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

Details

Stereochemistry ACHIRAL
Molecular Formula C34H52N18O2
Molecular Weight 744.8961
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 4
Charge 0

SHOW SMILES / InChI
Structure of SEMAPIMOD

SMILES

C\C(=N/NC(N)=N)C1=CC(=CC(NC(=O)CCCCCCCCC(=O)NC2=CC(=CC(=C2)C(\C)=N\NC(N)=N)C(\C)=N\NC(N)=N)=C1)C(\C)=N\NC(N)=N

InChI

InChIKey=PWDYHMBTPGXCSN-VCBMUGGBSA-N
InChI=1S/C34H52N18O2/c1-19(45-49-31(35)36)23-13-24(20(2)46-50-32(37)38)16-27(15-23)43-29(53)11-9-7-5-6-8-10-12-30(54)44-28-17-25(21(3)47-51-33(39)40)14-26(18-28)22(4)48-52-34(41)42/h13-18H,5-12H2,1-4H3,(H,43,53)(H,44,54)(H4,35,36,49)(H4,37,38,50)(H4,39,40,51)(H4,41,42,52)/b45-19+,46-20+,47-21+,48-22+

HIDE SMILES / InChI

Molecular Formula C34H52N18O2
Molecular Weight 744.8961
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 4
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:30:01 UTC 2023
Edited
by admin
on Fri Dec 15 18:30:01 UTC 2023
Record UNII
9SGW2H1K8P
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SEMAPIMOD
INN  
INN  
Official Name English
N,N'-BIS(3,5-BIS(1- (CARBAMIMIDOYLHYDRAZONO)ETHYL)PHENYL)DECANEDIAMIDE
Common Name English
semapimod [INN]
Common Name English
CPSI-2364 FREE BASE
Code English
Classification Tree Code System Code
NCI_THESAURUS C2149
Created by admin on Fri Dec 15 18:30:01 UTC 2023 , Edited by admin on Fri Dec 15 18:30:01 UTC 2023
Code System Code Type Description
WIKIPEDIA
SEMAPIMOD
Created by admin on Fri Dec 15 18:30:01 UTC 2023 , Edited by admin on Fri Dec 15 18:30:01 UTC 2023
PRIMARY
EPA CompTox
DTXSID70870333
Created by admin on Fri Dec 15 18:30:01 UTC 2023 , Edited by admin on Fri Dec 15 18:30:01 UTC 2023
PRIMARY
PUBCHEM
5745214
Created by admin on Fri Dec 15 18:30:01 UTC 2023 , Edited by admin on Fri Dec 15 18:30:01 UTC 2023
PRIMARY
SMS_ID
100000175237
Created by admin on Fri Dec 15 18:30:01 UTC 2023 , Edited by admin on Fri Dec 15 18:30:01 UTC 2023
PRIMARY
FDA UNII
9SGW2H1K8P
Created by admin on Fri Dec 15 18:30:01 UTC 2023 , Edited by admin on Fri Dec 15 18:30:01 UTC 2023
PRIMARY
INN
8349
Created by admin on Fri Dec 15 18:30:01 UTC 2023 , Edited by admin on Fri Dec 15 18:30:01 UTC 2023
PRIMARY
NCI_THESAURUS
C96535
Created by admin on Fri Dec 15 18:30:01 UTC 2023 , Edited by admin on Fri Dec 15 18:30:01 UTC 2023
PRIMARY
ChEMBL
CHEMBL2107779
Created by admin on Fri Dec 15 18:30:01 UTC 2023 , Edited by admin on Fri Dec 15 18:30:01 UTC 2023
PRIMARY
DRUG BANK
DB12094
Created by admin on Fri Dec 15 18:30:01 UTC 2023 , Edited by admin on Fri Dec 15 18:30:01 UTC 2023
PRIMARY
CAS
352513-83-8
Created by admin on Fri Dec 15 18:30:01 UTC 2023 , Edited by admin on Fri Dec 15 18:30:01 UTC 2023
PRIMARY
MESH
C097256
Created by admin on Fri Dec 15 18:30:01 UTC 2023 , Edited by admin on Fri Dec 15 18:30:01 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
TARGET -> AGONIST
CNI-1493 was found to be effective for resolving of endotoxic shock in a rat model. In a clinical trial, CNI-1493 was examined as a drug for the treatment of Crohn’s disease, a disease associated with inflammation. The investigators reported no plausible effect for CNI-1493 single and 3 day dosing. However, cumulative dosing brings some positive effects to Crohn’s disease therapy.
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY