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Home > Encyclopedia > Diclofenac sodium

Diclofenac sodium

pharmaceutical raw materials
Diclofenac sodium structure

Diclofenac sodium 

structure
  • CAS No:

    15307-79-6

  • Formula:

    C14H11Cl2NO2.Na

  • Chemical Name:

    Diclofenac sodium

  • Synonyms:

    Benzeneacetic acid,2-[(2,6-dichlorophenyl)amino]-,sodium salt (1:1);Acetic acid,[o-(2,6-dichloroanilino)phenyl]-,monosodium salt;Benzeneacetic acid,2-[(2,6-dichlorophenyl)amino]-,monosodium salt;N-(2,6-Dichlorophenyl)-o-aminophenylacetic acid sodium salt;GP 45840;[o-(2,6-Dichloroanilino)phenyl]acetic acid sodium salt;Diclofenac sodium;Voltaren;Diclophenac sodium;Sodium [o-(2,6-dichloroanilino)phenyl]acetate;Sodium diclofenac;Voltarol;Diclofenac sodium salt;Feloran;Orthofen;2-(2,6-Dichloroanilino)phenylacetic acid sodium salt;Orthophen;Hyanalgese D;Inflaban;Naclof;Diklovit;SR 318B;Diclofen SR 100;Sorelmon;Voltaren Ophtha CD;Voltaren Ophtha;Voveran;Voldal;Rhumalgan;Kriplex;Effekton;Duravolten;Dicloreum;Evofenac;Diclo-Puren;Valetan;Neriodin;Dichronic;Novapirina;Dolobasan;Primofenac;Diclord;Diclo-Phlogont;Delphimix;Assaren;Prophenatin;Diclobenin;Xenid;Allvoran;Benfofen;Tsudohmin;Profenac;Fortfen;Diclofenac-Na Emulgel;Diclofenacsodium Emulgel;Dyclo;Diclokalium;Diclorep;Diclodyn;Diacron;Dyloject;Diclobene;Naclofen;Dicloberl Retard;Dicloberl;Dicloran CP;Diclofenac retard;Declophen;Naclofen Duo;diclotard;Refen retard;Refen;Diclon;Dicloflex;Panamor;Modifenac;Abitren;Olfen;Dedolor;Deflamat;Dicloran Plus;Dolaut;Dikloron;Saffrac;Daispas;Bolabomin;Voltral;Diclogesic;2-[2-[(2,6-Dichlorophenyl)amino]phenyl]acetic acid sodium salt;Neurodiclovit;Neurofenac;Phlogin;Diclomol;Dynapar;Voveran Plus;1147187-62-9

  • Categories:

    Active Pharmaceutical Ingredients  >  Antipyretic Analgesics

Description

Diclofenac Sodium is a potent and nonselective anti-inflammatory agent, acts as a COX inhibitor, with IC50s of 4 nM, 1.3 nM for human COX-1 and COX-2 in CHO cells, and 5.1, 0.84 μM for ovine COX-1 and COX-2, respectively.


Diclofenac sodium is the sodium salt of diclofenac. It contains a diclofenac(1-).|Diclofenac Sodium is the sodium salt form of diclofenac, a benzene acetic acid derivate and nonsteroidal anti-inflammatory drug (NSAID) with analgesic, antipyretic and anti-inflammatory activity. Diclofenac sodium is a non-selective reversible and competitive inhibitor of cyclooxygenase (COX), subsequently blocking the conversion of arachidonic acid into prostaglandin precursors. This leads to an inhibition of the formation of prostaglandins that are involved in pain, inflammation and fever.|A non-steroidal anti-inflammatory agent (NSAID) with antipyretic and analgesic actions. It is primarily available as the sodium salt.

Diclofenac sodium Basic Attributes

318.13000

316.99900

239-346-4

QTG126297Q

DTXSID3037208

C47984

2922499990

Characteristics

52.16000

3.10240

white or off-white powder

0.563 g/cm3

283-285 °C

412ºC at 760 mmHg

203ºC

H2O: 50 mg/mL

Keep tightly closed.

157.2 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]

Safety Information

III

6.1(b)

UN 2811

3

R25

S22-S36/37-S45

AG6330000

T

Stable.

P301 + P310

H301

|Danger|H301 (77.32%): Toxic if swallowed [Danger Acute toxicity, oral]|P201, P202, P260, P264, P270, P273, P280, P281, P301+P310, P301+P312, P302+P352, P305+P351+P338, P308+P313, P314, P321, P330, P332+P313, P337+P313, P362, P391, P405, and P501|Aggregated GHS information provided by 291 companies from 38 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

Treatment of pain|Treatment of inflammation, Treatment of pain|Treatment of musculoskeletal and connective tissue pain and discomfort|Treatment of musculoskeletal and connective tissue pain|Rheumatoid arthritis, Ankylosing spondylitis, Osteoarthritis

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.)

Dichlofenal

Diclofenac sodium Use and Manufacturing

Uses

A nonsteroidal anti-inflammatory compound and cyclooxygenase (COX) inhibitor.This product is a powerful antipyretic analgesic and anti-inflammatory drug. Its anti-inflammatory effect is 2-2.5 times that of indomethacin, 26-50 times stronger than acetylsalicylic acid. It is suitable for rheumatoid arthritis, osteoarthropathy, pain relief after surgery and fever caused by various reasons. Used as an anti-inflammatory analgesic, standard NSAID and cyclooxygenase (COX) inhibitor; used as a selective matrix for CYP2C9

Human Drugs -> EU pediatric investigation plans|Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients|Animal Drugs -> FDA Approved Animal Drug Products (Green Book) -> Active Ingredients

Computed Properties

Molecular Weight:318.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:316.9986282
Monoisotopic Mass:316.9986282
Topological Polar Surface Area:52.2
Heavy Atom Count:20
Complexity:310
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

Downstream Products

Drug Function and Efficacy

Inhibits cyclooxygenase activity, thereby blocking the conversion of arachidonic acid to prostaglandins; promotes the combination of arachidonic acid and triglycerides, reduces the concentration of free arachidonic acid in cells, and indirectly inhibits the synthesis of leukotrienes

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • AMOLI ORGANICS (A DIVISION OF UMEDICA LABORATORIES PVT LTD)

    United States United States
    Active
  • SYN-TECH CHEM AND PHARM CO LTD

    United States United States
    Active
  • MACLEODS PHARMACEUTICALS LTD

    India India
    Active

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