Tyrosols and derivatives

Organic compounds that consist of a phenol ring with an ethyl functional group substitution that is subsequently bonded to a hydroxyl group.

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721 – 735 of 867 results

721

Sigma Aldrich Fine Chemicals Biosciences Metoprolol tartrate United States Pharmacopeia (USP) Reference Standard | 56392-17-7 | MFCD00056257 | 200MG

Metoprolol tartrate United States Pharmacopeia (USP) Reference Standard | Mol Wt: 684.81 | 56392-17-7 | MFCD00056257 | 200MG

Pricing & Availability

722

eMolecules 184163-80-2 | 4-(5-(2,6-Dimethoxyphenyl)-3-(methoxycarbonyl)-1h-pyrazol-1-yl)-3-isopropylbenzoic acid | Combi-Blocks, Inc.424.453 | C23H24N2O6 | 95.000 | COC(=O)c1cc(-c2c(OC)cccc2OC)n(n1)-c1ccc(cc1C(C)C)C(O)=O | 10g | 866383734

4-(5-(2,6-Dimethoxyphenyl)-3-(methoxycarbonyl)-1h-pyrazol-1-yl)-3-isopropylbenzoic acid | Combi-Blocks, Inc. | 184163-80-2424.453 | C23H24N2O6 | 95.000 | COC(=O)c1cc(-c2c(OC)cccc2OC)n(n1)-c1ccc(cc1C(C)C)C(O)=O | 10g | 866383734

Pricing & Availability

723

Apexbio Technology LLC VX-702 479543-46-9; 745833-23-2 25mg

VX-702 is a small-molecule inhibitor targeting p38 mitogen-activated protein kinase (MAPK) also known as MAPK14 It is designed to inhibit p38 MAPK thereby regulating cellular responses to cytokine signaling and various stressors VX-702 exerts its biological activity primarily through ATP-competitive inhibition In experimental models VX-702 demonstrates potent inhibition with reported IC50 values ranging from 4 to 20 nM Based on these pharmacological properties VX-702 holds research potential in the study of p38 MAPK-dependent pathways platelet storage lesions and renal excretion mechanisms

Pricing & Availability

724

Medchemexpress LLC 6-(N-carbamoyl-2,6-difluoroanilino)-2-(2,4-difluorophenyl)pyridine-3-carboxamide | 745833-23-2 | MFCD11616590 | 99.7% | 404.32 g/mol | C19H12F4N4O2 | 100 MG

VX-702 is a small-molecule research inhibitor selective for the p38α isoform of mitogen-activated protein kinase (MAPK). It is used to probe MAPK signaling and inflammatory cytokine production in preclinical and cellular studies. The compound is supplied as a powder with high reported purity and documented potency against p38α.