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AUNP-12 acetate

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Catalog No. TP1076L
Alias AUNP-12 acetate (1353563-85-5 Free base)

AUNP-12 acetate is a polypeptide inhibitor of PD-1 that is equivalent to PD-1 and PD-2 in inhibiting lymphocyte proliferation and effector fuction, in addition to immune activation and antitumor activity.

AUNP-12 acetate

AUNP-12 acetate

😃Good
Purity: 95.07%
Catalog No. TP1076LAlias AUNP-12 acetate (1353563-85-5 Free base)
AUNP-12 acetate is a polypeptide inhibitor of PD-1 that is equivalent to PD-1 and PD-2 in inhibiting lymphocyte proliferation and effector fuction, in addition to immune activation and antitumor activity.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$116In StockIn Stock
5 mg$326In StockIn Stock
10 mg$489-In Stock
25 mg$798-In Stock
50 mg$1,090InquiryInquiry
100 mg$1,480InquiryInquiry
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:95.07%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
AUNP-12 acetate is a polypeptide inhibitor of PD-1 that is equivalent to PD-1 and PD-2 in inhibiting lymphocyte proliferation and effector fuction, in addition to immune activation and antitumor activity.
In vitro
In vitro, AUNP-12 displayed equipotent antagonism toward PD-L1 and PD-L2 in the rescue of lymphocyte proliferation and effector functions. In human PBMC cells, AUNP-12 was also able to significantly rescue recombinant human PD-L1 and PD-L2 mediated inhibition in vitro, with average EC50 values of 63.3 nM and 44.1 nM against PD-L1 and PD-L2 respectively. [1]
In vivo
AUNP-12 acetate rescued the proliferation in the mouse splenocyte assay system, with average EC50 values of 17 nM and 16.6 nM against rmPD-L1 and rmPD-L2 respectively. AUNP-12 (6 hours) showed a Plasma protein binding of 93.9% with plasma stability of more than 60%. AUNP-12 exhibited a half-life of 90 minutes in mouse liver microsomes. In male Balb/c mice, AUNP-12 subcutaneous injection or intravenous injection as a concentration of 3 mg/kg for its PK study. As a result, AUNP-12 shows a low volume of distribution, and the peak plasma levels reach at 0.2-0.4 hours. The absolute bioavailability of AUNP-12 is about 77% in mice. [1]
SynonymsAUNP-12 acetate (1353563-85-5 Free base)
Chemical Properties
Molecular Weight3321.61
FormulaC144H230N40O50
SmilesO=C([C@@](NC([C@](NC([C@@](NC([C@@](NC([C@@](NC([C@@](NN)(CCC(O)=O)[H])=O)(CCCCN)[H])=O)([C@@](CC)(C)[H])[H])=O)(CCC(N)=O)[H])=O)(C)[H])=O)(CCCCN)[H])N1[C@@](CCC1)(C(N[C@@](C(C([C@@](NC([C@@](NC([C@@](NC([C@@](NC([C@@](NC([C@@](NC(C(CCCCNN[C@@](CC2=CC=CC=C2)(C(N([H])[C@](C(N[C@@](C(CC(O)=O)([H])[H])(C(N[C@](C(N[C@@]([C@@](O)(C)[H])(C(N[C@@](CC(N)=O)(C(N[C@@](CO)(C([H])=O)[H])=O)[H])=O)[H])=O)(CO)[H])=O)[H])=O)(CO)[H])=O)[H])NC([C@@](N([H])C([C@@](NC([C@@](NC([C@@](NC([C@@](NC([C@@](NC([C@@](N)(CO)[H])=O)(CC(N)=O)[H])=O)([C@@](O)(C)[H])[H])=O)(CO)[H])=O)(CCC(O)=O)[H])=O)(CO)[H])=O)(CC3=CC=CC=C3)[H])=O)=O)(CC4=CC=CC=C4)[H])=O)(CCCNC(N)=N)[H])=O)(C(C)(C)[H])[H])=O)([C@@](O)(C)[H])[H])=O)(CCC(N)=O)[H])=O)(CC(C)C)[H])=O)=O)(C)[H])=O)[H].CC(O)=O
SequenceSer-Asn-Thr-Ser-Glu-Ser-Phe-Lys(1)-Phe-Arg-Val-Thr-Gln-Leu-Ala-Pro-Lys-Ala-Gln-Ile-Lys-Glu-NH2.H-Ser-Asn-Thr-Ser-Glu-Ser-Phe-(1)
Sequence ShortSNTSESFKF(H-SNTSESF)RVTQLAPKAQIKE
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.
Solubility Information
DMSO: 100 mg/mL (30.11 mM), Sonication is recommended.
H2O: 25 mg/mL (7.53 mM), Sonication is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM0.3011 mL1.5053 mL3.0106 mL15.0529 mL
5 mM0.0602 mL0.3011 mL0.6021 mL3.0106 mL
DMSO
1mg5mg10mg50mg
10 mM0.0301 mL0.1505 mL0.3011 mL1.5053 mL
20 mM0.0151 mL0.0753 mL0.1505 mL0.7526 mL

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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 stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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Keywords

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