C75 (trans)|cas 191282-48-1|DC Chemicals

C75 (trans)|cas 191282-48-1|DC Chemicals

C75 trans is the trans form of C75; C75 is a potent  fatty-acid synthase(FASN) inhibitor with IC50 of 35.4 μM(LNCaP cell Proliferation inhibition).

IC50 value: 35.4 μM(LNCaP cel) [1]

Target: fatty-acid synthase inhibitor

in vitro: C75 exhibited apoptosis induction by reducing the levels of fatty acid without any change in the abundance of FASN expression along with increasing ROS production [2].

Product Name: C75 (trans)|Cat No: DC9528|Cas: 191282-48-1|Molecule Formular: C14H22O4|Molecule Weight: 254.3221|Other names: C75 (trans)

C75 trans is the trans form of C75; C75 is a potent  fatty-acid synthase(FASN) inhibitor with IC50 of 35.4 μM(LNCaP cell Proliferation inhibition).
in vitro: C75 exhibited apoptosis induction by reducing the levels of fatty acid without any change in the abundance of FASN expression along with increasing ROS production. C75 treatment decreased LA content, impaired mitochondrial function, increased reactive oxygen species content, and reduced cell viability. HsmtKAS but not FASN knockdown had an effect that was similar to C75 treatment. In addition, an LA supplement efficiently inhibited C75-induced mitochondrial dysfunction and oxidative stress.
in vivo: C75 (5 mg/kg body weight) or dimethyl sulfoxide (DMSO) (vehicle) was administered intraperitoneally from d 2 to 6. C75 significantly reduced body weight loss from 23% to 15% on d 8, compared with the vehicle group. The fecal bleeding, diarrhea and colon histological damage scores in the C75-treated group were significantly lower than scores in the vehicle animals. Colon shortening was significantly improved after C75 treatment. C75 protected colon tissues from DSS-induced apoptosis by inhibiting caspase-3 activity.

For research only, not for human use!