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(137)
- Aromatase(13)
- CRTH2(2)
- Estrogen/progestogen Receptor(147)
- GnRH(26)
- Opioid Receptor(175)
- RAAS(8)
- Thyroid hormone Receptor(59)
- TRH(2)
- ROR/RAR/RXR(94)
- FXR & LXR(69)
- Glucocorticoids & Mineralocorticoids(49)
- GPR(1)
Products for Endocrinology and Hormones
- Cat.No. Product Name Information
- 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.
- 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
- GC11390 BAM 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
- GC17588 Bavachin estrogen receptors ERα and ERβ activator
- GC14883 Bazedoxifene
- GC10852 Bazedoxifene acetate 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
-
GP10051
Beta-Lipotropin (1-10), porcine
Morphine-like substance
- GC52329 Betamethasone-d5 An internal standard for the quantification of betamethasone
- GC30639 Bevenopran (CB-5945) Bevenopran (CB-5945) is a peripheral μ-opioid receptor antagonist.
- GC10037 Bexarotene Retinoid Receptor agonist
- GC46923 Bexarotene-d4 A neuropeptide with diverse biological activities
- GC12271 Bicalutamide Androgen receptor antagonist
- GC46925 Bicalutamide-d4 An internal standard for the quantification of bicalutamide
- GC31577 Bifluranol (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.
- 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.
- GC11504 BMS 195614 BMS 195614 (BMS 614) is a neutral RARα-selective antagonist with a Ki of 2.5 nM.
- GC49654 BMS 270394 A RARγ agonist
- GC10656 BMS 453 RAR agonist
- GC15648 BMS 493 Pan-RAR inverse agonist
- GC14185 BMS 753 RARα-selective agonist
- GC17382 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.
- 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.
- GA20967 Boc-D-His-OH 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.
- GC35541 Boldenone Undecylenate
- GC46941 Bombesin (trifluoroacetate salt) 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
- GC16521 BW 373U86 Non-peptide delta agonist,potent and selective
- GC43127 Calcitonin (salmon) (trifluoroacetate salt) Calcitonin is a peptide hormone that lowers blood calcium level and inhibits bone resorption.
- GC16978 Candesartan Angiotensin II receptor 1 (AT1) antagonist
- GC16223 Captopril An ACE inhibitor
- GC43140 Captopril Disulfide 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
- 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.
- 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.
- 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.
- 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.
- 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.
- 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
- GC11464 CD 437 RARγ-selective agonist,potent and cell-permeable
- GC35637 Cebranopadol An analgesic NOP and opioid receptor agonist
- GC35638 Cebranopadol ((1α,4α)stereoisomer) Cebranopadol ((1α,4α)stereoisomer) is a stereoisomer of cebranopadol.
- GC19229 CERC-501 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) 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
- GC17985 Chenodeoxycholic Acid nuclear receptors(FXR) activator
- GC48424 Chenodeoxycholic Acid 24-Acyl-β-D-Glucuronide A metabolite of CDCA
- GC49853 Chenodeoxycholic Acid 3-Glucuronide A metabolite of CDCA
- GC48595 Chenodeoxycholic Acid MaxSpec® Standard A quantitative analytical standard guaranteed to meet MaxSpec® identity, purity, stability, and concentration specifications
- GC68212 Chenodeoxycholic acid-13C
- GC47076 Chenodeoxycholic Acid-d4 A quantitative analytical standard guaranteed to meet MaxSpec® identity, purity, stability, and concentration specifications
- GC11144 Chlormadinone acetate steroidal progestin with additional antiandrogen and antigonadotropic effects
- GC10012 Chlorotrianisene Estrogen agonist
- GC45409 Ciclesonide-d7
- 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).
-
GC17491
CITCO
Constitutive androstane receptor (CAR) agonist
- GC52351 Citrullinated α-Enolase (R8 + R14) (1-19)-biotin Peptide A biotinylated and citrullinated α-enolase peptide
- GC47097 CJC-1295 A synthetic peptide derivative of GHRH
- GC14560 Cl-4AS-1 steroidal androgen receptor agonist
- GC48496 Clobetasol Propionate-d5 An internal standard for the quantification of clobetasol propionate
- GC49680 Clobetasone Propionate A corticosteroid
- GC15366 Clomiphene citrate 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.
- GC18804 Cosyntropin (acetate) Cosyntropin (acetate) is a synthetic peptide stimulating the release of corticosteroids such as cortisol from the adrenal gland.
- GC10002 Coumestrol competitive binder of the estrogen receptors ERα
- GC45413 Cridanimod (sodium salt)
- GC52387 Crosstide (trifluoroacetate salt) A peptide substrate for Akt
- GC11535 CTAP Potent and selective μ opioid receptor antagonist
- GC60730 CTAP TFA CTAP TFA is a potent, highly selective, and BBB penetrant μ opioid receptor antagonist, with an IC50 of 3.5 nM.
- GC16888 CTOP Potent and selective μ opioid receptor antagonist
- GC60731 CTOP TFA CTOP TFA is a potent and highly selective μ-opioid receptor antagonist.
- GC10180 Cyclofenil Non-steroidal selective estrogen receptor modulator (SERM)
-
GC13189
Cyprodime hydrochloride
μ-opioid receptor antagonist
- GC47159 Cyprodinil An anilinopyrimidine fungicide