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Volumn 46, Issue 2, 2003, Pages 254-264

GnRH antagonists

Author keywords

[No Author keywords available]

Indexed keywords

ABARELIX; CETRORELIX; DANAZOL; GANIRELIX; GESTAGEN; GONADORELIN AGONIST; GONADORELIN ANTAGONIST; ITURELIX; ORAL CONTRACEPTIVE AGENT; PYRIDINE DERIVATIVE; QUINOLINE DERIVATIVE; RECOMBINANT FOLLITROPIN; TEVERELIX; TRIPTORELIN;

EID: 0038826226     PISSN: 00099201     EISSN: None     Source Type: Journal    
DOI: 10.1097/00003081-200306000-00007     Document Type: Review
Times cited : (6)

References (50)
  • 1
    • 0035225737 scopus 로고    scopus 로고
    • Gonadotrophin-releasing hormone antagonists for assisted conception
    • Al-Inany H, Aboulghar M. Gonadotrophin-releasing hormone antagonists for assisted conception. Cochrane Database Syst Rev. 2001;4.
    • (2001) Cochrane Database Syst Rev , pp. 4
    • Al-Inany, H.1    Aboulghar, M.2
  • 2
    • 0015229042 scopus 로고
    • Structure of the porcine LH and FSH releasing hormone. II. Confirmation of the proposed structure by conventional sequential analysis
    • Baba Y, et al. Structure of the porcine LH and FSH releasing hormone. II. Confirmation of the proposed structure by conventional sequential analysis. Biochem Biophys Res Commun. 1971;44:459-463.
    • (1971) Biochem Biophys Res Commun , vol.44 , pp. 459-463
    • Baba, Y.1
  • 3
    • 0018775596 scopus 로고
    • Inhibitory effects of long-term treatment with a LHRH agonist on the pituitary-gonadal axis in male and female rats
    • Cusan L, et al. Inhibitory effects of long-term treatment with a LHRH agonist on the pituitary-gonadal axis in male and female rats. Endocrinology. 1979;104:1369-1376.
    • (1979) Endocrinology , vol.104 , pp. 1369-1376
    • Cusan, L.1
  • 4
    • 0023485735 scopus 로고
    • Comparison of the mechanisms of action of LHRH analogs and steroids in the treatment of endometriosis
    • Bouchard P, Garcia E. Comparison of the mechanisms of action of LHRH analogs and steroids in the treatment of endometriosis. Contrib Gynecol Obstet. 1987;16:260-265.
    • (1987) Contrib Gynecol Obstet , vol.16 , pp. 260-265
    • Bouchard, P.1    Garcia, E.2
  • 5
    • 0023933472 scopus 로고
    • Inhibition of ovulation: Comparison between the mechanism of action of steroids and GnRH analogues
    • Bouchard P, Wolf JP, Hajri S. Inhibition of ovulation: comparison between the mechanism of action of steroids and GnRH analogues. Hum Reprod. 1988;3:503-506.
    • (1988) Hum Reprod , vol.3 , pp. 503-506
    • Bouchard, P.1    Wolf, J.P.2    Hajri, S.3
  • 6
    • 0022665939 scopus 로고
    • Gonadotropin-releasing hormone analog design. Structure-function studies toward the development of agonists and antagonists: Rationale and perspective
    • Karten MJ, Rivier JE. Gonadotropin-releasing hormone analog design. Structure-function studies toward the development of agonists and antagonists: rationale and perspective. Endocr Rev. 1986;7:44-66.
    • (1986) Endocr Rev , vol.7 , pp. 44-66
    • Karten, M.J.1    Rivier, J.E.2
  • 7
    • 0026671797 scopus 로고
    • Evolving role of GnRH antagonists
    • Gordon K, et al. Evolving role of GnRH antagonists. Trends in Endocrinol Metab. 1992;3:259-263.
    • (1992) Trends in Endocrinol Metab , vol.3 , pp. 259-263
    • Gordon, K.1
  • 9
    • 0024211812 scopus 로고
    • Antagonists of luteinizing hormone releasing hormone bind to rat mast cells and induce histamine release
    • Sundaram K, Didolkar A, Thau R, et al. Antagonists of luteinizing hormone releasing hormone bind to rat mast cells and induce histamine release. Agents Actions. 1988;25:307-313.
    • (1988) Agents Actions , vol.25 , pp. 307-313
    • Sundaram, K.1    Didolkar, A.2    Thau, R.3
  • 13
    • 0035430430 scopus 로고    scopus 로고
    • Applications for GnRH antagonists
    • Blithe DL. Applications for GnRH antagonists. Trends Endocrinol Metab. 2001;12:238-240.
