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Status:
US Previously Marketed
Source:
Aptrol by Smith Kline & French
(1949)
Source URL:
First approved in 1949
Source:
Aptrol by Smith Kline & French
Source URL:
Class (Stereo):
CHEMICAL (RACEMIC)
Status:
First approved in 1949
Class (Stereo):
CHEMICAL (ABSOLUTE)
Conditions:
Aurothioglucose (trade name Solganal), also known as gold thioglucose, is a glucose derivative formerly used to treat rheumatoid arthritis, that cannot be adequately controlled by other medicines. Aurothioglucose has been shown to inhibit protein kinase C, a metalloenzyme containing Zn(2+) bound to cysteine and histidine residues, which plays a crucial role in intracellular signal transduction by phosphorylating serine/threonine residues in the protein. The inhibition of protein kinase C has been suggested as a possible mode of action for the therapeutic antirheumatic action of gold drugs. In 2001, aurothioglucose was withdrawn from the Dutch market, where it had been the only injectable gold preparation available since 1943, forcing hospitals to change medication for a large number of patients to aurothiomalate. The drug had been in use for more than 70 years, and four years later the reasons for its sudden disappearance remained unclear.
Status:
First approved in 1949
Class (Stereo):
CHEMICAL (RACEMIC)
Conditions:
THIANTOIN (also known as phethenylate) is an anticonvulsant drug.
Status:
First approved in 1949
Class (Stereo):
CHEMICAL (ACHIRAL)
Nitrosulfathiazole, a sulfonamide drug, is an antibacterial agent. It was marketed under the brand name Nisulfazole (Sterling Winthrop). Nisulfazole was used in the treatment of ulcerative colitis.
Status:
US Previously Marketed
Source:
FLOROPRYL 0.1 PCT. by MSD
(1961)
Source URL:
First approved in 1949
Class (Stereo):
CHEMICAL (ACHIRAL)
Targets:
Conditions:
Isofluorophate (diisopropyl fluorophosphate) is an irreversile acetylcholinesterase inhibitor. It was used in ophthalmology as a miotic agent in treatment of chronic glaucoma.
Status:
US Previously Marketed
First approved in 1949
Class (Stereo):
CHEMICAL (RACEMIC)
Conditions:
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:
METUBINE IODIDE by LILLY
(1949)
Source URL:
First approved in 1949
Source:
METUBINE IODIDE by LILLY
Source URL:
Class (Stereo):
CHEMICAL (ABSOLUTE)
Targets:
Conditions:
Metocurine, also known as dimethyltubocurarine, is a non-depolarizing muscle relaxant through the neuromuscular blockade. It antagonizes the neurotransmitter action of acetylcholine by binding competitively with cholinergic receptor sites on the motor end-plate. Patients chronically receiving anticonvulsants are relatively resistant to metocurine.
Status:
First approved in 1949
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
PARATHIAZINE, a member of phenothiazines, is a histamine receptor antagonist used for the treatment of allergic diseases. Also, it can be used as an antiemetic agent.
Status:
US Previously Marketed
Source:
Benodaine by Merck Sharp & Dohme
(1949)
Source URL:
First approved in 1949
Source:
Benodaine by Merck Sharp & Dohme
Source URL:
Class (Stereo):
CHEMICAL (RACEMIC)
Piperoxan is the first antihistamine was discovered. Piperoxan protected guinea pigs against histamine-induced bronchospasm. The piperoxan has been used to provoke anxiety behaviors in the monkey. Piperoxan is an alpha-adrenergic antagonist. Piperoxan has been claimed to preferentially block presynaptic alpha-adrenoreceptors leading to an increase in noradrenaline release and by this way the postsynaptic alpha-adrenoreceptors blockade may be overcome. There was clear evidence that piperoxan enhanced myocardial performance. Piperoxan is a diagnostic aid used in studies of hypertension.
Status:
US Previously Marketed
Source:
RONIACOL W/AMINOPHYLLI NICOTINYL ALCOHOL by ROCHE
(1961)
Source URL:
First approved in 1949
Class (Stereo):
CHEMICAL (ACHIRAL)
Nicotinyl alcohol is a direct-acting vasolidator, that may decrease the blood pressure and it is a cholesterol-lowering agent. Nicotinyl alcohol as a tartrate salt led to the efficiency improvements in patients with intermittent claudication. In addition, nicotinyl alcohol alone or associated with other drugs was studied in the treatment of radicular syndromes; and was shown, that the effect had not been due to mechanical compression.