(+-)-3-Benzoyl-alpha-methylbenzeneacetic acid
CAS number: 22071-15-4
Groups: Pharmaceutical, All Chemicals, API Active Pharmaceutical Ingredients
Information:
IUPAC Name: 2-[3-(Benzoyl)phenyl]propanoic acid
CAS Number: 22161-86-0
Chemical Formula: C16H14O3
Synonyms: 172964-50-0, 19,583 RP, 19583 RP, 22071-15-4, 22161-86-0, 2-[3-(benzoyl)phenyl]propanoic acid, 2-(3-Benzoylphenyl)propanoic acid, 2-[3-(benzoyl)phenyl]propionic acid, 2-(3-Benzoylphenyl)propionic acid, 2-(3-phenylcarbonylphenyl)propanoic acid, 2-[3-(phenylcarbonyl)phenyl]propanoic acid, 2-(m-Benzoylphenyl)propionic acid, 34016_RIEDEL, (+-)-3-Benzoyl-alpha-methylbenzeneacetic acid, 3-BENZOYL-ALPHA-METHYLBENZENEACETIC ACID, 3-Benzoylhydratropic acid, AB00052249, Acide (benzoyl-3-phenyl)-2-propionique [French], Actron, Alrheumat, Alrheumum, Alrheumun, Aneol, Benzeneacetic acid, 3-benzoyl-.alpha.-methyl-, Benzeneacetic acid, 3-benzoyl-alpha-methyl-, Benzeneacetic acid, 3-benzoyl-alpha-methyl-, (+-)-, Benzoylhydratropic Acid, BIM-0050664.0001, BPBio1_000261, BSPBio_000237, BSPBio_003037, C01716, C16H14O3, Capisten, CCRIS 4508, CHEBI:6128, CID3825, D00132, DB01009, DivK1c_000598, EINECS 244-759-8, Epatec, EU-0100686, Hydratropic acid, m-benzoyl-, (+-)-, IDI1_000598, K1751_SIAL, K2012_SIAL, KBio1_000598, KBio2_001789, KBio2_004357, KBio2_006925, KBio3_002537, KBioGR_000435, KBioSS_001789, ketoprofen, Ketoprofen (+-), Ketoprofene, Ketoprofene [INN-French], Ketoprofen (JP15/USP/INN), Ketoprofeno [INN-Spanish], Ketoprofenum [INN-Latin], Ketoprofen [USAN:BAN:INN:JAN], Ketoprofen [USAN:INN:BAN:JAN], Ketoprophene, L'Acide (benzoyl-3-phenyl)-2-propionique, Lopac0_000686, LS-28621, LS-7470, (+-)-m-Benzoylhydratropic acid, m-Benzoylhydratropic acid, MLS000028446, MLS000079024, MLS001201752, MLS001306444, NCGC00094043-01, NCGC00094043-02, NCGC00094043-03, NCGC00094043-04, NINDS_000598, Oprea1_117113, Orudis, Orudis KT, Orudis (TN), Oruvail, Prestwick0_000219, Prestwick1_000219, Prestwick2_000219, Prestwick3_000219, Prestwick_617, Profenid, Propionic acid, 2-(3-benzoylphenyl)-, racemic-Ketoprofen, RP 19583, RP-19583, RU 4733, SMR000040181, SPBio_000952, SPBio_002158, Spectrum_001309, SPECTRUM1501215, Spectrum2_000956, Spectrum3_001479, Spectrum4_000028, Spectrum5_001254, STOCK2S-03814
Product Info: Ketoprofen is a drug belong to a class of NSAID (nonsteroidal anti-inflammatory drug) acts by inhibiting isoforms of cyclo-oxygenase 1 and 2. It has an activity to treat inflammatory rheumatoid diseases and relieve acute pain. It is effective against period pains, pain after surgery, and fever.
