Cas no 127103-11-1 (Ac-Ser-Asp-Lys-Pro-OH)
Ac-Ser-Asp-Lys-Pro-OH Chemical and Physical Properties
Names and Identifiers
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- L-Proline,N-acetyl-L-seryl-D-a-aspartyl-L-lysyl- (9CI)
- Ac-Ser-Asp-Lys-Pro-OH
- 1-[2-[[2-[(2-acetamido-3-hydroxypropanoyl)amino]-3-carboxypropanoyl]amino]-6-aminohexanoyl]pyrrolidine-2-carboxylic acid
- ACSDKP
- Thymosin β4 (1-4), Goralatide
- SDKP
- Ser-Asp-Lys-Pro
- Acetyl-Ser-Asp-Lys-Pro
- AC-SDKP
- GORALATIDE
- SERASPENIDE
- Acetyl-SDKP
- AC-SDKP-DELTA
- Thymosin β4 (1-4)
- AC-SER-ASP-LYS-PRO
- N-Ac-Ser-Asp-Lys-Pro-OH
- Acetyl-Ser-Asp-Lys-Pro, >=97% (HPLC)
- 127103-11-1
- DTXSID30402957
- DTXSID40861258
- N-Acetylseryl-alpha-aspartyllysylproline
- Acetyl-serinyl-aspartyl-lysinyl-proline
- N-acetyl-Ser-Asp-Lys-Pro
- Goralatide?
-
- MDL: MFCD28155524
- Inchi: 1S/C20H33N5O9/c1-11(27)22-14(10-26)18(31)24-13(9-16(28)29)17(30)23-12(5-2-3-7-21)19(32)25-8-4-6-15(25)20(33)34/h12-15,26H,2-10,21H2,1H3,(H,22,27)(H,23,30)(H,24,31)(H,28,29)(H,33,34)
- InChI Key: HJDRXEQUFWLOGJ-UHFFFAOYSA-N
- SMILES: O=C(C(CCCCN)NC(C(CC(=O)O)NC(C(CO)NC(C)=O)=O)=O)N1CCCC1C(=O)O
Computed Properties
- Exact Mass: 487.22799
- Monoisotopic Mass: 487.22782765g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 7
- Hydrogen Bond Acceptor Count: 14
- Heavy Atom Count: 34
- Rotatable Bond Count: 18
- Complexity: 776
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 4
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: 8
- XLogP3: -5.4
- Topological Polar Surface Area: 229?2
Experimental Properties
- Water Partition Coefficient: Soluble in water at 2mg/ml
- PSA: 228.46
Ac-Ser-Asp-Lys-Pro-OH Security Information
- WGK Germany:3
- Storage Condition:Please store the product under the recommended conditions in the Certificate of Analysis.
Ac-Ser-Asp-Lys-Pro-OH Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | TP1828-1 mg |
N-Acetyl-Ser-Asp-Lys-Pro |
127103-11-1 | 99.85% | 1mg |
¥487.00 | 2022-02-28 | |
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | TP1828-5 mg |
N-Acetyl-Ser-Asp-Lys-Pro |
127103-11-1 | 99.85% | 5mg |
¥987.00 | 2022-02-28 | |
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | TP1828-10 mg |
N-Acetyl-Ser-Asp-Lys-Pro |
127103-11-1 | 99.85% | 10mg |
¥1675.00 | 2022-02-28 | |
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | TP1828-25 mg |
N-Acetyl-Ser-Asp-Lys-Pro |
127103-11-1 | 99.85% | 25mg |
¥3457.00 | 2022-02-28 | |
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | TP1828-50 mg |
N-Acetyl-Ser-Asp-Lys-Pro |
127103-11-1 | 99.85% | 50mg |
¥5175.00 | 2022-02-28 | |
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | TP1828-100 mg |
N-Acetyl-Ser-Asp-Lys-Pro |
127103-11-1 | 99.85% | 100MG |
¥7763.00 | 2022-02-28 | |
| WU HAN AN JIE KAI Biomedical Technology Co., Ltd. | ajce52020-1mg |
N-Acetyl-Ser-Asp-Lys-Pro |
127103-11-1 | 98% | 1mg |
¥445.00 | 2023-09-07 | |
| WU HAN AN JIE KAI Biomedical Technology Co., Ltd. | ajce52020-5mg |
N-Acetyl-Ser-Asp-Lys-Pro |
127103-11-1 | 98% | 5mg |
¥981.00 | 2023-09-07 | |
| WU HAN AN JIE KAI Biomedical Technology Co., Ltd. | ajce52020-10mg |
N-Acetyl-Ser-Asp-Lys-Pro |
127103-11-1 | 98% | 10mg |
¥1559.00 | 2023-09-07 | |
| WU HAN AN JIE KAI Biomedical Technology Co., Ltd. | ajce52020-25mg |
N-Acetyl-Ser-Asp-Lys-Pro |
127103-11-1 | 98% | 25mg |
¥3388.00 | 2023-09-07 |
Ac-Ser-Asp-Lys-Pro-OH Related Literature
