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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. GC11282 β-Estradiol

    β-Estradiol, Estradiol, 17β-Oestradiol, E2

    Sex hormone

     β-Estradiol Chemical Structure
  3. GC49838 α-Cortolone

    20α-Cortolone, NSC 59872

     A metabolite of cortisol α-Cortolone Chemical Structure
  4. GC48292 α-MSH (human, mouse, rat, porcine, bovine, ovine) (trifluoroacetate salt)

    α-Melanocyte-stimulating Hormone, Ac-SYSMEHFRWGKPV-NH2

     α-MSH (α-Melanocyte-Stimulating Hormone) TFA, an endogenous neuropeptide, is an endogenous melanocortin receptor 4 (MC4R) agonist with anti-inflammatory and antipyretic activities. α-MSH (human, mouse, rat, porcine, bovine, ovine) (trifluoroacetate salt) Chemical Structure
  5. GC60391 β-Casomorphin, bovine TFA

    β-Casomorphin-7 (bovine) (TFA); Bovine β-casomorphin-7 TFA

     β-Casomorphin, bovine TFA Chemical Structure
  6. GC61484 β-Casomorphin, human TFA

    Human β-casomorphin 7 TFA

     β-Casomorphin, human TFA Chemical Structure
  7. GC45236 β-Endorphin (rat) β-Endorphin (β-EP) is an endogenous opioid neuropeptide with diverse biological activities. β-Endorphin (rat) Chemical Structure
  8. GC52494 β-Endorphin (rat) (trifluoroacetate salt) An opioid neuropeptide β-Endorphin (rat) (trifluoroacetate salt) Chemical Structure
  9. GC38005 β-Endorphin, equine β-Endorphin, equine is an endogenous opioid peptide, which binds at high affinity to both μ/δ opioid receptors. β-Endorphin, equine Chemical Structure
  10. GC38030 β-Endorphin, equine (TFA) β-Endorphin, equine (TFA) Chemical Structure
  11. GC72132 β-Endorphin, equine TFA β-Endorphin, equine TFA is an endogenous opioid peptide, which binds at high affinity to both μ/δ opioid receptors. β-Endorphin, equine TFA Chemical Structure
  12. GC45238 δ14-Triamcinolone acetonide

    14,15-dehydro Triamcinolone acetonide, Triamcinolone acetonide Impurity B

     δ14-Triamcinolone acetonide is a potential impurity found in commercial preparations of triamcinolone acetonide. δ14-Triamcinolone acetonide Chemical Structure
  13. GC45239 δ4-Abiraterone

    CB 7627, D4A

     δ4-Abiraterone is a major metabolite of abiraterone. δ4-Abiraterone is an inhibitor of CYP17A1, 3b-hydroxysteroid dehydrogenase (3βHSD) and steroid-5a-reductase (SRD5A) and also an antagonist of androgen receptor. δ4-Abiraterone Chemical Structure
  14. GC15975 α-Estradiol

    Alfatradiol, α-Estradiol, 17-epi Estradiol, NSC 20293, 17α-Oestradiol

     α-Estradiol is a weak estrogen and a 5α-reductase inhibitor which is used as a topical medication in the treatment of androgenic alopecia. α-Estradiol Chemical Structure
  15. GC33736 β-Casomorphin, bovine (β-Casomorphin-7 (bovine)) β-Casomorphin, bovine (β-Casomorphin-7 (bovine)) (β-Casomorphin-7 (bovine) ) is a opioid peptide with an IC50 of 14 μM in an Opioid receptors binding assay. β-Casomorphin, bovine (β-Casomorphin-7 (bovine)) Chemical Structure
  16. GC33784 β-Casomorphin, human (Human β-casomorphin 7)

    Human β-casomorphin 7

     is an opioid peptide, acts as an agonist of opioid receptor. β-Casomorphin, human (Human β-casomorphin 7) Chemical Structure
  17. GC31117 β-Endorphin, human β-Endorphin, human, a prominent endogenous peptide, existing in the hypophysis cerebri and hypothalamus, is an agonist of opioid receptor, with preferred affinity for μ-opioid receptor and δ-opioid receptor; β-Endorphin, human exhibits antinociception activity. β-Endorphin, human Chemical Structure
  18. GC15938 β-Funaltrexamine hydrochloride

