Displaying drugs 201 - 225 of 15057 in total
Alfuzosin
Benign prostatic hyperplasia (BPH) refers to a benign growth or hyperplasia of the prostate and leads to lower urinary tract symptoms in men, such as urgency, frequency and changes to urine flow. The prevalence of BPH is as high as 50%-60% for males in their 60's, and this prevalence increases...
Approved
Investigational
Matched Synonyms: … (±)-N-[3-[(4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino]propyl]tetrahydro-2-furamide ... N-[3-[(4-amino-6,7-dimethoxy-quinazolin-2-yl)- methyl-amino]propyl] tetrahydrofuran- 2-carboxamide …
Matched Iupac: … N-{3-[(4-amino-6,7-dimethoxyquinazolin-2-yl)(methyl)amino]propyl}oxolane-2-carboxamide …
Matched Description: … by relaxing the muscles in the prostate and bladder neck. ... [L31593] It was initially approved by the FDA in 2003 and is marketed by several pharmaceutical companies ... Benign prostatic hyperplasia (BPH) refers to a benign growth or hyperplasia of the prostate and leads …
Matched Categories: … Drugs Used in Benign Prostatic Hypertrophy …
Matched Iupac: … N-{3-[(4-amino-6,7-dimethoxyquinazolin-2-yl)(methyl)amino]propyl}oxolane-2-carboxamide …
Matched Description: … by relaxing the muscles in the prostate and bladder neck. ... [L31593] It was initially approved by the FDA in 2003 and is marketed by several pharmaceutical companies ... Benign prostatic hyperplasia (BPH) refers to a benign growth or hyperplasia of the prostate and leads …
Matched Categories: … Drugs Used in Benign Prostatic Hypertrophy …
Vardenafil
Vardenafil is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5) and an oral therapy for the treatment of erectile dysfunction.[L45563,L45568] During sexual stimulation, nitric oxide (NO) is released from nerve endings and endothelial cells in the corpus cavernosum, activating the enzyme guanylate cyclase and increasing the...
Approved
Matched Iupac: … -4-one ... 2-{2-ethoxy-5-[(4-ethylpiperazin-1-yl)sulfonyl]phenyl}-5-methyl-7-propyl-1H,4H-imidazo[4,3-f][1,2,4]triazin …
Matched Description: … Vardenafil is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase ... Compared to [sildenafil] and [tadalafil], vardenafil is a more potent inhibitor of PDE5; however, its ... [A258313] The use of vardenafil as a monotherapy for the treatment of pulmonary arterial hypertension …
Matched Categories: … Drugs Used in Erectile Dysfunction …
Matched Products: … Vardenafil 1 A Pharma 5 mg - Filmtabletten ... Vardenafil 1 A Pharma 10 mg - Filmtabletten ... Vardenafil 1 A Pharma 20 mg - Filmtabletten …
Matched Description: … Vardenafil is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase ... Compared to [sildenafil] and [tadalafil], vardenafil is a more potent inhibitor of PDE5; however, its ... [A258313] The use of vardenafil as a monotherapy for the treatment of pulmonary arterial hypertension …
Matched Categories: … Drugs Used in Erectile Dysfunction …
Matched Products: … Vardenafil 1 A Pharma 5 mg - Filmtabletten ... Vardenafil 1 A Pharma 10 mg - Filmtabletten ... Vardenafil 1 A Pharma 20 mg - Filmtabletten …
Difenoxin
Difenoxin is a 4-phenylpiperidine which is closely related to the opioid analgesic meperidine. Difenoxin alone is a USA Schedule I controlled drug, as it may be habit forming. However, it is listed as a Schedule IV controlled drug if combined with atropine, which is added to decrease deliberate misuse. Motofen(R)...
Approved
Illicit
Matched Synonyms: … 1-(3-cyano-3,3-diphenylpropyl)-4-phenylisonipecotic acid …
Matched Iupac: … 1-(3-cyano-3,3-diphenylpropyl)-4-phenylpiperidine-4-carboxylic acid …
Matched Description: … Difenoxin is a 4-phenylpiperidine which is closely related to the opioid analgesic meperidine. ... It is approved by the FDA to treat acute and chronic diarrhea. ... It works mostly in the periphery and activates opioid receptors in the intestine rather than the central …
Matched Salts cas: … 35607-36-4 …
Matched Iupac: … 1-(3-cyano-3,3-diphenylpropyl)-4-phenylpiperidine-4-carboxylic acid …
Matched Description: … Difenoxin is a 4-phenylpiperidine which is closely related to the opioid analgesic meperidine. ... It is approved by the FDA to treat acute and chronic diarrhea. ... It works mostly in the periphery and activates opioid receptors in the intestine rather than the central …
Matched Salts cas: … 35607-36-4 …
Oseltamivir
Oseltamivir (marketed as the product TamifluⓇ), is an antiviral neuraminidase inhibitor used for the treatment and prophylaxis of infection with influenza viruses A (including pandemic H1N1) and B. Oseltamivir exerts its antiviral activity by inhibiting the activity of the viral neuraminidase enzyme found on the surface of the virus, which...
Approved
Matched Synonyms: … Ethyl (3R,4R,5S)-4-acetamido-5-amino-3-(1-ethylpropoxy)-1-cyclohexene-1-carboxylate ... 1-Cyclohexene-1-carboxylic acid, 4-(acetylamino)-5-amino-3-(1-ethylpropoxy)-, ethyl ester, (3R-(3alpha …
Matched Iupac: … ethyl (3R,4R,5S)-5-amino-4-acetamido-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate …
Matched Description: … They recommend the use of oseltamivir in people with a higher risk of developing complications including ... Oseltamivir exerts its antiviral activity by inhibiting the activity of the viral neuraminidase enzyme ... is a self-limiting illness. …
Matched Iupac: … ethyl (3R,4R,5S)-5-amino-4-acetamido-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylate …
Matched Description: … They recommend the use of oseltamivir in people with a higher risk of developing complications including ... Oseltamivir exerts its antiviral activity by inhibiting the activity of the viral neuraminidase enzyme ... is a self-limiting illness. …
Azatadine
Antihistamines such as azatadine appear to compete with histamine for histamine H1- receptor sites on effector cells. The antihistamines antagonize those pharmacological effects of histamine which are mediated through activation of H1- receptor sites and thereby reduce the intensity of allergic reactions and tissue injury response involving histamine release.
Approved
Matched Synonyms: … 11-(1-Methyl-4-piperidinylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine ... 6,11-Dihydro-11-(1-methyl-4-piperidylidene)-5H-benzo(5,6)cyclohepta(1,2-b)pyridine …
Matched Iupac: … 2-(1-methylpiperidin-4-ylidene)-4-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3(8),4,6,11,13-hexaene …
Matched Iupac: … 2-(1-methylpiperidin-4-ylidene)-4-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3(8),4,6,11,13-hexaene …
Dasatinib
Dasatinib is an orally available multikinase inhibitor indicated for the treatment of Philadelphia chromosome (Ph)-positive leukemias.[A2224,L45171] Ph is a chromosomal abnormality found in patients with chronic myelogenous leukemia (CML) and acute lymphocytic leukemia (ALL), where the ABL tyrosine kinase and the breakpoint cluster region (BCR) gene transcribe the chimeric protein...
Approved
Investigational
Matched Synonyms: … N-(2-CHLORO-6-methylphenyl)-2-({6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl}amino)-1,3 …
Matched Iupac: … N-(2-chloro-6-methylphenyl)-2-({6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl}amino)-1,3 …
Matched Description: … [A2226] The use of dasatinib was first approved by the FDA in 2006.[L45171,L45186] ... [A2224,L45171] Ph is a chromosomal abnormality found in patients with chronic myelogenous leukemia (CML ... [A11377,A33432] Dasatinib also inhibits a spectrum of kinases involved in cancer, including several SRC-family …
Matched Categories: … P-glycoprotein substrates with a Narrow Therapeutic Index ... Cytochrome P-450 CYP1A2 Substrates with a Narrow Therapeutic Index ... Cytochrome P-450 CYP3A4 Substrates with a Narrow Therapeutic Index ... Cytochrome P-450 CYP3A5 Substrates with a Narrow Therapeutic Index …
Matched Iupac: … N-(2-chloro-6-methylphenyl)-2-({6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl}amino)-1,3 …
Matched Description: … [A2226] The use of dasatinib was first approved by the FDA in 2006.[L45171,L45186] ... [A2224,L45171] Ph is a chromosomal abnormality found in patients with chronic myelogenous leukemia (CML ... [A11377,A33432] Dasatinib also inhibits a spectrum of kinases involved in cancer, including several SRC-family …
Matched Categories: … P-glycoprotein substrates with a Narrow Therapeutic Index ... Cytochrome P-450 CYP1A2 Substrates with a Narrow Therapeutic Index ... Cytochrome P-450 CYP3A4 Substrates with a Narrow Therapeutic Index ... Cytochrome P-450 CYP3A5 Substrates with a Narrow Therapeutic Index …
Triamcinolone
Triamcinolone is a corticosteroid used to treat various inflammatory conditions in the body from allergic rhinitis to acute exacerbations of multiple sclerosis. Triamcinolone can be used as a one time adjunct treatment of osteoarthritic knee pain, or first line as a topical treatment of corticosteroid responsive dermatoses. Triamcinolone is more...
