Endocrinologia/Ormoni
Gli inibitori dell'endocrinologia/oromone sono composti che bloccano l'azione degli ormoni o interferiscono con le vie di segnalazione ormonale. Questi inibitori sono fondamentali per studiare la regolazione dei sistemi endocrini e per sviluppare trattamenti per malattie correlate agli ormoni, come il diabete, i disturbi della tiroide e i tumori ormono-dipendenti. Modulando l'attività ormonale, questi inibitori possono aiutare a chiarire le complesse interazioni all'interno del sistema endocrino. Presso CymitQuimica, offriamo un'ampia gamma di inibitori di alta qualità per endocrinologia/oromone per supportare le tue ricerche in endocrinologia, farmacologia e scienze mediche.
Sottocategorie di "Endocrinologia/Ormoni"
- Recettore degli androgeni(230 prodotti)
- Annessina A(16 prodotti)
- Aromatasi(23 prodotti)
- Recettore degli estrogeni/progestogeni(66 prodotti)
- GPR(1 prodotti)
- Recettore dei glucocorticoidi(164 prodotti)
- LHRH(2 prodotti)
- Recettore degli oppioidi(327 prodotti)
- Recettore della prostaglandina(126 prodotti)
- RAAS(89 prodotti)
- Riduttasi(51 prodotti)
- Somatostatina(57 prodotti)
- Recettore dell'ormone tiroideo (THR)(34 prodotti)
- Recettore della vasopressina(48 prodotti)
Mostrare 6 più sottocategorie
Trovati 3420 prodotti di "Endocrinologia/Ormoni"
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Dynorphin A (1-13) amide
CAS:Dynorphin A (1-13) amide, an endogenous opioid peptide, counteracts the analgesic effects of morphine [1].Formula:C75H127N25O14Peso molecolare:1602.97Neuropeptide AF (human) acetate
Neuropeptide AF (human) acetate (Neuropeptide AF (human) acetate (192387-38-5 Free base)) is an anti-opioid neuropeptide, a Neuropeptide AF (human) derivative,
Purezza:99.89%Colore e forma:SoildBAY 1003803
CAS:BAY 1003803 is a glucocorticoid receptor agonist for the topical treatment of psoriasis or severe atopic dermatitis.Formula:C21H18ClF5N2O4Colore e forma:SolidPeso molecolare:492.83PROTAC ERα Degrader-2
CAS:PROTAC ERα Degrader-2 is composed of a cIAP1 ligand binding group, a linker, and an estrogen receptor α (ERα) binding group, serving as an ERα degrader.Formula:C42H61N5O8Purezza:98%Colore e forma:SolidPeso molecolare:763.96Fluorphine
CAS:Fluorphine, an analog of Brorphine, binds to the μ-opioid receptor (MOR) with a Ki of 12.5 nM. It exhibits GTPγS binding activity with an EC50 of 75 nM and β-arrestin 2 recruitment activity with an EC50 of 377 nM, and it also has respiratory depressive effects.Formula:C20H22FN3OColore e forma:SolidPeso molecolare:339.41Neuropeptide EI, rat
CAS:Displays functional MCH-antagonist and MSH-agonist activity in different behavioral paradigms.Formula:C63H98N16O23Purezza:98%Colore e forma:SolidPeso molecolare:1447.55(1S,2R)-2-PCCA
(1S,2R)-2-PCCA is a novel and potent small molecule GPR88 receptor agonist with an EC50 value of 3 nM in the non-cellular system and 603 nM in the cellularFormula:C30H39Cl2N3OPurezza:99.91%Colore e forma:SoildPeso molecolare:528.56Awl 60
CAS:Awl 60 is a substance P (6-11) non-competitive antagonist.Formula:C57H65N9O8SPurezza:98%Colore e forma:SolidPeso molecolare:1036.25Raloxifene dimethyl ester hydrochloride
CAS:Raloxifene dimethyl ester hydrochloride is an analog of Raloxifene.Formula:C32H32ClNO6SColore e forma:SolidPeso molecolare:594.12WAY267464 HCl
CAS:WAY267464: nonpeptide OT agonist, anxiolytic, modulates selectivity, improves CNS entry and oral uptake.Formula:C32H37Cl2N7O4Purezza:98%Colore e forma:SolidPeso molecolare:654.59Hodgkinsine B
CAS:Hodgkinsine B, a pain-relieving alkaloid, increases tail-flick latency in mice at 10 mg/kg dose.Formula:C33H38N6Colore e forma:SolidPeso molecolare:518.70Dexamethasone phosphate
CAS:Dexamethasone phosphate is a synthetic adrenal corticosteroid. It also has potent anti-inflammatory properties.Formula:C22H30FO8PColore e forma:SolidPeso molecolare:472.44Cortodoxone-d7
Cortodoxone-d7 (11-Deoxycortisol-d7) is a deuterium-labeled form of Cortodoxone. Cortodoxone (11-Deoxycortisol; cortexolone) is both a glucocorticoid steroid hormone and a glucocorticoid antagonist. It enhances tryptophan oxygenase (TO) activity and stimulates the secretion of corticosterone. Additionally, Cortodoxone regulates the proliferation and activation of T cells.Formula:C21H23D7O4Colore e forma:SolidPeso molecolare:353.50GLL 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:C25H23BO4Purezza:98%Colore e forma:SolidPeso molecolare: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€BMS-903452
CAS:BMS-903452: potent GPR119 agonist, EC50 = 14 nM, treats rodent diabetes, no P450 inhibition, safe for liver cells.Formula:C21H19Cl2FN4O4SPurezza:98.69% - 99.76%Colore e forma:SolidPeso molecolare:513.37Ref: TM-T67791
1mg95,00€5mg207,00€1mL*10mM (DMSO)244,00€10mg295,00€25mg444,00€50mg600,00€100mg810,00€200mg1.063,00€[Met5]-Enkephalin, amide
CAS:[Met5]-Enkephalin, amide activates δ and ζ opioid receptors; has multiple forms and varying plasma levels.Formula:C27H36N6O6SPurezza:98%Colore e forma:SolidPeso molecolare:572.681,4-Dihydropyridine
1,4-Dihydropyridine acts as an antagonist for calcium channels (calcium channel), specifically blocking the L-type calcium channels. This action reduces the influx of calcium ions into cardiac and vascular smooth muscle cells, consequently decreasing cardiac contractility and heart rate, dilating blood vessels, and lowering blood pressure.Formula:C12H17NO4Colore e forma:SolidPeso molecolare:239.27PRL 3195
CAS:PRL 3195: Somatostatin antagonist, Ki: 6 nM (sst5), 17 nM (sst2), 66 nM (sst3), 1 μM (sst1/4).Formula:C58H69ClN12O9S2Colore e forma:SolidPeso molecolare:1177.8317-Epiestriol
CAS:17-Epiestriol, metabolite of estrone, forms via 16α-hydroxy intermediate and binds ERα and ERβ with affinity less than 17β-estradiol.Formula:C18H24O3Purezza:99.72%Colore e forma:SolidPeso molecolare:288.38Vasopressin Dimer (parallel) (TFA)
Vasopressin Dimer (parallel) TFA, a parallel dimer of Vasopressin, has the capability to activate four G protein-coupled receptors—namely, V1aR, V1bR, V2R, andFormula:C94H131F3N30O26S4Purezza:98%Colore e forma:SolidPeso molecolare:2282.49
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