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Details

Stereochemistry ACHIRAL
Molecular Formula C25H24F2N2O3
Molecular Weight 438.4665
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TUROFEXORATE ISOPROPYL

SMILES

CC(C)OC(=O)C1=CN(CC(C)(C)C2=C1NC3=C2C=CC=C3)C(=O)C4=CC=C(F)C(F)=C4

InChI

InChIKey=INASOKQDNHHMRE-UHFFFAOYSA-N
InChI=1S/C25H24F2N2O3/c1-14(2)32-24(31)17-12-29(23(30)15-9-10-18(26)19(27)11-15)13-25(3,4)21-16-7-5-6-8-20(16)28-22(17)21/h5-12,14,28H,13H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C25H24F2N2O3
Molecular Weight 438.4665
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.pharmacodia.com/yaodu/html/v1/chemicals/ba3c5e7b68dbdb900c4ee701df6cd6b5.html http://adisinsight.springer.com/drugs/800025892

Turofexorate Isopropyl (XL335) is a potent, selective, and orally bioavailable FXR agonist. Binds to the ligand-binding domain (LBD) of human FXR. Turofexorate Isopropyl resides in a predominately hydrophobic pocket with only a few polar atoms making contact with WAY-362450. Turofexorate Isopropyl promotes transcription of the human BSEP, human SHP, and mouse IBABP genes utilizing reporter constructs with EC50 of 17, 230, and 33 nM, respectively in promoter assays. Turofexorate Isopropyl had been in phase I clinical trials for the treatment of hyperlipidemia. This compound was originally discovered by Exelixis Pharmaceuticals, then licensed to Wyeth (now a wholly-owned subsidiary of Pfizer). However, the studies were discontinued.

Originator

Curator's Comment: # Exelixis

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
4.0 nM [EC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
A synthetic farnesoid X receptor (FXR) agonist promotes cholesterol lowering in models of dyslipidemia.
2009 Mar
Patents

Sample Use Guides

capsule, single oral doses from 10 mg to 450 mg
Route of Administration: Oral
Turofexorate Isopropyl (WAY-362450) at concentration of 1 μM significantly induces mRNAs encoding for BSEP, SHP, and IBABP in human cell cultures to 13-, 2-, and 20-fold, respectively. Turofexorate Isopropyl at concentration of 1 uM suppresses interleukin-6-induced CRP expression in human Hep3B hepatoma cells, and the inhibitory effect is attenuated when knockdown of FXR by short interfering RNA.
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:23:09 UTC 2023
Edited
by admin
on Sat Dec 16 17:23:09 UTC 2023
Record UNII
S6KDM312I5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TUROFEXORATE ISOPROPYL
INN   USAN   WHO-DD  
INN   USAN  
Official Name English
FXR-450
Code English
Isopropyl 3-(3,4-difluorobenzoyl)-1,1-dimethyl-1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylate
Systematic Name English
XL-335
Code English
XL335
Code English
AZEPINO(4,5-B)INDOLE-5-CARBOXYLIC ACID, 3-(3,4-DIFLUOROBENZOYL)-1,2,3,6-TETRAHYDRO-1,1-DIMETHYL-,1-METHYLETHYL ESTER
Common Name English
TUROFEXORATE ISOPROPYL [USAN]
Common Name English
WAY-362450
Code English
turofexorate isopropyl [INN]
Common Name English
Turofexorate isopropyl [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29703
Created by admin on Sat Dec 16 17:23:09 UTC 2023 , Edited by admin on Sat Dec 16 17:23:09 UTC 2023
Code System Code Type Description
DRUG BANK
DB12719
Created by admin on Sat Dec 16 17:23:09 UTC 2023 , Edited by admin on Sat Dec 16 17:23:09 UTC 2023
PRIMARY
CAS
629664-81-9
Created by admin on Sat Dec 16 17:23:09 UTC 2023 , Edited by admin on Sat Dec 16 17:23:09 UTC 2023
PRIMARY
FDA UNII
S6KDM312I5
Created by admin on Sat Dec 16 17:23:09 UTC 2023 , Edited by admin on Sat Dec 16 17:23:09 UTC 2023
PRIMARY
PUBCHEM
10026128
Created by admin on Sat Dec 16 17:23:09 UTC 2023 , Edited by admin on Sat Dec 16 17:23:09 UTC 2023
PRIMARY
EPA CompTox
DTXSID90978825
Created by admin on Sat Dec 16 17:23:09 UTC 2023 , Edited by admin on Sat Dec 16 17:23:09 UTC 2023
PRIMARY
INN
9095
Created by admin on Sat Dec 16 17:23:09 UTC 2023 , Edited by admin on Sat Dec 16 17:23:09 UTC 2023
PRIMARY
USAN
UU-51
Created by admin on Sat Dec 16 17:23:09 UTC 2023 , Edited by admin on Sat Dec 16 17:23:09 UTC 2023
PRIMARY
SMS_ID
300000034455
Created by admin on Sat Dec 16 17:23:09 UTC 2023 , Edited by admin on Sat Dec 16 17:23:09 UTC 2023
PRIMARY
NCI_THESAURUS
C81536
Created by admin on Sat Dec 16 17:23:09 UTC 2023 , Edited by admin on Sat Dec 16 17:23:09 UTC 2023
PRIMARY
ChEMBL
CHEMBL454138
Created by admin on Sat Dec 16 17:23:09 UTC 2023 , Edited by admin on Sat Dec 16 17:23:09 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY