Receptor de andrógenos
El receptor de andrógenos (AR) es un receptor hormonal nuclear que se activa al unirse a andrógenos, como la testosterona y la dihidrotestosterona. Este receptor juega un papel crucial en el desarrollo y mantenimiento de las características masculinas, así como en la regulación de varios procesos fisiológicos, incluyendo el crecimiento muscular, la libido y la densidad ósea. Los inhibidores del receptor de andrógenos son ampliamente estudiados en el contexto del cáncer de próstata, donde la señalización del AR a menudo está sobreexpresada. En CymitQuimica, ofrecemos una gama de moduladores del receptor de andrógenos de alta calidad para apoyar su investigación en endocrinología, biología del cáncer y regulación hormonal.
Se han encontrado 207 productos de "Receptor de andrógenos"
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MI-136
CAS:<p>MI-136 inhibits expression of androgen receptor (AR) target genes that DHT induced.</p>Fórmula:C23H21F3N6SPureza:98.63% - 99.12%Forma y color:SolidPeso molecular:470.51Apalutamide
CAS:<p>Apalutamide (ARN-509) is a small molecule and androgen receptor (AR) antagonist with potential antineoplastic activity.</p>Fórmula:C21H15F4N5O2SPureza:99.03% - 99.91%Forma y color:SolidPeso molecular:477.43S-23
CAS:<p>S-23 ((S)-3-(4-chloro-3-fluorophenoxy)-N-(4-cyano-3-(trifluoromethyl)phenyl)-2-hydroxy-2-methylpropanamide) is an oral selective androgen receptor modulator (</p>Fórmula:C18H13ClF4N2O3Pureza:99.55%Forma y color:SolidPeso molecular:416.75Iprodione
CAS:<p>Iprodione is a fungicide. Iprodione is also used in cannabis testing kits as a component of pesticide mixes.</p>Fórmula:C13H13Cl2N3O3Pureza:98.82%Forma y color:Colorless Crystals Cream To Colorless Odorless PowderPeso molecular:330.17Testosterone undecanoate
CAS:<p>Testosterone undecanoate is a metabolite of Testosterone, which is a promising androgen for male hormonal contraception.</p>Fórmula:C30H48O3Pureza:99.45% - 99.788%Forma y color:White Crystalline PowderPeso molecular:456.7CLP-3094
CAS:<p>CLP-3094 (2-([2-(4-CHLOROPHENOXY)ETHYL]THIO)-1H-BE) is a potent androgen receptor BF3 (binding function 3) inhibitor.</p>Fórmula:C15H13ClN2OSPureza:99.84%Forma y color:SolidPeso molecular:304.79AC-262536
CAS:<p>AC-262536 is a selective androgen receptor (SAR) modulator and exhibits potent agonist activity at the androgen receptor.</p>Fórmula:C18H18N2OPureza:99.88%Forma y color:SolidPeso molecular:278.35Triptophenolide
CAS:<p>Triptophenolide (Hypolide) is a compound isolated from Tripterygium wilfordii Hook with anti-inflammatory activity.</p>Fórmula:C20H24O3Pureza:98.07% - ≥95%Forma y color:White PowderPeso molecular:312.4Boldenone Undecylenate
CAS:<p>Boldenone Undecylenate (Parenabol) is a synthetic steroid.</p>Fórmula:C30H44O3Pureza:99.39%Forma y color:Light Yellow Oily MatterPeso molecular:452.67JNJ-63576253 free base
CAS:<p>JNJ-63576253 free base (TRC253) is a potent and orally active full antagonist of androgen receptor (AR). JNJ-63576253 can be used for the research of CRPC.</p>Fórmula:C23H21F3N6O2SPureza:98.32%Forma y color:SolidPeso molecular:502.51Dimethylcurcumin
CAS:<p>Dimethylcurcumin (ASC-J9) (ASC-J9) is an androgen receptor degradation enhancer.</p>Fórmula:C23H24O6Pureza:97.36% - 98.96%Forma y color:SolidPeso molecular:396.43Nandrolone phenylpropionate
CAS:<p>Nandrolone phenylpropionate (Nandrolone phenpropionate) is an androgen receptor agonist. It mainly used to treat women with breast cancer and osteoporosis</p>Fórmula:C27H34O3Pureza:99.2% - 99.46%Forma y color:White Or Milky Crystalline PowderPeso molecular:406.56JNJ-63576253
