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PNC-28

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Catalog No. T81435Cas No. 392661-17-5

PNC-28, a peptide derived from the mdm-2-binding domain of p53 protein (residues 17–26), incorporates a membrane-crossing penetratin sequence. This compound is utilized in pancreatic cancer research [1] [2].

PNC-28
Other Forms of PNC-28:
PNC-28 acetateT78028
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PNC-28

😃Good
Catalog No. T81435Cas No. 392661-17-5
PNC-28, a peptide derived from the mdm-2-binding domain of p53 protein (residues 17–26), incorporates a membrane-crossing penetratin sequence. This compound is utilized in pancreatic cancer research [1] [2].
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Product Introduction

Bioactivity
Description
PNC-28, a peptide derived from the mdm-2-binding domain of p53 protein (residues 17–26), incorporates a membrane-crossing penetratin sequence. This compound is utilized in pancreatic cancer research [1] [2].
In vitro
PNC-28 demonstrates activity by selectively binding to and penetrating cancer cell membranes, inducing apoptosis. This effect is notably absent in normal, non-cancerous cells due to the specific interaction with a distinct motif on the cancer cell surface. Additionally, PNC-28 facilitates the inhibition of tumor growth and metastasis.
In vivo
PNC-28, administered subcutaneously (SC) or intraperitoneally (IP) at a dose of 2 mg/mouse for 14 days, effectively impedes the growth of BMRPA1. Tuc3 cells in vivo [1]. Additionally, doses ranging from 1 to 20 mg/mouse, when given subcutaneously for the same duration, notably restrain BMRPA1. Tuc3 tumor proliferation, with pronounced efficacy when applied directly to the neoplasm [1].
Chemical Properties
Molecular Weight3509.14
FormulaC164H255N47O37S
Cas No.392661-17-5
SmilesC([C@H](NC([C@H](CC1=CC=CC=C1)NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@H](CC=2C=3C(NC2)=CC=CC3)NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@H](CC=4C=5C(NC4)=CC=CC5)NC([C@@H](NC([C@@H](NC([C@@H](NC([C@H](CC6=CC=CC=C6)NC([C@@H](NC([C@H](CCC(O)=O)N)=O)[C@@H](C)O)=O)=O)CO)=O)CC(O)=O)=O)CC(C)C)=O)=O)CCCCN)=O)CC(C)C)=O)CC(C)C)=O)CCCCN)=O)CCCCN)=O)=O)CCCCN)=O)CCSC)=O)CCCNC(=N)N)=O)CCCNC(=N)N)=O)CC(N)=O)=O)CCC(N)=O)=O)=O)C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@@H](CCCNC(=N)N)C(NCC(O)=O)=O)=O)CCC(N)=O)=O)[C@H](C)C)=O)CCCCN)=O)[C@@H](C)C)=O)C=7C=8C(NC7)=CC=CC8
Sequence ShortETFSDLWKLLKKWKMRRNQFWVKVQRG
Storage & Solubility Information
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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