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  • oxygen intoxication =o. poisoning
    »ê¼ÒÁßµ¶(¡­ñéÔ¸).
  • oxygen lack
    »ê¼ÒºÎÁ·, »ê¼Ò°áÇÌ.
  • oxygen manifold
    »ê¼Ò¹èºÐÀåÄ¡(¡­ÛÕÝ íûöÇ).
  • oxygen mask
    »ê¼Ò¸¶½ºÅ©.
  • oxygen meter
    »ê¼Ò¹ÌÅÍ, »ê¼Ò°è(ß«áÈͪ).
  • oxygen monitors
    »ê¼Ò °¨Áö±â
  • oxygen partial pressure
    »ê¼ÒºÐ¾Ð(ß«áÈ ÝÂäâ).
  • oxygen poisoning
    »ê¼ÒÁßµ¶(Áõ)(¡­ñéÔ¸ñø).
  • oxygen pressure
    »ê¼Ò¾Ð.
  • oxygen probe
    »ê¼ÒŽħ
  • oxygen requirement
    »ê¼Ò¿ä±¸(·®)
  • oxygen requirement
    »ê¼Ò¿ä±¸·®(¡­é©Ï´åÖ).
  • oxygen reserve
    »ê¼Ò¿¹ºñ
  • oxygen reserve
    »ê¼Ò¿¹ºñ(ß«áÈçãÝá).
  • oxygen room
    »ê¼Ò½Ç(ß«áÈãø).
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CMRO, CMRO2 cerebral metabolic rate of oxygen consumption
COD cause of death; cerebro-ocular dysplasia; chemical oxygen demand; codeine; condition on discharge
CVO central vein occlusion; central venous oxygen; Chief Veterinary Officer; credentialing verification ...
cvPO2, cvPO2 cerebral venous partial pressure of oxygen
DLO2 diffusing capacity of the lungs for oxygen
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HBO(2) Hyperbaric oxygen
HBOT Hyperbaric oxygen therapy
LOI Lactate-Oxygen-Index
LTOT Long Term Oxygen Therapy
LTO Long-term oxygen therapy
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 7
hexamethonium compounds <chemical> Compounds containing the hexamethylenebis(trimethylammonium) cation. Members of this group frequently act as antihypertensive agents and selective ganglionic blocking agents.
Pharmacological action: antihypertensive agents, ganglionic blockers.
(12 Dec 1998)
high energy compounds Classically, a group of phosphoric esters whose hydrolysis takes place with a standard free energy change of -5 to -15 kcal/mol (or, -20 to -63 kJ/mol) (in contrast to -1 to -4 kcal/mol or, -4 to -17 kJ/mol) for simple phosphoric esters like glucose-6-phosphate or alpha-glycerophosphates), thus being capable of driving energy-consuming reactions in living cells or reconstituted cell-free systems; adenosine 5'-triphosphate, with respect to the beta-and gamma-phosphates, is the best known and is regarded as the immediate energy source for most metabolic syntheses. The general types are acid anhydrides, phosphoric esters of enols, phosphamic acid (R-NH-PO3H2) derivatives, acyl thioesters (e.g., of coenzyme A), sulfonium compound's (R3-S+), and aminoacyl esters of ribosyl moieties.
See: high energy phosphates.
(05 Mar 2000)
selenium compounds Inorganic compounds that contain selenium as an integral part of the molecule.
(12 Dec 1998)
pyrvinium compounds <chemical> Pharmacological action: antinematodal agent.
(12 Dec 1998)
silicon compounds Inorganic compounds that contain silicon as an integral part of the molecule.
(12 Dec 1998)
silver compounds Inorganic compounds that contain silver as an integral part of the molecule.
(12 Dec 1998)
sodium compounds Inorganic compounds that contain sodium as an integral part of the molecule.
(12 Dec 1998)
spiro compounds A group of compounds consisting in part of two rings sharing one carbon atom in common.
(12 Dec 1998)
nitrogen compounds Inorganic compounds that contain nitrogen as an integral part of the molecule.
(12 Dec 1998)
nitrogen mustard compounds <chemical> A group of alkylating agents derived from mustard gas, with the sulfur replaced by nitrogen. They were formerly used as toxicants and vesicants, but now function as antineoplastic agent. These compounds are also powerful mutagens, teratogens, immunosuppressants, and carcinogens.
Pharmacological action: antineoplastic agent, alkylating, carcinogens, mutagens, teratogens.
(12 Dec 1998)
sulfhydryl compounds Compounds containing the -sh radical.
(12 Dec 1998)
sulfonium compounds Sulfur compounds in which the sulfur atom is attached to three organic radicals and an electronegative element or radical.
(12 Dec 1998)
sulfonylurea compounds <chemical> Pharmacological action: hypoglycaemic agents.
(12 Dec 1998)
sulfur compounds Inorganic or organic compounds that contain sulfur as an integral part of the molecule.
(12 Dec 1998)
dansyl compounds <chemical> Compounds that contain a 1-dimethylaminonaphthalene-5-sulfonyl group.
Pharmacological action: indicators and reagents.
(12 Dec 1998)
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