Endocrinology/Hormones
Endocrinology/hormone inhibitors are compounds that block the action of hormones or interfere with hormone signaling pathways. These inhibitors are essential for studying the regulation of endocrine systems and for developing treatments for hormone-related diseases, such as diabetes, thyroid disorders, and hormone-dependent cancers. By modulating hormone activity, these inhibitors can help elucidate the complex interactions within the endocrine system. At CymitQuimica, we offer a wide range of high-quality endocrinology/hormone inhibitors to support your research in endocrinology, pharmacology, and medical sciences.
Subcategories of "Endocrinology/Hormones"
- Androgen Receptor(230 products)
- Annexin A(16 products)
- Aromatase(23 products)
- Estrogen/progestogen Receptor(66 products)
- GPR(1 products)
- Glucocorticoid Receptor(165 products)
- LHRH(2 products)
- Opioid Receptor(327 products)
- Prostaglandin Receptor(126 products)
- RAAS(89 products)
- Reductase(51 products)
- Somatostatin(57 products)
- Thyroid hormone receptor(THR)(34 products)
- Vasopressin Receptor(48 products)
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Found 3427 products of "Endocrinology/Hormones"
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2-sec-Butylphenol
CAS:2-sec-Butylphenol is an inhibitor of the androgen receptor and P450 aromatase, and can be used in research and experiments in the field of life sciences.Formula:C10H14OColor and Shape:SolidMolecular weight:150.22Linuron
CAS:Linuron herbicide disrupts photosynthesis and acts as an androgen receptor antagonist.Formula:C9H10Cl2N2O2Purity:99.08%Color and Shape:White Crystalline Solid Linuron Is A Colorless Crystals Non Corrosive Used As An HerbicideMolecular weight:249.09Angiotensin II (5-8), human
CAS:Angiotensin II (5-8) is an endogenous C-terminal fragment of the peptide vasoconstrictor angiotensin IIFormula:C26H36N6O5Purity:98%Color and Shape:SolidMolecular weight:512.64',2-Dihydroxy-4,6-dimethoxydihydrochalcone
CAS:4',2-Dihydroxy-4,6-dimethoxydihydrochalcone, an estrogen-like compound, binds to bovine estrogen receptors, IC50 15 μM.Formula:C17H18O5Color and Shape:SolidMolecular weight:302.32Norethindrone acetate
CAS:Norethindrone acetate (19-Norethindroneacetate) is an oestrogen with inhibitory effects on adolescent menstruation and hepatic adenomas and is often used inFormula:C22H28O3Purity:99.56%Color and Shape:SolidMolecular weight:340.46[Sar1, Ile8]-Angiotensin II acetate
'[Sar1, Ile8]-Angiotensin II acetate triggers oxidases and prompts superoxide in muscles; has varied vascular impacts.Formula:C48H77N13O12Purity:99.36%Color and Shape:SolidMolecular weight:1028.2Ref: TM-T7575L1
2mg34.00€5mg46.00€10mg60.00€1mL*10mM (DMSO)90.00€25mg119.00€50mg192.00€100mg289.00€200mg415.00€GLL 398
CAS:GLL 398 is an orally active and selective degrader of estrogen receptor with an IC50 of 1.14 nM. GLL 398 blocks tumor growth in xenograft breast cancer models.Formula:C25H23BO4Purity:98%Color and Shape:SolidMolecular weight:398.26Ref: TM-T9997
1mg175.00€5mg394.00€1mL*10mM (DMSO)403.00€10mg590.00€25mg1,060.00€50mg1,591.00€100mg2,387.00€200mg3,580.00€D3R/MOR antagonist 2
Compound 121, a D3R/MOR antagonist with K i values of 361 nM and 85.2 nM for D3R and MOR respectively, has the potential for analgesic effects through MORFormula:C25H31ClN2OPurity:98%Color and Shape:SolidMolecular weight:410.98ARD-2585
CAS:ARD-2585 is an orally active and selective androgen receptor PROTAC degrader with anticancer activity for the study of prostate cancer.Formula:C41H43ClN8O5Color and Shape:SolidMolecular weight:763.28BWA-6047
BWA-6047 is a dual AR/AR-V7 and GSPT1 PROTAC-type degrader (AR: DC50= 3.7 nM; AR-V7: DC50= 3.0 nM; GSPT1: DC50= 1.2 nM). It facilitates the ubiquitination and degradation of AR/AR-V7 and, through molecular glue properties, induces a PPI between GSPT1 and CRBN, leading to GSPT1 degradation. BWA-6047 is applicable in prostate cancer research.Formula:C42H46ClN5O7Color and Shape:SolidMolecular weight:767.30858ZINC05925939
ZINC05925939 is an estrogen receptor β (ESR2) inhibitor used in breast cancer research.Formula:C17H17NO2Color and Shape:SolidMolecular weight:267.32Methylpiperidino pyrazole
CAS:Methylpiperidino pyrazole is an ERα inhibitor and can prevent the BPS-induced Rb phosphorylation and cell cycle progression.Formula:C29H31N3O3Purity:98.84%Color and Shape:SolidMolecular weight:469.57Perindoprilat
CAS:Perindoprilat (Perindoprilate) is an angiotensin-converting enzyme inhibitor.Formula:C17H28N2O5Purity:99.21%Color and Shape:SolidMolecular weight:340.41TRV055 acetate
TRV055 acetate is a ligand of angiotensin II type 1 receptor and stimulates cellular Gq-mediated signaling.Formula:C44H61N9O11Purity:99.84%Color and Shape:SolidMolecular weight:892.01Ref: TM-T40220L
1mg109.00€2mg154.00€5mg235.00€10mg349.00€1mL*10mM (DMSO)389.00€25mg532.00€50mg745.00€100mg999.00€200mg1,333.00€Nociceptin(1-7)
CAS:Bioactive metabolite of nociceptin, antagonist of nociceptin-induced hyperalgesiaFormula:C31H41N7O9Purity:98%Color and Shape:SolidMolecular weight:655.709AKR1C3-IN-10
AKR1C3-IN-10 (compound 5r), a selective inhibitor of AKR1C3 with an IC50 of 51 nM, demonstrates efficacy in a prostate cancer xenograft model [1].Formula:C24H20N4O3Color and Shape:SolidMolecular weight:412.44Histamine & Melatonin Receptor-Targeted Compound Library
A unique collection of xnum compounds targeting histaminergic receptor and melatonin receptor for high throughput screening (HTS) and high content screening (HCS
Color and Shape:Odour SolidPotassium Channel Targeted Library
A unique collection of xnum potassium channel blockers and agonists for high throughput and high content screening;Color and Shape:Odour SolidRef: TM-L7300
1mgTo inquire30μL*10mM (DMSO)To inquire50μL*10mM (DMSO)To inquire100μL*10mM (DMSO)To inquire250μL*10mM (DMSO)To inquireERα degrader 10
ERα degrader10 is a potent, selective, orally active estrogen receptor α (ERα) degrader. It demonstrates strong ERα binding affinity (IC50 of 24.0 nM) and degradation capability (EC50 of 5.3 nM). This compound degrades ERα through a proteasome-mediated pathway and is utilized in breast cancer research.Color and Shape:Odour SolidImidaprilate
CAS:Imidaprilate, an active TA-6366 metabolite, is a potent ACE inhibitor with an IC50 of 2.6 nM, researched for hypertension.Formula:C18H23N3O6Purity:98%Color and Shape:SolidMolecular weight:377.39
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