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Listado de productos por fabricante AbMole
(R)Ginsenoside-Rh2
20(R)-Ginsenoside Rh2, a matrix metalloproteinase (MMP) inhibitor, acts as an anti-proliferative agent in cells. It has anticancer effects by blocking cell proliferation and causing G1 phase arrest. 20(R)-Ginsenoside Rh2 induces apoptosis and has anti-inflammatory and antioxidant activities. 20(R)-Ginsenoside Rh2 inhibited the replication and...
(R,R)-Secoisolariciresinol diglucoside
(R,R)-Secoisolariciresinol diglucoside ((R,R)-SDG) is a minor subtype of Secoisolariciresinol diglucoside present in flaxseed. (R,R)-Secoisolariciresinol diglucoside ((R,R)-SDG) has antioxidant properties, free radical scavenging activity, and DNA-radiation protection. (R,R)-Secoisolariciresinol diglucoside ((R,R)-SDG) inhibits myeloperoxidase (MPO)...
(Rac)-Brassinazole
(Rac)-Brassinazole is a brassinosteroid (BR) biosynthesis inhibitor.
(Rac)-Brassinazole
(Rac)-Brassinazole is a brassinosteroid (BR) biosynthesis inhibitor.
(Rac)-Brassinazole
(Rac)-Brassinazole is a brassinosteroid (BR) biosynthesis inhibitor.
(Rac)-Brassinazole
(Rac)-Brassinazole is a brassinosteroid (BR) biosynthesis inhibitor.
(Rac)-Indoximod
(Rac)-Indoximod(1-methyl-DL-tryptophan) is an indoleamine 2, 3-dioxygenase (IDO) inhibitor.
(Rac)-Indoximod
(Rac)-Indoximod(1-methyl-DL-tryptophan) is an indoleamine 2, 3-dioxygenase (IDO) inhibitor.
(Rac)-JBJ-04-125-02
(Rac)-JBJ-04-125-02 is a racemate of JBJ-04-125-02, which is a potent, selectively mutated, allosteric and oral active EGFR inhibitor. The IC50 of EGFRL858R/T790M was 0.26 nM.
(Rac)-JBJ-04-125-02
(Rac)-JBJ-04-125-02 is a racemate of JBJ-04-125-02, which is a potent, selectively mutated, allosteric and oral active EGFR inhibitor. The IC50 of EGFRL858R/T790M was 0.26 nM.
(Rac)-NSC305787 hydrochloride
NSC305787 hydrochloride is an inhibitor of ezrin with a Kd of 5.85 μM, inhibits the phosphorylation of ezrin caused by PKCΙ with an IC50 of 8.3 μM, has antitumor activity.
(Rac)-NSC305787 hydrochloride
NSC305787 hydrochloride is an inhibitor of ezrin with a Kd of 5.85 μM, inhibits the phosphorylation of ezrin caused by PKCΙ with an IC50 of 8.3 μM, has antitumor activity.