    • (2001) Trends Endocrinol Metab , vol.12 , pp. 238-240
    • Blithe, D.L.1
  • 14
    • 0026343588 scopus 로고
    • The gonadotropin-releasing hormone antagonist (Nal-Glu) acutely blocks the luteinizing hormone surge but allows for resumption of folliculogenesis in normal women
    • Ditkoff EC, Cassidenti DL, Paulson RJ, et al. The gonadotropin-releasing hormone antagonist (Nal-Glu) acutely blocks the luteinizing hormone surge but allows for resumption of folliculogenesis in normal women. Am J Obstet Gynecol. 1991;165:1811-1817.
    • (1991) Am J Obstet Gynecol , vol.165 , pp. 1811-1817
    • Ditkoff, E.C.1    Cassidenti, D.L.2    Paulson, R.J.3
  • 15
    • 0028068645 scopus 로고
    • A single injection of a gonadotropin-releasing hormone (GnRH) antagonist (Cetrorelix) postpones the luteinizing hormone (LH) surge: Further evidence for the role of GnRH during the LH surge
    • Leroy I, d'Acremont M, Brailly-Tabard S, et al. A single injection of a gonadotropin-releasing hormone (GnRH) antagonist (Cetrorelix) postpones the luteinizing hormone (LH) surge: further evidence for the role of GnRH during the LH surge. Fertil Steril. 1994;62:461-467.
    • (1994) Fertil Steril , vol.62 , pp. 461-467
    • Leroy, I.1    D'Acremont, M.2    Brailly-Tabard, S.3
  • 16
    • 0034124210 scopus 로고    scopus 로고
    • Effect of gonadotrophin-releasing hormone (GnRH) antagonist during the LH surge in normal women and during controlled ovarian hyperstimulation
    • Christin-Maitre S, Olivennes F, Dubourdieu S, et al. Effect of gonadotrophin-releasing hormone (GnRH) antagonist during the LH surge in normal women and during controlled ovarian hyperstimulation. Clin Endocrinol (Oxf). 2000;52:721-726.
    • (2000) Clin Endocrinol (Oxf) , vol.52 , pp. 721-726
    • Christin-Maitre, S.1    Olivennes, F.2    Dubourdieu, S.3
  • 17
    • 84995853542 scopus 로고
    • Effect of administration of a gonadotropin-releasing hormone (GnRH) antagonist (Nal-Glu) during the periovulatory period: The luteinizing hormone surge requires secretion of GnRH
    • Dubourdieu S, Charbonnel B, D'Acremont MF, et al. Effect of administration of a gonadotropin-releasing hormone (GnRH) antagonist (Nal-Glu) during the periovulatory period: the luteinizing hormone surge requires secretion of GnRH. J Clin Endocrinol Metab. 1994;78:343-347.
    • (1994) J Clin Endocrinol Metab , vol.78 , pp. 343-347
    • Dubourdieu, S.1    Charbonnel, B.2    D'Acremont, M.F.3
  • 18
    • 0025340121 scopus 로고
    • Changes in gonadotropin and alpha-subunit secretion after a single administration of gonadotropin-releasing hormone antagonist in adult males
    • Lahlou N, Delivet S, Bardin CW, et al. Changes in gonadotropin and alpha-subunit secretion after a single administration of gonadotropin-releasing hormone antagonist in adult males. Fertil Steril. 1990;53:898-905.
    • (1990) Fertil Steril , vol.53 , pp. 898-905
    • Lahlou, N.1    Delivet, S.2    Bardin, C.W.3
  • 19
    • 0034975340 scopus 로고    scopus 로고
    • Comment on the debate article: Embryo implantation: The Rubicon for GnRH antagonists
    • Diedrich K, Frydman R, Devroey P, et al. Comment on the debate article: embryo implantation: the Rubicon for GnRH antagonists. Hum Reprod. 2001;16:1305-1306.
    • (2001) Hum Reprod , vol.16 , pp. 1305-1306
    • Diedrich, K.1    Frydman, R.2    Devroey, P.3
  • 20
    • 0034756166 scopus 로고    scopus 로고
    • The role of gonadotropin-releasing hormone antagonists in in vitro fertilization
    • Diedrich K, Ludwig M, Felberbaum RE. The role of gonadotropin-releasing hormone antagonists in in vitro fertilization. Semin Reprod Med. 2001;19:213-220.
