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Acalabrutinib M5 Metabolite

SZ CAT No SZ-A078004
Mol.F. C36H40N10O8S
Mol.Wt. 772.8
Inv. Status Custom Synthesis

Chemical Name: N5-((R)-3-(((Z)-4-((S)-2-(8-amino-1-(4-(pyridin-2-ylcarbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)pyrrolidin-1-yl)-4-oxobut-2-en-2-yl)thio)-1-((carboxymethyl)amino)-1-oxopropan-2-yl)-L-glutamine

Smiles: O=C(O)[C@@H](N)CCC(N[C@H](C(NCC(O)=O)=O)CS/C(C)=C\C(N1[C@H](C2=NC(C3=CC=C(C(NC4=NC=CC=C4)=O)C=C3)=C5C(N)=NC=CN52)CCC1)=O)=O

Inchi: InChI=1S/C21H19N5O3/c1-2-4-16(27)25-11-3-5-15(25)20-24-17(18-19(22)23-10-12-26(18)20)13-6-8-14(9-7-13)21(28)29/h6-10,12,15H,3,5,11H2,1H3,(H2,22,23)(H,28,29)/t15-/m0/s1

Development and validation of novel HPLC bioanalytical analysis method for acalabrutinib: an anticancer drug in human plasma
By Krishna, G. Atchutarama; Srinivasarao, P.; Patrudu, T. Benarji; Chidanandaswamy, R.
From Asian Journal of Chemistry (2020), 32(10), 2606-2610

Development and validation of UV-​spectrophotometric method for simultaneous determination of acamprosate calcium, disulfiram and ondansetron hydrochloride in bulk and tablet dosage forms
By Patil, Purushottam R.; Wagh, Milind P.; Chaudhari, Sanjay R.
From American Journal of PharmTech Research (2016), 6(2), 655-664