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Goserelin acetate

CAS No.
145781-92-6
Chemical Name:
Goserelin acetate
Synonyms
Fertilan;Goserelin HCl;Goserelin acetate;Gosorelin Acetate;Goserelin Acteate;Goserilyn acetate;ICI-118630 acetate;Goserelin acetate/Fertilan;Goserelin?Acetate impurity;Goserelin Acetate(acetate)
CBNumber:
CB1281026
Molecular Formula:
C61H88N18O16
Molecular Weight:
1329.49
MDL Number:
MFCD00867894
MOL File:
145781-92-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-27 17:00:41

Goserelin acetate Properties

Melting point >190°C (dec.)
storage temp. -20°C
solubility H2O: 20 mg/mL, clear, colorless
form white powder
color White to Off-White
Water Solubility H2O: 20mg/mL, clear, colorless
Stability Hygroscopic
InChIKey IKDXDQDKCZPQSZ-JHYYTBFNSA-N
NCI Dictionary of Cancer Terms goserelin acetate
FDA UNII 6YUU2PV0U8
NCI Drug Dictionary goserelin acetate
Proposition 65 List Goserelin Acetate
UNSPSC Code 51111800
NACRES NA.32

SAFETY

Risk and Safety Statements

Symbol(GHS)  Health Hazard (GHS08)
GHS08
Signal word  Danger
Hazard statements  H360
Precautionary statements  P201-P202-P280-P308+P313-P405-P501
PPE Eyeshields, Gloves, type N95 (US)
Safety Statements  22-24/25
WGK Germany  3
RTECS  OK6369800
HS Code  2937190000
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Repr. 1B
NFPA 704
0
2 0

Goserelin acetate price More Price(59)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0001473 Goserelin for NMR identification European Pharmacopoeia (EP) Reference Standard 145781-92-6 14 mg $127 2026-04-30 Buy
Sigma-Aldrich Y0000125 Goserelin European Pharmacopoeia (EP) Reference Standard 145781-92-6 2 mg $241 2026-04-30 Buy
Sigma-Aldrich PHR3776 Goserelin Acetate certified reference material, pharmaceutical secondary standard 145781-92-6 100MG $698 2026-04-30 Buy
Sigma-Aldrich G4919 Goserelin acetate ≥99% (HPLC), white powder 145781-92-6 5mg $306 2026-04-30 Buy
Sigma-Aldrich 1297205 Goserelin acetate United States Pharmacopeia (USP) Reference Standard 145781-92-6 100mg $1430 2026-04-30 Buy
Product number Packaging Price Buy
Y0001473 14 mg $127 Buy
Y0000125 2 mg $241 Buy
PHR3776 100MG $698 Buy
G4919 5mg $306 Buy
1297205 100mg $1430 Buy

Goserelin acetate Chemical Properties, Uses, Production

Description

Goserelin acetate, like leuprolide acetate, is a synthetic superagonist nonapeptide analogue of GnRH that possesses greater potency than the natural hormone. Note that it contains D-Ser(But) and NH-NHCONH2 in place of Gly6 and Gly10-NH2, respectively. That is, the C terminal modification simply has an NH substituting for the CH2 of Gly, and like the C-terminal change in leuprolide acetate, this inhibits enzymatic degradation of the peptide by the postproline carboxyamide peptidase.
Goserelin acetate is available in the form of a small, solid pellet that is administered as an SC implant for the palliative treatment of advanced, metastatic breast cancer in pre- and perimenopausal women or, similarly, as a palliative in advanced prostatic cancer. The rationale for this drug's use is, as described above, its ability as a superagonist to bring the levels of estradiol or testosterone to near castrate levels, thus slowing the progression of breast or prostate carcinoma, respectively. Additionally, goserelin acetate is approved for use in treating endometriosis for up to 6 months.

Description

Goserelin is a synthetic gonadotropin-releasing hormone (GNRH) agonist that binds to the GNRH receptor (GNRHR; Ki = 1.6 nM, in CHO cells expressing the human receptor). It binds to mouse pituitary αT3-1 cells and human placenta (Kds = 2 and 580 nM, respectively) and increases intracellular calcium in αT3-1 cells. Goserelin induces testosterone production in vitro within 4 h in rat Leydig cells (ED50 = 83 nM) but decreases testosterone plasma level in vivo in rats over a period of 2 to 24 weeks. It inhibits tumor growth in a DU145 human prostate carcinoma mouse xenograft model when administered at a dose of 100 μg per day. Formulations containing goserelin have been used in the treatment of hormone-dependent breast and prostate cancers, as well as endometriosis and uterine fibroids.

Chemical Properties

White Solid

Uses

Anticancer

Uses

injectable gonadotropin releasing hormone superagonist (GnRH agonist) or luteinizing hormone antiproliferative activity in breast, prostate and endometrial cancers

Uses

Synthetic peptide agonist analog of LH-RH. Antineoplastic (hormonal).

General Description

Goserelin acetate is a synthetic decapaptide, which is a potent analog of LHRH (luteinizing hormone releasing hormone).

Biochem/physiol Actions

Goserelin acetate peptide results in significant inhibition of gonadotropin release and suppresses steroidogenesis in ovaries and testis. Thus, it leads to a reduction of testosterone to castration levels and estrogen to postmenopausal levels. Therefore, this peptide is used for reducing testosterone levels in patients with locally advanced prostate cancer.

