Long-acting oxyntomodulin (OXM) hybrid peptide, preparation method of hybrid peptide and application of hybrid peptide serving as drug
A compound and drug technology, applied in the field of medicinal chemistry, can solve the problems of weak hypoglycemic activity and short half-life, and achieve the effects of long drug effect time, short synthesis cycle and cost saving
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Embodiment 1
[0089] His-Gly-Gln-Gly-Thr-Phe-Thr-Ser-Asp-Tyr-Ser-Lys-Tyr-Met-Asp-Cys-Arg-Arg-Ala-Gln-Asp-Phe-Val-Gln-Trp- Leu-Lys-Asn-Gly-Gly-Pro-Ser-Ser-Gly-Ala-Pro-Pro-Pro-Ser-NH 2 (SEQ.ID NO.1)
[0090] solid phase synthesis
[0091] (1) Swelling of the resin
[0092] Weigh 50mg of Fmoc-Rink amide-MBHA Resin (degree of substitution: 0.4mmol / g), swell with 7mL of DCM for 30min, filter to remove DCM, then swell with 10mL of NMP for 30min, rinse with NMP and 7mL of DCM respectively.
[0093] (2) Removal of Fmoc protecting group
[0094] Put the swollen resin into the reactor, add 25% piperidine / NMP (V / V) solution containing 0.1M HOBt to the resin to remove Fmoc, and wash it with NMP after the reaction. A resin free of the initially attached Fmoc protecting group is obtained.
[0095] (3) Synthesis of Fmoc-Ser(tBu)-Rink amide-MBHA Resin
[0096] Fmoc-Ser(tBu)-OH (15.4 mg, 0.04 mmol), HBTU (15.1 mg, 0.04 mmol), HOBt (5.4 mg, 0.04 mmol) and DIPEA (13.9 μL, 0.08 mmol) were dissolved in N...
Embodiment 2
[0102] His-Gly-Gln-Gly-Thr-Phe-Thr-Ser-Asp-Tyr-Ser-Lys-Tyr-Leu-Glu-Cys-Arg-Arg-Ala-Gln-Asp-Phe-Val-Gln-Trp- Leu-Lys-Asn-Gly-Gly-Pro-Ser-Ser-Gly-Ala-Pro-Pro-Pro-Ser-NH 2 (SEQ.ID NO.2)
[0103] The synthesis method was the same as in Example 1, and the collected solution was lyophilized to obtain 29.2 mg of the pure product. The theoretical relative molecular mass is 4269.7. ESI-MS m / z: Calcd.[M+3H] 3+ 1424.2, [M+4H] 4+ 1068.4; Found[M+3H] 3+ 1424.8, [M+4H] 4+ 1068.1.
Embodiment 3
[0105] His-Gly-Gln-Gly-Thr-Phe-Thr-Ser-Asp-Tyr-Ser-Lys-Tyr-Leu-Asp-Cys-Glu-Arg-Ala-Gln-Asp-Phe-Val-Gln-Trp- Leu-Lys-Asn-Gly-Gly-Pro-Ser-Ser-Gly-Ala-Pro-Pro-Pro-Ser-NH 2 (SEQ.ID NO.3)
[0106] The synthesis method was the same as in Example 1, and the collected solution was lyophilized to obtain 27.6 mg of the pure product. The theoretical relative molecular mass is 4228.6. ESI-MS m / z: Calcd.[M+3H] 3+ 1410.5, [M+4H] 4+ 1058.2; Found[M+3H] 3+ 1410.0, [M+4H] 4+ 1058.2.
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