GnRH antagonist 1
GnRH antagonist 1 (Relugolix impurity 1) is a GnRH receptor antagonist that blocks the binding of gonadotropin-releasing hormone (GnRH) in the anterior pituitary, thereby inhibiting the secretion of luteinizing hormone and follicle-stimulating hormone. GnRH antagonist 1 can be used for research on endometriosis, uterine fibroids, and prostate cancer.
For research use only. We do not sell to patients.
- CAS No.: 1801551-07-4
- Formula: C28H25F2N7O5S
- Molecular Weight:609.61
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
In Vitro
GnRH antagonist 1 (example 10) blocks the binding of gonadotropin-releasing hormone (GnRH) in the anterior pituitary, inhibiting the secretion of luteinizing hormone and follicle-stimulating hormone[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 1801551-07-4
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Molecular Weight 609.61
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Formula C28H25F2N7O5S
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SMILES
O=C1C=CC(=NN1)N2C(=O)C3=C(SC(C=4C=CC(=CC4)NC(=O)NOC)=C3CN(C)C)N(C2=O)CC=5C(F)=CC=CC5F
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Synonyms
Relugolix impurity 1
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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)
Keywords
- GnRH antagonist 1
- 1801551-07-4
- Relugolix impurity 1
- GnRH antagonist1
- GnRH antagonist-1
- Relugolix impurity1
- Relugolix impurity-1
- GnRH Receptor
- tetrahydrofuran solvate
- endometriosis
- luteinizing hormone
- uterine fibroid
- prostate cancer
- follicle stimulating hormone secretion
- anterior pituitary
- GnRH receptor antagonist
- dimethylsulfoxide
- gonadotropin releasing hormone binding
- Inhibitor
- inhibitor
- inhibit