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B2186

BL-1249

≥98% (HPLC)

Synonym(e):

(5,6,7,8-Tetrahydro-naphthalen-1-yl)-[2-(1H-tetrazol-5-yl)-phenyl]-amine

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Ihnen/SKUVerfügbarkeitPreis
10 mg
Warenkorb auf Verfügbarkeit prüfen
€ 257,00
50 mg
Warenkorb auf Verfügbarkeit prüfen
€ 1.020,00
€ 867,00

Über diesen Artikel

Empirische Formel (Hill-System):
C17H17N5
CAS-Nummer:
Molekulargewicht:
291.35
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
Assay:
≥98% (HPLC)
Form:
solid
Storage condition:
protect from light

€ 257,00


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Quality Segment

assay

≥98% (HPLC)

form

solid

storage condition

protect from light

color

pink to brown

solubility

DMSO: ~17.5 mg/mL, H2O: insoluble

storage temp.

−20°C

SMILES string

C1CCc2c(C1)cccc2Nc3ccccc3-c4nnn[nH]4

InChI

1S/C17H17N5/c1-2-8-13-12(6-1)7-5-11-15(13)18-16-10-4-3-9-14(16)17-19-21-22-20-17/h3-5,7,9-11,18H,1-2,6,8H2,(H,19,20,21,22)

InChI key

YYNRZIFBTOUICE-UHFFFAOYSA-N

General description

BL-1249 is a non-steroid anti-inflammatory drug and an inhibitor of the cyclooxygenase (COX) enzyme.

Application

BL-1249 has been used:
  • as an activator of mechano-gated K2P channel in contracted mouse ileum and colon tissues
  • as a TWIK related potassium channel (TREK2) modulator and in U-2 OS osteosarcoma cell line
  • as a TREK1 and TREK2 activator in mice.

Biochem/physiol Actions

BL-1249 also activates TWIK related potassium channel 2 (TREK2). It interacts with K2P channel at the negatively charged activator site and modulates channel opening.
BL-1249 is a potassium TREK-1 channel activator.
BL-1249 is a putative activator of potassium TREK-1 channel.

Features and Benefits

This compound is featured on the Potassium Channels page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

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Dieser Artikel
236005444800S8951
description

≥98% (HPLC)

description

The COX-1 Inhibitor, FR122047, also referenced under CAS 130717-51-0, controls the biological activity of COX-1. This small molecule/inhibitor is primarily used for Cell Signaling applications.

description

A cell-permeable, non-steroidal anti-inflammatory drug (NSAID) of the oxicam family which preferentially inhibits the inducible isoform of COX-2 (IC50 = 4.7 µM) relative to COX-1 (IC50 = 36.6 µM).

description

≥98% (HPLC)

form

solid

form

solid

form

solid

form

powder

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

solubility

H2O: insoluble, DMSO: ~17.5 mg/mL

solubility

DMSO: 5 mg/mL, 1 M HCl: 2 mg/mL, water: 4 mg/mL

solubility

DMSO: 10 mg/mL

solubility

DMSO: >28 mg/mL (warmed)

storage condition

protect from light

storage condition

protect from light, OK to freeze, desiccated (hygroscopic)

storage condition

OK to freeze, protect from light

storage condition

-


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Lagerklasse

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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