Details
Stereochemistry | EPIMERIC |
Molecular Formula | C9H16N2O6 |
Molecular Weight | 248.2331 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 4 / 5 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N2CCC(O)NC2=O
InChI
InChIKey=UCKYOOZPSJFJIZ-XVKVHKPRSA-N
InChI=1S/C9H16N2O6/c12-3-4-6(14)7(15)8(17-4)11-2-1-5(13)10-9(11)16/h4-8,12-15H,1-3H2,(H,10,16)/t4-,5?,6-,7-,8-/m1/s1
Molecular Formula | C9H16N2O6 |
Molecular Weight | 248.2331 |
Charge | 0 |
Count |
|
Stereochemistry | EPIMERIC |
Additional Stereochemistry | No |
Defined Stereocenters | 4 / 5 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/28880867Curator's Comment: The description was created based on several sources, including
https://clinicaltrials.gov/ct2/show/NCT03233724 | https://www.ncbi.nlm.nih.gov/pubmed/24520856 | https://clinicaltrials.gov/ct2/show/NCT02839694 | https://www.ncbi.nlm.nih.gov/pubmed/25567350 | https://www.ncbi.nlm.nih.gov/pubmed/26518542
Sources: https://www.ncbi.nlm.nih.gov/pubmed/28880867
Curator's Comment: The description was created based on several sources, including
https://clinicaltrials.gov/ct2/show/NCT03233724 | https://www.ncbi.nlm.nih.gov/pubmed/24520856 | https://clinicaltrials.gov/ct2/show/NCT02839694 | https://www.ncbi.nlm.nih.gov/pubmed/25567350 | https://www.ncbi.nlm.nih.gov/pubmed/26518542
Tetrahydrouridine is a potent competitive reversible inhibitor of cytidine deaminase. Tetrahydrouridine can inhibit cell proliferation by regulation of the cell cycle independent of cytidine deaminase (CDA) expression levels. Tetrahydrouridine may be useful for researching potential treatments for high CDA-expressing tumors. Tetrahydrouridine use, alone or in combination with the DNA methyltransferase inhibitor 5-fluoro-2’-deoxycytidine, is being evaluated in animal models and clinical trials for diseases, including cancer and mitochondrial DNA depletion syndrome.
CNS Activity
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL4502 Sources: https://www.ncbi.nlm.nih.gov/pubmed/24520856 |
0.34 µM [IC50] |
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 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
29.9 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26321472 |
30 mg/kg single, intravenous dose: 30 mg/kg route of administration: Intravenous experiment type: SINGLE co-administered: 5-FLUORO-2'-DEOXYCYTIDINE |
TETRAHYDROURIDINE plasma | Macaca fascicularis population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1428 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26321472 |
1750 mg/m² single, oral dose: 1750 mg/m² route of administration: Oral experiment type: SINGLE co-administered: 5-FLUORO-2'-DEOXYCYTIDINE |
TETRAHYDROURIDINE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
16452 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26321472 |
350 mg/m² single, intravenous dose: 350 mg/m² route of administration: Intravenous experiment type: SINGLE co-administered: 5-FLUORO-2'-DEOXYCYTIDINE |
TETRAHYDROURIDINE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
7.31 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26321472 |
500 mg/kg single, oral dose: 500 mg/kg route of administration: Oral experiment type: SINGLE co-administered: 5-FLUORO-2'-DEOXYCYTIDINE5-FLUORO-2'-DEOXYCYTIDINE |
TETRAHYDROURIDINE plasma | Macaca fascicularis population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
8969 mg × min/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26321472 |
30 mg/kg single, intravenous dose: 30 mg/kg route of administration: Intravenous experiment type: SINGLE co-administered: 5-FLUORO-2'-DEOXYCYTIDINE |
TETRAHYDROURIDINE plasma | Macaca fascicularis population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
1606 μg × min/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26321472 |
1750 mg/m² single, oral dose: 1750 mg/m² route of administration: Oral experiment type: SINGLE co-administered: 5-FLUORO-2'-DEOXYCYTIDINE |
TETRAHYDROURIDINE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
7969 μg × min/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26321472 |
350 mg/m² single, intravenous dose: 350 mg/m² route of administration: Intravenous experiment type: SINGLE co-administered: 5-FLUORO-2'-DEOXYCYTIDINE |
TETRAHYDROURIDINE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
4017 mg × min/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26321472 |
500 mg/kg single, oral dose: 500 mg/kg route of administration: Oral experiment type: SINGLE co-administered: 5-FLUORO-2'-DEOXYCYTIDINE5-FLUORO-2'-DEOXYCYTIDINE |
TETRAHYDROURIDINE plasma | Macaca fascicularis population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
3.85 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26321472 |
30 mg/kg single, intravenous dose: 30 mg/kg route of administration: Intravenous experiment type: SINGLE co-administered: 5-FLUORO-2'-DEOXYCYTIDINE |
TETRAHYDROURIDINE plasma | Macaca fascicularis population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
|
4.99 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/26321472 |
500 mg/kg single, oral dose: 500 mg/kg route of administration: Oral experiment type: SINGLE co-administered: 5-FLUORO-2'-DEOXYCYTIDINE5-FLUORO-2'-DEOXYCYTIDINE |
TETRAHYDROURIDINE plasma | Macaca fascicularis population: HEALTHY age: ADULT sex: FEMALE / MALE food status: UNKNOWN |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/28880867
Tetrahydrouridine 10 mg/kg was administered 60 minutes before oral decitabine at 0.01, 0.02, 0.04, 0.08, or 0.16 mg/kg. Repeat dose administration 2X/week for 8 weeks
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/22616006
Panc-1, MIAPaCa-2, BxPC-3, H322, H441, and H1299 cells were seeded in 96-well plates at 2,500-5,000 cells/well in triplicate. After incubating for 12 hrs, cell viability was determined by treating cells with stepwise 4-fold serial dilutions of gemcitabine (from 100 mkM), and incubating at 37uC for 96 hrs with or without Tetrahydrouridine (THU). To evaluate cell viability, all cells were fixed with 25% glutaraldehyde for 30 min at room temperature and then stained with 200 mkl of 0.05% methylene blue for 20 min. The dye was eluted with 0.33 M HCl for 20 min with agitation. Absorbance was measured in a microplate reader (model 3550, Bio-Rad, Tokyo, Japan) at 598 nm.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:02:19 GMT 2023
by
admin
on
Fri Dec 15 15:02:19 GMT 2023
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Record UNII |
0NIZ8H6OL8
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Record Status |
Validated (UNII)
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Record Version |
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Classification Tree | Code System | Code | ||
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FDA ORPHAN DRUG |
555916
Created by
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NCI_THESAURUS |
C1557
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EU-Orphan Drug |
EU/3/17/1881
Created by
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NCI_THESAURUS |
C2135
Created by
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FDA ORPHAN DRUG |
537716
Created by
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SUB33651
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18771-50-1
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D013767
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112907
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100000127578
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0NIZ8H6OL8
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29243
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DTXSID6021329
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C868
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DB12484
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