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SDZ 216-525
structure given in first source; a selective 5-HT(1A) receptor antagonist
Also Known As:
SDZ-216-525; methyl 4-(4-(4-(1,1,3-trioxo-2H-1,2-benzoisothiazol-2-yl)butyl)-1-piperazinyl)-1H-indole-2-carboxylate; 1H-Indole-2-carboxylic acid, 4-(4-(4-(3-oxo-1,2-benzisothiazol-2(3H)-yl)butyl)-1-piperazinyl)-, methyl ester, S,S-dioxide
Networked:
2
relevant articles (
0
outcomes,
0
trials/studies)
Bio-Agent Context: Research Results
Heterocyclic Compounds: 198
1-Ring Heterocyclic Compounds
Azoles: 2138
Thiazoles: 392
SDZ 216-525: 2
Fused-Ring Heterocyclic Compounds
2-Ring Heterocyclic Compounds
Indoles: 200
SDZ 216-525: 2
Organic Chemicals: 133
Sulfur Compounds: 278
Thiazoles: 392
SDZ 216-525: 2
Related Diseases
1.
Hypothermia
03/01/1993 - "
At postsynaptic 5-HT1A receptors mediating hypothermia, eltoprazine, WY 48,723, MDL 72832 and tandospirone are agonists, zalospirone is a partial agonist and (-)-tertatolol, WAY 100,135, MDL 73005 EF and SDZ 216-525 are antagonists.
"
2.
Bites and Stings (Sting)
12/01/1993 - "
Defensive evade was significantly attenuated at 20.0 mg/kg. SDZ 216-525 (0.025-1.0 mg/kg), a selective 5-HT1A antagonist, significantly attenuated offensive posturing and bite-attacks at 1.0 mg/kg, and all offensive behaviors nonsignificantly at the smaller doses tested.
"
Related Drugs and Biologics
1.
Serotonin 5-HT1 Receptor Antagonists
2.
zalospirone
3.
eltoprazine
4.
binospirone mesylate
5.
MDL 72832
6.
tandospirone
7.
tertatolol (Artex)