- 1. (+)-2-(2-((p-Chloro-alpha-methyl-alpha-phenylbenzyl)oxy)ethyl)-1-methyl Pyrrolidine Fumarate
- [A synthetic ethanolamine with anticholinergic, sedative, and histamine H1 antagonistic properties. Clemastine fumarate blocks the H1 histamine receptor and prevents the symptoms that are caused by histamine activity on capillaries, bronchial and gastrointestinal smooth muscles, including vasodilation, increased capillary permeability, bronchoconstriction, and spasmodic contraction of gastrointestinal smooth muscles. This drug also prevents histamine-induced pain and itching of mucous membranes. ( NCI )] (UMLS (NCI) C0546858) =Organic Chemical; Pharmacologic Substance =CLEMASTINE;
=CLEMASTINE FUMARATE 0.67 MG/5ML;
CLEMASTINE FUMARATE 1.34 MG;
CLEMASTINE FUMARATE 2.68 MG;
| - 5. 2-(p-Chloro-alpha-(2-(dimethylamino)ethoxy)benzyl)pyridine Bimaleate
- [An ethanolamine class of H1 antihistamines with mild antimuscarinic and sedative properties. Carbinoxamine diminishes the typical histaminergic effects on H1-receptors in bronchial smooth muscle, capillaries, and gastrointestinal smooth muscle, including vasodilation, bronchoconstriction, increased vascular permeability, pain, itching, and spasmodic contractions of gastrointestinal smooth muscle. Carbinoxamine maleate is used to provide symptomatic relieve of allergic symptoms. ( NCI )] (UMLS (NCI) C0304300) =Organic Chemical; Pharmacologic Substance ;
=CARBINOXAMINE;
=CARBINOXAMINE MALEATE 2 MG/ML;
CARBINOXAMINE MALEATE 4 MG;
CARBINOXAMINE MALEATE 4 MG/5ML;
CARBINOXAMINE MALEATE 8 MG;
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- 2. (+)-2-(p-Chloro-alpha-(2-(dimethylamino)ethyl)benzyl)pyridine Maleate(1:1)
- [The maleate salt form of dexchlorpheniramine, an alkylamine, and first-generation histamine antagonist with anti-allergic activity. Dexchlorpheniramine maleate competitively blocks H1 receptors, thereby preventing the actions of histamine on bronchial smooth muscle, capillaries and gastrointestinal (GI) smooth muscle. This prevents histamine-induced bronchoconstriction, vasodilation, increased capillary permeability, and GI smooth muscle spasms. ( NCI )] (UMLS (NCI) C0137440) =Organic Chemical; Pharmacologic Substance ;
=DEXCHLORPHENIRAMINE;
=DEXCHLORPHENIRAMINE MALEATE 2 MG/5ML;
DEXCHLORPHENIRAMINE MALEATE 2 MG;
DEXCHLORPHENIRAMINE MALEATE 4 MG;
DEXCHLORPHENIRAMINE MALEATE 6 MG;
| - 6. 2-[p-(2-Chloro-1,2-diphenylvinyl)phenoxy]triethylamine
- [USP lists as a gonad stimulating principle; is a fertility inhibitor in male and female rats, but is a fertility stimulant in women used to induce multiple births. ( CSP )] (UMLS (NCI) C0009008) =Organic Chemical; Pharmacologic Substance ;
=fertility promoting drug;
[HS400] GONADOTROPINS;
[HS800] PROGESTINS;
stilbene =2-[p-(2-Chloro-1,2-diphenylvinyl)phenoxy]triethylamine Citrate;
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- 3. 1-(p-Chlorobenzhydryl)-4-(2-(2-hydroxyethoxy)ethyl)diethylenediamine Hydrochloride
- [The hydrochloride salt form of hydroxyzine, a piperazine histamine H1-receptor antagonist with anti-allergic, antispasmodic, sedative, anti-emetic and anti-anxiety properties. Hydroxyzine hydrochloride blocks the H1 histamine receptor and prevents the symptoms that are caused by histamine activity on capillaries, bronchial smooth muscle, and gastrointestinal smooth muscle, including vasodilatation, increased capillary permeability, bronchoconstriction, and spasmodic contraction of gastrointestinal smooth muscle. In addition, hydroxyzine hydrochloride crosses the blood-brain barrier and acts on the histamine H1-receptors in the central nervous system. (NCI05) ( NCI )] (UMLS (NCI) C0600110) =Organic Chemical; Pharmacologic Substance =HYDROXYZINE;
=HYDROXYZINE HYDROCHLORIDE 100 MG;
HYDROXYZINE HYDROCHLORIDE 25 MG;
HYDROXYZINE HYDROCHLORIDE 50 MG;
HYDROXYZINE HYDROCHLORIDE 50 MG/ML;
HYDROXYZINE HYDROCHLORIDE 10 MG;
HYDROXYZINE HYDROCHLORIDE 25 MG/ML;
HYDROXYZINE HYDROCHLORIDE 10 MG/5ML | - 7. 2-[p-(2-Chloro-1,2-diphenylvinyl)phenoxy]triethylamine Citrate
- [The citrate salt form of clomiphene, a triphenylethylene nonsteroidal ovulatory stimulant evaluated for antineoplastic activity against breast cancer. Clomiphene has both estrogenic and anti-estrogenic activities that compete with estrogen for binding at estrogen receptor sites in target tissues. This agent causes the release of the pituitary gonadotropins follicle stimulating hormone (FSH) and luteinizing hormone (LH), leading to ovulation. (NCI04) ( NCI )] (UMLS (NCI) C0546859) =Organic Chemical; Pharmacologic Substance =2-[p-(2-Chloro-1,2-diphenylvinyl)phenoxy]triethylamine;
=CLOMIPHENE CITRATE 50 MG;
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- 4. 1-(p-Chlorophenyl)-5-isopropylbiguanide Hydrochloride
- [The hydrochloride salt form of proguanil, a synthetic biguanide derivative of pyrimidine and an folate antagonist with antimalarial property. Upon hydrolysis, proguanil is converted to its active cyclic triazine metabolite, cycloguanil, by a cytochrome P450 dependent reaction. Cycloguanil selectively inhibits the bifunctional dihydrofolate reductase-thymidylate synthase (DHFR-TS) of plasmodium parasite, thereby disrupting deoxythymidylate synthesis and ultimately blocking DNA and protein synthesis in the parasite. ( NCI )] (UMLS (NCI) C0546856) =Organic Chemical; Pharmacologic Substance
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