4-Aminobenzoic acid yroxine acyl glucuronide Smiles: [2H]C(NCC(O)COC1=CC=C(C=C1C(C)=O)NC(=O)CCC)(C([2H])([2H])[2H])C([2H])([2H])[2H]

Smiles: [2H]C(NCC(O)COC1=CC=C(C=C1C(C)=O)NC(=O)CCC)(C([2H])([2H])[2H])C([2H])([2H])[2H]

5 min) drives MAPK activation in GPR18-transfected HEK293 cells

Norswertianin induces GBM cells differentiation through oxidative stress and Akt/mTOR dependent autophagy

A-887826 potently blocks tetrodotoxin-resistant sodium (TTX-R Na(+)) currents (IC50=8 nM) from small diameter rat dorsal root ganglion (DRG) neurons in a voltage-dependent fashion

2'-Deoxyguanosine monohydrate is an endogenous metabolite

4-Aminobenzoic acid yroxine acyl glucuronide Smiles: [2H]C(NCC(O)COC1=CC=C(C=C1C(C)=O)NC(=O)CCC)(C([2H])([2H])[2H])C([2H])([2H])[2H]4 Aminobenzoic acid is an intermediate in the synthesis of folate by bacteria, plants, and fungi. Product information CAS Number: 150 13 0 Molecular Weight: 137. 14 Formula: C7H7NO2 Chemical Name: 4 aminobenzoic acid Smiles: NC1=CC=C(C=C1)C(O)=O InChiKey: ALYNCZNDIQEVRV UHFFFAOYSA N InChi: InChI=1S C7H7NO2 c8 6 3 1 5(2 4 6)7(9)10 h1 4H,8H2,(H,9,10) Technical Data Appearance: Solid Power Purity: 98% (or refer to the Certificate of Analysis) Solubility: