多肽定制(Tyr0)-Melanocyte-Stimulating Hormone-Release Inhibiting Factor 编码 [77133-61-0]

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名称 (Tyr0)-Melanocyte-Stimulating Hormone-Release Inhibiting Factor
编码 [77133-61-0]
别名 (Tyr0)-Melanocyte-Stimulating Hormone-Release Inhibiting Factor
纯度 80%,90%,95%,98%,99%
重量 1mg,5mg,10mg,50mg,100mg,1g
序列(单字母缩写) YPLG-NH2
序列(三字母缩写) D-Phe(4-Cl)Tyr-Pro-Leu-Gly-NH2
基本描述
溶解度
分子量 0
化学式
存储条件 Store at -20°C. Keep tightly closed. Store in a cool dry place.
注释
Documents (Tyr0)-Melanocyte-Stimulating Hormone-Release Inhibiting Factor          编码     [77133-61-0]
Figures (Tyr0)-Melanocyte-Stimulating Hormone-Release Inhibiting Factor          编码     [77133-61-0]
Reference
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多肽定制(D-Leu2)-Melanocyte-Stimulating Hormone-Release Inhibiting Factor 编码 [39705-60-7]

上海金畔生物科技有限公司可以定制不同序列多肽,可以访问官网了解更多产品信息。

名称 (D-Leu2)-Melanocyte-Stimulating Hormone-Release Inhibiting Factor
编码 [39705-60-7]
别名 (D-Leu2)-Melanocyte-Stimulating Hormone-Release Inhibiting Factor
纯度 80%,90%,95%,98%,99%
重量 1mg,5mg,10mg,50mg,100mg,1g
序列(单字母缩写) P-D-LG-NH2
序列(三字母缩写) D-Phe(4-Cl)Pro-D-Leu-Gly-NH2
基本描述
溶解度
分子量 0
化学式
存储条件 Store at -20°C. Keep tightly closed. Store in a cool dry place.
注释
Documents (D-Leu2)-Melanocyte-Stimulating Hormone-Release Inhibiting Factor          编码     [39705-60-7]
Figures (D-Leu2)-Melanocyte-Stimulating Hormone-Release Inhibiting Factor          编码     [39705-60-7]
Reference
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多肽定制[D-Leu2]-Melanocyte-Stimulating Hormone-Release Inhibiting Factor 编码 [39705-60-7]

上海金畔生物科技有限公司可以定制不同序列多肽,可以访问官网了解更多产品信息。

名称 [D-Leu2]-Melanocyte-Stimulating Hormone-Release Inhibiting Factor
编码 [39705-60-7]
别名 [D-Leu2]-Melanocyte-Stimulating Hormone-Release Inhibiting Factor
纯度 80%,90%,95%,98%,99%
重量 1mg,5mg,10mg,50mg,100mg,1g
序列(单字母缩写) PlG-NH2
序列(三字母缩写) Pro-D-Leu-Gly-NH2
基本描述
溶解度
分子量 284.36
化学式 C13H24N4O3
存储条件 Store at -20°C. Keep tightly closed. Store in a cool dry place.
注释
Documents [D-Leu2]-Melanocyte-Stimulating Hormone-Release Inhibiting Factor           编码     [39705-60-7]
Figures [D-Leu2]-Melanocyte-Stimulating Hormone-Release Inhibiting Factor           编码     [39705-60-7]
Reference
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多肽定制[Tyr0]-Melanocyte-Stimulating Hormone-Release Inhibiting Factor 编码 [77133-61-0]

上海金畔生物科技有限公司可以定制不同序列多肽,可以访问官网了解更多产品信息。

名称 [Tyr0]-Melanocyte-Stimulating Hormone-Release Inhibiting Factor
编码 [77133-61-0]
别名 [Tyr0]-Melanocyte-Stimulating Hormone-Release Inhibiting Factor
纯度 80%,90%,95%,98%,99%
重量 1mg,5mg,10mg,50mg,100mg,1g
序列(单字母缩写) YPLG-NH2
序列(三字母缩写) Tyr-Pro-Leu-Gly-NH2
基本描述
溶解度
分子量 447.54
化学式 C22H33N5O5
存储条件 Store at -20°C. Keep tightly closed. Store in a cool dry place.
注释
Documents [Tyr0]-Melanocyte-Stimulating Hormone-Release Inhibiting Factor           编码     [77133-61-0]
Figures [Tyr0]-Melanocyte-Stimulating Hormone-Release Inhibiting Factor           编码     [77133-61-0]
Reference
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多肽定制Melanocyte-Stimulating Hormone-Release Inh,MSH Release Inhibiting Factor, amide 编码 [2002-44-0]

上海金畔生物科技有限公司可以定制不同序列多肽,可以访问官网了解更多产品信息。

名称 Melanocyte-Stimulating Hormone-Release Inh,MSH Release Inhibiting Factor, amide
编码 [2002-44-0]
别名 Melanocyte-Stimulating Hormone-Release Inh,MSH Release Inhibiting Factor, amide
纯度 80%,90%,95%,98%,99%
重量 1mg,5mg,10mg,50mg,100mg,1g
序列(单字母缩写) PLG-NH2
序列(三字母缩写) H-Pro-Leu-Gly-NH2?(trifluoroacetate salt)
基本描述 Screening analogs of the cyclic lactam melanocortin agonist MTII led to the identification of the agoutimimetic SHU9119. The cyclopeptide SHU9119 shares pharmacological properties with the agouti peptide in that it is a potent antagonist of the melanocortin-4 receptor and a less potent antagonist of the melanocortin-3 receptor.
溶解度
分子量 284.36
化学式 C13H24N4O3
存储条件 Store at -20°C. Keep tightly closed. Store in a cool dry place.
注释
Documents Melanocyte-Stimulating Hormone-Release Inh,MSH Release Inhibiting Factor, amide          编码     [2002-44-0]
Figures Melanocyte-Stimulating Hormone-Release Inh,MSH Release Inhibiting Factor, amide          编码     [2002-44-0]
Reference S.Bj?rkman and H.Sievertsson, Naunyn-Schmiedeberg’s Arch. Pharmacol., 298, 79 (1977) T.A.Pugsley and W.Lippmann, Drug Res., 27 II, 2290 (1977) S.Chiu and R.K.Mishra, Eur. J. Pharmacol., 53, 119 (1979) R.Walter et al., Proc. Natl. Acad. Sci. USA, 76, 518 (1979) K.Dolbeare et al., Bioorg. Med. Chem., 11, 4103 (2003) R.S.Khan et al., Int. J. Pept., ID 537639 (2010)
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