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Details

Stereochemistry ABSOLUTE
Molecular Formula C28H30N2O6
Molecular Weight 490.5476
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PEMAFIBRATE

SMILES

CC[C@@H](OC1=CC=CC(CN(CCCOC2=CC=C(OC)C=C2)C3=NC4=CC=CC=C4O3)=C1)C(O)=O

InChI

InChIKey=ZHKNLJLMDFQVHJ-RUZDIDTESA-N
InChI=1S/C28H30N2O6/c1-3-25(27(31)32)35-23-9-6-8-20(18-23)19-30(28-29-24-10-4-5-11-26(24)36-28)16-7-17-34-22-14-12-21(33-2)13-15-22/h4-6,8-15,18,25H,3,7,16-17,19H2,1-2H3,(H,31,32)/t25-/m1/s1

HIDE SMILES / InChI
Pemafibrate (Parmodia®) is a novel, highly selective peroxisome proliferator-activated receptor (PPAR)-α modulator (SPPARM). It acts by binding to PPAR-α and regulating the expression of target genes that modulate lipid metabolism, thereby decreasing plasma triglyceride levels and increasing high-density lipoprotein cholesterol levels. Developed by Kowa Company, Ltd., oral pemafibrate has been approved in Japan for the treatment of hyperlipidaemia (including familial hyperlipidaemia). Pemafibrate is undergoing phase III development in a number of countries for the treatment of dyslipidaemias and is also in phase III development for the treatment of hypertriglyceridaemia.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
1.0 nM [EC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Parmodia

Approved Use

Indicated for the treatment of hyperlipidaemia.

Launch Date

2017
PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

The recommended dosage of oral pemafibrate is 0.1 mg twice daily (administered in the morning and evening); this dosage can be adjusted according to age and symptoms to a maximum dosage of 0.2 mg twice daily.
Route of Administration: Oral
In Vitro Use Guide
Curator's Comment: To test for a direct effect on apoB secretion by intestinal epithelial cells, polarized Caco-2/TC7 cells grown and polarized on a porous filter to mimic the human intestinal barrier, were treated with the different PPARα ligands added to the apical side. After 24 hours, medium in the basolateral compartment was collected, chylomicrons isolated by centrifugation and apoB quantified by ELISA.
Pemafibrate (K-877) (10uM) significantly decreased apoB secretion.
Name Type Language
PEMAFIBRATE
INN   WHO-DD  
INN  
Official Name English
K-13675, (R)-
Common Name English
(R)-K-13675
Code English
pemafibrate [INN]
Common Name English
Pemafibrate [WHO-DD]
Common Name English
(R)-2-(3-((N-(BENZOXAZOL-2-YL)-N-(3-(4-METHOXYPHENOXY)PROPYL)AMINO)METHYL)PHENOXY)BUTANOIC ACID
Systematic Name English
PEMAFIBRATE [MI]
Common Name English
PEMAFIBRATE [JAN]
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 934223
Created by admin on Fri Dec 15 21:32:10 GMT 2023 , Edited by admin on Fri Dec 15 21:32:10 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C166474
Created by admin on Fri Dec 15 21:32:10 GMT 2023 , Edited by admin on Fri Dec 15 21:32:10 GMT 2023
PRIMARY
DRUG CENTRAL
5248
Created by admin on Fri Dec 15 21:32:10 GMT 2023 , Edited by admin on Fri Dec 15 21:32:10 GMT 2023
PRIMARY
CAS
848259-27-8
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WIKIPEDIA
Pemafibrate
Created by admin on Fri Dec 15 21:32:10 GMT 2023 , Edited by admin on Fri Dec 15 21:32:10 GMT 2023
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INN
9692
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PRIMARY
SMS_ID
100000174784
Created by admin on Fri Dec 15 21:32:10 GMT 2023 , Edited by admin on Fri Dec 15 21:32:10 GMT 2023
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PUBCHEM
11526038
Created by admin on Fri Dec 15 21:32:10 GMT 2023 , Edited by admin on Fri Dec 15 21:32:10 GMT 2023
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MERCK INDEX
m12073
Created by admin on Fri Dec 15 21:32:10 GMT 2023 , Edited by admin on Fri Dec 15 21:32:10 GMT 2023
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EPA CompTox
DTXSID00233891
Created by admin on Fri Dec 15 21:32:10 GMT 2023 , Edited by admin on Fri Dec 15 21:32:10 GMT 2023
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FDA UNII
17VGG92R23
Created by admin on Fri Dec 15 21:32:10 GMT 2023 , Edited by admin on Fri Dec 15 21:32:10 GMT 2023
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DRUG BANK
DB15212
Created by admin on Fri Dec 15 21:32:10 GMT 2023 , Edited by admin on Fri Dec 15 21:32:10 GMT 2023
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ChEMBL
CHEMBL3545412
Created by admin on Fri Dec 15 21:32:10 GMT 2023 , Edited by admin on Fri Dec 15 21:32:10 GMT 2023
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