Non-steroidal anti-inflammatory drugs NSAID Chemical properties Mechanism Pharmacokinetics Uses Used in Particular Diseases Production method Synthetic routes Usage and dosage Adverse drug reaction Attention
ChemicalBook > CAS DataBase List > Etodolac

Etodolac

Non-steroidal anti-inflammatory drugs NSAID Chemical properties Mechanism Pharmacokinetics Uses Used in Particular Diseases Production method Synthetic routes Usage and dosage Adverse drug reaction Attention
Product Name
Etodolac
CAS No.
41340-25-4
Chemical Name
Etodolac
Synonyms
Lodine;Hypen;Etopen;Edolan;RAK-591;Osteluc;Etodine;Napilac;ay24236;Tedolan
CBNumber
CB3216064
Molecular Formula
C17H21NO3
Formula Weight
287.35
MOL File
41340-25-4.mol
More
Less

Etodolac Property

Melting point:
145-1480C
Boiling point:
507.9±45.0 °C(Predicted)
Density 
1.193±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
Practically insoluble in water, freely soluble in acetone and in ethanol (96 per cent)
pka
4.65(at 25℃)
form 
Solid
color 
White to Orange to Green
Water Solubility 
40mg/L(37 ºC)
Merck 
14,3874
BCS Class
2
InChIKey
NNYBQONXHNTVIJ-QGZVFWFLSA-N
CAS DataBase Reference
41340-25-4(CAS DataBase Reference)
EPA Substance Registry System
Pyrano[3,4-b]indole-1-acetic acid, 1,8-diethyl-1,3,4,9-tetrahydro- (41340-25-4)
More
Less

Safety

Hazard Codes 
T,Xi
Risk Statements 
23/24/25-40-36-25-36/37/38
Safety Statements 
22-36-45-26-36/37
RIDADR 
3249
WGK Germany 
3
RTECS 
UQ0360000
HazardClass 
6.1(b)
PackingGroup 
III
HS Code 
29349990
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P405Store locked up.

P501Dispose of contents/container to..…

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
E0516
Product name
Etodolac
Packaging
10mg
Price
$44
Updated
2024/03/01
Sigma-Aldrich
Product number
BP529
Product name
Etodolac
Purity
British Pharmacopoeia (BP) Reference Standard
Packaging
150MG
Price
$262
Updated
2024/03/01
Sigma-Aldrich
Product number
1268706
Product name
Etodolac
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
400mg
Price
$436
Updated
2024/03/01
TCI Chemical
Product number
E0858
Product name
Etodolac
Purity
>98.0%(HPLC)(T)
Packaging
5g
Price
$122
Updated
2024/03/01
TCI Chemical
Product number
E0858
Product name
Etodolac
Purity
>98.0%(HPLC)(T)
Packaging
25g
Price
$305
Updated
2024/03/01
More
Less

Etodolac Chemical Properties,Usage,Production

Non-steroidal anti-inflammatory drugs

Etodolac (trade name: Lodine), also known as ethoxycolic acid, indoleacetic acid, and rhododine, is a new generation of non-steroidal anti-inflammatory drug highly selective to COX-2. This product is a weak acidic drug, existing in a molecular form under the condition of lower pH value which is conducive to drug absorption. This product is widely used in the clinical treatment of postoperative pain. It has analgesic and anti-inflammatory effects, being able to relieve the symptoms of rheumatoid arthritis and osteoarthritis, delaying the pathological changes caused by arthritis. In inflammatory site, it can selectivity inhibit the prostaglandin synthesis to exert its anti-inflammatory effect. It is especially applicable to the elderly patients. This product appears as white crystalline powder with the melting point of 145~148 ℃.
Etodolac was first developed by a subsidiary of AHP in the United States. It had been successfully listed in the UK in 1985, followed by being listed in France, the United States, Germany, Japan and other countries.

