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ACTH (1-17) acetate
🥰Excellent
Catalog No. TP1011L
ACTH (1-17) acetate is a potent agonist at the human melanocortin 1 (MC1) receptor with high affinity(Ki = 0.21 nM).
ACTH (1-17) acetate
🥰Excellent
Purity: 98.53%
Catalog No. TP1011L
ACTH (1-17) acetate is a potent agonist at the human melanocortin 1 (MC1) receptor with high affinity(Ki = 0.21 nM).
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $122 | In Stock | |
| 5 mg | $411 | In Stock | |
| 10 mg | $587 | In Stock | |
| 25 mg | $1,057 | In Stock | |
| 50 mg | $1,585 | In Stock | |
| 100 mg | $2,377 | In Stock |
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Purity:98.53%
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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.Product Introduction
Bioactivity
Chemical Properties
| Description | ACTH (1-17) acetate is a potent agonist at the human melanocortin 1 (MC1) receptor with high affinity(Ki = 0.21 nM). |
| Targets&IC50 | MC1R (human):0.21 nM(Ki) |
| In vitro | ACTH (1-17) acetate induces a slight and not significant increase in growth hormone secretion even when micromolar concentrations of the peptide are employed in rat pituitary cultures[1]. ACTH (1-17) acetate showed an affinity for alpha-MSH with Ki of 0.13±0.005 nM[1]. |
| In vivo | When nocturnal animals became active, inhibition of DNA markers was noted when ACTH (1-17) acetate was administered 2 hours after the start of the daily dark span. When administered during this circadian phase, particularly larger doses were associated with a 24-hour lasting inhibition of DNA markers. When the same dose was injected 4 hours earlier, the inhibitory effect was much shorter [2]. |
| Molecular Weight | 2153.47 |
| Formula | C97H149N29O25S |
| Smiles | CC(O)=O.N=C(N)NCCC[C@@H](C(O)=O)NC([C@H](CCCCN)NC([C@H](CCCCN)NC(CNC([C@H](C(C)C)NC([C@H]1N(C([C@H](CCCCN)NC(CNC([C@H](CC2=CNC3=C2C=CC=C3)NC([C@H](CCCNC(N)=N)NC([C@H](CC4=CC=CC=C4)NC([C@H](CC5=CNC=N5)NC([C@H](CCC(O)=O)NC([C@H](CCSC)NC([C@H](CO)NC([C@H](CC6=CC=C(O)C=C6)NC([C@H](CO)N)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)CCC1)=O)=O)=O)=O)=O |
Storage & Solubility Information
| Storage | store at low temperature,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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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% 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 μLddH2O 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 μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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