Search Site
  • 0
    My Cart

    Click Here to Find How Many Items You Have Added:)

    image loader

    Adding item(s) to cart......

Home >> Signaling Pathways >> Endocrinology and Hormones

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

Targets for  Endocrinology and Hormones

Products for  Endocrinology and Hormones

  1. Cat.No. Product Name Information
  2. GC49123 Somatorelin (1-44) amide (human) (trifluoroacetate salt) A synthetic GHRH peptide Somatorelin (1-44) amide (human) (trifluoroacetate salt) Chemical Structure
  3. GC44914 Somatostatin-14 (acetate) Somatostatin-14 is a natural cyclic peptide hormone derived from the preprohormone, somatostatin. Somatostatin-14 (acetate) Chemical Structure
  4. 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
  5. 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
  6. GC63200 Spiradoline Spiradoline Chemical Structure
  7. GC12516 Spironolactone Competitive mineralocorticoid (aldosterone) receptor antagonist Spironolactone Chemical Structure
  8. GC45567 SR 1903   SR 1903 Chemical Structure
  9. GC13680 SR-9243 inverse agonist of LXR SR-9243 Chemical Structure
  10. GC14638 SR9238 inverse agonist of the two LXR isoforms, LXRα and LXRβ SR9238 Chemical Structure
  11. GC37687 Stanolone benzoate Stanolone benzoate Chemical Structure
  12. GC37691 Stigmasterol glucoside Stigmasterol glucoside is a sterol isolated from P. Stigmasterol glucoside Chemical Structure
  13. GC10596 T0901317 Liver X receptor agonist,potent and selective T0901317 Chemical Structure
  14. GC34822 T3-ATA S-isomer T3-ATA S-isomer is the S-isomer of T3-ATA, which is the active form of the thyroid hormone. T3-ATA S-isomer Chemical Structure
  15. GC34824 T4-ATA S-isomer T4-ATA S-isomer Chemical Structure
  16. GC16649 TAK-700 (Orteronel) A non-steroidal inhibitor of the 17,20-lyase activity of CYP17A1 TAK-700 (Orteronel) Chemical Structure
  17. GC17063 Talarozole Talarozole Chemical Structure
  18. GC17983 Taltirelin novel orally active TRH analogue Taltirelin Chemical Structure
  19. GC37732 Taltirelin acetate Taltirelin acetate (TA-0910 acetate) is a superagonist at thyrotropin-releasing hormone receptor (TRH-R) with an IC50 of 910 nM and EC50 of 36 nM for stimulating an increase in cytosolic Ca2+ concentration (Ca2+ release). Taltirelin acetate Chemical Structure
  20. GC13984 Tamibarotene A selective RARα agonist Tamibarotene Chemical Structure
  21. GC11669 Tamoxifen Citrate Antiestrogen drug Tamoxifen Citrate Chemical Structure
  22. GC40301 Tamoxifen N-oxide Tamoxifen is a selective estrogen receptor modulator that evokes tissue-dependent effects. Tamoxifen N-oxide Chemical Structure
  23. GC50558 TAN 452

    Potent and selective peripherally acting δ opioid antagonist; antianalgesic.

     TAN 452 Chemical Structure
  24. GC16847 Tanaproget Tanaproget Chemical Structure
  25. GC44999 Tauro-α-muricholic Acid (sodium salt) Tauro-α-muricholic acid (TαMCA) is an antagonist of the farnesoid X receptor (FXR; IC50 = 28 μM) and a taurine-conjugated form of the murine-specific primary bile acid α-muricholic acid. Tauro-α-muricholic Acid (sodium salt) Chemical Structure
  26. GC49011 Tauro-α-muricholic Acid-d4 (sodium salt) An internal standard for the quantification of tauro-α-muricholic acid Tauro-α-muricholic Acid-d4 (sodium salt) Chemical Structure
  27. GC45000 Tauro-β-muricholic Acid (sodium salt) Tauro-β-muricholic Acid sodium (T-βMCA sodium), a endogenous metabolite, is a competitive and reversible farnesoid X receptor (FXR) antagonist, with an IC50 of 40 μM. Tauro-β-muricholic Acid (sodium salt) Chemical Structure
  28. GC49012 Tauro-β-muricholic Acid-d4 (sodium salt) An internal standard for the quantification of tauro-β-muricholic acid Tauro-β-muricholic Acid-d4 (sodium salt) Chemical Structure
  29. GC44998 Tauro-Obeticholic Acid Tauro-obeticholic acid is a taurine-conjugated form of obeticholic acid, which is a farnesoid X receptor (FXR) agonist and semisynthetic derivative of chenodeoxycholic acid. Tauro-Obeticholic Acid Chemical Structure
  30. GC15459 Tazarotene Topical retinoid;antiproliferative;inducer of TIG3 tumor suppressor Tazarotene Chemical Structure
  31. GC45001 Tazarotenic Acid Tazarotenic acid is an active metabolite of tazarotene, an acetylenic retinoid prodrug that induces epidermal hyperplasia with an ED50 value of 100 nM. Tazarotenic Acid Chemical Structure
  32. GC10567 TCPOBOP constitutive androstane receptor (CAR) agonist TCPOBOP Chemical Structure
  33. GC49055 Tebuconazole-d9 An internal standard for the quantification of tebuconazole Tebuconazole-d9 Chemical Structure
  34. GC15023 Telmisattan Telmisattan is a potent, long lasting antagonist of angiotensin II type 1 receptor (AT1), selectively inhibiting the binding of 125I-AngII to AT1 receptors with IC50 of 9.2 nM. Telmisattan Chemical Structure
  35. GC46230 Terrelumamide A A peptide fungal metabolite Terrelumamide A Chemical Structure
  36. GC45935 Testosterone

    An Analytical Reference Material

     Testosterone Chemical Structure
  37. GC39451 Testosterone (propionate) Testosterone (propionate) Chemical Structure
  38. GC63935 Testosterone buciclate Testosterone buciclate Chemical Structure
  39. GC63217 Testosterone undecanoate Testosterone undecanoate Chemical Structure
  40. GC40341 Tetrahydro-11-deoxy Cortisol Tetrahydro-11-deoxy cortisol (THS) is the primary urinary metabolite of 11-deoxycortisol. Tetrahydro-11-deoxy Cortisol Chemical Structure
  41. GC12445 TFM-4AS-1 androgen receptor modulator TFM-4AS-1 Chemical Structure
  42. GC48174 Thiorphan-d5 An internal standard for the quantification of thiorphan Thiorphan-d5 Chemical Structure
  43. GC48358 Thymulin (acetate hydrate) A peptide hormone Thymulin (acetate hydrate) Chemical Structure
  44. GC10413 Thyroid Hormone Receptor Antagonist (1-850) Thyroid hormone receptor antagonist Thyroid Hormone Receptor Antagonist (1-850) Chemical Structure
  45. GC31328 Thyroxine sulfate (T4 Sulfate) Thyroxine sulfate (T4 Sulfate) is a thyroid hormone metabolite. Thyroxine sulfate (T4 Sulfate) Chemical Structure
  46. GC41153 Tibolone Tibolone is an estrogen-like compound used for the treatment of the symptoms associated with menopausal transition (i.e., climacteric symptoms) and also for the treatment of osteoporosis. Tibolone Chemical Structure
  47. GC15001 Tiratricol thyroid hormone analogue Tiratricol Chemical Structure
  48. GC13362 TOK-001 TOK-001 (TOK-001) is a multifunctional antiandrogen and CYP17 inhibitor (IC50=47 nM) in castration resistant prostate cancer (CRPC). TOK-001 Chemical Structure
  49. GC11544 Toremifene Toremifene Chemical Structure
  50. GC13835 Toremifene Citrate Oral selective estrogen receptor modulator (SERM) Toremifene Citrate Chemical Structure
  51. GC31402 TR antagonist 1 TR antagonist 1 is a high-affinity thyroid hormone receptor (TR) antagonist with IC50s of 36 and 22 nM for TRα and TRβ, respectively. TR antagonist 1 Chemical Structure
  52. GC65255 Trestolone Trestolone Chemical Structure
  53. GC18147 Tretinoin (Aberela) Tretinoin (Aberela) is a metabolite of vitamin A that plays important roles in cell growth, differentiation, and organogenesis. Tretinoin (Aberela) is a natural agonist of RAR nuclear receptors, with IC50s of 14 nM for RARα/β/γ. Tretinoin (Aberela) bind to PPARβ/δ with Kd of 17 nM. Tretinoin (Aberela) acts as an inhibitor of transcription factor Nrf2 through activation of retinoic acid receptor alpha. Tretinoin (Aberela) Chemical Structure
  54. GP10112 TRH Precursor Peptide

    Thyrotropin Releasing Hormone Precursor Peptide

     TRH Precursor Peptide Chemical Structure
  55. GC31935 Trifarotene (CD5789) Trifarotene (CD5789) (CD5789) is a potent and selective RARγ agonist. Trifarotene (CD5789) Chemical Structure
  56. GC10702 Trimebutine Antimuscarinic Trimebutine Chemical Structure
  57. GC37829 Trimebutine maleate Trimebutine maleate is a drug with antimuscarinic and weak mu opioid agonist effects. Trimebutine maleate Chemical Structure
  58. GN10268 Triptophenolide Triptophenolide Chemical Structure
  59. GC49475 Triptorelin (trifluoroacetate salt) A synthetic GNRH peptide agonist Triptorelin (trifluoroacetate salt) Chemical Structure
  60. GC32772 Triptorelin ([DTrp6]-LH-RH) A synthetic GNRH peptide agonist Triptorelin ([DTrp6]-LH-RH) Chemical Structure
  61. GC49389 Tritylolmesartan Medoxomil An intermediate in the synthesis of olmesartan medoxomil Tritylolmesartan Medoxomil Chemical Structure
  62. GC19363 Tropifexor Tropifexor is a novel and highly potent agonist of FXR with an EC50 of 0.2 nM. Tropifexor Chemical Structure
  63. GC14273 TTNPB (Arotinoid Acid) TTNPB (Arotinoid Acid) is a highly potent RAR agonist. Competitive binding assays using human RARs yield IC50s of α=5.1 nM, β= 4.5 nM, and γ=9.3 nM, respectively. TTNPB (Arotinoid Acid) Chemical Structure
  64. GC49329 Turkesterone (hydrate) A phytoecdysteroid with diverse biological activities Turkesterone (hydrate) Chemical Structure
  65. GC30816 Tyr-Gly-Gly-Phe-Met-OH (Met-Enkephalin) Tyr-Gly-Gly-Phe-Met-OH (Met-Enkephalin) regulates human immune function and inhibits tumor growth via binding to the opioid receptor. Tyr-Gly-Gly-Phe-Met-OH (Met-Enkephalin) Chemical Structure
  66. GC15512 U-54494A hydrochloride κ-opioid agonist and NMDA antagonist U-54494A hydrochloride Chemical Structure
  67. GC61586 UFP-101 TFA UFP-101 TFA is a potent, selective, and competitive antagonist of the N/OFQ peptide (NOP) receptor, with a pKi of 10.24. UFP-101 TFA Chemical Structure
  68. GC11677 Ulipristal acetate Novel selective progesterone receptor modulator (SPRM) Ulipristal acetate Chemical Structure
  69. GC48219 Ulipristal Acetate-d6 An internal standard for the quantification of ulipristal acetate Ulipristal Acetate-d6 Chemical Structure
  70. GC18231 Urocortin II (human) (trifluoroacetate salt) Urocortin II is a neuropeptide hormone and member of the corticotropin-releasing factor (CRF) family which includes mammalian CRF , urocortin , urocortin III , frog sauvagine, and piscine urotensin I. Urocortin II (human) (trifluoroacetate salt) Chemical Structure
  71. GC45588 Urocortin II (mouse) (trifluoroacetate salt)   Urocortin II (mouse) (trifluoroacetate salt) Chemical Structure
  72. GC45589 Urocortin III (human) (trifluoroacetate salt)   Urocortin III (human) (trifluoroacetate salt) Chemical Structure
  73. GC45590 Urocortin III (mouse) (free acid) (trifluoroacetate salt)   Urocortin III (mouse) (free acid) (trifluoroacetate salt) Chemical Structure
  74. GC45591 Urocortin III (mouse) (trifluoroacetate salt)   Urocortin III (mouse) (trifluoroacetate salt) Chemical Structure
  75. GC32908 UT-155 UT-155 is a selective and potent androgen receptor (AR) antagonist, with a Ki of 267 nM for UT-155 binding to AR-LBD. UT-155 Chemical Structure
  76. GC62124 UT-34 UT-34 is a potent, selective and orally active second-generation pan-androgen receptor (AR) antagonist and degrader with IC50s of 211.7 nM, 262.4 nM and 215.7 nM for wild-type, F876L and W741L AR, respectively. UT-34 Chemical Structure
  77. GC13199 UVI 3003 RXR antagonist UVI 3003 Chemical Structure
  78. GC52242 V-125 An RXR agonist V-125 Chemical Structure
  79. GC31126 Valorphin Valorphin is an endogenous hemoglobin β-chain (33-39) fragment with opioid analgesic activity, binds to rat mu-opioid receptor, with an IC50 of 14 nM; Valorphin also shows anti-tumor activity. Valorphin Chemical Structure
  80. GC30994 Vanilpyruvic acid (Vanylpyruvic acid) Vanilpyruvic acid (Vanylpyruvic acid) is a catecholamine metabolite and precursor to vanillactic acid. Vanilpyruvic acid (Vanylpyruvic acid) Chemical Structure
  81. GC45139 Vapreotide (trifluoroacetate salt) Vapreotide is a peptide neurokinin-1 receptor (NK1) antagonist and analog of somatostatin (IC50 = 330 nM in a radioligand binding assay). Vapreotide (trifluoroacetate salt) Chemical Structure
  82. GC37913 Vitamin A An intermediate in retinol metabolism 325,000 IU/g Vitamin A Chemical Structure
  83. GC70128 VPC-14228

    VPC-14228 is an effective androgen receptor DNA binding domain (AR-DBD) inhibitor that can interfere with the interaction between AR and androgen response elements, effectively blocking AR transcriptional activity. VPC-14228 can be used for research on prostate cancer.

     VPC-14228 Chemical Structure
  84. GC62329 VPC-14449 VPC-14449 is a potent and selective inhibitor of the DNA-binding domain of the androgen receptor (AR-DBD), with IC50 of 0.34 μM for full-length human AR. VPC-14449 reduces the ability of full-length AR as well as AR variants to interact with chromatin. VPC-14449 can be used for the research of prostate cancer. VPC-14449 Chemical Structure
  85. GC13309 WAY 200070 ERβ receptor agonist WAY 200070 Chemical Structure
  86. 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
  87. GC34862 WYC-209 WYC-209, a synthetic retinoid, is a retinoic acid receptor (RAR) agonist. WYC-209 induces apoptosis primarily via the caspase 3 pathway (IC50=0.19?μM for inmalignant murine melanoma TRCs), and has long-term effects with little toxicity. WYC-209 Chemical Structure
  88. GC10789 XCT790 ERRα agonist XCT790 Chemical Structure
  89. GC32459 XL041 (BMS-852927) XL041 (BMS-852927) (BMS-852927) is an LXRβ-selective agonist. XL041 (BMS-852927) Chemical Structure
  90. GC10760 XL335 XL335 (FXR-450) is a potent, selective, and orally bioavailable FXR agonist with EC50 of 4 nM. XL335 Chemical Structure
  91. GC10346 Y 134 estrogen receptor modulator Y 134 Chemical Structure
  92. GC70155 YCT529

    YCT529 is an effective, selective, and orally active RAR-α inhibitor.

     YCT529 Chemical Structure
  93. GC31442 YK11 A partial agonist of the androgen receptor YK11 Chemical Structure
  94. GC40293 Z3-Dodecenyl E2-butenoate Z3-Dodecenyl E2-butenoate is a female sex pheromone produced by the sweet potato weevil, C. Z3-Dodecenyl E2-butenoate Chemical Structure
  95. GC10684 Zearalanone estrogen receptor agonist Zearalanone Chemical Structure
  96. GC12767 Zearalenone Mycotoxin produced by several species of Fusarium fungi. Zearalenone Chemical Structure
  97. GC16742 ZK 164015 estrogen receptor silent antagonist ZK 164015 Chemical Structure
  98. GC31006 ZT 52656A hydrochloride ZT 52656A is a selective kappa opioid agonist, used for the prevention or alleviation of pain in the eye. ZT 52656A hydrochloride Chemical Structure
  99. GC52414 [Ala17]-MCH (trifluoroacetate salt) An MCH-derived peptide and MCH receptor agonist [Ala17]-MCH (trifluoroacetate salt) Chemical Structure
  100. GC11848 [D-Ala2]-Deltorphin II [D-Ala2]-Deltorphin II is a selective peptide agonist for the δ opioid receptor. [D-Ala2]-Deltorphin II Chemical Structure
  101. GC33081 [D-Ala2]leucine-enkephalin [D-Ala2]leucine-enkephalin, a delta opioid agonist, is a degradation resistant long-acting Leu-enkephalin. [D-Ala2]leucine-enkephalin Chemical Structure

Items 701 to 800 of 807 total

per page
  2. 5
  3. 6
  4. 7
  5. 8
  6. 9

Set Descending Direction