Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C20H26N4O4S |
Molecular Weight | 418.51 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12C[C@@]3(CNC(=O)N3CCNS(C)(=O)=O)CCN1CCC4=C2OC5=C4C=CC=C5
InChI
InChIKey=GTBKISRCRQUFNL-OXJNMPFZSA-N
InChI=1S/C20H26N4O4S/c1-29(26,27)22-8-11-24-19(25)21-13-20(24)7-10-23-9-6-15-14-4-2-3-5-17(14)28-18(15)16(23)12-20/h2-5,16,22H,6-13H2,1H3,(H,21,25)/t16-,20+/m0/s1
MK-467 (also known as Vatinoxan) is a peripheral α2 -adrenoceptor antagonist patented by American multinational pharmaceutical company Merck & Co., Inc. for treatment of hypertension, diabetes, obesity, and as blood platelet aggregation. In preclinical models Vatinoxan administration alleviate the unwanted cardiopulmonary effects of various α2-agonists (such as bradycardia, vasoconstriction, and hypoxemia). Because of its low lipophilicity MK-467 poorly penetrates the mammalian central nervous system and preserve the centrally mediated desired effects of α2-agonists. Simultaneous intramuscular injection of MK-467 hastened the absorption of α2-agonist drugs, which was manifested by rapid onset of sedation.
CNS Activity
Approval Year
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NCI_THESAURUS |
C29713
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FG-38
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300000023727
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C152839
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2601584
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10620
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342EYN0QFD
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342EYN0QFD
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163952
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DTXSID80921542
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114914-42-0
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ACTIVE MOIETY
SALT/SOLVATE (PARENT)