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SCH-23390: Difference between revisions

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Revision as of 05:39, 5 May 2010 editBogBot (talk | contribs)Bots53,132 editsm activated IUPHAR link← Previous edit Latest revision as of 03:20, 21 October 2024 edit undo76.174.0.57 (talk) See also. 
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{{chembox {{chembox
| Verifiedfields = changed
|ImageFile=SCH_23390.svg
| verifiedrevid = 360226113
|ImageSize=200px
| ImageFile=SCH_23390.svg
|IUPACName=7-chloro-3-methyl-1-phenyl-1,2,4,5-tetrahydro-3-benzazepin-8-ol
| ImageSize=200px
|OtherNames=
| IUPACName=7-chloro-3-methyl-1-phenyl-1,2,4,5-tetrahydro-3-benzazepin-8-ol
| OtherNames=
|Section1={{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo=87075-17-0 | CASNo=87075-17-0
| PubChem=5018
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = UGT5535REQ
| PubChem=5018
| ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 73297
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 62
| IUPHAR_ligand = 943 | IUPHAR_ligand = 943
| SMILES=CN1CCC2=CC(=C(C=C2C(C1)C3=CC=CC=C3)O)Cl | SMILES=CN1CCC2=CC(=C(C=C2C(C1)C3=CC=CC=C3)O)Cl
}} }}
|Section2={{Chembox Properties |Section2={{Chembox Properties
| Formula=C<sub>17</sub>H<sub>18</sub>ClNO | Formula=C<sub>17</sub>H<sub>18</sub>ClNO
| MolarMass=287.78 g/mol | MolarMass=287.78 g/mol
| Appearance= | Appearance=
| Density= | Density=
| MeltingPt= | MeltingPt=
| BoilingPt= | BoilingPt=
| Solubility= | Solubility=
}} }}
|Section3={{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards= | MainHazards=
| FlashPt= | FlashPt=
| AutoignitionPt =
| Autoignition=
}} }}
}} }}


'''SCH23390''' is a synthetic compound that acts as a ] ] and has either minimal or negligible effects on the ]. '''SCH-23390''' also known as halobenzazepine, is a synthetic compound that acts as a ] ] and has either minimal or negligible effects on the ].


In a 1990 study in rats SCH-23390 offered significant protection from death in ] overdosage, without providing protection from death by ] overdose. The compound provided significant protection from cocaine overdose in rats only at the lowest dose tested in the measurement series.
{{pharm-stub}}
This suggested that D-amphetamine and methamphetamine at high (lethal) doses have different mechanisms of toxicity in rats.<ref>{{ cite journal | pmid = 2215083 | year = 1990 | last1 = Derlet | first1 = R. W. | last2 = Albertson | first2 = T. E. | last3 = Rice | first3 = P. | title = The Effect of SCH 23390 Against Toxic Doses of Cocaine, d-Amphetamine and Methamphetamine | volume = 47 | issue = 9 | pages = 821–827 | journal = Life Sciences | doi = 10.1016/0024-3205(90)90555-6 }}</ref>


== References == ==See also==
* ] (NNC 22-0010)
{{reflist}}
* ] (SCH-39166)
* ] (ADX-10061)
* ] (NNC 01-0756)


==References==
{{Dopaminergics}}
{{Reflist}}



]
{{Dopamine receptor modulators}}
]

]
]
]
]
]

{{nervous-system-drug-stub}}
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