400-998-5282
专注多肽 服务科研
400-998-5282
专注多肽 服务科研
ADM (22-52) 是一种推定的肾上腺髓质素受体拮抗剂，可抑制由肾上腺髓质素引起的 cAMP 的产生。它是比 α-CGRP (8-37)（人）更有效的肾上腺髓质素和 CGRP 特异性受体拮抗剂。
编号：132320
CAS号：192871-80-0
单字母：H2N-LAHQIYQFTDKDKDNVAPRSKISPQGY-CONH2
ADM（22-52）是一种假定的肾上腺髓质素受体拮抗剂，可抑制肾上腺髓质素清除的cAMP的产生。它是比α-CGRP（8-37）（人）更有效的肾上腺髓质素和CGRP特异性受体拮抗剂。
ADM (22-52) is a putative adrenomedullin receptor antagonist that inhibits the production of cAMP elicted by adrenomedullin. It is a more effective antagonist for adrenomedullin- and CGRP-specific receptors than α-CGRP (8-37) (human).
肾上腺髓质素（26-52），人类捕获一个影响螺旋形成和受体结合行为的C末端区域。其序列支持对两亲性基序和结构灵活性的分析。该片段有助于绘制生物合成和构象转变的图谱。
Adrenomedullin (26-52), human captures a C-terminal region influential in helical formation and receptor-binding behavior. Its sequence supports analysis of amphipathic motifs and structural flexibility. The fragment aids in mapping biosynthesis and conformational transitions.
人肾上腺髓质素（26‑52）包含对螺旋形成和受体结合行为具有重要作用的 C 端区域。其序列可用于分析两亲性基序与结构柔性，助力定位生物合成与构象转变。应用包括多肽结构研究与配体工程。
Adrenomedullin (26-52), human captures a C-terminal region influential in helical formation and receptor-binding behavior. Its sequence supports analysis of amphipathic motifs and structural flexibility. The fragment aids in mapping biosynthesis and conformational transitions. Applications include peptide structure studies and ligand engineering.
Definition
Adrenomedullin (AM) is a pluripotent peptide and a hypotensive substance extracted from human adrenal tumour. Due to its origin of discovery, i.e. the medulla of the adrenal gland, the peptide is named adrenomedullin.
Discovery
AM was initially isolated from phaechromcytoma cells in 1993 by Kitmura K and his associates1.
Classification
AM is a member of the calcitonin family of peptides. In teleost fish, AM forms an independent subfamily consisting of five members viz. (AM1–AM5). This teleost AM family comprises three groups, AM1/AM4, AM2/AM3, and AM5 2,3.
Structural Characteristics
The peptide consists of 52 amino acids with a 6-member ring structure linked by a disulfide bond between amino acid 16 and 21 and amidated-COOH terminal4. It has 27 % homology with the calcitonin gene-related peptide (CGRP).
Mechanism of action
AM peptides act through specific receptors in the plasma membrane to activate adenylate cyclase activity and modulate Ca2+ flux in the target cells. The intracellular free Ca2+ increases on the activation of phospholipase C and formation of inositol 1, 4, 5-trisphosphate in the endothelial cells. The intracellular increase of Ca2+ activates endothelial nitric oxide synthase which leads to vascular relaxation5.
Function
AM is the most potent endogenous vasodilatory peptide found in the body6. They increase the tolerance of cells to oxidative stress, hypoxic injury and angiogenesis. It plays an important role in neurotransmission and ovarian function and in kidney, it acts as a diuretic and natriuretic7. AM is considered to play an important endocrine role in various tissues in maintaining electrolyte and fluid homeostasis8. It is used in the diagnosis and treatment of preeclampsia, type II diabetic patients and to promote fetal growth. They also play an important role in the regulation of insulin secretion and blood glucose metabolism.
References
1. Kitamura K, Kangawa K, Kawamoto M, Ichiki Y, Nakamura S, Matsuo H, Eto T (1993). Adrenomedullin: a novel hypotensive peptide isolated from human pheochromocytoma. Biochem Biophys Res Commun., 192 (2):553-560.
2. Ogoshi M, Nobata S, and Takei Y (2008). Potent osmoregulatory actions of homologous adrenomedullins administered peripherally and centrally in eels. Am J Physiol Regul Integr Comp Physiol, 295: 2075-2083.
3. Ogoshi M, Inoue K, Naruse K, Takei Y (2006). Evolutionary history of the calcitonin gene-related peptide family in vertebrates revealed by comparative genomic analyses. Peptides, 27 (12):3154-3164.
4. Cockcroft JR, Noon JP, Gardner-Medwin J, Bennett T (1997). Haemodynamic effects of adrenomedullin in human resistance and capacitance vessels. Br J Clin Pharmacol, 44(1):57-60.
5. Shimekake Y, Nagata K, Ohta S, Kambayashi Y, Teraoka H, Kitamura K, Eto T, Kangawa K, Matsuo H (1995). Adrenomedullin stimulates two signal transduction pathways, cAMP accumulation and Ca2+ mobilization, in bovine aortic endothelial cells. J Biol Chem, 270: 4412-4417.
6. Yanagawa B, Nagaya N (2007). Adrenomedullin: molecular mechanisms and its role in cardiac disease. Amino Acids, 32 (1):157-164.
7. Vesely DL (2003). Natriuretic peptides and acute renal failure. Am J Physiol Renal Physiol, 285 (2):167-177.
8. Ruzicska E, Toth M, Tulassay Z, Somogyi A (2001). Adrenomedullin and diabetes mellitus. Diabetes Metab Res Rev, 17 (5):321-329.
| DOI | 名称 | |
|---|---|---|
| 10.1093/oxfordjournals.jbchem.a124978 | Distribution and characterization of immunoreactive adrenomedullin in porcine tissue, and isolation of adrenomedullin 26-52 and adrenomedullin 34-52 from porcine duodenum | 下载 |
多肽H2N-Leu-Ala-His-Gln-Ile-Tyr-Gln-Phe-Thr-Asp-Lys-Asp-Lys-Asp-Asn-Val-Ala-Pro-Arg-Ser-Lys-Ile-Ser-Pro-Gln-Gly-Tyr-NH2的合成步骤：
1、合成MBHA树脂：取若干克的MBHA树脂（如初始取代度为0.5mmol/g）和1倍树脂摩尔量的Fmoc-Linker-OH加入到反应器中，加入DMF，搅拌使氨基酸完全溶解。再加入树脂2倍量的DIEPA，搅拌混合均匀。再加入树脂0.95倍量的HBTU，搅拌混合均匀。反应3-4小时后，用DMF洗涤3次。用2倍树脂体积的10%乙酸酐/DMF 进行封端30分钟。然后再用DMF洗涤3次，甲醇洗涤2次，DCM洗涤2次，再用甲醇洗涤2次。真空干燥12小时以上，得到干燥的树脂{Fmoc-Linker-MHBA Resin}，测定取代度。这里测得取代度为 0.3mmol/g。结构如下图：
2、脱Fmoc：取2.09g的上述树脂，用DCM或DMF溶胀20分钟。用DMF洗涤2遍。加3倍树脂体积的20%Pip/DMF溶液，鼓氮气30分钟，然后2倍树脂体积的DMF 洗涤5次。得到 H2N-Linker-MBHA Resin 。（此步骤脱除Fmoc基团，茚三酮检测为蓝色，Pip为哌啶）。结构图如下：
3、缩合：取1.88mmol Fmoc-Tyr(tBu)-OH 氨基酸，加入到上述树脂里，加适当DMF溶解氨基酸，再依次加入3.76mmol DIPEA，1.79mmol HBTU。反应30分钟后，取小样洗涤，茚三酮检测为无色。用2倍树脂体积的DMF 洗涤3次树脂。（洗涤树脂，去掉残留溶剂，为下一步反应做准备）。得到Fmoc-Tyr(tBu)-Linker-MBHA Resin。氨基酸：DIPEA：HBTU：树脂=3：6：2.85：1（摩尔比）。结构图如下：
