B5313
BIX-01338 hydrate
≥98% (HPLC)
Synonym(s):
1-{2-[4-(4-Methoxybenzoyloxy)phenyl]ethyl}-2-(4-trifluoromethylbenzoylamino)-1H-benzoimidazole-5-carboxylic acid hydrate
About This Item
Recommended Products
assay
≥98% (HPLC)
form
powder
color
off-white to light tan
solubility
DMSO: >10 mg/mL
storage temp.
2-8°C
SMILES string
O.COc1ccc(cc1)C(=O)Oc2ccc(CCn3c(NC(=O)c4ccc(cc4)C(F)(F)F)nc5cc(ccc35)C(O)=O)cc2
InChI
1S/C32H24F3N3O6.H2O/c1-43-24-13-6-21(7-14-24)30(42)44-25-11-2-19(3-12-25)16-17-38-27-15-8-22(29(40)41)18-26(27)36-31(38)37-28(39)20-4-9-23(10-5-20)32(33,34)35;/h2-15,18H,16-17H2,1H3,(H,40,41)(H,36,37,39);1H2
InChI key
LLTPCGBKXOESTJ-UHFFFAOYSA-N
Biochem/physiol Actions
Features and Benefits
Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Articles
Epigenetic modifications are thought to occur through two key interconnected processes—DNA methylation and the covalent modification of histones.
Related Content
We offer a variety of small molecule research tools, such as transcription factor modulators, inhibitors of chromatin modifying enzymes, and agonists/antagonists for target identification and validation in gene regulation research; a selection of these research tools is shown below.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service