CAS:<p>JNJ-63576253 is a Clinical Stage Androgen Receptor Antagonist for F877L Mutant and Wild-Type Castration-Resistant Prostate Cancer (mCRPC).</p>Fórmula:C23H22ClF3N6O2SPureza:98.71%Forma y color:SolidPeso molecular:538.97Ailanthone
CAS:<p>Ailanthone (Δ13-Dehydrochaparrinone) is an effective inhibitor of both full-length androgen receptor (AR) (IC50: 69 nM) and constitutively active truncated AR</p>Fórmula:C20H24O7Pureza:99.71% - 99.96%Forma y color:SolidPeso molecular:376.43-(7,7-dimethyl-5-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-2-yl)-1H-indole-7-carbonitrile
CAS:<p>3-[7 ,7- dimethyl-5-oxo -6H-pyrrolo[3,4-b]pyridin-2-yI]-1H-indole-7 -carbonitrile is an androgen receptor modulator.</p>Fórmula:C18H14N4OPureza:98.41%Forma y color:SolidPeso molecular:302.33ARD-2128
CAS:<p>ARD-2128: potent oral PROTAC that degrades AR, curbing prostate cancer growth with no toxicity.</p>Fórmula:C45H50ClN7O6Pureza:98.8%Forma y color:SolidPeso molecular:820.372-hydroxy Flutamide
CAS:<p>2-hydroxy Flutamide is competitive inhibition of androgen receptor (AR) for the treatment of prostate cancer</p>Fórmula:C11H11F3N2O4Pureza:99.45% - 99.82%Forma y color:SolidPeso molecular:292.21AH-3960
CAS:<p>AH-3960 是一种甲状腺激素受体 1 (PTHR1) 激动剂。</p>Fórmula:C13H22N4O3Pureza:98.44%Forma y color:SolidPeso molecular:282.34DSRM-3716
CAS:<p>Isoquinoline, 5-iodo- (9CI) is a potent and selective inhibitor of SARM1(IC50 = 75 nM) by preventing axonal degeneration and by allowing functional recovery of</p>Fórmula:C9H6INPureza:97.28% - 99.785%Forma y color:SolidPeso molecular:255.06Bavdegalutamide
CAS:<p>Bavdegalutamide (ARV-110) is a PROTAC degrader of androgen receptor (AR).</p>Fórmula:C41H43ClFN9O6Pureza:97.17% - 99.04%Forma y color:SolidPeso molecular:812.29N-desmethyl Enzalutamide
CAS:<p>N-desmethyl Enzalutamide (N-desmethyl MDV 3100) is the active Enzalutamide metabolite.It is the active metabolite of Enzalutamide.</p>Fórmula:C20H14F4N4O2SPureza:99.74%Forma y color:SolidPeso molecular:450.41Enzalutamide carboxylic acid
CAS:<p>Enzalutamide carboxylic acid is an antagonist of androgen receptor (AR) .</p>Fórmula:C20H13F4N3O3SPureza:97.88%Forma y color:SolidPeso molecular:451.39Clascoterone
CAS:<p>Clascoterone (CB-03-01) is a new topical and peripherally selective androgen antagonist.</p>Fórmula:C24H34O5Pureza:99.2% - 99.64%Forma y color:SolidPeso molecular:402.52LY2452473
CAS:<p>LY2452473 (OPK 88004) is an orally available and selective androgen receptor modulator with potential anticancer activity for the study of prostate cancer.</p>Fórmula:C22H22N4O2Pureza:99.72%Forma y color:SolidPeso molecular:374.44Masofaniten
CAS:<p>Masofaniten (EPI-7386) is an orally active androgen receptor (AR) inhibitor with antitumor activity for the study of prostate and breast cancer.</p>Fórmula:C24H24Cl2N4O4SPureza:98.42% - 98.66%Forma y color:SolidPeso molecular:535.44AR antagonist 6
CAS:<p>AR antagonist 6 (compound 6i), a diphenyl ether androgen receptor (AR) antagonist, binds to the AR with an affinity of 120 nM. It demonstrates low toxicity and effective in vitro activity in the golden Syrian hamster ear model. [19] [1]</p>Fórmula:C16H12F3NO2Forma y color:SolidPeso molecular:307.27GDC-2992
CAS:<p>GDC-2992 is a selective androgen receptor (AR) degradator that degrades AR and inhibits proliferation in VCaP cells,CRPC.</p>Fórmula:C45H51ClN8O5Pureza:99.82%Forma y color:SoildPeso molecular:819.39Estromustine
