Phenethylamine

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Phenethylamine
Chemical name	2-Phenyl-ethylamine or 2-phenylethanamine
Chemical formula	C8H11N
Molecular mass	121.18 g/mol
Density	0.965 g/ml
Melting point	-60 °C
Boiling point	200 °C
CAS number	64-04-0
SMILES	c1ccccc1CCN
Image:Phenethylamine structure.png

Phenethylamine (β-Phenylethylamine) is an alkaloid and monoamine. In the human brain, it is believed to function as a neuromodulator or neurotransmitter (trace amine). A colorless liquid that forms a solid carbonate salt with carbon dioxide (CO₂) upon exposure to air, phenethylamine in nature is synthesized from the amino acid phenylalanine by enzymatic decarboxylation. It is also found in many foods, especially after microbial fermentation, e.g., in chocolate. It has been suggested that phenethylamine from food (e.g., chocolate) may have psychoactive effects in sufficient quantities. However, it is quickly metabolized by the enzyme MAO-B, preventing significant concentrations from reaching the brain.

Substituted phenethylamines are a broad and diverse class of compounds that include neurotransmitters, hormones, stimulants, hallucinogens, entactogens, anorectics, bronchodilators, and antidepressants.

The phenethylamine structure can also be found as part of more complex ring systems such as the ergoline system of LSD or the morphinan system of morphine.

It is commonly known as the Love Molecule.

Contents 1 Substituted phenethylamines 2 Pharmacology 3 Substitution table 4 See also 5 External links 6 Categorization

Substituted phenethylamines

Image:Phenethylamine rests.png

Substituted phenethylamines carry additional chemical modifications at the phenyl ring, the sidechain, or the amino group:

• Amphetamines are homologues of phenethylamines carrying an alpha-methyl (α-CH₃) group at the sidechain carbon atom next to the amino group.
• Catecholamines are phenethylamines carrying two hydroxy groups in positions 3 and 4 of the phenyl ring. Examples are the hormones and neurotransmitters dopamine, epinephrine (adrenaline), and norepinephrine (noradrenaline).
• The aromatic amino acids phenylalanine and tyrosine are phenethylamines carrying a carboxyl group (COOH) in alpha position.

Pharmacology

Many substituted phenethylamines are pharmacologically active drugs due to their similarity to the monoamine neurotransmitters:

• Stimulants like the plant alkaloids ephedrine and cathinone and the synthetic drugs amphetamine (speed, benzedrine) and methylphenidate
• Hallucinogens like the plant alkaloid mescaline and the synthetic drug 2C-B
• Empathogen/Entactogens like MDMA (ecstasy) and MDA
• Anorectics like phentermine, fenfluramine, and amphetamine
• Bronchodilators like salbutamol and ephedrine
• Antidepressants like bupropion and the monoamine oxidase inhibitors phenelzine and tranylcypromine.

Substitution table

Some of the more important phenethylamines are tabulated below. For simplicity, the stereochemistry of the sidechain is not covered in the table. Hundreds of other simple synthetic phenethylamines are known. This is due in part to the pioneering work of Alexander Shulgin, much of which is described in the book PiHKAL.

Substituted phenethylamines, tabulated by structure

Short Name	Rα	Rβ	R2	R3	R4	R5	RN	Full Name
Tyramine					OH			4-hydroxy-phenethylamine
Dopamine				OH	OH			3,4-dihydroxy-phenethylamine
Epinephrine (Adrenaline)		OH		OH	OH		CH3	β,3,4-trihydroxy-N-methyl-phenethylamine
Norepinephrine (Noradrenaline)		OH		OH	OH			β,3,4-trihydroxyphenethylamine
Salbutamol		OH			OH	CH2CH2OH	C(CH3)3	4-(2-(tert-Butylamino)-1-hydroxyethyl)-2-(hydroxymethyl)phenol
Amphetamine	CH3							α-methyl-phenethylamine
Methamphetamine	CH3						CH3	N-methyl-amphetamine
Levmetamfetamine	CH3						CH3	N-methyl-amphetamine
Ephedrine, pseudoephedrine	CH3	OH					CH3	N-methyl-β-hydroxy-amphetamine
Cathine	CH3	OH						β-hydroxy-amphetamine
Cathinone	CH3	=O						β-keto-amphetamine
Methcathinone	CH3	=O					CH3	N-methyl-β-keto-amphetamine
Bupropion	CH3	=O		Cl			C(CH3)3	3-chloro-N-tert-butyl-β-keto-amphetamine
Fenfluramine	CH3			CF3			CH2CH3	3-trifluoromethyl-N-ethyl-amphetamine
Phentermine	CH3,CH3							α,α-dimethyl-phenethylamine
Mescaline				OCH3	OCH3	OCH3		3,4,5-trimethoxy-phenethylamine
MDA	CH3			-O-CH2-O-				3,4-methylenedioxy-amphetamine
MDMA	CH3			-O-CH2-O-			CH3	3,4-methylenedioxy-N-methyl-amphetamine
DOM	CH3		OCH3		CH3	OCH3		2,5-dimethoxy-4-methyl-amphetamine
DOB	CH3		OCH3		Br	OCH3		2,5-dimethoxy-4-bromo-amphetamine
2C-B			OCH3		Br	OCH3		2,5-dimethoxy-4-bromo-phenethylamine
2C-C			OCH3		Cl	OCH3		2,5-dimethoxy-4-chloro-phenethylamine
DOI	CH3		OCH3		I	OCH3		2,5-dimethoxy-4-iodo-amphetamine
2C-I			OCH3		I	OCH3		2,5-dimethoxy-4-iodo-phenethylamine
2C-D			OCH3		CH3	OCH3		2,5-dimethoxy-4-methyl-phenethylamine
2C-E			OCH3		CH2CH3	OCH3		2,5-dimethoxy-4-ethyl-phenethylamine
2C-N			OCH3		NO2	OCH3		2,5-dimethoxy-4-Nitro-phenethylamine
2C-T-2			OCH3		SCH2CH3	OCH3		2,5-dimethoxy-4-ethylthio-phenethylamine
2C-T-4			OCH3		SCHCH3CH3	OCH3		2,5-dimethoxy-4-(i)-propylthio-phenethylamine
2C-T-7			OCH3		SCH2CH2CH3	OCH3		2,5-dimethoxy-4-propylthio-phenethylamine
2C-T-8			OCH3		SCH2CHCH2CH2	OCH3		2,5-dimethoxy-4-cyclopropylmethylthio-phenethylamine
2C-T-9			OCH3		S-(CH3)3C	OCH3		2,5-dimethoxy-4-(t)-Butylthio-phenethylamine
2C-T-21			OCH3		SCH2CH2F	OCH3		2,5-dimethoxy-4-(2-fluoroethylthio)-phenethylamine

Image:Overview Phenethylamines.png

See also

• Catecholamines
• PiHKAL
• Alexander Shulgin
• Venom (comics) The alien symbiote relies on this chemical.
• chocolate This substance is found in chocolate.

External links

• Book II of PiHKAL online
• Review and summary of PiHKAL, including table of 300+ phenethylamines: ascii postscript
• A Structural Tour of PiHKAL

Categorization

Template:Phenethylamines Template:Hallucinogenic phenethylaminescs:Fenylethylamin de:Phenethylamin es:Fenetilamina fr:Phényléthylamine pl:Fenyloetyloamina fi:Fenetyyliamiini sv:Fenetylamin