Từ điển y khoa

Thuật ngữ y khoa chuẩn hóa theo MeSH, ICD-11, SNOMED CT.

62,341 terms indexed

• C5795505-allyl-5'-(2-hydroxy-1-methoxypropyl) (1,1-biphenyl)-2,2'-diolMeSH

  has antiviral activity; isolated from Streblus asper; structure in first source

• D0588915-alpha Reductase InhibitorsMeSH

  Drugs that inhibit 3-OXO-5-ALPHA-STEROID 4-DEHYDROGENASE. They are commonly used to reduce the production of DIHYDROTESTOSTERONE.

• D0435825-alpha-DihydroprogesteroneMeSH

  A biologically active 5-alpha-reduced metabolite of plasma PROGESTERONE. It is the immediate precursor of 5-alpha-pregnan-3-alpha-ol-20-one (ALLOPREGNANOLONE), a neuroactive steroid that binds with GABA(A) RECEPTOR.

• C5855805-amino-1-(1-cyanopiperidin-3-yl)-3-(4-(2,4-difluorophenoxy)phenyl)-1H-pyrazole-4-carboxamideMeSH

  inhibits Bruton's tyrosine kinase; structure in first source

• C5791795-amino-1-(4-methylphenylsulfonyl)-4-pyrazolin-3-oneMeSH

  structure in first source

• C5854065-amino-4-(1,3-benzothiazol-2-yl)-1-(3-methoxyphenyl)-1,2-dihydro-3H-pyrrol-3-oneMeSH

  a protein tyrosine kinase inhibitor; structure in first source

• C5611335-amino-4-acetylamino-3-(4-methylphenylamino)1H-pyrazoleMeSH

  structure in first source

• C5837115-amino-6-methoxy-2-(3',4',5'-trimethoxybenzoyl)quinolineMeSH

  a microtubule inhibitor; structure in first source

• C5705385-amino-6-methoxy-2-(3',4',5'-trimethoxyphenylsulfonyl)quinolineMeSH

  a tubulin polymerization inhibitor; structure in first source

• C5758495-amino-N-cyclopropyl-3-(4-fluorophenyl)-4-oxo-3,4-dihydrothieno(3,4-d)pyridazine-1-carboxamideMeSH

  structure in first source

• C5724645-amino-exo-3-azatricyclo(5.2.1.0(2,6))decan-4-oneMeSH
• C5824405-androsten-3,17,19-triolMeSH

  a translocator protein inhibitor

• C5619625-benzoylcarbonylfluoresceinMeSH

  structure in first source

• C5760595-benzyl-5H-indeno(1,2-b)indole-6,9,10-trioneMeSH

  structure in first source

• C5844125-benzylglycinyl amilorideMeSH

  structure in first source

• C5844865-benzylidene thiazolidine-2,4-dioneMeSH

  structure in first source

• C5682975-bis(4-hydroxy-3-methoxybenzylidene)-N-methyl-4-piperidoneMeSH

  has antineoplastic activity; structure in first source

• C5874235-bromo-1-((phenyl)sulfonyl)-2-((4-nitrophenoxy)methyl)-1H-benzimidazoleMeSH

  structure in first source

• C5617005-bromo-2-(4-chlorobenzoyl)-(Z)-3-(2-cyano-3-hydroxybut-2-enonyl)aminobenzo(b)furanMeSH

  structure in first source

• C5696835-bromo-3-((3,4,5-trimethoxyphenyl)thio)-1H indoleMeSH

  structure in first source

• C5727585-bromo-3-(3-hydroxyprop-1-ynyl)-2H-pyran-2-oneMeSH

  a radiosensitizing agent; structure in first source

• C5599225-bromo-N-(1-(3-fluoro-2-methoxybenzoyl)-5-methylpiperidin-2-yl)methylpyridin-2-amineMeSH

  an orexin-1 receptor antagonist

• C5867645-bromoimidazo(1,2-a)pyridineMeSH

  structure in first source

• C5695075-butyl-2-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-3,8-dimethoxyphenanthridin-6(5H)-oneMeSH

  has antiviral activity against hepatitis C virus; structure in first source

• C5768345-carboethoxymethyl-4',7-dihydroxyflavoneMeSH

  from Rhizophora mucronata; structure in first source

• C5768335-carbomethoxymethyl-7-hydroxy-2-pentylchromoneMeSH

  from the herb Selaginella moellendorffii; structure in first source

• C5609745-carboxylcytosineMeSH

  structure in first source

• C5705925-carboxymethyl-7,4'-dihydroxyflavonone-7-O-glucopyranosideMeSH

  increases glucose consumption in insulin-resistant cells; isolated from Selaginella moellendorffii; structure in first source

