U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C23H32ClN5O3
Molecular Weight 461.985
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DASOLAMPANEL ETIBUTIL

SMILES

[H][C@@]12CC[C@@H](C[C@]1([H])C[C@H](NC2)C(=O)OCC(CC)CC)OC3=C(C4=NN=NN4)C(Cl)=CC=C3

InChI

InChIKey=HPBRMCFZIGUGTK-ZMMAXQRCSA-N
InChI=1S/C23H32ClN5O3/c1-3-14(4-2)13-31-23(30)19-11-16-10-17(9-8-15(16)12-25-19)32-20-7-5-6-18(24)21(20)22-26-28-29-27-22/h5-7,14-17,19,25H,3-4,8-13H2,1-2H3,(H,26,27,28,29)/t15-,16+,17-,19-/m0/s1

HIDE SMILES / InChI

Molecular Formula C23H32ClN5O3
Molecular Weight 461.985
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Dasolampanel (NGX-426) is an orally available competitive antagonist of the AMPA and kainate receptors. The dug originated at Eli Lilly and Horizon Pharma and was developed for the treatment of migraine and neuropathic pain. Dasalompanel was reduced capsaicin-induced pain and hyperalgesia in human volunteers but failed to achieve positive results in phase 2 clinical trials in patients with pain due to osteoarthritis of the knee and diabetic peripheral neuropathic pain.

Approval Year

Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:40:32 GMT 2023
Edited
by admin
on Sat Dec 16 01:40:32 GMT 2023
Record UNII
M7BFC308LR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DASOLAMPANEL ETIBUTIL
USAN  
USAN  
Official Name English
3-ISOQUINOLINECARBOXYLIC ACID, 6-(3-CHLORO-2-(2H-TETRAZOL-5-YL)PHENOXY)DECAHYDRO-, 2-ETHYLBUTYL ESTER, (3S,4AS,6S,8AR)-
Common Name English
3-ISOQUINOLINECARBOXYLIC ACID, 6-(3-CHLORO-2-(1H-TETRAZOL-5-YL)PHENOXY)DECAHYDRO-, 2-ETHYLBUTYL ESTER, (3S,4AS,6S,8AR)-
Common Name English
LY-545694
Code English
DASOLAMPANEL ETIBUTIL [USAN]
Common Name English
LY545694
Code English
Code System Code Type Description
SMS_ID
100000156623
Created by admin on Sat Dec 16 01:40:32 GMT 2023 , Edited by admin on Sat Dec 16 01:40:32 GMT 2023
PRIMARY
ChEMBL
CHEMBL3545161
Created by admin on Sat Dec 16 01:40:32 GMT 2023 , Edited by admin on Sat Dec 16 01:40:32 GMT 2023
PRIMARY
FDA UNII
M7BFC308LR
Created by admin on Sat Dec 16 01:40:32 GMT 2023 , Edited by admin on Sat Dec 16 01:40:32 GMT 2023
PRIMARY
PUBCHEM
53307207
Created by admin on Sat Dec 16 01:40:32 GMT 2023 , Edited by admin on Sat Dec 16 01:40:32 GMT 2023
PRIMARY
DRUG BANK
DB12049
Created by admin on Sat Dec 16 01:40:32 GMT 2023 , Edited by admin on Sat Dec 16 01:40:32 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107328
Created by admin on Sat Dec 16 01:40:32 GMT 2023 , Edited by admin on Sat Dec 16 01:40:32 GMT 2023
PRIMARY
NCI_THESAURUS
C174696
Created by admin on Sat Dec 16 01:40:32 GMT 2023 , Edited by admin on Sat Dec 16 01:40:32 GMT 2023
PRIMARY
CAS
503291-52-9
Created by admin on Sat Dec 16 01:40:32 GMT 2023 , Edited by admin on Sat Dec 16 01:40:32 GMT 2023
PRIMARY
EVMPD
SUB130581
Created by admin on Sat Dec 16 01:40:32 GMT 2023 , Edited by admin on Sat Dec 16 01:40:32 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT