Likewise dihydroreductase inhibitors, e.g., sulfasalazine, methotrexate, triamterene, and
aminopterin, that block conversion of folate to its more active metabolites, are known to cause NTDs.
These drugs include
aminopterin sulfasalazine, pyrimethamine, triamterene, trimethoprim, and methotrexate (N.
These drugs include
aminopterin, sulfasalazine, pyrimethamine, triamterene, trimethoprim, and methotrexate, they reported (N.
During the 1940s childhood leukemias had a uniformly rapid fatal course over a short period of time, thus the designation of the term "acute."[5] In the late 1940s, Farber and colleagues[6] found that
aminopterin (a folic acid antagonist) could induce temporary remissions in leukemia.
*
aminopterin in Phase II in patients with persistent, recurrent or refractory endometrial carcinoma
Here's why: n A drug that prevents the body from using folic acid (
aminopterin) causes NTDS in mice, cats, and rats.
Hybridomas were selected in hypoxanthine
aminopterin thymidine (HAT) medium.
Good examples of vitamin antagonists include isonicotinic acid hydrazide (antagonist of pyridoxine),
aminopterin (folate antagonist), dicumarol (vitamin K antagonist), and avidin (interferes with biotin absorption).
wheat gluten contaminated with
aminopterin, a toxin used in some countries as rat poison.
The federal government prohibits using
aminopterin for killing rodents in the United States.
* In utero exposure to
aminopterin, an antagonist of folic acid, has been associated with anencephaly, meningocele, hydrocephalus, and cleft lip and palate (Thiersch 1952; Warkany et al.