- 1. 1,1'-Thiobis(2-chloroethane)
- [A pale yellow, oily, highly toxic, volatile, liquid alkylating compound with a sweet to garlic-like odor that evaporates to a poisonous gas. Mustard gas is a vesicant that was first used in chemical warfare in World War I, but is now only used in small amounts in research studies involving alkylating agents. Exposure to this substance is corrosive to the eyes, skin and lungs and leads to blindness and blistering of the skin and can cause severe and sometimes fatal respiratory damage. Mustard gas is a mutagen and is a known carcinogen that is associated with an increased risk of developing lung and other respiratory tract cancers. (NCI05) ( NCI )] (UMLS (NCI) C0026874) =Organic Chemical; Hazardous or Poisonous Substance ;
| - 51. Thioflavine-S stain
- [Stain, Thioflavine-S ( HL7V3.0 )] (UMLS (HL7) C1294425) =Laboratory Procedure =ObservationMethod;
|
- 2. 1,3, 4-Thiadiazol-2-amine (9CI)
- [A synthetic derivative of nicotinamide adenine dinucleotide (NAD). Aminothiadiazole competitively inhibits inosine 5-monophosphate dehydrogenase, thereby disrupting the regulation of cell proliferation and differentiation in a number of cells. This agent is also a selective human adenosine A3 receptor antagonist. (NCI04) ( NCI )] (UMLS (NCI) C0092419) =Organic Chemical; Pharmacologic Substance
| - 52. Thiofozil
- (UMLS (NCI) C0729088) =Organophosphorus Compound; Pharmacologic Substance; Hazardous or Poisonous Substance
|
- 3. 2,4 thiazolidinedione
- [ ] (UMLS (CSP) C0289779) =Organic Chemical; Pharmacologic Substance ;
| - 53. thiofuran
- [5-membered aromatic ring structure with a sulfur heteroatom. ( CSP )] (UMLS (CSP) C0599532) =Organic Chemical; Pharmacologic Substance =sulfurous heterocyclic compound;
=(+)-Biotin;
CLOPIDOGREL;
|
- 4. 2-Thiophenecarboxylic Acid, 4-Methyl-3-((1-oxo-2-(propylamino)propyl)amino)-, Methyl Ester, Monohydrochloride
- [The hydrochloride salt form of articaine, an amide-type local anesthetic. Articaine hydrochloride reversibly blocks nerve impulse conduction by binding to specific membrane sodium ion channels thereby interfering with the electrical excitation in the nerve, slowing the propagation of the nerve impulse and reducing the rate of rise of the action potential. This results in a loss of sensation at the injection site. Articaine hydrochloride is used for relief of pain in minor operations, usually in combination with the vasoconstrictor epinephrine. ( NCI )] (UMLS (NCI) C0007300) =Organic Chemical; Pharmacologic Substance ;
| - 54. thiol disulfide oxidoreductase
- [ ] (UMLS (CSP) C0087081) =Amino Acid, Peptide, or Protein; Enzyme ;
|
- 5. 2-Thiourea
- [(NH2)2C=S; precursor and metabolite of 2-thiouracil, used for similar purposes. ( CSP )] (UMLS (NCI) C0039958) =Organic Chemical; Indicator, Reagent, or Diagnostic Aid =sulfur compound;
| - 55. Thiola
- (UMLS (NCI) C0733414) =Amino Acid, Peptide, or Protein; Pharmacologic Substance
|
- 6. 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid, 3,3-dimethyl-7-oxo-, 4,4-dioxide, Sodium Salt,(2S-cis)-
- [The sodium salt form of sulbactam, a beta-lactam with weak antibacterial property. Sulbactam sodium contains a beta-lactam ring and irreversibly binds to beta-lactamase at or near its active site, thereby blocking enzyme activity and preventing metabolism of other beta-lactam antibiotics. Combining this agent with a beta-lactamase sensitive antibiotic such as penicillins and cephalosporins against penicillinase-producing and beta-lactamase-producing organisms, results in a decreased turnover rate of the sensitive antibiotic and enhances its antibacterial property. ( NCI )] (UMLS (NCI) C0282355) =Organic Chemical; Antibiotic ;
