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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. GC43213 CCK (26-30) (sulfated)

    N-Acetyl Cholecystokinin (26-30)

     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
  3. GC43214 CCK (26-31) (non-sulfated)

    N-Acetyl Cholecystokinin (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
  4. GC18553 CCK (26-31) (sulfated)

    N-Acetyl Cholecystokinin (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
  5. GC18384 CCK (27-33) (non-sulfated)

    Cholecystokinin (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
  6. GC43215 CCK Octapeptide (non-sulfated), (trifluoroacetate salt)

    Cholecystokinin Octapeptide (26-33), Pancreozymin (C-terminal) Octapeptide, SQ 19,265

     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
  7. GC11794 CD 1530 RAR receptor agonist CD 1530 Chemical Structure
  8. GC10080 CD 2314 RARβ agonist,potent and selective CD 2314 Chemical Structure
  9. GC12072 CD 2665 Selective RARβ/γ antagonist CD 2665 Chemical Structure
  10. GC17730 CD 3254 RXRα agonist,potent and selective CD 3254 Chemical Structure
  11. GC11464 CD 437

    CD437

     RARγ-selective agonist,potent and cell-permeable CD 437 Chemical Structure
  12. GC35637 Cebranopadol

    GRT6005

     An analgesic NOP and opioid receptor agonist Cebranopadol Chemical Structure
  13. GC35638 Cebranopadol ((1α,4α)stereoisomer)

    GRT6005 (1α,4α)stereoisomer

     Cebranopadol ((1α,4α)stereoisomer) is a stereoisomer of cebranopadol. Cebranopadol ((1α,4α)stereoisomer) Chemical Structure
  14. GC19229 CERC-501

    CERC-501, JNJ-67953964, LY2456302

     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
  15. GC33467 Cetrorelix Acetate (SB-075 acetate)

    SB-75

     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
  16. 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
  17. GC11053 Ch 55 RAR agonist Ch 55 Chemical Structure
  18. GC17985 Chenodeoxycholic Acid

    CDCA

     nuclear receptors(FXR) activator Chenodeoxycholic Acid Chemical Structure
  19. GC48424 Chenodeoxycholic Acid 24-Acyl-β-D-Glucuronide

    CDCA-24G, CDCA-24-glucuronide

     A metabolite of CDCA Chenodeoxycholic Acid 24-Acyl-β-D-Glucuronide Chemical Structure
  20. GC49853 Chenodeoxycholic Acid 3-Glucuronide

    CDCA-3G, CDCA-3-Glucuronide

     A metabolite of CDCA Chenodeoxycholic Acid 3-Glucuronide Chemical Structure
  21. GC68212 Chenodeoxycholic acid-13C

    CDCA-13C

     Chenodeoxycholic acid-13C Chemical Structure
  22. GC47076 Chenodeoxycholic Acid-d4

    CDCA-d4

     A quantitative analytical standard guaranteed to meet MaxSpec® identity, purity, stability, and concentration specifications Chenodeoxycholic Acid-d4 Chemical Structure
  23. GC11144 Chlormadinone acetate

    NSC 92338

     steroidal progestin with additional antiandrogen and antigonadotropic effects Chlormadinone acetate Chemical Structure
  24. GC10012 Chlorotrianisene

    NSC 10108, TACE, Tri-p-anisylchloroethylene

     Estrogen agonist Chlorotrianisene Chemical Structure
  25. GC45409 Ciclesonide-d7

    CIC-d7

       Ciclesonide-d7 Chemical Structure
  26. GC18212 Cilofexor

    GS-9674

     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
  27. GC47090 Cinacalcet-d3 (hydrochloride)

    AMG 073-d3

     A neuropeptide with diverse biological activities Cinacalcet-d3 (hydrochloride) Chemical Structure
  28. GC17491 CITCO

    Constitutive androstane receptor (CAR) agonist

     CITCO Chemical Structure
  29. GC52351 Citrullinated α-Enolase (R8 + R14) (1-19)-biotin Peptide

    Citrullinated Enolase-1-biotin, α-Enolase Peptide (Citrulline Residues 8 + 14)