Nonsteroidal Antiinflammatory Drugs (NSAIDs); chemically heterogeneous large groups of drugs which suppress inflammation in a manner similar to steroids, but less side effects of sedation, respiratory depression, or addiction than steroids. They are widely used for the treatment of inflammatory disorders and painful conditions such as rheumatoid arthritis, gout, bursitis, painful menstruation, and headache. They are effective in the relief of pain and fever. NSAIDs inhibit the cyclooxygenase (COX) activity resulting in decreased synthesis of prostaglandin, leukotriene and thromboxane precursors such as the ubiquitous enzyme which catalyzes the initial step in the synthesis of prostanoids. Prostanoid is any of a group of C-20 fatty acids complex with an internal five or six carbon rings such as prostaglandins, prostanoic acid, prostacyclins, and thromboxane; derived from arachidonic acid (C-20 polyunsaturated fatty acid with four cis double bonds). The action or the synthesis of prostanoids are involved in the modulation of a variety of pathophysiologic processes including inflammation, hemostasis, thrombosis, cytoprotection, ulceration, hemodynamics and other the progression of kidney diseases. Thus, NSAIDs as non-selective inhibitors of the cyclooxygenases (both the cyclooxygenase-1 and cyclooxygenase-2 isoenzymes) may have beneficial as well as untoward effects on a variety of human diseases. Low stomach prostanoid levels caused by COX-1 inhibitors can result in ulceration and internal bleeding and perforation. The selective COX-2 inhibitors such as oxicam, meloxicam, and coxibs (celecoxib, rofecoxib, valdecoxib, parecoxib and etoricoxib) do not interfere with COX-1. The most prominent NSAID is aspirin. Nonaspirin NSAIDs can be classified based on chemical structures.
Nonsteroidal Anti-Inflammatory Drugs (NSAID) by chemical structure
Carboxylic Acid Groups
Salicylates (Acetylsalicylate, Choline salicylate, Diflunisal, Magnesium choline salicylate, Magnesium salicylate, Salsalate)
Acetic Acids (Bendazac, Diclofenac, Etodolac, Indomethacin, Ketorolac, Nabumetone, Sulindac, Tolmetin)
Propionic acids (Carprofen, Fenoprofen, Flurbiprofen, Ibuprofen, Ketoprofen, Loxoprofen, Naproxen, Naproxen sodium, Oxaprozin, Vedaprofen)
Anthranilic acids (Meclofenamic acid, Meclofenamate sodium, Tolfenamic acid)
Phenylacetic acids
Aminonicotinic acids (Flunixin)
Indole Analogs (Indomethacin, Nabumetone, Ketorolac, Etodolac,)
Enolic Acid Groups (which doesn't have carboxylic group but acid due to the enolic hydroxy substituent)
Pyrazolones (Phenylbutazone, Oxyphenbutazone, Dipyrone, Ramifenazone)
Oxicams (Meloxicam, Piroxicam, Tenoxicam)
Coxibs
Celecoxib, Rofecoxib, Valdecoxib, Parecoxib, Etoricoxib
Gold Salts
Auranofin, Gold sodium thiomalate, Aurothioglucose
ASK FOR QUOTATIONGroups: Pharmaceutical, All Chemicals, API Active Pharmaceutical Ingredients
Information:
IUPAC Name: 2-[3-(Benzoyl)phenyl]propanoic acid
CAS Number: 22161-86-0
Chemical Formula: C16H14O3
Synonyms: 172964-50-0, 19,583 RP, 19583 RP, 22071-15-4, 22161-86-0, 2-[3-(benzoyl)phenyl]propanoic acid, 2-(3-Benzoylphenyl)propanoic acid, 2-[3-(benzoyl)phenyl]propionic acid, 2-(3-Benzoylphenyl)propionic acid, 2-(3-phenylcarbonylphenyl)propanoic acid, 2-[3-(phenylcarbonyl)phenyl]propanoic acid, 2-(m-Benzoylphenyl)propionic acid, 34016_RIEDEL, (+-)-3-Benzoyl-alpha-methylbenzeneacetic acid, 3-BENZOYL-ALPHA-METHYLBENZENEACETIC ACID, 3-Benzoylhydratropic acid, AB00052249, Acide (benzoyl-3-phenyl)-2-propionique [French], Actron, Alrheumat, Alrheumum, Alrheumun, Aneol, Benzeneacetic acid, 3-benzoyl-.alpha.