Naproxen sodium
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Naproxen sodium
structure -
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CAS No:
26159-34-2
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Formula:
C14H14O3.Na
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Chemical Name:
Naproxen sodium
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Synonyms:
2-Naphthaleneacetic acid,6-methoxy-α-methyl-,sodium salt (1:1),(αS)-;2-Naphthaleneacetic acid,6-methoxy-α-methyl-,sodium salt,L-(-)-;2-Naphthaleneacetic acid,6-methoxy-α-methyl-,sodium salt,(S)-;2-Naphthaleneacetic acid,6-methoxy-α-methyl-,sodium salt,(αS)-;Naproxen sodium;Sodium naproxen;Naprosyn sodium;Sodium naprosyn;Sodium (+)-6-methoxy-2-naphthalenepropionate;Sodium d-2-(6-methoxy-2-naphthyl)propionate;Apranax;Aleve;Xenobid;Anaprox;Anaprox DS;Naprelan;Flanax Forte;Naprogesic;Apraxin;Uniflam;Lefaine;Sutolin;Duk-F;Agilxen;Synflex;Apronax;Licorax;Flanax;Anax;Dafloxen;Narocin;Gynestrel;Axer;Miranax;RS 3560;Primeral;(2S)-2-(6-Methoxy-2-naphthyl)propanoic acid sodium salt;Aflaxen;Synflex Forte;Sunprox;(+)-(S)-Naproxen sodium salt
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CAS No:
Description
White Powder
Naproxen sodium is an organic sodium salt consisting of equimolar amounts of naproxen(1-) anions and sodium anions. It has a role as a non-narcotic analgesic, a cyclooxygenase 2 inhibitor, a cyclooxygenase 1 inhibitor, an antipyretic and a non-steroidal anti-inflammatory drug. It contains a naproxen(1-).|Naproxen Sodium is the sodium salt form of naproxen, a member of the arylacetic acid group of non-steroidal anti-inflammatory drugs (NSAIDs) with anti-inflammatory analgesic and antipyretic properties. Naproxen sodium reversibly and competitively inhibits cyclooxygenases (COX), thereby blocking the conversion of arachidonic acid to pro-inflammatory prostaglandins. This inhibits the formation of prostaglandins that are involved in pain, inflammation and fever.|An anti-inflammatory agent with analgesic and antipyretic properties. Both the acid and its sodium salt are used in the treatment of rheumatoid arthritis and other rheumatic or musculoskeletal disorders, dysmenorrhea, and acute gout.
Naproxen sodium Basic Attributes
252.24
252.076
247-486-2
9TN87S3A3C
DTXSID7045576
C48006
2918992090
Characteristics
49.4
1.70180
white powder
244-246 °C
403.9ºC at 760 mmHg
154.5ºC
Soluble in water up to 100mg/mlSoluble in methanol and chloroform. Slightly soluble in ether. Insoluble in water.
Commercially available naproxen and naproxen sodium conventional tablets and naproxen delayed-release (enteric-coated) tablets should be stored in well-closed containers at 15 - 30 deg C; the containers for the delayed-release tablets also should be light resistant. Extended-release naproxen sodium tablets should be stored in well-closed containers at 20 - 25 deg C. Naproxen oral suspension should be stored in light-resistant containers at 15 - 30 deg C, and temperatures exceeding 40 deg C shoul
1.89X10-6 mm Hg at 25 deg C (est)
Safety Information
III
6.1(b)
UN 3249
3
R22
53-45
QJ1047000
Xn,T
P201, P202, P261, P264, P270, P271, P280, P281, P301+P312, P302+P352, P304+P340, P305+P351+P338, P308+P313, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501
H302
|Danger|H302 (61.48%): Harmful if swallowed [Warning Acute toxicity, oral]|P201, P202, P261, P264, P270, P271, P280, P281, P301+P312, P302+P352, P304+P340, P305+P351+P338, P308+P313, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 136 companies from 15 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)|Compounds or agents that combine with cyclooxygenase (PROSTAGLANDIN-ENDOPEROXIDE SYNTHASES) and thereby prevent its substrate-enzyme combination with arachidonic acid and the formation of eicosanoids, prostaglandins, and thromboxanes. (See all compounds classified as Cyclooxygenase Inhibitors.)|Agents that increase uric acid excretion by the kidney (URICOSURIC AGENTS), decrease uric acid production (antihyperuricemics), or alleviate the pain and inflammation of acute attacks of gout. (See all compounds classified as Gout Suppressants.)
Aleve
Naproxen sodium Use and Manufacturing
Used as anti-inflammatory analgesic Naproxen (Aleve, Anaprox) is a COX inhibitor for COX-1 and COX-2 with IC50 of 8.7 μM and 5.2 μM, respectively An anti-inflammatory, analgesic, antipyretic. A non-steroidal anti-inflammatory
Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients
Computed Properties
Molecular Weight:252.24
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:252.07623855
Monoisotopic Mass:252.07623855
Topological Polar Surface Area:49.4
Heavy Atom Count:18
Complexity:282
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Drug Function and Efficacy
This product is a non-steroidal anti-inflammatory drug that can inhibit the synthesis of prostaglandins and exert anti-inflammatory and analgesic effects.
Registered Holders
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HETERO LABS LTD
Active
United States
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APITORIA PHARMA PRIVATE LTD
Active
United States
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DIVIS LABORATORIES LTD
Active
United States
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