Fmoc-HoCys(ACM)-OH Catalog No.:M27349-C 4)41(60-42(64)32(52)23-39(62)63)48(70)57-36(20-27-10-6-5-7-11-27)44(66)56-37(22-29-24-53-33-13-9-8-12-31(29)33)46(68)54-34(18-19-51)43(65)55-35(45(67)58-38)21-28-14-16-30(61)17-15-28/h5-17

4)41(60-42(64)32(52)23-39(62)63)48(70)57-36(20-27-10-6-5-7-11-27)44(66)56-37(22-29-24-53-33-13-9-8-12-31(29)33)46(68)54-34(18-19-51)43(65)55-35(45(67)58-38)21-28-14-16-30(61)17-15-28/h5-17

12-decahydro-1H-2-benzoxacyclotetradecin-1-one

indicating that the anti-HBV mechanisms are associated with and dependent on the rate of HBcAg inhibition

InChiKey: MVOWQBJZZKOQNU-UHFFFAOYSA-N

Fmoc-HoCys(ACM)-OH Catalog No.:M27349-C 4)41(60-42(64)32(52)23-39(62)63)48(70)57-36(20-27-10-6-5-7-11-27)44(66)56-37(22-29-24-53-33-13-9-8-12-31(29)33)46(68)54-34(18-19-51)43(65)55-35(45(67)58-38)21-28-14-16-30(61)17-15-28/h5-17Fmoc 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