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Home > Kinase Inhibitors > BUB1 (Budding Uninhibited by Benzimidazoles 1)(Mitotic checkpoint serine/threonine-protein kinase) > BAY-1816032 (BAY1816032)

BAY-1816032 (BAY1816032)

BAY-1816032 is an orally available, highly potent and selective BUB1 (Mitotic checkpoint serine/threonine-protein kinase) inhibitor, with an enzymatic IC50 of 7 nM, and highly selective against other 395 kinases. Mechanistically BAY 1816032 abrogated nocodazole-induced Thr-120 phosphorylation of the major BUB1 target protein histone H2A in HeLa cells with an IC50 of 29 nM, induced lagging chromosomes and mitotic delay (ref 1). Demonstrated in vitro and in vivo antitumor efficacy when applied in combination with taxanes (ref 1).

Catalog NO:	CT-BAY181
Synonym:
CAS NO:	1891087-61-8
Mol. Formula:	C27H24F2N6O4
MW:	534.5 (or refer to Certificate of Analysis, batch specific)

** 99.9% Purity. in vivo Quality material. A white crystalline powder (pic attached), hemihydrate* (validated by a spot-on microanalysis), clean and impeccable (see attached QC Docs). Bulk stock! Same day shipping.

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NO	Size	Price	In Stock	Quantity
1	5 mg	$125.00	YES
2	10 mg	$175.00	YES
3	50 mg	$495.00	YES
4	100 mg	$895.00	YES

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Solubility : refer to certificate of analysis

Storage : refer to certificate of analysis

Purity : 99.9% (HPLC at 214 and 254 nm)

Original QC Data : HPLC-MS, NMR and Quantitative Elemental Analysis

Please Pick Batch NO:

BAY-1816032. Lot 01, Certificate of Analysis.pdf
BAY-1816032, Lot 01, Visual Appearance.pdf

1. Gerhard Siemeister, et al, Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. Abstract 287: BAY 1816032, a novel BUB1 kinase inhibitor with potent antitumor activity

* confirmed by a spot-on high precision quantitative elemental analysis.

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