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Corticotropin-releasing factor (human) acetate
🥰Excellent
Catalog No. TP1144L
Alias Corticotropin-releasing factor (human) acetate (86784-80-7 Free base)
Corticotropin-releasing factor (human) acetate stimulates to synthesize and secret adrenocorticotropin in the anterior pituitary.
Corticotropin-releasing factor (human) acetate
Corticotropin-releasing factor (human) acetate
🥰Excellent
Purity: 98.30%
Catalog No. TP1144LAlias Corticotropin-releasing factor (human) acetate (86784-80-7 Free base)
Corticotropin-releasing factor (human) acetate stimulates to synthesize and secret adrenocorticotropin in the anterior pituitary.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $148 | In Stock | |
| 5 mg | $497 | In Stock | |
| 10 mg | $747 | In Stock | |
| 25 mg | $1,342 | In Stock | |
| 50 mg | $1,997 | In Stock |
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K 41498 aceate
TP2009L
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Astressin acetate
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Urocortin (rat) acetate
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Purity:98.30%
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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 | Corticotropin-releasing factor (human) acetate stimulates to synthesize and secret adrenocorticotropin in the anterior pituitary. |
| In vitro | Corticotropin-releasing factor (human) acetate caused pain-induced aversive responses through the increase of excitability of type II dlBNST neurons and the activation of the AC-cAMP-PKA pathway[2]. |
| In vivo | The time spent in the drug-paired compartment during the test session (314±22 s) is significantly shorter than the time spent in that compartment during the preconditioning session (520±18 s) in rats injected with Corticotropin-releasing factor (human) acetate (1 nmol/side)[2]. |
| Alias | Corticotropin-releasing factor (human) acetate (86784-80-7 Free base) |
| Relative Density. | no data available |
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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