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Details

Stereochemistry ACHIRAL
Molecular Formula C23H32N6
Molecular Weight 392.5404
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TOREFORANT

SMILES

CN1CCC(CCCNC2=NC=C(C3=NC4=C(C)C=C(C)C=C4N3)C(C)=N2)CC1

InChI

InChIKey=FCRFVPZAXGJLPW-UHFFFAOYSA-N
InChI=1S/C23H32N6/c1-15-12-16(2)21-20(13-15)27-22(28-21)19-14-25-23(26-17(19)3)24-9-5-6-18-7-10-29(4)11-8-18/h12-14,18H,5-11H2,1-4H3,(H,27,28)(H,24,25,26)

HIDE SMILES / InChI

Molecular Formula C23H32N6
Molecular Weight 392.5404
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Toreforant (JNJ-38518168) is an orally active, selective histamine H4 receptor antagonist. Toreforant was investigated as an agent for the treatment of active rheumatoid arthritis. While some improvement in rheumatoid arthritis signs/symptoms through week 12 was observed in the phase IIa study, no efficacy was observed with toreforant at lower doses in a subsequent phase IIb study. Toreforant has been tested in clinical studies in patients with asthma and psoriasis. Toreforant failed to provide therapeutic benefit in population of patients with uncontrolled, eosinophilic, persistent asthma. Toreforant efficacy at 30 and 60 mg was greater than placebo but did not meet predefined success criterion in patients with moderate-to-severe psoriasis.

Approval Year

PubMed

PubMed

TitleDatePubMed
Clinical Development of Histamine H(4) Receptor Antagonists.
2017
Efficacy and Safety of Toreforant, a Selective Histamine H4 Receptor Antagonist, for the Treatment of Moderate-to-Severe Plaque Psoriasis: Results from a Phase 2 Multicenter, Randomized, Double-blind, Placebo-controlled Trial.
2018 Aug 1
Toreforant, an orally active histamine H(4)-receptor antagonist, in patients with active rheumatoid arthritis despite methotrexate: mechanism of action results from a phase 2, multicenter, randomized, double-blind, placebo-controlled synovial biopsy study.
2019 Apr
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:11:25 UTC 2023
Edited
by admin
on Sat Dec 16 09:11:25 UTC 2023
Record UNII
U6LA7G393X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TOREFORANT
INN   USAN   WHO-DD  
USAN   INN  
Official Name English
TOREFORANT [USAN]
Common Name English
JNJ-38518168
Code English
Toreforant [WHO-DD]
Common Name English
toreforant [INN]
Common Name English
2-PYRIMIDINAMINE, 5-(5,7-DIMETHYL-1H-BENZIMIDAZOL-2-YL)-4-METHYL-N-(3-(1-METHYL-4-PIPERIDINYL)PROPYL)-
Systematic Name English
5-(4,6-DIMETHYL-1H-BENZIMIDAZOL-2-YL)-4-METHYL-N-(3-(1-METHYL-4-PIPERIDINYL)PROPYL)-2-PYRIMIDINAMINE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29708
Created by admin on Sat Dec 16 09:11:25 UTC 2023 , Edited by admin on Sat Dec 16 09:11:25 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C152698
Created by admin on Sat Dec 16 09:11:25 UTC 2023 , Edited by admin on Sat Dec 16 09:11:25 UTC 2023
PRIMARY
INN
10046
Created by admin on Sat Dec 16 09:11:25 UTC 2023 , Edited by admin on Sat Dec 16 09:11:25 UTC 2023
PRIMARY
ChEMBL
CHEMBL3301609
Created by admin on Sat Dec 16 09:11:25 UTC 2023 , Edited by admin on Sat Dec 16 09:11:25 UTC 2023
PRIMARY
WIKIPEDIA
Toreforant
Created by admin on Sat Dec 16 09:11:25 UTC 2023 , Edited by admin on Sat Dec 16 09:11:25 UTC 2023
PRIMARY
SMS_ID
300000034367
Created by admin on Sat Dec 16 09:11:25 UTC 2023 , Edited by admin on Sat Dec 16 09:11:25 UTC 2023
PRIMARY
CAS
952494-46-1
Created by admin on Sat Dec 16 09:11:25 UTC 2023 , Edited by admin on Sat Dec 16 09:11:25 UTC 2023
PRIMARY
FDA UNII
U6LA7G393X
Created by admin on Sat Dec 16 09:11:25 UTC 2023 , Edited by admin on Sat Dec 16 09:11:25 UTC 2023
PRIMARY
PUBCHEM
23650961
Created by admin on Sat Dec 16 09:11:25 UTC 2023 , Edited by admin on Sat Dec 16 09:11:25 UTC 2023
PRIMARY
EPA CompTox
DTXSID701336756
Created by admin on Sat Dec 16 09:11:25 UTC 2023 , Edited by admin on Sat Dec 16 09:11:25 UTC 2023
PRIMARY
USAN
BC-68
Created by admin on Sat Dec 16 09:11:25 UTC 2023 , Edited by admin on Sat Dec 16 09:11:25 UTC 2023
PRIMARY
DRUG BANK
DB12522
Created by admin on Sat Dec 16 09:11:25 UTC 2023 , Edited by admin on Sat Dec 16 09:11:25 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY