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"propoxyphene hydrochloride compound"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • ¿µ¹®
    ÇѱÛ
  • chloroquine hydrochloride
    ¿°»êŬ·Î·ÎÄý
  • ethylnorepinephrine hydrochloride
    ¿°»ê¿¡Æ¿³ë¸£¿¡Çdz×ÇÁ¸°
  • hydrochloride
    ¿°»ê¿°
  • naloxone hydrochloride
    ³¯·Ï¼Õ
  • piperoxane hydrochloride
    ¿°»êÇÇÆä·Ï»ê
  • pyridoxine hydrochloride
    ¿°»êÇǸ®µ¶½Å
  • quinacrine hydrochloride
    Äû³ªÅ©¸°È÷µå·ÎŬ·Î¶óÀ̵å
  • verapamil hydrochloride
    º£¶óÆÄ¹Ð¿°»ê¿°
  • aromatic compound
    ¹æÇâÁ·È­ÇÕ¹°
  • asymmetric compound
    ºñ´ëĪȭÇÕ¹°
  • acyclic compound
    ¹«°í¸®È­ÇÕ¹°
  • addition compound
    ÷°¡È­ÇÕ¹°
  • adsorption compound
    ÈíÂøÈ­ÇÕ¹°
  • aliphatic compound
    Áö¹æÁ·È­ÇÕ¹°
  • amphoteric compound
    ¾ç¼ºÈ­ÇÕ¹°
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  • ¿µ¹®
    ÇѱÛ
  • verapamil hydrochloride
    ¿°»êº£¶óÆÄ¹Ð, º£¶óÆÄ¹ÐÈ÷µå·ÎŬ·Î¶óÀ̵å
  • compound
    º¹Àâ, º¹ÇÕ, È­ÇÕ¹°
  • organic compound
    À¯±âÈ­ÇÕ¹°
  • compound nevus
    º¹ÇÕ¸ð¹Ý
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  • ¿µ¹®
    ÇѱÛ
  • chloroquine hydrochloride
    ¿°»êŬ·Î·ÎÄý
  • ethylmorphine hydrochloride
    ¿¡Æ¿¸ð¸£ÇÉ¿°»ê¿°
  • ethylnorepinephrine hydrochloride
    ¿°»ê¿¡Æ¿³ë¸£¿¡Çdz×ÇÁ¸°
  • piperoxane hydrochloride
    ¿°»êÇÇÆä·Ï»ê
  • pyridoxine hydrochloride
    ¿°»êÇǸ®µ¶½Å
  • quinacrine hydrochloride
    Äû³ªÅ©¸°ÇÏÀ̵å·ÎŬ·Î¶óÀ̵å
  • acyclic compound
    ¹«°í¸®È­ÇÕ¹°
  • addition compound
    ÷°¡È­ÇÕ¹°
  • adsorption compound
    ÈíÂøÈ­ÇÕ¹°
  • aliphatic compound
    Áö¹æÁ·È­ÇÕ¹°
  • amphoteric compound
    ¾ç¼ºÈ­ÇÕ¹°
  • aromatic compound
    ¹æÇâÁ·È­ÇÕ¹°
  • asymmetric compound
    ºñ´ëĪȭÇÕ¹°
  • compound astigmatism
    º¹ÇÕ³­½Ã
  • compound
    º¹Àâ, º¹ÇÕ, È­ÇÕ¹°
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  • ¿µ¹®
    ÇѱÛ
  • harmol hydrochloride
    ¿°»êÇϸ£¸ô.
  • phentolamine hydrochloride
    ¿°»ê(ç¤ß«)ÆæÅç¶ó¹Î.
  • phenylephrine hydrochloride
    ¿°»êÆä´Ò ¿¡ÇÁ¸°.
  • piperoxane hydrochloride
    ¿°»êÇÇÆä·Ï»ê.
  • pyridoxine hydrochloride
    ¿°»ê(ç¤ß«)ÇǸ® µ¶½Å.
  • acyclic compound
    ºñȯ»óÈ­ÇÕ¹°.
