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Procedure for obtaining a compound Peptide to antagonize the in vivo Response of an animal to the Antidiuretic Action of ADH.
Procedure for obtaining a compound Peptide to antagonize the in vivo Response of an animal to the Antidiuretic Action of ADH.
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机译:获得用于对抗动物对ADH的抗利尿作用的体内应答的化合物肽的方法。
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摘要
Procedure for obtaining a compound Peptide to antagonize the in vivo Response of an animal to the Antidiuretic Action of ADH.Consists of: (a) treat by Solid Phase Synthesis of BOC Gly Resin and Neutralization and coupling with an amino acid to produce BOC PHE Val ASN CY (Bzl) - W (d or L - (coughing) - Arg - Gly - Resin); (b) addressing the previous composite in a cycle of Vulnerability,Neutralize with BOC and attach x to produce TERT butoxycarbonyl (BOC octapeptidil Resin Formula X - Phe Val ASN CY (Bzl) - w or L D -) (coughing) Arg Gly resin); (c) amonolizar Compound obtained in (b) to produce a compound of formula Boc - xphe Val ASN CY (Bzl) - W - (D - or L - (coughing) - Arg - Gly - NH2); (d) conve As the compound obtained in (c) a compound of formula (ii); and (e) convert the compound (d)A Peptide of formula (i).
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机译:获得用于对抗动物对ADH的抗利尿作用的体内应答的化合物肽的程序,包括:(a)通过BOC甘油树脂的固相合成和中和处理并与氨基酸偶联以产生BOC PHE Val ASN CY(Bzl)-W(d或L-(咳嗽)-Arg-Gly-树脂); (b)在脆弱性循环中处理先前的复合材料,用BOC中和并连接x以产生TERT丁氧羰基(BOC八肽树脂X-Phe Val ASN CY(Bzl)-w或LD-)(咳嗽)Arg Gly树脂) ; (c)在(b)中获得的阿莫诺扎尔化合物,以产生式Boc-xphe Val ASN CY(Bzl)-W-(D-或L-(咳嗽)-Arg-Gly-NH2)的化合物; (d)将式(ii)的化合物作为(c)中获得的化合物; (e)转化式(i)的化合物(d)A肽。
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