research use only
Cat.No.S4507
| Related Targets | Adrenergic Receptor GPR Androgen Receptor Glucocorticoid Receptor ACE RAAS Progesterone Receptor Opioid Receptor PGES THR |
|---|---|
| Other Estrogen/progestogen Receptor Inhibitors | Elacestrant (RAD1901) Dihydrochloride MPP dihydrochloride Cholesterol Endoxifen HCl G15 Chrysin Licochalcone A AZD9496 PHTPP Liquiritigenin |
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In vitro |
DMSO
: 66 mg/mL
(199.72 mM)
Ethanol : 66 mg/mL Water : Insoluble |
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In vivo |
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Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
Calculation results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.
| Molecular Weight | 330.46 | Formula | C21H30O3 |
Storage (From the date of receipt) | |
|---|---|---|---|---|---|
| CAS No. | 68-96-2 | Download SDF | Storage of Stock Solutions |
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| In vitro |
17α-OHP is an agonist of the progesterone receptor (PR) similarly to progesterone, albeit weakly in comparison.
It is a chemical intermediate in the biosynthesis of steroid hormones, including the androgen and estrogen sex hormones and the glucocorticoids and mineralocorticoids.
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| In vivo |
17-Hydroxyprogesterone is a potent steroid inducer of GVBD (germinal vesicle breakdown).
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References |
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(data from https://clinicaltrials.gov, updated on 2024-05-22)
| NCT Number | Recruitment | Conditions | Sponsor/Collaborators | Start Date | Phases |
|---|---|---|---|---|---|
| NCT06402344 | Recruiting | Hormones; Abuse|Cardiovascular Diseases |
Hospital Israelita Albert Einstein |
May 27 2024 | -- |
| NCT05907291 | Recruiting | Congenital Adrenal Hyperplasia|Classic Congenital Adrenal Hyperplasia |
Crinetics Pharmaceuticals Inc. |
July 3 2023 | Phase 2 |
| NCT05669950 | Recruiting | Congenital Adrenal Hyperplasia |
H. Lundbeck A/S |
December 19 2022 | Phase 1 |
| NCT05299554 | Enrolling by invitation | Congenital Adrenal Hyperplasia |
Diurnal Limited |
April 1 2022 | Phase 3 |
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