    • (2001) Semin Reprod Med , vol.19 , pp. 213-220
    • Diedrich, K.1    Ludwig, M.2    Felberbaum, R.E.3
  • 21
    • 0026715032 scopus 로고
    • Spontaneous luteinizing hormone surges can be reliably prevented by the timely administration of a gonadotrophin releasing hormone antagonist (Nal-Glu) during the late follicular phase
    • Frydman R, Cornel C, de Ziegler D, et al. Spontaneous luteinizing hormone surges can be reliably prevented by the timely administration of a gonadotrophin releasing hormone antagonist (Nal-Glu) during the late follicular phase. Hum Reprod. 1992;7:930-933.
    • (1992) Hum Reprod , vol.7 , pp. 930-933
    • Frydman, R.1    Cornel, C.2    De Ziegler, D.3
  • 22
    • 0033971301 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone antagonist: New tools versus old habits
    • Bouchard P, Fauser BC. Gonadotropin-releasing hormone antagonist: new tools versus old habits. Fertil Steril. 2000;73:18-20.
    • (2000) Fertil Steril , vol.73 , pp. 18-20
    • Bouchard, P.1    Fauser, B.C.2
  • 23
    • 0033954654 scopus 로고    scopus 로고
    • Prospective, randomized, controlled study of in vitro fertilization/embryo transfer with a single dose of a luteinizing hormone-releasing hormone (LH-RH) antagonist (cetrorelix) or a depot formula of an LH-RH agonist (triptorelin)
    • Olivennes F, Belaisch-Allart J, Emperaire JC, et al. Prospective, randomized, controlled study of in vitro fertilization/embryo transfer with a single dose of a luteinizing hormone-releasing hormone (LH-RH) antagonist (cetrorelix) or a depot formula of an LH-RH agonist (triptorelin). Fertil Steril. 2000;73:314-320.
    • (2000) Fertil Steril , vol.73 , pp. 314-320
    • Olivennes, F.1    Belaisch-Allart, J.2    Emperaire, J.C.3
  • 25
    • 0029027250 scopus 로고
    • Scheduled administration of a gonadotrophin-releasing hormone antagonist (Cetrorelix) on day 8 of in-vitro fertilization cycles: A pilot study
    • Olivennes F, Fanchin R, Bouchard P, et al. Scheduled administration of a gonadotrophin-releasing hormone antagonist (Cetrorelix) on day 8 of in-vitro fertilization cycles: a pilot study. Hum Reprod. 1995;10:1382-1386.
    • (1995) Hum Reprod , vol.10 , pp. 1382-1386
    • Olivennes, F.1    Fanchin, R.2    Bouchard, P.3
  • 26
    • 0031661436 scopus 로고    scopus 로고
    • The use of a GnRH antagonist (Cetrorelix) in a single dose protocol in IVF-embryo transfer: A dose-finding study of 3 versus 2 mg
    • Olivennes F, Alvarez S, Bouchard P, et al. The use of a GnRH antagonist (Cetrorelix) in a single dose protocol in IVF-embryo transfer: a dose-finding study of 3 versus 2 mg. Hum Reprod. 1998;13:2411-2414.
    • (1998) Hum Reprod , vol.13 , pp. 2411-2414
    • Olivennes, F.1    Alvarez, S.2    Bouchard, P.3
  • 27
    • 0034053260 scopus 로고    scopus 로고
    • Ovarian stimulation with HMG: A prospective randomized phase III European study comparing the luteinizing hormone releasing hormone (LHRH) antagonist cetrorelix and the LHRH-agonist buserelin
    • Albano C, Felberbaum R, Smitz J. Ovarian stimulation with HMG: a prospective randomized phase III European study comparing the luteinizing hormone releasing hormone (LHRH) antagonist cetrorelix and the LHRH-agonist buserelin. Hum Reprod. 2000;15:526-531.
    • (2000) Hum Reprod , vol.15 , pp. 526-531
    • Albano, C.1    Felberbaum, R.2    Smitz, J.3
  • 28
    • 0033807688 scopus 로고    scopus 로고
    • Treatment with gonadotropin releasing hormone antagonist cetrorelix in women undergoing ovarian stimulation with recombinant follicle stimulating hormone is effective, safe and convenient: Results of a controlled randomized, multicenter trial
    • The European Orgalutran Study Group. Treatment with gonadotropin releasing hormone antagonist cetrorelix in women undergoing ovarian stimulation with recombinant follicle stimulating hormone is effective, safe and convenient: results of a controlled randomized, multicenter trial. Hum Reprod. 2000;15:1490-1498.