     A biotinylated and citrullinated α-enolase peptide Citrullinated α-Enolase (R8 + R14) (1-19)-biotin Peptide Chemical Structure
  30. GC47097 CJC-1295

    Modified GRF (1-29), CJC-1295-no DAC, GHRH (1-29)-NH2

     A synthetic peptide derivative of GHRH CJC-1295 Chemical Structure
  31. GC14560 Cl-4AS-1 steroidal androgen receptor agonist Cl-4AS-1 Chemical Structure
  32. GC48496 Clobetasol Propionate-d5

    CCI-4725-d5, CGP 9555-d5, Clobetasol 17-propionate-d5

     An internal standard for the quantification of clobetasol propionate Clobetasol Propionate-d5 Chemical Structure
  33. GC49680 Clobetasone Propionate

    Clobetasone 17-Propionate

     A corticosteroid Clobetasone Propionate Chemical Structure
  34. GC15366 Clomiphene citrate

    Clomifene, Omifin, NSC 35770

     Selective estrogen receptor modulator Clomiphene citrate Chemical Structure
  35. GC62209 CLP-3094 CLP-3094 is a potent BF3 (binding function 3)-directed inhibitor of the androgen receptor (AR). CLP-3094 Chemical Structure
  36. GC65587 CO23 CO23 is a selective thyroid hormone receptor (TR) α agonist and used for growth and development regulation. CO23 Chemical Structure
  37. GC43310 Corticostatin (human) (trifluoroacetate salt)

    DEFA4 Protein, α-Defensin 4, Defensin HNP-4, Human Neutrophil Peptide 4, Neutrophil Defensin 4

     Corticostatin is a corticostatic peptide that has been found in human granulocytes. Corticostatin (human) (trifluoroacetate salt) Chemical Structure
  38. GC60725 Cortisone

    17α-hydroxy-11-Dehydrocorticosterone, Kendall’s Compound E, 4-Pregnene-17α,21-diol-3,11,20-trione, Reichstein’s Substance Fa

     A precursor and metabolite of cortisol Cortisone Chemical Structure
  39. 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
  40. 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
  41. GC18804 Cosyntropin (acetate)

    ACTH (1-24), Adrenocorticotropic Hormone 1-24, Tetracosactide

     Cosyntropin (acetate) is a synthetic peptide stimulating the release of corticosteroids such as cortisol from the adrenal gland. Cosyntropin (acetate) is currently used for the research of ulcerative colitis and Crohn's disease, juvenile/adult rheumatoid arthritis and osteoarthrosis. Cosyntropin (acetate) Chemical Structure
  42. GC10002 Coumestrol

    NSC 22842

     competitive binder of the estrogen receptors ERα Coumestrol Chemical Structure
  43. GC45413 Cridanimod (sodium salt)

    10-Carboxymethyl-9-Acridanone

       Cridanimod (sodium salt) Chemical Structure
  44. GC52387 Crosstide (trifluoroacetate salt)

    Gly-Arg-Pro-Arg-Thr-Ser-Ser-Phe-Ala-Glu-Gly-OH, GRPRTSSFAEG-OH

     A peptide substrate for Akt Crosstide (trifluoroacetate salt) Chemical Structure
  45. GC11535 CTAP Potent and selective μ opioid receptor antagonist CTAP Chemical Structure
  46. 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
  47. GC16888 CTOP Potent and selective μ opioid receptor antagonist CTOP Chemical Structure
  48. GC60731 CTOP TFA CTOP TFA is a potent and highly selective μ-opioid receptor antagonist. CTOP TFA Chemical Structure
  49. GC10180 Cyclofenil

    ICI 48213, NSC 86464

     Non-steroidal selective estrogen receptor modulator (SERM) Cyclofenil Chemical Structure
  50. GC91460 CYN 154806 (trifluoroacetate salt)