• C5837865-chloro-1-(1-(3-(7-chloroquinolin-4-ylamino)propyl)-1H-(1,2,3)triazol-4-ylmethyl)-1H-indole-2,3-dioneMeSH

  structure in first source

• C5796515-chloro-2-(3,5-dimethylphenyl)-4-(4-methoxyphenoxy)pyridazin-3(2H)-oneMeSH

  structure in first source

• C5818375-chloro-2-(9H-fluoren-9-yl)-4-(4-methoxyphenoxy)pyridazin-3(2H)-oneMeSH

  an NPBWR1 antagonist; structure in first source

• C5682135-chloro-2-hydroxybenzamideMeSH

  structure in first source

• C5682175-chloro-2-hydroxybenzoic acidMeSH

  structure in first source

• C5732765-chloro-2-methylbenzoxazoleMeSH
• C5756615-chloro-3-(2-(4-methylpiperazin-1-yl)-2-oxoethyl)benzo(d)thiazol-2(3H)-oneMeSH

  structure in first source

• C5798085-chloro-3-ethyl-1-methyl-N-(4-(piperidin-1-yl)phenethyl)-1H-indole-2-carboxamideMeSH

  a CB1 receptor ligand; structure in first source

• C5725045-chloro-3-ethyl-1H-indole-2-carboxylic acid (2-(4-piperidin-1-yl-phenyl)ethyl)amideMeSH

  structure in first source

• C5796435-chloro-3-methyl-1-phenyl-1H-pyrazole-4-carbaldehydeMeSH

  structure in first source

• C5798095-chloro-3-pentyl-N-(4-(piperidin-1-yl)phenethyl)-1H-indole-2-carboxamideMeSH

  a CB1 receptor ligand; structure in first source

• C5780715-chloro-6-(1-hydroxy-1,3-dihydrobenzo(c)(1,2)oxaborol-5-yloxy)-2-(2-isopropoxyethoxy)nicotinonitrileMeSH

  structure in first source

• C5866755-chloro-6-(4-(1-(4-chlorobenzyl)piperidin-4-yl)-3-ethylpiperazin-1-yl)-N-ethylnicotinamideMeSH

  structure in first source

• C5606855-chloro-8-hydroxy-6-methoxy-3-pentylisocoumarinMeSH

  structure in first source

• C5790855-chloro-8-hydroxyquinolinium chlorideMeSH

  structure in first source

• C5736405-chloro-N-(4-(N-(4,6-dimethylpyrimidin-2-yl)sulfamoyl)phenyl)-2-hydroxybenzamideMeSH

  has antibacterial activity; structure in first source

• C5868395-chloro-N-(4-(dimethylamino)phenethyl)-3-pentyl-1H-indole-2-carboxamideMeSH

  a CB1 receptor modulator; structure in first source

• C5779195-chloro-armeniaspirole AMeSH

  isolated from Streptomyces armeniacus; structure in first source

• C5738935-chlorochromenoneMeSH

  structure in first source

• C5833965-chloromuconolactone dehalogenase, Rhodococcus opacusMeSH

  catalyzes the conversion of 5-chloromuconolactone into cis-dienelactone

• C5867395-chlorothiophene-2-carboxylic acid (2-(2-methyl-3-(2-oxopyrrolidin-1-yl)benzenesulfonylamino)-3-(4-methylpiperazin-1-yl)-3-oxopropyl)amideMeSH

  structure in first source

• C5862735-cyanobenzenesulfonylureaMeSH

  structure in first source