  • addition compound
    ÷°¡È­ÇÕ¹°(ôÕÊ¥ ûùùêÚª).
  • adsorption compound
    ÈíÂøÈ­ÇÕ¹°.
  • aliphatic compound
    Áö¹æÁ·È­ÇÕ¹°.
  • amino compound
    ¾Æ¹Ì³ëÈ­ÇÕ¹°(¡­ûùùêÚª).
  • amphoteric compound
    ¾ç¼ºÈ­ÇÕ¹°(¡­ûùùêÚª).
  • antimuscarinic compound
    Ç×¹«½ºÄ«¸°Á¦.
  • aromatic compound
    ¹æÇâÁ·È­ÇÕ¹°.
  • heme compound
    ÇðÈ­ÇÕ¹°
  • heterocyclic compound
    ÇìÅ×·Î°í¸®È­ÇÕ¹°, ÀÌÁ¾¿øÀÚ°í¸®È­ÇÕ¹°.
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  • ¿µ¹®
    ÇѱÛ
  • cassantin =diethazine hydrochloride
    ¿°È­µð¿¡ ŸÁø.
  • cinchonamina hydrochloride
    ¿°»ê(ç¤ß«)½ÅÄÚ³ª¹Î.
  • cocaine hydrochloride
    ¿°»ê(ç¤ß«)ÄÚÄ«ÀÎ.
  • ephedrine hydrochloride
    ¿°»ê(ç¤ß«)¿¡Æäµå¸°.
  • ethylmorphine hydrochloride
    ¿¡Æ¿¸ð¸£ÇÉ¿°»ê¿°.
  • ethylnorepinephrine hydrochloride
    ¿°»ê(ç¤ß«)¿¡Æ¿³ë¸£¿¡Çdz×ÇÁ¸°.
  • harmol hydrochloride
    ¿°»êÇϸ£¸ô.
  • phentolamine hydrochloride
    ¿°»ê(ç¤ß«)ÆæÅç¶ó¹Î.
  • phenylephrine hydrochloride
    ¿°»êÆä´Ò ¿¡ÇÁ¸°.
  • phenylhyrazine hydrochloride
    ¿°»ê¿°Æä´ÒÈ÷µå¶óÁø.
  • piperoxane hydrochloride
    ¿°»êÇÇÆä·Ï»ê.
  • pyridoxine hydrochloride
    ¿°»ê(ç¤ß«)ÇǸ® µ¶½Å.
  • trihexyphenidyl hydrochloride
    ¿°»ê(ç¤ß«)Æ®¸®Çí½ÃÆä´Ïµô.
  • tyramine hydrochloride
    ¿°»ê Ƽ¶ó¹Î
  • acyclic compound
    ºñȯ»óÈ­ÇÕ¹°.
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  • ¿µ¹®
    ÇѱÛ
  • Compound gland
    º¹ÇÕ»ù
    [¿¾ ¿ë¾î] º¹ÇÕ¼±
  • Compound intercellular junction
    º¹ÇÕ¼¼Æ÷»çÀÌ¿¬Á¢
    [¿¾ ¿ë¾î] º¹ÇÕ¼¼Æ÷°£°áÇÕ[¿¬Á¢]
  • Compound intercellular junction
    º¹ÇÕ¼¼Æ÷»çÀÌ¿¬Á¢
    [¿¾ ¿ë¾î] º¹ÇÕ¼¼Æ÷¿¬Á¢
  • Compound joint
    º¹ÇÕ°üÀý
    [¿¾ ¿ë¾î] º¹°üÀý
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  • ¿µ¹®
    ÇѱÛ
  • emetine hydrochloride
    ¿¡¸ÞƾÇÏÀ̵å·ÎŬ·Î¶óÀ̵å
  • quinacrine hydrochloride (Atabrine)
    Äû³ªÅ©¸°ÇÏÀ̵å·ÎŬ·Î¶óÀ̵å(¾ÆÅº기)
  • carbamate compound
    Ä«¹Ù¸ÞÀÌÆ®°è »ìÃæÁ¦
  • chlorinated hydrocarbon compound
    À¯±â¿°¼Ò°è»ìÃæÁ¦
  • organophosphorus compound
    À¯±âÀΰè»ìÃæÁ¦
  • pyrethroid compound
    ÇÇ·¹½º·ÎÀ̵å°è»ìÃæÁ¦
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  • ¿µ¹®
