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Biological activity of substance P methyl ester.

作者信息

Cascieri M A, Goldenberg M M, Liang T

出版信息

Mol Pharmacol. 1981 Nov;20(3):457-9.

PMID:6173735
Abstract
摘要

相似文献

1
Biological activity of substance P methyl ester.
Mol Pharmacol. 1981 Nov;20(3):457-9.
2
Tachyphylaxis due to the D-Phe7 analogue of substance P.P物质的D-苯丙氨酸7类似物引起的快速耐受性。
J Pharm Pharmacol. 1980 May;32(5):376-7. doi: 10.1111/j.2042-7158.1980.tb12945.x.
3
[Differentiation of the biological activity of eledoisin and substance-P analogs in affinity and intrinsic activity on isolated guinea pig ileum and comparison with the activity on rat colon].
Experientia. 1974 Nov 15;30(11):1315-7. doi: 10.1007/BF01945205.
4
Contracting activity of C-terminal fragments and a C-terminal hexapeptide analogue of substance P on non-stimulated and electrically stimulated isolated guinea-pig ileum.
Gen Pharmacol. 1981;12(2):119-21. doi: 10.1016/0306-3623(81)90110-5.
5
Novel substance P analogues inhibit circular muscle contraction of guinea pig ileum and depolarization of new born rat spinal cord induced by substance P.新型P物质类似物可抑制豚鼠回肠的环形肌收缩以及P物质诱导的新生大鼠脊髓去极化。
Regul Pept. 1993 Jul 2;46(1-2):321-5. doi: 10.1016/0167-0115(93)90073-h.
6
Synthesis of substance P analogs with arginine in position eleven.
Chem Pharm Bull (Tokyo). 1984 Oct;32(10):4144-8. doi: 10.1248/cpb.32.4144.
7
Inhibition of smooth muscle contractions induced by capsaicin and electrical transmural stimulation by a substance P antagonist.P物质拮抗剂对辣椒素和电透壁刺激诱导的平滑肌收缩的抑制作用。
Acta Physiol Scand Suppl. 1983;515:11-6.
8
Synthesis of substance P antagonists: [D-Pro4, D-Trp7,9,Nle11]-substance P(4-11).
Pharmazie. 1984 Jan;39(1):65-7.
9
Synthesis and biological activities of substance P antagonists.P物质拮抗剂的合成与生物活性
J Med Chem. 1982 Nov;25(11):1313-6. doi: 10.1021/jm00353a008.
10
Specific recognition of SP or NKB receptors by analogues of SP substituted at positions 8 and 9.在第8和9位被取代的速激肽类似物对速激肽或神经激肽B受体的特异性识别。
Eur J Pharmacol. 1986 Jun 24;125(3):461-2. doi: 10.1016/0014-2999(86)90804-6.

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A Biomimetic C-Terminal Extension Strategy for Photocaging Amidated Neuropeptides.一种模拟生物的酰胺化神经肽光笼化 C 端扩展策略。
J Am Chem Soc. 2023 Sep 13;145(36):19611-19621. doi: 10.1021/jacs.3c03913. Epub 2023 Aug 31.
2
Structures of neurokinin 1 receptor in complex with G and G proteins reveal substance P binding mode and unique activation features.神经激肽1受体与G蛋白和G蛋白复合物的结构揭示了P物质的结合模式和独特的激活特征。
Sci Adv. 2021 Dec 10;7(50):eabk2872. doi: 10.1126/sciadv.abk2872. Epub 2021 Dec 8.
3
The substance P receptor on rat mast cells and in human skin.
大鼠肥大细胞和人类皮肤中的P物质受体。
Agents Actions. 1984 Apr;14(3-4):420-4. doi: 10.1007/BF01973842.
4
Subtypes and excitation-contraction coupling mechanisms for neurokinin receptors in smooth muscle of the guinea-pig Taenia caeci.豚鼠盲肠带平滑肌中神经激肽受体的亚型及兴奋-收缩偶联机制
Naunyn Schmiedebergs Arch Pharmacol. 1991 Aug;344(2):225-34. doi: 10.1007/BF00167223.
5
Novel selective agonists and antagonists confirm neurokinin NK1 receptors in guinea-pig vas deferens.新型选择性激动剂和拮抗剂证实了豚鼠输精管中的神经激肽NK1受体。
Br J Pharmacol. 1991 Feb;102(2):511-7. doi: 10.1111/j.1476-5381.1991.tb12202.x.
6
Pharmacological specificity of novel, synthetic, cyclic peptides as antagonists at tachykinin receptors.新型合成环肽作为速激肽受体拮抗剂的药理学特异性
Br J Pharmacol. 1991 Oct;104(2):355-60. doi: 10.1111/j.1476-5381.1991.tb12435.x.
7
A pharmacological study of NK1 and NK2 tachykinin receptor characteristics in the rat isolated urinary bladder.大鼠离体膀胱中NK1和NK2速激肽受体特性的药理学研究
Br J Pharmacol. 1992 Nov;107(3):777-84. doi: 10.1111/j.1476-5381.1992.tb14523.x.