General description This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate.
General description This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate.
Biochem/physiol Actions TAPI-0 inhibit peptide deformylase (PDF) activity and retard the growth Chlamydia trachomatis , which is an obligate intracellular bacterium responsible for a number of human diseases. TAPI-0 is a metalloproteinase
Biochem/physiol Actions TAPI-0 inhibit peptide deformylase (PDF) activity and retard the growth Chlamydia trachomatis , which is an obligate intracellular bacterium responsible for a number of human diseases. TAPI-0 is a metalloproteinase
Biochem/physiol Actions ONO-AE3-208 is an orally active prostaglandin E2 receptor 4 (EP4)-selective antagonist (Ki in nM = 1.3/EP4, 30/EP3, 790/FP and 2400/TP: Ki >:10 μ:M for prostanoid receptors DP, EP1, EP2, IP).
Biochem/physiol Actions ONO-AE3-208 is an orally active prostaglandin E2 receptor 4 (EP4)-selective antagonist (Ki in nM = 1.3/EP4, 30/EP3, 790/FP and 2400/TP: Ki >:10 μ:M for prostanoid receptors DP, EP1, EP2, IP).
Biochem/physiol Actions ONO-AE3-208 is an orally active prostaglandin E2 receptor 4 (EP4)-selective antagonist (Ki in nM = 1.3/EP4, 30/EP3, 790/FP and 2400/TP: Ki >:10 μ:M for prostanoid receptors DP, EP1, EP2, IP).
Biochem/physiol Actions ONO-AE3-208 is an orally active prostaglandin E2 receptor 4 (EP4)-selective antagonist (Ki in nM = 1.3/EP4, 30/EP3, 790/FP and 2400/TP: Ki >:10 μ:M for prostanoid receptors DP, EP1, EP2, IP).
Biochem/physiol Actions XIE62-1004 is a synthetic sequestosome-1 (p62, SQSTM1) ZZ domain ligand that induces disulfide bond-linked and PB1 domain-dependent p62 self-aggregation, leading to interaction with LC3 on autophagic membranes and
Biochem/physiol Actions XIE62-1004 is a synthetic sequestosome-1 (p62, SQSTM1) ZZ domain ligand that induces disulfide bond-linked and PB1 domain-dependent p62 self-aggregation, leading to interaction with LC3 on autophagic membranes and
Biochem/physiol Actions XIE62-1004 is a synthetic sequestosome-1 (p62, SQSTM1) ZZ domain ligand that induces disulfide bond-linked and PB1 domain-dependent p62 self-aggregation, leading to interaction with LC3 on autophagic membranes and
Biochem/physiol Actions XIE62-1004 is a synthetic sequestosome-1 (p62, SQSTM1) ZZ domain ligand that induces disulfide bond-linked and PB1 domain-dependent p62 self-aggregation, leading to interaction with LC3 on autophagic membranes and
Biochem/physiol Actions ONO-2506 (arundic acid: (R)-2-propyloctanoic acid) is an inhibitory astrocytes-modulating agent that exerts glioprotective effects against amyloid-β:-peptide (Aβ:)-induced glial death in astrocyte cultures (50
Biochem/physiol Actions ONO-2506 (arundic acid: (R)-2-propyloctanoic acid) is an inhibitory astrocytes-modulating agent that exerts glioprotective effects against amyloid-β:-peptide (Aβ:)-induced glial death in astrocyte cultures (50
Biochem/physiol Actions ONO-2506 (arundic acid: (R)-2-propyloctanoic acid) is an inhibitory astrocytes-modulating agent that exerts glioprotective effects against amyloid-β:-peptide (Aβ:)-induced glial death in astrocyte cultures (50
Biochem/physiol Actions ONO-2506 (arundic acid: (R)-2-propyloctanoic acid) is an inhibitory astrocytes-modulating agent that exerts glioprotective effects against amyloid-β:-peptide (Aβ:)-induced glial death in astrocyte cultures (50
General description Standardized, concentrated cell culture supernatant which has been diafiltered with phosphate buffered saline. For the formulation of Anti-K blood typing reagents or devices.
General description Standardized, concentrated cell culture supernatant which has been diafiltered with phosphate buffered saline. For the formulation of Anti-K blood typing reagents or devices.