    ÇѱÛ
  • alicyclic compound
    ºñ(Þª)°í¸®Çü(û¡)È­ÇÕ¹°(ûùùêÚª)
  • anticancer compound
    Ç×¾ÏÈ­ÇÕ¹°(ù÷äßûùùêÚª)
  • antithyroid compound
    Ç×°©»ó¼± È­ÇÕ¹°(ù÷Ë£ßÒàÍûùùêÚª)
  • azo compound
    ¾ÆÁ¶È­ÇÕ¹°(ûùùêÚª)
  • carbamino compound
    Ä«¸£¹Ù¸¶À̵å È­ÇÕ¹°(ûùùêÚª)
  • compound
    È­ÇÕ¹°(ûùùêÚª)
  • compound lipid
    "È­ÇÕÁöÁú(ûùùêò·òõ), (ÔÒ) complex lipid"
  • compound microscope
    º¹ÇÕÇö¹Ì°æ(ÜÜùêúéÚ°Ìð)
  • diazo compound
    µð¾ÆÁ¶ È­ÇÕ¹°(ûùùêÚª)
  • diazonium compound
    µð¾ÆÁ¶´½ È­ÇÕ¹°(ûùùêÚª) (ÔÒ) diazonium salt
  • energy-poor compound
    ºó(Þ¸)¿¡³ÊÁö È­ÇÕ¹°(ûùùêÚª)
  • energy-rich compound
    ºÎ(Ý£)¿¡³ÊÁö È­ÇÕ¹°(ûùùêÚª)
  • enzyme-substrate compound
    È¿¼Ò-±âÁú È­ÇÕ¹° (ý£áÈÐñòõûùùêÚª)
  • high-energy compound
    °í(ÍÔ)¿¡³ÊÁö È­ÇÕ¹°(ûùùêÚª)
  • Kendall's compound
    ÄË´Þ È­ÇÕ¹°(ûùùêÚª)
KI ÀÇÇпë¾î »çÀü °Ë»ö À¯»ç °Ë»ö °á°ú : 6 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
  • compound
    È­ÇÕ¹°, ÄÄÆÄ¿îµå
  • compound scan
    º¹ÇÕ½ºÄµ
  • compound scan motion
    º¹ÇÕ½ºÄµ¿îµ¿
  • compound sector
    º¹ÇÕ ºÎä²Ã
  • contact compound scan
    Á¢Ã˺¹ÇÕ½ºÄµ
  • inorganic compound
    ¹«±âÈ­ÇÕ¹°
KMLE ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
PCC Pasteur Culture Collection; percutaneous cecostomy; pheochromocytoma; phosphate carrier compound; pl...
Cyclo C cyclocytidine hydrochloride
DBI development at birth index; phenformin hydrochloride
DHAD mitoxantrone hydrochloride
EHC enterohepatic circulation; enterohepatic clearance; essential hypercholesterolemia; ethylhydrocuprei...
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 1
C 48/80 Compound 48/80
CAP Compound Action Potential
CMAP Compound motor action potential
CMAP Compound muscle action potential
CNAP Compound nerve action potential
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • acecainide hydrochloride
    ¿°»ê ¾Æ¼¼ÄÉÀ̳ªÀ̵å
    Ç׺ÎÁ¤¸Æ¼º ½ÉÀå ¾ïÁ¦Á¦.
  • bupivacaine hydrochloride
    ¿°»ê ºÎÇǹÙÄÉÀÎ
    ¹é»ö °áÁ¤¼º ºÐ¸». ¸»ÃʽŰæ Â÷´ÜÁ¦, ħÀ±, ±³°¨½Å°æ, ¹ÌÃø, °æ¸·¿Ü Â÷´Ü µî¿¡ »ç¿ëµÈ´Ù.
