Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C15H23N3O4S.ClH |
| Molecular Weight | 377.887 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCN1CCC[C@@H]1CNC(=O)C2=C(OC)C=CC(=C2)S(N)(=O)=O
InChI
InChIKey=PFHZICSPLHQCDZ-RFVHGSKJSA-N
InChI=1S/C15H23N3O4S.ClH/c1-3-18-8-4-5-11(18)10-17-15(19)13-9-12(23(16,20)21)6-7-14(13)22-2;/h6-7,9,11H,3-5,8,10H2,1-2H3,(H,17,19)(H2,16,20,21);1H/t11-;/m1./s1
| Molecular Formula | C15H23N3O4S |
| Molecular Weight | 341.426 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Molecular cloning and characterization of a novel dopamine receptor (D3) as a target for neuroleptics. | 1990 Sep 13 |
|
| Unique binding characteristics of antipsychotic agents interacting with human dopamine D2A, D2B, and D3 receptors. | 1993 May |
|
| Expression and pharmacological characterization of the human D3 dopamine receptor. | 1994 Jan |
|
| Identification and pharmacological characterization of [125I]L-750,667, a novel radioligand for the dopamine D4 receptor. | 1996 Dec |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:33:00 GMT 2023
by
admin
on
Sat Dec 16 11:33:00 GMT 2023
|
| Record UNII |
9964K1S45E
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
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9964K1S45E
Created by
admin on Sat Dec 16 11:33:00 GMT 2023 , Edited by admin on Sat Dec 16 11:33:00 GMT 2023
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PRIMARY | |||
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119026019
Created by
admin on Sat Dec 16 11:33:00 GMT 2023 , Edited by admin on Sat Dec 16 11:33:00 GMT 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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RACEMATE -> ENANTIOMER |