=SULBACTAM;
=SULBACTAM SODIUM 1.5 GM/VIL;
SULBACTAM SODIUM 3 GM/VIL;
SULBACTAM SODIUM 5 GM;
| - 56. thioltransferase
- [ ] (UMLS (CSP) C0076484) =Amino Acid, Peptide, or Protein; Enzyme
|
- 7. 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid, 3,3-dimethyl-7-oxo-6-((phenylacetyl)amino)-,(2S-(2alpha,5alpha,6beta))-, Monosodium Salt
- [The sodium salt form of benzylpenicillin, a semi-synthetic, broad-spectrum penicillin antibiotic with bactericidal activity. Benzylpenicillin sodium binds to and inactivates penicillin-binding proteins (PBP) located on the inner membrane of the bacterial cell wall. Inactivation of PBPs interferes with the cross-linkage of peptidoglycan chains necessary for bacterial cell wall strength and rigidity. This results in the weakening of the bacterial cell wall and causes cell lysis. ( NCI )] (UMLS (NCI) C0037540) =Organic Chemical; Antibiotic ;
=Penicillin G Benzathine;
PENICILLIN G PROCAINE;
PENICILLIN;
=PENICILLIN G SODIUM 5000000 UNT | - 57. thione
- [compounds of the type R-(C=S)-R. ( CSP )] (UMLS (CSP) C0039921) =Organic Chemical ;
=sulfur compound;
=3H-1,2-Dithiole-3-thione, 4-methyl-5-pyrazinyl- |
- 8. 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-, Monopotassium Salt
- [The potassium salt form of penicillin G, a broad-spectrum penicillin antibiotic. Penicillin G potassium binds to penicillin binding proteins (PBP), the enzymes that catalyze the synthesis of peptidoglycan, which is a critical component of the bacterial cell wall. This leads to the interruption of cell wall synthesis, consequently leading to bacterial cell growth inhibition and cell lysis. ( NCI )] (UMLS (NCI) C0700462) =Organic Chemical; Antibiotic =Penicillin G Benzathine;
PENICILLIN G PROCAINE;
PENICILLIN;
=PENICILLIN G POTASSIUM 40000 UNT/ML;
PENICILLIN G POTASSIUM 20000 UNT/ML;
PENICILLIN G POTASSIUM 30000 UNT/ML;
PENICILLIN G POTASSIUM 5000000 UNT;
PENICILLIN G POTASSIUM 20000000 UNT;
PENICILLIN G POTASSIUM 1000000 UNT;
| - 58. thiopental
- [ultra-short acting barbiturate used as an anesthetic, anticonvulsant, and narcoanalysis. ( CSP )] (UMLS (CSP) C0039925) =Organic Chemical; Pharmacologic Substance =[CN200] ANESTHETICS;
[CN400] ANTICONVULSANTS;
barbiturate;
Thiobarbiturates;
[CN202] BARBITURIC ACID DERIVATIVE, ANESTHETICS;
=thiobutabarbital;
THIOPENTAL SODIUM;
|
- 9. 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid, 6-(((1-aminocyclohexyl)carbonyl)amino)-3,3-dimethyl-7-oxo-,(2S-(2alpha,5alpha,6beta))-
- [A semi-synthetic beta-lactam aminocyclohexylpenicillin antibiotic. Cyclacillin is bactericidal and binds to specific penicllin-binding proteins, thereby inhibiting transpeptidation during peptidoglycan synthesis. This leads to an interruption of the bacterial cell wall, causing instability of bacterial cell wall and results in cell lysis. Cyclacillin is beta-lactamase susceptible. ( NCI )] (UMLS (NCI) C0010523) =Organic Chemical; Antibiotic ;
=Penicillanic Acid;
[AM052] PENICILLINS, AMINO DERIVATIVES | - 59. thiophenol
- [ ] (UMLS (CSP) C0076506) =Organic Chemical; Pharmacologic Substance
|
- 10. 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid, 6-((2,6-dimethoxybenzoyl)amino)-3,3-dimethyl-7-oxo-, Monosodium Salt, Monohydrate,(2S-(2alpha,5alpha,6beta))-