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Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
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Chao-Han Cheng,Wen-Zhen Wang,Shie-Ming Peng,I-Chia Chen Phys. Chem. Chem. Phys., 2017,19, 25471-25477
-
Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng Cai Chem. Commun., 2013,49, 11086-11088
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Chung-Sung Yang,Mong-Shian Shih,Fang-Yi Chang New J. Chem., 2006,30, 729-735
Additional information on Ac-Ser-Asp-Lys-Pro-OH
Recent Advances in the Study of 127103-11-1 and Ac-Ser-Asp-Lys-Pro-OH in Chemical Biology and Medicine
The compound 127103-11-1 and the peptide Ac-Ser-Asp-Lys-Pro-OH (AcSDKP) have garnered significant attention in recent years due to their potential therapeutic applications in various medical fields. This research brief aims to summarize the latest findings related to these molecules, focusing on their biological activities, mechanisms of action, and clinical relevance.
127103-11-1, a small molecule with a unique chemical structure, has been investigated for its role in modulating specific biochemical pathways. Recent studies suggest that it may act as an inhibitor of certain enzymes involved in inflammatory processes, making it a potential candidate for treating chronic inflammatory diseases. The precise mechanism of action is still under investigation, but preliminary data indicate promising results in preclinical models.
Ac-Ser-Asp-Lys-Pro-OH, commonly known as AcSDKP, is a naturally occurring tetrapeptide with demonstrated roles in hematopoiesis and tissue repair. Recent research has expanded our understanding of its biological functions, revealing its potential in mitigating fibrosis and promoting stem cell proliferation. A 2023 study published in the Journal of Medicinal Chemistry highlighted its efficacy in reducing collagen deposition in animal models of pulmonary fibrosis, suggesting a novel therapeutic avenue for fibrotic disorders.
One of the most groundbreaking developments involves the synergistic effects of 127103-11-1 and AcSDKP in combination therapies. A recent in vitro study demonstrated that the co-administration of these compounds enhanced their individual anti-fibrotic properties, potentially through complementary pathways. This finding opens new possibilities for developing multi-targeted treatment strategies for complex diseases.
From a pharmaceutical development perspective, significant progress has been made in improving the stability and bioavailability of AcSDKP. Novel formulation approaches, including nanoparticle encapsulation and PEGylation, have shown promise in overcoming the peptide's inherent metabolic instability. These advancements are crucial for translating laboratory findings into clinically viable therapies.
In conclusion, the ongoing research on 127103-11-1 and Ac-Ser-Asp-Lys-Pro-OH continues to reveal their multifaceted therapeutic potential. While challenges remain in terms of clinical translation and safety profiling, the accumulating evidence supports further investigation of these compounds as promising candidates for various medical applications. Future studies should focus on elucidating their precise molecular mechanisms and optimizing their pharmacological properties for human use.
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