    Ac-4NO2-Phe-c(D-Cys-Tyr-D-Trp-Lys-Thr-Cys)-D-Tyr-NH2

     CYN 154806 is a cyclic peptide somatostatin receptor 2 (SST2) antagonist (IC50 = 2.62 nM). CYN 154806 (trifluoroacetate salt) Chemical Structure
  51. GC13189 Cyprodime hydrochloride

    μ-opioid receptor antagonist

     Cyprodime hydrochloride Chemical Structure
  52. GC47159 Cyprodinil An anilinopyrimidine fungicide Cyprodinil Chemical Structure
  53. GC13971 Cyproterone Acetate

    CPA, Cyprostat, NSC 81430, SH 714

     Androgen receptor antagonist Cyproterone Acetate Chemical Structure
  54. GC17677 DADLE

    D-Ala2, D-Leu5-Enkephalin

     δ-opioid receptor agonist DADLE Chemical Structure
  55. GC47168 Daidzein-d4 An internal standard for the quantification of daidzein Daidzein-d4 Chemical Structure
  56. GC72209 DALDA acetate DALDA acetate is a potent and highly selective μ-opioid receptor agonist with a Ki of 1.69 nM. DALDA acetate Chemical Structure
  57. GC10803 DAMGO μ opioid receptor agonist DAMGO Chemical Structure
  58. 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
  59. GC10785 Danazol

    Danocrine,Ladogal,NSC 270916,WIN 17,757

     A derivative of testosterone and ethisterone Danazol Chemical Structure
  60. GC35828 Degarelix Degarelix is a competitive and reversible gonadotropin-releasing hormone receptor (GnRHR/LHRHR) antagonist. Degarelix Chemical Structure
  61. GC18556 Degarelix (acetate)

    FE 200486

     Degarelix is a synthetic gonadotropin-releasing hormone receptor (GNRHR) antagonist (IC50 = 3 nM in HEK293 cells expressing the human receptor). Degarelix (acetate) Chemical Structure
  62. GC11070 Dehydroepiandrosterone (DHEA)

    Androstenolone, trans-Dehydroandrosterone, DHEA, Diandrone, NSC 9896, Prasterone, Psicosterone

     Dehydroepiandrosterone (DHEA) and its sulfate ester, DHEAS, together represent the most abundant steroid hormones in the human body . Dehydroepiandrosterone (DHEA) Chemical Structure
  63. 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
  64. GC61954 Deltorphin 2 TFA

    [D-Ala2]-Deltorphin II TFA

     Deltorphin 2 TFA is a selective peptide agonist for the δ opioid receptor. Deltorphin 2 TFA Chemical Structure
  65. GC12143 Deltorphin I

    Deltorphin 1; Deltorphin C

     δ-opioid receptor agonist Deltorphin I Chemical Structure
  66. GC90700 Dendrogenin A

    A selective LXR modulator and ChEH inhibitor

     Dendrogenin A Chemical Structure
  67. GC31168 Dermorphin

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

     Dermorphin Chemical Structure
  68. GC34223 Dermorphin Analog Dermorphin Analog is an analog of Dermorphin. Dermorphin Analog Chemical Structure
  69. GC49143 Deslorelin (acetate)

    D-Trp6-Pro9-des-Gly10-GnRH ethylamide, pGlu-His-Trp-Ser-Tyr-D-Trp-Leu-Arg-Pro-NHEt

     A peptide agonist of GnRH Deslorelin (acetate) Chemical Structure
  70. GC49459 Desmopressin (trifluoroacetate salt)

    Adiuretin, DDAVP

     A vasopressin receptor agonist Desmopressin (trifluoroacetate salt) Chemical Structure
  71. GC49025 Desogestrel-13C2-d2 An internal standard for the quantification of desogestrel Desogestrel-13C2-d2 Chemical Structure
  72. GC47198 Desoximetasone-d3

