GOSERELIN ACETATE

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C59H84N18O14.C2H4O2
Molecular Weight	1329.4648
Optical Activity	UNSPECIFIED
Defined Stereocenters	9 / 9
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CC(O)=O.CC(C)C[C@H](NC(=O)[C@@H](COC(C)(C)C)NC(=O)[C@H](CC1=CC=C(O)C=C1)NC(=O)[C@H](CO)NC(=O)[C@H](CC2=CNC3=C2C=CC=C3)NC(=O)[C@H](CC4=CNC=N4)NC(=O)[C@@H]5CCC(=O)N5)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N6CCC[C@H]6C(=O)NNC(N)=O

InChI

InChIKey=IKDXDQDKCZPQSZ-JHYYTBFNSA-N

InChI=1S/C59H84N18O14.C2H4O2/c1-31(2)22-40(49(82)68-39(12-8-20-64-57(60)61)56(89)77-21-9-13-46(77)55(88)75-76-58(62)90)69-54(87)45(29-91-59(3,4)5)74-50(83)41(23-32-14-16-35(79)17-15-32)70-53(86)44(28-78)73-51(84)42(24-33-26-65-37-11-7-6-10-36(33)37)71-52(85)43(25-34-27-63-30-66-34)72-48(81)38-18-19-47(80)67-38;1-2(3)4/h6-7,10-11,14-17,26-27,30-31,38-46,65,78-79H,8-9,12-13,18-25,28-29H2,1-5H3,(H,63,66)(H,67,80)(H,68,82)(H,69,87)(H,70,86)(H,71,85)(H,72,81)(H,73,84)(H,74,83)(H,75,88)(H4,60,61,64)(H3,62,76,90);1H3,(H,3,4)/t38-,39-,40-,41-,42-,43-,44-,45+,46-;/m0./s1

HIDE SMILES / InChI

Molecular Formula	C2H4O2
Molecular Weight	60.052
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Molecular Formula	C59H84N18O14
Molecular Weight	1269.4128
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	9 / 9
E/Z Centers	0
Optical Activity	UNSPECIFIED

Description
Sources: http://www.drugbank.ca/drugs/DB00014
Curator's Comment: Description was created based on several sources, including https://www.drugs.com/zoladex.html

Goserelin is a synthetic decapeptide analogue of LHRH. Goserelin acts as a potent inhibitor of pituitary gonadotropin secretion when administered in the biodegradable formulation. The result is sustained suppression of LH and serum testosterone levels. Goserelin is used to treat hormone-sensitive cancers of the breast (in pre- and peri- menopausal women) and prostate, and some benign gynaecological disorders (endometriosis, uterine fibroids and endometrial thinning). In addition, goserelin is used in assisted reproduction and in the treatment of precocious puberty. Goserelin is marketed under the brand names Zoladex, by AstraZeneca, or goserelin acetate.

CNS Activity

Originator

Approval Year

Targets

Primary Target	Pharmacology	Potency
Luteinizing hormone/Choriogonadotropin receptor 2 Target ID: CHEMBL1854 Sources: http://www.drugbank.ca/drugs/DB00014	Agonist 2752
LNCaP 3 Target ID: CHEMBL612518 Sources: https://www.ncbi.nlm.nih.gov/pubmed/1320049	Inhibitor 8504	0.82 nM [IC50]
Gonadotropin-releasing hormone receptor 41 Target ID: CHEMBL1855 Sources: http://www.drugbank.ca/drugs/DB00014	Agonist 2752	1.6 nM [Ki]

Conditions

Condition	Modality	Targets	Highest Phase	Product
Locally confined carcinoma of the prostate 2 Sources: http://www.accessdata.fda.gov/drugsatfda_docs/label/2013/020578s034,020578s035lbl.pdf	Primary		Approved 8583	ZOLADEX Approved Use ZOLADEX is a Gonadotropin Releasing Hormone (GnRH) agonist indicated for: Use in combination with flutamide for the management of locally confined carcinoma of the prostate Use as palliative treatment of advanced carcinoma of the prostate Launch Date 1997
Advanced carcinoma of the prostate 2 Sources: http://www.accessdata.fda.gov/drugsatfda_docs/label/2013/020578s034,020578s035lbl.pdf	Palliative		Approved 8583	ZOLADEX Approved Use ZOLADEX is a Gonadotropin Releasing Hormone (GnRH) agonist indicated for: Use in combination with flutamide for the management of locally confined carcinoma of the prostate Use as palliative treatment of advanced carcinoma of the prostate Launch Date 1997

C_max

Value	Dose	Analyte	Population
7.79 μg/L REVIEW https://pubmed.ncbi.nlm.nih.gov/10926349	250 μg single, subcutaneous dose: 250 μg route of administration: Subcutaneous experiment type: SINGLE co-administered:	GOSERELIN serum	Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN
13.9 μg/L REVIEW https://pubmed.ncbi.nlm.nih.gov/10926349	250 μg single, subcutaneous dose: 250 μg route of administration: Subcutaneous experiment type: SINGLE co-administered:	GOSERELIN serum	Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN
7.5 μg/L REVIEW https://pubmed.ncbi.nlm.nih.gov/10926349	250 μg single, subcutaneous dose: 250 μg route of administration: Subcutaneous experiment type: SINGLE co-administered:	GOSERELIN plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN
9.5 μg/L REVIEW https://pubmed.ncbi.nlm.nih.gov/10926349	250 μg 1 times / day multiple, subcutaneous dose: 250 μg route of administration: Subcutaneous experiment type: MULTIPLE co-administered:	GOSERELIN plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN
2.84 ng/mL DRUG LABEL https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/019726s050s051s052lbl.pdf	3.6 mg single, subcutaneous dose: 3.6 mg route of administration: Subcutaneous experiment type: SINGLE co-administered:	GOSERELIN plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN
1.46 ng/mL DRUG LABEL https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/019726s050s051s052lbl.pdf	3.6 mg single, subcutaneous dose: 3.6 mg route of administration: Subcutaneous experiment type: SINGLE co-administered:	GOSERELIN plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE food status: UNKNOWN
8.85 ng/mL DRUG LABEL https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/019726s059,020578s037lbl.pdf	10.8 mg single, subcutaneous dose: 10.8 mg route of administration: Subcutaneous experiment type: SINGLE co-administered:	GOSERELIN plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN
3 ng/mL DRUG LABEL https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/019726s059,020578s037lbl.pdf	3.6 mg single, subcutaneous dose: 3.6 mg route of administration: Subcutaneous experiment type: SINGLE co-administered:	GOSERELIN plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN

AUC

Value	Dose	Analyte	Population
36.9 μg × h/L REVIEW https://pubmed.ncbi.nlm.nih.gov/10926349	250 μg single, subcutaneous dose: 250 μg route of administration: Subcutaneous experiment type: SINGLE co-administered:	GOSERELIN serum	Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN
41.3 μg × h/L REVIEW https://pubmed.ncbi.nlm.nih.gov/10926349	250 μg single, subcutaneous dose: 250 μg route of administration: Subcutaneous experiment type: SINGLE co-administered:	GOSERELIN serum	Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN
44.5 μg × h/L REVIEW https://pubmed.ncbi.nlm.nih.gov/10926349	250 μg single, subcutaneous dose: 250 μg route of administration: Subcutaneous experiment type: SINGLE co-administered:	GOSERELIN plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN
44 μg × h/L REVIEW https://pubmed.ncbi.nlm.nih.gov/10926349	250 μg 1 times / day multiple, subcutaneous dose: 250 μg route of administration: Subcutaneous experiment type: MULTIPLE co-administered:	GOSERELIN plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN
27.8 ng × day/mL DRUG LABEL https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/019726s050s051s052lbl.pdf	3.6 mg single, subcutaneous dose: 3.6 mg route of administration: Subcutaneous experiment type: SINGLE co-administered:	GOSERELIN plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN
18.5 ng × day/mL DRUG LABEL https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/019726s050s051s052lbl.pdf	3.6 mg single, subcutaneous dose: 3.6 mg route of administration: Subcutaneous experiment type: SINGLE co-administered:	GOSERELIN plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE food status: UNKNOWN

T_1/2

Value	Dose	Analyte	Population
4.2 h REVIEW https://pubmed.ncbi.nlm.nih.gov/10926349	250 μg single, subcutaneous dose: 250 μg route of administration: Subcutaneous experiment type: SINGLE co-administered:	GOSERELIN serum	Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN
2.3 h REVIEW https://pubmed.ncbi.nlm.nih.gov/10926349	250 μg single, subcutaneous dose: 250 μg route of administration: Subcutaneous experiment type: SINGLE co-administered:	GOSERELIN serum	Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: UNKNOWN
4.6 h REVIEW https://pubmed.ncbi.nlm.nih.gov/10926349	250 μg single, subcutaneous dose: 250 μg route of administration: Subcutaneous experiment type: SINGLE co-administered:	GOSERELIN plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN
5 h REVIEW https://pubmed.ncbi.nlm.nih.gov/10926349	250 μg 1 times / day multiple, subcutaneous dose: 250 μg route of administration: Subcutaneous experiment type: MULTIPLE co-administered:	GOSERELIN plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN

