunati et al., 2008; Yang et al., 2012; 2013)
SEW2871 (S1PR1 agonist) (Ding et al., 2016)
W146 (S1PR1 antagonist) (King et al., 2017; Liu et al., 2011; Yang et al., 2012; 2013)
JTE-013 (S1PR2 antagonist) (Kageyama et al., 2012; Wang et al., 2017a; Xu et al., 2016; Yang et al., 2015)
Suramin (S1PR3 antagonist) (Li et al., 2009a; 2009b)
KRP203 (FTY720 analog) (Kaneko et al., 2006; Khattar et al., 2013)
CAY-10444 (S1PR3 antagonist) (Yang et al., 2015)
VPC24191 (S1PR1 and S1PR3 antagonist) (Al Fadel et al., 2016)
Other inhibitor Pertussis toxin (PTX; G-protein-coupled receptor signaling inhibitor) (Brunati et al., 2008; Gonzalez-Fernandez et al., 2017; Yang et al., 2015)
Melatonin (melatonin receptors agonist)