4、依次循环步骤二、步骤三，依次得到
H2N-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Gln(Trt)-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Gln(Trt)-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Tyr(tBu)-Gln(Trt)-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Tyr(tBu)-Gln(Trt)-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Ile-Tyr(tBu)-Gln(Trt)-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Ile-Tyr(tBu)-Gln(Trt)-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Gln(Trt)-Ile-Tyr(tBu)-Gln(Trt)-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Gln(Trt)-Ile-Tyr(tBu)-Gln(Trt)-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-His(Trt)-Gln(Trt)-Ile-Tyr(tBu)-Gln(Trt)-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-His(Trt)-Gln(Trt)-Ile-Tyr(tBu)-Gln(Trt)-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Ala-His(Trt)-Gln(Trt)-Ile-Tyr(tBu)-Gln(Trt)-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
H2N-Ala-His(Trt)-Gln(Trt)-Ile-Tyr(tBu)-Gln(Trt)-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
Fmoc-Leu-Ala-His(Trt)-Gln(Trt)-Ile-Tyr(tBu)-Gln(Trt)-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin
以上中间结构，均可在专肽生物多肽计算器-多肽结构计算器中，一键画出。
最后再经过步骤二得到 H2N-Leu-Ala-His(Trt)-Gln(Trt)-Ile-Tyr(tBu)-Gln(Trt)-Phe-Thr(tBu)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Lys(Boc)-Asp(OtBu)-Asn(Trt)-Val-Ala-Pro-Arg(Pbf)-Ser(tBu)-Lys(Boc)-Ile-Ser(tBu)-Pro-Gln(Trt)-Gly-Tyr(tBu)-Linker-MBHA Resin，结构如下：
5、切割：6倍树脂体积的切割液（或每1g树脂加8ml左右的切割液），摇床摇晃 2小时，过滤掉树脂，用冰无水乙醚沉淀滤液，并用冰无水乙醚洗涤沉淀物3次，最后将沉淀物放真空干燥釜中，常温干燥24小试，得到粗品H2N-Leu-Ala-His-Gln-Ile-Tyr-Gln-Phe-Thr-Asp-Lys-Asp-Lys-Asp-Asn-Val-Ala-Pro-Arg-Ser-Lys-Ile-Ser-Pro-Gln-Gly-Tyr-NH2。结构图见产品结构图。
切割液选择：1）TFA：H2O=95%：5%
2）TFA：H2O：TIS=95%：2.5%：2.5%
3）三氟乙酸：茴香硫醚：1，2-乙二硫醇：苯酚：水=87.5%：5%：2.5%：2.5%：2.5%
（前两种适合没有容易氧化的氨基酸，例如Trp、Cys、Met。第三种适合几乎所有的序列。）
6、纯化冻干：使用液相色谱纯化，收集目标峰液体，进行冻干，获得蓬松的粉末状固体多肽。不过这时要取小样复测下纯度 是否目标纯度。
7、最后总结：
杭州专肽生物技术有限公司（ALLPEPTIDE https://www.allpeptide.com）主营定制多肽合成业务，提供各类长肽，短肽，环肽，提供各类修饰肽，如：荧光标记修饰（CY3、CY5、CY5.5、CY7、FAM、FITC、Rhodamine B、TAMRA等），功能基团修饰肽（叠氮、炔基、DBCO、DOTA、NOTA等），同位素标记肽（N15、C13），订书肽（Stapled Peptide）,脂肪酸修饰肽（Pal、Myr、Ste），磷酸化修饰肽（P-Ser、P-Thr、P-Tyr），环肽（酰胺键环肽、一对或者多对二硫键环），生物素标记肽，PEG修饰肽，甲基化修饰肽等。
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