Carbosulfan te) TFA Smiles: [2H]C([2H])([2H])C1=C([2H])C([2H])=C(/C(=C\CN2CCCC2)/C2=CC=CC(/C=C/C(O)=O)=N2)C([2H])=C1[2H]

Smiles: [2H]C([2H])([2H])C1=C([2H])C([2H])=C(/C(=C\CN2CCCC2)/C2=CC=CC(/C=C/C(O)=O)=N2)C([2H])=C1[2H]

7(7):671-5

possesses anti-inflammatory activities

Smiles: CC(=O)[C@]1(N)CC2=C([C@H](C1)O[C@H]1C[C@H](O)[C@H](O)CO1)C(O)=C1C(C(=O)C3=CC=CC=C3C1=O)=C2O

Carbosulfan te) TFA Smiles: [2H]C([2H])([2H])C1=C([2H])C([2H])=C(/C(=C\CN2CCCC2)/C2=CC=CC(/C=C/C(O)=O)=N2)C([2H])=C1[2H]Carbosulfan inhibited relatively potently CYP3A4 and moderately CYP1A1 2 and CYP2C19 in pooled HLM (human livers). Carbosulfan activation is predominantly catalyzed in humans by CYP3A4. Product information CAS Number: 55285 14 8 Molecular Weight: 380. 54 Formula: C20H32N2O3S Chemical Name: 2,2 dimethyl 2,3 dihydro 1 benzofuran 7 yl N [(dibutylamino)sulfanyl] N methylcarbamate Smiles: CN(SN(CCCC)CCCC)C(=O)OC1C=CC=C2CC(C)(C)OC2=1 InChiKey: