(3S,6S,9R,12S,15S,23S)-15-[(N-Acetyl-L-norleucyl)amino]-9-benzyl-6-(3-carbamimidamidopropyl)-12-(1H-imidazol-5-ylmethyl)-3-(1H-indol-3-ylmethyl)-2,5,8,11,14,17-hexaoxo-1,4,7,10,13,18-hexaazacyclotrico sane-23-carboxylic acid acetate (1:1)(CAS: 1607799-13-2)
![(3S,6S,9R,12S,15S,23S)-15-[(N-Acetyl-L-norleucyl)amino]-9-benzyl-6-(3-carbamimidamidopropyl)-12-(1H-imidazol-5-ylmethyl)-3-(1H-indol-3-ylmethyl)-2,5,8,11,14,17-hexaoxo-1,4,7,10,13,18-hexaazacyclotrico
sane-23-carboxylic acid acetate (1:1) (3S,6S,9R,12S,15S,23S)-15-[(N-Acetyl-L-norleucyl)amino]-9-benzyl-6-(3-carbamimidamidopropyl)-12-(1H-imidazol-5-ylmethyl)-3-(1H-indol-3-ylmethyl)-2,5,8,11,14,17-hexaoxo-1,4,7,10,13,18-hexaazacyclotrico
sane-23-carboxylic acid acetate (1:1)](https://cnstatic.chemtradehub.com/structs/160/1607799-13-2-ed5d.webp)
CAS号
相关产品
(2S,3S,4R,5R,6S)-6-[[(1S,2R,19R,22S,34S,37R,40R,52S)-5,32-dichloro-52-[3-(dimethylamino)propylcarbamoyl]-2,26,31,44,49-pentahydroxy-22-(methylamino)-21,35,38,54,56,59-hexaoxo-47-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,13,28-trioxa-20,36,39,53,55,58-hexazaundecacyclo[38.14.2.23,6.214,17.219,34.18,12.123,27.129,33.141,45.010,37.046,51]hexahexaconta-3,5,8,10,12(64),14(63),15,17(62),23(61),24,26,29(60),30,32,41(57),42,44,46(51),47,49,65-henicosaen-64-yl]oxy]-3,4-dihydroxy-5-(10-methylundecanoylamino)oxane-2-carboxylic acid
CAS号: 171500-79-1
其他供应商提供的 (3S,6S,9R,12S,15S,23S)-15-[(N-Acetyl-L-norleucyl)amino]-9-benzyl-6-(3-carbamimidamidopropyl)-12-(1H-imidazol-5-ylmethyl)-3-(1H-indol-3-ylmethyl)-2,5,8,11,14,17-hexaoxo-1,4,7,10,13,18-hexaazacyclotrico sane-23-carboxylic acid acetate (1:1)
基本信息
分子式
C52H72N14O12
分子量
1085.23 g/mol
化学标识符
SMILES
CC(=O)O.CCCC[C@@H](C(=O)N[C@H]1CC(=O)NCCCC[C@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](NC(=O)[C@@H](NC1=O)Cc1[nH]cnc1)Cc1ccccc1)CCCNC(=N)N)Cc1c[nH]c2c1cccc2)C(=O)O)NC(=O)C
InChIKey
MAYUSRUHXFWITM-GBRHMYBBSA-N
数据库引用
MDL号
MFCD29472571
常见问题
Bremelanotide (Acetate) 是一种复杂的有机化合物,具有多个手性中心,其结晶形态为固体。分子量约为1000 g/mol。该化合物在水中的溶解度较低,但在有机溶剂如DMSO中有较好的溶解性。其反应活性主要体现在与特定受体的结合能力上,表现为较强的生物活性。
Bremelanotide (Acetate) 的合成通常涉及多步反应,包括酰胺化、环化、氨基甲酸酯化等步骤。常用的方法包括使用保护基进行修饰,然后在适当的条件下进行脱保护和偶联反应。最终通过结晶纯化得到目标化合物。该合成路线的选择性和产率较高。
Bremelanotide (Acetate) 主要应用于医药行业,作为药物候选物。它具有治疗性功能,能够刺激内源性黑色素生成,用于治疗色素性皮肤病。此外,它还可能在生物传感器和生物材料领域有潜在应用。
在处理Bremelanotide (Acetate) 时,应佩戴适当的个人防护装备(PPE),如手套、护目镜和实验服。操作应在通风橱内进行,以减少吸入或皮肤接触的风险。若发生泄漏,应立即关闭通风橱,使用适当的吸附剂清理,并遵守化学品泄漏处理指南。参考物质安全数据表(SDS)获取详细的安全信息。
安全须知
使用前请验证产品规格和安全数据。联系供应商获取详细安全信息。
请始终遵循正确的操作程序
联系信息
联系人
杨
邮箱
394537118@qq.com


![(2S,3S,4R,5R,6S)-6-[[(1S,2R,19R,22S,34S,37R,40R,52S)-5,32-dichloro-52-[3-(dimethylamino)propylcarbamoyl]-2,26,31,44,49-pentahydroxy-22-(methylamino)-21,35,38,54,56,59-hexaoxo-47-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,13,28-trioxa-20,36,39,53,55,58-hexazaundecacyclo[38.14.2.23,6.214,17.219,34.18,12.123,27.129,33.141,45.010,37.046,51]hexahexaconta-3,5,8,10,12(64),14(63),15,17(62),23(61),24,26,29(60),30,32,41(57),42,44,46(51),47,49,65-henicosaen-64-yl]oxy]-3,4-dihydroxy-5-(10-methylundecanoylamino)oxane-2-carboxylic acid](https://cnstatic.chemtradehub.com/structs/171/171500-79-1-998b.webp)


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