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Showing 1 - 9 of 9 results

Status:
US Approved Rx (2000)
First approved in 1983

Class (Stereo):
CHEMICAL (ACHIRAL)



Ranitidine, a histamine H2-receptor antagonist, is now well established as a potent inhibitor of gastric acid secretion effective in the treatment and prophylaxis of gastrointestinal lesions aggravated by gastric acid secretion.
Status:
Investigational

Class (Stereo):
CHEMICAL (ABSOLUTE)


Ecopipam (SCH-39166) is a selective D1 dopamine receptor antagonist both in vitro and in vivo. Additionally, it exhibits saturable, high-affinity binding to D5 receptors. Ecopipam was studied clinically for a variety of indications, including schizop...
Status:
Other

Class (Stereo):
CHEMICAL (ABSOLUTE)

Conditions:

Benazepril Related Compound A, it is an Impurity. Benazepril is a prodrug which is metabolized by the liver into its active form benazeprilat via cleavage of the drug's ester group. Benazepril and Benazeprilat inhibit angiotensin-converting enzyme (A...
Status:
US Approved Rx (2000)
First approved in 1983

Class (Stereo):
CHEMICAL (ACHIRAL)



Ranitidine, a histamine H2-receptor antagonist, is now well established as a potent inhibitor of gastric acid secretion effective in the treatment and prophylaxis of gastrointestinal lesions aggravated by gastric acid secretion.
Status:
US Approved Rx (2000)
First approved in 1983

Class (Stereo):
CHEMICAL (ACHIRAL)



Ranitidine, a histamine H2-receptor antagonist, is now well established as a potent inhibitor of gastric acid secretion effective in the treatment and prophylaxis of gastrointestinal lesions aggravated by gastric acid secretion.
Status:
Investigational

Class (Stereo):
CHEMICAL (ABSOLUTE)


Ecopipam (SCH-39166) is a selective D1 dopamine receptor antagonist both in vitro and in vivo. Additionally, it exhibits saturable, high-affinity binding to D5 receptors. Ecopipam was studied clinically for a variety of indications, including schizop...
Status:
Other

Class (Stereo):
CHEMICAL (ABSOLUTE)

Conditions:

Benazepril Related Compound A, it is an Impurity. Benazepril is a prodrug which is metabolized by the liver into its active form benazeprilat via cleavage of the drug's ester group. Benazepril and Benazeprilat inhibit angiotensin-converting enzyme (A...
Status:
US Approved Rx (2004)
First approved in 1991

Class (Stereo):
CHEMICAL (RACEMIC)



BENAZEPRIL, (±)- is an impurity referred to as Related Compound B, which is a diastereomer of benazepril, an ACE inhibitor, under the brand name Lotensin used primarily in treatment of hypertension, congestive heart failure, and heart attacks, and al...