| DS | dead air space; dead space; deep sedative; deep sleep; defined substrate; dehydroepiandrosterone sul... |
|---|---|
| AS | acetylstrophanthidin; acidified serum; acoustic schwannoma; acoustic stimulation; active sarcoidosis... |
| DHEAS | Di-Hydro-Epi-Androsterone Sulfate |
| DS | 1) Dead Space 2) Dehydroisoandrosterone Sulfate |
| H2S | Hydrogen Sulfate; Ȳȼö¼Ò |
| MHPG-SO4 | 3-methoxy-4-hydroxy-phenylethylene glycol sulfate |
|---|---|
| S | 3-sulfate |
| SDS | 6%-sodium dodecyl sulfate |
| AS | Ammonium sulfate |
| CS | Cholesterol sulfate |
| hyoscyamine sulfate | <drug> An antispasmodic, hypnotic, and sedative, also used in parkinsonism to relieve tremor, rigidity, and excessive salivation. (05 Mar 2000) |
|---|---|
| hyoscyamine | <chemical> A chemical with the formula C17H23O3N which is a white powder at room temperature and which melts at 108.5 degrees C. It comes from plants such as henbane and belladona. Hyoscyamine is used medically as the levorotatory isomer of racemic atropine and as an anticholinergic alkaloid. (08 Mar 2000) |
| hyoscyamine (6S)-dioxygenase | <enzyme> A 2-oxoglutarate-dependent dioxygenase that catalyses hydroxylation of l-hyoscyamine to 6beta-hydroxyhyoscyamine in biosynthetic pathway to scopolamine; requires fe2+ Registry number: EC 1.14.11.11 Synonym: hyoscyamine 6beta-hydroxylase, hyoscyamine 6 beta-hydroxylase (26 Jun 1999) |
| dl-hyoscyamine | <drug> A toxic alkaloid extracted from belladonna and other members of thenightshade family, it is typically used to dilate the eye and to stopmuscular spasms. Pharmacologic action: Parasympatholytic. Competitive blockade of acetylcholine at muscarinic receptors. Increases sinus node automaticity and AV conduction. Uses: Treat bradycardia, asystole, and AV block Dose: 0.5 - 1.0 mg for bradycardia every 3 - 5 min to a total dose of 0.04 mg/kg. Doses smaller than 0.5 mg can cause a paradoxical bradycardia due to sympathomimetic effects Typically 3 mg is adequate to completely block vagal effects Atropine is well absorbed via endotracheal route - administer 1-2 mg diluted in 10 mL sterile water or normal saline. Potential complications: 1. Tachyarrhythmias 2. Exacerbation of myocardial ischemia 3. Low dose may cause paradoxical bradycardia 4. Dry mouth, urinary retention, flushed and hot skin 5. Crosses blood-brain barrier which can cause delirium Note: The denervated heart will not respond to atropine. (15 Mar 2000) |
| acid sulfate | A salt containing HSO4-. Synonym: acid sulfate. (05 Mar 2000) |
| active sulfate | 3'-phosphoadenosine 5'-phosphosulfate;an intermediate in the formation of urinary ethereal sulfates, notable for containing a "high energy" sulfate bond; the 3'-OH of adenosine is replaced by -OPO3H2, the 5'-OH by -OP(O2H)-OSO3H. Synonym: active sulfate. Acronym: PAPS (05 Mar 2000) |
| adenine sulfate | Adenine conjugated with sulfuric acid; used to stimulate leukocyte production in agranulocytosis. (05 Mar 2000) |
| adenylyl sulfate-ammonia adenylyltransferase | <enzyme> Forms adenosine 5'-phosphoramidate Registry number: EC 2.7.7.- Synonym: adenylyl sulphate-ammonia adenylyltransferase, as-aat (26 Jun 1999) |
| aluminum ammonium sulfate | AlNH4(SO4)2;an astringent. (05 Mar 2000) |
| aluminum potassium sulfate | AlK(SO4)2;an astringent and styptic; also used in veterinary medicine for ulcerative stomatitis, leukorrhoea, and conjunctivitis. Synonym: potassium alum. (05 Mar 2000) |
| aluminum sulfate octadecahydrate | Astringent detergent for skin ulcers. Synonym: cake alum. (05 Mar 2000) |
| amikacin sulfate | An aminoglycoside antibiotic agent with antimicrobial activity similar to that of kanamycin; also effective against Pseudomonas aeruginosa. (05 Mar 2000) |
| ammonium ferric sulfate | An astringent and styptic. Synonym: ammonium ferric sulfate, ferric alum, iron alum. (05 Mar 2000) |
| ammonium sulfate | <chemical> Sulfuric acid diammonium salt. It is used in fractionation of proteins. Chemical name: Sulfuric acid diammonium salt (12 Dec 1998) |
| atropine sulfate | An anticholinergic; a widely used soluble salt of atropine. (05 Mar 2000) |
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