NSAID

Etodolac (Etodolac), also known as indole acetic acid, indole acetic acid pyran and rodin etc, and the tradename is Lodine, a new generation of non-steroidal anti-inflammatory drugs which has a high selective of COX-2. This product is a kind of weak acid drug and has the form of molecular at lower pH values which is conducive to drug absorption. This product is widely used in the clinical treatment of pain after surgery, has a good effect of analgesic and anti-inflammatory that can relieve symptoms of rheumatoid arthritis and osteoarthritis, delay the bone pathology caused by arthritis and synthesis the prostaglandin at the sites of inflammation selectively. The product apply to the elderly patients. The etodolac is white crystalline powder, has the melting point of 145~148 ℃.
Etodolac was first developed by the subsidiary of AHP and successfully listed in the UK in 1985. The product have been listed in many countries like France, the United States, Germany and Japan etc.

Chemical properties

It is crystallized by the hexane-chloroform, with the melting point of 145~148 ℃.

Mechanism

This product is non-steroidal anti-inflammatory drugs. Its effects is similar to aspirin. It can inactivated the cyclooxygenase at the sites of inflammation thereby inhibit the biosynthesis of prostaglandins selectively.The product has little side effect for the gastrointestinal since its inhibition of PGE2 is mild and transient. It can be quickly absorbed by oral with a single dose of 200mg.It has the Tmax of 1 h, Cmax of 18.6 μg/ml, T1/2 of 7.4 h and PPB of 95%. The product do not accumulate in the body and 60% of the dose can be excreted after 24hr by the cellular metabolism, among the them, 74% is excreted in urine by the kidneys and 19% in feces. The product can reduce the incidence and damage of bone and joint and improce the condition of patients. The current study shows that the product has no teratogenic effect in  animal experiments and has little impact on fertility and reproductive function.

Pharmacokinetics

According to the current study abroad, the drug is well absorbed orally and has the the systemic bioavailability of 80% or more. The dosage should be within 600mg every 12 hours, the area under the curve of plasma concentration-time is in direct proportion to the dosage. More than 99% of etodolac can combine with the plasma protein, the free fraction is less than 1%. The single dose is at the range of 200-600mg and the the average peak plasma concentration (Cmax) within 80 ± 30 the minute is in the scope of 14 ± 4-37 ± 9μg/ml range. The average plasma clearance rate is 47 (± 16) ml/hr/kg and the elimination half-life is 7.3 (± 4.0) hours. Etodolac can be metabolized by the liver and 16% of the dose excreted by the faeces. The dose of the product is not determined by the weight, but the recommended dosage can use the body weight as reference.

Uses

(1) The non-steroidal anti-inflammatory drugs of Indole acetic acid class has the analgesic and anti-inflammatory effect. It can inhibit prostaglandin synthesis at the site of inflammation selectively. The product can be absorbed rapidly and has no signs of drug savings. It can be used for the treatment of rheumatoid arthritis, rheumatoid arthritis, osteoarthritis and postoperative pain relief etc. It is a medicament that suitable for elderly patients.
(2) Using as anti-inflammatory drugs.

Used in Particular Diseases

Acute Gouty Arthritis:
Dosage and Frequency: 300 mg twice daily

Production method

The acylation reaction of o-ethyl aniline, chloral hydrate and hydroxylamine can form the oxime, after the cyclization by using the sulfuric as the catalyst and the reduction by lithium aluminium hydride , oxime can turn into the indole derivatives. The reaction with the oxalyl chloride and ethanol can bring 1,2-carbonyl side chain in 3 bit and then be restored to hydroxyethyl by lithium aluminium hydride, after the condensation , cyclization with  ethyl propionylacetate and hydrolyzation. The final product-etodolac can be obtained.

Synthetic routes

The etodolac ester should be prepared at first, and the final product can be obtained after the hydrolyzation, acidification, crystallization of the organic phase and rectification by the toluene (or benzene)-refined petroleum ether. Using the industrial 7-Ethyl tryptophol and  ethyl propionylacetateas as the raw material to synthesis the etodolac ethyl, and get the crude etodolac by hydrolyzation and acidification. The refined etodolac can be obtained by recrystallization with isopropanol-water.

