![4-phenyl-5-methyl-1, 2, 3-Thiadiazole ylpropionic acid Smiles: COC1=C(OC)C(O)=CC([C@H]2CC3=CC=C(C=C3OC2)OC)=C1O](https://cdn.shopify.com/s/files/1/0389/1897/9723/products/M22636_1635327712.gif?v=1635327714)
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Smiles: COC1=C(OC)C(O)=CC([C@H]2CC3=CC=C(C=C3OC2)OC)=C1O
InChi: InChI=1S/C21H16ClF3N4O3/c1-26-19(30)18-11-15(8-9-27-18)32-14-5-2-12(3-6-14)28-20(31)29-13-4-7-17(22)16(10-13)21(23
InChi: InChI=1S/C32H38O14/c1-13(2)5-10-17-18(33)11-19(34)21-24(38)29(27(44-28(17)21)15-6-8-16(41-4)9-7-15)45-32-30(25(39)22(36)14(3)43-32)46-31-26(40)23(37)20(35)12-42-31/h5-9
ALPS(N-Ethyl-N-sulfopropylaniline sodium salt) is a bio-chemical reagents/chromogenic reagent
anti-inflammatory and insecticidal activities
4-phenyl-5-methyl-1, 2, 3-Thiadiazole ylpropionic acid Smiles: COC1=C(OC)C(O)=CC([C@H]2CC3=CC=C(C=C3OC2)OC)=C1O4 phenyl 5 methyl 1,2,3 Thiadiazole is a CYP2B4 and CYP2E1 inhibitor. Cytochrome P450 (CYP450) enzymes, a superfamily of oxidative catalysts, are important in the biosynthesis and metabolism of a wide range of endogenous molecules and the metabolism of xenobiotics. CYP2B4 can metabolize substituted amines, while CYP2E1 metabolizes various alcohols and halogenated alkenes. In vitro: 4 phenyl 5 methyl 1,2,3 Thiadiazole (PMT) was found to be slightly
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