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Endocrinology and Hormones

Endocrinology and Hormones

Endocrinology and Hormones

The endocrine system is an information signaling system that coordinates most bodily functions. It senses environmental changes and secretes corresponding hormones to coordinate metabolism, maintain homeostasis, and regulate growth and development.read more

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Products for  Endocrinology and Hormones

  1. Cat.No. Product Name Information
  2. GC13971 Cyproterone Acetate Androgen receptor antagonist Cyproterone Acetate  Chemical Structure
  3. GC17677 DADLE δ-opioid receptor agonist DADLE  Chemical Structure
  4. GC47168 Daidzein-d4 An internal standard for the quantification of daidzein Daidzein-d4  Chemical Structure
  5. GC10803 DAMGO μ opioid receptor agonist DAMGO  Chemical Structure
  6. GC35805 DAMGO (TFA) DAMGO (TFA) is a μ-opioid receptor (μ-OPR ) selective agonist with a Kd of 3.46 nM for native μ-OPR. DAMGO (TFA)  Chemical Structure
  7. GC10785 Danazol A derivative of testosterone and ethisterone Danazol  Chemical Structure
  8. GC35828 Degarelix Degarelix is a competitive and reversible gonadotropin-releasing hormone receptor (GnRHR/LHRHR) antagonist. Degarelix  Chemical Structure
  9. GC18556 Degarelix (acetate) Degarelix is a synthetic gonadotropin-releasing hormone receptor (GNRHR) antagonist (IC50 = 3 nM in HEK293 cells expressing the human receptor). Degarelix (acetate)  Chemical Structure
  10. GC11070 Dehydroepiandrosterone (DHEA) Dehydroepiandrosterone (DHEA) and its sulfate ester, DHEAS, together represent the most abundant steroid hormones in the human body . Dehydroepiandrosterone (DHEA)  Chemical Structure
  11. GC34005 Dehydroisoandrosterone 3-acetate (Dehydroepiandrosterone 3-acetate) Dehydroepiandrosterone 3-acetate is a testosterone/estrogen precursor and known modulator of vertebrate aggression. Dehydroisoandrosterone 3-acetate (Dehydroepiandrosterone 3-acetate)  Chemical Structure
  12. GC61954 Deltorphin 2 TFA Deltorphin 2 TFA is a selective peptide agonist for the δ opioid receptor. Deltorphin 2 TFA  Chemical Structure
  13. GC12143 Deltorphin I δ-opioid receptor agonist Deltorphin I  Chemical Structure
  14. GC31168 Dermorphin

    Dermorphin is a natural heptapeptide μ-opioid receptor (MOR) agonist found in amphibian skin.