Approved
Vet approved
Matched International brands: … Omcilon-A …
Matched Iupac: … trihydroxy-1-(2-hydroxyacetyl)-9a,11a-dimethyl-1H,2H,3H,3aH,3bH,4H,5H,7H,9aH,9bH,10H,11H,11aH-cyclopenta[a] …
Matched Description: … Triamcinolone is a corticosteroid used to treat various inflammatory conditions in the body from allergic ... [L8243] In October 2021, a suspension of triamcinolone acetonide was approved for suprachoroidal injection ... or first line as a topical treatment of corticosteroid responsive dermatoses. …
Matched Mixtures name: … Mlp A-2 ... Mlp A-1 ... Pro-C-Dure 4 Kit …
Matched Products: … Volon 4 mg - Tabletten ... ไซมาคอร์ท (4 มก. ชนิดเม็ด) ... KENALOG IN ORABASE …
Matched Iupac: … trihydroxy-1-(2-hydroxyacetyl)-9a,11a-dimethyl-1H,2H,3H,3aH,3bH,4H,5H,7H,9aH,9bH,10H,11H,11aH-cyclopenta[a] …
Matched Description: … Triamcinolone is a corticosteroid used to treat various inflammatory conditions in the body from allergic ... [L8243] In October 2021, a suspension of triamcinolone acetonide was approved for suprachoroidal injection ... or first line as a topical treatment of corticosteroid responsive dermatoses. …
Matched Mixtures name: … Mlp A-2 ... Mlp A-1 ... Pro-C-Dure 4 Kit …
Matched Products: … Volon 4 mg - Tabletten ... ไซมาคอร์ท (4 มก. ชนิดเม็ด) ... KENALOG IN ORABASE …
Nilutamide
Nilutamide is an antineoplastic hormonal agent primarily used in the treatment of prostate cancer. Nilutamide is a pure, nonsteroidal anti-androgen with affinity for androgen receptors (but not for progestogen, estrogen, or glucocorticoid receptors). Consequently, Nilutamide blocks the action of androgens of adrenal and testicular origin that stimulate the growth of...
Approved
Investigational
Matched Synonyms: … 5,5-Dimethyl-3-(α,α,α-trifluoro-4-nitro-m-tolyl)hydantoin …
Matched Iupac: … 5,5-dimethyl-3-[4-nitro-3-(trifluoromethyl)phenyl]imidazolidine-2,4-dione …
Matched Description: … Nilutamide is an antineoplastic hormonal agent primarily used in the treatment of prostate cancer. ... Nilutamide is a pure, nonsteroidal anti-androgen with affinity for androgen receptors (but not for progestogen …
Matched Iupac: … 5,5-dimethyl-3-[4-nitro-3-(trifluoromethyl)phenyl]imidazolidine-2,4-dione …
Matched Description: … Nilutamide is an antineoplastic hormonal agent primarily used in the treatment of prostate cancer. ... Nilutamide is a pure, nonsteroidal anti-androgen with affinity for androgen receptors (but not for progestogen …
Methylparaben
Methylparaben is used in allergenic testing.
Approved
Matched Synonyms: … Methyl 4-hydroxybenzoate …
Matched Iupac: … methyl 4-hydroxybenzoate …
Matched Description: … Methylparaben is used in allergenic testing. …
Matched Categories: … Compounds used in a research, industrial, or household setting …
Matched Iupac: … methyl 4-hydroxybenzoate …
Matched Description: … Methylparaben is used in allergenic testing. …
Matched Categories: … Compounds used in a research, industrial, or household setting …
Famciclovir
Famciclovir, marketed as Famvir by Novartis, is a guanine analogue used to treat herpes virus infections. It is most commonly used to treat herpes zoster (shingles). Famciclovir is a prodrug of penciclovir with higher oral bioavailability.
Approved
Investigational
Matched Synonyms: … 9-[4-acetoxy-3-(acetoxymethyl)but-1-yl]-2-aminopurine ... acetic acid 2-acetoxymethyl-4-(2-amino-purin-9-yl)-butyl ester …
Matched Iupac: … 2-[(acetyloxy)methyl]-4-(2-amino-9H-purin-9-yl)butyl acetate …
Matched Description: … Famciclovir, marketed as Famvir by Novartis, is a guanine analogue used to treat herpes virus infections ... Famciclovir is a prodrug of penciclovir with higher oral bioavailability. …
Matched Iupac: … 2-[(acetyloxy)methyl]-4-(2-amino-9H-purin-9-yl)butyl acetate …
Matched Description: … Famciclovir, marketed as Famvir by Novartis, is a guanine analogue used to treat herpes virus infections ... Famciclovir is a prodrug of penciclovir with higher oral bioavailability. …
Phloxine B
Phloxine B (commonly known simply as phloxine, also known as D&C RED NO. 28) is a color additive which is used both as an inactive ingredient to provide color to products, or as a colorant in dental disclosing tablets. These tablets allow patients to visualise areas where more brushing and...
Approved
Matched Synonyms: … Disodium 2',4',5',7'-tetrabromo-4,5,6,7-tetrachlorofluorescein …
Matched Description: … is used both as an inactive ingredient to provide color to products, or as a colorant in dental disclosing ... Phloxine B (commonly known simply as phloxine, also known as D&C RED NO. 28) is a color additive which …
Matched Categories: … Compounds used in a research, industrial, or household setting …
Matched Description: … is used both as an inactive ingredient to provide color to products, or as a colorant in dental disclosing ... Phloxine B (commonly known simply as phloxine, also known as D&C RED NO. 28) is a color additive which …
Matched Categories: … Compounds used in a research, industrial, or household setting …
Chlorpropamide
Chlorpropamide is an oral antihyperglycemic agent used for the treatment of non-insulin-dependent diabetes mellitus (NIDDM). It belongs to the sulfonylurea class of insulin secretagogues, which act by stimulating β cells of the pancreas to release insulin. Sulfonylureas increase both basal insulin secretion and meal-stimulated insulin release. Medications in this class...
Approved
Investigational
Matched Synonyms: … N-(4-chlorophenylsulfonyl)-N'-propylurea ... 4-chloro-N-((propylamino)carbonyl)benzenesulfonamide ... 4-chloro-N-[(propylamino)carbonyl]benzenesulfonamide …
Matched Iupac: … 1-(4-chlorobenzenesulfonyl)-3-propylurea …
Matched Description: … It belongs to the sulfonylurea class of insulin secretagogues, which act by stimulating β cells of the ... Medications in this class differ in their dose, rate of absorption, duration of action, route of elimination ... dose is excreted in urine as unchanged drug and metabolites. …
Matched Categories: … Drugs Used in Diabetes …
Matched Iupac: … 1-(4-chlorobenzenesulfonyl)-3-propylurea …
Matched Description: … It belongs to the sulfonylurea class of insulin secretagogues, which act by stimulating β cells of the ... Medications in this class differ in their dose, rate of absorption, duration of action, route of elimination ... dose is excreted in urine as unchanged drug and metabolites. …
Matched Categories: … Drugs Used in Diabetes …
Valproic acid
Valproic acid, or valproate, is an fatty acid derivative and anticonvulsant originally synthesized in 1881 by Beverly S. Burton. It enjoyed use as a popular organic solvent in industry and pharmaceutical manufacturing for nearly a century. In 1963, a serendipitous discovery was made by George Carraz during his investigations into...
Approved
Investigational
Matched Synonyms: … 4-heptanecarboxylic acid …
Matched Description: … In 1963, a serendipitous discovery was made by George Carraz during his investigations into the anticonvulsant ... 1881 by Beverly S. ... is the subject of many clinical trials in a variety of cancer types. …
Matched Mixtures name: … Depakine Chronosphere 50 mg Retardgranulat in Beuteln ... Depakine Chronosphere 50 mg Retardgranulat in Beuteln ... Depakine Chronosphere 250 mg Retardgranulat in Beuteln …
Matched Categories: … UGT1A1 Substrates with a Narrow Therapeutic Index ... UGT1A3 Substrates with a Narrow Therapeutic Index ... UGT1A6 Substrates with a Narrow Therapeutic Index ... UGT1A9 Substrates with a Narrow Therapeutic Index ... UGT2B7 Substrates with a Narrow Therapeutic Index …
Matched Products: … DEPAKINE (400MG/4 ML) ... 4 ADET ÇÖZÜCÜ AMPUL ... DEPAKİN 400 MG/4 ML IV ENJEKSİYONLUK ÇÖZELTİ İÇİN LİYOFLİZE TOZ VE ÇÖZÜCÜ, 4 ADET …
Matched Description: … In 1963, a serendipitous discovery was made by George Carraz during his investigations into the anticonvulsant ... 1881 by Beverly S. ... is the subject of many clinical trials in a variety of cancer types. …
Matched Mixtures name: … Depakine Chronosphere 50 mg Retardgranulat in Beuteln ... Depakine Chronosphere 50 mg Retardgranulat in Beuteln ... Depakine Chronosphere 250 mg Retardgranulat in Beuteln …
Matched Categories: … UGT1A1 Substrates with a Narrow Therapeutic Index ... UGT1A3 Substrates with a Narrow Therapeutic Index ... UGT1A6 Substrates with a Narrow Therapeutic Index ... UGT1A9 Substrates with a Narrow Therapeutic Index ... UGT2B7 Substrates with a Narrow Therapeutic Index …
Matched Products: … DEPAKINE (400MG/4 ML) ... 4 ADET ÇÖZÜCÜ AMPUL ... DEPAKİN 400 MG/4 ML IV ENJEKSİYONLUK ÇÖZELTİ İÇİN LİYOFLİZE TOZ VE ÇÖZÜCÜ, 4 ADET …
Metipranolol
A beta-adrenergic antagonist effective for both beta-1 and beta-2 receptors. It is used as an antiarrhythmic, antihypertensive, and antiglaucoma agent.
Approved
Matched Synonyms: … Acetic acid 4-(2-hydroxy-3-isopropylamino-propoxy)-2,3,6-trimethyl-phenyl ester …
Matched Iupac: … 4-{2-hydroxy-3-[(propan-2-yl)amino]propoxy}-2,3,6-trimethylphenyl acetate …
Matched Description: … A beta-adrenergic antagonist effective for both beta-1 and beta-2 receptors. …
Matched Iupac: … 4-{2-hydroxy-3-[(propan-2-yl)amino]propoxy}-2,3,6-trimethylphenyl acetate …
Matched Description: … A beta-adrenergic antagonist effective for both beta-1 and beta-2 receptors. …
Parecoxib
Parecoxib is a water-soluble and injectable prodrug of valdecoxib. It is marketed as Dynastat in the European Union. Parecoxib is a COX2 selective inhibitor in the same category as celecoxib (Celebrex) and rofecoxib (Vioxx). As it is injectable, it can be used perioperatively when patients are unable to take oral...
Approved
Matched Synonyms: … N-((p-(5-methyl-3-phenyl-4-isoxazolyl)phenyl)sulfonyl)propionamide …
Matched Iupac: … N-[4-(5-methyl-3-phenyl-1,2-oxazol-4-yl)benzenesulfonyl]propanamide …
Matched Description: … A letter of non-approval for parecoxib was issued by the FDA in 2005. ... Parecoxib is a COX2 selective inhibitor in the same category as celecoxib (Celebrex) and rofecoxib (Vioxx ... Parecoxib is a water-soluble and injectable prodrug of valdecoxib. …
Matched Iupac: … N-[4-(5-methyl-3-phenyl-1,2-oxazol-4-yl)benzenesulfonyl]propanamide …
Matched Description: … A letter of non-approval for parecoxib was issued by the FDA in 2005. ... Parecoxib is a COX2 selective inhibitor in the same category as celecoxib (Celebrex) and rofecoxib (Vioxx ... Parecoxib is a water-soluble and injectable prodrug of valdecoxib. …
Polyethylene glycol
Polyethylene glycol (PEG) is a synthetic polymer produced via polymerization of ethylene oxide molecules to make joining units of ethylene glycol by an ether linkage.[A190975,A190978] PEGs are water-soluble polymers that can form hydrogen bonds in a ratio of 100 water molecules per one PEG molecule. Molecular weights of PEGs vary...
Approved
Vet approved
Matched Description: … [A190975,A190978] PEGs are water-soluble polymers that can form hydrogen bonds in a ratio of 100 water ... to make joining units of ethylene glycol by an ether linkage. ... [A190975] Molecular weights of PEGs vary by time of the polymerization process and the molecular weight …
Matched Categories: … Compounds used in a research, industrial, or household setting …
Matched Products: … Mix-In Laxative Packets ... Lax-A-day ... Lax-A-day Men …
Matched Categories: … Compounds used in a research, industrial, or household setting …
Matched Products: … Mix-In Laxative Packets ... Lax-A-day ... Lax-A-day Men …
Lomefloxacin
Lomefloxacin is a fluoroquinolone antibiotic, used to treat bacterial infections including bronchitis and urinary tract infections (UTIs). Additionally, it has been employed for the prophylaxis of UTIs prior to surgery as well.
