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| | Naproxen Chemical Properties |
| Melting point | 152-154 °C (lit.) | | alpha | D +66° (in chloroform) | | Boiling point | 332.25°C (rough estimate) | | density | 1.1450 (rough estimate) | | refractive index | 67.5 ° (C=1, CHCl3) | | Fp | 9℃ | | storage temp. | 2-8°C | | solubility | Practically insoluble in water, soluble in ethanol (96 per cent) and in methanol. | | pka | pKa 4.28± 0.02(H2O,t =25,I=0.01) (Uncertain) | | form | powder | | color | White to Almost white | | optical activity | [α]25/D +66°, c = 1 in chloroform | | Water Solubility | Insoluble in water. | | Merck | 14,6417 | | BRN | 3591067 | | BCS Class | 2 | | LogP | 3.18 | | CAS DataBase Reference | 22204-53-1(CAS DataBase Reference) | | NIST Chemistry Reference | Naproxen(22204-53-1) | | EPA Substance Registry System | 2-Naphthaleneacetic acid, 6-methoxy-.alpha.-methyl-, (.alpha.S)- (22204-53-1) |
| | Naproxen Usage And Synthesis |
| Non-steroidal anti-inflammatory drugs | Naproxen is a non-steroidal anti-inflammatory drug ,it is a PG synthase inhibitor, which can inhibit prostaglandin synthetase, it has significant analgesic and antipyretic effects, oral absorption is rapid and complete, 2 to 4 hours after a dose ,plasma concentration reaches the peak, in the blood , more than 99% is bound to plasma proteins, t1/2 is 13 to 14 hours, about 95% is discharged from the urine with the prototype and metabolites.it is clinically used For the treatment of rheumatic and rheumatoid arthritis , osteoarthritis, ankylosing spondylitis, gout, arthritis, tenosynovitis.it can also be used to alleviate pain caused by musculoskeletal sprains, contusions,damages and dysmenorrhea . But it should be noted that like other non-steroidal anti-inflammatory drugs, the same serious gastrointestinal adverse reactions could occur at any time while taking naproxen during treatment, so the active gastroduodenal ulcer patients are hanged, other gastrointestinal tract disease patients should take this drug under close medical supervision.
The above information is edited by the Chemicalbook of Tian Ye.
| | Chemical Properties | White crystal or crystalline powder. Melting point 155.3 ℃. Soluble in acetone, soluble in methanol, ethanol, acetic acid, insoluble in benzene, practically insoluble in water. In case of light,it is color-graded, odorless, tasteless.
| | Uses | It is a non-steroidal anti-inflammatory drug for the relief of fever and inflammation and pain associated with arthritis or other symptoms , it has anti-inflammatory, antipyretic and analgesic effects. Naproxen plays a role by inhibiting the cyclooxygenase, which generates prostaglandin and is one kind of enzymes related to inflammatory mediators . It is recommended to take the drug during meals to reduce stomach irritation.
| | Used in Particular Diseases | Acute Gouty Arthritis:
Dosage and Frequency: 500 mg twice daily for 3 days, then 250–500 mg daily for 4–7 days
| | production method | by methylation, acetylation With 2-naphthol , 6-methoxy-2-acetonaphthone is produced, then it is condensed with acid ester, then generate the product through isomerization, hydrolysis, oxidation, and split and other reactions.
| | Category | Toxic substances
| | Toxicity grading | Highly toxic
| | Acute toxicity | Oral-rat LD50 248 mg/kg; Oral-Mouse LD50: 360 mg/kg
| | Flammability and hazard characteristics | Combustible; combustion produces toxic and acrid smoke.
| | Storage Characteristics | Ventilated, low-temperature ,dry storeroom, it should be stored and transported from food raw materials separately.
