1. Vitamin D Related/Nuclear Receptor
  2. Progesterone Receptor
  3. EIDD-1723

EIDD-1723 is a Progesterone (HY-N0437) analogues, that binds progesterone receptor (PR) with an IC50 of 2.25 μM. EIDD-1723 is the prodrug of EIDD-036 (HY-17649). EIDD-1723 may exert its neuroprotective effects not solely through progesterone receptor (PR)-dependent pathways but also via non-genomic mechanisms, such as modulation of inflammatory responses and oxidative stress. EIDD-1723 can be used for the study of traumatic brain injury (TBI).

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EIDD-1723

EIDD-1723 Chemical Structure

CAS No. : 1659302-89-2

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Description

EIDD-1723 is a Progesterone (HY-N0437) analogues, that binds progesterone receptor (PR) with an IC50 of 2.25 μM. EIDD-1723 is the prodrug of EIDD-036 (HY-17649). EIDD-1723 may exert its neuroprotective effects not solely through progesterone receptor (PR)-dependent pathways but also via non-genomic mechanisms, such as modulation of inflammatory responses and oxidative stress. EIDD-1723 can be used for the study of traumatic brain injury (TBI)[1][2][3].

In Vitro

ANT308 (1-10 μM, 48 h) significantly enhances CD69 and Ki67 expressions in CD4+ and CD8+ T cells[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Parmacokinetics[2]
Species Dose Route Indicator value
Rat 10 mg/kg i.m. Cmax 1362 ng/mL
Rat 2 mg/kg i.v. Cmax 182 ng/mL
Rat 10 mg/kg i.m. AUClast 724 ng·h/mL
Rat 2 mg/kg i.v. AUClast 48 ng·h/mL
In Vivo

EIDD-1723 (3-30 mg/kg, i.m., 2 mg/kg, i.v., 30 mg/kg, p.o., single dose) after administered by intramuscular injection rapidly and completely transforms into the active metabolite EIDD-036, which is capable of crossing the blood-brain barrier[1][3].
EIDD-1723 (10 mg/kg, i.m., for 9 doses) significantly reduces cerebral edema and improved recovery from motor, sensory and spatial learning deficits in rats[1][3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: TBI model induced by controlled cortical impact (CCI) established in male SD rats weighing 200-350 g[1][3]
Dosage: 10 mg/kg
Administration: Intramuscular injection (i.m.), at 1, 6, and 24 h and 2, 3, 4, 5, 6, and 7 days post-injury
Result: Significantly reduced cerebral edema, improved motor function, shortened the delay time of sensory neglect, and enhanced spatial learning ability.
Significantly reduced brain tissue damage and weakened the activation of astrocytes and microglia cells.
Molecular Weight

483.45

Formula

C22H32NNa2O6P

CAS No.
SMILES

C[C@@]12[C@](CC[C@@H]2/C(C)=N/OCOP(O[Na])(O[Na])=O)([H])[C@@]3([H])[C@@](CC1)([H])[C@@]4(C(CC3)=CC(CC4)=O)C

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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
EIDD-1723
Cat. No.:
HY-125547
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