    • (2000) Hum Reprod , vol.15 , pp. 1490-1498
  • 29
    • 0035161913 scopus 로고    scopus 로고
    • Efficacy and safety of ganirelix acetate vs. leuprolide acetate in women undergoing controlled ovarian hyperstimulation
    • The North American Ganirelix Study Group. Efficacy and safety of ganirelix acetate vs. leuprolide acetate in women undergoing controlled ovarian hyperstimulation. Fertil Steril. 2001;75:38-45.
    • (2001) Fertil Steril , vol.75 , pp. 38-45
  • 30
    • 0035070776 scopus 로고    scopus 로고
    • Comparable clinical outcome using the GnRH antagonist ganirelix or a long protocol of the GnRH agonist triptorelin for the prevention of premature LH surges in women undergoing ovarian stimulation
    • European And Middle East Orgalutran Study Group. Comparable clinical outcome using the GnRH antagonist ganirelix or a long protocol of the GnRH agonist triptorelin for the prevention of premature LH surges in women undergoing ovarian stimulation. Hum Reprod. 2001;16:644-651.
    • (2001) Hum Reprod , vol.16 , pp. 644-651
  • 31
    • 0036104055 scopus 로고    scopus 로고
    • GnRH antagonist in assisted reproduction: A Cochrane review
    • Al-Inany H, Aboulghar M. GnRH antagonist in assisted reproduction: a Cochrane review. Hum Reprod. 2002;17:874-885.
    • (2002) Hum Reprod , vol.17 , pp. 874-885
    • Al-Inany, H.1    Aboulghar, M.2
  • 32
    • 0033994130 scopus 로고    scopus 로고
    • A pilot study involving minimal ovarian stimulation for in vitro fertilization: Extending the follicle-stimulating hormone window combined with the gonadotropin-releasing hormone antagonist cetrorelix
    • de Jong D, Macklon NS, Fauser BC. A pilot study involving minimal ovarian stimulation for in vitro fertilization: extending the follicle-stimulating hormone window combined with the gonadotropin-releasing hormone antagonist cetrorelix. Fertil Steril. 2000;73:1051-1054.
    • (2000) Fertil Steril , vol.73 , pp. 1051-1054
    • De Jong, D.1    Macklon, N.S.2    Fauser, B.C.3
  • 33
    • 0037244594 scopus 로고    scopus 로고
    • A randomized comparison of two ovarian stimulation protocols with gonadotropin-releasing hormone (GnRH) antagonist co-treatment for in vitro fertilization commencing recombinant follicle-stimulating hormone on cycle day 2 or 5 with the standard long GnRH agonist protocol
    • Hohmann FP, Macklon NS, Fauser BC. A randomized comparison of two ovarian stimulation protocols with gonadotropin-releasing hormone (GnRH) antagonist co-treatment for in vitro fertilization commencing recombinant follicle-stimulating hormone on cycle day 2 or 5 with the standard long GnRH agonist protocol. J Clin Endocrinol Metab. 2003;88:166-173.
    • (2003) J Clin Endocrinol Metab , vol.88 , pp. 166-173
    • Hohmann, F.P.1    Macklon, N.S.2    Fauser, B.C.3
  • 34
    • 0342302492 scopus 로고    scopus 로고
    • Revival of the natural cycles in invitro fertilization with the use of a new gonadotrophin-releasing hormone antagonist (Cetrorelix): A pilot study with minimal stimulation
    • Rongieres-Bertrand C, Olivennes F, Righini C, et al. Revival of the natural cycles in invitro fertilization with the use of a new gonadotrophin-releasing hormone antagonist (Cetrorelix): a pilot study with minimal stimulation. Hum Reprod. 1999;14:683-688.
    • (1999) Hum Reprod , vol.14 , pp. 683-688
    • Rongieres-Bertrand, C.1    Olivennes, F.2    Righini, C.3
  • 35
    • 0029954772 scopus 로고    scopus 로고
    • Triggering of ovulation by a gonadotropin-releasing hormone (GnRH) agonist in patients pretreated with a GnRH antagonist
    • Olivennes F, Fanchin R, Bouchard P, et al. Triggering of ovulation by a gonadotropin-releasing hormone (GnRH) agonist in patients pretreated with a GnRH antagonist. Fertil Steril. 1996;66:151-153.
    • (1996) Fertil Steril , vol.66 , pp. 151-153
    • Olivennes, F.1    Fanchin, R.2    Bouchard, P.3
  • 36
    • 0029810408 scopus 로고    scopus 로고
    • Comparison of gonadotrophin-releasing hormone analogues and human chorionic gonadotrophin for the induction of ovulation and prevention of ovarian hyperstimulation syndrome: A case-control study
    • Lewit N, Kol S, Manor D, Itskovitz-Eldor J. Comparison of gonadotrophin-releasing hormone analogues and human chorionic gonadotrophin for the induction of ovulation and prevention of ovarian hyperstimulation syndrome: a case-control study. Hum Reprod. 1996;11:1399-1402.
    • (1996) Hum Reprod , vol.11 , pp. 1399-1402
    • Lewit, N.1    Kol, S.2    Manor, D.3    Itskovitz-Eldor, J.4
  • 37
    • 19044367534 scopus 로고    scopus 로고
    • Comparison of the nonsupplemented luteal phase characteristics after recombinant (r)hCG, rLH on GnRH agonist for oocyte maturation in IVF
    • Beckers NGM. Comparison of the nonsupplemented luteal phase characteristics after recombinant (r)hCG, rLH on GnRH agonist for oocyte maturation in IVF. Hum Reprod. 2002:157.
    • (2002) Hum Reprod , pp. 157
    • Beckers, N.G.M.1
  • 38
    • 0036286393 scopus 로고    scopus 로고
    • Impact of ovarian stimulation on corpus luteum function and embryonic implantation
    • Tavaniotou A, Albano C, Smitz J, Devroey P. Impact of ovarian stimulation on corpus luteum function and embryonic implantation. J Reprod Immunol. 2002;55:123-130.
    • (2002) J Reprod Immunol , vol.55 , pp. 123-130
    • Tavaniotou, A.1    Albano, C.2    Smitz, J.3    Devroey, P.4
  • 39
    • 0036634088 scopus 로고    scopus 로고
    • Use of GnRH antagonists in the treatment of endometriosis
    • Kupker W, Felberbaum R, Krapp M, et al. Use of GnRH antagonists in the treatment of endometriosis. Reprod Biomed Online. 2002;5:12-16.
    • (2002) Reprod Biomed Online , vol.5 , pp. 12-16
    • Kupker, W.1    Felberbaum, R.2    Krapp, M.3
  • 40
    • 0038651804 scopus 로고    scopus 로고
    • Will GnRH antagonists assist in the treatment of benign gynaecological diseases?
    • Felberbaum R, Kupker W, Diedrich K. Will GnRH antagonists assist in the treatment of benign gynaecological diseases? Reprod Biomed Online. 2002;5:68-72.
    • (2002) Reprod Biomed Online , vol.5 , pp. 68-72
    • Felberbaum, R.1    Kupker, W.2    Diedrich, K.3
  • 41
    • 0025999887 scopus 로고
    • Suppression of the pituitary-gonadal axis in children with central precocious puberty: Effects on growth, growth hormone, insulin-like growth factor-I, and prolactin secretion
    • Sklar CA RS, Blumberg D, Oberfield SE, et al. Suppression of the pituitary-gonadal axis in children with central precocious puberty: effects on growth, growth hormone, insulin-like growth factor-I, and prolactin secretion. J Clin Endocrinol Metab. 1991;73:734-738.
    • (1991) J Clin Endocrinol Metab , vol.73 , pp. 734-738
    • Sklar, C.A.R.S.1    Blumberg, D.2    Oberfield, S.E.3
  • 42
    • 0034501385 scopus 로고    scopus 로고
    • Hormonal contraception in the male
    • Anderson RA. Hormonal contraception in the male. Br Med Bull. 2000;56:717-728.
    • (2000) Br Med Bull , vol.56 , pp. 717-728
    • Anderson, R.A.1
  • 43
    • 0035657262 scopus 로고    scopus 로고
    • Suppression of spermatogenesis to azoospermia by combined administration of GnRH antagonist and 19-nortestosterone cannot be maintained by this non-aromatizable androgen alone
    • Behre HM, Kliesch S, Lemcke B, et al. Suppression of spermatogenesis to azoospermia by combined administration of GnRH antagonist and 19-nortestosterone cannot be maintained by this non-aromatizable androgen alone. Hum Reprod. 2001;16:2570-2577.
