Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C10H14FN3O4 |
Molecular Weight | 259.2343 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 4 / 4 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@]1(F)[C@H](O)[C@@H](CO)O[C@H]1N2C=CC(N)=NC2=O
InChI
InChIKey=NYPIRLYMDJMKGW-VPCXQMTMSA-N
InChI=1S/C10H14FN3O4/c1-10(11)7(16)5(4-15)18-8(10)14-3-2-6(12)13-9(14)17/h2-3,5,7-8,15-16H,4H2,1H3,(H2,12,13,17)/t5-,7-,8-,10-/m1/s1
Molecular Formula | C10H14FN3O4 |
Molecular Weight | 259.2343 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 4 / 4 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Mericitabine is a specific inhibitor of hepatitis C virus (HCV) replication that target NS5B polymerase. Mericitabine, a prodrug, is hydrolyzed in vivo to produce PSI-6130. It had been studied in phase II clinical trials for the treatment of chronic hepatitis C. However, while it showed a good safety profile in clinical trials, it was not sufficiently effective to be used as a standalone agent.
Originator
Approval Year
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
0.557 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24025983 |
1000 mg single, oral dose: 1000 mg route of administration: Oral experiment type: SINGLE co-administered: |
RO5012433 plasma | Homo sapiens population: HEALTHY age: ADOLESCENT sex: FEMALE / MALE food status: FASTED |
|
0.854 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24025983 |
2000 mg single, oral dose: 2000 mg route of administration: Oral experiment type: SINGLE co-administered: |
RO5012433 plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
0.361 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24025983 |
500 mg single, oral dose: 500 mg route of administration: Oral experiment type: SINGLE co-administered: |
RO5012433 plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
10.2 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24025983 |
2000 mg single, oral dose: 2000 mg route of administration: Oral experiment type: SINGLE co-administered: |
RO4995855 plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
4.23 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24025983 |
500 mg single, oral dose: 500 mg route of administration: Oral experiment type: SINGLE co-administered: |
RO4995855 plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
11.2 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24025983 |
1000 mg single, oral dose: 1000 mg route of administration: Oral experiment type: SINGLE co-administered: |
RO5012433 plasma | Homo sapiens population: HEALTHY age: ADOLESCENT sex: FEMALE / MALE food status: FASTED |
|
20.5 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24025983 |
2000 mg single, oral dose: 2000 mg route of administration: Oral experiment type: SINGLE co-administered: |
RO5012433 plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
6.35 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24025983 |
500 mg single, oral dose: 500 mg route of administration: Oral experiment type: SINGLE co-administered: |
RO5012433 plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
113 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24025983 |
2000 mg single, oral dose: 2000 mg route of administration: Oral experiment type: SINGLE co-administered: |
RO4995855 plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
28.8 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24025983 |
500 mg single, oral dose: 500 mg route of administration: Oral experiment type: SINGLE co-administered: |
RO4995855 plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
22.7 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24025983 |
1000 mg single, oral dose: 1000 mg route of administration: Oral experiment type: SINGLE co-administered: |
RO5012433 plasma | Homo sapiens population: HEALTHY age: ADOLESCENT sex: FEMALE / MALE food status: FASTED |
|
21.8 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24025983 |
2000 mg single, oral dose: 2000 mg route of administration: Oral experiment type: SINGLE co-administered: |
RO5012433 plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
19 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24025983 |
500 mg single, oral dose: 500 mg route of administration: Oral experiment type: SINGLE co-administered: |
RO5012433 plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
5.54 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24025983 |
2000 mg single, oral dose: 2000 mg route of administration: Oral experiment type: SINGLE co-administered: |
RO4995855 plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
4.96 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/24025983 |
500 mg single, oral dose: 500 mg route of administration: Oral experiment type: SINGLE co-administered: |
RO4995855 plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
PubMed
Title | Date | PubMed |
---|---|---|
Tetrazole and triazole as bioisosteres of carboxylic acid: discovery of diketo tetrazoles and diketo triazoles as anti-HCV agents. | 2013 Aug 15 |
|
Highly efficient infectious cell culture of three hepatitis C virus genotype 2b strains and sensitivity to lead protease, nonstructural protein 5A, and polymerase inhibitors. | 2014 Feb |
|
The combination of alisporivir plus an NS5A inhibitor provides additive to synergistic anti-hepatitis C virus activity without detectable cross-resistance. | 2014 Jun |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20942646
1500 mg doses twice daily for 2 weeks
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18285474
A stable HCV 1b replicon cell (Gt 1b Con1) line was treated with the NS5B nucleoside inhibitor R7128 (prodrug PSI-6130). Inhibition of HCV replicon-encoded Renilla luciferase reporter activity after 3 days of incubation was calculated - EC50 = 0.61 uM.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:15:26 GMT 2023
by
admin
on
Fri Dec 15 18:15:26 GMT 2023
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Record UNII |
05J68784G1
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Record Status |
Validated (UNII)
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Record Version |
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-
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05J68784G1
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DTXSID10231287
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admin on Fri Dec 15 18:15:26 GMT 2023 , Edited by admin on Fri Dec 15 18:15:26 GMT 2023
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817204-33-4
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admin on Fri Dec 15 18:15:26 GMT 2023 , Edited by admin on Fri Dec 15 18:15:26 GMT 2023
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6481236
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admin on Fri Dec 15 18:15:26 GMT 2023 , Edited by admin on Fri Dec 15 18:15:26 GMT 2023
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PSI-6130
Created by
admin on Fri Dec 15 18:15:26 GMT 2023 , Edited by admin on Fri Dec 15 18:15:26 GMT 2023
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TARGET ORGANISM->INHIBITOR |
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TARGET -> INHIBITOR |
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Related Record | Type | Details | ||
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PRODRUG -> METABOLITE ACTIVE |
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