ligands acting on targets

(S)-JQ-35 (TEN-010) is an inhibitor of the Bromodomain and Extra-Terminal (BET) family bromodomain-containing proteins with potential antineoplastic activity.Form:Solid.

(S)-JQ-35 (TEN-010) is an inhibitor of the Bromodomain and Extra-Terminal (BET) family bromodomain-containing proteins with potential antineoplastic activity.

(S)-Ketorolac is R-enantiomer of Ketorolac. The (S)-enantiomer is about 60 times more potent than (R)-enantiomer. A prostaglandin biosynthesis inhibitor. Analgesic and anti-inflammatory. (S)-Ketorolac is an inhibitor of Cox-1 and Cox-2.

(S)-Lercanidipine Hydrochloride is a calcium channel protein inhibitor.

(S)-Lisinopril-d5 Sodium is an angiotensin-converting enzyme (ACE) inhibitor.

(S)-Mapracorat is a selective and less active glucocorticoid receptor agonist.In Vitro(S)-Mapracorat concentration dependently inhibited TNFα secretion from activated canine PBMC with IC 50 value of approximately 0.2 nM. MCE has not independently

(S)-Mapracorat is a selective and less active glucocorticoid receptor agonist.In Vitro(S)-Mapracorat concentration dependently inhibited TNFα secretion from activated canine PBMC with IC 50 value of approximately 0.2 nM. MCE has not independently

(S)-Mapracorat is a selective and less active glucocorticoid receptor agonist.In Vitro(S)-Mapracorat concentration dependently inhibited TNFα secretion from activated canine PBMC with IC 50 value of approximately 0.2 nM. MCE has not independently

(S)-Methyl 2-amino-3-(naphthalen-2-yl)propanoate hydrochloride.

(S)-Methyl 2-amino-3-(naphthalen-2-yl)propanoate hydrochloride.

(S)-Methyl 2-amino-3-(naphthalen-2-yl)propanoate hydrochloride.

(S)-Methyl 2-amino-3-(naphthalen-2-yl)propanoate hydrochloride.