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C4397

Chlorzoxazone

Sinonimo/i:

5-Chloro-2(3H)-benzoxazolone, 5-Chloro-2-hydroxybenzoxazole

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Taglio della confezioneSKUDisponibilitàPrezzo
25 g
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CHF 89.50
100 g
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CHF 282.00
CHF 239.70

Informazioni su questo articolo

Formula empirica (notazione di Hill):
C7H4ClNO2
Numero CAS:
Peso molecolare:
169.57
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
202-403-9
MDL number:
Assay:
≥98% (TLC)
Form:
powder

CHF 89.50


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assay

≥98% (TLC)

Quality Segment

form

powder

color

white to off-white

mp

191-192 °C (lit.)

solubility

DMSO: 50 mg/mL, clear

originator

Johnson & Johnson

storage temp.

room temp

SMILES string

Clc1ccc2OC(=O)Nc2c1

InChI

1S/C7H4ClNO2/c8-4-1-2-6-5(3-4)9-7(10)11-6/h1-3H,(H,9,10)

InChI key

TZFWDZFKRBELIQ-UHFFFAOYSA-N

Gene Information

human ... KCNN4(3783)

Application

Chlorzoxazone may be used:
  • as a calcium-activated potassium (KCa) channel activator in patch-clamp electrophysiology to test its effect on dendritic hyperexcitability[1]
  • as a substrate for cytochrome P450 2E1 (CYP2E1) enzyme in cultured human hepatocytes[2]
  • as a benzimidazolone compound to test its effect on epithelial sodium (Na+) transport[3]

Biochem/physiol Actions

Chlorzoxazone inhibits the multisynaptic reflex arcs primarily in the spinal cord and brain subcortical areas.[4] It is an activator of calcium activated potassium channels and may contribute to the aortic artery relaxation in mice.[5] Chlorzoxazone also activates the calcium-activated potassium (KCa) channel and small conductance calcium-activated potassium channels (SK).[1] It is metabolized by cytochrome P450 2E1 (CYP2E1) and serves as a probe for monitoring this enzyme function.[6]
Chlorzoxazone is a skeletal muscle relaxant.

Features and Benefits

This compound is a featured product for ADME Tox research. Click here to discover more featured ADME Tox products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
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.
This compound was developed by Johnson & Johnson. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

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Questo articolo
UC148SML1616SML0866
Chlorzoxazone

Sigma-Aldrich

C4397

Chlorzoxazone

ICA-069673 ≥98% (HPLC)

Sigma-Aldrich

SML1616

ICA-069673

BMS-191011 ≥98% (HPLC)

Sigma-Aldrich

SML0866

BMS-191011

assay

≥98% (TLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

form

powder

form

solid

form

powder

form

powder

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100

storage temp.

room temp

storage temp.

2-8°C

storage temp.

room temp

storage temp.

room temp

solubility

DMSO: 50 mg/mL, clear

solubility

methanol: soluble

solubility

DMSO: 20 mg/mL, clear

solubility

DMSO: 20 mg/mL, clear (warmed)

originator

Johnson & Johnson

originator

-

originator

-

originator

-


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pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Classe di stoccaggio

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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Numero articolo commerciale globale

SKUGTIN
C4397-100G04061832574141
C4397-25G04061833492093

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