Misplaced Pages

RS-102221: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editContent deleted Content addedVisualWikitext
Revision as of 20:28, 13 January 2011 editHarbinary (talk | contribs)1,113 edits cat← Previous edit Latest revision as of 20:48, 5 April 2024 edit undoحسن علي البط (talk | contribs)Extended confirmed users, Pending changes reviewers19,940 edits added Category:Heterocyclic compounds with 2 rings using HotCat 
(29 intermediate revisions by 22 users not shown)
Line 1: Line 1:
{{Short description|Chemical compound}}
{{drugbox |
{{Drugbox
| IUPAC_name = ''N''-{5-dec-8-yl)pentanoyl] -2,4-dimethoxyphenyl}-4-(trifluoromethyl)benzenesulfonamide
| Verifiedfields = changed
| image = RS-102,221_structure.png
| verifiedrevid = 407718072
| width = 250
| IUPAC_name = ''N''-{5-dec-8-yl)pentanoyl] -2,4-dimethoxyphenyl}-4-(trifluoromethyl)benzenesulfonamide
| CAS_number = 185376-97-0
| image = RS-102221.svg
| synonyms = <small>RS-102,221; 8--1,3,8-triazaspirodecane-2,4-dione</small>
| width = 250
| ATC_prefix =

| ATC_suffix =
<!--Clinical data-->
| PubChem = 3693566
| tradename =
| pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X -->
| pregnancy_US = <!-- A / B / C / D / X -->
| pregnancy_category =
| legal_AU = <!-- Unscheduled / S2 / S3 / S4 / S5 / S6 / S7 / S8 / S9 -->
| legal_CA =
| legal_UK =
| legal_US =
| legal_status =
| routes_of_administration =

<!--Pharmacokinetic data-->
| bioavailability =
| protein_bound =
| metabolism =
| elimination_half-life =
| excretion =

<!--Identifiers-->
| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 185376-97-0
| ATC_prefix =
| ATC_suffix =
| PubChem = 3693566
| IUPHAR_ligand = 187 | IUPHAR_ligand = 187
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank = | DrugBank =
| C = 27 | H = 33 | F = 3 | N = 4 | O = 7 | S = 1
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| molecular_weight = 614.632 g/mol
| ChEMBL = 88402
| smiles = c4cc(C(F)(F)F)ccc4S(=O)(=O)Nc(c(OC)cc2OC)cc2C(=O)CCCCN(CC3)CCC13NC(=O)NC1=O
| bioavailability = | ChemSpiderID = 2925610

| protein_bound =
<!--Chemical data-->
| metabolism =
| C=27 | H=33 | F=3 | N=4 | O=7 | S=1
| elimination_half-life =
| smiles = c4cc(C(F)(F)F)ccc4S(=O)(=O)Nc(c(OC)cc2OC)cc2C(=O)CCCCN(CC3)CCC13NC(=O)NC1=O
| excretion =
| StdInChI = 1S/C27H31F3N4O7S/c1-40-22-16-23(41-2)20(33-42(38,39)18-8-6-17(7-9-18)27(28,29)30)15-19(22)21(35)5-3-4-12-34-13-10-26(11-14-34)24(36)31-25(37)32-26/h6-9,15-16,33H,3-5,10-14H2,1-2H3,(H2,31,32,36,37)
| pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X -->
| StdInChIKey = HZZZZODVDSHQRG-UHFFFAOYSA-N
| pregnancy_US = <!-- A / B / C / D / X -->
| synonyms = <small>RS-102,221; 8--1,3,8-triazaspirodecane-2,4-dione</small>
| pregnancy_category=
| legal_AU = <!-- Unscheduled / S2 / S3 / S4 / S5 / S6 / S7 / S8 / S9 -->
| legal_CA =
| legal_UK =
| legal_US =
| legal_status =
| routes_of_administration =
}} }}


