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3-Mercaptopropionyl-beta-3-pyridyl-D-ala-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2 is a peptide chemical compound composed of nine amino acids, including an additional 3-mercaptopropionyl group attached to the N-terminal amino acid. 3-MERCAPTOPROPIONYL-BETA-3-PYRIDYL-D-ALA-PHE-GLN-ASN-CYS-PRO-ARG-GLY-NH2 is a derivative of beta-3-pyridyl-D-ala-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2 and has potential applications in various fields, such as medical research, drug development, cancer treatment, neurobiology, and biochemical studies related to the targeted delivery of bioactive molecules. Its unique molecular structure and properties make it a valuable tool for understanding and manipulating biological processes, with the potential for targeted therapeutic interventions.

136105-89-0

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136105-89-0 Usage

Uses

Used in Medical Research and Drug Development:
3-Mercaptopropionyl-beta-3-pyridyl-D-ala-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2 is used as a research tool for studying the molecular mechanisms of various diseases and developing new therapeutic agents. Its unique structure allows for the investigation of protein-protein interactions, enzyme activities, and other biological processes.
Used in Cancer Treatment:
In the field of oncology, 3-Mercaptopropionyl-beta-3-pyridyl-D-ala-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2 is used as a potential therapeutic agent for targeting cancer cells. Its ability to bind specifically to certain cellular receptors or proteins may enable the development of targeted cancer therapies with reduced side effects compared to conventional chemotherapy.
Used in Neurobiology:
3-Mercaptopropionyl-beta-3-pyridyl-D-ala-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2 is used as a research tool in neurobiology to study the molecular mechanisms underlying neurological disorders and to develop new treatments for these conditions. Its potential to modulate neurotransmitter release, receptor binding, or other neuronal processes makes it a valuable compound for understanding the pathophysiology of various neurological diseases.
Used in Biochemical Studies:
In biochemical research, 3-Mercaptopropionyl-beta-3-pyridyl-D-ala-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2 is used as a probe to investigate the structure and function of various biomolecules, such as enzymes, receptors, and signaling pathways. Its unique properties may facilitate the discovery of novel bioactive compounds and the elucidation of their mechanisms of action.
Used in Targeted Drug Delivery:
3-Mercaptopropionyl-beta-3-pyridyl-D-ala-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2 is used as a component in the development of targeted drug delivery systems. Its ability to bind specifically to certain cellular receptors or proteins may enable the design of drug delivery systems that selectively target diseased cells or tissues, improving the therapeutic efficacy and reducing the side effects of various treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 136105-89-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,1,0 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 136105-89:
(8*1)+(7*3)+(6*6)+(5*1)+(4*0)+(3*5)+(2*8)+(1*9)=110
110 % 10 = 0
So 136105-89-0 is a valid CAS Registry Number.
InChI:InChI=1/C45H63N15O11S2/c46-34(61)13-12-28-39(66)58-31(21-35(47)62)42(69)59-32(44(71)60-17-6-11-33(60)43(70)56-27(10-5-16-52-45(49)50)38(65)53-23-36(48)63)24-73-72-18-14-37(64)54-29(20-26-9-4-15-51-22-26)40(67)57-30(41(68)55-28)19-25-7-2-1-3-8-25/h1-4,7-9,15,22,27-33H,5-6,10-14,16-21,23-24H2,(H2,46,61)(H2,47,62)(H2,48,63)(H,53,65)(H,54,64)(H,55,68)(H,56,70)(H,57,67)(H,58,66)(H,59,69)(H4,49,50,52)

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