| | Extinguishing agent | Water, dry powder, foam,sand
| | Description | Naproxen is synthesized from 2-methoxynaphthalene and the (+)-isomer obtained by resolution with cinchonidine
(61). It was introduced in the United States in 1976 and, as a generic drug, has consistently been among the more
popular NSAIDs. It is marketed as the S-(+)-enantiomer, but interestingly, the sodium salt of the (–)-isomer also is on
the market as Anaprox. As an inhibitor of prostaglandin biosynthesis, it is 12 times more potent than aspirin, 10 times
more potent than phenylbutazone, three to four times more potent than ibuprofen, and four times times more potent
than fenoprofen, but it is approximately 300 times less potent than indomethacin. | | Chemical Properties | white to light yellow crystal powde | | Originator | Naprosyn,Syntex,UK,1973 | | Uses | An anti-inflammatory, analgesic, antipyretic. A non-steroidal anti-inflammatory | | Uses | (S)-(+)-2-(6-Methoxy-2-naphthyl)propionic acid is a non-selective cyclooxygenase (COX-1 and COX-2) inhibitor. | | Uses | Being analogous to other drugs of this series, naproxene exhibits analgesic, fever-reducing, and long-lasting anti-inflammatory action. It causes reduction and removal of
painful symptoms including joint pain, stiffness, and swelling in the joints. It is used in
the same indications as ibuprofen. | | Definition | ChEBI: A methoxynaphthalene that is 2-methoxynaphthalene substituted by a carboxy ethyl group at position 6. Naproxen is a non-steroidal anti-inflammatory drug commonly used for the reduction of pain, fever, inflammation and stiffness caused by conditions such a
osteoarthritis, kidney stones, rheumatoid arthritis, psoriatic arthritis, gout, ankylosing spondylitis, menstrual cramps, tendinitis, bursitis, and for the treatment of primary dysmenorrhea. It works by inhibiting both the COX-1 and COX-2 enzymes. | | Indications | Naproxen (Naprosyn) also has pharmacological
properties and clinical uses similar to those of ibuprofen.
It exhibits approximately equal selectivity for
COX-1 and COX-2 and is better tolerated than certain
NSAIDs, such as indomethacin. Adverse reactions related
to the GI tract occur in about 14% of all patients,
and severe GI bleeding has been reported. CNS complaints
(headache, dizziness, drowsiness), dermatological
effects (pruritus, skin eruptions, echinoses), tinnitus,
edema, and dyspnea also occur. | | Manufacturing Process | According to US Patent 3,658,858, a solution of 24 grams of 2-bromo-6-
methoxynaphthalene in 300 ml of tetrahydrofuran is slowly added to 2.5
grams of magnesium turnings and 100 ml of tetrahydrofuran at reflux
temperature. After the addition is complete, 20 grams of cadium chloride is
added, and the resultant mixture is refluxed for 10 minutes to yield a solution
of di-(6-methoxy-2-naphthyl)cadmium (which can be separated by
conventional chromatography, although separation is unnecessary).
A solution of 18 grams of ethyl 2-bromopropionate in 20 ml of tetrahydrofuran
is then added to the cooled reaction mixture. After 24 hours at 20°C, the
product is hydrolyzed by adding 200 ml of 5 weight percent methanolic
sodium hydroxide followed by heating to reflux for 1 hour. The reaction
mixture is then diluted with excess 1 N sulfuric acid and extracted with ether.
The ether phase is separated, evaporated to dryness and the residue is
recrystallized from acetone-hexane to yield 2-(6-methoxy-2-
naphthyl)propionic acid. | | Brand name | Naprosyn (Roche). | | Therapeutic Function | Antiinflammatory | | Synthesis Reference(s) | Tetrahedron, 49, p. 8433, 1993 DOI: 10.1016/S0040-4020(01)81926-8 | | General Description | Naproxen (Naprosyn, Anaprox), marketed as the (S)-enantiomer,is well absorbed after oral administration, givingpeak plasma levels in 2 to 4 hours and a half-life of 13 hours.Naproxen is highly protein bound and displaces most protein-bound drugs. It is recommended for use in RA, OA, acute gouty inflammation, and in primary dysmenorrhea. Itshows good analgesic activity (i.e., 400 mg is comparable to75–150 mg of oral meperidine and superior to 65 mg ofpropoxyphene and 325 mg of aspirin plus 30 mg of codeine).It is also available OTC as 200-mg tablets (Aleve). | | Pharmacokinetics | Naproxen is almost completely absorbed following oral administration. Peak plasma levels are achieved within 2 to 4
hours following administration. Like most of the acidic NSAIDs (pKa = 4.2), it is highly bound (99.6%) to plasma