CAS:<p>Estromustine, an active metabolite of estramustine phosphate, is used to treat prostate cancer.</p>Fórmula:C23H29Cl2NO3Forma y color:SolidPeso molecular:438.39Procymidone
CAS:<p>Procymidone is a broad-spectrum fungicide that inhibits fungal glycerol triester synthesis, thereby disrupting hyphal growth. androgen receptor (AR) antagonist</p>Fórmula:C13H11Cl2NO2Pureza:99.86%Forma y color:Colorless SolidPeso molecular:284.14JNJ-37654032
CAS:<p>JNJ-37654032: orally active, nonsteroidal SARM. Mixed AR agonist/antagonist. Selective for muscle, grows levator ani, max at 3mg/kg, ED(50) 0.8mg/kg.</p>Fórmula:C11H7Cl2F3N2OForma y color:SolidPeso molecular:311.09BMS-564929
CAS:<p>BMS-564929 is an AR agonist that upregulates the expression and activity of fat-producing enzymes, reducing VAT content and lipid levels.</p>Fórmula:C14H12ClN3O3Pureza:98.17%Forma y color:SolidPeso molecular:305.72(R)-Bicalutamide
CAS:<p>(R)-Bicalutamide, an AR antagonist with antitumor properties, is crucial in prostate cancer research.</p>Fórmula:C18H14F4N2O4SForma y color:SolidPeso molecular:430.37LG-121071
CAS:<p>LG-121071: oral SARM, high-affinity AR full agonist, Ki=17 nM.</p>Fórmula:C15H15F3N2OPureza:98%Forma y color:SolidPeso molecular:296.29Honokiol DCA
CAS:<p>Honokiol DCA inhibits DRP1, enhances respiration via mitochondrial repair, and is active against Vemurafenib-resistant melanoma.</p>Fórmula:C22H18Cl4O4Forma y color:SolidPeso molecular:488.19Lubabegron fumarate
CAS:<p>Lubabegron (LY591281, LY488756 fumarate) is a beta-agonist approved in 2018 to lower ammonia in cattle waste, aiding environment and health.</p>Fórmula:C29H29N3O3SC4H4O4Forma y color:SolidPeso molecular:557.66Gumelutamide
CAS:<p>Gumelutamide, a tetrahydropyridopyrimidine compound, functions as both an antiandrogen and an antineoplastic agent by acting as an androgen antagonist.</p>Fórmula:C22H21ClN6OForma y color:SolidPeso molecular:420.89TFM-4AS-1
CAS:<p>androgen receptor modulator</p>Fórmula:C27H33F3N2O2Pureza:98%Forma y color:SolidPeso molecular:474.56HG122
CAS:<p>HG122 promotes AR degradation via proteasome, inhibiting castration-resistant prostate cancer.</p>Fórmula:C15H13N5O5Forma y color:SolidPeso molecular:343.29Androgen receptor antagonist 4
CAS:<p>Compound AT2 is an AR inhibitor with anticancer effects, blocking DHT action and AR nuclear translocation (IC50=0.15μM).</p>Fórmula:C22H18ClNForma y color:SolidPeso molecular:331.84AZD3514
CAS:<p>AZD3514 is a potent and oral androgen receptor downregulator with Ki of 2.2 μM and has ability of reducing AR protein expression.Phase 1.</p>Fórmula:C25H32F3N7O2Pureza:98.09%Forma y color:SolidPeso molecular:519.56AR antagonist 2
CAS:<p>AR antagonist 2 (compound 58) is a potent inhibitor of the androgen receptor (AR) (IC50: 0.95 μM).</p>Fórmula:C22H17ClFN5O2SForma y color:SolidPeso molecular:469.92AR antagonist 5
CAS:<p>Compound 30a, known as AR Antagonist 5, is a selective androgen receptor (AR) antagonist that demonstrates an IC 50 value of 134.8 nM. It exhibits favorable pharmacokinetic properties, characterized by high skin exposure and low plasma exposure [1].</p>Fórmula:C23H21F3N6O2Forma y color:SolidPeso molecular:470.45CSRM617
CAS:<p>CSRM617: selective ONECUT2 inhibitor, Kd 7.43 uM, binds OC2-HOX, induces apoptosis, tolerable in mouse prostate cancer model.</p>Fórmula:C10H13N3O5Pureza:98%Forma y color:SolidPeso molecular:255.23MK-4541
CAS:<p>MK-4541: oral, selective AR modulator, blocks 5α-reductase, curbs AR+ prostate cancer growth, effective in mouse model.</p>Fórmula:C22H31F3N2O3Forma y color:SolidPeso molecular:428.49(R)-UT-155
