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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

Products for  Endocrinology and Hormones

  1. Cat.No. Product Name Information
  2. GC68427 GSK1521498 free base GSK1521498 free base  Chemical Structure
  3. GC68337 Parathyroid hormone (1-34) (rat) acetate Parathyroid hormone (1-34) (rat) acetate  Chemical Structure
  4. GC68212 Chenodeoxycholic acid-13C Chenodeoxycholic acid-13C  Chemical Structure
  5. GC67956 Endomorphin 1 acetate Endomorphin 1 acetate  Chemical Structure
  6. GC67907 CCG258747 CCG258747  Chemical Structure
  7. GC67703 Adrenocorticotropic hormone TFA Adrenocorticotropic hormone TFA  Chemical Structure
  8. GC67698 Androgen receptor-IN-2 Androgen receptor-IN-2  Chemical Structure
  9. GC52506 Ghrelin (human) (trifluoroacetate salt) A growth hormone releasing peptide Ghrelin (human) (trifluoroacetate salt)  Chemical Structure
  10. GC52494 β-Endorphin (rat) (trifluoroacetate salt) An opioid neuropeptide β-Endorphin (rat) (trifluoroacetate salt)  Chemical Structure
  11. GC52490 Glucagon (hydrochloride) A peptide hormone Glucagon (hydrochloride)  Chemical Structure
  12. GC52420 Drospirenone-13C3 An internal standard for the quantification of drospirenone Drospirenone-13C3  Chemical Structure
  13. GC52415 Angiotensin A (trifluoroacetate salt) An AT1 and AT2 receptor agonist and active metabolite of angiotensin II Angiotensin A (trifluoroacetate salt)  Chemical Structure
  14. GC52414 [Ala17]-MCH (trifluoroacetate salt) An MCH-derived peptide and MCH receptor agonist [Ala17]-MCH (trifluoroacetate salt)  Chemical Structure
  15. GC52390 Spexin 1 (human, mouse, rat, bovine) (acetate) An endogenous peptide and agonist of GAL2 and GAL3 Spexin 1 (human, mouse, rat, bovine) (acetate)  Chemical Structure
  16. GC52388 [D-Lys3]-GHRP-6 (trifluoroacetate salt) An antagonist of GHS-R1a [D-Lys3]-GHRP-6 (trifluoroacetate salt)  Chemical Structure
  17. GC52387 Crosstide (trifluoroacetate salt) A peptide substrate for Akt Crosstide (trifluoroacetate salt)  Chemical Structure
  18. GC52365 4-tert-Octylphenol monoethoxylate An alkylphenolethoxylate and a degradation product of non-ionic surfactants 4-tert-Octylphenol monoethoxylate  Chemical Structure
  19. GC52351 Citrullinated α-Enolase (R8 + R14) (1-19)-biotin Peptide A biotinylated and citrullinated α-enolase peptide Citrullinated α-Enolase (R8 + R14) (1-19)-biotin Peptide  Chemical Structure
  20. GC52329 Betamethasone-d5 An internal standard for the quantification of betamethasone Betamethasone-d5  Chemical Structure
  21. GC52325 MeTC7 A vitamin D receptor antagonist MeTC7  Chemical Structure
  22. GC52281 Losartan Azide A potential impurity in commercial preparations of losartan Losartan Azide  Chemical Structure
  23. GC52242 V-125 An RXR agonist V-125  Chemical Structure
  24. GC66679 2,6-Dimethyl-L-tyrosine 2,6-Dimethyl-L-tyrosine (Dmt) is a tyrosine derivative that enhances receptor affinity, functional bioactivity and in vivo analgesia of opioid peptides. 2,6-Dimethyl-L-tyrosine  Chemical Structure
  25. GC66433 Ro 41-5253 Ro 41-5253 is an orally active selective retinoic acid receptor alpha (RARα) antagonist. Ro 41-5253 can bind RARα without inducing transcription or affecting RAR/RXR heterodimerization and DNA binding. Ro 41-5253 can inhibit cancer cell proliferation and induce apoptosis, has antitumor activity. Ro 41-5253  Chemical Structure
  26. GC66207 Atraric acid Atraric acid (Methyl atrarate) is a specific androgen receptor (AR) antagonist with anti-inflammatory and anticancer effects. Atraric acid represses the expression of the endogenous prostate specific antigen gene in both LNCaP and C4-2 cells. Atraric acid can also inhibit the synthesis of NO and cytokine, and suppress the MAPK-NFκB signaling pathway. Atraric acid can be used to research prostate diseases and inflammatory diseases. Atraric acid  Chemical Structure
  27. GC65936 Larsucosterol (trimethylamine) Larsucosterol (DUR-928) trimethylamine, a cholesterol metabolite, is a potent liver X receptor (LXR) antagonist. Larsucosterol trimethylamine as a potent endogenous regulator decreases lipogenesis. Larsucosterol trimethylamine inhibits the cholesterol biosynthesis via decreasing mRNA levels and inhibiting the activation of SREBP-1. Larsucosterol (trimethylamine)  Chemical Structure
  28. GC52189 Nomegestrol Nomegestrol is a potent and orally available progestin, acts as a selective full progesterone receptor agonist, with a Kd of 5.44 nM for rat uterine progesterone receptor, and has moderate antiandrogenic activity and strong antiestrogenic activity. Nomegestrol  Chemical Structure
  29. GC52185 (R,S)-Anatabine-d4 (R,S)-Anatabine-d4  Chemical Structure
  30. GC52180 WAY-169916 WAY-169916 is a pathway-selective ligand of ER (estrogen receptor) that acts by inhibiting NF-kB transcriptional activity. WAY-169916  Chemical Structure
  31. GC52129 3-Amino-5-hydroxybenzoic Acid 3-Amino-5-hydroxybenzoic Acid  Chemical Structure
  32. GC65587 CO23 CO23 is a selective thyroid hormone receptor (TR) α agonist and used for growth and development regulation. CO23  Chemical Structure
  33. 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
  34. GC65255 Trestolone Trestolone  Chemical Structure
  35. 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
  36. GC64600 SK33 SK33, a trifluoromethylated enobosarm analog, is a potent, and tissue selective anti-androgen. SK33reduces androgen receptor (AR) transcriptional activity. SK33  Chemical Structure
  37. GC64586 Nandrolone laurate Nandrolone laurate  Chemical Structure
  38. GC64540 Ar-V7-IN-1 Ar-V7-IN-1 is a potent inhibitor of Ar-V7. AR-V7 is a hormone-independent splice variant of the androgen receptor. Ar-V7-IN-1 has the potential for the research of various indications, in particular cancers such as prostate cancer (extracted from patent WO2018114781A1, compound 43). Ar-V7-IN-1  Chemical Structure
  39. GC52083 21-Deoxycortisone A corticosteroid metabolite of 11-keto progesterone 21-Deoxycortisone  Chemical Structure
  40. GC52043 Hydrocortisone Aceponate Hydrocortisone aceponate (Hydrocortisone 17-propionate 21-acetate) is a potent topical glucocorticoid. Hydrocortisone Aceponate  Chemical Structure
  41. GC52021 L-Thyroxine-N-methylamide A potential impurity found in commercial preparations of L-thyroxine L-Thyroxine-N-methylamide  Chemical Structure
  42. GC64301 DS08210767 DS08210767 is a highly potent, orally bioavailable PTHR1 antagonist with IC50 of 90 nM. DS08210767  Chemical Structure
  43. GC64147 Acetyl tetrapeptide-15 Acetyl tetrapeptide-15 is a synthetic peptide used in the cosmetics for sensitive skin. Acetyl tetrapeptide-15  Chemical Structure
  44. GC64007 (±)-U-50488 hydrate hydrochloride (±)-U-50488 hydrate hydrochloride  Chemical Structure
  45. GC63935 Testosterone buciclate Testosterone buciclate  Chemical Structure
  46. GC63932 Amsilarotene Amsilarotene (TAC-101; Am 555S), an orally active synthetic retinoid, has selective affinity for retinoic acid receptor α (RAR-α) binding with Ki of 2.4, 400 nM for RAR-α and RAR-β. Amsilarotene induces the apoptotic of human gastric cancer, hepatocellular carcinoma and ovarian carcinoma cells. Amsilarotene can be used for the research of cancer. Amsilarotene  Chemical Structure