    • (2001) Hum Reprod , vol.16 , pp. 2570-2577
    • Behre, H.M.1    Kliesch, S.2    Lemcke, B.3
  • 44
    • 0036843858 scopus 로고    scopus 로고
    • Effect of ovarian stimulation with recombinant follicle-stimulating hormone, gonadotropin releasing hormone antagonists, and human chorionic gonadotropin on endometrial maturation on the day of oocyte pickup
    • Kolibianakis E, Bourgain C, Albano C, et al. Effect of ovarian stimulation with recombinant follicle-stimulating hormone, gonadotropin releasing hormone antagonists, and human chorionic gonadotropin on endometrial maturation on the day of oocyte pickup. Fertil Steril. 2002;78:1025-1029.
    • (2002) Fertil Steril , vol.78 , pp. 1025-1029
    • Kolibianakis, E.1    Bourgain, C.2    Albano, C.3
  • 45
    • 0034268038 scopus 로고    scopus 로고
    • Embryo implantation and GnRH antagonists: GnRH antagonists in ART: Lower embryo implantation?
    • Kol S. Embryo implantation and GnRH antagonists: GnRH antagonists in ART: lower embryo implantation? Hum Reprod. 2000;15:1881-1882.
    • (2000) Hum Reprod , vol.15 , pp. 1881-1882
    • Kol, S.1
  • 46
    • 0035164682 scopus 로고    scopus 로고
    • Health of 227 children born after controlled ovarian stimulation for in vitro fertilization using the luteinizing hormone-releasing hormone antagonist cetrorelix
    • Ludwig M, Riethmuller-Winzen H, Felberbaum RE, et al. Health of 227 children born after controlled ovarian stimulation for in vitro fertilization using the luteinizing hormone-releasing hormone antagonist cetrorelix. Fertil Steril. 2001;75:18-22.
    • (2001) Fertil Steril , vol.75 , pp. 18-22
    • Ludwig, M.1    Riethmuller-Winzen, H.2    Felberbaum, R.E.3
  • 47
    • 0034883163 scopus 로고    scopus 로고
    • Perinatal outcome of pregnancy after GnRH antagonist (ganirelix) treatment during ovarian stimulation for conventional IVF or ICSI: A preliminary report
    • Olivennes F, Mannaerts B, Struijs M, et al. Perinatal outcome of pregnancy after GnRH antagonist (ganirelix) treatment during ovarian stimulation for conventional IVF or ICSI: a preliminary report. Hum Reprod. 2001;16:1588-1591.
    • (2001) Hum Reprod , vol.16 , pp. 1588-1591
    • Olivennes, F.1    Mannaerts, B.2    Struijs, M.3
  • 48
    • 0034618152 scopus 로고    scopus 로고
    • Quinolones as gonadotropin releasing hormone (GnRH) antagonists: Simultaneous optimization of the C(3)-aryl and C(6)-substituents
    • Young JR, Huang SX, Chen I, et al. Quinolones as gonadotropin releasing hormone (GnRH) antagonists: simultaneous optimization of the C(3)-aryl and C(6)-substituents. Bioorg Med Chem Lett. 2000;10:1723-1727.
    • (2000) Bioorg Med Chem Lett , vol.10 , pp. 1723-1727
    • Young, J.R.1    Huang, S.X.2    Chen, I.3
  • 49
    • 0036316840 scopus 로고    scopus 로고
    • Acyline: The first study in humans of a potent, new gonadotropin-releasing hormone antagonist
    • Herbst KL, Anawalt BD, Amory JK, Bremner WJ. Acyline: the first study in humans of a potent, new gonadotropin-releasing hormone antagonist. J Clin Endocrinol Metab. 2002;87:3215-3220.
    • (2002) J Clin Endocrinol Metab , vol.87 , pp. 3215-3220
    • Herbst, K.L.1    Anawalt, B.D.2    Amory, J.K.3    Bremner, W.J.4
  • 50
    • 0037413559 scopus 로고    scopus 로고
    • Discovery of a thieno[2,3-d]pyrimidine-2,4-dione bearing a p-methoxyureidophenyl moiety at the 6-position: A highly potent and orally bioavailable non-peptide antagonist for the human luteinizing hormone-releasing hormone receptor
    • Sasaki S, Cho N, Nara Y, et al. Discovery of a thieno[2,3-d]pyrimidine-2,4-dione bearing a p-methoxyureidophenyl moiety at the 6-position: a highly potent and orally bioavailable non-peptide antagonist for the human luteinizing hormone-releasing hormone receptor. J Med Chem. 2003;46:113-124.
    • (2003) J Med Chem , vol.46 , pp. 113-124
    • Sasaki, S.1    Cho, N.2    Nara, Y.3


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