proteins. Approximately 70% of an administered dose is eliminated as either unchanged drug (60%) or as conjugates
of unchanged drug (10%). The remainder is converted to the 6-O-desmethyl metabolite by both CYP3A4 and CYP1A2
and, further, to the glucuronide conjugate of the demethylated metabolite. The 6-O-desmethyl metabolite lacks
anti-inflammatory activity. Like most of the arylalkanoic acids, the most common side effect associated with the use
of naproxen is irritation to the GI tract. The most common other adverse reactions are associated with CNS
disturbances (e.g., nausea and dizziness). | | Clinical Use | Naproxen is indicated for the treatment of rheumatoid arthritis, osteoarthritis, juvenile arthritis, ankylosing
spondylitis, tendinitis, bursitis, acute gout, and primary dysmenorrhea and for the relief of mild to moderate pain. | | Synthesis | Naproxene, 2-(6-methoxy-2-naphthyl)-propionic acid (3.2.15) can be synthesized by the methods of synthesis described for ibuprofen as well as by the methods of
fenoprofen (3.2.21) and ketoprofen (3.2.27) synthesis that will be described below from
2-acetyl or 2-chloromethyl-6-methoxynaphthaline [99–101]. | | Veterinary Drugs and Treatments | The manufacturer lists the following indications: “…for the relief
of inflammation and associated pain and lameness exhibited with
myositis and other soft tissue diseases of the musculoskeletal system
of the horse.” (Package Insert; Equiproxen?—Syntex). It has
also been used as an antiinflammatory/analgesic in dogs for the
treatment of osteoarthritis and other musculoskeletal inflammatory
diseases (see adverse reactions below). | | Drug interactions | Potentially hazardous interactions with other drugs
ACE inhibitors and angiotensin-II antagonists:
antagonism of hypotensive effect; increased risk of
nephrotoxicity and hyperkalaemia
.
Analgesics: avoid concomitant use of 2 or more
NSAIDs, including aspirin (increased side effects);
avoid with ketorolac (increased risk of side effects
and haemorrhage).
Antibacterials: possibly increased risk of convulsions
with quinolones.
Anticoagulants: effects of coumarins and
phenindione enhanced; possibly increased risk of
bleeding with heparins, dabigatran and edoxaban -
avoid long term use with edoxaban.
Antidepressants: increased risk of bleeding with
SSRIs and venlaflaxine.
Antidiabetic agents: effects of sulphonylureas
enhanced.
Antiepileptics: possibly increased phenytoin
concentration.
Antivirals: increased risk of haematological toxicity
with zidovudine; concentration possibly increased by
ritonavir.
Ciclosporin: may potentiate nephrotoxicity
Cytotoxics: reduced excretion of methotrexate;
increased risk of bleeding with erlotinib.
Diuretics: increased risk of nephrotoxicity;
antagonism of diuretic effect; hyperkalaemia with
potassium-sparing diuretics.
Lithium: excretion decreased.
Pentoxifylline: increased risk of bleeding.
Probenecid: excretion reduced by probenecid.
Tacrolimus: increased risk of nephrotoxicity. | | Metabolism | Naproxen is extensively metabolised in the liver
to 6-0-desmethyl naproxen. Both naproxen and
6-0-desmethyl naproxen are further metabolised to their
respective acylglucuronide conjugated metabolites.
About 95% of a dose is excreted in urine as naproxen and
6-O-desmethylnaproxen and their conjugates. Less than
5% of a dose appears in the faeces. | | references | [1] barnett j, chow j, ives d, et al. purification, characterization and selective inhibition of human prostaglandin g/h synthase 1 and 2 expressed in the baculovirus system[j]. biochimica et biophysica acta (bba)-protein structure and molecular enzymology, 1994, 1209(1): 130-139.
[2] laneuville o, breuer d k, dewitt d l, et al. differential inhibition of human prostaglandin endoperoxide h synthases-1 and-2 by nonsteroidal anti-inflammatory drugs[j]. journal of pharmacology and experimental therapeutics, 1994, 271(2): 927-934.
[3] dubois r n, abramson s b, crofford l, et al. cyclooxygenase in biology and disease[j]. the faseb journal, 1998, 12(12): 1063-1073.
[4] agdeppa e d, kepe v, petri a, et al. in vitro detection of (s)-naproxen and ibuprofen binding to plaques in the alzheimer’s brain using the positron emission tomography molecular imaging probe 2-(1-{6-[(2-[18 f] fluoroethyl)(methyl) amino]-2-naphthyl} ethylidene) malononitrile[j]. neuroscience, 2003, 117(3): 723-730. |
| | Naproxen Preparation Products And Raw materials |
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