    Dermorphin  Chemical Structure
  15. GC34223 Dermorphin Analog Dermorphin Analog is an analog of Dermorphin. Dermorphin Analog  Chemical Structure
  16. GC49143 Deslorelin (acetate) A peptide agonist of GnRH Deslorelin (acetate)  Chemical Structure
  17. GC49459 Desmopressin (trifluoroacetate salt) A vasopressin receptor agonist Desmopressin (trifluoroacetate salt)  Chemical Structure
  18. GC49025 Desogestrel-13C2-d2 An internal standard for the quantification of desogestrel Desogestrel-13C2-d2  Chemical Structure
  19. GC17688 Diarylpropionitrile(DPN) Diarylpropionitrile(DPN) (Diarylpropionitrile) is a non-steroidal estrogen receptor β (ERβ) selective ligand, with an EC50 of 0.85 nM. Diarylpropionitrile(DPN)  Chemical Structure
  20. GP10126 Diazepam-Binding Inhibitor Fragment, human Diazepam-Binding Inhibitor (DBI) Fragment is encoded by the DBI gene in human. Diazepam-Binding Inhibitor Fragment, human  Chemical Structure
  21. GC15578 Dienogest Orally active synthetic progesterone Dienogest  Chemical Structure
  22. GC47215 Dienogest-d8 An internal standard for the quantification of dienogest Dienogest-d8  Chemical Structure
  23. GC40867 Diflorasone Diacetate Diflorasone is a corticosteroid with anti-inflammatory activity. Diflorasone Diacetate  Chemical Structure
  24. GC10663 Dihydrodaidzein estrogen receptor agonist Dihydrodaidzein  Chemical Structure
  25. GC47231 Dimethomorph A morpholine fungicide Dimethomorph  Chemical Structure
  26. GC17553 DIPPA hydrochloride κ receptor antagonist DIPPA hydrochloride  Chemical Structure
  27. GC31441 DJ-V-159 DJ-V-159 is an agonist for G protein-coupled receptor family C group 6 member A (GPRC6A). DJ-V-159  Chemical Structure
  28. GC50178 DPC AJ1951 Potent parathyroid hormone (PTH) receptor agonist DPC AJ1951  Chemical Structure
  29. GC43567 DPC-AJ1951 (trifluoroacetate salt) DPC-AJ1951 is a peptide agonist of the parathyroid hormone (PTH)/PTH-related peptide receptor (PPR; EC50 = 0.15 nM in HEK293 cells expressing human PPR). DPC-AJ1951 (trifluoroacetate salt)  Chemical Structure
  30. GC10333 DPDPE Prototypical selective δ-opioid receptor agonist peptide DPDPE  Chemical Structure
  31. GC63431 DPDPE TFA DPDPE TFA, an opioid peptide, is a selective δ-opioid receptor?(DOR) agonist?with anticonvulsant effects. DPDPE TFA  Chemical Structure
  32. GC12379 Drospirenone Synthetic progestin Drospirenone  Chemical Structure
  33. GC52420 Drospirenone-13C3 An internal standard for the quantification of drospirenone Drospirenone-13C3  Chemical Structure
  34. GC64301 DS08210767 DS08210767 is a highly potent, orally bioavailable PTHR1 antagonist with IC50 of 90 nM. DS08210767  Chemical Structure
  35. GC14774 DSLET δ Opioid receptor agonist DSLET  Chemical Structure
  36. GC10893 Dutasteride 5-alpha-reductase inhibitor Dutasteride  Chemical Structure
  37. GC13546 Dynorphin A Endogenous kappa receptor agonist Dynorphin A  Chemical Structure
  38. GC35917 Dynorphin A (1-10) TFA Dynorphin A (1-10) TFA  Chemical Structure
  39. GA21407 Dynorphin A (1-8) Dynorphin A (1-8) is the predominant opioid peptide identified in placental tissue extracts. Dynorphin A (1-8)  Chemical Structure
  40. GC35918 Dynorphin A 1-10 Dynorphin A 1-10 an endogenous opioid neuropeptide, binds to extracellular loop 2 of the κ-opioid receptor. Dynorphin A 1-10  Chemical Structure
  41. GC15078 Dynorphin B endogenous agonist for the kappa opioid receptor Dynorphin B  Chemical Structure
  42. GC35919 Dynorphin B (1-13) (TFA) Dynorphin B (1-13) TFA acts as an agonist on opioid κ-receptor. Dynorphin B (1-13) (TFA)  Chemical Structure
  43. GC11676 EC 23 retinoic acid receptors agonist EC 23  Chemical Structure
  44. GC65260 EDP-305 EDP-305 is an orally active, potent and selective farnesoid X receptor (FXR) agonist, with EC50 values of 34 nM (chimeric FXR in CHO cells) and 8 nM (full-length FXR in HEK cells). EDP-305  Chemical Structure
  45. GC19135 Elagolix Elagolix is a highly potent, selective, orally-active, short-duration, non-peptide antagonist of the gonadotropin-releasing hormone receptor (GnRHR) (KD = 54 pM). Elagolix  Chemical Structure
  46. GC19136 Elagolix sodium Elagolix sodium is a human GnRH receptor (GnRHR) antagonist with an IC50 and Ki of 0.25 and 3.7 nM, respectively. Elagolix sodium  Chemical Structure
  47. GC67956 Endomorphin 1 acetate Endomorphin 1 acetate  Chemical Structure
  48. GC35986 Endomorphin 2 TFA Endomorphin 2 TFA, a high affinity, highly selective agonist of the μ-opioid receptor, displays reasonable affinities for kappa3 binding sites, with Ki value between 20 and 30 nM. Endomorphin 2 TFA  Chemical Structure
  49. GP10065 Endomorphin-1 Endomorphin-1  Chemical Structure
  50. GC10059 Endomorphin-2

