Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C20H18FNO4 |
| Molecular Weight | 355.3596 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC(=CC=C1)C2=CC=C(NC(=O)C3=C(CCC3)C(O)=O)C(F)=C2
InChI
InChIKey=XPRDUGXOWVXZLL-UHFFFAOYSA-N
InChI=1S/C20H18FNO4/c1-26-14-5-2-4-12(10-14)13-8-9-18(17(21)11-13)22-19(23)15-6-3-7-16(15)20(24)25/h2,4-5,8-11H,3,6-7H2,1H3,(H,22,23)(H,24,25)
| Molecular Formula | C20H18FNO4 |
| Molecular Weight | 355.3596 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/23078909Curator's Comment: description was created based on several sources, including
http://www.4sc.de/wp-content/uploads/Poster-Tokyo.pdf
Sources: https://www.ncbi.nlm.nih.gov/pubmed/23078909
Curator's Comment: description was created based on several sources, including
http://www.4sc.de/wp-content/uploads/Poster-Tokyo.pdf
Vidofludimus (SC12267; 4SC-101) is a novel oral immunomodulator inhibiting dihydroorotate dehydrogenase (DHODH) and the expression of proinflammatory cytokines including interleukin-17 (IL17A and IL17F) and interferon-gamma. This drug is in the clinical trial for the treatment of inflammatory bowel diseases and Rheumatoid arthritis.
Originator
Approval Year
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
6.543 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32361977 |
28.4 mg 1 times / day multiple, oral dose: 28.4 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
VIDOFLUDIMUS plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
10.911 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32361977 |
37.8 mg 1 times / day multiple, oral dose: 37.8 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
VIDOFLUDIMUS plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
10.783 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32361977 |
47.3 mg 1 times / day multiple, oral dose: 47.3 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
VIDOFLUDIMUS plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
100.294 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32361977 |
28.4 mg 1 times / day multiple, oral dose: 28.4 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
VIDOFLUDIMUS plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
158.686 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32361977 |
37.8 mg 1 times / day multiple, oral dose: 37.8 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
VIDOFLUDIMUS plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
166.401 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32361977 |
47.3 mg 1 times / day multiple, oral dose: 47.3 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
VIDOFLUDIMUS plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
30.414 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32361977 |
28.4 mg 1 times / day multiple, oral dose: 28.4 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
VIDOFLUDIMUS plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
28.566 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32361977 |
37.8 mg 1 times / day multiple, oral dose: 37.8 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
VIDOFLUDIMUS plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: FASTED |
|
29.805 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/32361977 |
47.3 mg 1 times / day multiple, oral dose: 47.3 mg route of administration: Oral experiment type: MULTIPLE co-administered: |
VIDOFLUDIMUS plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
Overview
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
Drug as perpetrator
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
| inconclusive [IC50 26.837 uM] | ||||
| inconclusive [IC50 26.837 uM] | ||||
| inconclusive [IC50 8.1995 uM] | ||||
| weak | ||||
| yes [IC50 0.02 uM] | ||||
| yes [IC50 21.3174 uM] | ||||
| yes |
Drug as victim
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
| major | ||||
| minor |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20310011
Curator's Comment: Peripheral blood mononuclear cells (PBMCs) from healthy human donors were used to evaluate cellular proliferation and cytokine (IL-17, TNF-α) production. 4SC-101 (VIDOFLUDIMUS) is a potent inhibitor of human Dihydroorotate dehydrogenase (DHODH), inhibits lymphocyte proliferation, and uniquely blocks phytohemagglutinin-stimulated IL-17 production by lymphocytes.
Unknown
| Substance Class |
Chemical
Created
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Edited
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8Y1PJ3VG81
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TARGET -> INHIBITOR | |||
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |