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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. GC42870 Atrazine Mercapturate Atrazine mercapturate is a major, glutathione-derived metabolite of atrazine, an herbicide that is effective in controlling a broad range of weeds. Atrazine Mercapturate Chemical Structure
  3. GC49321 AZ-GHS-22 An inverse agonist of GHS-R1a AZ-GHS-22 Chemical Structure
  4. GC32801 AZ876 An LXR agonist AZ876 Chemical Structure
  5. GC12434 AZD1981 CRTh2 antagonist,potent and selective AZD1981 Chemical Structure
  6. GC10372 AZD3514 Androgen receptor downregulator AZD3514 Chemical Structure
  7. GC14405 AZD9496 estrogen receptor inhibitor, orally active AZD9496 Chemical Structure
  8. GC11390 BAM 22P Potent endogenous agonist peptide for the newly identified sensory neuron specific receptor (SNSR); BAM 22P Chemical Structure
  9. GC15926 BAN ORL 24 A nociceptin receptor antagonist BAN ORL 24 Chemical Structure
  10. GC30565 BAR502 A dual agonist of GP-BAR1 and FXR BAR502 Chemical Structure
  11. GC17588 Bavachin estrogen receptors ERα and ERβ activator Bavachin Chemical Structure
  12. GC14883 Bazedoxifene Bazedoxifene Chemical Structure
  13. GC10852 Bazedoxifene acetate A selective estrogen receptor modulator Bazedoxifene acetate Chemical Structure
  14. GC10245 Bazedoxifene HCl Bazedoxifene HCl (TSE-424 hydrochloride) is an oral active, BBB-penetrant nonsteroidal selective estrogen receptor modulator (SERM), with IC50s of 23 nM and 99 nM for ERα and ERβ, respectively. Bazedoxifene HCl can be used for the research of osteoporosis. Bazedoxifene HCl acts as an inhibitor of IL-6/GP130 protein-protein interactions. Bazedoxifene HCl can be used for the research of pancreatic cancer. Bazedoxifene HCl Chemical Structure
  15. GC49757 Bazedoxifene N-oxide An oxidative degradation product of bazedoxifene Bazedoxifene N-oxide Chemical Structure
  16. GC46907 Bazedoxifene-d4 An internal standard for the quantification of bazedoxifene Bazedoxifene-d4 Chemical Structure
  17. GC46909 BE-26263 A fungal metabolite BE-26263 Chemical Structure
  18. GP10051 Beta-Lipotropin (1-10), porcine

    Morphine-like substance

     Beta-Lipotropin (1-10), porcine Chemical Structure
  19. GC52329 Betamethasone-d5 An internal standard for the quantification of betamethasone Betamethasone-d5 Chemical Structure
  20. GC30639 Bevenopran (CB-5945) Bevenopran (CB-5945) is a peripheral μ-opioid receptor antagonist. Bevenopran (CB-5945) Chemical Structure
  21. GC10037 Bexarotene Retinoid Receptor agonist Bexarotene Chemical Structure
  22. GC46923 Bexarotene-d4 A neuropeptide with diverse biological activities Bexarotene-d4 Chemical Structure
  23. GC12271 Bicalutamide Androgen receptor antagonist Bicalutamide Chemical Structure
  24. GC46925 Bicalutamide-d4 An internal standard for the quantification of bicalutamide Bicalutamide-d4 Chemical Structure
  25. GC31577 Bifluranol (BX341) Bifluranol (BX341) (BX341) is an anti-androgen. Bifluranol (BX341) Chemical Structure
  26. GC60076 Bigelovin Bigelovin, a sesquiterpene lactone isolated from Inula helianthus-aquatica, is a selective retinoid X receptor α agonist. Bigelovin suppresses tumor growth through inducing apoptosis and autophagy via the inhibition of mTOR pathway regulated by ROS generation. Bigelovin Chemical Structure
  27. GC42943 Bischloroanthrabenzoxocinone Bacterial type II fatty acid synthesis (FAS-II) is mediated by a series of enzymes, each of which may be targeted by potential antibiotics. Bischloroanthrabenzoxocinone Chemical Structure
  28. GC11504 BMS 195614 BMS 195614 (BMS 614) is a neutral RARα-selective antagonist with a Ki of 2.5 nM. BMS 195614 Chemical Structure
  29. GC49654 BMS 270394 A RARγ agonist BMS 270394 Chemical Structure
  30. GC10656 BMS 453 RAR agonist BMS 453 Chemical Structure
  31. GC15648 BMS 493 Pan-RAR inverse agonist BMS 493 Chemical Structure
  32. GC14185 BMS 753 RARα-selective agonist BMS 753 Chemical Structure
  33. GC17382 BMS 961 Selective RARγ agonist BMS 961 Chemical Structure
  34. GC35534 BMS-564929 BMS-564929 is an androgen receptor (AR) agonist, binds to androgen receptor (AR) with a Ki of 2.11±0.16 nM. BMS-564929 Chemical Structure
  35. GC31372 BMS-779788 (EXEL04286652) BMS-779788 (EXEL04286652) is a LXR partial agonist with IC50 values of 68 nM for LXRα and 14 nM for LXRβ. BMS-779788 (EXEL04286652) Chemical Structure
  36. GA20967 Boc-D-His-OH An amino acid building block Boc-D-His-OH Chemical Structure
  37. GA20972 Boc-D-Leu-OSu An amino acid-containing building block Boc-D-Leu-OSu Chemical Structure
  38. GC41187 Boldenone Cypionate Boldenone is an anabolic androgenic steroid and synthetic derivative of testosterone that was originally developed for veterinary use. Boldenone Cypionate Chemical Structure
  39. GC35541 Boldenone Undecylenate Boldenone Undecylenate Chemical Structure
  40. GC46941 Bombesin (trifluoroacetate salt) A neuropeptide with diverse biological activities Bombesin (trifluoroacetate salt) Chemical Structure
  41. GC38741 BPR1M97 BPR1M97 is a dual-acting mu opioid receptor (MOP) and nociceptin-orphanin FQ peptide (NOP) receptor agonist with Ki values of 1.8 and 4.2 nM, respectively. BPR1M97 Chemical Structure
  42. GC15313 BRL 52537 hydrochloride κ/μ opioid receptor agonist,potent and selective BRL 52537 hydrochloride Chemical Structure
  43. GC46956 Budesonide-d8 An internal standard for the quantification of budesonide Budesonide-d8 Chemical Structure
  44. GC34099 Buserelin Acetate Buserelin Acetate Chemical Structure
  45. GC46104 Butyric Acid-d7 An internal standard for the quantification of sodium butyrate Butyric Acid-d7 Chemical Structure
  46. GC16521 BW 373U86 Non-peptide delta agonist,potent and selective BW 373U86 Chemical Structure
  47. GC43127 Calcitonin (salmon) (trifluoroacetate salt) Calcitonin is a peptide hormone that lowers blood calcium level and inhibits bone resorption. Calcitonin (salmon) (trifluoroacetate salt) Chemical Structure
  48. GC16978 Candesartan Angiotensin II receptor 1 (AT1) antagonist Candesartan Chemical Structure
  49. GC16223 Captopril An ACE inhibitor Captopril Chemical Structure
  50. GC43140 Captopril Disulfide Captopril disulfide is a metabolite and symmetrical disulfide form of the angiotensin converting enzyme (ACE) inhibitor captopril. Captopril Disulfide Chemical Structure
  51. GC48348 Carbetocin (acetate) A peptide oxytocin receptor agonist Carbetocin (acetate) Chemical Structure
  52. GC48426 CAY10771 A dual agonist of FXR and PPARδ CAY10771 Chemical Structure
  53. GC67907 CCG258747 CCG258747 Chemical Structure
  54. GC43213 CCK (26-30) (sulfated) CCK (26-30) is an N-terminal fragment of CCK, a peptide hormone found in the intestine and brain that stimulates digestion, mediates satiety, and is involved in anxiety. CCK (26-30) (sulfated) Chemical Structure
  55. GC43214 CCK (26-31) (non-sulfated) CCK (26-31) is an N-terminal fragment of CCK , a peptide hormone found in the intestine and brain that stimulates digestion, mediates satiety, and is involved in anxiety. CCK (26-31) (non-sulfated) Chemical Structure
  56. GC18553 CCK (26-31) (sulfated) CCK (26-31) is an N-terminal fragment of CCK , a peptide hormone found in the intestine and brain that stimulates digestion, mediates satiety, and is involved in anxiety. CCK (26-31) (sulfated) Chemical Structure
  57. GC18384 CCK (27-33) (non-sulfated) CCK (27-33) is a C-terminal fragment of CCK , a peptide hormone found in the intestine and brain that stimulates digestion, mediates satiety, and is involved in anxiety. CCK (27-33) (non-sulfated) Chemical Structure
  58. GC43215 CCK Octapeptide (non-sulfated), (trifluoroacetate salt) Cholecystokinin (CCK) octapeptide is a peptide hormone found in the intestine and brain that stimulates digestion, mediates satiety, and is involved in anxiety. CCK Octapeptide (non-sulfated), (trifluoroacetate salt) Chemical Structure
  59. GC11794 CD 1530 RAR receptor agonist CD 1530 Chemical Structure
  60. GC10080 CD 2314 RARβ agonist,potent and selective CD 2314 Chemical Structure
  61. GC12072 CD 2665 Selective RARβ/γ antagonist CD 2665 Chemical Structure
  62. GC17730 CD 3254 RXRα agonist,potent and selective CD 3254 Chemical Structure
  63. GC11464 CD 437 RARγ-selective agonist,potent and cell-permeable CD 437 Chemical Structure
  64. GC35637 Cebranopadol An analgesic NOP and opioid receptor agonist Cebranopadol Chemical Structure
  65. GC35638 Cebranopadol ((1α,4α)stereoisomer) Cebranopadol ((1α,4α)stereoisomer) is a stereoisomer of cebranopadol. Cebranopadol ((1α,4α)stereoisomer) Chemical Structure
  66. GC19229 CERC-501 CERC-501 (CERC-501) is a potent and centrally-penetrant kappa opioid receptor antagonist with a Ki of 0.807 nM. CERC-501 Chemical Structure
  67. GC33467 Cetrorelix Acetate (SB-075 acetate) Cetrorelix Acetate (SB-075 acetate) (SB-75 acetate) is a potent gonadotropin-releasing hormone (GnRH) receptor antagonist with an IC50 of 1.21 nM. Cetrorelix Acetate (SB-075 acetate) Chemical Structure
  68. GC32422 CGP-53153 CGP-53153 is a steroidal inhibitor of 5 alpha reductase with IC50s of 36 and 262 nM in rat and human prostatic tissue, respectively. CGP-53153 Chemical Structure
  69. GC11053 Ch 55 RAR agonist Ch 55 Chemical Structure
  70. GC17985 Chenodeoxycholic Acid nuclear receptors(FXR) activator Chenodeoxycholic Acid Chemical Structure
  71. GC48424 Chenodeoxycholic Acid 24-Acyl-β-D-Glucuronide A metabolite of CDCA Chenodeoxycholic Acid 24-Acyl-β-D-Glucuronide Chemical Structure
  72. GC49853 Chenodeoxycholic Acid 3-Glucuronide A metabolite of CDCA Chenodeoxycholic Acid 3-Glucuronide Chemical Structure
  73. GC48595 Chenodeoxycholic Acid MaxSpec® Standard A quantitative analytical standard guaranteed to meet MaxSpec® identity, purity, stability, and concentration specifications Chenodeoxycholic Acid MaxSpec® Standard Chemical Structure
  74. GC68212 Chenodeoxycholic acid-13C Chenodeoxycholic acid-13C Chemical Structure
  75. GC47076 Chenodeoxycholic Acid-d4 A quantitative analytical standard guaranteed to meet MaxSpec® identity, purity, stability, and concentration specifications Chenodeoxycholic Acid-d4 Chemical Structure
  76. GC11144 Chlormadinone acetate steroidal progestin with additional antiandrogen and antigonadotropic effects Chlormadinone acetate Chemical Structure
  77. GC10012 Chlorotrianisene Estrogen agonist Chlorotrianisene Chemical Structure
  78. GC45409 Ciclesonide-d7   Ciclesonide-d7 Chemical Structure
  79. GC18212 Cilofexor Cilofexor inhibits binding of a synthetic peptide, comprising residues 676-700 of the steroid receptor coactivator 1 (SRC-1), to the farnesoid X receptor (FXR; EC50 = <25 nM in a FRET activity assay). Cilofexor Chemical Structure
  80. GC17491 CITCO