  47. GC63884 Linzagolix Linzagolix (KLH-2109; OBE-2109) is a potent, non-peptide, and orally active GnRH antagonist. Linzagolix  Chemical Structure
  48. GC49680 Clobetasone Propionate A corticosteroid Clobetasone Propionate  Chemical Structure
  49. GC49679 Sauvagine (trifluoroacetate salt) A neuropeptide hormone Sauvagine (trifluoroacetate salt)  Chemical Structure
  50. GC49676 6β-hydroxy Budesonide A metabolite of budesonide 6β-hydroxy Budesonide  Chemical Structure
  51. GC49671 2,3-Oxidosqualene An intermediate in the biosynthesis of sterols 2,3-Oxidosqualene  Chemical Structure
  52. GC49654 BMS 270394 A RARγ agonist BMS 270394  Chemical Structure
  53. GC49653 Ramipril Diketopiperazine A potential impurity found in commercial preparations of ramipril Ramipril Diketopiperazine  Chemical Structure
  54. GC49648 Enobosarm-d4 An internal standard for the quantification of enobosarm Enobosarm-d4  Chemical Structure
  55. GC49634 Isoflupredone Isoflupredone belongs to the class of corticosteroids and exerts its effect by binding to glucocorticoid and mineralocorticoid receptors of animals, such as horses. Isoflupredone  Chemical Structure
  56. GC49631 Fluocortolone A glucocorticoid Fluocortolone  Chemical Structure
  57. GC49629 6β-hydroxy Prednisolone A metabolite of prednisolone 6β-hydroxy Prednisolone  Chemical Structure
  58. GC49611 21-Deoxycortisol-d8 An internal standard for the quantification of 21-deoxycortisol 21-Deoxycortisol-d8  Chemical Structure
  59. GC49609 2-bromo 17β-Estradiol A synthetic steroid and inhibitor of estrogen 2-hydroxylase 2-bromo 17β-Estradiol  Chemical Structure
  60. GC49592 Sermorelin (acetate) A growth hormone-releasing hormone analog Sermorelin (acetate)  Chemical Structure
  61. GC49574 Somatostatin-28 (human, mouse, rat, porcine, bovine, ovine) (trifluoroacetate salt) A cyclic neuropeptide hormone Somatostatin-28 (human, mouse, rat, porcine, bovine, ovine) (trifluoroacetate salt)  Chemical Structure
  62. GC49563 Fenhexamid Fenhexamid, a botryticide, is a sterol biosynthesis inhibitor. Fenhexamid  Chemical Structure
  63. GC49562 4-methoxy Estrone An active metabolite of estrone 4-methoxy Estrone  Chemical Structure
  64. GC49542 5α-Androstan-3β-ol A steroidal androgen 5α-Androstan-3β-ol  Chemical Structure
  65. GC49520 (S)-Equol An estrogen receptor β agonist (S)-Equol  Chemical Structure
  66. GC49475 Triptorelin (trifluoroacetate salt) A synthetic GNRH peptide agonist Triptorelin (trifluoroacetate salt)  Chemical Structure
  67. GC49459 Desmopressin (trifluoroacetate salt) A vasopressin receptor agonist Desmopressin (trifluoroacetate salt)  Chemical Structure
  68. GC63764 7-α-Methylthio Spironolactone-D3 7-α-Methylthio Spironolactone-D3  Chemical Structure
  69. GC63755 Exemestane-D2 Exemestane-D2  Chemical Structure
  70. GC63686 Naloxone methiodide Naloxone methiodide  Chemical Structure
  71. GC63595 NH-3 NH-3 is an orally active, reversible thyroid hormone receptor (THR) antagonist with an IC50 of 55 nM. NH-3  Chemical Structure
  72. GC63579 Linuron Linuron is a phenylurea herbicide that is widely used to control the growth of grass and weeds in various agriculture crops and in orchards. Linuron  Chemical Structure
  73. GC63431 DPDPE TFA DPDPE TFA, an opioid peptide, is a selective δ-opioid receptor?(DOR) agonist?with anticonvulsant effects. DPDPE TFA  Chemical Structure
  74. GC63402 Rezvilutamide Rezvilutamide (SHR3680) is an androgen receptor antagonist. Rezvilutamide (SHR3680) is used for the study of prostate cancer. Rezvilutamide  Chemical Structure
  75. GC63292 (rac)-PF-998425 (Rac)-PF-998425 is a potent, selective, nonsteroidal androgen receptor (AR) antagonist. (rac)-PF-998425  Chemical Structure