'''RS-102,221''' is a drug developed by ], which was one of the first compounds discovered that acts as a potent and selective ] at the ] ] ], with around 100x selectivity over the closely related ] and ] receptors.<ref>Bonhaus DW, Weinhardt KK, Taylor M, DeSouza A, McNeeley PM, Szczepanski K, Fontana DJ, Trinh J, Rocha CL, Dawson MW, Flippin LA, Eglen RM. RS-102221: a novel high affinity and selective, 5-HT2C receptor antagonist. ''Neuropharmacology''. 1997 Apr-May;36(4-5):621-9. PMID 9225287</ref> It has ] effects in animal studies,<ref>Kuznetsova EG, Amstislavskaya TG, Shefer EA, Popova NK. Effect of 5-HT2C receptor antagonist RS 102221 on mouse behavior. ''Bulletin of Experimental Biology and Medicine''. 2006 Jul;142(1):76-9. PMID 17369908</ref> increases the effectiveness of ] antidepressants,<ref>Cremers TI, Giorgetti M, Bosker FJ, Hogg S, Arnt J, Mørk A, Honig G, Bøgesø KP, Westerink BH, den Boer H, Wikstrom HV, Tecott LH. Inactivation of 5-HT(2C) receptors potentiates consequences of serotonin reuptake blockade. ''Neuropsychopharmacology''. 2004 Oct;29(10):1782-9. PMID 15138437</ref> and shows a complex interaction with ], increasing some effects but decreasing others, reflecting a role for the 5-HT<sub>2C</sub> receptor in regulation of the ] signalling system in the brain.<ref>Filip M, Cunningham KA. Serotonin 5-HT(2C) receptors in nucleus accumbens regulate expression of the hyperlocomotive and discriminative stimulus effects of cocaine. ''Pharmacology, Biochemistry and Behaviour''. 2002 Apr;71(4):745-56. PMID 11888566</ref><ref>Filip M, Cunningham KA. Hyperlocomotive and discriminative stimulus effects of cocaine are under the control of serotonin(2C) (5-HT(2C)) receptors in rat prefrontal cortex. ''Journal of Pharmacology and Experimental Therapeutics''. 2003 Aug;306(2):734-43. PMID 12721337</ref><ref>Morita K, Hamamoto M, Arai S, Kitayama S, Irifune M, Kawahara M, Kihira K, Dohi T. Inhibition of serotonin transporters by cocaine and meprylcaine through 5-TH2C receptor stimulation facilitates their seizure activities. ''Brain Research''. 2005 Sep 28;1057(1-2):153-60. PMID 16125150</ref><ref>Dremencov E, Weizmann Y, Kinor N, Gispan-Herman I, Yadid G. Modulation of dopamine transmission by 5HT2C and 5HT3 receptors: a role in the antidepressant response. ''Current Drug Targets''. 2006 Feb;7(2):165-75. PMID 16475958</ref> '''RS-102221''' is a drug developed by ], which was one of the first compounds discovered that acts as a potent and selective ] at the ] ] ], with around 100× selectivity over the closely related ] and ] receptors.