    Constitutive androstane receptor (CAR) agonist

     CITCO Chemical Structure
  81. 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
  82. GC47097 CJC-1295 A synthetic peptide derivative of GHRH CJC-1295 Chemical Structure
  83. GC14560 Cl-4AS-1 steroidal androgen receptor agonist Cl-4AS-1 Chemical Structure
  84. GC48496 Clobetasol Propionate-d5 An internal standard for the quantification of clobetasol propionate Clobetasol Propionate-d5 Chemical Structure
  85. GC49680 Clobetasone Propionate A corticosteroid Clobetasone Propionate Chemical Structure
  86. GC15366 Clomiphene citrate Selective estrogen receptor modulator Clomiphene citrate Chemical Structure
  87. GC62209 CLP-3094 CLP-3094 is a potent BF3 (binding function 3)-directed inhibitor of the androgen receptor (AR). CLP-3094 Chemical Structure
  88. GC65587 CO23 CO23 is a selective thyroid hormone receptor (TR) α agonist and used for growth and development regulation. CO23 Chemical Structure
  89. GC43312 Cortistatin-29 (1-13) (rat) (trifluoroacetate salt) Cortistatin-29 (1-13) is a neuropeptide and cleavage product of cortistatin-29, which is a cleavage product of procortistatin. Cortistatin-29 (1-13) (rat) (trifluoroacetate salt) Chemical Structure
  90. GC43313 Cortistatin-29 (rat) (trifluoroacetate salt) Cortistatin-29 is a neuropeptide that is structurally similar to somatostatin-28. Cortistatin-29 (rat) (trifluoroacetate salt) Chemical Structure
  91. GC18804 Cosyntropin (acetate) Cosyntropin (acetate) is a synthetic peptide stimulating the release of corticosteroids such as cortisol from the adrenal gland. Cosyntropin (acetate) Chemical Structure
  92. GC10002 Coumestrol competitive binder of the estrogen receptors ERα Coumestrol Chemical Structure
  93. GC45413 Cridanimod (sodium salt)   Cridanimod (sodium salt) Chemical Structure
  94. GC52387 Crosstide (trifluoroacetate salt) A peptide substrate for Akt Crosstide (trifluoroacetate salt) Chemical Structure
  95. GC11535 CTAP Potent and selective μ opioid receptor antagonist CTAP Chemical Structure
  96. GC60730 CTAP TFA CTAP TFA is a potent, highly selective, and BBB penetrant μ opioid receptor antagonist, with an IC50 of 3.5 nM. CTAP TFA Chemical Structure
  97. GC16888 CTOP Potent and selective μ opioid receptor antagonist CTOP Chemical Structure
  98. GC60731 CTOP TFA CTOP TFA is a potent and highly selective μ-opioid receptor antagonist. CTOP TFA Chemical Structure
  99. GC10180 Cyclofenil Non-steroidal selective estrogen receptor modulator (SERM) Cyclofenil Chemical Structure
  100. GC13189 Cyprodime hydrochloride

    μ-opioid receptor antagonist

     Cyprodime hydrochloride Chemical Structure
  101. GC47159 Cyprodinil An anilinopyrimidine fungicide Cyprodinil Chemical Structure

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