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Transdermal Peptide TD-1 HCl

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Catalog No. T37766L
Alias Transdermal Peptide TD-1 HCl(918629-48-8 Free base), TD1 (peptide) HCl, TD 1 (peptide) HCl

Transdermal Peptide TD-1 HCl is a novel peptide for enhanced transdermal drug delivery that facilitates the penetration of the skin barrier by several drugs and large hydrophilic proteins, such as insulin and human growth hormoneb.

Transdermal Peptide TD-1 HCl

Transdermal Peptide TD-1 HCl

🥰Excellent
Catalog No. T37766LAlias Transdermal Peptide TD-1 HCl(918629-48-8 Free base), TD1 (peptide) HCl, TD 1 (peptide) HCl
Transdermal Peptide TD-1 HCl is a novel peptide for enhanced transdermal drug delivery that facilitates the penetration of the skin barrier by several drugs and large hydrophilic proteins, such as insulin and human growth hormoneb.
Pack SizePriceAvailabilityQuantity
1 mg$32 In Stock
5 mg$70 In Stock
10 mg$107 In Stock
25 mg$180 In Stock
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Product Introduction

Bioactivity
Description
Transdermal Peptide TD-1 HCl is a novel peptide for enhanced transdermal drug delivery that facilitates the penetration of the skin barrier by several drugs and large hydrophilic proteins, such as insulin and human growth hormoneb.
In vitro
In vitro, 0.5 mg/mL Transdermal Peptide TD-1 HCl markedly enhanced the transdermal penetration of curcumin liposomes (Cur-Lips) in mouse skin models (Qₙ = 2.20 μg/cm²/h), and maintained strong anti-melanoma activity even in the presence of 150 mM NaCl and serum. Transdermal Peptide TD-1 HCl combined with Cur-Lips significantly inhibited B16F10 melanoma cell proliferation (P < 0.001), while Transdermal Peptide TD-1 HCl alone showed no cytotoxicity at low concentrations[1].
In vivo
In vivo, topical application of Transdermal Peptide TD-1 HCl (0.5 mg/mL) with Cur-Lips gel twice daily for 12 days significantly reduced tumor volume and weight in B16F10 melanoma-bearing mice (P < 0.001), induced tumor cell apoptosis, and downregulated serum VEGF levels[1].
AliasTransdermal Peptide TD-1 HCl(918629-48-8 Free base), TD1 (peptide) HCl, TD 1 (peptide) HCl
Chemical Properties
Molecular Weight1099.63
FormulaC40H67ClN14O16S2
SmilesC[C@H](N)C(N[C@@H](CS)C(N[C@@H](CO)C(N[C@@H](CO)C(N[C@@H](CO)C(N1[C@@H](CCC1)C(N[C@@H](CO)C(N[C@@H](CCCCN)C(N[C@H](C(N[C@@H](CS)C(NCC(O)=O)=O)=O)CC2=CN=CN2)=O)=O)=O)=O)=O)=O)=O)=O.Cl
Storage & Solubility Information
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
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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