- [The sodium salt form of methicillin, a semisynthetic beta-lactam penicillin antibiotic with beta-lactamase resistant activity. Methicillin sodium is bactericidal and binds to specific penicillin-binding proteins on the bacterium and inhibits the transpeptidation enzyme, thereby preventing the cross-linking of peptidoglycans. This leads to an interruption of the bacterial cell wall and causes bacterial lysis. Methicillin sodium is active against beta-lactamase producing staphylococci. ( NCI )] (UMLS (NCI) C0887175) Celbenin;
METHICILLIN SODIUM;
METHICILLIN SODIUM PREPARATION;
=Organic Chemical; Antibiotic ;
=2,6 dimethoxyphenylpenicillin;
| - 60. thiophosphate
- [phosphate in which one or more O atoms has been replaced by S. ( CSP )] (UMLS (CSP) C0145675) =Inorganic Chemical =sulfur compound;
phosphorus compound |
- 11. 4-Thiazolidine Carboxylic Acid
- [A cyclic sulfur amino acid derivative with potential antineoplastic and antioxidant activity. Thiazolidine carboxylic acid (TCA) acts on cellular membranes of malignant cells through an unknown mechanism to induce reverse transformation, a term denoting changes in morphological and growth characteristics that cause malignant cells to revert back to an untransformed state. TCA produces anti-proliferative effects by restoring contact inhibition, a phenomenon characterized by the paracrine inhibition of mitosis following the formation of a critical cell mass, which is presumably the result of cell-to-cell signal transfer. This drug may also produce antioxidant effects secondary to its release of cysteine and restoration of glutathione concentrations, an important protective property useful against DNA-damaging agents, including chemotherapy and radiation. ( NCI )] (UMLS (NCI) C0076425) =Organic Chemical; Pharmacologic Substance
| - 61. thiopurine
- [ ] (UMLS (CSP) C0597573) =Nucleic Acid, Nucleoside, or Nucleotide; Pharmacologic Substance =sulfur compound;
purine analog =1,7-Dihydro-6H-purine-6-thione |
- 12. 4-Thiazolidinecarboxamide, N-(1,1-dimethylethyl)-3- [2-hydroxy-3-[[2-[[(5-isoquinolinyloxy)acetyl]amino]-3- (methylthio)-1-oxopropyl]amino]-1-oxo-4-phenylbutyl]-,[4R-[3[2S*, 3S*(R*)],4R*]]
- [A synthetic peptide-based antiviral agent. As a peptidomimetic substrate containing an unnatural amino acid, allophenylnorstatine, KNI-272 selectively binds to and inhibits the human immunodeficiency virus (HIV) 1 and 2 proteases, thereby preventing cleavage of the gag-pol viral polyprotein and resulting in the release of immature, noninfectious virions. (NCI04) ( NCI )] (UMLS (NCI) C0174543) =Amino Acid, Peptide, or Protein; Pharmacologic Substance
| - 62. Thiopurine Methyltransferase Deficiency
- (UMLS (NCI) C0342801) =Disease or Syndrome
|
- 13. 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid, 3-(((aminocarbonyl)oxy)methyl)-7-((2-furanyl(methoxyimino)acetyl)amino)-8-oxo-, Monosodium Salt(6R-(6alpha,7beta(Z)))-
- [The sodium salt form of cefuroxime and a semi-synthetic, broad-spectrum, beta-lactamase resistant, second-generation cephalosporin antibiotic with bactericidal activity. Cefuroxime sodium inhibits bacterial cell wall synthesis by inactivating penicillin binding proteins (PBPs) thereby interfering with the final transpeptidation step required for cross-linking of peptidoglycan units which are a component of the cell wall. Lack of cross-linking results in a reduction of cell wall stability and leads to cell lysis. ( NCI )] (UMLS (NCI) C0701852) =Organic Chemical; Antibiotic =CEFUROXIME;
Cefuroxime Axetil =Cefuroxime 1.5 MG/ML Injectable Solution;
CEFUROXIME SODIUM 7.5 GM/VIL;
CEFUROXIME SODIUM 30 MG/ML;
CEFUROXIME SODIUM 15 MG/ML;
CEFUROXIME SODIUM 7.5 MG/ML;
CEFUROXIME SODIUM 7.5 GM;
CEFUROXIME SODIUM 750 MG | - 63. thiopurine nucleoside
- [ ] (UMLS (CSP) C0597574) =Nucleic Acid, Nucleoside, or Nucleotide; Pharmacologic Substance =sulfur compound;
nucleoside analog |
- 14. 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid, 7-(((2,3-dihydro-2-imino-4-thiazolyl)(methoxyimino)acetyl)amino)-8-oxomonosodium Salt,(6R-(6alpha,7beta(Z)))-
- [The sodium salt form of ceftizoxime and a semi-synthetic, broad-spectrum, beta-lactamase resistant, third-generation cephalosporin antibiotic with bactericidal activity. Ceftizoxime sodium inhibits bacterial cell wall synthesis by inactivating penicillin binding proteins (PBPs) thereby interfering with the final transpeptidation step required for cross-linking of peptidoglycan units which are a component of the cell wall. Lack of cross-linking results in a reduction of cell wall stability and leads to cell lysis. ( NCI )] (UMLS (NCI) C0282391) =Organic Chemical; Antibiotic ;
=CEFTIZOXIME;
=ceftizoxime 1 gm injectable powder for injection;
ceftizoxime 10 gm injectable powder for injection;
CEFTIZOXIME SODIUM 2 GM/VIL;
CEFTIZOXIME SODIUM 20 MG/ML;
CEFTIZOXIME SODIUM 40 MG/ML;
CEFTIZOXIME SODIUM 1 GM;
CEFTIZOXIME SODIUM 2 GM;
CEFTIZOXIME SODIUM 500 MG | - 64. Thiopurine S-Methyltransferase Gene
- [This gene plays a role in the metabolism of thiopurine drugs. ( NCI )] (UMLS (NCI) C1336663) TPMT;
TPMT Gene =Gene or Genome ;
|
- 15. 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid, 7-(((2-amino-4-thiazolyl)(methoxyimino)acetyl)amino)-3-((1Z)-2-(4-methyl-5-thiazolyl)ethenyl)-8-oxo-,2,2-dimethyl-1-oxopropoxy)methyl Ester,(6R,7R)-
- [A semi-synthetic, broad-spectrum, beta-lactamase resistant, third-generation cephalosporin antibiotic with bactericidal activity. Cefditoren pivoxil is a prodrug that is rapidly hydrolyzed by intestinal esterases during absorption to the microbiologically active cefditoren, an active aminothiazolyl cephalosporin. Cefditoren inactivates penicillin binding proteins (PBPs) thereby interfering with peptidoglycan synthesis and inhibiting bacterial cell wall synthesis. Another consequence of beta-lactam exposure results in the loss of lipoteichoic acids from the cell wall. Lipoteichoic acids inhibit murein hydrolase activity and their absence from the cell wall triggers uncontrolled autolytic activity rendering bacterial cells susceptible to osmotic shock. This results in a reduction of cell wall stability and causes cell lysis. ( NCI )] (UMLS (NCI) C0245519) =Organic Chemical; Antibiotic ;
=CEFDITOREN;
Unclassified Ingredients | - 65. thiopyrimidine
- [ ] (UMLS (CSP) C0597575) =Nucleic Acid, Nucleoside, or Nucleotide; Pharmacologic Substance =sulfur compound;
pyrimidine analog =thiouracil |
- 16. 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7-(((4-(2-amino-1-carboxy-2-oxoethylidene)-1,3-dithietan-2-yl)carbonyl)amino)-7-methoxy-3-(((1-methyl-1H-tetrazol-5-yl)thio)methyl)-8-oxo-, Disodium Salt,(6R-(6alpha,7alpha))-
- [The disodium salt form of cefotetan and a semi-synthetic, broad-spectrum, beta-lactamase-resistant, second-generation cephalosporin antibiotic with bactericidal activity. Cefotetan disodium causes inhibition of bacterial cell wall synthesis by inactivating penicillin binding proteins (PBPs) thereby interfering with the final transpeptidation step required for cross-linking of peptidoglycan units which are a component of the cell wall. This results in a reduction of cell wall stability and causes cell lysis. ( NCI )] (UMLS (NCI) C0700471) =Organic Chemical; Antibiotic =CEFOTETAN;
=CEFOTETAN DISODIUM 1 GM/VIL;
CEFOTETAN DISODIUM 2 GM/VIL;
CEFOTETAN DISODIUM 1 GM/50ML;
CEFOTETAN DISODIUM 2 GM/50ML;
CEFOTETAN DISODIUM 10 GM/VIL;
CEFOTETAN DISODIUM 2 GM;
CEFOTETAN DISODIUM 1 GM;
| - 66. thioredoxin
- [family of small (13 kD) electron carrier proteins which mediate a number of reactions, including the conversion of ribonucleotides (RNA precursors) to deoxyribonucleotides (DNA precursors) by ribonucleotide reductase. ( CSP )] (UMLS (CSP) C0039938) =Amino Acid, Peptide, or Protein; Biologically Active Substance =redoxin;
|
- 17. 6 thiopurine riboside
- [ ] (UMLS (CSP) C0599534) =Nucleic Acid, Nucleoside, or Nucleotide; Pharmacologic Substance
| - 67. Thioredoxin Gene
- [This gene plays a role in intercellular signaling, signal transduction and protection against cellular oxidative stress. ( NCI )] (UMLS (NCI) C1336690) TXN;
TXN Gene =Gene or Genome ;
|
- 18. THIACETARSAMIDE
- [Proposed chemotherapeutic agent against filaria and trichomonas. ( MSH )] (UMLS (NCI) C0003815) =Organic Chemical; Pharmacologic Substance
| - 68. thioredoxin reductase
- [A FLAVOPROTEIN enzyme that catalyzes the oxidation of THIOREDOXINS to thioredoxin disulfide in the presence of NADP+. It was formerly listed as EC 1.6.4.5 ( MSH )] (UMLS (CSP) C0039941) =Amino Acid, Peptide, or Protein; Enzyme
|
- 19. thiadiazine
- [6-membered aromatic ring structure with 2 nitrogen and 1 sulfur heteroatoms. ( CSP )] (UMLS (CSP) C0039836) =Organic Chemical =nitrogenous heterocyclic compound;
sulfurous heterocyclic compound =thiazide | - 69. THIORIDAZINE
- [phenothiazine compound having antipsychotic and sedative effects, used in treatment of schizophrenia and acute psychotic episodes, for relief of anxiety, agitiation and depression in mood disorders, and for treatment of disruptive behavior disorders in children. ( CSP )] (UMLS (NCI) C0039943) =Organic Chemical; Pharmacologic Substance =[CN300] SEDATIVES/HYPNOTICS;
Phenothiazine;
[CN700] ANTIPSYCHOTICS;
[CN701] PHENOTHIAZINES/RELATED, ANTIPSYCHOTICS =THIORIDAZINE HYDROCHLORIDE |
- 20. Thiamin Metabolism
- [The chemical reactions and pathways involving thiamin (vitamin B1), a water soluble vitamin present in fresh vegetables and meats, especially liver. [GOC:jl, ISBN:0198506732 "Oxford Dictionary of Biochemistry and Molecular Biology"] ( GO )] (UMLS (NCI) C1159439) Thiamin Metabolism Pathway =Molecular Function
| - 70. thiosemicarbazone
- [ ] (UMLS (CSP) C0039946) =Organic Chemical ;
=hydrazone;
|
- 21. Thiamine and niacin deficiency states
- [ ] (UMLS (ICD9CM) C0154239) =Disease or Syndrome
| - 71. thiosugar
- [Sugar analogs in which the ring oxygen is replaced by a sulfur. ( MSH )] (UMLS (CSP) C0597576) =Carbohydrate ;
=carbohydrate;
sulfur compound =aurothioglucose |
- 22. thiamine deficiency
- [nutritional condition produced by a deficiency of thiamine in the diet, characterized by anorexia, irritability, and weight loss; later, patients experience weakness, peripheral neuropathy, headache, and tachycardia; in addition to being caused by a poor diet, thiamine deficiency in the United States most commonly occurs as a result of alcoholism, since ethanol interferes with thiamine absorption. ( CSP )] (UMLS (CSP) C0039841) =Disease or Syndrome =Deficiency of B-complex components;
=Korsakoff Syndrome;
Beri Beri;
Wernicke Encephalopathy | - 72. thiosulfate
- [sulfate group in which one or more oxygen atoms is replaced by sulfur. ( CSP )] (UMLS (CSP) C0039950) =Inorganic Chemical ;
=SULFATE;
sulfate =lime sulfur;
Disodium thiosulfate;
|
- 23. Thiamiprine
- [A cytotoxic purine antagonist that has both immunosuppressive and antiarthritic activity. (NCI) ( NCI )] (UMLS (NCI) C0076415) =Organic Chemical; Pharmacologic Substance
