国产毛片毛片精品天天看软件丨色情无码www视频无码区小黄鸭丨国产99青青成人a在线丨porno中国ⅹxxxx偷拍丨亚洲性无码一区二区三区丨91九色蝌蚪在线丨久久精品欧美一区丨国产 日韩 欧美 制服 另类丨97国产精品视频丨色哟哟在线观看丨91在线播放视频丨日本极品级片丨www.久久av丨a午夜丨精品区一区二区丨久久午夜免费视频丨欧美激情15p丨影音先锋啪啪看片资源丨97免费视频观看丨人人鲁免费播放视频

Cat#：215P13
序列（三字母）：Myristoyl-His-Ser-Asp-Ala-Val-Phe-Thr-Asp-Asn-Tyr-Thr-Lys-Leu-Arg-Lys-Gln-Met-Ala-Val-Lys-Lys-Tyr-Leu-Asn-Ser-Ile-Lys-Lys-Gly-Gly-Thr-OH trifluoroacetate salt
序列（單字母）：Myristoyl-HSDAVFTDNYTKLRKQMAVKKYLNSIKKGGT
類似名：PG 99-465
分子式：C???H???N??O??S
分子量：3753.47
合成方法：Synthetic
存儲(chǔ)條件：-20 ± 5 °C
應(yīng)用：Cancer Research
描述：PG 99-465 is a high affinity, selective VPAC2 receptor antagonist. It exhibited a 100-fold preference for the VPAC2 over the VPAC1 receptor. The compound showed partial agonistic activity on the VPAC1 receptor and was inactive on the VPAC2 receptor transfected in CHO cells, as well as on naturally expressed human VPAC2 receptors in the SUP T1 cell line. Dickson et al. observed an agonistic effect of PG99-465 on the human VPAC1 and PAC1 receptors. When applied singly, PG99-465 increased [cAMP](i) at all three hVPAC/PAC receptor subtypes.