TTT20171 | Inhibitor of SDHC
RATINGS:
Cellular Use: (3 reviews)

In Model Organisms: (2 reviews)
In Vivo
Vendors

Probe Summary

Targets Biochemical/Biophysical Potency Cellular Potency
SDHC
  • IC50:3.3 nM
  • IC50:5400 nM
Up to 2 uM

Selectivity

In Vitro Selectivity Assessment

Potency: IC50 - Mitochondrial Complex I: >10,000 nM

Potency Assay Off-Target:
Spectrophotometric assay in frozen-thawed mouse heart mitochondria.

Potency
Cellular
In Vitro

SDHC

Mode of Action: Inhibitor

Structure-Activity-Relationship data available? No

Negative Control Compounds

Compound 24
Notes: The inactive control compound 24 displayed no growth inhibition effect upon treatment of DU-145 cells up to 30 μg mL−1

Chemical Information

Molecular Formula C20H33NO5
SMILEs CCCCCCCCCCCCC(=O)c1c(O)c(OC)c(OC)[nH]c1=O
InChI InChI=1S/C20H33NO5/c1-4-5-6-7-8-9-10-11-12-13-14-15(22)16-17(23)18(25-2)20(26-3)21-19(16)24/h4-14H2,1-3H3,(H2,21,23,24)
Molecular weight 367.24 Da
AlogP 4.591400000000003
HBond acceptors 6
HBond donors 2
Atoms 59

References

Expert Reviews


(on 18 Aug 2017)
Cellular Use Rating
In Model Organisms
TTT20171 (compound 16k Wang et al., ChemMedChem 2017) displays nanomolar inhibition of CII but lacks cellular potency. In cell assays, the most sensitive cells (22Rv1 prostate cancer cells) are inhibited...
(on 11 Nov 2020)
Cellular Use Rating
In Model Organisms
(The reviewer did not leave any public comments)
(on 24 Apr 2023)
Cellular Use Rating
This work demonstrates a potent in vitro inhibitor of SDH activity against isolated mitochondria (IC50 < 10nM). While cellular anti-proliferative and mitochondrial functional data are presented, there...
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