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Buserelin Acetate

Known as: Acetate, Buserelin, BSRL Acetate, D-Ser (Bu(t))(6) Pro(9) NEt LHRH Acetate 
National Institutes of Health

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Broader (1)

Buserelin

Narrower (2)

HOE-766Suprefact

Papers overview

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2014
2014
Induction of ovulation with buserelin in jennies: in search of the minimum effective dose.
2008
2008
Delayed treatment with GnRH agonist, hCG and progesterone and reduced embryonic mortality in buffaloes.
1997
1997
Spectroscopic Characterization of the Inclusion Complex of a Luteinizing Hormone-Releasing Hormone Agonist, Buserelin Acetate, with Dimethyl-β-cyclodextriin
Inclusion complexation of buserelin acetate, an agonist of luteinizing hormone-releasing hormone, with dimethyl-β-cyclodextrin… 
1997
1997
Protection Afforded by Maltosyl-β-cyclodextrin Against α-Chymotrypsin-Catalyzed Hydrolysis of a Luteinizing Hormone-Releasing Hormone Agonist, Buserelin Acetate
AbstractPurpose. The present study addresses how maltosyl-β-cyclodextrin (G2-β-CyD) impacts upon the α-chymotrypsin-catalyzed… 
1995
1995
In Vivo CD3+CD25+ Lymphocyte Subpopulation Is Down‐regulated Without Increased Serum‐Soluble Interleukin‐2 Receptor (sIL‐2R) by Gonadotropin Releasing Hormone Agonist (GnRH‐a)
PROBLEM: To test further whether the suppression of the CD3+CD25+ lymphocyte sub‐population by gonadotropin‐releasing hormone… 
1994
1994
Use of follicle-stimulating hormone alone (urofollitropin) to stimulate the ovaries for assisted conception after pituitary desensitization.
1994
1994
Effect of gonadotropin-releasing hormone agonist on the bone mineral density of patients with endometriosis.
Highly Cited
1993
Highly Cited
1993
The long protocol of administration of gonadotropin‐releasing hormone agonist is superior to the short protocol for ovarian stimulation for in vitro fertilization
Highly Cited
1991
Highly Cited
1991
Correlation of endometrial histology, morphometry, and ultrasound appearance after different stimulation protocols for in vitro fertilization.
1989
1989
Sustained release of buserelin acetate, a luteinizing hormone‐releasing hormone agonist, from an injectable oily preparation utilizing ethylated β‐cyclodextrin
Abstract— The possible use of heptakis (2,6‐di‐O‐ethyl)‐β‐cyclodextrin (DE‐β‐CyD) as a parenteral sustained‐release carrier for… 
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