-methyl-, Benzeneacetic acid, 3-benzoyl-alpha-methyl-, Benzeneacetic acid, 3-benzoyl-alpha-methyl-, (+-)-, Benzoylhydratropic Acid, BIM-0050664.0001, BPBio1_000261, BSPBio_000237, BSPBio_003037, C01716, C16H14O3, Capisten, CCRIS 4508, CHEBI:6128, CID3825, D00132, DB01009, DivK1c_000598, EINECS 244-759-8, Epatec, EU-0100686, Hydratropic acid, m-benzoyl-, (+-)-, IDI1_000598, K1751_SIAL, K2012_SIAL, KBio1_000598, KBio2_001789, KBio2_004357, KBio2_006925, KBio3_002537, KBioGR_000435, KBioSS_001789, ketoprofen, Ketoprofen (+-), Ketoprofene, Ketoprofene [INN-French], Ketoprofen (JP15/USP/INN), Ketoprofeno [INN-Spanish], Ketoprofenum [INN-Latin], Ketoprofen [USAN:BAN:INN:JAN], Ketoprofen [USAN:INN:BAN:JAN], Ketoprophene, L'Acide (benzoyl-3-phenyl)-2-propionique, Lopac0_000686, LS-28621, LS-7470, (+-)-m-Benzoylhydratropic acid, m-Benzoylhydratropic acid, MLS000028446, MLS000079024, MLS001201752, MLS001306444, NCGC00094043-01, NCGC00094043-02, NCGC00094043-03, NCGC00094043-04, NINDS_000598, Oprea1_117113, Orudis, Orudis KT, Orudis (TN), Oruvail, Prestwick0_000219, Prestwick1_000219, Prestwick2_000219, Prestwick3_000219, Prestwick_617, Profenid, Propionic acid, 2-(3-benzoylphenyl)-, racemic-Ketoprofen, RP 19583, RP-19583, RU 4733, SMR000040181, SPBio_000952, SPBio_002158, Spectrum_001309, SPECTRUM1501215, Spectrum2_000956, Spectrum3_001479, Spectrum4_000028, Spectrum5_001254, STOCK2S-03814
Product Info: Ketoprofen is a drug belong to a class of NSAID (nonsteroidal anti-inflammatory drug) acts by inhibiting isoforms of cyclo-oxygenase 1 and 2. It has an activity to treat inflammatory rheumatoid diseases and relieve acute pain. It is effective against period pains, pain after surgery, and fever.
Nonsteroidal Antiinflammatory Drugs (NSAIDs); chemically heterogeneous large groups of drugs which suppress inflammation in a manner similar to steroids, but less side effects of sedation, respiratory depression, or addiction than steroids. They are widely used for the treatment of inflammatory disorders and painful conditions such as rheumatoid arthritis, gout, bursitis, painful menstruation, and headache. They are effective in the relief of pain and fever. NSAIDs inhibit the cyclooxygenase (COX) activity resulting in decreased synthesis of prostaglandin, leukotriene and thromboxane precursors such as the ubiquitous enzyme which catalyzes the initial step in the synthesis of prostanoids. Prostanoid is any of a group of C-20 fatty acids complex with an internal five or six carbon rings such as prostaglandins, prostanoic acid, prostacyclins, and thromboxane; derived from arachidonic acid (C-20 polyunsaturated fatty acid with four cis double bonds). The action or the synthesis of prostanoids are involved in the modulation of a variety of pathophysiologic processes including inflammation, hemostasis, thrombosis, cytoprotection, ulceration, hemodynamics and other the progression of kidney diseases. Thus, NSAIDs as non-selective inhibitors of the cyclooxygenases (both the cyclooxygenase-1 and cyclooxygenase-2 isoenzymes) may have beneficial as well as untoward effects on a variety of human diseases. Low stomach prostanoid levels caused by COX-1 inhibitors can result in ulceration and internal bleeding and perforation. The selective COX-2 inhibitors such as oxicam, meloxicam, and coxibs (celecoxib, rofecoxib, valdecoxib, parecoxib and etoricoxib) do not interfere with COX-1. The most prominent NSAID is aspirin. Nonaspirin NSAIDs can be classified based on chemical structures.
Nonsteroidal Anti-Inflammatory Drugs (NSAID) by chemical structure
Carboxylic Acid Groups
Salicylates (Acetylsalicylate, Choline salicylate, Diflunisal, Magnesium choline salicylate, Magnesium salicylate, Salsalate)
Acetic Acids (Bendazac, Diclofenac, Etodolac, Indomethacin, Ketorolac, Nabumetone, Sulindac, Tolmetin)
Propionic acids (Carprofen, Fenoprofen, Flurbiprofen, Ibuprofen, Ketoprofen, Loxoprofen, Naproxen, Naproxen sodium, Oxaprozin, Vedaprofen)
Anthranilic acids (Meclofenamic acid, Meclofenamate sodium, Tolfenamic acid)
Phenylacetic acids
Aminonicotinic acids (Flunixin)
Indole Analogs (Indomethacin, Nabumetone, Ketorolac, Etodolac,)
Enolic Acid Groups (which doesn't have carboxylic group but acid due to the enolic hydroxy substituent)
Pyrazolones (Phenylbutazone, Oxyphenbutazone, Dipyrone, Ramifenazone)
Oxicams (Meloxicam, Piroxicam, Tenoxicam)
Coxibs
Celecoxib, Rofecoxib, Valdecoxib, Parecoxib, Etoricoxib
Gold Salts
Auranofin, Gold sodium thiomalate, Aurothioglucose
Leave some information and we will contact you ASAP about the quotation of this product!
