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Request The Product List ofStearoyl-CoA Desaturase (SCD) Stearoyl-CoA Desaturase (SCD)

Cat. No. Product Name Information
PC-60369

T-3764518

T-3764518 (T 3764518, T3764518) is a novel potent, orally active SCD1 inhibitor with binding IC50 of 4.7 nM for hSCD1.
PC-45850

A-939572

SCD1 inhibitor

A-939572 is a potent, specific and orally bioavailable SCD1 inhibitor with IC50 of <4 nM and 37 nM for rSCD1 and hSCD1, respectively.
PC-20383

CAY10566

SCD1 inhibitor

CAY10566 is a potent, selective and orally bioavailable stearoyl-CoA desaturase 1 (SCD1) inhibitor with IC50 of 4.5 and 26 nM for mouse and human SCD1, respectively.
PC-20382

(R)-SW203668

SCD inhibitor

(R)-SW203668 (SCD inhibitor (R)-27) is a potent, tumor-specific, irreversible stearoyl CoA desaturase (SCD) inhibitor with high sensitity to H2122 cell (IC50=11 nM).
PC-20381

SW208108

SCD inhibitor

SW208108 (SW 208108) is a potent, tumor-specific, irreversible stearoyl CoA desaturase (SCD) inhibitor with high sensitity to H2122 cell (IC50=14 nM).
PC-20380

SW203668

SCD inhibitor

SW203668 (SW 203668) is a potent, tumor-specific, irreversible stearoyl CoA desaturase (SCD) inhibitor with high sensitity to H2122 cell (IC50=22 nM).
PC-20379

MF-438

SCD1 inhibitor

MF-438 (MF438) is a potent and orally bioavailable stearoyl-CoA desaturase 1 (SCD1) inhibitor with IC50 of 2.3 nM.
PC-38545

CVT-11127

SCD inhibitor

CVT-11127 (FMK13918) is a specfiic small molecule stearoyl-CoA desaturase (SCD) inhibitor with IC50 of 210 and 410 nM against rat microsomal SCD and HepG2 SCD, respectively.
PC-72680

YTX-7739

SCD inhibitor

YTX-7739 is a potent, selective stearoyl-CoA desaturase (SCD) inhibitor with IC50 of 12 nM.
PC-35915

YTX-465

YTX-465 (YTX465) is a specific small molecule that rescues yeast from a-Syn cytotoxicity with EC50 of 15 nM, via inhibiting Ole1, the yeast homolog of human stearoyl-CoA desaturase (SCD).
PC-43378

MK-8245 trifluoroacetate

MK-8245 trifluoroacetate is a potent, selective liver-targeted stearoyl-CoA desaturase (SCD) inhibitor with IC50 of 3, 3 and 1 nM for rat, mouse and human SCD1 enzyme, respectively.
PC-43373

MK-8245

MK-8245 is a potent, selective liver-targeted stearoyl-CoA desaturase (SCD) inhibitor with IC50 of 3, 3 and 1 nM for rat, mouse and human SCD1 enzyme, respectively.

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