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| Product | Description | |
|---|---|---|
| Flufenamic acid | Flufenamic Acid is an anti-inflammatory agent, and also acts as an ion channel modulator. Synonyms: Flufenamic Acid; CI-440; CN-27554; INF-1837; CI 440; CN 27554; INF 1837; CI440; CN27554; INF1837. Grades: >98%. CAS No. 530-78-9. Molecular formula: C14H10F3NO2. Mole weight: 281.23. |  |
| Flufenamic acid | Flufenamic acid is a non-steroidal anti-inflammatory agent, inhibits cyclooxygenase (COX), activates AMPK, and also modulates ion channels, blocking chloride channels and L-type Ca2+ channels, modulating non-selective cation channels (NSC), activating K+ channels. Flufenamic acid binds to the central pocket of TEAD2 YBD and inhibits both TEAD function and TEAD-YAP-dependent processes, such as cell migration and proliferation. Group: Inhibitors. Alternative Names: inf1837;Lanceat;Meralen;N-((m-Trifluoromethyl)phenyl)-2-aminobenzoic acid;N-(alpha, alpha, alpha-Trifluoro-m-tolyl)anthranilate;n-(alpha, alpha, alpha-trifluoro-m-tolyl)-anthranilicaci;n-(m-trifluoromethylphenyl)-2-aminobenzoicacid;Nichisedan. CAS No. 530-78-9. Molecular formula: C14H10F3NO2. Mole weight: 281.23. Purity: 0.9985. Catalog: ACM530789. |  |
| Flufenamic acid | Flufenamic acid is a non-steroidal anti-inflammatory agent, inhibits cyclooxygenase ( COX ), activates AMPK , and also modulates ion channels, blocking chloride channels and L-type Ca 2+ channels , modulating non-selective cation channels ( NSC ), activating K + channels. Flufenamic acid binds to the central pocket of TEAD2 YBD and inhibits both TEAD function and TEAD-YAP-dependent processes, such as cell migration and proliferation. Uses: Scientific research. Group: Signaling pathways. CAS No. 530-78-9. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1221. |  |
| Flufenamic Acid | Anti-inflammatory; analgesic. Group: Biochemicals. Alternative Names: 2-[[3- (Trifluoromethyl) phenyl]amino]benzoic Acid; 2-[3- (Trifluoromethyl) anilino]benzoic Acid; 3'-Trifluoro methyl diphenylamine-2-carboxylic Acid; Fullsafe; INF 1837; Meralen; Sastridex; Surika; Tecramine. Grades: Highly Purified. CAS No. 530-78-9. Pack Sizes: 5g. US Biological Life Sciences. |  Worldwide |
| Flufenamic acid butyl ester | Flufenamic acid butyl ester. Group: Biochemicals. Alternative Names: ufenamate. Grades: Highly Purified. CAS No. 67330-25-0. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C18H18F3NO2. US Biological Life Sciences. | Worldwide |
| Flufenamic acid-d4 | Flufenamic acid-d4 is deuterium labeled Flufenamic acid. Flufenamic acid is a non-steroidal anti-inflammatory agent, inhibits cyclooxygenase (COX), activates AMPK, and also modulates ion channels, blocking chloride channels and L-type Ca2+ channels, modulating non-selective cation channels (NSC), activating K+ channels. Group: Isotope-labeled synthetic intermediates. CAS No. 1185071-99-1. Molecular formula: C14H6D4F3NO2. Mole weight: 285.25. Canonical SMILES: OC (C (C ([2H])=C ([2H])C ([2H])=C1[2H])=C1NC2=CC (C (F) (F)F)=CC=C2)=O. Catalog: ACM1185071991. | |
| Flufenamic Acid Glucuronide | Flufenamic Acid Glucuronide is an emtabolite of Flufenamic Acid, an anti-inflammatory and analgesic agent. Synonyms: 1-[2-[[3- (Trifluoromethyl) phenyl]amino]benzoate]-β -D-glucopyranuronic Acid. Grades: 95%. CAS No. 87816-74-8. Molecular formula: C20H18F3NO8. Mole weight: 457.35. | |
| 4-Phenylsulfonylaniline | 4-Phenylsulfonylaniline is used in the preparation of novel Flufenamic acid analogues as inhibitors of androgen receptor mediated transcription. Group: Biochemicals. Alternative Names: 4- (Phenylsulfonyl) benzenamine; p- (Phenylsulfonyl) aniline; 4- (Benzenesulfonyl) aniline; 4- (Benzenesulphonyl) phenylamine; 4- (Phenylsulfonyl) benzenamine; 4-Aminodiphenyl Sulfone; 4-Aminophenyl Phenyl Sulfone; 4-Phenylsulfonylaniline; Phenyl p-Aminophenyl Sulfone; [4- (Phenylsulfonyl) phenyl]amine; p-Aminodiphenyl Sulfone; p-Aminophenyl Phenyl Sulfone; p-Phenylsulfonylaniline. Grades: Highly Purified. CAS No. 7019-1-4. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| Dapsone Impurity 4 | 4-Phenylsulfonylaniline is used in the preparation of novel Flufenamic acid analogues as inhibitors of androgen receptor mediated transcription. Synonyms: 4-Phenylsulfonylaniline; 4-(Phenylsulfonyl)benzenamine; p-(Phenylsulfonyl)aniline; 4-(Benzenesulfonyl)aniline; 4-(Benzenesulphonyl)phenylamine; 4-(Phenylsulfonyl)benzenamine; 4-Aminodiphenyl Sulfone; 4-Aminophenyl Phenyl Sulfone; 4-Phenylsulfonylaniline. Grades: > 95%. CAS No. 7019-1-4. Molecular formula: C12H11NO2S. Mole weight: 233.29. | |
| LM-41 | LM-41 is a Flufenamic acid-derived TEAD inhibitor hat strongly reduce the expression of CTGF, Cyr61, Axl and NF2. LM-41 inhibits migration of human MDA-MB-231 breast cancer cells [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2996821-30-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-155309. | |
| Ufenamate | Ufenamate is a topical analgesic. Uses: A topical analgesic. Synonyms: Benzoic acid,2-[[3-(trifluoromethyl)phenyl]amino]-, butyl ester; Flufenamic acid butyl ester. Grades: ≥95%. CAS No. 67330-25-0. Molecular formula: C18H18F3NO2. Mole weight: 337.37. | |
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