  • buspirone hydrochloride
    ¿°»ê ºÎ½ºÆÄÀÌ·Ð
    ½Å°æ¾ÈÁ¤Á¦.
  • butaclamol hydrochloride
    ¿°»êºÎŸŬ¶ó¸ô
    ½Å°æ¾ÈÁ¤Á¦.
  • butamisole hydrochloride
    ¿°»ê ºÎŸ¸ñ¼¼ÀÎ
    ½Å°æ¾ÈÁ¤Á¦.
  • butoxamine hydrochloride
    ¿°»ê ºÎÅå»ç¹Î
    ¾Æµå·¹³¯¸° º£Å¸ ¼ö¿ëü Â÷´ÜÁ¦.
  • chlorphenoxamine hydrochloride
    ¿°»ê Ŭ·Î¸£Ææ¿Á»ç¹Î
    2-[1-
  • cocaine hydrochloride
    ¿°»ê ÄÚÄ«ÀÎ
  • diltiazem hydrochloride
    ¿°»ê ´ÙÀÏÆ¼¾ÆÁª
    °ü»ó Ç÷°ü È®ÀåÁ¦, Çù½ÉÁõÀÇ ´ëÁõ¿ä¹ý¿¡ »ç¿ëÇÑ´Ù,
  • dimethisoquin hydrochloride
    ¿°»ê ´ÙÀÌ¸ÞÆ¼¼ÒÄý
    ¹é»ö ¹«ÃëÀÇ ºÐ¸». ¹°, ¾ËÄÝ, Ŭ·Î·ÎÆ÷¸§¿¡³ìÀ¸¸ç ±¹¼Ò¸¶ÃëÁ¦·Î »ç¿ëµÈ´Ù.
  • diphenhydramine hydrochloride
    ¿°»ê ´ÙÀÌÆæÇÏÀ̵å¶ó¹Î
    ¹é»ö ¹«ÃëÀÇ °áÁ¤¼º ºÐ¸». ¸¶Ã뼺 Áö»çÁ¦
  • ephedrine hydrochloride
    ¿°»ê ¿¡Æäµå¸°
  • ethylmorphine hydrochloride
    ¿¡Æ¿ ¸ð¸£ÇÉ ¿°»ê ¿°
  • hydralazine : ¹«»ö °¡½º»óÀÇ diamine. H2N?NH2. ¶ÇÇÑ ±× À¯µµÃ¼ÀÇ Àϱºµµ Æ÷ÇÔÇÑ´Ù.

    hydralazine hydrochloride

    ¿°»ê ÇÏÀ̵å¶ö¶óÁø
    ¹é»ö ¹«ÃëÀÇ ºÐ¸». ¹°¿¡ ³ì±â ¾î·Á¿ì¸ç, Ç÷¾Ð °­ÇÏÁ¦·Î¼­ °íÇ÷¾Ð Ä¡·á¿¡ »ç¿ëÇÑ´Ù.
  • Labetalol hydrochloride

    labia (À½¼ø, ÀÔ¼ú, ±¸¼ø

    ÀÔ¼úÀÇ, ÀÔ¼ú¿¡ °üÇÑ, ÀÔ¼úÀ» ÇâÇÑ.
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 1
propoxyphene hydrochloride (+)-alpha-4-(dimethylamino)-3-methyl-1,2-diphenyl-2-butanol propionate hydrochloride;a nonantipyretic, orally effective weak narcotic analgesic structurally related to methadone and used for the relief of mild to moderate pain; it is less effective than codeine.
Synonym: dextropropoxyphene hydrochloride.
(05 Mar 2000)
propoxyphene <chemical> A narcotic analgesic structurally related to methadone. Only the dextro-isomer has an analgesic effect; the levo-isomer appears to exert an antitussive effect.
Pharmacological action: analgesics, opioid, antitussive agents, narcotics.