Approved
Investigational
Matched Synonyms: … (±)-1-ethyl-6,8-difluoro-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxo-3-quinolinecarboxylic acid ... 1,4-Dihydro-6,8-difluoro-1-ethyl-7-(3-methyl-1-piperazinyl)-4-oxo-3-quinolinecarboxylic acid …
Matched Iupac: … 1-ethyl-6,8-difluoro-7-(3-methylpiperazin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid …
Matched Description: … Lomefloxacin is a fluoroquinolone antibiotic, used to treat bacterial infections including bronchitis …
Matched Iupac: … 1-ethyl-6,8-difluoro-7-(3-methylpiperazin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid …
Matched Description: … Lomefloxacin is a fluoroquinolone antibiotic, used to treat bacterial infections including bronchitis …
Enmetazobactam
Enmetazobactam is a penicillanic acid sulfone extended-spectrum beta (β)-lactamase (ESBL) inhibitor. Because ESBL enzymes can hydrolyze important antibiotics such as penicillins, broad-spectrum cephalosporins and monobactams, ESBL-producing bacteria poses challenges in the treatment of serious infections. The combination product of enmetazobactam and cefepime was first approved by the FDA on February...
Approved
Matched Synonyms: … (2s,3s,5r)-3-methyl-3-((3-methyltriazol-3-ium-1-yl)methyl)-4,4,7-trioxo-4^6-thia-1-azabicyclo(3.2.0)heptane ... 1h-1,2,3-triazolium, 3-(((2s,3s,5r)-2-carboxy-3-methyl-4,4-dioxido-7-oxo-4-thia-1-azabicyclo(3.2.0)hept …
Matched Description: … Enmetazobactam is a penicillanic acid sulfone extended-spectrum beta (β)-lactamase (ESBL) inhibitor. ... penicillins, broad-spectrum cephalosporins and monobactams, ESBL-producing bacteria poses challenges in ... [L50126] Enmetazobactam is used as cefepime-sparing therapy by preventing its breakdown by ESBL. …
Matched Description: … Enmetazobactam is a penicillanic acid sulfone extended-spectrum beta (β)-lactamase (ESBL) inhibitor. ... penicillins, broad-spectrum cephalosporins and monobactams, ESBL-producing bacteria poses challenges in ... [L50126] Enmetazobactam is used as cefepime-sparing therapy by preventing its breakdown by ESBL. …
Copanlisib
Copanlisib is a selective pan-Class I phosphoinositide 3-kinase (PI3K) inhibitor with preferential activity against the alpha and delta isoforms. PI3K, a lipid kinase that activates downstream signalling pathways involved in cell survival and growth, that exists in different isoforms and is often overexpressed in hematological malignancies. Copanlisib was granted accelerated...
Approved
Investigational
Matched Synonyms: … 2-AMINO-N-(7-METHOXY-8-(3-(MORPHOLIN-4-YL)PROPOXY)-2,3-DIHYDROIMIDAZO(1,2-C)QUINAZOLIN-5-YL(PYRIMIDINE ... 2-AMINO-N-(7-METHOXY-8-(3-MORPHOLIN-4-YLPROPOXY)-2,3-DIHYDROIMIDAZO(1,2-C)QUINAZOLIN-5-YL)PYRIMIDINE- ... 5-PYRIMIDINECARBOXAMIDE, 2-AMINO-N-(2,3-DIHYDRO-7-METHOXY-8-(3-(4-MORPHOLINYL)PROPOXY)IMIDAZO(1,2-C)QUINAZOLIN …
Matched Iupac: … 2-amino-N-{7-methoxy-8-[3-(morpholin-4-yl)propoxy]-2H,3H-imidazo[1,2-c]quinazolin-5-yl}pyrimidine-5-carboxamide …
Matched Description: … [A261730] Copanlisib was granted accelerated approval by the FDA in September 2017 for the treatment ... PI3K, a lipid kinase that activates downstream signalling pathways involved in cell survival and growth ... Copanlisib is a selective pan-Class I phosphoinositide 3-kinase (PI3K) inhibitor with preferential activity …
Matched Categories: … P-glycoprotein substrates with a Narrow Therapeutic Index ... Cytochrome P-450 CYP3A4 Substrates with a Narrow Therapeutic Index ... Cytochrome P-450 CYP3A5 Substrates with a Narrow Therapeutic Index ... Cytochrome P-450 CYP3A7 Substrates with a Narrow Therapeutic Index …
Matched Iupac: … 2-amino-N-{7-methoxy-8-[3-(morpholin-4-yl)propoxy]-2H,3H-imidazo[1,2-c]quinazolin-5-yl}pyrimidine-5-carboxamide …
Matched Description: … [A261730] Copanlisib was granted accelerated approval by the FDA in September 2017 for the treatment ... PI3K, a lipid kinase that activates downstream signalling pathways involved in cell survival and growth ... Copanlisib is a selective pan-Class I phosphoinositide 3-kinase (PI3K) inhibitor with preferential activity …
