EGIS-7625 - WHC

EGIS-7625

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EGIS-7625

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SMILES:CC1=CC([N+](=O)[O-])=C(N2CCN(CC3=CC=CC=C3)CC2)C=C1N

InChI:InChI=1S/C18H22N4O2/c1-14-11-18(22(23)24)17(12-16(14)19)21-9-7-20(8-10-21)13-15-5-3-2-4-6-15/h2-6,11-12H,7-10,13,19H2,1H3

InChI key:ZEFXWOMFCPRXJW-UHFFFAOYSA-N

Categories (non-exhaustive):

Substituted piperazine Substituted phenylmorpholine Substituted cathinone Methylphenidate analogue Aminorex analogue Imidazopyridine DOx Benzimidazole opioid Arylcyclohexylamine Xanthine Tryptamine Tropane Tricyclic Thiobarbiturate Cyclopyrrolone Pyrazolopyrimidine Substituted phenethylamine Lysergamide Diphenylbutylpiperidine Racetam Benzodiazepine Barbiturate Alkyl nitrite 25nb 2c Substituted amphetamine Naphthoylindole Phenylacetylindole Benzoylindole Cyclohexylphenol Check naphthoylpyrrole Naphthylmethylindene Tetramethylcyclopropanoylindoles Adamantoylindoles Indole3carboxylate ester Indazole3carboxamide Morphinan

Legal statuses

For each country, we look for references and regulations related to this molecule, of to families of compounds that this molecule belongs to.

Disclaimer: The information provided on this website regarding the legal references of molecules is for informational purposes only and does not constitute legal advice. While we strive to keep the information up-to-date and accurate, laws and regulations may change over time. Therefore, we cannot guarantee the completeness, accuracy, or applicability of the information provided. It is important to always refer to the original legal texts and consult with a qualified legal professional before making any decisions based on the information provided on this website.

Always double check the sources provided, there can be classification errors. Our system may also have missed certain references. : This molecule was added in the legislation: This molecule was removed from the legislation

Country:

Type of legislation

Narcotics

The system hasn't detected any mention of this drug in France as a Narcotics but you should always double check by yourself.

Psychotropes

The system hasn't detected any mention of this drug in France as a Psychotropes but you should always double check by yourself.

Advanced insights

In the following we provide more advanced analysis about the interactions of a molecule with the human metabolism, docking sites etc.

Interaction of this molecule with metabolism

We use a Deep Learning model to predict the interactions of this molecule with metabolism. Refer to the source to understand the methodology.

Reactions that metabolize this molecule

Nitroreduction of nitroarene to hydroxylamine BTMR1222

Enzymes: 1.6.2.4

Reagents

Metabolite: InChI=1S/C18H24...

N-Acetylation of arylamine BTMR0187

Enzymes: Unspecified acetyltransferase

Reagents

Metabolite: InChI=1S/C20H24...

Glucuronidation of primary aromatic amine BTMR0171

Enzymes: 2.4.1.17

Reagents

Metabolite: InChI=1S/C24H30...

N-Dealkylation of mixed tertiary amine BTMR1145

Enzymes: CYP1A2 CYP2A6 CYP2B6 CYP2C8 CYP2C9 CYP2C19 CYP2D6 CYP3A4

Reagents

Metabolite: InChI=1S/C18H22...

O-Hydroxylation of monosubstituted benzene BTMR1034

Enzymes: CYP1A2 CYP2C8 CYP2C9 CYP2C19 CYP3A4

Reagents

Metabolite: InChI=1S/C18H22...

Hydroxylation of non-terminal aliphatic carbon adjacent to aromatic ring BTMR1077

Enzymes: CYP1A2 CYP2C8 CYP2C9 CYP2D6 CYP3A4

Reagents

Metabolite: InChI=1S/C18H22...

Aliphatic hydroxylation of methyl carbon adjacent to aromatic ring BTMR1058

Enzymes: CYP1A2 CYP2A6 CYP2B6 CYP2C8 CYP2C9 CYP2C19 CYP2D6 CYP2E1 CYP3A4

Reagents

Metabolite: InChI=1S/C18H22...

N-Oxidation of alicyclic tertiary amine BTMR1099

Enzymes: CYP1A2 CYP2C8 CYP2C19 CYP2D6 CYP3A4

Reagents

Metabolite: InChI=1S/C18H22...

N-Oxidation of alicyclic tertiary amine BTMR1099

Enzymes: CYP1A2 CYP2C8 CYP2C19 CYP2D6 CYP3A4

Reagents

Metabolite: InChI=1S/C18H22...

N-Dealkylation of alicyclic tertiary amine BTMR1144

Enzymes: CYP1A2 CYP2A6 CYP2B6 CYP2C8 CYP2C9 CYP2C19 CYP2D6 CYP3A4

Reagents

Metabolite: InChI=1S/C11H16...

N-Dealkylation of alicyclic tertiary amine BTMR1144

Enzymes: CYP1A2 CYP2A6 CYP2B6 CYP2C8 CYP2C9 CYP2C19 CYP2D6 CYP3A4

Reagents

isomerdesign

BAL

pubchem

Benzaldehyde

Hydroxylation of benzene on carbon ortho to electron donating group BTMR1045

Enzymes: CYP1A2 CYP2C8 CYP2C9 CYP2C19 CYP2D6 CYP3A4

Reagents

Metabolite: InChI=1S/C18H22...

Hydroxylation of benzene on carbon ortho to electron donating group BTMR1045

Enzymes: CYP1A2 CYP2C8 CYP2C9 CYP2C19 CYP2D6 CYP3A4

Reagents

Metabolite: InChI=1S/C18H22...

Hydroxylation of benzene on carbon ortho to electron donating group BTMR1045

Enzymes: CYP1A2 CYP2C8 CYP2C9 CYP2C19 CYP2D6 CYP3A4

Reagents

Metabolite: InChI=1S/C18H22...

Hydroxylation of benzene on carbon para to electron donating group BTMR1047

Enzymes: CYP1A2 CYP2C8 CYP2C9 CYP2D6 CYP3A4

Reagents

Metabolite: InChI=1S/C18H22...

Hydroxylation of heteroalicyclic secondary carbon BTMR1070

Enzymes: CYP1A2 CYP2A6 CYP2C9 CYP2D6 CYP3A4

Reagents

Metabolite: InChI=1S/C18H22...

Hydroxylation of heteroalicyclic secondary carbon BTMR1070

Enzymes: CYP1A2 CYP2A6 CYP2C9 CYP2D6 CYP3A4

Reagents

Metabolite: InChI=1S/C18H22...

N-Hydroxylation of primary arylamine BTMR0042

Enzymes: CYP1A2 CYP2A6 CYP2B6 CYP2C9 CYP2C19 CYP2E1 CYP3A4

Reagents

Metabolite: InChI=1S/C18H22...

Nitroreduction of nitroarene to nitrosoarene BTMR1293

Enzymes: Bacterial oxygen-insensitive NADPH nitroreductase

Reagents

Metabolite: InChI=1S/C18H22...