<ref>{{cite journal | vauthors = Bonhaus DW, Weinhardt KK, Taylor M, DeSouza A, McNeeley PM, Szczepanski K, Fontana DJ, Trinh J, Rocha CL, Dawson MW, Flippin LA, Eglen RM | display-authors = 6 | title = RS-102221: a novel high affinity and selective, 5-HT2C receptor antagonist | journal = Neuropharmacology | volume = 36 | issue = 4–5 | pages = 621–9 | pmid = 9225287 | doi = 10.1016/s0028-3908(97)00049-x | year = 1997 | s2cid = 24930608 }}</ref> It has ] effects in animal studies,<ref>{{cite journal | vauthors = Kuznetsova EG, Amstislavskaya TG, Shefer EA, Popova NK | title = Effect of 5-HT2C receptor antagonist RS 102221 on mouse behavior | journal = Bulletin of Experimental Biology and Medicine | volume = 142 | issue = 1 | pages = 76–9 | date = July 2006 | pmid = 17369908 | doi = 10.1007/s10517-006-0296-8 | s2cid = 36424571 }}</ref> increases the effectiveness of ] antidepressants,<ref>{{cite journal | vauthors = Cremers TI, Giorgetti M, Bosker FJ, Hogg S, Arnt J, Mørk A, Honig G, Bøgesø KP, Westerink BH, den Boer H, Wikstrom HV, Tecott LH | display-authors = 6 | title = Inactivation of 5-HT(2C) receptors potentiates consequences of serotonin reuptake blockade | journal = Neuropsychopharmacology | volume = 29 | issue = 10 | pages = 1782–9 | date = October 2004 | pmid = 15138437 | doi = 10.1038/sj.npp.1300474 | doi-access = free }}</ref> and shows a complex interaction with ], increasing some effects but decreasing others, reflecting a role for the 5-HT<sub>2C</sub> receptor in regulation of the ] signalling system in the brain.<ref>{{cite journal | vauthors = Filip M, Cunningham KA | title = Serotonin 5-HT(2C) receptors in nucleus accumbens regulate expression of the hyperlocomotive and discriminative stimulus effects of cocaine | journal = Pharmacology, Biochemistry, and Behavior | volume = 71 | issue = 4 | pages = 745–56 | date = April 2002 | pmid = 11888566 | doi = 10.1016/s0091-3057(01)00741-9 | s2cid = 292398 }}</ref><ref>{{cite journal | vauthors = Filip M, Cunningham KA | title = Hyperlocomotive and discriminative stimulus effects of cocaine are under the control of serotonin(2C) (5-HT(2C)) receptors in rat prefrontal cortex | journal = The Journal of Pharmacology and Experimental Therapeutics | volume = 306 | issue = 2 | pages = 734–43 | date = August 2003 | pmid = 12721337 | doi = 10.1124/jpet.102.045716 | s2cid = 8338748 }}</ref><ref>{{cite journal | vauthors = Morita K, Hamamoto M, Arai S, Kitayama S, Irifune M, Kawahara M, Kihira K, Dohi T | display-authors = 6 | title = Inhibition of serotonin transporters by cocaine and meprylcaine through 5-TH2C receptor stimulation facilitates their seizure activities | journal = Brain Research | volume = 1057 | issue = 1–2 | pages = 153–60 | date = September 2005 | pmid = 16125150 | doi = 10.1016/j.brainres.2005.07.049 | s2cid = 30437231 | url = http://ir.lib.hiroshima-u.ac.jp/files/public/0/115/20141016115526561231/Brain-Res_1057-1-2_153-160_2005-9-28.pdf }}</ref><ref>{{cite journal | vauthors = Dremencov E, Weizmann Y, Kinor N, Gispan-Herman I, Yadid G | title = Modulation of dopamine transmission by 5HT2C and 5HT3 receptors: a role in the antidepressant response | journal = Current Drug Targets | volume = 7 | issue = 2 | pages = 165–75 | date = February 2006 | pmid = 16475958 | doi = 10.2174/138945006775515491 }}</ref>