Chemical name: Benzeneethanol, alpha-(2-(dimethylamino)-1-methylethyl)-alpha-phenyl-, propanoate (ester), (S-(R*,S*))-
(12 Dec 1998)
propoxyphene napsylate Mono-2-naphthalenesulfonate monohydrate salt of propoxyphene;a weak narcotic analgesic.
Synonym: dextropropoxyphene napsylate.
(05 Mar 2000)
acetone compound <biochemistry> Any of the three compounds created by acetyl coenzyme A (acetoacetate, hydroxybutyrate, and acetone) which are water-soluble cellular fuels normally exported by the liver.
They can build up in the blood and body tissues because of starvation, untreated diabetes mellitus, or other disorders that interfere with carbohydrate metabolism. The body rids itself of ketones mainly through urine, but it rids itself of acetone through the lungs, which gives the breath a characteristic fruity odour. If ketones build up in the body long enough, they cause serious illness and coma (see ketoacidosis.)
(09 Oct 1997)
acyclic compound An organic compound in which the chain does not form a ring.
Synonym: aliphatic compound, open chain compound.
(05 Mar 2000)
addition compound Strictly, a complex of two or more complete molecules in which each preserves its fundamental structure and no covalent bonds are made or broken (e.g., hydrates of salts, adducts), loosely, association of acids with basic organic compound's (e.g., amines with HCl), more loosely, addition of two molecules without loss of any atom, but forming new covalent bonds (e.g., CH2==CH2 + Br2 &rarr; BrCH2-CH2Br).
(05 Mar 2000)
aliphatic compound An organic compound in which the chain does not form a ring.
Synonym: aliphatic compound, open chain compound.
(05 Mar 2000)
APC compound An analgesic tablet drug combination containing aspirin, phenacetin and caffeine. Very widely used in the 1940's through 1960's; original constituents of popular over-the-counter pain remedies. Use currently much diminished due to concerns about potential renal injury due to the phenacetin.
(05 Mar 2000)
aromatic compound Any compound in which the constituent atoms, or any part of them, form a ring. Used mainly in organic chemistry where: 1) numerous compound's contain rings of carbon atoms (carbocyclic compound's) or carbon atoms plus one or more atoms of other types (heterocyclic compound's), usually nitrogen, oxygen, or sulfur; 2) where the atoms in the ring are all of the same element (homocyclic or isocyclic compound); 3) where the ring is saturated or contains nonconjugated double bonds (alicyclic compound), the compound is similar in properties to the corresponding acyclic compound (e.g., cyclohexane resembles hexane); 4) where the ring contains conjugated double bonds in a closed loop in which there are 4n + 2 (where n is an integer) delocalised &pi; electrons (Huckel's rule) (aromatic compound; e.g., benzene, pyridine), it is more stable than the corresponding saturated ring and exhibits unusual chemical properties characteristic of itself and not of other types of rings or of acyclic compound's. These aromatic compounds have the ability to sustain an induced ring current.
Synonym: closed chain compound, ring compound.
(05 Mar 2000)
binary compound <chemistry> This refers to any compound that is composed of only two elements.
(09 Oct 1997)
calcium compound Inorganic compounds that contain calcium as an integral part of the molecule.
(12 Dec 1998)
carbamino compound Any carbamic acid derivative formed by the combination of carbon dioxide with a free amino group to form an N-carboxy group, -NH-COOH, as in haemoglobin forming carbaminohemoglobin.
(05 Mar 2000)
carbocyclic compound See: cyclic compound.
(05 Mar 2000)
genetic compound In medical genetics, the presence of two different mutant alleles at the same loci.
Synonym: genetic compound.
(05 Mar 2000)
Reichstein's compound One of several steroids; e.g., Reichstein's substance F (cortisone), Reichstein's substance H (corticosterone), Reichstein's substance M (cortisol), Reichstein's substance Q (cortexone), and Reichstein's substance S (cortexolone).
Synonym: Reichstein's compound.
(05 Mar 2000)
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  • hydrochloride
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  • compound
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    µÎ»óÈ­;°ã²É(±¹È­°ú ½Ä¹°µîÀÇ)
  • compound fraction
    COMPLEX FRACTION
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