Eperisone hydrochloride

(&plusmn)12(13)-EpOME is the 12,13-cis epoxide of linoleic acid, generated by neutrophils during the oxidative burst. The toxicity and biosynthesis of (&plusmn)12(13)-EpOME have not been well differentiated from (&plusmn)9(10)-EpOME, but have

Description(2R,3R)-Diethyl 2,3-epoxysuccinate may be used in the preparation of ethyl (2R,3S)-4-hydroxy-2,3-epoxybutyrate via reduction using sodium borohydride.

Misoprostol is a widely sold analog of PGE1 which has potent but relatively non-selective agonist activity with respect to the prostanoid EP receptor subgroup. Misoprostol has been used therapeutically for many years in humans for the treatment of

17-phenyl trinor 8-iso PGE2 is the C-8 epimer of 17-phenyl trinor PGE2, a synthetic analog of PGE2. 17-phenyl trinor PGE2 is an EP1 and EP3 receptor agonist that causes contraction of the guinea pig ileum at a concentration of 11 &microM.

3- epi -25-Hydroxyvitamin D 2 (C-3 epimer) is a metabolite of vitamin D 2 . It is an epimer of 25-hydroxyvitamin D 2 which differs only at the C-3 position.

3- epi -25-Hydroxyvitamin D 3 (C 3 -epimer) is a metabolite of vitamin D 3 . It is an epimer of 25-hydroxyvitamin D 3 which differs only at C-3 position wherein -OH group&nbspat C-3 carbon is in the &#945 orientation rather than in the &#946

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the

7-epi-Isogarcinol is a polycyclic polyprenylated acylphloroglucinol (PPAP), with moderate antiproliferative activity. 7-epi-Isogarcinol blocks STAT3 signaling pathway, to induce apoptosis and inhibit cell migrationIC50&amp: Target:STAT3.

7-epi-Isogarcinol is a polycyclic polyprenylated acylphloroglucinol (PPAP), with moderate antiproliferative activity. 7-epi-Isogarcinol blocks STAT3 signaling pathway, to induce apoptosis and inhibit cell migrationIC50&amp: Target:STAT3.

Biochem/physiol Actions ALW-II-41-27 is an RG-25 (RG25) structural analog that exhibits enhanced type II kinase inhibitor activity against ephrin type-A receptor 2/EphA2/ECK (IC50 = 11 nM vs 770 nM with NG25) by targeting the ATP-binding pocket

ALW-II-49-7 is a selective EphB2 kinase inhibitor with an EC 50 value of 40 nM in cellIn VitroALW-II-49-7 (compound 9) exhibits selectivity profile of binding to a set of kinases including b-raf, CSF1R, DDR1, DDR2, EphA2, EphA5, EphA8, EphB1, EphB2,

General description This gene encodes a member of the ephrin family. The protein is composed of a signal sequence, a receptor-binding region, a spacer region, and a hydrophobic region.