== See also ==
{{pharm-stub}}
* ]
* ]
*]


== References == == References ==
{{reflist}} {{Reflist|2}}


{{Serotonergics}} {{Serotonergics}}
Line 45: Line 66:
] ]
] ]
] ]
]
]
]
]

Latest revision as of 20:48, 5 April 2024

Chemical compound Pharmaceutical compound
RS-102221
Clinical data
Other namesRS-102,221; 8--1,3,8-triazaspirodecane-2,4-dione
Identifiers
IUPAC name
  • N-{5-dec-8-yl)pentanoyl] -2,4-dimethoxyphenyl}-4-(trifluoromethyl)benzenesulfonamide
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC27H33F3N4O7S
Molar mass614.64 g·mol
3D model (JSmol)
SMILES
  • c4cc(C(F)(F)F)ccc4S(=O)(=O)Nc(c(OC)cc2OC)cc2C(=O)CCCCN(CC3)CCC13NC(=O)NC1=O
InChI
  • InChI=1S/C27H31F3N4O7S/c1-40-22-16-23(41-2)20(33-42(38,39)18-8-6-17(7-9-18)27(28,29)30)15-19(22)21(35)5-3-4-12-34-13-10-26(11-14-34)24(36)31-25(37)32-26/h6-9,15-16,33H,3-5,10-14H2,1-2H3,(H2,31,32,36,37)
  • Key:HZZZZODVDSHQRG-UHFFFAOYSA-N
  (what is this?)  (verify)

RS-102221 is a drug developed by Hoffmann–La Roche, which was one of the first compounds discovered that acts as a potent and selective antagonist at the serotonin 5-HT2C receptor, with around 100× selectivity over the closely related 5-HT2A and 5-HT2B receptors. It has anxiolytic effects in animal studies, increases the effectiveness of SSRI antidepressants, and shows a complex interaction with cocaine, increasing some effects but decreasing others, reflecting a role for the 5-HT2C receptor in regulation of the dopamine signalling system in the brain.

See also

References

  1. Bonhaus DW, Weinhardt KK, Taylor M, DeSouza A, McNeeley PM, Szczepanski K, et al. (1997). "RS-102221: a novel high affinity and selective, 5-HT2C receptor antagonist". Neuropharmacology. 36 (4–5): 621–9. doi:10.1016/s0028-3908(97)00049-x. PMID 9225287. S2CID 24930608.
  2. Kuznetsova EG, Amstislavskaya TG, Shefer EA, Popova NK (July 2006). "Effect of 5-HT2C receptor antagonist RS 102221 on mouse behavior". Bulletin of Experimental Biology and Medicine. 142 (1): 76–9. doi:10.1007/s10517-006-0296-8. PMID 17369908. S2CID 36424571.
  3. Cremers TI, Giorgetti M, Bosker FJ, Hogg S, Arnt J, Mørk A, et al. (October 2004). "Inactivation of 5-HT(2C) receptors potentiates consequences of serotonin reuptake blockade". Neuropsychopharmacology. 29 (10): 1782–9. doi:10.1038/sj.npp.1300474. PMID 15138437.
  4. Filip M, Cunningham KA (April 2002). "Serotonin 5-HT(2C) receptors in nucleus accumbens regulate expression of the hyperlocomotive and discriminative stimulus effects of cocaine". Pharmacology, Biochemistry, and Behavior. 71 (4): 745–56. doi:10.1016/s0091-3057(01)00741-9. PMID 11888566. S2CID 292398.
  5. Filip M, Cunningham KA (August 2003). "Hyperlocomotive and discriminative stimulus effects of cocaine are under the control of serotonin(2C) (5-HT(2C)) receptors in rat prefrontal cortex". The Journal of Pharmacology and Experimental Therapeutics. 306 (2): 734–43. doi:10.1124/jpet.102.045716. PMID 12721337. S2CID 8338748.
  6. Morita K, Hamamoto M, Arai S, Kitayama S, Irifune M, Kawahara M, et al. (September 2005). "Inhibition of serotonin transporters by cocaine and meprylcaine through 5-TH2C receptor stimulation facilitates their seizure activities" (PDF). Brain Research. 1057 (1–2): 153–60. doi:10.1016/j.brainres.2005.07.049. PMID 16125150. S2CID 30437231.
  7. Dremencov E, Weizmann Y, Kinor N, Gispan-Herman I, Yadid G (February 2006). "Modulation of dopamine transmission by 5HT2C and 5HT3 receptors: a role in the antidepressant response". Current Drug Targets. 7 (2): 165–75. doi:10.2174/138945006775515491. PMID 16475958.
Serotonin receptor modulators
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Categories: