Aminobenzoic acids and derivatives
Apexbio Technology LLC Sennoside A 81-27-6 10mM (in 1mL DMSO)
Sennoside A (CAS 81-27-6) is a small-molecule inhibitor targeting HIV-1 replication It is designed to inhibit HIV-1 reverse transcriptase (RT)-related DNA polymerase (RDDP) activity and ribonuclease H thereby suppressing viral replication pathways Sennoside A exerts its biological activity primarily through competitive inhibition of both DNA polymerase and ribonuclease H activities of HIV-1 RT In in vitro studies Sennoside A demonstrates inhibitory activity with IC50 values of 3 8 M for HIV-1 replication 1 9 M for DNA polymerase activity and 5 3 M for ribonuclease H activity Based on these pharmacological properties Sennoside A holds research potential in antiviral studies targeting HIV-1
eMolecules ChemScene / (4-Amino-2-methylphenyl)methanol / 100mg / 582645498 / CS-0098091 / 0.000 / 63405-88-9 / MFCD11110504 / 137.182 / C8H11NO
ChemScene / (4-Amino-2-methylphenyl)methanol / 100mg / 582645498 / CS-0098091 / 0.000 / 63405-88-9 / MFCD11110504 / 137.182 / C8H11NO
Medchemexpress LLC N-acetyl-L-valyl-L-alpha-glutamyl-L-isoleucyl-L-aspart-1-al | 00-00-0 | MFCD01318861 | 99.8% | 614.57 g/mol | C24H37F3N4O11 | 10 MG
Ac-VEID-CHO TFA is a peptide-derived reversible caspase inhibitor for biochemical research, commonly used to probe caspase activity and mechanisms relevant to neurodegeneration. It is formulated as a salt suitable for in vitro enzymatic assays and VEIDase activity studies.
- Peptide-derived reversible caspase inhibitor.
- Biochemical IC50 values: caspase-3 13.6 nM, caspase-6 16.2 nM, caspase-7 162.1 nM.
- High purity (≈99.8%).
- White to off-white solid, soluble in water with sonication and warming.
- Limited cellular accumulation; low activity in intact cell assays (>100 μM).
- Recommended storage: sealed, -80°C for long term, -20°C for up to 1 year.
Apexbio Technology LLC Ac-Endothelin-1 (16-21), human 1mg
Ac-Endothelin-1 16-21 human is a selective agonist targeting the ETB subtype of G protein-coupled endothelin receptors It is designed to activate ETB receptors thereby modulating phospholipase C-mediated signaling pathways and vascular function Ac-Endothelin-1 16-21 human exerts its biological activity primarily through selective ETB receptor activation leading to vasoconstrictive effects Based on these pharmacological properties Ac-Endothelin-1 16-21 human holds research potential in studies analyzing vascular function as well as investigations of cardiovascular and renal pathophysiology