Goserelin acetate
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Goserelin acetate
structure -
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CAS No:
145781-92-6
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Formula:
C59H84N18O14
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Chemical Name:
Goserelin acetate
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Synonyms:
PYR-HIS-TRP-SER-TYR-D-SER(TBU)-LEU-ARG-PRO-AZAGLY-NH2;[(T-BU)DSER6, (AZA)GLY10]-LH-RH;[(T-BU)DSER6, (AZA)GLY10]-LUTEINIZING HORMONE-RELEASING HORMONE;GLP-HIS-TRP-SER-TYR-D-SER(TBU)-LEU-ARG-PRO-AZA-GLY-NH2;(D-SER(TBU)6,AZAGLY10)-LHRH;(D-Ser(tBu)6,Azagly10)-LHRH acetate salt;Goserelin HCl;GOSERELIN HCL[PYR-HIS-TRP-SER-TYR-D-SER(T-BU)-LEU-ARG-PRO-AZAGLY-NH2]
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Categories:
Active Pharmaceutical Ingredients > Hormones and the Endocrine System
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CAS No:
Characteristics
493.39000
-0.95
white powder
1.5±0.1 g/cm3
>190°C (dec.)
1695.5ºC at 760mmHg
1.692
H2O: 20 mg/mL, clear, colorless
−20°C
Goserelin acetate Use and Manufacturing
Synthetic peptide agonist analog of LH-RH. Antineoplastic (hormonal).
Drug Function and Efficacy
This drug is a synthetic analog of luteinizing hormone-releasing hormone. Long-term use can inhibit the secretion of luteinizing hormone from the pituitary gland, thereby causing a decrease in male serum testosterone and female serum estradiol. This effect is reversible after discontinuation of the drug. About 21 days after the first dose of the drug, the testosterone concentration of male patients can be reduced to the level after castration. During the treatment process of taking the drug once every 28 days, the testosterone concentration has been maintained within the concentration range after castration. This testosterone inhibition can cause prostate tumors to regress and symptoms to improve in most patients. About 21 days after the first dose of the drug, the serum estradiol concentration of female patients is suppressed and maintained at the postmenopausal level during the subsequent 28-day treatment. This inhibition is associated with hormone-dependent breast cancer and endometriosis.
Registered Holders
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AstraZeneca Pharmaceuticals LP
Active
United States
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Bachem AG
Active
Switzerland
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Chinese Peptide Co., Ltd.
Active
China
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