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Merck
CN

A7980

AC-41848 hydrate

≥98% (HPLC), solid

Synonym(s):

1-[(2,4-Dichlorophenyl)methyl]-6,7,8,9-tetrahydro-3-phenyl-5H-imidazo[1,2-a]azepinium bromide hydrate

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About This Item

Empirical Formula (Hill Notation):
C21H21BrCl2N2 · xH2O
CAS Number:
Molecular Weight:
452.21 (anhydrous basis)
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
Assay:
≥98% (HPLC)
Form:
solid
Storage condition:
desiccated, under inert gas
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Quality Segment

assay

≥98% (HPLC)

form

solid

storage condition

desiccated, under inert gas

solubility

DMSO: ~14 mg/mL, H2O: >5 mg/mL

storage temp.

2-8°C

SMILES string

[Br-].[H]O[H].Clc1ccc(C[n+]2cc(-c3ccccc3)n4CCCCCc24)c(Cl)c1

InChI

1S/C21H21Cl2N2.BrH.H2O/c22-18-11-10-17(19(23)13-18)14-24-15-20(16-7-3-1-4-8-16)25-12-6-2-5-9-21(24)25;;/h1,3-4,7-8,10-11,13,15H,2,5-6,9,12,14H2;1H;1H2/q+1;;/p-1

InChI key

FPOBEBBUBSFIIA-UHFFFAOYSA-M

Application

AC-41848 is a potent, cell permeable, and subtype selective retinoic acid receptor RARγ agonist.

Biochem/physiol Actions

AC-41848 is a potent, cell permeable, subtype selective retinoic acid receptor RARγ agonist. AC-41848 has high selectivity (92%) for RARγ. EC50 = 5.9 μM.
Potent, cell permeable, subtype selective retinoic acid receptor RARγ agonist. High selectivity (92%) for RARγ. EC50 = 5.9 μM.

Features and Benefits

This compound is featured on the Nuclear Receptors (Non-Steroids) page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Global Trade Item Number

SKUGTIN
A7980-20MG04061832258096
A7980-5MG04061832952963