It is known that amino acids and pe

It is known that amino acids and peptides are being taxonomically natural, physiologically nontoxic and chemically multifunctional, their rationalized conjugates with biologically active synthetic organic agents, are hypothesized to be more potent, particularly less toxic than their parent biologicals [8]. Further, thiophene de-rivatives have received interest because of their potential pharmacological utility and their incorporation in syn-thetic peptides [9-11]. Several thiophene derivatives are

*Corresponding author.


known and have been used as antibiotic, anti-allergic, anti-migraine, antioxidant agents [12-14].

結果 (中文) 1:

它已知氨基酸和多肽正在分类学自然，生理上无毒和化学多功能，具有生物活性的合成有机剂，及其合理化的复合物假设，以成为更有力的特别是较少毒性比其父生物制品 [8]。进一步，噻吩 de rivatives 由于其潜在的药理实用程序并将其纳入合成肽 [9-11] 中的收到利息。几种噻吩衍生物是* 相应的作者。众所周知，一直被用作抗生素、 抗过敏、 抗偏头痛，抗氧剂 [12-14]。

結果 (中文) 2:

已知的是氨基酸和肽正在分类学天然的，生理学无毒和化学官能，其具有生物活性的合成有机剂合理化缀合物，被假定为比其母体生物制剂更有效，特别是毒性较低的[8]。此外，噻吩去rivatives已收到，因为其潜在的药理效用和他们的SYN-正题肽[9-11]掺入的兴趣。几个噻吩衍生物是

*通讯作者。


已知的，并且已被用作抗生素，抗过敏，抗偏头痛，抗氧化剂[12-14]。

結果 (中文) 3:

它是已知的氨基酸和肽是天然无毒、化学分类学、生理功能、合理化合物，具有生物活性的有机合成剂，被认为是更有效的，比他们的父母，[ 8 ]特别是毒性较低的。此外，噻吩衍生品因其具有潜在的药理效用及其在合成肽[9-11]公司收到利息。几个噻吩衍生物*通讯作者。已知和已用抗生素、抗过敏、抗偏头痛、抗氧化剂[ 14 ]。