    μ opioid receptor antagonist

     β-Funaltrexamine hydrochloride Chemical Structure
  19. GC45713 (±)-α-Tocopherol Acetate

    all-rac-α-Tocopherol Acetate, DL-α-Tocopherol Acetate, DL-Vitamin E acetate

     (±)-α-Tocopherol Acetate ((±)-Vitamin E acetate), is a orally active synthetic form of vitamin E. (±)-α-Tocopherol Acetate Chemical Structure
  20. GC41671 (±)-Equol 4'-sulfate (sodium salt)

    R,S-Equol 4'-Sulfate

    (±)-Equol 4'-sulfate is a gut-mediated phase II metabolite of the isoflavonoid phytoestrogen (±)-equol.

     (±)-Equol 4'-sulfate (sodium salt) Chemical Structure
  21. GC50708 (±)-ML 209 An RORγt antagonist (±)-ML 209 Chemical Structure
  22. GC64007 (±)-U-50488 hydrate hydrochloride

    (±)-Trans-(1R,2R)-U-50488 hydrate hydrochloride

     (±)-U-50488 hydrate hydrochloride Chemical Structure
  23. GC15885 (±)-U-50488 hydrochloride

    (±)-Trans-(1R,2R)-U-50488 hydrochloride

    κ-opioid receptor agonist, selective

     (±)-U-50488 hydrochloride Chemical Structure
  24. GC34960 (+)-Talarozole (+)-Talarozole is a potent inhibitor of retinoic acid metabolism extracted from patent WO 1997049704 A1. (+)-Talarozole Chemical Structure
  25. GC12688 (+)-U-50488 hydrochloride

    (+)-Trans-(1R,2R)-U-50488 hydrochloride

     Selective κ-opioid agonist (+)-U-50488 hydrochloride Chemical Structure
  26. GC31386 (-)-PX20606 trans isomer ((-)-PX-102 trans isomer) (-)-PX20606 trans isomer ((-)-PX-102 trans isomer) is a FXR agonist with EC50s of 18 and 29 nM for FXR in FRET and M1H assay, respectively. (-)-PX20606 trans isomer ((-)-PX-102 trans isomer) Chemical Structure
  27. GC15944 (-)-U-50488 hydrochloride

    (-)-Trans-(1S,2S)-U-50488 hydrochloride

     κ-opioid receptor agonist, selective (-)-U-50488 hydrochloride Chemical Structure
  28. GC70081 (1R,2R)-U-50488 hydrochloride

    (1R,2R)-U-50488 hydrochloride is the absolute configuration of (±)-U-50488 hydrochloride. (±)-U-50488 hydrochloride is a κ opioid receptor agonist.

     (1R,2R)-U-50488 hydrochloride Chemical Structure
  29. GC34965 (20S)-Protopanaxatriol

    20(S)-APPT, 20(S)-PPT

     An active ginsenoside metabolite (20S)-Protopanaxatriol Chemical Structure
  30. GA20156 (D-Ser(tBu)⁶,Azagly¹⁰)-LHRH (free base) (D-Ser(tBu)⁶,Azagly¹⁰)-LHRH (free base) Chemical Structure
  31. GA20164 (D-Trp¹²,Tyr³⁴)-pTH (7-34) amide (bovine) (D-Trp¹²,Tyr³⁴)-pTH (7-34) amide (bovine) is a potent and competitive antagonist of parathyroid hormone (PTH), with a Ki of 69 nM in bovine renal cortical membrane. (D-Trp¹²,Tyr³⁴)-pTH (7-34) amide (bovine) Chemical Structure
  32. GC15373 (E)-2-Decenoic acid

    trans-2-Decylenic Acid

     An unsaturated fatty acid found in royal jelly (E)-2-Decenoic acid Chemical Structure
  33. GC46336 (E)-Guggulsterone A farnesoid X receptor antagonist (E)-Guggulsterone Chemical Structure
  34. GC49189 (E/Z)-4-hydroxy Tamoxifen-d5

    Afimoxifene-d5, 4-OHT-d5

     An internal standard for the quantification of (E/Z)-4-hydroxy tamoxifen (E/Z)-4-hydroxy Tamoxifen-d5 Chemical Structure
  35. GC40833 (E/Z)-Endoxifen

    (E/Z)-N-desmethyl-4-hydroxy Tamoxifen

     (E/Z)-Endoxifen is an active metabolite of tamoxifen produced by the sequential action of cytochrome P450 (CYP) isoforms, including CYP2D6. (E/Z)-Endoxifen Chemical Structure
  36. GC61491 (R)-Bicalutamide (R)-Bicalutamide is the (R)-enantiomer of Bicalutamide. (R)-Bicalutamide is an androgen receptor (AR) antagonist, with antineoplastic activity. (R)-Bicalutamide is widely used for the research of prostate cancer. (R)-Bicalutamide Chemical Structure
  37. GC13373 (R)-DPN estrogen receptor (ER) β agonist (R)-DPN Chemical Structure
  38. GC30710 (R)-UT-155 (R)-UT-155 (compound 11) is a selective androgen receptor degrader (SARD) ligand. Less active than the S-isomer. (R)-UT-155 Chemical Structure
  39. GC18003 (R,R)-THC ERα receptor agonist (R,R)-THC Chemical Structure
  40. GC52185 (R,S)-Anatabine-d4

    (±)-Anatabine-d4

     (R,S)-Anatabine-d4 Chemical Structure
  41. GC63292 (rac)-PF-998425 (Rac)-PF-998425 is a potent, selective, nonsteroidal androgen receptor (AR) antagonist. (rac)-PF-998425 Chemical Structure
  42. GC69798 (Rac)-SNC80

    (Rac)-NIH 10815

    (Rac)-SNC80 is the racemic form of SNC80. SNC80 (NIH 10815) is an effective and highly selective non-peptide delta-opioid receptor agonist with a Ki of 1.78 nM and IC50 of 2.73 nM. SNC80 has anti-nociceptive, anti-hyperalgesic, and antidepressant-like effects, and can be used in research on various types of headaches.

     (Rac)-SNC80 Chemical Structure
  43. GC49520 (S)-Equol

    4',7Dihydroxyisoflavan, (-)Equol, 4',7Isoflavandiol

    An estrogen receptor β agonist

     (S)-Equol Chemical Structure
  44. GC16372 (Z)-4-Hydroxytamoxifen

    ICI 79280, trans-4-hydroxy Tamoxifen

     (Z)-4-Hydroxytamoxifen is a metabolite of Tamoxifen. (Z)-4-Hydroxytamoxifen shows higher affinity for the ER than Tamoxifen. (Z)-4-Hydroxytamoxifen induces a non-apoptotic cytotoxic effect in human endometrial adenocarcinoma cells. (Z)-4-Hydroxytamoxifen Chemical Structure
  45. 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
  46. GC48787 11β-Hydroxyetiocholanolone

    NSC 53897

     A metabolite of hydrocortisone 11β-Hydroxyetiocholanolone Chemical Structure
  47. GC48710 11-Dehydrocorticosterone

    11-DHC, DHCS, Kendall's Compound A, NSC 9702

     An endogenous mineralocorticoid 11-Dehydrocorticosterone Chemical Structure
  48. GC49161 16α-hydroxy Dehydroepiandrosterone

    16α-hydroxy DHEA

     A metabolite of dehydroepiandrosterone 16α-hydroxy Dehydroepiandrosterone Chemical Structure
  49. GC41950 16α-hydroxy Estrone

    16α-hydroxy E1, 16αOHE1

     The naturally-occurring estrogens are estrone, estradiol, and estriol. 16α-hydroxy Estrone Chemical Structure
  50. GC46456 16α-Hydroxyetiocholanolone A metabolite of 16α-DHEA and androstenedione 16α-Hydroxyetiocholanolone Chemical Structure
  51. GC40454 16(S)-HETE

    16(S)-Hydroxyeicosatetraenoic Acid

     Electrolyte and fluid transport in the kidney are regulated in part by arachidonic acid and its metabolites. 16(S)-HETE Chemical Structure
  52. GC49068 16-Epiestriol