| - 73. Thiosulfil
- (UMLS (NCI) C0729139) =Organic Chemical; Pharmacologic Substance
|
- 24. THIAMPHENICOL
- [A methylsulfonyl analog of CHLORAMPHENICOL. It is an antibiotic and immunosuppressive agent. ( MSH )] (UMLS (NCI) C0039854) =Organic Chemical; Antibiotic ;
| - 74. Thiotepa/Vinblastine
- (UMLS (NCI) C0280263) =Therapeutic or Preventive Procedure
|
- 25. THIAMYLAL
- [A barbiturate that is administered intravenously for the production of complete anesthesia of short duration, for the induction of general anesthesia, or for inducing a hypnotic state. (From Martindale, The Extra Pharmacopoeia, 30th ed, p919) ( MSH )] (UMLS (NCI) C0039855) =Organic Chemical; Pharmacologic Substance ;
=Thiobarbiturates;
[CN202] BARBITURIC ACID DERIVATIVE, ANESTHETICS =Thiamylal Sodium | - 75. Thiotepa/Vincristine
- (UMLS (NCI) C0280690) =Therapeutic or Preventive Procedure
|
- 26. Thiamylal Sodium
- (UMLS (NCI) C0700559) =Organic Chemical; Pharmacologic Substance ;
=THIAMYLAL;
| - 76. thiouracil
- [antimetabolite used to treat hyperthyroidism, angina pectoris, and congestive heart failure, and as an experimental metabolic probe. ( CSP )] (UMLS (CSP) C0039957) =Organic Chemical; Pharmacologic Substance =2, 4-Dioxopyrimidine;
thiopyrimidine;
uracil analog;
=6-Propyl-2-thiouracil |
- 27. thiazide
- [family of bicyclic compounds in which one ring has a sulfony l and 2 nitrogen heteroatoms; they inhibit renal sodium resorption, and so are used as diuretics and antihypertensives. ( CSP )] (UMLS (CSP) C0541746) =Organic Chemical; Pharmacologic Substance =[CV700] DIURETICS;
thiadiazine =chlorothiazide;
3-Methyl-7-chloro-1,2,4-benzothiadiazine 1,1-Dioxide;
| - 77. thiourea analog
- [ ] (UMLS (CSP) C0597838) =Organic Chemical; Indicator, Reagent, or Diagnostic Aid ;
|
- 28. thiazine
- [6-membered aromatic ring structure with 1 nitrogen and 1 sulfur heteroatoms. ( CSP )] (UMLS (CSP) C0039858) =Organic Chemical =Heterocyclic Compounds, 1-Ring;
nitrogenous heterocyclic compound;
sulfurous heterocyclic compound;
=Phenothiazine;
4-Hydroxy-2-methyl-N-2-pyridinyl-2H-1,2-benzothiazine-3-carboximide-1,1-dioxide;
CHLORMEZANONE;
4-Hydroxy-2-methyl-N-2-pyridinyl-2H-1,2-benzothiazine-3-carboximide-1,1-dioxide;
4-Hydroxy-2-methyl-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide;
azopt;
| - 78. thioxanthone
- [tricyclic xanthene analog with a sulfur atom at one bridge point and a carbonyl carbon at the other. ( CSP )] (UMLS (CSP) C0597577) =Organic Chemical ;
=sulfurous heterocyclic compound;
|
- 29. thiazole
- [5-membered aromatic ring structure with 1 nitrogen and 1 sulfur heteroatoms. ( CSP )] (UMLS (CSP) C0039859) =Organic Chemical =azole;
Heterocyclic Compounds, 1-Ring;
sulfurous heterocyclic compound;
=acetazolamide;
[VT105] THIAMINE;
Rosiglitazone;
epothilon;
Famotidine;
(S)-2,3,5,6-Tetrahydro-6-phenylimidazo[2,1-b]thiazole;
Saccharin;
Sulfathiazoles;
TBZ;
Thiadiazoles;
Pioglitazone;
2-Amino-6-(trifluoromethoxy)benzothiazole;
pramipexol;
4-Hydroxy-2-methyl-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide;
NIZATIDINE;
5-[[4-[4(3,4-Dihydro-6-hydroxy-2,5,7,8-tetramethyl-2H-1-benzopyran-2-yl)methoxy]phenyl]methyl\-2,4-thiazolidinedione;
BRL 49653;
RIT;
2H-Indol-2-one, 5-(2-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)ethyl)-6-chloro-1,3-dihydro- | - 79. THIRAM
- [A dithiocarbamate chemical, used commercially in the rubber processing industry and as a fungicide. In vivo studies indicate that it inactivates the enzyme GLUTATHIONE REDUCTASE. It has mutagenic activity and may induce chromosomal aberrations. ( MSH )] (UMLS (NCI) C0039962) =Organic Chemical; Pharmacologic Substance; Hazardous or Poisonous Substance