  76. GC63217 Testosterone undecanoate Testosterone undecanoate  Chemical Structure
  77. GC63200 Spiradoline Spiradoline  Chemical Structure
  78. GC63115 Nociceptin (1-13), amide TFA Nociceptin (1-13), amide TFA is a potent ORL1 receptor (opioid receptor-like 1 receptor, OP4) agonist with a pEC50 of 7.9 for mouse vas deferens and a Ki of 0.75 nM for binding to rat forebrain membranes. Nociceptin (1-13), amide TFA  Chemical Structure
  79. GC63096 Nandrolone phenylpropionate Nandrolone phenylpropionate  Chemical Structure
  80. GC63072 Methyl-6-alpha-Naltrexol Methyl-6-alpha-Naltrexol  Chemical Structure
  81. GC63066 Methenolone acetate Methenolone acetate  Chemical Structure
  82. GC62992 Glutaurine Glutaurine containing glutamine and taurine residues is an orally active hormone of the parathyroid. Glutaurine  Chemical Structure
  83. GC62761 1α-Hydroxy-3-epi-vitamin D3 1α-Hydroxy-3-epi-vitamin D3, a natural metabolite of 1alpha,25-dihydroxyvitamin D3, is a potent suppressor of parathyroid hormone (PTH) secretion. 1α-Hydroxy-3-epi-vitamin D3  Chemical Structure
  84. GC49427 3,5-Diiodo-L-thyronine 3,5-Diiodo-L-thyronine is an endogenous metabolite. 3,5-Diiodo-L-thyronine  Chemical Structure
  85. GC49423 Metanephrine-d3 (hydrochloride) An internal standard for the quantification of metanephrine Metanephrine-d3 (hydrochloride)  Chemical Structure
  86. GC49408 Ramipril Diketopiperazine Acid A potential impurity found in commercial preparations of ramipril Ramipril Diketopiperazine Acid  Chemical Structure
  87. GC49399 N-Desbutyl Dronedarone (hydrochloride) Debutyldronedarone (SR35021) hydrochloride, the main metabolite of Dronedarone, is a selective thyroid hormone receptor α1 (TRα1) inhibitor. N-Desbutyl Dronedarone (hydrochloride)  Chemical Structure
  88. GC49393 all-trans-13,14-Dihydroretinol A metabolite of all-trans retinoic acid all-trans-13,14-Dihydroretinol  Chemical Structure
  89. GC49391 7α-Thiospironolactone An active metabolite of spironolactone 7α-Thiospironolactone  Chemical Structure
  90. GC49389 Tritylolmesartan Medoxomil An intermediate in the synthesis of olmesartan medoxomil Tritylolmesartan Medoxomil  Chemical Structure
  91. GC49385 Halometasone A synthetic corticosteroid Halometasone  Chemical Structure
  92. GC49342 Glucagon-d9 (trifluoroacetate salt) An internal standard for the quantification of glucagon Glucagon-d9 (trifluoroacetate salt)  Chemical Structure
  93. GC49329 Turkesterone (hydrate) A phytoecdysteroid with diverse biological activities Turkesterone (hydrate)  Chemical Structure
  94. GC49326 5β-Dihydroprogesterone A progesterone receptor agonist and metabolite of progesterone 5β-Dihydroprogesterone  Chemical Structure
  95. GC49321 AZ-GHS-22 An inverse agonist of GHS-R1a AZ-GHS-22  Chemical Structure
  96. GC49306 Isopimaric Acid A diterpenoid resin acid Isopimaric Acid  Chemical Structure
  97. GC49303 Ganoderic Acid DM A triterpenoid with diverse biological activities Ganoderic Acid DM  Chemical Structure
  98. GC49254 Estrone-3-Glucuronide (sodium salt hydrate) A metabolite of 17β-estradiol Estrone-3-Glucuronide (sodium salt hydrate)  Chemical Structure
  99. GC49207 Lumisterol 3 A photoisomer of previtamin D3 Lumisterol 3  Chemical Structure
  100. GC49206 7α-hydroxy Dehydroepiandrosterone An active metabolite of dehydroepiandrosterone 7α-hydroxy Dehydroepiandrosterone  Chemical Structure
  101. GC49189 (E/Z)-4-hydroxy Tamoxifen-d5 An internal standard for the quantification of (E/Z)-4-hydroxy tamoxifen (E/Z)-4-hydroxy Tamoxifen-d5  Chemical Structure

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