1.0 2011-09-21 01:45:01 UTC 2015-07-21 06:59:32 UTC FDB028792 (R)-Amphetamine ==(R)==-Amphetamine is an enantiomer of amphetamine that is urinary metabolite from selegeline (drug used for the treatment of early-stage Parkinson's disease, depression and senile dementia). ==(R)==-Amphetamine as stereoisomer is not considered psychoactive and has little abuse potential. The stimulatory effect on locomotor activity and dopamine synthesis may be contributed to by the action of R-methamphetamine. If anyone is prescribed and takes selegiline, they can and will test positive for amphetamine/methamphetamine on most drug tests. [HMDB] (-)-Amphetamine (-)-Phenylisopropylamine (R)-a-Methyl-benzeneethanamine (R)-a-Methylbenzeneethanamine (R)-a-Methylphenethylamine (R)-alpha-Methyl-benzeneethanamine (R)-alpha-Methylbenzeneethanamine (R)-alpha-Methylphenethylamine (R)-Amphetamine (R)-Phenaminum (R)-Phenylisopropylamine (R)-α-methylbenzeneethanamine (R)-α-methylphenethylamine L-(R)-Amphetamine L-a-Methylphenethylamine L-alpha-Methylphenethylamine L-Amphetamine Levamfetamine Levamphetamine C9H13N 135.2062 135.104799421 (2R)-1-phenylpropan-2-amine (-)-amphetamine 156-34-3 C[C@@H](N)CC1=CC=CC=C1 InChI=1S/C9H13N/c1-8(10)7-9-5-3-2-4-6-9/h2-6,8H,7,10H2,1H3/t8-/m1/s1 KWTSXDURSIMDCE-MRVPVSSYSA-N belongs to the class of organic compounds known as amphetamines and derivatives. These are organic compounds containing or derived from 1-phenylpropan-2-amine. Amphetamines and derivatives Organic compounds Benzenoids Benzene and substituted derivatives Phenethylamines Aromatic homomonocyclic compounds Aralkylamines Hydrocarbon derivatives Monoalkylamines Organopnictogen compounds Phenylpropanes Amine Amphetamine or derivatives Aralkylamine Aromatic homomonocyclic compound Hydrocarbon derivative Organic nitrogen compound Organonitrogen compound Organopnictogen compound Phenylpropane Primary aliphatic amine Primary amine amphetamine Solid logp 1.85 ALOGPS logs -1.89 ALOGPS solubility 1.74e+00 g/l ALOGPS logp 1.8 ChemAxon pka_strongest_basic 10.01 ChemAxon iupac (2R)-1-phenylpropan-2-amine ChemAxon average_mass 135.2062 ChemAxon mono_mass 135.104799421 ChemAxon smiles C[C@@H](N)CC1=CC=CC=C1 ChemAxon formula C9H13N ChemAxon inchi InChI=1S/C9H13N/c1-8(10)7-9-5-3-2-4-6-9/h2-6,8H,7,10H2,1H3/t8-/m1/s1 ChemAxon inchikey KWTSXDURSIMDCE-MRVPVSSYSA-N ChemAxon polar_surface_area 26.02 ChemAxon refractivity 43.71 ChemAxon polarizability 16.18 ChemAxon rotatable_bond_count 2 ChemAxon acceptor_count 1 ChemAxon donor_count 1 ChemAxon physiological_charge 1 ChemAxon formal_charge 0 ChemAxon Specdb::MsIr 14 Specdb::MsIr 2631 Specdb::MsIr 2632 Specdb::MsIr 2633 Specdb::CMs 17913 Specdb::CMs 146884 Specdb::NmrOneD 95398 Specdb::NmrOneD 95399 Specdb::NmrOneD 95400 Specdb::NmrOneD 95401 Specdb::NmrOneD 95402 Specdb::NmrOneD 95403 Specdb::NmrOneD 95404 Specdb::NmrOneD 95405 Specdb::NmrOneD 95406 Specdb::NmrOneD 95407 Specdb::NmrOneD 95408 Specdb::NmrOneD 95409 Specdb::NmrOneD 95410 Specdb::NmrOneD 95411 Specdb::NmrOneD 95412 Specdb::NmrOneD 95413 Specdb::NmrOneD 95414 Specdb::NmrOneD 95415 Specdb::NmrOneD 95416 Specdb::NmrOneD 95417 Specdb::MsMs 305689 Specdb::MsMs 305690 Specdb::MsMs 305691 Specdb::MsMs 349147 Specdb::MsMs 349148 Specdb::MsMs 349149 Specdb::MsMs 2705705 Specdb::MsMs 2705706 Specdb::MsMs 2705707 Specdb::MsMs 3003747 Specdb::MsMs 3003748 Specdb::MsMs 3003749 HMDB12128 42724 FRD #<Reference:0x000055ce328dfa80> #<Reference:0x000055ce328df7b0> #<Reference:0x000055ce328df558> #<Reference:0x000055ce328df350> #<Reference:0x000055ce328df0f8>