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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
Structure of VIDOFLUDIMUS

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)

HIDE SMILES / InChI

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

Description
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.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
134.0 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
Unknown

Approved Use

Unknown
Palliative
Unknown

Approved Use

Unknown
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
6.543 μg/mL
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
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
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

AUC

ValueDoseCo-administeredAnalytePopulation
100.294 μg × h/mL
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
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
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

T1/2

ValueDoseCo-administeredAnalytePopulation
30.414 h
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
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
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

Overview

OverviewOther

Other InhibitorOther SubstrateOther Inducer





Drug as perpetrator​Drug as victim

Drug as victim

TargetModalityActivityMetaboliteClinical evidence
major
minor
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
4SC-101, a novel immunosuppressive drug, inhibits IL-17 and attenuates colitis in two murine models of inflammatory bowel disease.
2010-10
New preclinical findings with vidofludimus.
2010-07
Patents

Sample Use Guides

at a dose of 35 mg once daily
Route of Administration: Oral
In Vitro Use Guide
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
by admin
on Mon Mar 31 21:11:36 GMT 2025
Edited
by admin
on Mon Mar 31 21:11:36 GMT 2025
Record UNII
8Y1PJ3VG81
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4SC-101
Preferred Name English
VIDOFLUDIMUS
INN   WHO-DD  
INN  
Official Name English
SC-12267
Code English
vidofludimus [INN]
Common Name English
1-CYCLOPENTENE-1-CARBOXYLIC ACID, 2-(((3-FLUORO-3'-METHOXY(1,1'-BIPHENYL)-4-YL)AMINO)CARBONYL)-
Common Name English
NSC-717824
Code English
SC12267
Code English
IMU-838
Code English
Vidofludimus [WHO-DD]
Common Name English
Code System Code Type Description
FDA UNII
8Y1PJ3VG81
Created by admin on Mon Mar 31 21:11:36 GMT 2025 , Edited by admin on Mon Mar 31 21:11:36 GMT 2025
PRIMARY
NCI_THESAURUS
C152873
Created by admin on Mon Mar 31 21:11:36 GMT 2025 , Edited by admin on Mon Mar 31 21:11:36 GMT 2025
PRIMARY
CAS
717824-30-1
Created by admin on Mon Mar 31 21:11:36 GMT 2025 , Edited by admin on Mon Mar 31 21:11:36 GMT 2025
PRIMARY
INN
9315
Created by admin on Mon Mar 31 21:11:36 GMT 2025 , Edited by admin on Mon Mar 31 21:11:36 GMT 2025
PRIMARY
MESH
C553728
Created by admin on Mon Mar 31 21:11:36 GMT 2025 , Edited by admin on Mon Mar 31 21:11:36 GMT 2025
PRIMARY
PUBCHEM
9820008
Created by admin on Mon Mar 31 21:11:36 GMT 2025 , Edited by admin on Mon Mar 31 21:11:36 GMT 2025
PRIMARY
DRUG BANK
DB05125
Created by admin on Mon Mar 31 21:11:36 GMT 2025 , Edited by admin on Mon Mar 31 21:11:36 GMT 2025
PRIMARY
EPA CompTox
DTXSID50431325
Created by admin on Mon Mar 31 21:11:36 GMT 2025 , Edited by admin on Mon Mar 31 21:11:36 GMT 2025
PRIMARY
NSC
717824
Created by admin on Mon Mar 31 21:11:36 GMT 2025 , Edited by admin on Mon Mar 31 21:11:36 GMT 2025
PRIMARY
SMS_ID
100000184316
Created by admin on Mon Mar 31 21:11:36 GMT 2025 , Edited by admin on Mon Mar 31 21:11:36 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
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ACTIVE MOIETY