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RTI-353

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Chemical compound Pharmaceutical compound
RTI-353
Identifiers
IUPAC name
  • methyl (1R,2S,3S,5S)-3-(4-ethyl-3-iodophenyl)-8-azabicyclooctane-2-carboxylate
CAS Number
PubChem CID
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC17H22INO2
Molar mass399.272 g·mol
3D model (JSmol)
SMILES
  • CCC1=C(C=C(C=C1)2C3CC(2C(=O)OC)N3)I
  (verify)

RTI(-4229)-353 is a phenyltropane derived drug which acts as an SSRI. Tamagnan et al. also made some phenyltropanes with high activity and selectivity for the SERT (pM affinity).

See also

References

  1. Navarro HA, Xu H, Zhong D, Blough BE, Ross WP, Kuhar MJ, Carroll FI (September 2001). "3beta-(4-ethyl-3-iodophenyl)nortropane-2beta-carboxylic acid methyl ester (EINT): a potent and selective radioligand for the brain serotonin transporter". Synapse. 41 (3). New York, N.Y.: 241–7. doi:10.1002/syn.1081. PMID 11418937. S2CID 2323766.
  2. Tamagnan G, Alagille D, Fu X, Kula NS, Baldessarini RJ, Innis RB, Baldwin RM (January 2006). "Synthesis and monoamine transporter affinity of new 2beta-carbomethoxy-3beta-phenyltropanes". Bioorganic & Medicinal Chemistry Letters. 16 (1): 217–20. doi:10.1016/j.bmcl.2005.09.016. PMID 16236497.


Phenyltropanes (classifications)
2-Carboxymethyl Esters
(3,4-Disubstituted Phenyl)-tropanes
Arylcarboxy
Carboxyalkyl
Acyl
β,α Stereochemistry
α,β Stereochemistry
Heterocycles: 3-Substituted-isoxazol-5-yl
Heterocycles: 3-Substituted-1,2,4-oxadiazole
N-alkyl
N-replaced (S,O,C)
Irreversible
Nortropanes (N-demethylated)
Monoamine reuptake inhibitors
DATTooltip Dopamine transporter
(DRIsTooltip Dopamine reuptake inhibitors)
NETTooltip Norepinephrine transporter
(NRIsTooltip Norepinephrine reuptake inhibitors)
SERTTooltip Serotonin transporter
(SRIsTooltip Serotonin reuptake inhibitors)
VMATsTooltip Vesicular monoamine transporters
Others
See also: Receptor/signaling modulatorsMonoamine releasing agentsAdrenergicsDopaminergicsSerotonergicsMonoamine metabolism modulatorsMonoamine neurotoxins
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