F_unbound

Value	Dose	Co-administered	Analyte	Population
73% DRUG LABEL https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/019726s059,020578s037lbl.pdf	10.8 mg single, subcutaneous dose: 10.8 mg route of administration: Subcutaneous experiment type: SINGLE co-administered:		GOSERELIN plasma	Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN

Doses

Dose	Population	Adverse events
3.6 mg 1 times / day steady, subcutaneous Recommended Dose: 3.6 mg, 1 times / day Route: subcutaneous Route: steady Dose: 3.6 mg, 1 times / day Sources: https://pubmed.ncbi.nlm.nih.gov/25738668/	unhealthy, 18 - 49 years Health Status: unhealthy Age Group: 18 - 49 years Sex: F Sources: https://pubmed.ncbi.nlm.nih.gov/25738668/	Other AEs: Fatigue, Hot flashes... Other AEs: Fatigue (grade 2, 2 patients) Hot flashes (grade 2, 29 patients) Menses irregular (grade 2, 5 patients) Libido decreased (grade 2, 9 patients) Agitation (grade 2, 6 patients) Anxiety (grade 2, 9 patients) Depression (grade 2, 8 patients) Muscle pain (grade 2, 1 patient) Headache (grade 2, 12 patients) Sweating (grade 2, 10 patients) Thromboembolism (grade 4, 1 patient) Dryness vaginal (grade 2, 12 patients) Hot flashes (grade 3, 4 patients) Menses irregular (grade 3, 2 patients) Depression (grade 3, 1 patient) Sources: https://pubmed.ncbi.nlm.nih.gov/25738668/
10.8 mg 1 times / day steady, subcutaneous Recommended Dose: 10.8 mg, 1 times / day Route: subcutaneous Route: steady Dose: 10.8 mg, 1 times / day Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/020578s034,020578s035lbl.pdf	unhealthy, adult Health Status: unhealthy Age Group: adult Sex: M Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/020578s034,020578s035lbl.pdf	Other AEs: Gastrointestinal disorder (NOS), Bladder disorder NOS... Other AEs: Gastrointestinal disorder (NOS) (80%) Bladder disorder NOS (58%) Skin and subcutaneous conditions NEC (37%) Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/020578s034,020578s035lbl.pdf
10.8 mg 1 times / day steady, subcutaneous Recommended Dose: 10.8 mg, 1 times / day Route: subcutaneous Route: steady Dose: 10.8 mg, 1 times / day Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/020578s034,020578s035lbl.pdf	unhealthy, adult Health Status: unhealthy Age Group: adult Sex: M Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/020578s034,020578s035lbl.pdf	Other AEs: Diarrhea, Cystitis... Other AEs: Diarrhea (36%) Cystitis (16%) Bleeding rectal (14%) Proctitis (8%) Hematuria (7%) Sources: https://www.accessdata.fda.gov/drugsatfda_docs/label/2013/020578s034,020578s035lbl.pdf

AEs

Sourcing

Vendor/Aggregator	ID	URL
3B Scientific (Wuhan) Corp	3B2-0290	http://www.3bsc.com/index/pro_info.php?id=19646
abcr GmbH	AB477773	http://www.abcr.de/shop/en/AB477773
Achemtek	0104-042050	http://www.achemtek.com/65807-02-5
Acorn PharmaTech	ACN-057301	http://www.acornpharmatech.com/
AHH Chemical co.,ltd	API-1276	http://www.ahhchemical.com/product/API-1276.html
Alfa Chemistry	145781-92-6	https://www.alfa-chemistry.com/goserelin-acetate-cas-145781-92-6-item-290306.htm
Alfa Chemistry	AP145781926	https://reagents.alfa-chemistry.com/product/goserelin-acetate-cas-145781-92-6-5107.html
ApexBio Technology	B3723	http://www.apexbt.com/goserelin-acetate.html
AvaChem Scientific	2222	http://www.avachem.com/productSearch.asp?2222
BOC Sciences	145781-92-6	https://www.bocsci.com/goserelin-acetate-cas-145781-92-6-item-58990.html
Chem Scene	CS-3114	http://www.chemscene.com/65807-02-5.html
Chemspace	CSSB02125551064	https://chem-space.com/CSSB02125551064
Glentham Life Sciences	GK2378	http://www.glentham.com/products/product/GK2378/
iChemical	EBD22503	http://www.ichemical.com/chemicals/cas-65807-02-5
Lab Network	LN01254447	https://labnetwork.com/frontend-app/p/#!/moleculedetails/LN01254447
MedChem Express	HY-13673	https://www.medchemexpress.com/Goserelin.html
MolPort	MolPort-006-823-831	https://www.molport.com/shop/molecule-link/MolPort-006-823-831
MuseChem	I004480	https://www.musechem.com/product/I004480.html
OChem	20403	http://www.ocheminc.com/index.php?act=psearch&pid=807G025
OChem	7371	http://www.ocheminc.com/index.php?act=psearch&pid=81G926
Smolecule	S529156	http://www.smolecule.com/products/s529156
THE BioTek	bt-269569	https://www.thebiotek.com/product/inhibitors/bt-269569
Yuhao Chemical	JZ0501	http://www.chemyuhao.com/145781-92-6.html

PubMed

Title	Date	PubMed
Death due to liver failure during endocrine therapy for premenopausal breast cancer.	2010-08	20482225
A comparative study of the effect of raloxifene and gosereline on uterine leiomyoma volume changes and estrogen receptor, progesterone receptor, bcl-2 and p53 expression immunohistochemically in premenopausal women.	2007-11	16973256
Prostate specific antigen expression does not necessarily correlate with prostate cancer cell growth.	2006-07	16753443
Gonadotrophin-releasing hormone agonist treatment of aggression in Alzheimer's disease: a case report.	2005-06	16050439
A randomised factorial trial of sequential doxorubicin and CMF vs CMF and chemotherapy alone vs chemotherapy followed by goserelin plus tamoxifen as adjuvant treatment of node-positive breast cancer.	2005-02-14	15668708
Quality of life compared during pharmacological treatments and clinical monitoring for non-localized prostate cancer: a randomized controlled trial.	2004-05	15142146
Fatal acute tumor lysis syndrome, hepatic encephalopathy and flare phenomenon following combined androgen blockade.	2004-04	15017238
Cirrhosis with steatohepatitis following longterm stilboestrol treatment.	2003-08	12890826
Altered cognitive function in men treated for prostate cancer with luteinizing hormone-releasing hormone analogues and cyproterone acetate: a randomized controlled trial.	2002-09	12175403
Randomized trial of adjuvant tamoxifen and/or goserelin in premenopausal breast cancer--self-rated physiological effects and symptoms.	2000	11207003
Frequency of flutamide induced hepatotoxicity in patients with prostate carcinoma.	1999-03	10215102
[A case of fulminant hepatitis caused by antiandrogen, flutamide in a patient with prostate cancer].	1997-07	9267134
Anxiety and mood disorders associated with gonadotropin-releasing hormone agonist therapy.	1997	9230649
[Severe toxic hepatitis during flutamide (Eulexin) treatment].	1989-01-16	2911917

Patents

Sample Use Guides

In Vivo Use Guide

ZOLADEX (Goserelin), at a dose of 3.6 mg, should be administered subcutaneously every 28 days into the anterior abdominal wall below the navel line using an aseptic technique under the supervision of a physician

Route of Administration: Other

In Vitro Use Guide

Goserelin significantly inhibited LNCaP cell proliferation at doses between 10(-9)-10(-6) M.

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:15:14 GMT 2025` Edited by `admin` on `Mon Mar 31 18:15:14 GMT 2025`
Record UNII	6YUU2PV0U8
Record Status	`FAILED`
Record Version

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Name

Type

Language

FERTILAN

Preferred Name

English

GOSERELIN ACETATE

Common Name

English

Goserelin acetate [WHO-DD]

Common Name

English

GOSERELIN ACETATE [USP MONOGRAPH]

Common Name

English

GOSERELIN ACETATE [VANDF]

Common Name

English

GOSERELIN ACETATE [USP-RS]

Common Name

English

GOSERELIN ACETATE [JAN]

Common Name

English

GOSERELIN ACETATE [MART.]

Common Name

English

GOSERELIN ACETATE [ORANGE BOOK]

Common Name

English

ZOLADEX

Brand Name

English

1-9-LUTEINIZING HORMONE-RELEASING FACTOR (SWINE), 6-(O-(1,1-DIMETHYLETHYL)-D-SERINE)-, 2-(AMINOCARBONYL)HYDRAZIDE, ACETATE (SALT)

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C1910