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

    {{facet.count}}
    {{facet.count}}

    {{facet.count}}
    {{facet.count}}

    {{facet.count}}
    {{facet.count}}

    {{facet.count}}
    {{facet.count}}

    {{facet.count}}
    {{facet.count}}
Status:
Investigational
Source:
INN:naprodoxime [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Naprodoxime is an antidepressant, antiaggressive agent.
Status:
US Previously Marketed
Source:
Dichlor Mapharsen by Parke-Davis
(1945)
Source URL:
First approved in 1945
Source:
Dichlor Mapharsen by Parke-Davis
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Dichlorophenarsine is a potent anti-syphilitic drug, which exhibits a rapid effect on the serological reactions of the blood in early syphilis. Dichlorophenarsine was more rapid than thiacetarsamide sodium in its action against the canine heartworms infections. Dichlorophenarsine was used for the treatment of canine filariasis - emesia, nausea, and shock occurred several to 30 minutes after injection. Ascorbic acid and hesperidin methyl chalcone when used as a combined therapy afforded a definite protection in mice against the toxic effect of a single dose of intravenously administered dichlorophenarsine hydrochloride.
Status:
Investigational
Source:
INN:naprodoxime [INN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Naprodoxime is an antidepressant, antiaggressive agent.
Status:
US Previously Marketed
Source:
Dichlor Mapharsen by Parke-Davis
(1945)
Source URL:
First approved in 1945
Source:
Dichlor Mapharsen by Parke-Davis
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Dichlorophenarsine is a potent anti-syphilitic drug, which exhibits a rapid effect on the serological reactions of the blood in early syphilis. Dichlorophenarsine was more rapid than thiacetarsamide sodium in its action against the canine heartworms infections. Dichlorophenarsine was used for the treatment of canine filariasis - emesia, nausea, and shock occurred several to 30 minutes after injection. Ascorbic acid and hesperidin methyl chalcone when used as a combined therapy afforded a definite protection in mice against the toxic effect of a single dose of intravenously administered dichlorophenarsine hydrochloride.