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Ketorolac tris salt - ≥99%, high purity , Cyclooxygenase inhibitor, CAS No.74103-07-4, Cyclooxygenase inhibitor

  • ≥99%
Item Number
K129289
Grouped product items
SKUSizeAvailabilityPrice Qty
K129289-1g
1g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$94.90
K129289-5g
5g
In stock
$379.90
K129289-25g
25g
In stock
$1,710.90

Selective COX-1 inhibitor

Basic Description

SynonymsKetorolac tromethamine|74103-07-4|Ketorolac tris salt|Toradol|Acular|Ketorolac (tromethamine salt)|Acular LS|Ketorolac tromethamine salt|Acuvail|Lixidol|Ketorolac trometamol|Acular PF|Syntex|Dolac|SPRIX|Tarasyn|Godek|Acular Preservative Free|Tromethamine
Specifications & Purity≥99%
Storage TempProtected from light,Store at -20°C
Shipped InDry ice
Action TypeINHIBITOR
Mechanism of actionCyclooxygenase inhibitor
Product Description

Ketorolac (tromethamine salt) inhibits both isoforms of Cox in recombinant rat and human enzyme systems. Ketorolac inhibits rat Cox-1 (IC50 of 0.27 μM), rat Cox-2 (IC50 of 2.06 μM), human Cox-1 (IC50 of 1.23 μM) and human Cox-2 (IC50 of 3.50 μM). The (S) enantiomer of Ketorolac with rat Cox-1 (IC50 of 0.10 μM) is approximately twice as potent as the racemate, whereas the (R)-enantiomer (IC50 of > 100 μM) is virtually without activity. Ketorolac shows inhibition of eicosanoid formation in HEL cells (Cox-1, IC50 of 0.025 μM) and LPS-stimulated Mono Mac 6 cells (Cox-2, IC50 of 0.039 μM), but does not significantly inhibit NO accumulation in supernatants of LPS-stimulated RAW 264.7 cells up to 300 μM. Ketorolac significantly inhibits thymidine incorporation of human osteoblasts (hOBs) upon 24 hours treatment in a dose-dependent manner, and inhibits proliferation and arrests cell cycle at G0/G1 phase in hOBs.
A non selective inhibitior of Cox-1 and Cox-2.

Associated Targets

PTGS2 Tclin Prostaglandin G/H synthase 2 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 2-amino-2-(hydroxymethyl)propane-1,3-diol;5-benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid
INCHI InChI=1S/C15H13NO3.C4H11NO3/c17-14(10-4-2-1-3-5-10)13-7-6-12-11(15(18)19)8-9-16(12)13;5-4(1-6,2-7)3-8/h1-7,11H,8-9H2,(H,18,19);6-8H,1-3,5H2
InChi Key BWHLPLXXIDYSNW-UHFFFAOYSA-N
Canonical SMILES C1CN2C(=CC=C2C(=O)C3=CC=CC=C3)C1C(=O)O.C(C(CO)(CO)N)O
Isomeric SMILES C1CN2C(=CC=C2C(=O)C3=CC=CC=C3)C1C(=O)O.C(C(CO)(CO)N)O
WGK Germany 3
RTECS UY7759900
PubChem CID 84003
Molecular Weight 376.4
Reaxy-Rn 6463165

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

4 results found

Lot NumberCertificate TypeDateItem
H2203398Certificate of AnalysisMay 13, 2024 K129289
H2203402Certificate of AnalysisMay 13, 2024 K129289
G1516073Certificate of AnalysisJan 17, 2023 K129289
L2009180Certificate of AnalysisOct 17, 2022 K129289

Chemical and Physical Properties

SolubilitySoluble in ethanol (~7 mg/ml), DMF (~50 mg/ml), DMSO (~7 mg/ml), water (15 mg/ml), and methanol.
Sensitivitylight &Moisture sensitive
Melt Point(°C)160-162°C

Safety and Hazards(GHS)

Pictogram(s) GHS06,   GHS07
Signal Danger
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

H301:Toxic if swallowed

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P271:Use only outdoors or in a well-ventilated area.

P270:Do not eat, drink or smoke when using this product.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P403+P233:Store in a well-ventilated place. Keep container tightly closed.

P362+P364:Take off contaminated clothing and wash it before reuse.

P330:Rinse mouth.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P301+P316:IF SWALLOWED: Get emergency medical help immediately.

P337+P317:If eye irritation persists: Get medical help.

P332+P317:If skin irritation occurs: Get medical help.

P319:Get medical help if you feel unwell.

WGK Germany 3
RTECS UY7759900
Reaxy-Rn 6463165
Merck Index 5306

Related Documents

References

1. Bagayoko S et al..  (2021)  Host phospholipid peroxidation fuels ExoU-dependent cell necrosis and supports Pseudomonas aeruginosa-driven pathology..  PLoS Pathog,  17  (9): (e1009927).  [PMID:34516571]

Solution Calculators