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Details

Stereochemistry ABSOLUTE
Molecular Formula C31H34NO4.Br
Molecular Weight 564.51
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENTONIUM BROMIDE

SMILES

[Br-].C[N@+]3(CC(=O)C1=CC=C(C=C1)C2=CC=CC=C2)[C@H]4CC[C@@H]3C[C@@H](C4)OC(=O)[C@H](CO)C5=CC=CC=C5

InChI

InChIKey=MPLNGQBULSHWQW-QRAMOEPWSA-M
InChI=1S/C31H34NO4.BrH/c1-32(20-30(34)25-14-12-23(13-15-25)22-8-4-2-5-9-22)26-16-17-27(32)19-28(18-26)36-31(35)29(21-33)24-10-6-3-7-11-24;/h2-15,26-29,33H,16-21H2,1H3;1H/q+1;/p-1/t26-,27+,28+,29-,32-;/m1./s1

HIDE SMILES / InChI

Molecular Formula BrH
Molecular Weight 80.912
Charge 0
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C31H33NO4
Molecular Weight 483.598
Charge 0
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 4 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Description

Fentonium is an anticholinergic, antispasmodic and anti-ulcerogenic agent. It is quaternary analog of hyoscyamine, is a blocker of muscarinic activity and an allosteric blocker of α12βγε nicotinic receptors. It increases the spontaneous release of acetylcholine at the motor endplate without depolarizing the muscle or inhibiting cholinesterase activity. Fentonium inhibited transmitter release and depressed twitch without changing the responsiveness to noradrenaline or ATP. It is a K(+)-channel opener. Administration of fentonium bromide in rats receiving naloxone after chronic morphine treatment reduced the intensity of withdrawal signs such as increased defecation or micturition, salivation and wet-dog shakes, and elevated the nociceptive threshold values.

Approval Year

PubMed

Sample Use Guides

In Vivo Use Guide
Single dose - 1, 3 or 9 mg/kg
Route of Administration: Intraperitoneal
Substance Class Chemical
Record UNII
XS152O7VCZ
Record Status Validated (UNII)
Record Version