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CAS RN: 38194-50-2 | Product Number: U0099
Sulindac
![Sulindac No-Image](/medias/U0099.jpg?context=bWFzdGVyfHJvb3R8NTM1MjR8aW1hZ2UvanBlZ3xhR1V6TDJnMk9DODRPVEl6TmprM09UQTFOamswTDFVd01EazVMbXB3Wnd8MjY5MGFkODY2OTVkNGU5ZWM1Yzc3ODI3NWNlNGU0MTU2MzZjMGI0NjQ5MDRlNGY0ZTFmMzMyYzA2YTZkZTEwZA)
Purity: >98.0%(T)(HPLC)
Synonyms:
- (Z)-5-Fluoro-2-methyl-1-[(p-methylsulfinyl)benzylidene]-1H-indene-3-acetic Acid
- (Z)-2-[5-Fluoro-2-methyl-1-[4-(methylsulfinyl)benzylidene]-1H-inden-3-yl]acetic Acid
Product Documents:
Size | Unit Price | Shanghai | Tianjin | Japan* |
---|---|---|---|---|
10G |
¥330.00
|
2 | 7 | 7 |
50G |
¥1,030.00
|
2 | Contact Us | 7 |
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Product Number | U0099 |
Purity / Analysis Method | >98.0%(T)(HPLC) |
Molecular Formula / Molecular Weight | C__2__0H__1__7FO__3S = 356.41 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
CAS RN | 38194-50-2 |
PubChem Substance ID | 354334891 |
Merck Index (14) | 8982 |
MDL Number | MFCD00599589 |
Specifications
Appearance | Light yellow to Brown powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(Neutralization titration) | min. 98.0 % |
Melting point | 182.0 to 186.0 °C |
Properties (reference)
Melting Point | 184 °C |
Maximum Absorption Wavelength | 327(0.05mol/L methanolic HCl) nm |
Solubility in water | Insoluble |
GHS
Pictogram |
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Signal Word | Danger |
Hazard Statements | H301 : Toxic if swallowed. H361 : Suspected of damaging fertility or the unborn child. H317 : May cause an allergic skin reaction. H334 : May cause allergy or asthma symptoms or breathing difficulties if inhaled. |
Precautionary Statements | P501 : Dispose of contents/ container to an approved waste disposal plant. P261 : Avoid breathing dust/ fume/ gas/ mist/ vapors/ spray. P272 : Contaminated work clothing should not be allowed out of the workplace. P270 : Do not eat, drink or smoke when using this product. P202 : Do not handle until all safety precautions have been read and understood. P201 : Obtain special instructions before use. P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection. P284 : Wear respiratory protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P308 + P313 : IF exposed or concerned: Get medical advice/ attention. P362 + P364 : Take off contaminated clothing and wash it before reuse. P304 + P340 : IF INHALED: Remove person to fresh air and keep comfortable for breathing. P333 + P313 : If skin irritation or rash occurs: Get medical advice/ attention. P301 + P310 + P330 : IF SWALLOWED: Immediately call a POISON CENTER/doctor. Rinse mouth. P405 : Store locked up. |
Related Laws:
RTECS# | NK8226000 |
Transport Information:
UN Number | UN2811 |
Class | 6.1 |
Packing Group | III |
Customs Control Conditions (Q) |
Application
Sulindac: A Nonsteroidal Anti-Inflammatory Drug (NSAID) with Unique Metabolisms
Sulindac is a nonsteroidal anti-inflammatory drug that has anti-inflammatory, analgesic and antipyretic activities. The mechanism of action, like that of other NSAIDs, is not completely understood but may be related to prostaglandin synthetase inhibition. Sulindac is a unique prodrug. Slindac is reversibly metabolized to sulindac sulfide [S0906] which has anti-inflammatory and analgesic properties and is irreversibly metabolized to sulindac sulfone which has been suggested to possess antiproliferative effects against tumors. (The product is for research purpose only.)
References
- The disposition of sulindac
- Chemical and biological studies on indomethacin, sulindac and their analogs (a review)
- Cyclooxygenase-2 overexpression and tumor formation are blocked by sulindac in a murine model of familial adenomatous polyposis
- Sulindac and its derivatives: a novel class of anticancer agents (a review)
- NSAID sulindac and its analog bind RXRα and inhibit RXRα-dependent AKT signaling
- Combination of sulindac and dichloroacetate kills cancer cells via oxidative damage
- Sulindac (a review on the synthesis, physical properties, methods of detection, drug metabolism, pharmacokinetics, etc.)
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