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Veliflapon

Cat. No.: DC28965

Chemical Structure

128253-31-6

For research use only. We do not sell to patients.

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Field of application

Veliflapon (BAY X 1005; DG-031) is an orally active and selective 5-lipoxygenase activating protein (FLAP) inhibitor. Veliflapon inhibits the synthesis of the leukotrienes B4 and C4.

Chemicals Properties Biological activity Related products COA MSDS Datasheet

Cas No.:	128253-31-6
Chemical Name:	(R)-2-(4-(Quinolin-2-yl-methoxy)phenyl)-2-cyclopentylacetic acid
Synonyms:	Bay X1005; Bay X-1005; Bay X 1005; DG 031; DG-031; DG031; Veliflapon;
Formula:	C₂₃H₂₃NO₃
M.Wt:	361.441
Sotrage:	2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Cat. No.	Product name	Field of application
DC28965	Veliflapon	Veliflapon (BAY X 1005; DG-031) is an orally active and selective 5-lipoxygenase activating protein (FLAP) inhibitor. Veliflapon inhibits the synthesis of the leukotrienes B4 and C4.
DC28608	(S)-BI 665915	(S)-BI 665915 is an orally active oxadiazole-containing 5-lipoxygenase-activating protein (FLAP) inhibitor with an IC50 of 1.7 nM for FLAP binding. (S)-BI 665915 inhibits FLAP functional in human whole blood with an IC50 of 45 nM. (S)-BI 665915 demonstrates an excellent cross-species drug metabolism and pharmacokinetics (DMPK) profile and a dose-dependent inhibition of LTB4 production.

Products are chemical reagents for research use only and are not intended for human use. We do not sell to patients.