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SML2416

Sigma-Aldrich

HET0016

≥95% (HPLC)

Synonym(s):

HET 0016, HET-0016, N′-(4-Butyl-2-methylphenyl)-N-hydroxymethanimidamide, N-(4-Butyl-2-methylphenyl)-N′-hydroxyformamidine, N-(4-Butyl-2-methylphenyl)-N′-hydroxymethanimidamide, N-Hydroxy-N′-(4-n-butyl-2-methylphenyl)formamidine

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About This Item

Empirical Formula (Hill Notation):
C12H18N2O
CAS Number:
Molecular Weight:
206.28
UNSPSC Code:
12352200
NACRES:
NA.77

Assay

≥95% (HPLC)

form

powder

storage condition

desiccated

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

−20°C

SMILES string

CCCCC1=CC=C(C(C)=C1)/N=C/NO

InChI

1S/C12H18N2O/c1-3-4-5-11-6-7-12(10(2)8-11)13-9-14-15/h6-9,15H,3-5H2,1-2H3,(H,13,14)

InChI key

LYNOGBKNFIHKLE-UHFFFAOYSA-N

Biochem/physiol Actions

HET0016 is a potent and selective inhibitor against cytochrome P450 (CYP450) ω-hydroxylases (human CYP4A11/4A22/4F2/4F3, rat CYP4A1/4A2/4A3/4A8)-mediated 20-hydroxyeicosatetraenoic acid (20-HETE) biosynthesis (IC50 = 8.9/35 nM using human/rat renal microsomes), exhibiting much reduced potency against epoxyeicosatrienoic acids (EETs) biosynthesis (IC50 = 2.8 μM/rat microsome) or the enzyme activities of CYP2C9/2D6/3A4 and COX (IC50 = 3.3/83.9/71 μM and 2.3 μM). HET0016 is widely employed both in cultures (1-10 μM) and in aminals in vivo (1-10 mg/kg via i.v., i.m., i.p. or s.c.) for probing 20-HETE-dependent physiological and pathological processes.
Potent and selective inhibitor against cytochrome P450 (CYP450) ω-hydroxylases-mediated 20-hydroxyeicosatetraenoic acid (20-HETE) biosynthesis.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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