Name: Name:2-Bromo-N-(3-butanamidophenyl)benzamide
Brand: AABLOCKS
SKU: AA00C9OE
Rating: 90 (10 reviews)

Catalog No.: AA00C9OE

423735-93-7 | 2-Bromo-N-(3-butanamidophenyl)benzamide

Pack Size： 1mg

Purity： 98%

in stock

$6.00 $4.00

Pack Size： 250mg

Purity： 98%

in stock

$73.00 $51.00

Quantity

- +

Add to Card

Order Now

bulk Quotation Request

Technical Information

Catalog Number: AA00C9OE

Chemical Name: 2-Bromo-N-(3-butanamidophenyl)benzamide

CAS Number: 423735-93-7

Molecular Formula: C17H17BrN2O2

Molecular Weight: 361.2331

MDL Number: MFCD03063772

SMILES: CCCC(=O)Nc1cccc(c1)NC(=O)c1ccccc1Br

Properties

Complexity: 389

Covalently-Bonded Unit Count: 1

Heavy Atom Count: 22

Hydrogen Bond Acceptor Count: 2

Hydrogen Bond Donor Count: 2

Rotatable Bond Count: 5

XLogP3: 3.5

Upstream Synthesis Route

93469-29-5

88-65-3

423735-93-7

[1]ACSMedicinalChemistryLetters,2012,vol.3,#3,p.232-237

[2]Patent:US9422262,2016,B2,.Locationinpatent:Page/Pagecolumn33;34;35

99-09-2

423735-93-7

[1]ACSMedicinalChemistryLetters,2012,vol.3,#3,p.232-237

[2]Patent:US9422262,2016,B2,

107829-09-4

423735-93-7

[1]ACSMedicinalChemistryLetters,2012,vol.3,#3,p.232-237

Literature fold

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology20060501

Title: Gandhi DM, et al. Characterization of Protease-Activated Receptor (PAR) ligands: Parmodulins are reversible allosteric inhibitors of PAR1-driven calcium mobilization in endothelial cells. Bioorg Med Chem. 2018 May 15;26(9):2514-2529.

Title: Susanna F Gunnink, et al. Allosteric inhibition of protease activated receptor 1: a new antiplatelet therapy.

Title: Aisiku O, et al. Parmodulins inhibit thrombus formation without inducing endothelial injury caused by vorapaxar. Blood. 2015 Mar 19;125(12):1976-85.