Search results
Results from the WOW.Com Content Network
[4] [7] Conversely, extended-release forms of phenylpropanolamine reach peak levels after 3.0 to 4.5 hours. [4] The pharmacokinetics of phenylpropanolamine are linear across an oral dose range of 25 to 100 mg. [4] Steady-state levels of phenylpropanolamine are achieved within 12 hours when the drug is taken once every 4 hours. [4]
Bucinnazine (AP-237, 1-butyryl-4-cinnamylpiperazine) is an opioid analgesic drug that was widely used in China to treat pain in cancer patients as of 1986. [1] It is one of the most potent compounds among a series of piperazine- amides first synthesized and reported in Japan in the 1970s.
100 mg testosterone decanoate [1] Cumulatively, a 1 ml of the oil solution contains exactly 250 mg of above mentioned testosterone esters. [2] [3] This particular numerical value is clearly depicted in the name of the product, Sustanon 250. [4] They are provided as an oil solution and are administered by intramuscular injection. [5]
Testosterone phenylpropionate (BAN Tooltip British Approved Name; TPP) (brand name Testolent), or testosterone phenpropionate, also known as testosterone hydrocinnamate, is a synthetic anabolic-androgenic steroid (AAS) and an androgen ester – specifically, the C17β phenyl propionate ester of testosterone – which was formerly marketed in Romania.
This drug article relating to the nervous system is a stub. You can help Wikipedia by expanding it.
Caramiphen is an anticholinergic drug used in the treatment of Parkinson's disease. [1] In combination with phenylpropanolamine it is used as a cough suppressant and nasal decongestant to treat symptoms associated with respiratory illnesses such as cold, allergies, hay fever, and sinusitis. [2]
Benzyl (2E)-3-phenylprop-2-enoate. Other names Benzyl cinnamate Cinnamein Benzyl cinnamoate Benzyl 3-phenylpropenoate 3-Phenyl-2-propenoic acid phenylmethyl ester
Halogenation of the alcohol in muriatic acid afforded 4-Chlorobenzhydryl chloride [134-83-8] (3). Alkylation with one equivalent of piperazine gives 1-(4-Chlorobenzhydryl)piperazine [303-26-4] ( 4 ). Alkylation of the remaining nitrogen with Cinnamyl Bromide [4392-24-9] ( 5 ) completed the synthesis of Clocinizine ( 6 ).