G Protein-Coupled Receptor Ligands

Quinabactin View larger

Quinabactin

AOB6476

CAS: 946270-26-4

Chemical Name: LC-66C6; ABA mimics 1; AM1; N-(2-oxo-1-propyl-1,2,3,4-tetrahydroquinolin-6-yl)-1-p-tolylmethanesulfonamide

More details

Molarity Calculation Cart®

HOW TO ORDER

$59.00

$59.00 per mg

Quantity Discount Table - Order More To Get More Price Discount

Quantity (mg or Unit)Unit Price ($/mg or $/Unit)Final Price
100 $26.55 Total: $2,655.00
50 $30.68 Total: $1,534.00
25 $35.99 Total: $899.75
10 $42.48 Total: $424.80
5 $50.15 Total: $250.75

Data sheet

Molecular FormulaC20H24N2O3S
Molecular Weight372.48
CAS Numbers946270-26-4
Storage Condition0°C (short term), -20°C (long term), desiccated
SolubilityDMSO
Purity98% by HPLC
SynonymQuinabactin; LC-66C6; LC 66C6; LC66C6; ABA mimics 1; AM1; AM-1; AM 1;
IUPAC/Chemical NameN-(2-oxo-1-propyl-1,2,3,4-tetrahydroquinolin-6-yl)-1-p-tolylmethanesulfonamide
InChl Key IVHKSUMLZQXFPR-UHFFFAOYSA-N
InChl CodeInChI=1S/C20H24N2O3S/c1-3-12-22-19-10-9-18(13-17(19)8-11-20(22)23)21-26(24,25)14-16-6-4-15(2)5-7-16/h4-7,9-10,13,21H,3,8,11-12,14H2,1-2H3
SMILES CodeO=S(CC1=CC=C(C)C=C1)(NC2=CC3=C(N(CCC)C(CC3)=O)C=C2)=O
References1) Vaidya AS, et al., A Rationally Designed Agonist Defines Subfamily IIIA Abscisic Acid Receptors As Critical Targets for Manipulating Transpiration. ACS Chem Biol. 2017 Nov 17;12(11):2842-2848.2) Helander JD, et al.,. Chemical manipulation of plant water use. Bioorg Med Chem. 2016 Feb 1;24(3):493-500.

More info

Aba-mimicking agonist, preferentially activating dimeric ABA receptors and possesses ABA-like potency in vivo