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
- 5-alpha Reductase(8)
- Smoothened Receptors(3)
- Androgen Receptor(141)
- Aromatase(12)
- CRTH2(2)
- Estrogen/progestogen Receptor(163)
- GnRH(26)
- Opioid Receptor(176)
- RAAS(7)
- Thyroid hormone Receptor(62)
- TRH(1)
- ROR/RAR/RXR(92)
- FXR & LXR(82)
- Glucocorticoids & Mineralocorticoids(66)
- GPR(1)
- Androgen/Estrogen Receptor Modulators(1)
Products for Endocrinology and Hormones
- Cat.No. Product Name Information
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GC31762
Asimadoline (EMD-61753)
EMD 61753
Asimadoline (EMD-61753) (EMD-61753) is an orally active, selective and peripherally active κ-opioid agonist with IC50s of 5.6 nM (guinea pig) and 1.2 nM (human recombinant). - GC61397 Asimadoline hydrochloride Asimadoline (EMD-61753) hydrochloride is an orally active, selective and peripherally active κ-opioid agonist with IC50s of 5.6 nM (guinea pig) and 1.2 nM (human recombinant).
- GC46892 ATRA-BA Hybrid A prodrug form of all-trans retinoic acid and butyric acid
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GC66207
Atraric acid
Methyl atrarate
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. -
GC42870
Atrazine Mercapturate
ATR Mercapturate
Atrazine mercapturate is a major, glutathione-derived metabolite of atrazine, an herbicide that is effective in controlling a broad range of weeds. - GC49321 AZ-GHS-22 An inverse agonist of GHS-R1a
- GC32801 AZ876 An LXR agonist
- GC12434 AZD1981 CRTh2 antagonist,potent and selective
- GC10372 AZD3514 Androgen receptor downregulator
- GC14405 AZD9496 estrogen receptor inhibitor, orally active
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GC11390
BAM 22P
Bovine adrenal medulla-22P
Potent endogenous agonist peptide for the newly identified sensory neuron specific receptor (SNSR); - GC15926 BAN ORL 24 A nociceptin receptor antagonist
- GC30565 BAR502 A dual agonist of GP-BAR1 and FXR
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GC17588
Bavachin
Corylifolin
estrogen receptors ERα and ERβ activator - GC14883 Bazedoxifene
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GC10852
Bazedoxifene acetate
TSE 424
A selective estrogen receptor modulator - 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.
- GC49757 Bazedoxifene N-oxide An oxidative degradation product of bazedoxifene
- GC46907 Bazedoxifene-d4 An internal standard for the quantification of bazedoxifene
- GC46909 BE-26263 A fungal metabolite
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GP10051
Beta-Lipotropin (1-10), porcine
H2N-Glu-Leu-Ala-Gly-Ala-Pro-Pro-Glu-Pro-Ala-OH
Morphine-like substance
-
GC20142
Beta-Sitosterol (purity>98%)
β-Sitosterol (purity>98%); 22,23-Dihydrostigmasterol (purity>98%))
-
GC52329
Betamethasone-d5
β-Methasone-d5, SCH 4831-d5
An internal standard for the quantification of betamethasone -
GC30639
Bevenopran (CB-5945)
CB-5945; ADL-5945
Bevenopran (CB-5945) is a peripheral μ-opioid receptor antagonist. -
GC10037
Bexarotene
LG 100069, LGD 1069, Ro 264455, SR 11247
Retinoid Receptor agonist -
GC46923
Bexarotene-d4
LGD1069 D4
A neuropeptide with diverse biological activities -
GC12271
Bicalutamide
ICI 176334, ZD 176334
Androgen receptor antagonist - GC46925 Bicalutamide-d4 An internal standard for the quantification of bicalutamide
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GC31577
Bifluranol (BX341)
BX341
Bifluranol (BX341) (BX341) is an anti-androgen. - 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.
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GC42943
Bischloroanthrabenzoxocinone
BABX, (―)-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. -
GC11504
BMS 195614
BMS 614
BMS 195614 (BMS 614) is a neutral RARα-selective antagonist with a Ki of 2.5 nM. - GC49654 BMS 270394 A RARγ agonist
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GC10656
BMS 453
BMS 189453
RAR agonist -
GC15648
BMS 493
BMS 204493
Pan-RAR inverse agonist - GC14185 BMS 753 RARα-selective agonist
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GC17382
BMS 961
BMS 961
Selective RARγ agonist - 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.
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GC31372
BMS-779788 (EXEL04286652)
EXEL04286652; XL-652; BMS-788
BMS-779788 (EXEL04286652) is a LXR partial agonist with IC50 values of 68 nM for LXRα and 14 nM for LXRβ. -
GC68785
BMS-986121
BMS-986121 is a positive allosteric modulator (PAM) of the μ opioid receptor, derived from patent WO2014107344. BMS-986121 is built on a chemical scaffold and represents a new chemical type of μ receptor PAMs.
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GC68781
BMS641
BMS-209641
BMS641 (BMS-209641) is a selective RARβ agonist. BMS641 has 100 times higher affinity for RARβ (Kd, 2.5 nM) than for RARα (Kd, 225 nM) or RARγ (Kd, 223 nM).
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GA20967
Boc-D-His-OH
N-(tert-Butoxycarbonyl)-D-histidine, N-(t-Butoxycarbonyl)-D-histidine, Nα-tert-Butoxycarbonyl-D-histidine
An amino acid building block - GA20972 Boc-D-Leu-OSu An amino acid-containing building block
- GC41187 Boldenone Cypionate Boldenone is an anabolic androgenic steroid and synthetic derivative of testosterone that was originally developed for veterinary use.
