Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C7H16N4O2 |
| Molecular Weight | 188.2275 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CNC(=N)NCCC[C@H](N)C(O)=O
InChI
InChIKey=NTNWOCRCBQPEKQ-YFKPBYRVSA-N
InChI=1S/C7H16N4O2/c1-10-7(9)11-4-2-3-5(8)6(12)13/h5H,2-4,8H2,1H3,(H,12,13)(H3,9,10,11)/t5-/m0/s1
| Molecular Formula | C7H16N4O2 |
| Molecular Weight | 188.2275 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/18808317Curator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/12620067 | https://www.ncbi.nlm.nih.gov/pubmed/12182860 | https://clinicaltrials.gov/ct2/show/NCT00112281
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18808317
Curator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/12620067 | https://www.ncbi.nlm.nih.gov/pubmed/12182860 | https://clinicaltrials.gov/ct2/show/NCT00112281
Tilarginine is L-N-monomethyl arginine (L -NMMA), a non-selective inhibitor of nitric oxide synthase (NOS), which has been studied in the treatment of septic shock and cardiogenic shock complicating myocardial infarction. Despite strong evidence that excessive nitric oxide (NO) production plays a pivotal role in the pathogenesis of septic shock and may contribute to the pathogenesis of cardiogenic shock complicating myocardial infarction, outcome studies in these two disorders have proved disappointing. Tilarginine therapy was associated with an excess mortality, particularly at doses > 5 mg/(kg h), in septic shock, whereas the effects of a lower dose (1 mg/(kg h)) in cardiogenic shock complicating myocardial infarction were neutral. The excess mortality in patients with septic shock was almost certainly the result of unfavorable hemodynamic changes induced by Tilarginine (decreased cardiac output, increased pulmonary vascular resistance and reduced tissue oxygen delivery) whereas the lack of benefit in patients with cardiogenic shock complicating myocardial infarction may have been because the dose of Tilarginine was too low.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL3568 Sources: https://www.ncbi.nlm.nih.gov/pubmed/12620067 |
90.0 nM [IC50] | ||
Target ID: CHEMBL4481 Sources: https://www.ncbi.nlm.nih.gov/pubmed/12182860 |
1000.0 nM [IC50] | ||
Target ID: CHEMBL4803 Sources: https://www.ncbi.nlm.nih.gov/pubmed/12182860 |
540.0 nM [IC50] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
|||
| Primary | Unknown Approved UseUnknown |
|||
| Primary | Unknown Approved UseUnknown |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
12.9 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10336578/ |
3 mg/kg single, intravenous dose: 3 mg/kg route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
2.03 μg/mL CLINICAL TRIAL https://pubmed.ncbi.nlm.nih.gov/9951425/ |
1 mg/kg/h single, intravenous dose: 1 mg/kg/h route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
5.53 μg/mL CLINICAL TRIAL https://pubmed.ncbi.nlm.nih.gov/9951425/ |
2.5 mg/kg/h single, intravenous dose: 2.5 mg/kg/h route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
22.9 μg/mL CLINICAL TRIAL https://pubmed.ncbi.nlm.nih.gov/9951425/ |
5 mg/kg/h single, intravenous dose: 5 mg/kg/h route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
51.9 μg/mL CLINICAL TRIAL https://pubmed.ncbi.nlm.nih.gov/9951425/ |
10 mg/kg/h single, intravenous dose: 10 mg/kg/h route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
128 μg/mL CLINICAL TRIAL https://pubmed.ncbi.nlm.nih.gov/9951425/ |
20 mg/kg/h single, intravenous dose: 20 mg/kg/h route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
260.4 μg × min/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10336578/ |
3 mg/kg single, intravenous dose: 3 mg/kg route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
16.6 μg × h/mL CLINICAL TRIAL https://pubmed.ncbi.nlm.nih.gov/9951425/ |
1 mg/kg/h single, intravenous dose: 1 mg/kg/h route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
40.8 μg × h/mL CLINICAL TRIAL https://pubmed.ncbi.nlm.nih.gov/9951425/ |
2.5 mg/kg/h single, intravenous dose: 2.5 mg/kg/h route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
175 μg × h/mL CLINICAL TRIAL https://pubmed.ncbi.nlm.nih.gov/9951425/ |
5 mg/kg/h single, intravenous dose: 5 mg/kg/h route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
443 μg × h/mL CLINICAL TRIAL https://pubmed.ncbi.nlm.nih.gov/9951425/ |
10 mg/kg/h single, intravenous dose: 10 mg/kg/h route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
1640 μg × h/mL CLINICAL TRIAL https://pubmed.ncbi.nlm.nih.gov/9951425/ |
20 mg/kg/h single, intravenous dose: 20 mg/kg/h route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
63.5 min EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/10336578/ |
3 mg/kg single, intravenous dose: 3 mg/kg route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
2.3 h CLINICAL TRIAL https://pubmed.ncbi.nlm.nih.gov/9951425/ |
1 mg/kg/h single, intravenous dose: 1 mg/kg/h route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
2.1 h CLINICAL TRIAL https://pubmed.ncbi.nlm.nih.gov/9951425/ |
2.5 mg/kg/h single, intravenous dose: 2.5 mg/kg/h route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
3.1 h CLINICAL TRIAL https://pubmed.ncbi.nlm.nih.gov/9951425/ |
5 mg/kg/h single, intravenous dose: 5 mg/kg/h route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
2.4 h CLINICAL TRIAL https://pubmed.ncbi.nlm.nih.gov/9951425/ |
10 mg/kg/h single, intravenous dose: 10 mg/kg/h route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
7.6 h CLINICAL TRIAL https://pubmed.ncbi.nlm.nih.gov/9951425/ |
20 mg/kg/h single, intravenous dose: 20 mg/kg/h route of administration: Intravenous experiment type: SINGLE co-administered: |
TILARGININE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
Overview
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
OverviewOther
| Other Inhibitor | Other Substrate | Other Inducer |
|---|---|---|
Drug as perpetrator
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
Page: 12.0 |
inconclusive [IC50 15.8489 uM] | |||
Page: 31.0 |
inconclusive | |||
Page: 42.0 |
no | |||
Page: 48.0 |
no | |||
Page: 42.0 |
no |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18808317
Tilarginine was given as an intravenous infusion starting with a dose of 2.5 mg/(kg h), which could be subsequently increased in an incremental manner up to a maximum dose of 20 mg/(kg h).
Route of Administration:
Intravenous
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/12620067
L-NMMA (Tilarginine) was assayed for ability to inhibit NO production in human colorectal adenocarcinoma (DLD-1) cells preincubated with a cytokine cocktail. Cells were grown to confluence in 12-well plates. Cytokines or other agents were added to fresh media (1 mL/well). At 18-24-h postinduction, culture supernatants were harvested and stored at -20 C for nitrite analysis. Nitrite was measured spectrophotometrically using the Griess reagent
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:59:49 GMT 2025
by
admin
on
Mon Mar 31 17:59:49 GMT 2025
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| Record UNII |
27JT06E6GR
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| Record Status |
Validated (UNII)
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NCI_THESAURUS |
C29574
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DB11815
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100000177267
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CHEMBL312870
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CHEMBL256147
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17035-90-4
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SUB10833MIG
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C1178
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DTXSID3040560
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7672
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132862
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Methylarginine
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m7366
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27JT06E6GR
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28229
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