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Details

Stereochemistry ACHIRAL
Molecular Formula C12H6ClF3N4O3
Molecular Weight 346.649
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of JNJ-42041935

SMILES

OC(=O)C1=CN(N=C1)C2=NC3=CC(OC(F)(F)F)=C(Cl)C=C3N2

InChI

InChIKey=FXHHASJVTYRJHH-UHFFFAOYSA-N
InChI=1S/C12H6ClF3N4O3/c13-6-1-7-8(2-9(6)23-12(14,15)16)19-11(18-7)20-4-5(3-17-20)10(21)22/h1-4H,(H,18,19)(H,21,22)

HIDE SMILES / InChI

Molecular Formula C12H6ClF3N4O3
Molecular Weight 346.649
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

JNJ 42041935 is a potent, 2-oxoglutarate competitive, reversible, and selective inhibitor of PHD enzymes. Administration of JNJ-42041935 to rats for 5 consecutive days resulted in a 2-fold increase in reticulocytes, an increase in hemoglobin, and an increase in the hematocrit. It may be an effective means to treat anemia of various origin, in which current treatments are ineffective or not optimal.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
7.91 null [pKi]
7.29 null [pKi]
7.65 null [pKi]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
The stabilization of hypoxia inducible factor modulates differentiation status and inhibits the proliferation of mouse embryonic stem cells.
2016 Jan 25
Patents

Sample Use Guides

100 uM/kg, once a day for 14 days
Route of Administration: Oral
JNJ-42041935 was highly selective for PHD relative to factor-inhibiting hypoxia-inducible factor (FIH) (pIC50 = 4).
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:06:15 GMT 2023
Edited
by admin
on Sat Dec 16 09:06:15 GMT 2023
Record UNII
T4PPL01131
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
JNJ-42041935
Common Name English
1H-PYRAZOLE-4-CARBOXYLIC ACID, 1-(6-CHLORO-5-(TRIFLUOROMETHOXY)-1H-BENZIMIDAZOL-2-YL)-
Systematic Name English
Code System Code Type Description
PUBCHEM
45102710
Created by admin on Sat Dec 16 09:06:15 GMT 2023 , Edited by admin on Sat Dec 16 09:06:15 GMT 2023
PRIMARY
CAS
1193383-09-3
Created by admin on Sat Dec 16 09:06:15 GMT 2023 , Edited by admin on Sat Dec 16 09:06:15 GMT 2023
PRIMARY
FDA UNII
T4PPL01131
Created by admin on Sat Dec 16 09:06:15 GMT 2023 , Edited by admin on Sat Dec 16 09:06:15 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY