Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C8H12N4O5 |
Molecular Weight | 244.2047 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 4 / 4 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)C1=NN(C=N1)[C@H]2O[C@@H](CO)[C@H](O)[C@@H]2O
InChI
InChIKey=IWUCXVSUMQZMFG-RGDLXGNYSA-N
InChI=1S/C8H12N4O5/c9-6(16)7-10-2-12(11-7)8-5(15)4(14)3(1-13)17-8/h2-5,8,13-15H,1H2,(H2,9,16)/t3-,4-,5-,8-/m0/s1
Levovirin is a guanosine nucleoside analog and the L-enantiomer of ribavirin. It is an investigational drug for the treatment of hepatitis C virus-mediated diseases. Levovirin has a similar immunomodulatory potency to ribavirin in vitro without accumulating in red blood cells or causing hemolytic anemia, a known side effect of ribavirin. Levovirin has been shown to stimulate host immune responses (enhanced Th1 and reduced Th2 cytokine expression). Significantly improved oral absorption of levovirin was achieved following administration of a valine ester prodrug of levovirin R1518. Levovirin was found more potent to inhibit Tick-borne encephalitis virus (TBEV) on the basis of robust binding affinity between protein-drug interactions. This finding may help to understand the nature of helicase and development of specific anti-TBEV therapies.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: GO:0002369 Sources: https://www.ncbi.nlm.nih.gov/pubmed/10715165 |
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Target ID: Q01299 Gene ID: NA Gene Symbol: NA Target Organism: Tick-borne encephalitis virus (strain Hypr) (TBEV) Sources: https://www.ncbi.nlm.nih.gov/pubmed/20640834 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
0.66 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
3000 mg single, oral dose: 3000 mg route of administration: Oral experiment type: SINGLE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FED |
|
19.62 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
1500 mg 2 times / day steady-state, oral dose: 1500 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
0.89 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
3000 mg single, oral dose: 3000 mg route of administration: Oral experiment type: SINGLE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
28.22 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
1500 mg 2 times / day steady-state, oral dose: 1500 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
|
35.13 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
3000 mg 2 times / day steady-state, oral dose: 3000 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
10.02 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
750 mg 2 times / day steady-state, oral dose: 750 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
13.65 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
750 mg 2 times / day steady-state, oral dose: 750 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
1.68 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
3000 mg single, oral dose: 3000 mg route of administration: Oral experiment type: SINGLE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FED |
|
193.1 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
1500 mg 2 times / day steady-state, oral dose: 1500 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
2.09 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
3000 mg single, oral dose: 3000 mg route of administration: Oral experiment type: SINGLE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
275.7 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
1500 mg 2 times / day steady-state, oral dose: 1500 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
|
371.7 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
3000 mg 2 times / day steady-state, oral dose: 3000 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
94.5 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
750 mg 2 times / day steady-state, oral dose: 750 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
98 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
750 mg 2 times / day steady-state, oral dose: 750 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
0.8 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
3000 mg single, oral dose: 3000 mg route of administration: Oral experiment type: SINGLE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FED |
|
9.9 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
1500 mg 2 times / day steady-state, oral dose: 1500 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
0.65 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
3000 mg single, oral dose: 3000 mg route of administration: Oral experiment type: SINGLE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
21.1 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
1500 mg 2 times / day steady-state, oral dose: 1500 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
|
8.5 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
3000 mg 2 times / day steady-state, oral dose: 3000 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
7.7 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
750 mg 2 times / day steady-state, oral dose: 750 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
15.1 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/15831782/ |
750 mg 2 times / day steady-state, oral dose: 750 mg route of administration: Oral experiment type: STEADY-STATE co-administered: |
LEVOVIRIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
Overview
CYP3A4 | CYP2C9 | CYP2D6 | hERG |
---|---|---|---|
OverviewOther
Other Inhibitor | Other Substrate | Other Inducer |
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Drug as perpetrator
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
no | ||||
no | ||||
no | ||||
no | ||||
no | ||||
no | ||||
Sources: https://pubmed.ncbi.nlm.nih.gov/14635270/ |
no | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/14635270/ |
no | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/14635270/ |
no | |||
Sources: https://pubmed.ncbi.nlm.nih.gov/14635270/ |
no |
PubMed
Title | Date | PubMed |
---|---|---|
Single- and multiple-dose pharmacokinetics of levovirin valinate hydrochloride (R1518) in healthy volunteers. | 2005 May |
|
Hepatitis-C patients have reduced growth hormone (GH) secretion which improves during long-term therapy with pegylated interferon-alpha. | 2007 Dec |
|
Structural modeling of the NS 3 helicase of Tick-borne encephalitis virus and their virtual screening of potent drugs using molecular docking. | 2009 Sep |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10770762
Rat: 180 mg/kg of body weight for 4 weeks
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/16634069
Levovirin has a very low transport rate through Caco-2 cell monolayers (1.2x10(-7) cm/s). For bi-directional transport studies from basolateral to apical side, 1.25 mL of 20 uM drug solution in pH 7.4 buffer was placed in the basolateral chamber, and 0.5 mL pH 6.5 buffer was put into the apical chamber. There are no significant differences between apical (A) to basolateral (B) and B to A permeability values for levovirin.
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ACTIVE MOIETY