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preprosomatostatin
Compounds 1 and 2 significantly reduced melanin production in a dose-dependent manner with IC50 values of 13
2 ng/μL) accelerates the formation of multinucleated cells and promotes the exit of mitosis in taxol-treated HBV-positive HCC cells
Smiles: CC(C)C[C@@H]1NC(=O)[C@@H](CC2=CC=CC=C2)NC(=O)[C@H](CCN)NC(=O)[C@H](CCNC(=O)[C@@H](NC(=O)[C@H](CCN)NC(=O)[C@H](CCN)NC1=O)[C@@H](C)O)NC(=O)[C@@H](CO)NC(=O)[C@@H](NC(C)=O)[C@@H](C)O
(R)-Amlodipine-d4 Size:Contact [email protected] for quotation preprosomatostatinProduct information CAS Number: 1346616 97 4 Molecular Weight: 412. 90 Formula: C20H25ClN2O5 Chemical Name: 3 ethyl 5 methyl (4S) 2 {[2 amino(1,1,2,2 H)ethoxy]methyl} 4 (2 chlorophenyl) 6 methyl 1,4 dihydropyridine 3,5 dicarboxylate Smiles: [2H]C([2H])(OCC1NC(C)=C([C@@H](C=1C(=O)OCC)C1=CC=CC=C1Cl)C(=O)OC)C([2H])([2H])N InChiKey: HTIQEAQVCYTUBX MIHJCSFKSA N InChi: InChI=1S C20H25ClN2O5 c1 4 28 20(25)18 15(11 27 10 9 22)23 12(2)16(19(24)26 3)17(18)13 7
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