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Structure Cat No. Product Name CAS No. Product Description
AG-17724 V83243 AG-17724 884033-66-3 AG17724 is a novel and potent peptidyl-prolyl isomerase (PPIase) Pin1 inhibitor.
AI-10-49 V1895 AI-10-49 1256094-72-0 AI-10-49 is a potent and selective inhibitor of the binding of CBFβ-SMMHC to RUNX1 with IC50 of 260 nM.
Amelenodor (NX-13) V83223 Amelenodor (NX-13) 2389235-01-0 NX-13 is an orally bioactive NLRX1 agonist.
BRD7552 V1898 BRD7552 1137359-47-7 BRD7552 is an inducer of transcription factor PDX1, which increases insulin expression.
Cetiedil V83208 Cetiedil 14176-10-4 Cetiedil is a potent vasodilator which displays weak muscarinic receptor antagonist activity and inhibits the release of acetylcholine.
CY5.5羧基 V2154 CY5.5 carboxylic acid 1144107-80-1 CY5.5 carboxylic acid (Cyanine5.5 carboxylic acid) is a novel and potent Far-red emitting fluorescent dye with Ex/Em wavelength 673nm/707nm.
DCZ-5418 V83237 DCZ-5418 2883709-99-5 DCZ5418 is a potent inhibitor of TRIP13 with anti-multiple myeloma activity in vitro and in vivo.
FH1 (BRD-K4477) V1963 FH1 (BRD-K4477) 2719-05-3 FH1 (also known as NSC 12407, BRD-K4477) can enhance the functions of cultured hepatocytes bypromoting differentiation of iPS-derived hepatocytes.
FPH1 (BRD-6125) V1943 FPH1 (BRD-6125) 708219-39-0 FPH1 (also known as BRD-6125) is a small molecule that promotes expansion of iPS-derived hepatocytes.
FPH2 (BRD-9424) V1930 FPH2 (BRD-9424) 957485-64-2 FPH2 (also known as BRD-9424) is able to promote differentiation of iPS-derived hepatocytes.
LB-100 V1901 LB-100 1632032-53-1 LB-100 (LB100) is a water soluble small-molecular protein phosphatase 2A (PP2A) inhibitor with anticancer activity.
Mebufotenin V83225 Mebufotenin 2568048-63-3 Mebufotenin is biochemical for resistant depression.
ML241 V2109 ML241 1346528-06-0 ML241 is a novel and potent p97inhibitor which inhibits p97 ATPase with an IC50 value of 100 nM.
MRTX-849 analog 24 V51206 MRTX-849 analog 24 2490716-96-4 MRTX849 analog 24 is a probe containing an alkyne moiety for click reaction, can be used for synthesis of KRAS G12C PROTAC MRTX849.
Sudoterb (LL3858) V2056 Sudoterb (LL3858) 676266-31-2 Sudoterb (formerly also known as LL3858; LL-3858) is a novel and potent drug candidate with the potential for treating Tuberculosis (TB).
Tinlarebant V83218 Tinlarebant 1821327-95-0 Tinlarebant is an orally bioactive, potent and specific non-retinoid antagonist of RPB4.
TRC051384 V2151 TRC051384 1333327-56-2 TRC051384 is an inducer of heat shock protein Hsp70, activating heat shock factor-1 and enhancing Hsp72 expression in neurons and glial cells.
Vidoflufolastat (18F) V83226 Vidoflufolastat (18F) 1628717-59-8 Vidoflufolastat (18F) is a novel 18F-Labeled imaging agent with phosphoramidate core targeting prostate-specific membrane antigen in prostate cancer.
依托贝特 V1967 Etofibrate 31637-97-5 Etofibrate, the ethandiol-1,2 diester of the nicotinic and clofibric acid, is a combination of conjugated clofibrate and niacin that is used to treat hyperlipemia.
依替唑仑 V1920 Etizolam 40054-69-1 Discontinued (DEA controlled substance).
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