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GC35541
Boldenone Undecylenate
Boldenone 10-Undecenoate
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GC46941
Bombesin (trifluoroacetate salt)
Glp-Gln-Arg-LeuGly-Asn-GlnTrp-Ala-ValGly-His-LeuMet-NH2
A neuropeptide with diverse biological activities - 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.
- GC15313 BRL 52537 hydrochloride κ/μ opioid receptor agonist,potent and selective
- GC46956 Budesonide-d8 An internal standard for the quantification of budesonide
- GC34099 Buserelin Acetate
- GC46104 Butyric Acid-d7 An internal standard for the quantification of sodium butyrate
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GC16521
BW 373U86
SNC86
Non-peptide delta agonist,potent and selective -
GC43127
Calcitonin (salmon) (trifluoroacetate salt)
Calcitonin (1-32) (salmon), Salcatonin, sCT, Thyrocalcitonin (salmon)
Calcitonin is a peptide hormone that lowers blood calcium level and inhibits bone resorption. -
GC16978
Candesartan
Candesartan M1, CV-11974
Angiotensin II receptor 1 (AT1) antagonist -
GC16223
Captopril
SA 333, SQ 14,225
An ACE inhibitor -
GC43140
Captopril Disulfide
SQ 14,551
Captopril disulfide is a metabolite and symmetrical disulfide form of the angiotensin converting enzyme (ACE) inhibitor captopril. - GC48348 Carbetocin (acetate) A peptide oxytocin receptor agonist
- GC48426 CAY10771 A dual agonist of FXR and PPARδ
- GC67907 CCG258747
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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. -
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. -
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. -
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. -
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. - GC11794 CD 1530 RAR receptor agonist
- GC10080 CD 2314 RARβ agonist,potent and selective
- GC12072 CD 2665 Selective RARβ/γ antagonist
- GC17730 CD 3254 RXRα agonist,potent and selective
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GC11464
CD 437
CD437
RARγ-selective agonist,potent and cell-permeable -
GC35637
Cebranopadol
GRT6005
An analgesic NOP and opioid receptor agonist -
GC35638
Cebranopadol ((1α,4α)stereoisomer)
GRT6005 (1α,4α)stereoisomer
Cebranopadol ((1α,4α)stereoisomer) is a stereoisomer of cebranopadol. -
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. -
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. - 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.
- GC11053 Ch 55 RAR agonist
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GC17985
Chenodeoxycholic Acid
CDCA
nuclear receptors(FXR) activator -
GC48424
Chenodeoxycholic Acid 24-Acyl-β-D-Glucuronide
CDCA-24G, CDCA-24-glucuronide
A metabolite of CDCA -
GC49853
Chenodeoxycholic Acid 3-Glucuronide
CDCA-3G, CDCA-3-Glucuronide
A metabolite of CDCA -
GC48595
Chenodeoxycholic Acid MaxSpec® Standard
CDCA
A quantitative analytical standard guaranteed to meet MaxSpec® identity, purity, stability, and concentration specifications -
GC68212
Chenodeoxycholic acid-13C
CDCA-13C
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GC47076
Chenodeoxycholic Acid-d4
CDCA-d4
A quantitative analytical standard guaranteed to meet MaxSpec® identity, purity, stability, and concentration specifications -
GC11144
Chlormadinone acetate
NSC 92338
steroidal progestin with additional antiandrogen and antigonadotropic effects -
GC10012
Chlorotrianisene
NSC 10108, TACE, Tri-p-anisylchloroethylene
Estrogen agonist -
GC45409
Ciclesonide-d7
CIC-d7
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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). -
GC17491
CITCO
Constitutive androstane receptor (CAR) agonist
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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 -
GC47097
CJC-1295
Modified GRF (1-29), CJC-1295-no DAC, GHRH (1-29)-NH2
A synthetic peptide derivative of GHRH - GC14560 Cl-4AS-1 steroidal androgen receptor agonist
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GC48496
Clobetasol Propionate-d5
CCI-4725-d5, CGP 9555-d5, Clobetasol 17-propionate-d5
An internal standard for the quantification of clobetasol propionate -
GC49680
Clobetasone Propionate
Clobetasone 17-Propionate
A corticosteroid -
GC15366
Clomiphene citrate
Clomifene, Omifin, NSC 35770
Selective estrogen receptor modulator - GC62209 CLP-3094 CLP-3094 is a potent BF3 (binding function 3)-directed inhibitor of the androgen receptor (AR).
- GC65587 CO23 CO23 is a selective thyroid hormone receptor (TR) α agonist and used for growth and development regulation.
- 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.
- GC43313 Cortistatin-29 (rat) (trifluoroacetate salt) Cortistatin-29 is a neuropeptide that is structurally similar to somatostatin-28.
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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. -
GC10002
Coumestrol
NSC 22842
competitive binder of the estrogen receptors ERα -
GC45413
Cridanimod (sodium salt)
10-Carboxymethyl-9-Acridanone
-
GC52387
Crosstide (trifluoroacetate salt)
Gly-Arg-Pro-Arg-Thr-Ser-Ser-Phe-Ala-Glu-Gly-OH, GRPRTSSFAEG-OH
A peptide substrate for Akt