Colestipol hydrochloride

Application This allylboration reagent is a convenient, salt-free, stable solution of a chiral allyl borane for asymmetric allylation of aldehydes leading to chiral homoallylic alcohols. Other Notes Material may become hazy upon cooler storage,

General description Componentof stevia. This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities).

(2S,3R)-Voruciclib hydrochloride is the enantiomer of Voruciclib hydrochloride. (2S,3R)-Voruciclib is an orally active CDK inhibitor.Appearance:SolidBiological Activity:(2S,3R)-Voruciclib hydrochloride is the enantiomer of Voruciclib hydrochloride.

(2S,3R)-Voruciclib hydrochloride is the enantiomer of Voruciclib hydrochloride. (2S,3R)-Voruciclib is an orally active CDK inhibitor.Appearance:SolidBiological Activity:(2S,3R)-Voruciclib hydrochloride is the enantiomer of Voruciclib hydrochloride.

(2S,3R)-Voruciclib hydrochloride is the enantiomer of Voruciclib hydrochloride. (2S,3R)-Voruciclib is an orally active CDK inhibitor.Appearance:SolidBiological Activity:(2S,3R)-Voruciclib hydrochloride is the enantiomer of Voruciclib hydrochloride.

(2S,3R)-Voruciclib hydrochloride is the enantiomer of Voruciclib hydrochloride. (2S,3R)-Voruciclib is an orally active CDK inhibitor.Appearance:SolidBiological Activity:(2S,3R)-Voruciclib hydrochloride is the enantiomer of Voruciclib hydrochloride.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

An unsaturated diacylglycerol with linoleic acid (18:2) side-chains attached at both the C-1 and C-3 positions that is useful for lipid research.

An unsaturated diacylglycerol with linoleic acid (18:2) side-chains attached at both the C-1 and C-3 positions that is useful for lipid research.

An unsaturated diacylglycerol with linoleic acid (18:2) side-chains attached at both the C-1 and C-3 positions that is useful for lipid research.

Preferred phospholipid substrate for cPLA2 an important source of activation-induced arachidonate released as a substrate for COX-2 mediated signaling.