Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C23H20ClN3O3S |
| Molecular Weight | 453.941 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(C=CC(=C1)N2C=NC3=C(SC(=C3)C4=CC=C(Cl)C=C4)C2=O)N5CC[C@@H](O)C5
InChI
InChIKey=JOAYEJZDGOLEDZ-QGZVFWFLSA-N
InChI=1S/C23H20ClN3O3S/c1-30-20-10-16(6-7-19(20)26-9-8-17(28)12-26)27-13-25-18-11-21(31-22(18)23(27)29)14-2-4-15(24)5-3-14/h2-7,10-11,13,17,28H,8-9,12H2,1H3/t17-/m1/s1
| Molecular Formula | C23H20ClN3O3S |
| Molecular Weight | 453.941 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Tue Apr 01 16:30:56 GMT 2025
by
admin
on
Tue Apr 01 16:30:56 GMT 2025
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| Record UNII |
2BN5Z6HFX3
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| Record Status |
Validated (UNII)
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| Record Version |
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2BN5Z6HFX3
Created by
admin on Tue Apr 01 16:30:56 GMT 2025 , Edited by admin on Tue Apr 01 16:30:56 GMT 2025
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11419640
Created by
admin on Tue Apr 01 16:30:56 GMT 2025 , Edited by admin on Tue Apr 01 16:30:56 GMT 2025
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851690-21-6
Created by
admin on Tue Apr 01 16:30:56 GMT 2025 , Edited by admin on Tue Apr 01 16:30:56 GMT 2025
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
Class: Pyrimidinone, Pyrrolidine, Small molecule; Mechanism of Action: MCHR1 protein inhibitor
Highest Development Phase: No development reported for Obesity; Most Recent Events: 18 Apr 2011 No development reported - Preclinical for Obesity in USA (PO), 01 Sep 2010 Preclinical development is ongoing in USA, 31 Oct 2007 Data presented at the 2007 Annual Meeting of the North American Association for the Study of Obesity (NAASO-2007) added to the Obesity pharmacodynamics section
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ACTIVE MOIETY |
The observations that mice with overexpression of MCH1-R are obese, MCH1-R knockout animals become lean and can develop a hypophagia (208,209) and leaness may occur also in consequence to ablation of melanin-concentrating hormone neurons (210) accelerated the efforts in search for suitable antagonistic agents up to date. Among these GW 856464 (211), AMG076 (212)and NGD-4715 (213) achieved phase 1 clinical investigations.
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