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SML2072

OX03050

≥98% (HPLC)

Synonym(s):

(E)-3-(4-Styrylphenoxy)propan-1-ol, 3-[4-[(1E)-2-Phenylethenyl]phenoxy]-1-propanol

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25 mg

Available to ship TODAYfromMILWAUKEE

$356.00
$302.60

About This Item

Empirical Formula (Hill Notation):
C17H18O2
CAS Number:
1357581-47-5
Molecular Weight:
254.32
NACRES:
NA.77
UNSPSC Code:
12352200
Assay:
≥98% (HPLC)
Form:
powder

$302.60

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assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 2 mg/mL, clear (warmed)

storage temp.

2-8°C

Biochem/physiol Actions

OX03050 is a metabolically stable, potent and selective squalene synthase inhibitor that upregulates the Low-Density Lipoprotein Receptor (LDLR) in mouse and in human liver cell lines. OX03050 used in conjunction with statin acts synergistically to increase LDLR expression
metabolically stable, potent and selective squalene synthase inhibitor that upregulates the LDLR in mouse and in human liver cell lines.

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OX03050 ≥98% (HPLC)

Sigma-Aldrich

SML2072

OX03050

UNC0642 ≥98% (HPLC)

Sigma-Aldrich

SML1037

UNC0642

RWJ 67657 ≥98% (HPLC)

Sigma-Aldrich

SML2212

RWJ 67657

NSC49652 ≥98% (HPLC)

Sigma-Aldrich

SML2544

NSC49652

description

≥98% (HPLC)

description

≥98% (HPLC)

description

≥98% (HPLC)

description

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

form

powder

form

powder

form

powder

form

powder

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

solubility

DMSO: 2 mg/mL, clear (warmed)

solubility

DMSO: 5 mg/mL, clear (warmed)

solubility

DMSO: 2 mg/mL, clear

solubility

DMSO: 2 mg/mL, clear

color

white to beige

color

white to beige

color

white to beige

color

white to beige

(E)-3-(4-Styrylphenoxy)propan-1-ol

-

RWJ 67657 4-(4-Fluorophenyl)-1-(3-Phenylpropyl)-imidazole, RWJ 67657 CAS 215303-72-3, RWJ 67657 TNF-α IL-1β release inhibitor, RWJ 67657 anti-inflammatory agent for research, RWJ 67657 cardioprotective compound, RWJ 67657 for laboratory use, RWJ 67657 inhibitor p38 MAP kinase, RWJ 67657 p38 MAP kinase selective inhibitor, RWJ 67657 p38α p38β inhibitor, Sigma-Aldrich RWJ 67657 MAP kinase inhibitor, high purity RWJ 67657 for scientific research, p38 MAPK inhibitor RWJ 67657 in vivo studies, p38 MAPK inhibitor for inflammatory disease studies, research grade RWJ 67657 inhibitor

-

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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