Figure 1 shows the synthetic route of etodolac

Usage and dosage

The usage are various with the different applications, as follows:
1. For pain: The recommended dose is 0.2-0.4g every 8 hours for acute pain , the maximum daily dose should not exceed 1.2g. The maximum daily dose for the patients who weight under 60kg should not exceed 20mg per kilogram of body weight. The etodolac still has analgesic effect on some patients.
2. For chronic diseases such as osteoarthritis and rheumatoid arthritis: The recommended dose of daily is 0.4-1.2g in divided doses orally, the maximum daily dose should not exceed 1.2g. The maximum daily dose for the patients who weight over 60kg should not exceed 20mg per kilogram of body weight. The daily dose for etodolac is 0.4g or less in divided doses.It has a certain effect for some patients.

Adverse drug reaction

The product may cause some side effect like the allergic symptoms include the rash, eczema, itching and redness etc; nausea, diarrhea, abdominal pain, heartburn, indigestion, bloating, abdominal pain, stomach cramps, constipation and vomiting for the gastrointestinal system; headache , dizziness, drowsiness, insomnia, nervousness, anxiety, depression, general malaise, fatigue, weakness, frequent urination, palpitations, edema and tinnitus for the central nervous system. The side effect like the increasing of the ALT, AST and BUN , the decline of the hemoglobin, white blood cells, red blood cells and thrombocytopenia are rarely.
The mechanism of action of Etodolac, the route of synthesis, adverse reactions, etc., were edited by Baoquan, Chemicalbook. (2016-11-18)

Attention

The drug security of pregnant and lactating women has not been established and should be used with caution. The first three months of pregnancy should not use this drug. The patients who allergic to aspirin and other NSAIDs or have the active peptic ulcer can not use this product disabled. The patients with the history of gastrointestinal disease include peptic ulcer should be closely monitored and be discontinued immediately when the peptic ulcer come. Even it has no direct effect on platelets, but the inhibition of prostaglandin biosynthesis can interfere the platelet function in some ways. The patients who has liver and kidney dysfunction sjpi;d adjust the dose according to need.

Description

Etodolac (etodolic acid) is a non-steroidal antiinflammatory/analgesic agent useful in the treatment of various inflammatory conditions, including rheumatoid and osteoarthritis.

Chemical Properties

Crystalline Solid

Originator

Ayerst (USA)

Uses

betaadrenergic agonist

Uses

Etodolac is a non-steroidal anti-inflammatory drug (NSAID) that selectively inhibits cyclooxygenase-2 (COX-2). Etodolac displays anti-inflammatory effects in both adjuvant arthritic and normal rats. E todolac is an anti-inflammatory; analgesic.

Uses

For acute and long-term management of signs and symptoms of osteoarthritis and rheumatoid arthritis, as well as for the management of pain.

Uses

Etodolac is a non-steroidal anti-inflammatory drug (NSAID). Product Data Sheet

Definition

ChEBI: A monocarboxylic acid that is acetic acid in which one of the methyl hydrogens is substituted by a 1,8-diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indol-1-yl moiety. A preferential inhibitor of cyclo-oxygenase 2 and non-steroidal anti-inflammatory, it is used for the treatment of rheumatoid arthritis and osteoarthritis, and for the alleviation of postoperative pain. Administered as the racemate, only the (S)-enantiomer is active.

Indications

Etodolac (Lodine) is indicated for the treatment of osteoarthritis, rheumatoid arthritis, and acute pain. It inhibits COX-2 with slightly more selectivity than COX-1 and therefore produces less GI toxicity than many other NSAIDs. Common adverse effects include skin rashes and CNS effects.

brand name

Lodine(Wyeth).

General Description

Etodolac (Lodine, Ultradol), a chiral, COX-2 selectiveNSAID drug that is marketed as a racemate, possesses an indolering as the aryl portion of this group of NSAID drugs.It shares many similar properties of this group and is indicatedfor short- and long-term management of pain and OA.
Similar to ketorolac, etodolac exhibits several uniqueenantioselective pharmacokinetic properties. For example,the “inactive” (R)-enantiomer has approximately a 10-foldhigher plasma concentration than the active (S)-enantiomer.Furthermore, the active (S)-enantiomer is less protein boundthan its (R)-enantiomer and therefore has a very large volumeof distribution. It is well absorbed with an elimination halflifeof 6 to 8 hours. Etodolac is extensively metabolized intothree major inactive metabolites, 6-hydroxy etodolac (via aromatichydroxylation), 7-hydroxy-etodolac (via aromatic hydroxylation),and 8-(1'-hydroxylethyl) etodolac (via benzylichydroxylation), which are eliminated as the correspondingether glucuronides. Its unstable, acyl glucuronide, however,is subject to enterohepatic circulation and reactivation tothe parent drug, similar to other NSAIDS in this class.