Clinical Use

Goserelin acetate also is used in combination with the antiandrogen flutamide for shrinking prostate carcinoma before radiation therapy. This maximal androgen blockade combination is used when the prostate carcinoma has been staged as locally confined to the prostate gland, with one or both lobes as well as the seminal vesicles involved. The treatment should start 8 weeks before radiation treatment begins and be continued throughout the radiation therapy.
Furthermore, women who are to undergo hysterectomy for menorrhagia can benefit from previous treatment with goserelin acetate, because it is able to induce endometrial thinning. This thinning of the endometrium improves the operating environment by causing less intrauterine bleeding, increased postoperative amenorrhea, and decreased dysmenorrhea following surgery, which is why goserelin acetate is approved for inducing endometrial thinning prior to a patient undergoing a hysterectomy for heavy menstrual bleeding.

References

[1] INDIRA NEDERPELT. Characterization of 12 GnRH peptide agonists – a kinetic perspective[J]. British Journal of Pharmacology, 2015, 173 1: 128-141. DOI: 10.1111/bph.13342
[2] E CHATZAKI. The expression of gonadotropin-releasing hormone and its receptor in endometrial cancer, and its relevance as an autocrine growth factor.[J]. Cancer research, 1996, 56 9: 2059-2065.
[3] M H SULLIVAN  B A C. The role of calcium in luteinizing hormone-releasing hormone agonist (ICI 118630)-stimulated steroidogenesis in rat Leydig cells.[J]. Biochemical Journal, 1984, 218 2: 621-624. DOI: 10.1042/bj2180621
[4] JERRY A. WARD. Prolonged Suppression of Rat Testis Function by a Depot Formulation of Zoladex, a GnRH Agonist[J]. Journal of andrology, 1989, 10 6: 478-486. DOI: 10.1002/j.1939-4640.1989.tb00144.x
[5] DONATELLA DONDI. Growth-inhibitory effects of luteinizing hormone-releasing hormone (LHRH) agonists on xenografts of the DU 145 human androgen-independent prostate cancer cell line in nude mice[J]. International Journal of Cancer, 1998, 76 4: 506-511. DOI: 10.1002/(sici)1097-0215(19980518)76:4<506::aid-ijc11>3.0.co;2-5

Goserelin acetate Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 285)
Supplier Tel Email Country ProdList Advantage
Chengdu Jinglin Biotechnology Co., Ltd. 17711399154 3211919385@qq.com China 1815 58
Chinese Peptide Company 0571-86737118-8680 15988144796 sales@chinesepeptide.com China 10 58
Suzhou Tianma Pharma Group Tianji Bio-Pharmaceutical Co., Ltd. 0512-68322275 15850786624 danielzhao@tianmapharma.com China 30 58
Hybio Pharmaceutical(Wuhan)Co., Ltd. 0755-26586015 13924639140 sales@hybio.com China 300 58
Fuan Bio 15002819872 2845971812@qq.com China 2103 58
SU ZHOU MOTIF BIOTECH CO.,LTD 18151592215 18516107567 info@motifbiotech.com China 999 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037 3bsc@sina.com China 15813 69
Chembest Research Laboratories Limited 021-20908456 sales@BioChemBest.com China 5996 61
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32273 50

View Latest Price from Goserelin acetate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Goserelin acetate pictures 2026-09-14 Goserelin acetate
145781-92-6
2kg 98% up by HPLC, EP 20tons Sinoway Industrial co., ltd.
Goserelin acetate pictures 2026-09-14 Goserelin acetate
145781-92-6
1G 99% 1 ton/year Forest chemical technology
Goserelin acetate pictures 2026-08-12 Goserelin acetate
145781-92-6
$1413.00 1g 98% 1kg Baoji Guokang Healthchem Co., Ltd.

Goserelin acetate Spectrum

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 ICI-118630 acetate GOSERELIN HCL[PYR-HIS-TRP-SER-TYR-D-SER(T-BU)-LEU-ARG-PRO-AZAGLY-NH2] 1-9-Luteinizing hormone-releasing factor (swine), 6-(o-(1,1-dimethylethyl)-D-serine)-, 2-(aminocarbonyl)hydrazide, acetate (salt) Fertilan 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 Acetate (100 mg) (COLD SHIPMENT REQUIRED) (2S)-1-[(2R)-2-[(2R)-2-[(2R)-3-(tert-butoxy)-2-[(2R)-2-[(2R)-3-hydroxy-2-[(2S)-2-[(2S)-3-(1H-iMidazol-5-yl)-2-{[(2R)-5-oxopyrrolidin-2-yl]forMaMido}propanaMido]-3-(1H-indol-3-yl)propanaMido]propanaMido]-3-(4-hydroxyphenyl)propanaMido]propanaMido]-4-Methyl Goserelin acetate Gosorelin Acetate Goserelin Acteate Goserelin for NMR identification Goserelin acetate (ICI-118630 acetate) Goserelin acetate/Fertilan Goserelin?Acetate impurity Goserilyn acetate Goserelin acetate USP/EP/BP Goserelin Acetate(acetate) (D-Ser(tBu)?,Azagly??)-LHRH acetate salt HIS-TRP-SER-TYR-D-SER(TBU)-LEU-ARG-PRO-AZA-GLY-NH2 Goserelin acetate, 10 mM in DMSO 145781-92-6 C61H88N18O16 C59H84N18O14C2H4O2 C59H84N18O14xC2H4O2 C59H84N18O14xH2O Other Protein/Peptide Hormones Cell Biology Cell Signaling and Neuroscience BioChemical Hormones Cytokines, Growth Factors and Hormones Peptide Pepetides Amino Acid Derivatives Intermediates & Fine Chemicals Peptides Pharmaceuticals