|
- 30. thiazolidine carboxylate
- [ ] (UMLS (CSP) C0599531) =Organic Chemical ;
| - 80. Third
- [Following the second position in an ordering or series; coming next after the second and just before the fourth in position. ( NCI )] (UMLS (NCI) C0205437) =Quantitative Concept
|
- 31. Thibenzole
- (UMLS (NCI) C0733600) =Organic Chemical; Pharmacologic Substance ;
| - 81. third assistant
- [In a typical surgery setting there is rarely a third assistant (e.g., in some Hip operations the third assistant postures the affected leg). ( HL7V3.0 )] (UMLS (HL7) C1550494) =Professional or Occupational Group =ParticipationFunction;
|
- 32. Thick Filament
- (UMLS (NCI) C1179120) =Cell Component ;
| - 82. Third Cerebral Ventricle
- [A centrally placed component of the ventricular system of the brain located in the diencephalon. Cerebrospinal fluid from the lateral ventricles flows into the third ventricle via the foramina of Monroe and exits the third ventricle via the aqueduct of Sylvius. The thalamus and hypothalamus border the lateral walls of the third ventricle. ( NCI )] (UMLS (NCI) C0149555) =Body Space or Junction
|
- 33. Thickness
- [The dimension between two surfaces of an object, usually the smallest dimension as opposed to the width or the length: also, viscous consistency. ( NCI )] (UMLS (NCI) C1280412) =Qualitative Concept
| - 83. Third Degree Uterine Prolapse
- (UMLS (NCI) C0392530) =Acquired Abnormality ;
|
- 34. THIETHYLPERAZINE
- [A piperazine phenothiazine derivative and a dopamine antagonist used as antiemetic. Thiethylperazine blocks postsynaptic dopamine 2 (D2) receptors in the medullary chemoreceptor trigger zone (CTZ), thereby decreasing stimulation of the vomiting center in the brain. Peripherally, thiethylperazine blocks the vagus nerve in the gastrointestinal tract. In addition, this agent also shows antagonistic activities mediated through muscarinic receptors, H1-receptors, and alpha(1)-receptors. ( NCI )] (UMLS (NCI) C0039865) =Organic Chemical; Pharmacologic Substance ;
=[GA700] ANTIEMETICS;
Phenothiazine;
Piperazines;
=THIETHYLPERAZINE MALATE | - 84. Third major medical
- (UMLS (HL7) C1549484) =Idea or Concept =Policy type;
|
- 35. THIETHYLPERAZINE MALATE
- [The maleate salt form of triethylperazine, a piperazine phenothiazine derivative and a dopamine antagonist used as antiemetic. Thiethylperazine blocks postsynaptic dopamine 2 (D2) receptors in the medullary chemoreceptor trigger zone (CTZ), thereby decreasing stimulation of the vomiting center in the brain. Peripherally, thiethylperazine blocks the vagus nerve in the gastrointestinal tract. In addition, this agent also shows antagonistic activities mediated through muscarinic receptors, H1-receptors, and alpha(1)-receptors. ( NCI )] (UMLS (NCI) C0242518) =Organic Chemical; Pharmacologic Substance =THIETHYLPERAZINE;
=THIETHYLPERAZINE MALEATE 10 MG;
THIETHYLPERAZINE MALEATE 5 MG/ML;
| - 85. Third Molar
- [Any one of the rearmost molars on each side of the upper and lower jaw in humans. ( NCI )] (UMLS (NCI) C0026369) =Body Part, Organ, or Organ Component ;
|
- 36. Thigh
- (UMLS (HL7) C0039866) =Body Location or Region =Body Part;
| - 86. Third or oculomotor nerve palsy, total
- [ ] (UMLS (ICD9CM) C0271371) =Disease or Syndrome
|
- 37. THIGH REATTACHMENT
- [ ] (UMLS (ICD9CM) C0177657) =Therapeutic or Preventive Procedure
| - 87. Third Party
- (UMLS (HL7) C1698594) =Intellectual Product =RoleCode;
|
- 38. Thin