Biological Activity

Non-steroidal anti-inflammatory drug (NSAID) that selectively inhibits cyclooxygenase-2 (COX-2) (IC 50 values are 53 and >100 μ M for COX-2 and COX-1 respectively). Displays anti-inflammatory effects in both adjuvant arthritic and normal rats.

Biochem/physiol Actions

Non-steroidal anti-inflammatory compound that is a non-selective inhibitor of COX-1 and COX-2.

Mechanism of action

The primary mechanism of action appears to be inhibition of the biosynthesis of prostaglandins at the cyclooxygenase step, with no inhibition of the lipoxygenase system. Etodolac, however, possesses a more favorable ratio of inhibition of prostaglandin biosynthesis in human rheumatoid synoviocytes and chondrocytes than by cultured human gastric mucosal cells compared to ibuprofen, indomethacin, naproxen, diclofenac, and piroxicam.

Pharmacokinetics

Etodolac is rapidly absorbed following oral administration, with maximum serum levels being achieved within 1 to 2 hours, and it is highly bound to plasma proteins (99%) with pKa 4.7. The penetration of etodolac into synovial fluid is greater than or equal to that of tolmetin, piroxicam, or ibuprofen. Only diclofenac appears to provide greater penetration.

Clinical Use

Etodolac is promoted as the first of a new chemical class of anti-inflammatory drugs, the pyranocarboxylic acids. Although not strictly an arylacetic acid derivative (because there is a two-carbon atom separation between the carboxylic acid function and the hetero-aromatic ring), it still possesses structural characteristics similar to those of the heteroarylacetic acids and is classified here. It was introduced in the United States in 1991 for acute and long-term use in the management of osteoarthritis and as an analgetic. It also possesses antipyretic activity. Etodolac is marketed as a racemic mixture, although only the S-(+)-enantiomer possesses anti-inflammatory activity in animal models. Etodolac also displays a high degree of enantioselectivity in its inhibitory effects on the arachidonic acid cyclooxygenase system.

Veterinary Drugs and Treatments

Etodolac is labeled for the management of pain and inflammation associated with osteoarthritis in dogs. It may find uses, however, for a variety of conditions where pain and/or inflammation should be treated.

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 heparin, dabigatran and edoxaban - avoid long term use with edoxaban.
Antidepressants: increased risk of bleeding with SSRIs and venlafaxine.
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
Cytotoxic agents: 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
Tacrolimus: increased risk of nephrotoxicity.

Metabolism

Etodolac is metabolized to three hydroxylated metabolites and to glucuronide conjugates, none of which possesses important pharmacological activity. Metabolism appears to be the same in the elderly as in the general population, so no dosage adjustment appears necessary. Etodolac is indicated for the management of the signs and symptoms of osteoarthritis and for the management of pain.

References

[1] kumagai k1, kubo m, imai s, toyoda f, maeda t, okumura n, matsuura h, matsusue y.the cox-2 selective blocker etodolac inhibits tnfα-induced apoptosis in isolated rabbit articular chondrocytes. int j mol sci. 2013 sep 30;14(10):19705-15.
[2] hakozaki m1, hojo h, kikuchi s, abe m. etodolac, a selective cyclooxygenase-2 inhibitor, induces apoptosis by activating caspases in human malignant rhabdoid tumor cells (frtk-1). oncol rep. 2007 jan;17(1):169-73.