    16-epi Estriol, 16-EpiE3, 16β-hydroxy-17α-Estradiol, NSC 26646

     A metabolite of estrone 16-Epiestriol Chemical Structure
  53. GC49848 16-Ketoestradiol

    16-keto E2, NSC 51169, 16-Oxoestradiol

     An active metabolite of estrone 16-Ketoestradiol Chemical Structure
  54. GC17557 17 alpha-propionate

    CB-03-01

     A peripherally selective androgen receptor antagonist 17 alpha-propionate Chemical Structure
  55. GC41321 17α,20β-Dihydroxy-4-pregnen-3-one

    17α,20β-DHP，17α,20β-dihydroxy Progesterone

     An endogenous, maturation-inducing steroid 17α,20β-Dihydroxy-4-pregnen-3-one Chemical Structure
  56. GC46470 17β-Estradiol-d2

    2,4-Dideuteriostradiol, E2-d2, Estradiol-d2, β-Estradiol-d2, 17β-Oestradiol-d2

     17β-Estradiol-d2 (β-17β-Estradiol-d2) is the deuterium labeled Estradiol. 17β-Estradiol-d2 Chemical Structure
  57. GC41300 17β-hydroxy Exemestane 17β-hydroxy Exemestane is the primary active metabolite of exemestane. 17β-hydroxy Exemestane Chemical Structure
  58. GC48819 17-Epiestriol

    16α-hydroxy-17α-Estradiol, 16α,17α-Estriol, 17α-Estriol, 17-epi-Estriol, NSC 84051

     A metabolite of estrone 17-Epiestriol Chemical Structure
  59. GC17475 17-Hydroxyprogesterone

    NSC 15468, 17-OHP, 17-hydroxy Progesterone

     An endogenous progestogen and chemical intermediate 17-Hydroxyprogesterone Chemical Structure
  60. GC18635 18-hydroxy-11-deoxy Corticosterone

    18-Hydroxydeoxycorticosterone, 18-OH-DOC

     18-hydroxy-11-deoxy Corticosterone (18-OH-DOC) is a mineralocorticoid secreted by the zona fasciculata of the adrenal gland. 18-hydroxy-11-deoxy Corticosterone Chemical Structure
  61. GC35069 2,2,5,7,8-Pentamethyl-6-Chromanol 2,2,5,7,8-Pentamethyl-6-Chromanol (PMC) is the anti-oxidant moiety of vitamin E (α-tocopherol). 2,2,5,7,8-Pentamethyl-6-Chromanol has potent androgen receptor (AR) signaling modulation and anti-cancer activity against prostate cancer cell lines. 2,2,5,7,8-Pentamethyl-6-Chromanol Chemical Structure
  62. GC49671 2,3-Oxidosqualene

    (3R,S)-Oxidosqualene, Squalene 2,3-oxide

     An intermediate in the biosynthesis of sterols 2,3-Oxidosqualene Chemical Structure
  63. GC66679 2,6-Dimethyl-L-tyrosine

    Dmt

     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
  64. GC49609 2-bromo 17β-Estradiol

    2-bromo E2, 2-bromo β-Estradiol, 2-bromo Estradiol, NSC 105460, 2-bromo 17β-Oestradiol

     A synthetic steroid and inhibitor of estrogen 2-hydroxylase 2-bromo 17β-Estradiol Chemical Structure
  65. GC49172 2-hydroxy Estrone

    Catecholestrone, 2-hydroxy E1, 2-OHE1

     An active metabolite of estrone 2-hydroxy Estrone Chemical Structure
  66. GC17160 2-hydroxy Flutamide

    Hydroxyniphtholide,SCH 16423

     2-hydroxy Flutamide (HF), an active metabolite of Flutamide, is a potent androgen receptor antagonist (IC50=700 nM). 2-hydroxy Flutamide can be used for the research of prostate cancer. 2-hydroxy Flutamide Chemical Structure
  67. GC48910 2-Hydroxyanthraquinone

    2-hydroxy-9,10-Anthraquinone, 2-hATQ, β-Hydroxyanthraquinone, NSC 2595

     An anthraquinone with antibacterial and estrogenic activities 2-Hydroxyanthraquinone Chemical Structure
  68. GC40960 20α-dihydro Prednisolone

