U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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There is one exact (name or code) match for methoxamine

 
Status:
US Previously Marketed
Source:
Vasoxyl by Burroughs Wellcome
(1949)
Source URL:
First approved in 1949
Source:
Vasoxyl by Burroughs Wellcome
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)



Methoxamine is an alpha-adrenergic agonist that induces prolonged peripheral vasoconstriction, and can also stimulate the release of arginine vasopressin in humans. In clinical trials, methoxamine was found to improve fecal incontinence. It had been marketed by Glaxo-Smith-Kline under the brand name Vasoxyl but has been discontinued. Methoxamine was also found to stimulate the induction of hiPSC-derived hepatoblasts to ALBUMIN+ cells.
Status:
US Previously Marketed
Source:
Vasoxyl by Burroughs Wellcome
(1949)
Source URL:
First approved in 1949
Source:
Vasoxyl by Burroughs Wellcome
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)



Methoxamine is an alpha-adrenergic agonist that induces prolonged peripheral vasoconstriction, and can also stimulate the release of arginine vasopressin in humans. In clinical trials, methoxamine was found to improve fecal incontinence. It had been marketed by Glaxo-Smith-Kline under the brand name Vasoxyl but has been discontinued. Methoxamine was also found to stimulate the induction of hiPSC-derived hepatoblasts to ALBUMIN+ cells.
Status:
Other

Class (Stereo):
CHEMICAL (ABSOLUTE)

Status:
US Previously Marketed
Source:
Vasoxyl by Burroughs Wellcome
(1949)
Source URL:
First approved in 1949
Source:
Vasoxyl by Burroughs Wellcome
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)



Methoxamine is an alpha-adrenergic agonist that induces prolonged peripheral vasoconstriction, and can also stimulate the release of arginine vasopressin in humans. In clinical trials, methoxamine was found to improve fecal incontinence. It had been marketed by Glaxo-Smith-Kline under the brand name Vasoxyl but has been discontinued. Methoxamine was also found to stimulate the induction of hiPSC-derived hepatoblasts to ALBUMIN+ cells.