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Details

Stereochemistry RACEMIC
Molecular Formula C17H37N7O3
Molecular Weight 387.5208
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GUSPERIMUS

SMILES

NCCCNCCCCNC(=O)C(O)NC(=O)CCCCCCNC(N)=N

InChI

InChIKey=IDINUJSAMVOPCM-UHFFFAOYSA-N
InChI=1S/C17H37N7O3/c18-9-7-11-21-10-5-6-12-22-15(26)16(27)24-14(25)8-3-1-2-4-13-23-17(19)20/h16,21,27H,1-13,18H2,(H,22,26)(H,24,25)(H4,19,20,23)

HIDE SMILES / InChI

Molecular Formula C17H37N7O3
Molecular Weight 387.5208
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 17:24:50 UTC 2023
Edited
by admin
on Fri Dec 15 17:24:50 UTC 2023
Record UNII
UJ0ZJ76DO9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GUSPERIMUS
INN   MI   WHO-DD  
INN  
Official Name English
Gusperimus [WHO-DD]
Common Name English
(±)-N-(((4-((3-AMINOPROPYL)AMINO)BUTYL)CARBAMOYL)HYDROXYMETHYL)-7-GUANIDINOHEPTANAMIDE
Systematic Name English
(±)-15-DEOXYSPERGUALIN
Common Name English
HEPTANAMIDE, 7-((AMINOIMINOMETHYL)AMINO)-N-(2-((4-((3-AMINOPROPYL)AMINO)BUTYL)AMINO)-1-HYDROXY-2-OXOETHYL)-
Systematic Name English
GUSPERIMUS [MI]
Common Name English
gusperimus [INN]
Common Name English
(±)-DEOXYSPERGUALIN
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 96896
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
WHO-ATC L04AA19
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
WHO-VATC QL04AA19
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
NCI_THESAURUS C574
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID60861078
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
PRIMARY
NCI_THESAURUS
C128052
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
PRIMARY
FDA UNII
UJ0ZJ76DO9
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
PRIMARY
CAS
104317-84-2
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
SUPERSEDED
DRUG CENTRAL
1347
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
PRIMARY
SMS_ID
100000085438
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
PRIMARY
WIKIPEDIA
GUSPERIMUS
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
PRIMARY
MESH
C037258
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
PRIMARY
CAS
98629-43-7
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
PRIMARY
PUBCHEM
55362
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
PRIMARY
INN
6941
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
PRIMARY
MERCK INDEX
m5887
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
PRIMARY Merck Index
EVMPD
SUB07991MIG
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
PRIMARY
DRUG BANK
DB12692
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
PRIMARY
ChEMBL
CHEMBL406117
Created by admin on Fri Dec 15 17:24:50 UTC 2023 , Edited by admin on Fri Dec 15 17:24:50 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY