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RTI-177

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
RTI-177
Identifiers
  • (1R,2S,3S,5S)-3-(4-chlorophenyl)-8-methyl-2-(3-phenyl-1,2-oxazol-5-yl)-8-azabicyclo[3.2.1]octane
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC23H23ClN2O
Molar mass378.90 g·mol−1
3D model (JSmol)
  • CN1[C@H]2CC[C@@H]1[C@H]([C@H](C2)C3=CC=C(C=C3)Cl)C4=CC(=NO4)C5=CC=CC=C5
  • InChI=1S/C23H23ClN2O/c1-26-18-11-12-21(26)23(19(13-18)15-7-9-17(24)10-8-15)22-14-20(25-27-22)16-5-3-2-4-6-16/h2-10,14,18-19,21,23H,11-13H2,1H3/t18-,19+,21+,23-/m0/s1
  • Key:ZGCYMNJHHKQEGA-KPYOPSEVSA-N

RTI(-4229)-177 (2β-(3-phenylisoxazol-5-yl)-3β-(4-chlorophenyl)tropane,β-CPPIT) is a syntheticstimulant drug from thephenyltropane family, which acts as aDRI with micromolar affinity for theSERT.[1] RTI-177 has an unusually long duration of action of 20 hours or more, substantially longer than the related compoundRTI-336 from which it differs in molecular structure only by the absence of ap-methyl group.[2]

"the nonselectivemonoamine transporter inhibitorRTI-126 and theDAT-selective inhibitorsRTI-150 and RTI-336 both had a faster rate of onset (30 min) and a short duration of action (4h). In contrast, the nonselective monoamine transporter inhibitorRTI-112 had a slower rate of onset (30–60 min) and a longer duration of action (10h). The DAT-selective inhibitorsRTI-171 and RTI-177 also had slower rates of onset (30–120 min), but RTI-171 had a short duration of action (2.5 h) while RTI-177 had a very long duration of action (20 h)."[3]

Update

[edit]

Lower reinforcing strength of the phenyltropane cocaine analogs RTI-336 and RTI-177 compared to cocaine in nonhuman primates.

Comparison of six MAT inhibitors

[edit]
RTIXR[3H]CFT[3H]Nisoxetine[3H]Paroxetine
Coc89.13298 (1986)1045 (45)
177Clphenyl1.28504 (304)2420 (220)
176Mephenyl1.58398 (239)5110 (465)
354Meethyl1.62299 (180)6400 (582)
336Clp-cresyl4.091714 (1033)5741 (522)
386Mep-anisoyl3.93756 (450)4027 (380)

In the Lindsey paper, RTI-177 was wrongly considered to be a dual inhibitor of theNET, although this was later found out to be incorrect.[citation needed]

"In acute toxicity studies in male rats, 3β-(4-chlorophenyl)-2β-[3-(4’-methylphenyl)isoxazol-5-yl]tropane (RTI-336) possessed an LD50 of 180 mg/kg after oral administration, compared with 49 mg/kg for RTI-177 (unpublished results, Howell 2005; Table 9). These results suggested that RTI-336 was a better candidate than RTI-177 for further preclinical development."[2]

Also the potency of theheterocyclic compounds is not as great as would be predicted based onin vitro test results.

References

[edit]
  1. ^Lindsey KP, Wilcox KM, Votaw JR, Goodman MM, Plisson C, Carroll FI, et al. (June 2004)."Effects of dopamine transporter inhibitors on cocaine self-administration in rhesus monkeys: relationship to transporter occupancy determined by positron emission tomography neuroimaging"(PDF).The Journal of Pharmacology and Experimental Therapeutics.309 (3):959–69.doi:10.1124/jpet.103.060293.PMID 14982963.S2CID 39794215. Archived fromthe original(PDF) on 2010-06-11.
  2. ^abCarroll FI, Howard JL, Howell LL, Fox BS, Kuhar MJ (March 2006)."Development of the dopamine transporter selective RTI-336 as a pharmacotherapy for cocaine abuse".The AAPS Journal.8 (1): E196-203.doi:10.1208/aapsj080124.PMC 2751440.PMID 16584128. Archived fromthe original on 2010-09-20. Retrieved2009-07-17.
  3. ^Kimmel HL, O'Connor JA, Carroll FI, Howell LL (January 2007)."Faster onset and dopamine transporter selectivity predict stimulant and reinforcing effects of cocaine analogs in squirrel monkeys".Pharmacology, Biochemistry, and Behavior.86 (1):45–54.doi:10.1016/j.pbb.2006.12.006.PMC 1850383.PMID 17258302.
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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
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)
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