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N-Acetyl-S-(2-hydroxyethyl)-L-cysteine-d4 dicyclohexylamine salt Size:Contact [email protected] for quotation InChi: InChI=1S/C25H21N5O3/c31-25(19-8-14-32-17-19)29-11-9-28(10-12-29)24-16-21(22-7-4-13-33-22)26-23-15-20(27-30(23)24)18-5-2-1-3-6-18/h1-8

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Description

InChi: InChI=1S/C25H21N5O3/c31-25(19-8-14-32-17-19)29-11-9-28(10-12-29)24-16-21(22-7-4-13-33-22)26-23-15-20(27-30(23)24)18-5-2-1-3-6-18/h1-8

in the molar ratio of about 1:2

20)/t14-/m1/s1

Carbachol increases basolateral K+ efflux by activating two different K+ transport pathways on the basolateral membrane in T84 cell monolayers

N-Acetyl-S-(2-hydroxyethyl)-L-cysteine-d4 dicyclohexylamine salt Size:Contact [email protected] for quotation InChi: InChI=1S/C25H21N5O3/c31-25(19-8-14-32-17-19)29-11-9-28(10-12-29)24-16-21(22-7-4-13-33-22)26-23-15-20(27-30(23)24)18-5-2-1-3-6-18/h1-8Product information CAS Number: 1331894 57 5 Molecular Weight: 392. 59 Formula: C19H36N2O4S Chemical Name: (2R) 2 acetamido 3 {[2 hydroxy(1,1,2,2 H)ethyl]sulfanyl}propanoic acid; N cyclohexylcyclohexanamine Smiles: [2H]C([2H])(O)C([2H])([2H])SC[C@H](NC(C)=O)C(O)=O. C1CCCCC1NC1CCCCC1 InChiKey: XLGHARKAPCCVFZ XAEDZKCESA N InChi: InChI=1S C12H23N. C7H13NO4S c1 3 7 11(8 4 1)13 12 9 5 2 6 10 12; 1 5(10)8 6(7(11)12)4 13 3 2 9 h11 13H,1 10H2; 6,9H,2

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