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64790-15-4

中文名稱 ALA-GLN-ASP-PHE-VAL-GLN-TRP-LEU-MET-ASN-THR
英文名稱 H-ALA-GLN-ASP-PHE-VAL-GLN-TRP-LEU-MET-ASN-THR-OH
CAS 64790-15-4
分子式 C61H89N15O18S
分子量 1352.51
MOL 文件 64790-15-4.mol
更新日期 2026/07/10 13:20:56
64790-15-4 結(jié)構(gòu)式 64790-15-4 結(jié)構(gòu)式

基本信息

中文別名
GLUCAGON (19-29) (人)
英文別名
AQDFVQWLMNT
glucagon(19-29
GLUCAGON (19-29), HUMAN
Miniglucagon (huMan, rat, porcine)
Glucagon (19-29) (human, rat, porcine)
GLUCAGON (19-29), BOVINE, HUMAN, PORCINE
GLUCAGON (19-29) (HUMAN, BOVINE, PORCINE)
PHE-VAL-GLN-TRP-LEU-MET-ASN-THR: FVQWLMNT
ALA-GLN-ASP-PHE-VAL-GLN-TRP-LEU-MET-ASN-THR
H-ALA-GLN-ASP-PHE-VAL-GLN-TRP-LEU-MET-ASN-THR-OH

物理化學(xué)性質(zhì)

沸點1828.5±65.0 °C(Predicted)
密度1.339±0.06 g/cm3(Predicted)
儲存條件-15°C
溶解度insoluble in EtOH; insoluble in H2O; ≥135.2 mg/mL in DMSO
酸度系數(shù)(pKa)3.19±0.10(Predicted)
形態(tài)粉末
顏色White to off-white
序列Ala-Gln-Asp-Phe-Val-Gln-Trp-Leu-Met-Asn-Thr
ALA-GLN-ASP-PHE-VAL-GLN-TRP-LEU-MET-ASN-THR價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2026/06/05HY-P0150ALA-GLN-ASP-PHE-VAL-GLN-TRP-LEU-MET-ASN-THR
Glucagon (19-29), human
64790-15-45mg420元
2026/06/05HY-P0150ALA-GLN-ASP-PHE-VAL-GLN-TRP-LEU-MET-ASN-THR
Glucagon (19-29), human
64790-15-410mg600元
2026/06/05HY-P0150ALA-GLN-ASP-PHE-VAL-GLN-TRP-LEU-MET-ASN-THR
Glucagon (19-29), human
64790-15-425mg950元

常見問題列表

生物活性
Glucagon (19-29), human是高效的胰島素分泌抑制劑。
靶點

Insulin secretion

體外研究

Glucagon (19-29), from 0.1 pM to 1 nM, exerts a potent negative inotropic action. The most striking observation is a 45% increase in the amplitude of cell contractility elicited by the combination of 30 nM glucagon with 1 nM Glucagon (19-29).

體內(nèi)研究

Glucagon (19-29), also named Miniglucagon, is the COOH-terminal (19-29) fragment processed from glucagon. Glucagon (19-29) dose-dependently inhibits insulin secretion stimulated by 8.3 M glucose, with no change in the perfusion flow rate. A concentration of 1 nM Glucagon (19-29) has a significant inhibitory effect on a 1 nM glucagon-like peptide 1 (7-36) amide–potentiated insulin secretion. Glucagon (19-29) is a highly potent and efficient inhibitor of insulin release by closing, via hyperpolarization, voltage-dependent Ca 2+ channels linked to a pathway involving a pertussis toxin-sensitive G protein.

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