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Somatostatin 1-28 acetate
🥰Excellent
Catalog No. TP2124L
Alias Somatostatin 1-28 acetate(74315-46-1 Free base)
Somatostatin 1-28 acetate circulates in human plasma. Approximately 46% of the total somatostatin-like immunoreactivity in plasma is due to Somatostatin 1-28 acetate.
Somatostatin 1-28 acetate
🥰Excellent
Purity: 99.51%
Catalog No. TP2124LAlias Somatostatin 1-28 acetate(74315-46-1 Free base)
Somatostatin 1-28 acetate circulates in human plasma. Approximately 46% of the total somatostatin-like immunoreactivity in plasma is due to Somatostatin 1-28 acetate.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $508 | In Stock | |
| 5 mg | $1,030 | In Stock | |
| 10 mg | $1,390 | In Stock | |
| 25 mg | $2,080 | In Stock | |
| 50 mg | $2,810 | In Stock |
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CYN 154806 TFA
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Somatostatin acetate
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BIM-23190 aceate
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- $195
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L-796,778
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L-796,778 is an SST3 agonist and a selective ligand of SST3, which can increase the level of cAMP in the body.
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L-797,591 hydrochloride
L-797,591 hydrochloride(217480-24-5 Free base)
T27787LIn house
L-797,591 hydrochloride is active for somatostatin receptor isoform 1 (SSTR1). L-797,591 hydrochloride is commonly used in combination with AG1478 to enhance p-ERK5 expression in SSTR1 cells. L-797,591 hydrochloride significantly enhanced p38 phosphorylation in cotransfected cells, and this effect was reversed in combination with AG1478.
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Cyclosomatostatin Acetate
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T11800217480-26-7
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Purity:99.51%
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Product Introduction
Bioactivity
Chemical Properties
| Description | Somatostatin 1-28 acetate circulates in human plasma. Approximately 46% of the total somatostatin-like immunoreactivity in plasma is due to Somatostatin 1-28 acetate. |
| Alias | Somatostatin 1-28 acetate(74315-46-1 Free base) |
| Smiles | C[C@@H](O)[C@H]1C(N[C@@H](CC2=CC=CC=C2)C(N[C@@H]([C@H](O)C)C(N[C@@H](CO)C(N[C@H](C(O)=O)CSSC[C@H](NC(CNC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H]3CCCN3C([C@@H](NC([C@@H](NC([C@@H](NC([C@@H]4CCCN4C([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](NC([C@@H](N)CO)=O)C)=O)CC(N)=O)=O)CO)=O)CC(N)=O)=O)=O)C)=O)CCSC)=O)C)=O)=O)CCCNC(N)=N)=O)CCC(O)=O)=O)CCCNC(N)=N)=O)CCCCN)=O)C)=O)=O)C(N[C@@H](CCCCN)C(N[C@@H](CC(N)=O)C(N[C@@H](CC5=CC=CC=C5)C(N[C@@H](CC6=CC=CC=C6)C(N[C@@H](CC7=CNC8=CC=CC=C87)C(N[C@@H](CCCCN)C(N1)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O.CC(O)=O |
| Relative Density. | no data available |
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. |
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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:
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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