Carnitine chloride

Methyl-&#946-cyclodextrin is a heptasaccharide, soluble in water, and has more affinity to cholesterol due to the presence of hydrophobic core. Cyclodextrins are cyclic oligosaccharides consisting of 6, 7, or 8 glucopyranose units, usually

Methyl-&#946-cyclodextrin is a heptasaccharide, soluble in water, and has more affinity to cholesterol due to the presence of hydrophobic core. Cyclodextrins are cyclic oligosaccharides consisting of 6, 7, or 8 glucopyranose units, usually

General description Methyl-&#946:-cyclodextrin is a small cyclic heptasaccharide. Application Methyl-&#946:-cyclodextrin has been used as a cholesterol chelator: to study its effects on mice cardiomyocytes to study its effects on human

application：β-Carotene has been used:as standard for quantification of b-carotene using HPLC analysisas a standard for the identification and quantification of authentic standards for carotenoid groupsfor standard curve preparation in the

application：β-Carotene has been used:as standard for quantification of b-carotene using HPLC analysisas a standard for the identification and quantification of authentic standards for carotenoid groupsfor standard curve preparation in the

application：β-Carotene has been used:as standard for quantification of b-carotene using HPLC analysisas a standard for the identification and quantification of authentic standards for carotenoid groupsfor standard curve preparation in the

application：β-Carotene has been used:as standard for quantification of b-carotene using HPLC analysisas a standard for the identification and quantification of authentic standards for carotenoid groupsfor standard curve preparation in the

NSC 23766 is a cell-permeable, reversible and specific inhibitor of Rac GTPase, used for cancer treatment.Application：The compound blocks activation by the guanine nucleotide exchange factors Trio and Tiam1, but does not affect interactions with

NSC 23766 is a cell-permeable, reversible and specific inhibitor of Rac GTPase, used for cancer treatment.Application：The compound blocks activation by the guanine nucleotide exchange factors Trio and Tiam1, but does not affect interactions with

Solid phase extraction apparatus uses glass vials or tubes for sample collection and concentration. Some sorbents require large desorption volume than small SPE cartridges in such case SPE tubes were used.

PROTAC RIPK degrader-2 is a nonpeptidic PROTAC based on von Hippel-Lindau ligand which potently targets serine-threonine kinase RIPK2 and has highly selective for RIPK2 degradationForm:SolidIC50&amp: Target:VHL.

R -Alpine-Borane &#174 is a chiral reducing agent, synthesized from (+)-&#945-pinene via hydroboration. Application R -Alpine-Borane &#174 may be used in the preparation of (22 R )-hydroxy-23-acetylenic steroids with high stereoselectivity.