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Nadolol EP Impurity D

Nadolol EP Impurity D

Product Description
CAT No.
ALN-N002005
CAS No.
67247-26-1
Mol. F.
C30H43NO8
Mol. Wt.
545.7
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RFQ
Chemical Name : 5,5′-[[(1,1-Dimethylethyl)imino]bis[(2-hydroxypropane-1,3-diyl)oxy]]bis(cis-1,2,3,4-tetrahydronaphthalene-2,3-diol) (as per EP)
Smiles : OC(CN(C(C)(C)C)CC(O)COC1=C(C[C@H](O)[C@H](O)C2)C2=CC=C1)COC3=CC=CC4=C3C[C@@H](O)[C@@H](O)C4
Inchi : InChI=1S/C23H28O7/c24-15(11-29-22-5-1-3-13-7-18(25)20(27)9-16(13)22)12-30-23-6-2-4-14-8-19(26)21(28)10-17(14)23/h1-6,15,18-21,24-28H,7-12H2/t15?,18-,19+,20+,21-

Nadolol: high-pressure liquid chromatographic methods for assay, racemate composition and related compounds

pauline m. lacroix,t norman m. curran and edward g. loveringnJournal of Pharmaceutical & Biomedical Analysis Vol. 10, Nos 10-12, pp. 917-924, 1992

The nonmetabolized u03b2u2011blocker nadolol is a substrate of oct1, oct2, mate1, mate2-k, and pu2011glycoprotein, but not of oatp1b1 and oatp1b3

Shingen Misaka, Jana Knop, Katrin Singer, Eva Hoier, Markus Keiser, Fabian Mu?ller, Hartmut Glaeser, Jo? rg Ko? nig, and Martin F. Fromm – Mol. Pharmaceutics 2016, 13, 2, 512–519

Separation of nadolol racemates by high pH reversed-phase preparative chromatography

Rami S. Arafaha,b , António E. Ribeiroa,b , Alírio E. Rodriguesc , Luís S. Pais – Separation and Purification Technology Volume 233, 15 February 2020, 116018

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