Matched Categories: … P-glycoprotein substrates with a Narrow Therapeutic Index ... Cytochrome P-450 CYP3A4 Substrates with a Narrow Therapeutic Index ... Cytochrome P-450 CYP3A5 Substrates with a Narrow Therapeutic Index ... Cytochrome P-450 CYP3A7 Substrates with a Narrow Therapeutic Index …
Thiethylperazine
A dopamine antagonist that is particularly useful in treating the nausea and vomiting associated with anesthesia, mildly emetic cancer chemotherapy agents, radiation therapy, and toxins. This piperazine phenothiazine does not prevent vertigo or motion sickness. (From AMA Drug Evaluations Annual, 1994, p457)
Approved
Withdrawn
Matched Synonyms: … 2-(ethylthio)-10-[3-(4-methylpiperazin-1-yl)propyl]-10H-phenothiazine …
Matched Iupac: … 2-(ethylsulfanyl)-10-[3-(4-methylpiperazin-1-yl)propyl]-10H-phenothiazine …
Matched Description: … A dopamine antagonist that is particularly useful in treating the nausea and vomiting associated with …
Matched Iupac: … 2-(ethylsulfanyl)-10-[3-(4-methylpiperazin-1-yl)propyl]-10H-phenothiazine …
Matched Description: … A dopamine antagonist that is particularly useful in treating the nausea and vomiting associated with …
Abatacept
Abatacept is a soluble fusion protein, which links the extracellular domain of human cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) to the modified Fc (hinge, CH2, and CH3 domains) portion of human immunoglobulin G1 (IgG1).[L20504,L42715] Structurally, abatacept is a glycosylated fusion protein with a MALDI-MS molecular weight of 92,300 Da and it...
Approved
Matched Description: … antigen 4 (CTLA-4) to the modified Fc (hinge, CH2, and CH3 domains) portion of human immunoglobulin ... It is produced through recombinant DNA technology in mammalian CHO cells. ... [L20504,L42715] Structurally, abatacept is a glycosylated fusion protein with a MALDI-MS molecular weight …
Matched Products: … ORENCIA Injection 125mg/ml in Prefilled Syringe ... ORENCIA SUBKUTAN 125 MG ENJEKSIYONLUK COZELTI ICEREN KULLANIMA HAZIR ENJEKTOR 4 ADET …
Matched Products: … ORENCIA Injection 125mg/ml in Prefilled Syringe ... ORENCIA SUBKUTAN 125 MG ENJEKSIYONLUK COZELTI ICEREN KULLANIMA HAZIR ENJEKTOR 4 ADET …
Nisoldipine
Nisoldipine is a 1,4-dihydropyridine calcium channel blocker. It acts primarily on vascular smooth muscle cells by stabilizing voltage-gated L-type calcium channels in their inactive conformation. By inhibiting the influx of calcium in smooth muscle cells, nisoldipine prevents calcium-dependent smooth muscle contraction and subsequent vasoconstriction. Nisoldipine may be used in alone...
Approved
Matched Synonyms: … isobutyl methyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate …
Matched Iupac: … 3-methyl 5-(2-methylpropyl) 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate …
Matched Description: … Nisoldipine is a 1,4-dihydropyridine calcium channel blocker. ... By inhibiting the influx of calcium in smooth muscle cells, nisoldipine prevents calcium-dependent smooth ... It acts primarily on vascular smooth muscle cells by stabilizing voltage-gated L-type calcium channels …
Matched Iupac: … 3-methyl 5-(2-methylpropyl) 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate …
Matched Description: … Nisoldipine is a 1,4-dihydropyridine calcium channel blocker. ... By inhibiting the influx of calcium in smooth muscle cells, nisoldipine prevents calcium-dependent smooth ... It acts primarily on vascular smooth muscle cells by stabilizing voltage-gated L-type calcium channels …
Hydroxyprogesterone caproate
Hydroxyprogesterone caproate is a synthetic steroid hormone that is similar to medroxyprogesterone acetate and megestrol acetate. It is an ester derivative of 17α-hydroxyprogesterone formed from caproic acid (hexanoic acid). Hydroxyprogesterone caproate was previously marketed under the trade name Delalutin by Squibb, which was approved by the U.S. Food and Drug...
