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17-Hydroxyprogesterone Estrogen/progestogen Receptor agonist

Cat.No.S4507

17-Hydroxyprogesterone (17-OHP) is an endogenous progestogen as well as chemical intermediate in the biosynthesis of other steroid hormones, including the corticosteroids and the androgens and the estrogens.
17-Hydroxyprogesterone Estrogen/progestogen Receptor agonist Chemical Structure

Chemical Structure

Molecular Weight: 330.46

Quality Control

Batch: S450701 DMSO]66 mg/mL]false]Ethanol]66 mg/mL]false]Water]Insoluble]false Purity: 99.94%
99.94

Chemical Information, Storage & Stability

Molecular Weight 330.46 Formula

C21H30O3

Storage (From the date of receipt)
CAS No. 68-96-2 Download SDF Storage of Stock Solutions

Solubility

In vitro
Batch:

DMSO : 66 mg/mL (199.72 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 66 mg/mL

Water : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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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.

Mechanism of Action

In vitro
17α-OHP is an agonist of the progesterone receptor (PR) similarly to progesterone, albeit weakly in comparison[1]. It is a chemical intermediate in the biosynthesis of steroid hormones, including the androgen and estrogen sex hormones and the glucocorticoids and mineralocorticoids.
In vivo
17-Hydroxyprogesterone is a potent steroid inducer of GVBD (germinal vesicle breakdown)[3].
References

Clinical Trial Information

(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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