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

Stereochemistry ABSOLUTE
Molecular Formula C25H37N5O6
Molecular Weight 503.5912
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of APIMOSTINEL

SMILES

C[C@@H](O)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N2CCC[C@@]2(CC3=CC=CC=C3)C(=O)N[C@@H]([C@@H](C)O)C(N)=O

InChI

InChIKey=DVBUEXCIEIAXPM-PJUQSVSOSA-N
InChI=1S/C25H37N5O6/c1-15(31)19(26)23(35)29-12-6-10-18(29)22(34)30-13-7-11-25(30,14-17-8-4-3-5-9-17)24(36)28-20(16(2)32)21(27)33/h3-5,8-9,15-16,18-20,31-32H,6-7,10-14,26H2,1-2H3,(H2,27,33)(H,28,36)/t15-,16-,18+,19+,20+,25-/m1/s1

HIDE SMILES / InChI

Molecular Formula C25H37N5O6
Molecular Weight 503.5912
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 23:14:28 GMT 2025
Edited
by admin
on Mon Mar 31 23:14:28 GMT 2025
Record UNII
TTT1F11FZB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
APIMOSTINEL
INN   WHO-DD  
INN  
Official Name English
apimostinel [INN]
Preferred Name English
Apimostinel [WHO-DD]
Common Name English
NRX-1074
Code English
THREONYL-PROLYL-2R-(2-BENZYL)-PROLYL-THREONINE AMIDE
Common Name English
L-THREONINAMIDE, L-THREONYL-L-PROLYL-2-(PHENYLMETHYL)-L-PROLYL-
Systematic Name English
APIMOSTINEL [USAN]
Common Name English
NRX1074
Code English
L-THREONYL-L-PROLYL-2-BENZYL-L-PROLYL-L-THREONINAMIDE N-METHYL-D-ASPARTATE
Systematic Name English
Code System Code Type Description
ChEMBL
CHEMBL3545230
Created by admin on Mon Mar 31 23:14:28 GMT 2025 , Edited by admin on Mon Mar 31 23:14:28 GMT 2025
PRIMARY
DRUG BANK
DB11784
Created by admin on Mon Mar 31 23:14:28 GMT 2025 , Edited by admin on Mon Mar 31 23:14:28 GMT 2025
PRIMARY
USAN
EF-85
Created by admin on Mon Mar 31 23:14:28 GMT 2025 , Edited by admin on Mon Mar 31 23:14:28 GMT 2025
PRIMARY
EPA CompTox
DTXSID101031863
Created by admin on Mon Mar 31 23:14:28 GMT 2025 , Edited by admin on Mon Mar 31 23:14:28 GMT 2025
PRIMARY
SMS_ID
100000174618
Created by admin on Mon Mar 31 23:14:28 GMT 2025 , Edited by admin on Mon Mar 31 23:14:28 GMT 2025
PRIMARY
INN
10362
Created by admin on Mon Mar 31 23:14:28 GMT 2025 , Edited by admin on Mon Mar 31 23:14:28 GMT 2025
PRIMARY
FDA UNII
TTT1F11FZB
Created by admin on Mon Mar 31 23:14:28 GMT 2025 , Edited by admin on Mon Mar 31 23:14:28 GMT 2025
PRIMARY
NCI_THESAURUS
C169785
Created by admin on Mon Mar 31 23:14:28 GMT 2025 , Edited by admin on Mon Mar 31 23:14:28 GMT 2025
PRIMARY
PUBCHEM
71249967
Created by admin on Mon Mar 31 23:14:28 GMT 2025 , Edited by admin on Mon Mar 31 23:14:28 GMT 2025
PRIMARY
WIKIPEDIA
NRX-1074
Created by admin on Mon Mar 31 23:14:28 GMT 2025 , Edited by admin on Mon Mar 31 23:14:28 GMT 2025
PRIMARY
CAS
1421866-48-9
Created by admin on Mon Mar 31 23:14:28 GMT 2025 , Edited by admin on Mon Mar 31 23:14:28 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY