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Details

Stereochemistry RACEMIC
Molecular Formula C20H34N2O4
Molecular Weight 366.495
Optical Activity ( + / - )
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SPIRIPROSTIL

SMILES

CCCCCC[C@H]1CC[C@]2(NC(=O)NC2=O)[C@@H]1CCCCCCC(O)=O

InChI

InChIKey=FFUQYYWTQVXVNM-YRNRMSPPSA-N
InChI=1S/C20H34N2O4/c1-2-3-4-7-10-15-13-14-20(18(25)21-19(26)22-20)16(15)11-8-5-6-9-12-17(23)24/h15-16H,2-14H2,1H3,(H,23,24)(H2,21,22,25,26)/t15-,16+,20-/m0/s1

HIDE SMILES / InChI

Molecular Formula C20H34N2O4
Molecular Weight 366.495
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Spiriprostil (IBI-P-01028 or R,S-cis-6-(6'-carboxyhexyl)-7-trans-n-hexyl-1,3-diazaspiro-[4-4]-nona n-2,4- dione) is a cytoprotective agent. It is an anti-ulcer agent.

Approval Year

PubMed

PubMed

TitleDatePubMed
Mass spectrometric identification of urinary and plasma metabolites of 6-(6'-carboxyhexyl)-7-n-hexyl-1,3-diazaspiro-[4-4]-nonan-2,4-dione, a new cytoprotective agent.
1991 Sep-Oct
Patents

Patents

Sample Use Guides

Dogs: after a single oral dose of 50 mg/kg, the compound is rapidly adsorbed and reaches a maximum blood concentration after 90 min. Drug accumulation was assessed in dogs given multiple 50 mg/kg doses; this dose showed cytoprotective activities in laboratory animals.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:39:38 GMT 2023
Edited
by admin
on Fri Dec 15 18:39:38 GMT 2023
Record UNII
Q2LN8K1MS7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SPIRIPROSTIL
INN  
INN  
Official Name English
spiriprostil [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C78568
Created by admin on Fri Dec 15 18:39:38 GMT 2023 , Edited by admin on Fri Dec 15 18:39:38 GMT 2023
NCI_THESAURUS C29701
Created by admin on Fri Dec 15 18:39:38 GMT 2023 , Edited by admin on Fri Dec 15 18:39:38 GMT 2023
Code System Code Type Description
CAS
122946-42-3
Created by admin on Fri Dec 15 18:39:38 GMT 2023 , Edited by admin on Fri Dec 15 18:39:38 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104909
Created by admin on Fri Dec 15 18:39:38 GMT 2023 , Edited by admin on Fri Dec 15 18:39:38 GMT 2023
PRIMARY
NCI_THESAURUS
C66564
Created by admin on Fri Dec 15 18:39:38 GMT 2023 , Edited by admin on Fri Dec 15 18:39:38 GMT 2023
PRIMARY
EPA CompTox
DTXSID00153803
Created by admin on Fri Dec 15 18:39:38 GMT 2023 , Edited by admin on Fri Dec 15 18:39:38 GMT 2023
PRIMARY
INN
6569
Created by admin on Fri Dec 15 18:39:38 GMT 2023 , Edited by admin on Fri Dec 15 18:39:38 GMT 2023
PRIMARY
PUBCHEM
6445090
Created by admin on Fri Dec 15 18:39:38 GMT 2023 , Edited by admin on Fri Dec 15 18:39:38 GMT 2023
PRIMARY
FDA UNII
Q2LN8K1MS7
Created by admin on Fri Dec 15 18:39:38 GMT 2023 , Edited by admin on Fri Dec 15 18:39:38 GMT 2023
PRIMARY
SMS_ID
100000083826
Created by admin on Fri Dec 15 18:39:38 GMT 2023 , Edited by admin on Fri Dec 15 18:39:38 GMT 2023
PRIMARY
EVMPD
SUB10626MIG
Created by admin on Fri Dec 15 18:39:38 GMT 2023 , Edited by admin on Fri Dec 15 18:39:38 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY