![Fmoc-HoCys(ACM)-OH Catalog No.:M27349-C 1]octan-8-yl]oxy}-4-{[(1R](https://cdn.shopify.com/s/files/1/0389/1897/9723/products/M27349_1635995107.gif?v=1635995110)
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1]octan-8-yl]oxy}-4-{[(1R
Smiles: [2H]C([2H])([2H])N1C(C)=C(N)C(=O)N1C1C=CC=CC=1
Smiles: CN1C[C@@H](C[C@H]1COC1N=C2CN(CCC2=C(N=1)N1C[C@H](CC#N)N(CC1)C(=O)OC(C)(C)C)C1C=CC=C2C=CC=CC2=1)OCCOCCOCCOCCN
Ipriflavone also promotes the deposition of calcium and the formation of mineralized nodules by newborn rat calvarial osteoblast-like cells as well as the activity of alkaline phosphatase
indicating that the anti-HBV mechanisms are associated with and dependent on the rate of HBcAg inhibition
Fmoc-HoCys(ACM)-OH Catalog No.:M27349-C 1]octan-8-yl]oxy}-4-{[(1RFmoc HoCys(ACM) OH, a homolog of cysteine, is synthesized from L methionine. Fmoc HoCys(ACM) OH also can be used for the synthesis of solid phase peptide. Product information CAS Number: 150281 21 3 Molecular Weight: 428. 50 Formula: C22H24N2O5S Chemical Name: (2S) 4 [(acetamidomethyl)sulfanyl] 2 ({[(9H fluoren 9 yl)methoxy]carbonyl}amino)butanoic acid Smiles: CC(=O)NCSCC[C@H](NC(=O)OCC1C2=CC=CC=C2C2=CC=CC=C21)C(O)=O InChiKey: LKXJXPIRDOELQS
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