Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C25H27F4N3O3S |
| Molecular Weight | 525.559 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(F)C[C@H](N[C@@H](C1=CC=C(C=C1)C2=CC=C(C=C2)S(C)(=O)=O)C(F)(F)F)C(=O)NC3(CC3)C#N
InChI
InChIKey=FWIVDMJALNEADT-SFTDATJTSA-N
InChI=1S/C25H27F4N3O3S/c1-23(2,26)14-20(22(33)32-24(15-30)12-13-24)31-21(25(27,28)29)18-6-4-16(5-7-18)17-8-10-19(11-9-17)36(3,34)35/h4-11,20-21,31H,12-14H2,1-3H3,(H,32,33)/t20-,21-/m0/s1
| Molecular Formula | C25H27F4N3O3S |
| Molecular Weight | 525.559 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
DescriptionSources: http://adisinsight.springer.com/drugs/800024552Curator's Comment: Description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/18226527 | https://www.ncbi.nlm.nih.gov/pubmed/27681784
Sources: http://adisinsight.springer.com/drugs/800024552
Curator's Comment: Description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/18226527 | https://www.ncbi.nlm.nih.gov/pubmed/27681784
Odanacatib is a potent, selective, and neutral cathepsin K inhibitor, an enzyme involved in bone resorption. Merck & Co was developing odanacatib, a once-weekly, oral Odanacatib, for the treatment of postmenopausal osteoporosis and osteoporosis in men. Merck & Co. has discontinued development of its cathepsin K inhibitor odanacatib, citing an increased risk of cardiovascular events for the osteoporosis drug.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL268 Sources: https://www.ncbi.nlm.nih.gov/pubmed/18226527 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
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| Primary | Unknown Approved UseUnknown |
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| Primary | Unknown Approved UseUnknown |
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| Primary | Unknown Approved UseUnknown |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
183 nM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
50 mg single, oral dose: 50 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: HIGH-FAT |
|
353.5 nM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
477.3 nM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
600 mg single, oral dose: 600 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
738.5 nM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
200 mg single, oral dose: 200 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: HIGH-FAT |
|
630.4 nM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: HIGH-FAT |
|
839.2 nM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
300 mg single, oral dose: 300 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: HIGH-FAT |
|
154.7 nM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
25 mg single, oral dose: 25 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
344.7 nM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
25 mg single, oral dose: 25 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: HIGH-FAT |
|
56.2 nM EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27402726 |
1 mg single, intravenous dose: 1 mg route of administration: Intravenous experiment type: SINGLE co-administered: ODANACATIB |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
3 μM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
50 mg single, oral dose: 50 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: HIGH-FAT |
|
6.4 μM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
9.4 μM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
600 mg single, oral dose: 600 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
13.6 μM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
200 mg single, oral dose: 200 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: HIGH-FAT |
|
11.3 μM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: HIGH-FAT |
|
16.1 μM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
300 mg single, oral dose: 300 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: HIGH-FAT |
|
3.2 μM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
25 mg single, oral dose: 25 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
6.7 μM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
25 mg single, oral dose: 25 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: HIGH-FAT |
|
2.7 μM × h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27402726 |
1 mg single, intravenous dose: 1 mg route of administration: Intravenous experiment type: SINGLE co-administered: ODANACATIB |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
78.8 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
50 mg single, oral dose: 50 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: HIGH-FAT |
|
96.7 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24553380/ |
25 mg single, oral dose: 25 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
59.2 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
600 mg single, oral dose: 600 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
50.5 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
200 mg single, oral dose: 200 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: HIGH-FAT |
|
48.2 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
100 mg single, oral dose: 100 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: HIGH-FAT |
|
62.6 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/23013236 |
300 mg single, oral dose: 300 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: HIGH-FAT |
|
104.4 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/27402726 |
1 mg single, intravenous dose: 1 mg route of administration: Intravenous experiment type: SINGLE co-administered: ODANACATIB |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
Funbound
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
2.5% EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24553380/ |
25 mg single, oral dose: 25 mg route of administration: Oral experiment type: SINGLE co-administered: |
ODANACATIB plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
Doses
| Dose | Population | Adverse events |
|---|---|---|
50 mg 1 times / week multiple, oral Studied dose Dose: 50 mg, 1 times / week Route: oral Route: multiple Dose: 50 mg, 1 times / week Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M Food Status: UNKNOWN Sources: |
Disc. AE: Myalgia... AEs leading to discontinuation/dose reduction: Myalgia (0.7%) Sources: |
300 mg 1 times / day multiple, oral Highest recorded dose Dose: 300 mg, 1 times / day Route: oral Route: multiple Dose: 300 mg, 1 times / day Sources: |
healthy |
Other AEs: Abdominal pain, Application-site erosion... Other AEs: Abdominal pain (5.4%) Sources: Application-site erosion (5.4%) Application-site erythema (17.9%) Pruritus (7.1%) |
50 mg 1 times / week multiple, oral Studied dose Dose: 50 mg, 1 times / week Route: oral Route: multiple Dose: 50 mg, 1 times / week Sources: |
unhealthy |
Disc. AE: Basal cell carcinoma... AEs leading to discontinuation/dose reduction: Basal cell carcinoma (3.6%) Sources: |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Myalgia | 0.7% Disc. AE |
50 mg 1 times / week multiple, oral Studied dose Dose: 50 mg, 1 times / week Route: oral Route: multiple Dose: 50 mg, 1 times / week Sources: |
unhealthy, ADULT Health Status: unhealthy Age Group: ADULT Sex: M Food Status: UNKNOWN Sources: |
| Application-site erythema | 17.9% | 300 mg 1 times / day multiple, oral Highest recorded dose Dose: 300 mg, 1 times / day Route: oral Route: multiple Dose: 300 mg, 1 times / day Sources: |
healthy |
| Abdominal pain | 5.4% | 300 mg 1 times / day multiple, oral Highest recorded dose Dose: 300 mg, 1 times / day Route: oral Route: multiple Dose: 300 mg, 1 times / day Sources: |
healthy |
| Application-site erosion | 5.4% | 300 mg 1 times / day multiple, oral Highest recorded dose Dose: 300 mg, 1 times / day Route: oral Route: multiple Dose: 300 mg, 1 times / day Sources: |
healthy |
| Pruritus | 7.1% | 300 mg 1 times / day multiple, oral Highest recorded dose Dose: 300 mg, 1 times / day Route: oral Route: multiple Dose: 300 mg, 1 times / day Sources: |
healthy |
| Basal cell carcinoma | 3.6% Disc. AE |
50 mg 1 times / week multiple, oral Studied dose Dose: 50 mg, 1 times / week Route: oral Route: multiple Dose: 50 mg, 1 times / week Sources: |
unhealthy |
Overview
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
OverviewOther
| Other Inhibitor | Other Substrate | Other Inducer |
|---|---|---|
Drug as perpetrator
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
| no | no (co-administration study) Comment: Coadministration did not affect R( )- and S(-)-warfarin exposure. Sources: https://pubmed.ncbi.nlm.nih.gov/24142206/ |
|||
| no | no (co-administration study) Comment: Coadministration did not affect R( )- and S(-)-warfarin exposure. Sources: https://pubmed.ncbi.nlm.nih.gov/24142206/ |
|||
| no | no (co-administration study) Comment: Coadministration did not affect R( )- and S(-)-warfarin exposure. Sources: https://pubmed.ncbi.nlm.nih.gov/24142206/ |
|||
| no | no (co-administration study) Comment: Coadministration did not affect R( )- and S(-)-warfarin exposure. Sources: https://pubmed.ncbi.nlm.nih.gov/24142206/ |
Drug as victim
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
| major | ||||
| minor | ||||
| yes |
Tox targets
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Sample Use Guides
In Vivo Use Guide
Sources: http://adisinsight.springer.com/drugs/800024552
Merck is conducting a long-term phase II trial that is assessing four different doses of odanacatib (3mg, 10mg, 25mg and 50mg once-weekly for 2 years) in women with postmenopausal osteoporosis (NCT00112437; EudraCT2005-001511-22). Results from this phase IIb study showed that odanacatib 50mg increased bone mineral density (BMD) from baseline, and was generally safe and well tolerated.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25394885
1 nM odanacatib had suppressive effects on the expression levels of inflammatory cytokines in murine RAW 264.7 cells were cultured in the presence of the receptor activator of NF-kB and lipopolysaccharide
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:19:04 GMT 2025
by
admin
on
Mon Mar 31 18:19:04 GMT 2025
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| Record UNII |
N673F6W2VH
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| Record Status |
Validated (UNII)
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| Record Version |
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NCI_THESAURUS |
C67439
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NCI_THESAURUS |
C783
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8962
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100000128030
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ODANACATIB
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DB06670
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603139-19-1
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C66981
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TT-63
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DTXSID40209075
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N673F6W2VH
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CHEMBL481611
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C527128
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m8131
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10152654
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SUB34600
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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TARGET -> INHIBITOR |
SELECTIVE
IC50
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METABOLIC ENZYME -> SUBSTRATE |
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BINDER->LIGAND |
BINDING
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EXCRETED UNCHANGED |
URINE
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TRANSPORTER -> SUBSTRATE |
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OFF TARGET->WEAK INHIBITOR |
IC50
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EXCRETED UNCHANGED |
FECAL
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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METABOLITE -> PARENT |
URINE
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METABOLITE -> PARENT |
URINE
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METABOLITE -> PARENT |
URINE
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METABOLITE -> PARENT |
FECAL
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METABOLITE -> PARENT |
URINE
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
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| Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
|---|---|---|---|---|---|---|
| Biological Half-life | PHARMACOKINETIC |
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ORAL ADMINISTRATION |
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| Tmax | PHARMACOKINETIC |
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ORAL ADMINISTRATION |
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