Cart
sales@molnova.com
Tebufelone
CAS No. 112018-00-5
Tebufelone( —— )
Catalog No. M36237 CAS No. 112018-00-5
Tebufelone is a potent in vitro inhibitor of CO , a novel non-steroidal anti-inflammatory drug (NSAID) belonging to the di-tert-butylphenol (DTBP) class that has shown potent anti-inflammatory, analgesic and anti-reticulitis properties in various animal models.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 187 | In Stock |
|
| 5MG | 117 | In Stock |
|
| 10MG | 173 | In Stock |
|
| 25MG | 282 | In Stock |
|
| 50MG | 424 | In Stock |
|
| 100MG | 612 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 1265 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameTebufelone
-
NoteResearch use only, not for human use.
-
Brief DescriptionTebufelone is a potent in vitro inhibitor of CO , a novel non-steroidal anti-inflammatory drug (NSAID) belonging to the di-tert-butylphenol (DTBP) class that has shown potent anti-inflammatory, analgesic and anti-reticulitis properties in various animal models.
-
DescriptionTebufelone (NE-11740), a nonsteroidal anti-inflammatory drug (NSAID), is a selective dual COX-2/5-lipoxygenase inhibitor. Tebufelone displays potent anti-inflammatory, analgesic and anti-pyretic properties.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayImmunology/Inflammation
-
TargetLTR
-
RecptorLTR | Prostaglandin Receptor
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number112018-00-5
-
Formula Weight300.44
-
Molecular FormulaC20H28O2
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESOC1=C(C(C)(C)C)C=C(C(CCCC#C)=O)C=C1C(C)(C)C
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. S M Weisman, et al. Effects of tebufelone (NE-11740), a new anti-inflammatory drug, on arachidonic acid metabolism. Agents Actions. 1994 May;41(3-4):156-63. ?
molnova catalog
related products
-
FPL 55712
FPL 55712 is a leukotriene receptor and SRS-A antagonist that inhibits bronchoconstriction and can be used in studies of asthma and coronary artery thrombosis.
-
YM 16638
YM 16638 is an orally active leukotriene (LT) antagonist with triglyceride-lowering and peroxisome-increasing effects that can be used to study antigen-induced early and late airway responses in allergic sheep.
-
JNJ-7777120
JNJ-7777120 is the first potent and selective non-imidazole histamine H4 receptor antagonist with Ki of 4.5 nM, exhibits >1000-fold selectivity over the other histamin receptors.
