GLPBio

GnRH

GnRH (gonadotropin-releasing hormone) is a neuhormone that stimulates the secretion of LH (luteinizing hormone) and FSH (follicle-stimulating hormone). GnRH mutation is linked to hypogonadotropic hypogonadism.

Products Related to GnRH(28)

  • GA20156 structure
    GA20156(D-Ser(tBu)⁶,Azagly¹⁰)-LHRH (free base)
    CAS: 65807-02-5
    Purity: >98%
  • GC10076 structure
    GC10076Leuprolide Acetate
    CAS: 74381-53-6
    Purity: >98%

    A synthetic GnRH receptor agonist

  • GC12374 structure
    GC12374Alarelin Acetate
    CAS: 79561-22-1
    Purity: >98.00%

    Alarelin Acetate is a synthetic gonadotropin-releasing hormone (GnRH) agonist.

  • GC19135 structure
    GC19135Elagolix
    CAS: 834153-87-6
    Purity: >98.00%

    Elagolix is a highly potent, selective, orally-active, short-duration, non-peptide antagonist of the gonadotropin-releasing hormone receptor (GnRHR) (KD = 54 pM).

  • GC19136 structure
    GC19136Elagolix sodium
    CAS: 832720-36-2
    Purity: >98.00%

    Elagolix sodium is a highly potent, selective, orally-active, short-duration, non-peptide antagonist of the gonadotropin-releasing hormone receptor (GnRHR) (IC 50 =0.94nM).

  • GC32029 structure
    GC32029opigolix
    CAS: 912587-25-8
    Purity: >98%

    Opigolix is a Gonadotropin-releasing hormone (GnRH) receptor antagonist, used for the research of endometriosis and rheumatoid arthritis.

  • GC32843 structure
    GC32843Abarelix (R3827)
    CAS: 183552-38-7
    Purity: >98%

    Abarelix (R3827) (R3827; PPI 149) is a potent gonadotrophin-releasing hormone (GnRH) antagonist, used for prostate cancer treatment.

  • GC32934 structure
    GC32934Relugolix (TAK-385)
    CAS: 737789-87-6
    Purity: >99.50%

    Relugolix (TAK-385) (TAK-385)is a potent, orally active, nonpeptidic gonadotropin-releasing hormone (GnRH) antagonist.

  • GC33034 structure
    GC33034Lecirelin
    CAS: 61012-19-9
    Purity: >99.50%

    Lecirelin, a synthetic gonadotropin-releasing hormone (GnRH) analogue, acts as a GnRH agonist.

  • GC33467 structure
    GC33467Cetrorelix Acetate (SB-075 acetate)
    CAS: 145672-81-7
    Purity: >99.00%

    Cetrorelix Acetate (SB-075 acetate) (SB-75 acetate) is a potent gonadotropin-releasing hormone (GnRH) receptor antagonist with an IC50 of 1.21 nM.

  • GC34001 structure
    GC34001Gonadorelin acetate
    CAS: 34973-08-5
    Purity: >98.00%

    Gonadorelin acetate is a synthetic decapeptide analog of gonadotropin-releasing hormone (GnRH) and acts as a specific agonist for the GnRH receptor.

  • GC34099 structure
    GC34099Buserelin Acetate
    CAS: 68630-75-1
    Purity: >98%
  • GC35217 structure
    GC35217Abarelix Acetate
    CAS: 785804-17-3
    Purity: >99.50%

    Abarelix Acetate (PPI 149 Acetate; R 3827 Acetate) is a potent gonadotrophin-releasing hormone (GnRH) antagonist, used for prostate cancer research.

  • GC35828 structure
    GC35828Degarelix
    CAS: 214766-78-6
    Purity: >98.00%

    Degarelix is a synthetic peptide gonadotropin-releasing hormone (GnRH; IC 50 =3nM) receptor antagonist. Degarelix reversibly binds to pituitary GnRH receptors, thereby inhibiting the release of gonadotropins.

  • GC36180 structure
    GC36180Goserelin acetate
    CAS: 145781-92-6
    Purity: >99.00%

    A synthetic GNRH agonist

  • GC45778 structure
    GC45778Abarelix (acetate)
    CAS: 785804-17-3
    Purity: >99.50%

    A synthetic GnRHR antagonist

  • GC62644 structure
    GC62644GnRH antagonist 2
    CAS: 1709823-61-9
    Purity: >98.00%

    GnRH antagonist 2 (formula I) is a GnRH receptor antagonist that can be used for endometriosis research.

  • GC63884 structure
    GC63884Linzagolix
    CAS: 935283-04-8
    Purity: >99.00%

    Linzagolix (KLH-2109; OBE-2109) is a potent, non-peptide, and orally active GnRH antagonist.

  • GC69334 structure
    GC69334Kisspeptin-54(human) TFA
    Purity: >99.00%

    Kisspeptin-54 (human) TFA (Metastin (human) TFA) is an endogenous ligand for the Kisspeptin receptor (KISS1, GPR54), which binds with high affinity to rat and human GPR54 receptors with Ki values of 1.81 nM and 1.45 nM, respectively. Kisspeptin-54 (human) TFA can inhibit tumor metastasis and stimulate gonadotropin secretion.

  • GC69883 structure
    GC69883sGnRH-A acetate
    Purity: >99.00%

    sGnRH-A acetate is a salmon gonadotropin-releasing hormone (GnRH) analog. It can stimulate growth hormone secretion and can also be used as an artificial insemination ovulation inducer.

  • GC71463 structure
    GC71463Acyline TFA
    Purity: >99.00%

    Acyline TFA, a GnRH peptide analogue, is a GnRH antagonist that inhibits gonadotropin and testosterone (T) levels.

  • GC72225 structure
    GC72225Fsh receptor-binding inhibitor fragment(bi-10)
    CAS: 163973-98-6
    Purity: >99.00%

    FSH receptor-binding inhibitor fragment(bi-10) is a potent FSH antagonist.

  • GC72293 structure
    GC72293Phoenixin-14
    CAS: 1415039-79-0
    Purity: >99.00%

    Phoenixin-14 (PNX-14) is one of the endogenous active isoform, and generates anxiolytic effect via the activation of the AHA GnRH system in mice.

  • GC74323 structure
    GC74323Zebrafish Kisspeptin-1
    CAS: 1071873-79-4
    Purity: >96.00%

    Zebrafish Kisspeptin-1 is the core sequence of the neuropeptide kisspeptin-1, which participate in the regulation of gonadotropin-releasing hormone (GnRH) release, and regulates the reproductive system.