    17-deoxy Dexamethasone-d3

     A neuropeptide with diverse biological activities Desoximetasone-d3 Chemical Structure
  73. GC31639 Dexamethasone (Hexadecadrol) An acetate form of dexamethasone Dexamethasone (Hexadecadrol) Chemical Structure
  74. GC47202 Dexamethasone-d4 A neuropeptide with diverse biological activities Dexamethasone-d4 Chemical Structure
  75. GC17688 Diarylpropionitrile(DPN)

    diarylpropionitrile

     Diarylpropionitrile(DPN) (Diarylpropionitrile) is a non-steroidal estrogen receptor β (ERβ) selective ligand, with an EC50 of 0.85 nM. Diarylpropionitrile(DPN) Chemical Structure
  76. GP10126 Diazepam-Binding Inhibitor Fragment, human

    H2N-Gln-Ala-Thr-Val-Gly-Asp-Ile-Asn-Thr-Glu-Arg-Pro-Gly-Met-Leu-Asp-Phe-Thr-Gly-Lys-OH

    Diazepam-Binding Inhibitor (DBI) Fragment is encoded by the DBI gene in human. Diazepam-Binding Inhibitor Fragment, human Chemical Structure
  77. GC15578 Dienogest

    STS 557

     Orally active synthetic progesterone Dienogest Chemical Structure
  78. GC47215 Dienogest-d8 An internal standard for the quantification of dienogest Dienogest-d8 Chemical Structure
  79. GC40867 Diflorasone Diacetate

    U-34865

     Diflorasone is a corticosteroid with anti-inflammatory activity. Diflorasone Diacetate Chemical Structure
  80. GC10663 Dihydrodaidzein

    (±)-Dihydrodaidzein,4',7-dihydroxy Isoflavanone

     estrogen receptor agonist Dihydrodaidzein Chemical Structure
  81. GC47231 Dimethomorph A morpholine fungicide Dimethomorph Chemical Structure
  82. GC17553 DIPPA hydrochloride κ receptor antagonist DIPPA hydrochloride Chemical Structure
  83. 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
  84. GC50178 DPC AJ1951 Potent parathyroid hormone (PTH) receptor agonist DPC AJ1951 Chemical Structure
  85. 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
  86. GC69007 DPC-AJ1951 TFA

    DPC-AJ1951 TFA is a peptide containing 14 amino acids that can act as an effective agonist for the parathyroid hormone (PTH)/PTH-related peptide receptor (PPR) and has been shown to have effects in both in vitro and in vivo bone resorption assays.

     DPC-AJ1951 TFA Chemical Structure
  87. GC10333 DPDPE Prototypical selective δ-opioid receptor agonist peptide DPDPE Chemical Structure
  88. GC63431 DPDPE TFA DPDPE TFA, an opioid peptide, is a selective δ-opioid receptor?(DOR) agonist?with anticonvulsant effects. DPDPE TFA Chemical Structure
  89. GC12379 Drospirenone

    1,2-dihydro Spirorenone, ZK 30595

     Synthetic progestin Drospirenone Chemical Structure
  90. GC52420 Drospirenone-13C3

    1,2-dihydro Spirorenone-13C3, ZK 30595-13C3

     An internal standard for the quantification of drospirenone Drospirenone-13C3 Chemical Structure
  91. GC64301 DS08210767 DS08210767 is a highly potent, orally bioavailable PTHR1 antagonist with IC50 of 90 nM. DS08210767 Chemical Structure
  92. GC73163 DS69910557 DS69910557 is a potent, selective and orally activehuman paratroid hormone receptor 1 (hPTHR1) antagonist. DS69910557 Chemical Structure
  93. GC14774 DSLET δ Opioid receptor agonist DSLET Chemical Structure
  94. GC10893 Dutasteride 5-alpha-reductase inhibitor Dutasteride Chemical Structure
  95. GC13546 Dynorphin A Endogenous kappa receptor agonist Dynorphin A Chemical Structure
  96. GC35917 Dynorphin A (1-10) TFA Dynorphin A (1-10) TFA Chemical Structure
  97. 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
  98. 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
  99. GC15078 Dynorphin B

    Dynorphin B-13, Rimorphin

     endogenous agonist for the kappa opioid receptor Dynorphin B Chemical Structure
  100. 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
  101. GC11676 EC 23

    AGN 190205, BASF 46928

     retinoic acid receptors agonist EC 23 Chemical Structure

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