    20α-DHP, 20α-dihydro-PRED, 20(R)-hydroxy Prednisolone, 20α-hydroxy Prednisolone

     20α-dihydro Prednisolone is a metabolite of prednisolone. 20α-dihydro Prednisolone Chemical Structure
  69. GC46526 21-Deoxycortisol

    21-Dehydrohydrocortisone

     A corticosteroid metabolite of 17-hydroxyprogesterone 21-Deoxycortisol Chemical Structure
  70. GC49611 21-Deoxycortisol-d8

    21-Dehydrohydrocortisone-d8

     An internal standard for the quantification of 21-deoxycortisol 21-Deoxycortisol-d8 Chemical Structure
  71. GC52083 21-Deoxycortisone

    21-Desoxycortisone, NSC 38722

     A corticosteroid metabolite of 11-keto progesterone 21-Deoxycortisone Chemical Structure
  72. GC40968 21-hydroxy Eplerenone 21-hydroxy Eplerenone is a major metabolite of the mineralocorticoid receptor antagonist eplerenone. 21-hydroxy Eplerenone Chemical Structure
  73. GC14972 22(R)-hydroxy Cholesterol

    Narthesterol

     endogenous agonist for LXRs 22(R)-hydroxy Cholesterol Chemical Structure
  74. GC18270 22(S)-hydroxy Cholesterol

    22β-hydroxy Cholesterol

     A synthetic oxysterol and LXR modulator 22(S)-hydroxy Cholesterol Chemical Structure
  75. GC17827 24(R)-hydroxy Cholesterol

    24-Epicerebrosterol

    LXRα and LXRβ nuclear receptors activator

     24(R)-hydroxy Cholesterol Chemical Structure
  76. GC40571 24(S),25-epoxy Cholesterol

    24(S)-24,25-EC

    24(S),25-epoxy Cholesterol is an oxysterol and the most abundant oxysterol in mouse ventral midbrain.

     24(S),25-epoxy Cholesterol Chemical Structure
  77. GC18076 24(S)-hydroxy Cholesterol

    Cerebrosterol

    LXRα and LXRβ nuclear receptors activator

     24(S)-hydroxy Cholesterol Chemical Structure
  78. GC33673 24-Hydroxycholesterol 24-Hydroxycholesterol is a natural sterol, which serves as a positive allosteric modulator of N-Methyl-d-Aspartate (NMDA) receptorsR, and a potent activator of the transcription factors LXR. 24-Hydroxycholesterol Chemical Structure
  79. GC13431 24α-methyl Cholesterol

    Campesterol,NSC 224330

     24α-methyl Cholesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects. 24α-methyl Cholesterol Chemical Structure
  80. GC13887 25(R)-27-hydroxy Cholesterol

    (25R)-26-hydroxy cholesterol

     25(R)-27-hydroxy Cholesterol is a selective estrogen receptor modulator and an agonist of the liver X receptor. 25(R)-27-hydroxy Cholesterol Chemical Structure
  81. GC11700 25(S)-27-hydroxy Cholesterol

    (25S)-26-hydroxy cholesterol

     liver x receptors (LXRα and LXRβ) activator 25(S)-27-hydroxy Cholesterol Chemical Structure
  82. GC10384 3,3',5'-Triiodo-L-thyronine

    Reverse T3,rT3,3,3’,5’-T3

     3,3',5'-Triiodo-L-thyronine is a thyroid hormone generated by deiodination of the prohormone thyroxine. 3,3',5'-Triiodo-L-thyronine Chemical Structure
  83. GC48395 3,3',5-Triiodo-L-thyronine (sodium salt hydrate)

    Liothyronine, T3, L3,3',5Triiodothyronine

     3,3',5-Triiodo-L-thyronine (sodium salt hydrate) is an active form of thyroid hormone. 3,3',5-Triiodo-L-thyronine (sodium salt hydrate) Chemical Structure
  84. GC12791 3,3'-Diindolylmethane

    DIM

     A phytochemical with antiradiation and chemopreventative effects 3,3'-Diindolylmethane Chemical Structure
  85. GC49427 3,5-Diiodo-L-thyronine

