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HSDVHK-NH2 acetate
🥰Excellent
Catalog No. TP1879L1
Alias P-11 Acetate
P11 acetate is an integrin αvβ3-vitronectin interaction antagonist(IC50 = 2.74 nM).
HSDVHK-NH2 acetate
🥰Excellent
Purity: 99.5%
Catalog No. TP1879L1Alias P-11 Acetate
P11 acetate is an integrin αvβ3-vitronectin interaction antagonist(IC50 = 2.74 nM).
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $82 | In Stock | |
| 5 mg | $167 | In Stock | |
| 10 mg | $283 | In Stock | |
| 25 mg | $512 | In Stock | |
| 50 mg | $743 | In Stock | |
| 100 mg | $1,050 | In Stock |
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Purity:99.5%
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Product Introduction
Bioactivity
Chemical Properties
| Description | P11 acetate is an integrin αvβ3-vitronectin interaction antagonist(IC50 = 2.74 nM). |
| Targets&IC50 | αvβ3 integrin:2.74 nM |
| In vitro | P11 acetate showed a strong antagonism against avb3-GRGDSP interaction(IC50 = 25.72 nM)[1]. P11 acetate inhibited the HUVEC proliferation due to the induction of HUVEC cell death through caspases activations and its mechanism is related with increased p53 expression[2].P11 acetate significantly inhibited bFGF-induced cell migration compared to the PBS control group[3]. |
| Synonyms | P-11 Acetate |
| Molecular Weight | 780.39 |
| Formula | C32H52N12O11 |
| Smiles | N[C@@H](CC1=CN=CN1)C(N[C@@H](CO)C(N[C@@H](CC(O)=O)C(N[C@@H](C(C)C)C(N[C@H](C(N[C@H](C(N)=O)CCCCN)=O)CC2=CN=CN2)=O)=O)=O)=O.CC(O)=O |
| Relative Density. | no data available |
| Sequence | His-Ser-Asp-Val-His-Lys |
| Sequence Short | HSDVHK |
Storage & Solubility Information
| Storage | keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||
| Solubility Information | DMSO: 7.24 mg/mL (9.28 mM), Sonication is recommended.  | |||||||||||||||
Solution Preparation Table | ||||||||||||||||
DMSO
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In Vivo Formulation Calculator (Clear solution)
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:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
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 DMSO (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.
(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 DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
Dose Conversion
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Tech Support
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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