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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H16N2OS2
Molecular Weight 268.398
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of APRIKALIM

SMILES

CNC(=S)[C@@]1(CCCC[S@+]1[O-])C2=CN=CC=C2

InChI

InChIKey=GKEMHVLBZNVZOI-SJKOYZFVSA-N
InChI=1S/C12H16N2OS2/c1-13-11(16)12(6-2-3-8-17(12)15)10-5-4-7-14-9-10/h4-5,7,9H,2-3,6,8H2,1H3,(H,13,16)/t12-,17-/m1/s1

HIDE SMILES / InChI
Aprikalim [RP 52891, RPG 52891] is a potent, specific, and selective opener of ATP-sensitive K+ (KATP) channels. By virtue of this pharmacological property, aprikalim affords cardioprotection in experimental models of ischemia/reperfusion injury, and, at higher doses, also causes peripheral or coronary vasodilatation. It is undergoing phase II clinical trials with Aventis Pharma for the treatment of asthma; heart failure; hypertension; myocardial ischaemia.

Approval Year

PubMed

PubMed

TitleDatePubMed
Effect of subarachnoid hemorrhage on dilatation of rat basilar artery in vivo.
1996-07
In vivo reactivity of resistance arterioles to activation of ATP-sensitive K+ channels.
1993-09-21
Role of ATP-sensitive potassium channels in the basilar artery.
1993-01
Cross tolerance between cromakalim and RP49356 in the uterus of the rat in vivo and in vitro.
1992-09-04

Sample Use Guides

In Vitro Use Guide
When smooth muscle cells of the rat portal vein were clamped at -10 mV, aprikalim (3 uM) induced a slowly-developing K-current (IKCO), the noise of which gradually increased. Aprikalim (3 uM) inhibited the slowly activating, slowly inactivating delayed rectifier current, ITO.
Name Type Language
APRIKALIM
INN  
INN  
Official Name English
aprikalim [INN]
Preferred Name English
(-)-(1R,2R)-TETRAHYDRO-N-METHYL-2-(3-PYRIDYL)THIO-2H-THIOPYRAN-2-CARBOXAMIDE 1-OXIDE
Systematic Name English
2H-THIOPYRAN-2-CARBOTHIOAMIDE, TETRAHYDRO-N-METHYL-2-(3-PYRIDINYL)-, 1-OXIDE, (1R,2R)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C270
Created by admin on Mon Mar 31 18:42:33 GMT 2025 , Edited by admin on Mon Mar 31 18:42:33 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID60869099
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PRIMARY
SMS_ID
100000087181
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CAS
132562-26-6
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INN
6716
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EVMPD
SUB05541MIG
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MESH
C061043
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NCI_THESAURUS
C77145
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PUBCHEM
9571083
Created by admin on Mon Mar 31 18:42:33 GMT 2025 , Edited by admin on Mon Mar 31 18:42:33 GMT 2025
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FDA UNII
374BH4KVRG
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ChEMBL
CHEMBL302180
Created by admin on Mon Mar 31 18:42:33 GMT 2025 , Edited by admin on Mon Mar 31 18:42:33 GMT 2025
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