    μ-opioid receptors agonist

    Endomorphin-2  Chemical Structure
  51. GC12140 Endoxifen Endoxifen Z-isomer is the most important Tamoxifen metabolite responsible for eliciting the anti-estrogenic effects of this drug in breast cancer cells expressing estrogen receptor-alpha (ERα). Endoxifen  Chemical Structure
  52. GC49648 Enobosarm-d4 An internal standard for the quantification of enobosarm Enobosarm-d4  Chemical Structure
  53. GC64854 Enzalutamide-d3 Enzalutamide D3 is a deuterium labeled Enzalutamide (MDV3100). Enzalutamide is an androgen receptor (AR) antagonist with an IC50 of 36 nM in LNCaP prostate cells. Enzalutamide-d3  Chemical Structure
  54. GC16631 EPI-001 AR antagonist EPI-001  Chemical Structure
  55. GC13072 Epiandrosterone steroid hormone with weak androgenic activity Epiandrosterone  Chemical Structure
  56. GC32953 Epristeride (ONO-9302) Epristeride (ONO-9302) (ONO-9302) is a selective, specific and orally active uncompetitive inhibitor of human steroid 5 alpha-reductase isoform 2. Epristeride (ONO-9302) has inhibitory effects for SR isoenzymes types 2 with Ki value of 0.7-2 nM. Epristeride (ONO-9302) can be used for the research of prostatic hyperplasia and acne. Epristeride (ONO-9302)  Chemical Structure
  57. GC33764 Eprotirome (KB2115) Eprotirome (KB2115) (KB2115) is a liver-selective thyroid hormone receptor (TR) agonist. Eprotirome (KB2115)  Chemical Structure
  58. GC18333 Equilenin Equilenin is an equine estrogen found in the urine of pregnant mares. Equilenin  Chemical Structure
  59. GC16292 Equol non-steroidal estrogen Equol  Chemical Structure
  60. GC12577 ER 50891 RARα receptor antagonist ER 50891  Chemical Structure
  61. GC10389 ERB 041 ERB 041 (ERB-041) is a potent and selective estrogen receptor (ER) β agonist with IC50s of 5.4, 3.1 and 3.7 nM for human, rat and mouse ERβ, respectively. ERB 041 displays >200-fold selectivity for ERβ over ERα. ERB 041 is a potent skin cancer chemopreventive agent that acts by dampening the WNT/β-catenin signaling pathway. ERB 041 induces ovarian cancer apoptosis. ERB 041  Chemical Structure
  62. GC11822 Erteberel (LY500307) Erteberel (LY500307) (LY500307) is a potent and selective estrogen receptor beta (ERβ) agonist with Ki and EC50 of 1.54 nM and 3.61 nM, respectively. Erteberel (LY500307)  Chemical Structure
  63. GC47309 Estetrol (hydrate) A naturally occurring estrogen Estetrol (hydrate)  Chemical Structure
  64. GC48979 Estradiol 17-(β-D-Glucuronide) (sodium salt hydrate) A substrate of multidrug resistance protein 2 Estradiol 17-(β-D-Glucuronide) (sodium salt hydrate)  Chemical Structure
  65. GC43629 Estradiol 3-sulfate 17β-Glucuronide (potassium salt) Estradiol 3-sulfate is a sulfated form of the steroid hormone 17β-estradiol, and is common in fetal plasma and in the breast tissues of patients with mammary carcinoma. Estradiol 3-sulfate 17β-Glucuronide (potassium salt)  Chemical Structure
  66. GC10139 Estradiol Cypionate Estrogen receptor inhibitor Estradiol Cypionate  Chemical Structure
  67. GC11796 Estradiol valerate Estradiol valerate (β-estradiol 17-valerate) is a synthetic estrogen widely used in combination with other steroid hormones in hormone replacement therapy drugs. Estradiol valerate  Chemical Structure
  68. GC12182 Estriol Estrogen receptor antagonist Estriol  Chemical Structure
  69. GC43630 Estriol 3-β-D-Glucuronide (sodium salt) Estriol 3-β-D-glucuronide is a metabolite of estriol. Estriol 3-β-D-Glucuronide (sodium salt)  Chemical Structure
  70. GC45450 Estriol-d2 Estriol-d2 is the deuterium labeled Estriol. Estriol is an antagonist of the G-protein coupled estrogen receptor in estrogen receptor-negative breast cancer cells. Estriol-d2  Chemical Structure
  71. GC14385 Estrone Estrogenic hormone Estrone  Chemical Structure
