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69698-54-0

中文名稱(chēng) PHE-THR-ASP-ASN-TYR-THR-ARG-LEU-ARG-LYS-GLN-MET-ALA-VAL-LYS-LYS-TYR-LEU-ASN-SER-ILE-LEU-ASN-NH2
英文名稱(chēng) VIP (6-28) (HUMAN, BOVINE, PORCINE, RAT)
CAS 69698-54-0
分子式 C126H207N37O34S
分子量 2816.28
MOL 文件 69698-54-0.mol
更新日期 2024/12/22 20:23:43
69698-54-0 結(jié)構(gòu)式 69698-54-0 結(jié)構(gòu)式

基本信息

中文別名
血管活性腸肽6-28
VIP(血管活性腸肽)(6-28)三氟乙酸鹽
血管活性腸肽VIP(6-28)(HUMAN, RAT, PORCINE, BOVINE)
英文別名
vip 6-28
Aviptadil (6-28)
M.W. 2816.31 C126H207N37O34S
VIP (6-28) (huMan, Mouse, rat)
VIP (6-28) (HUMAN, BOVINE, PORCINE, RAT)
VIP (6-28) (HUMAN, RAT, PORCINE, BOVINE)
VIP(6-28)(HUMAN, RAT, PORCINE, BOVINE)?, >98%
vasoactive intestinal peptide*fragment 6-28 porci
6-28-Vasoactive intestinal octacosapeptide (swine)
VASOACTIVE INTESTINAL PEPTIDE FRAGMENT 6-28 PORCINE

物理化學(xué)性質(zhì)

儲(chǔ)存條件−20°C
形態(tài)粉末
顏色White to off-white
水溶解性Soluble to 1 mg/ml in water
序列H-Phe-Thr-Asp-Asn-Tyr-Thr-Arg-Leu-Arg-Lys-Gln-Met-Ala-Val-Lys-Lys-Tyr-Leu-Asn-Ser-Ile-Leu-Asn-NH2

安全數(shù)據(jù)

WGK Germany3

常見(jiàn)問(wèn)題列表

生物活性
VIP(6-28)(human, rat, porcine, bovine) 是一種有效的外源性血管活性腸肽 (VIP) 拮抗劑。
靶點(diǎn)

VIP

體外研究

VIP(6-28) is an effective VIP antagonist in the superior cervical ganglion (SCG) , and results obtained using this analog indicate that endogenous VIP can participate in a positive feedback loop in injured sympathetic neurons in which it enhances its own expression. VIP(6-28), when added to short-term cultures of adult SCG at a concentration of 10, 30, or 100 μM, reduces the increase in cAMP levels produced by stimulation with 10 μM VIP by 52, 64, or 81%, respectively. At any of these concentrations tested, VIP(6-28) by itself does not alter cAMP levels. In contrast to its ability to reduce the VIP-stimulated elevation in cAMP levels by 64%, the addition of 30 μM VIP(6-28) to culture medium does not significantly alter cAMP levels measured after stimulation of adult ganglia with either isoproterenol or forskolin (10 μM each). Similar results on the ability of VIP(6-28) to block VIP-stimulated increases in cAMP levels are obtained in neuron-enriched and in non-neuronal cell-enriched dissociated cultures.

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