- (UMLS (NCI) C0205168) =Qualitative Concept
| - 88. Third Pharyngeal Pouch
- (UMLS (NCI) C0231070) =Embryonic Structure
|
- 39. Thin Filament
- (UMLS (NCI) C1179121) =Cell Component ;
| - 89. Third Portion of Duodenum
- (UMLS (NCI) C0227302) =Body Part, Organ, or Organ Component
|
- 40. thin layer chromatography
- [Chromatography, Thin Layer ( HL7V3.0 )] (UMLS (CSP) C0008569) =Laboratory Procedure =chromatography;
ObservationMethod | - 90. THIRD-STAGE HEM-POSTPART
- [ ] (UMLS (ICD9CM) C0269898) =Pathologic Function ;
|
- 41. Thin-Walled Branching Vascular Pattern
- (UMLS (NCI) C1336736) =Finding ;
| - 91. THIRD-STAGE HEM-UNSPEC
- [ ] (UMLS (ICD9CM) C0157392) =Injury or Poisoning
|
- 42. thinking
- [mental activity, not predominantly perceptual, by which one apprehends some aspect of an object or situation based on past learning and experience. ( CSP )] (UMLS (CSP) C0039869) =Mental Process =cognition;
| - 92. Third-stage postpartum hemorrhage, with delivery
- [ ] (UMLS (ICD9CM) C0157393) =Pathologic Function
|
- 43. thioacid
- [ ] (UMLS (CSP) C0599508) =Organic Chemical ;
| - 93. thirst
- [sensation associated with a craving to drink, ordinarily interpreted as a desire for water. ( CSP )] (UMLS (CSP) C0039971) =Physiologic Function =hunger;
|
- 44. thioamide
- [compounds of the type R-(C=S)-N=. ( CSP )] (UMLS (CSP) C0039875) =Organic Chemical =sulfur compound;
| - 94. thirst regulation
- [ ] (UMLS (CSP) C0599535) =Physiologic Function ;
|
- 45. Thiobacillus
- [A genus of gram-negative, rod-shaped bacteria that derives energy from the oxidation of one or more reduced sulfur compounds. Many former species have been reclassified to other classes of PROTEOBACTERIA. ( MSH )] (UMLS (CSP) C0039877) =Bacterium
| - 95. thirst regulatory center
- [a region of the hypothalamus that is responsible for the regulation of water intake; osmoreceptors in that region are stimulated by an increased osmotic pressure of the body fluids to initiate thirst and drinking. ( CSP )] (UMLS (CSP) C0597578) =Body Location or Region ;
=brain regulatory center;
|
- 46. thiocarbamate
- [carbamates in which either or both O atoms are replaced by S. ( CSP )] (UMLS (CSP) C0039882) =Organic Chemical =carbamate;
sulfur compound =Bis(diethylthiocarbamoyl) Disulfide;
DDTC;
Carbamothioic Acid, methyl(3-methylphenyl)-, O-2-naphthalenyl Ester | - 96. This APC is not paid
- (UMLS (HL7) C1547525) =Intellectual Product =Reimbursement Type Code;
|
- 47. Thiocolchicine
- [An antimitotic alkaloid that binds to microtubules and inhibits tubulin polymerization and induces apoptosis. (NCI) ( NCI )] (UMLS (NCI) C0076451) =Organic Chemical ;
| - 97. This is an actuation time
- (UMLS (HL7) C1547531) =Intellectual Product =TQ conjunction ID;
|
- 48. thiocyanate
- [compounds of the type R-S=C=N. ( CSP )] (UMLS (CSP) C0039887) =Organic Chemical =sulfur compound;
| - 98. This is the default, indicating that there is no character set switching occurring in this message.
- (UMLS (HL7) C1549933) =Idea or Concept =Alternate character set handling scheme;
|
- 49. thioester
- [esters where either or both O atoms are replaced by S. ( CSP )] (UMLS (CSP) C0597572) =Organic Chemical ;
=sulfur compound;
| - 99. This observation/service is not on the formulary
- (UMLS (HL7) C1547534) =Idea or Concept =Formulary Status;
|
- 50. thioether
- [any compound of the type R-S-R. ( CSP )] (UMLS (CSP) C0039894) =Organic Chemical =sulfide;
| - 100. This observation/service is on the formulary
- (UMLS (HL7) C1547536) =Idea or Concept =Formulary Status;
|
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