Etodolac Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Etodolac Suppliers

Gensenta Ilac Sanayii A.S.
Tel
--
Fax
--
Email
info@gensenta.com.tr
Country
Turkey
ProdList
4
Advantage
58
Ulkar Kimya Sanayii Ve Ticaret Anonim Sirketi
Tel
--
Fax
--
Email
info@ulkarkimya.com.tr
Country
Turkey
ProdList
7
Advantage
58
ULKAR KIMYA SANAYII VE TICARET AS
Tel
--
Fax
--
Email
info@ulkarkimya.com.tr
Country
Turkey
ProdList
7
Advantage
58
More
Less

View Lastest Price from Etodolac manufacturers

Hebei Chuanghai Biotechnology Co,.LTD
Product
Etodolac 41340-25-4
Price
US $1.90/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 ton
Release date
2024-08-20
Xiamen Wonderful Bio Technology Co., Ltd.
Product
Etodolac 41340-25-4
Price
US $88.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
330T
Release date
2023-07-21
Hong Kong Tiansheng New Material Trading Co., Ltd
Product
Etodolac 41340-25-4
Price
US $4.99/KG
Min. Order
1KG
Purity
99%
Supply Ability
100KG
Release date
2021-12-23

41340-25-4, EtodolacRelated Search:


  • (R)-2-(1,8-diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indol-1-yl)acetic acid
  • 22α-Hydroxyerythrodiol Solution, 100ppm
  • Etodolac Imp.(EP)
  • Etodolac impurity
  • 1,8-DIETHYL-1,3,4,9-TETRAHYDRO-PYRANO[3,4-B]INDOLE-1-ACETIC ACID
  • 1,3,4,9-tetrahydro-1,8-diethylpyrano(3,4-b)indole-1-aceticacid
  • 4-b)indole-1-aceticacid,1,3,4,9-tetrahydro-1,8-diethyl-pyrano(
  • 4-b]indole-1-aceticacid,1,8-diethyl-1,3,4,9-tetrahydro-pyrano[
  • 1,8-Diethyl-1,3,4,9-tetrahydropyran-(3,4-b)indol-1-acetic acid
  • Etodolac micronized
  • Pyrano(3,4-b)indole-1-acetic acid, 1,3,4,9-tetrahydro-1,8-diethyl-
  • (1R)-1,8-Diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid
  • RAK-591
  • Akomicol
  • Etopen
  • Hypen
  • Osteluc
  • rac Etodolac
  • (RS)-2-(1,8-Diethyl-4,9-dihydro-3H-pyrano[3,4-b]indol-1-yl)aceticacid
  • Etodolac,1,8-Diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid
  • Etodolac (400 mg)
  • Etodolac(Lodine)
  • Eccoxolac
  • Etodine
  • Lodin XL
  • Napilac
  • Etodlic Acid 1,8-Diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic Acid
  • AY-24236:Ramodar
  • ETODOLIC ACID
  • ETODOLAC
  • 2-[(1R)-1,8-diethyl-4,9-dihydro-3H-pyrano[3,4-b]indol-1-yl]acetic acid
  • ay24236
  • ultradol
  • ETODOLAC 8-METHYL ANALOGUE BP(CRM STANDARD)
  • ETODOLAC, BP STANDARD
  • ETODOLAC 1-METHYL ANALOGUE BP(CRM STANDARD)
  • ETODOLAC, ACID DIMER BP STANDARD
  • ETODOLAC, USP STANDARD
  • ETODOLAC, RELATED COMPOUND A(±)-8-ETHYL-L-METHYL-1,3,4,9-TETRAHYDROPYRANO[3,4-BETA]-INDOLE-1-ACETIC ACID USP STANDARD
  • ETODOLAC, EP STANDARD
  • ETODOLAC, IMPURITY H2-(7-ETHYLINDOL-3-YL)ETHANOL EP STANDARD
  • 1,8-diethyl-1,3,4,9-tetrahydropyrano-[3,4-6]indole-1-aceticacid
  • 1,8-Diethyl-1,3,4,9-tetrahydropyrano[3.4-b]indoleaceticacid
  • (1,8-Diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indol-1-yl)acetic acid
  • 1,8-Diethyl-1,3,4,9-tetrahydropyrano[3,4-β]indole-1-acetic Acid
  • Etogesic
  • Lodine
  • Tedolan
  • Ultrado
  • Etodolic
  • Pyrano3,4-bindole-1-acetic acid, 1,8-diethyl-1,3,4,9-tetrahydro-
  • ETODOLAC (DMF)
  • ETODOLAC ETODOLIC ACID
  • (RS)-Etodolic acid
  • Edolan
  • NIH 9918
  • NSC 282126
  • Ramodar