Approved
Investigational
Matched Synonyms: … 17alpha-Caproyloxypregn-4-ene-3,20-dione …
Matched Iupac: … 11aS)-1-acetyl-9a,11a-dimethyl-7-oxo-1H,2H,3H,3aH,3bH,4H,5H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a] …
Matched Description: … of preterm delivery in women with a history of preterm delivery, sparking a pricing controversy. ... was approved by the U.S. ... FDA approved Makena from KV Pharmaceutical (previously named as Gestiva) on February 4, 2011 for prevention …
Matched Iupac: … 11aS)-1-acetyl-9a,11a-dimethyl-7-oxo-1H,2H,3H,3aH,3bH,4H,5H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a] …
Matched Description: … of preterm delivery in women with a history of preterm delivery, sparking a pricing controversy. ... was approved by the U.S. ... FDA approved Makena from KV Pharmaceutical (previously named as Gestiva) on February 4, 2011 for prevention …
Celiprolol
Celiprolol is indicated for the management of mild to moderate hypertension and effort-induced angina pectoris. It is simultaneously a selective β1 receptor antagonist, a β2 receptor partial agonist and a weak α2 receptor antagonist. In 2010 a clinical trial has suggested a use for this medication in the prevention of...
Approved
Investigational
Matched Synonyms: … RS)-N'-{3-acetyl-4-[3-(tert-butylamino)-2-hydroxypropoxy]phenyl}-N,N-diethylurea …
Matched Iupac: … 1-{3-acetyl-4-[3-(tert-butylamino)-2-hydroxypropoxy]phenyl}-3,3-diethylurea …
Matched Description: … Celiprolol is not approved for use by the FDA in the treatment of vascular Ehlers–Danlos syndrome. ... In 2010 a clinical trial has suggested a use for this medication in the prevention of vascular complications ... It is simultaneously a selective β1 receptor antagonist, a β2 receptor partial agonist and a weak α2 …
Matched Iupac: … 1-{3-acetyl-4-[3-(tert-butylamino)-2-hydroxypropoxy]phenyl}-3,3-diethylurea …
Matched Description: … Celiprolol is not approved for use by the FDA in the treatment of vascular Ehlers–Danlos syndrome. ... In 2010 a clinical trial has suggested a use for this medication in the prevention of vascular complications ... It is simultaneously a selective β1 receptor antagonist, a β2 receptor partial agonist and a weak α2 …
Linezolid
Linezolid is a synthetic antibiotic which is used for the treatment of infections caused by aerobic Gram-positive bacteria. Its effects are bacteriostatic against both enterococci and staphylococci and bactericidal against most isolates of streptococci. Linezolid exerts its antibacterial activity by inhibiting the initiation of bacterial protein synthesis - more specifically,...
Approved
Investigational
Matched Synonyms: … N-(((S)-3-(3-Fluoro-4-morpholinophenyl)-2-oxo-5-oxazolidinyl)methyl)acetamide …
Matched Iupac: … N-{[(5S)-3-[3-fluoro-4-(morpholin-4-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide …
Matched Description: … [A233425] A second member of this class, [tedizolid], was approved by the FDA in 2014 and is considered ... Linezolid is a synthetic antibiotic which is used for the treatment of infections caused by aerobic Gram-positive ... [L32965] Linezolid exerts its antibacterial activity by inhibiting the initiation of bacterial protein …
Matched Categories: … Monoamine Oxidase A Inhibitors for interaction with Monoamine Oxidase A substrates …
Matched Iupac: … N-{[(5S)-3-[3-fluoro-4-(morpholin-4-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide …
Matched Description: … [A233425] A second member of this class, [tedizolid], was approved by the FDA in 2014 and is considered ... Linezolid is a synthetic antibiotic which is used for the treatment of infections caused by aerobic Gram-positive ... [L32965] Linezolid exerts its antibacterial activity by inhibiting the initiation of bacterial protein …
Matched Categories: … Monoamine Oxidase A Inhibitors for interaction with Monoamine Oxidase A substrates …
Displaying drugs 201 - 225 of 15057 in total