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Details

Stereochemistry ABSOLUTE
Molecular Formula C16H22N6O7
Molecular Weight 410.3819
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TEOPRANITOL

SMILES

CN1C2=C(N(CCCN[C@H]3CO[C@@H]4[C@H](CO[C@H]34)O[N+]([O-])=O)C=N2)C(=O)N(C)C1=O

InChI

InChIKey=XTEGRRHNMFDROI-YRRQLQLVSA-N
InChI=1S/C16H22N6O7/c1-19-14-11(15(23)20(2)16(19)24)21(8-18-14)5-3-4-17-9-6-27-13-10(29-22(25)26)7-28-12(9)13/h8-10,12-13,17H,3-7H2,1-2H3/t9-,10-,12+,13+/m0/s1

HIDE SMILES / InChI

Molecular Formula C16H22N6O7
Molecular Weight 410.3819
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Teopranitol, a coronary vasodilator that was studied for the treatment of the acute myocardial ischemia. Animal experiments have shown that this compound stimulated the release of prostacyclin (PGI2)-like antiplatelet activity. However, the development of teopranitol was discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed
Stimulation of coronary vascular PGI2 by organic nitrates.
1988-01
Successful treatment of acute myocardial ischaemia with teopranitol--a novel organic nitrate.
1986-05
[Changes in scintigraphically determined regional blood volume in coronary patients treated with the new substance teopranitol].
1984-06
Stereospecific stimulation of coronary vascular PGI2 by organic nitrates--studies with the new compound teopranitol (KC-046).
1984
Substance Class Chemical
Created
by admin
on Wed Apr 02 07:55:22 GMT 2025
Edited
by admin
on Wed Apr 02 07:55:22 GMT 2025
Record UNII
631R1KON85
Record Status Validated (UNII)
Record Version
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Name Type Language
teopranitol [INN]
Preferred Name English
TEOPRANITOL
INN  
INN  
Official Name English
Classification Tree Code System Code
NCI_THESAURUS C29707
Created by admin on Wed Apr 02 07:55:22 GMT 2025 , Edited by admin on Wed Apr 02 07:55:22 GMT 2025
Code System Code Type Description
FDA UNII
631R1KON85
Created by admin on Wed Apr 02 07:55:22 GMT 2025 , Edited by admin on Wed Apr 02 07:55:22 GMT 2025
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EPA CompTox
DTXSID20868624
Created by admin on Wed Apr 02 07:55:22 GMT 2025 , Edited by admin on Wed Apr 02 07:55:22 GMT 2025
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CAS
81792-35-0
Created by admin on Wed Apr 02 07:55:22 GMT 2025 , Edited by admin on Wed Apr 02 07:55:22 GMT 2025
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EVMPD
SUB10902MIG
Created by admin on Wed Apr 02 07:55:22 GMT 2025 , Edited by admin on Wed Apr 02 07:55:22 GMT 2025
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SMS_ID
100000082680
Created by admin on Wed Apr 02 07:55:22 GMT 2025 , Edited by admin on Wed Apr 02 07:55:22 GMT 2025
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NCI_THESAURUS
C66586
Created by admin on Wed Apr 02 07:55:22 GMT 2025 , Edited by admin on Wed Apr 02 07:55:22 GMT 2025
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MESH
C042286
Created by admin on Wed Apr 02 07:55:22 GMT 2025 , Edited by admin on Wed Apr 02 07:55:22 GMT 2025
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INN
5431
Created by admin on Wed Apr 02 07:55:22 GMT 2025 , Edited by admin on Wed Apr 02 07:55:22 GMT 2025
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PUBCHEM
3034007
Created by admin on Wed Apr 02 07:55:22 GMT 2025 , Edited by admin on Wed Apr 02 07:55:22 GMT 2025
PRIMARY
ChEMBL
CHEMBL2107483
Created by admin on Wed Apr 02 07:55:22 GMT 2025 , Edited by admin on Wed Apr 02 07:55:22 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY