Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C22H19FN4O3 |
| Molecular Weight | 406.4097 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
FC1=CC=CC=C1N2C=CC(NC(=O)[C@H]3CC[C@@]4(CC3)OC(=O)C5=CC=NC=C45)=N2
InChI
InChIKey=RMYZIRFUCOMQRH-CAJLXGCNSA-N
InChI=1S/C22H19FN4O3/c23-17-3-1-2-4-18(17)27-12-8-19(26-27)25-20(28)14-5-9-22(10-6-14)16-13-24-11-7-15(16)21(29)30-22/h1-4,7-8,11-14H,5-6,9-10H2,(H,25,26,28)/t14-,22-
| Molecular Formula | C22H19FN4O3 |
| Molecular Weight | 406.4097 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
MK-0557, trans-N-[1-(2-fluorophenyl)-3-pyrazolyl]-3-oxospiro [6 azaisobenzofuran-1(3H),10-cyclohexane]-40-carboxamide, is an orally available Neuropeptide Y (NPY5) receptor antagonist. MK-0557 was studied in the clinical trials for the treatment of obesity, however, MK-0557 did not significantly increase the weight loss efficacy. MK-0557 safety and effectiveness were studied in a trial for the treatment of cognitive impairment in patients with schizophrenia. It seems MK-0557 development was discontinued.
Originator
Sources: https://www.google.com/patents/US6723847
Curator's Comment: reference retrieved from https://www.ncbi.nlm.nih.gov/pubmed/17011500
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL4561 Sources: https://www.ncbi.nlm.nih.gov/pubmed/17011500 |
1.3 nM [Ki] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
|||
| Primary | Unknown Approved UseUnknown |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
0.07 μM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17011500 |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
MK-0557 plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
1.13 μM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17011500 |
750 mg single, oral dose: 750 mg route of administration: Oral experiment type: SINGLE co-administered: |
MK-055 plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
1.13 μM EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/17011500 |
750 mg single, oral dose: 750 mg route of administration: Oral experiment type: SINGLE co-administered: |
MK-0557 plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
2.8 μM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17011500 |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
MK-0557 plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
62.8 μM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17011500 |
750 mg single, oral dose: 750 mg route of administration: Oral experiment type: SINGLE co-administered: |
MK-055 plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
62.8 μM × h EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/17011500 |
750 mg single, oral dose: 750 mg route of administration: Oral experiment type: SINGLE co-administered: |
MK-0557 plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
19 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17011500 |
10 mg single, oral dose: 10 mg route of administration: Oral experiment type: SINGLE co-administered: |
MK-0557 plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
30 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17011500 |
750 mg single, oral dose: 750 mg route of administration: Oral experiment type: SINGLE co-administered: |
MK-055 plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
30 h EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/17011500 |
750 mg single, oral dose: 750 mg route of administration: Oral experiment type: SINGLE co-administered: |
MK-0557 plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Discovery of trans-N-[1-(2-fluorophenyl)-3-pyrazolyl]-3-oxospiro[6-azaisobenzofuran-1(3H),1'-cyclohexane]-4'-carboxamide, a potent and orally active neuropeptide Y Y5 receptor antagonist. | 2009-10-01 |
|
| Obesity and the central nervous system. | 2007-09-01 |
|
| NPY5R antagonism does not augment the weight loss efficacy of orlistat or sibutramine. | 2007-08 |
|
| Effect of NPY5R antagonist MK-0557 on weight regain after very-low-calorie diet-induced weight loss. | 2007-04 |
|
| Neuropeptide Y5 receptor antagonism does not induce clinically meaningful weight loss in overweight and obese adults. | 2006-10 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/17011500
The initial series of experiments reported herein, including a multiple-dose positron-emission tomography study and a 12 week proof-of concept/dose-ranging study, suggested an optimal MK-0557 dose of 1 mg/day. The hypothesis was then tested in a 52 week, multicenter, randomized, double-blind, placebo-controlled trial involving 1661 overweight and obese patients. Although statistically significant at 52 weeks, the magnitude of induced weight loss was not clinically meaningful.
Route of Administration:
Oral
| Substance Class |
Chemical
Created
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HVE36P8422
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