  72. GC45451 Estrone 3-methyl ether   Estrone 3-methyl ether  Chemical Structure
  73. GC43631 Estrone 3-sulfate (sodium salt) Estrone sulfate, a biologically inactive form of estrogen, is a major circulating plasma estrogen that is converted into the biologically active estrogen, estrone (E1) by steroid sulfatase (STS). strone sulfate can be used for the research of breast cancer. Estrone 3-sulfate (sodium salt)  Chemical Structure
  74. GC49254 Estrone-3-Glucuronide (sodium salt hydrate) A metabolite of 17β-estradiol Estrone-3-Glucuronide (sodium salt hydrate)  Chemical Structure
  75. GC45452 Estrone-d2   Estrone-d2  Chemical Structure
  76. GC16852 Estropipate Estrogen receptor agonist Estropipate  Chemical Structure
  77. GC12148 Ethinyl Estradiol Ethinyl Estradiol (17α-Ethynylestradiol;Ethynylestradiol) is an orally bio-active estrogen used in almost all modern formulations of combined oral contraceptive pills. Ethinyl Estradiol  Chemical Structure
  78. GC11436 Ethisterone Progestogen hormone Ethisterone  Chemical Structure
  79. GC12000 Ethynodiol diacetate Progestogen receptor agonist Ethynodiol diacetate  Chemical Structure
  80. GC47320 Ethynyl Estradiol 3-β-D-Glucuronide (hydrate) A metabolite of ethynyl estradiol Ethynyl Estradiol 3-β-D-Glucuronide (hydrate)  Chemical Structure
  81. GC13303 Etonogestrel steroidal progestin Etonogestrel  Chemical Structure
  82. GC32451 Examorelin (Hexarelin) A peptide agonist of GHS-R Examorelin (Hexarelin)  Chemical Structure
  83. GC11813 Exemestane Steroidal aromatase inhibitor,selective and irreversible Exemestane  Chemical Structure
  84. GC63755 Exemestane-D2 Exemestane-D2  Chemical Structure
  85. GC19151 Fadrozole A potent, selective and nonsteroidal inhibitor of aromatase Fadrozole  Chemical Structure
  86. GC18301 Fadrozole (hydrochloride) Fadrozole is a non-steroidal aromatase inhibitor (IC50s = 5 and 1.4 nM for human placental and rat ovarian microsomal aromatase, respectively). Fadrozole (hydrochloride)  Chemical Structure
  87. GC25410 Fasiglifam (TAK-875) Fasiglifam (TAK-875) is a selective GPR40 agonist with EC50 of 14 nM in human GPR40 expressing CHO cell line, 400-fold more potent than oleic acid. Fasiglifam (TAK-875)  Chemical Structure
  88. GC49563 Fenhexamid Fenhexamid, a botryticide, is a sterol biosynthesis inhibitor. Fenhexamid  Chemical Structure
  89. GC17143 Fenretinide A synthetic retinoic acid derivative Fenretinide  Chemical Structure
  90. GC14131 FERb 033 ERβ receptor agonist FERb 033  Chemical Structure
  91. GC18641 Ferutinin Ferutinin is a plant-derived ester of a sesquiterpenic alcohol that acts as an agonist for estrogen receptor (ER) α (IC50 = 33.1 nM) and an agonist/antagonist for ERβ (IC50 = 180.5 nM). Ferutinin  Chemical Structure
  92. GC10755 Fexaramine farnesoid X receptor agonist Fexaramine  Chemical Structure
  93. GC16248 Finasteride Inhibitor of Type II 5α-reductase Finasteride  Chemical Structure
  94. GC17572 Finasteride acetate 5α-reductase inhibitor Finasteride acetate  Chemical Structure
  95. GC15874 FIT δ-opioid agonist, irreversible FIT  Chemical Structure
  96. GC38682 Flavanone Flavanone is a naturally occurring flavone. Flavanone has inhibitory activity for human estrogen synthetase (aromatase). Flavanone  Chemical Structure
  97. GC47361 Fludioxonil A fungicide Fludioxonil  Chemical Structure
  98. GC49631 Fluocortolone A glucocorticoid Fluocortolone  Chemical Structure
  99. GC11694 Fluorobexarotene

    RXR agonist

    Fluorobexarotene  Chemical Structure
  100. GC10618 Fluoxymesterone androgen receptor agonist Fluoxymesterone  Chemical Structure
  101. GC10064 Flurizan A COX-inactive enantiomer of flurbiprofen Flurizan  Chemical Structure

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