    3,5-Diiodothyronine, NSC 90469, 3,5-T2

     3,5-Diiodo-L-thyronine is an endogenous metabolite. 3,5-Diiodo-L-thyronine Chemical Structure
  86. GC18205 3,5-Diiodothyroacetic Acid

    Diac, NSC 90463, T2A, TA2

     3,5-Diiodothyroacetic acid (diac) is the acetic acid variant of thyroxine. 3,5-Diiodothyroacetic Acid Chemical Structure
  87. GC18696 3,5-Diiodothyropropionic Acid

    DITPA

     3,5-Diiodothyropropionic acid (DITPA) is an inotropic thyroid hormone analogue of L-thyroxine that binds to the thyroid hormone receptors TRα and TRβ (Kas = 2.4 and 4.06 x 107 M-1, respectively, for human recombinant receptors). 3,5-Diiodothyropropionic Acid Chemical Structure
  88. GC52129 3-Amino-5-hydroxybenzoic Acid

    AHBA

     3-Amino-5-hydroxybenzoic Acid Chemical Structure
  89. GC49180 3-epi-25-hydroxy Vitamin D3

    3-epi-25(OH)D3, 3-epi-25-hydroxy Cholecalciferol

     The C-3 epimer of 25-hydroxy vitamin D3 3-epi-25-hydroxy Vitamin D3 Chemical Structure
  90. GC18462 3-Formylsalicylic Acid

    NSC 55753

     3-Formylsalicylic acid is a non-competitive inhibitor of estrone sulfatase (IC50 = 150 nM; Ki = 120 nM), the enzyme that converts estrone sulfate to estrone. 3-Formylsalicylic Acid Chemical Structure
  91. GC42294 3-Iodothyronamine (hydrochloride)

    T1AM

     3-Iodothyronamine is derived from the deiodination and decarboxylation of endogenous thyroxine. 3-Iodothyronamine (hydrochloride) Chemical Structure
  92. GC48824 4-hydroxy Estrone

    4-hydroxy E1, 4-OHE1

     A metabolite of estrone 4-hydroxy Estrone Chemical Structure
  93. GC17803 4-Hydroxytamoxifen

    Afimoxifene, 4-OHT

     4-Hydroxytamoxifen (Afimoxifene) is a racemic compound of (Z)-4-Hydroxytamoxifen and (E)-4-Hydroxytamoxifen isomers. 4-Hydroxytamoxifen is an estrogen receptor modulator. 4-Hydroxytamoxifen Chemical Structure
  94. GC49562 4-methoxy Estrone

    4-MeOE1, 4-methoxy E1

     An active metabolite of estrone 4-methoxy Estrone Chemical Structure
  95. GC11606 4-Methylbenzylidene camphor

    Enzacamene|Eusolex 6300|4-MBC|Neo Heliopan MBC|Parsol 500|Uvinul MBC 95

     ultraviolet light blocker used in cosmetics and sunscreen preparations that also has estrogenic activities. 4-Methylbenzylidene camphor Chemical Structure
  96. GC42473 4-tert-Octylphenol diethoxylate

    OP2EO

     4-tert-Octylphenol diethoxylate is a degradation product of the multi-purpose surfactant, Triton X. 4-tert-Octylphenol diethoxylate Chemical Structure
  97. GC52365 4-tert-Octylphenol monoethoxylate

    NSC 5259, OP1EO

     An alkylphenolethoxylate and a degradation product of non-ionic surfactants 4-tert-Octylphenol monoethoxylate Chemical Structure
  98. GC13917 4’-hydroxy Tamoxifen metabolite of tamoxifen, an estrogen receptor modulator 4’-hydroxy Tamoxifen Chemical Structure
  99. GC40053 5α,6α-epoxy Cholestanol

    NSC 18176

     An oxysterol and a metabolite of cholesterol produced by oxidation 5α,6α-epoxy Cholestanol Chemical Structure
  100. GC42569 5α-Androst-16-en-3-one

    Androstenone

     5α-Androst-16-en-3-one is a mammalian pheromone released as a volatile chemical cue in boar saliva to facilitate social and sexual interactions. 5α-Androst-16-en-3-one Chemical Structure
  101. GC49542 5α-Androstan-3β-ol

    NSC 50887

     A steroidal androgen 5α-Androstan-3β-ol Chemical Structure

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