Org 214444-0
Org 214444-0 is an orally active, nanomolar-potent and selective FSHR agonist, with EC50 values of 2.0 nM and 1.2 nM in human and rat (measured in CHO cells). Org 214444-0 activates human granulosa cells in vitro, supports rat follicular development and induces ovulation in vivo. Org 214444-0 can be used for the research of infertility.
For research use only. We do not sell to patients.
- CAS No.: 914093-78-0
- Formula: C30H32BrF2N3O5S
- Molecular Weight:664.56
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
In Vitro
Org 214444-0 (1 h) stimulates cAMP production in CHO cells expressing human FSHR, with an EC50 of 5 nM[1].
Org 214444-0 (2 h) induces internalization of EGFP-tagged rat FSHR in U2OS cells, with an EC50 of 97 nM[1].
Org 214444-0 (1 nM-10 mM; 48 h) stimulates estradiol production in human granulosa cells, with an EC50 of approximately 8.3 nM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. .
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Orga rats (mature female)[1]
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Dosage:0.1 mg/kg; 0.25 mg/kg; 0.5 mg/kg; 1.0 mg/kg (s.c.); 1.0 mg/kg (p.o.)
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Administration:s.c.; twice daily on met-estrus and diestrus, once on proestrus morning; p.o.; every 4 hours
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Result:Caused a dose-dependent increase in the number of ovulated ova per rat.
Chemical Information
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CAS No. 914093-78-0
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Molecular Weight 664.56
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Formula C30H32BrF2N3O5S
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SMILES
N#CC1=C(C)NC(C[C@@H](CC2=O)CCC)=C2[C@@H]1C3=CC(OCC)=C(C(Br)=C3)OCC4=C(C=C(C(F)=C4)F)NS(C)(=O)=O
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)