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Nadolol USP Related Compound C

Nadolol USP Related Compound C

Product Description
CAT No.
ALN-N002017
CAS No.
NA
Mol. F.
C23H28O7
Mol. Wt.
416.5
Stock
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RFQ
Chemical Name : (2SR,3RS)-5-(3-{[(6RS,7SR)-6,7-Dihydroxy-5,6,7,8-tetrahydronaphthalen-1-yl]oxy}-2-hydroxypropoxy)- 1,2,3,4-tetrahydronaphthalene-2,3-diol) and (1,3-Bis[(6R,7S)-6,7-dihydroxy-5,6,7,8-tetrahydronaphthalene-1-yloxy]propane-2-ol
Smiles : O[C@H](C1)[C@@H](O)CC2=C1C(OCC(O)COC3=C(C[C@H](O)[C@H](O)C4)C4=CC=C3)=CC=C2.O[C@@H](C5)[C@H](O)CC6=C5C(OCC(O)COC7=C(C[C@H](O)[C@H](O)C8)C8=CC=C7)=CC=C6
Inchi : InChI=1S/C12H8F2/c13-10-7-4-8-11(14)12(10)9-5-2-1-3-6-9/h1-8H

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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