CAS:<p>(R)-UT-155 is a selective androgen receptor degrader (SARD) ligand.</p>Fórmula:C20H15F4N3O2Forma y color:SolidPeso molecular:405.35Carbazole derivative 1
CAS:<p>Carbazole derivative 1 is used to reduce androgen or oestrogen levels in mammals.</p>Fórmula:C18H13FN2Pureza:98%Forma y color:SolidPeso molecular:276.31VPC-3033
CAS:<p>VPC-3033 is an antagonist of the androgen receptor. It acts by inhibiting the LNCaP cell line as well as cell lines with the wild-type androgen receptor.</p>Fórmula:C21H14O2Pureza:98%Forma y color:SolidPeso molecular:298.33Androgen receptor antagonist 3
CAS:<p>Androgen receptor antagonist 3 (Compound C18) has anticancer activities that is an antagonist of androgen receptor (AR) (IC 50 = 2.4 μM) [1].</p>Fórmula:C22H18ClNForma y color:SolidPeso molecular:331.84RU 58642
CAS:<p>RU 58642 is an effective systemic antiandrogen for androgen-dependent disorders.</p>Fórmula:C15H11F3N4O2Pureza:98%Forma y color:SolidPeso molecular:336.27VPC-13789
CAS:<p>VPC-13789: potent, selective oral antiandrogen for CRPC with 0.19 μM IC50 in LNCaP cells.</p>Fórmula:C21H16F3N3OForma y color:SolidPeso molecular:383.37Topterone
CAS:<p>Topterone (Win 17,665) is a potent topical antiandrogen that inhibits the stimulation of lumbar organ development by testosterone and dihydrotestosterone in</p>Fórmula:C22H34O2Pureza:>99.99%Forma y color:SolidPeso molecular:330.5Ar-V7-IN-1
CAS:<p>Ar-V7-IN-1 (compound 47) is a potent inhibitor of Ar-V7,associated with resistance to AR-targeted therapy with desmoplasia-resistant prostate cancer (mCRPC).</p>Fórmula:C10H10Br2N4OSForma y color:SolidPeso molecular:394.09Prochloraz
CAS:<p>Prochloraz: broad-spectrum imidazole fungicide; blocks placental aromatase (IC50=40nM), estrogen/androgen receptors; activates aryl hydrocarbon receptors.</p>Fórmula:C15H16Cl3N3O2Pureza:99.75% - 99.79%Forma y color:Colorless SolidPeso molecular:376.67Androgen receptor antagonist 1
CAS:<p>Androgen receptor antagonist 1, an oral full AR antagonist (IC50 59 nM), for PROTAC synthesis, reducing AR protein by 24–47% in LNCaP cells at 1–10 μM.</p>Fórmula:C21H25ClN4O3Pureza:99.054%Forma y color:SolidPeso molecular:416.9Bromopropylate
CAS:<p>Bromopropylate is an insecticide. Bromopropylate is the active substance in fumigant strips for mites.</p>Fórmula:C17H16Br2O3Pureza:98%Forma y color:White Crystalline Solid Yellowish CrystalsPeso molecular:428.11Dimethomorph
CAS:<p>Dimethomorph is a fungicide and sterol biosynthesis inhibitor that inhibits fungal cell wall formation,. inhibits androgen receptor (AR) .</p>Fórmula:C21H22ClNO4Pureza:99.2%Forma y color:Solid CrystallinePeso molecular:387.86MK-3984
CAS:<p>MK-3984 is a selective androgen receptor modulator, used in the study of conditions caused by androgen deficiency.</p>Fórmula:C17H12F7NO2Pureza:99.91%Forma y color:SolidPeso molecular:395.27Bifluranol
CAS:<p>Bifluranol (BX341) has anti-androgenic activity and has shown significant anti-prostatic activity in in vivo studies for the treatment of benign prostatic</p>Fórmula:C17H18F2O2Pureza:99.77%Forma y color:SolidPeso molecular:292.32VPC-14449
CAS:<p>VPC-14449 is a selective androgen receptor DNA-binding domain (AR-DBD) inhibitor, useful in prostate cancer research.</p>Fórmula:C10H10Br2N4OSPureza:99.56%Forma y color:SolidPeso molecular:394.09Ralaniten
CAS:<p>Ralaniten (EPI-002), a potent AR-NTD antagonist, inhibits AR with IC50 of 7.4 μM, for CRPC study.</p>Fórmula:C21H27ClO5Pureza:99.77%Forma y color:SolidPeso molecular:394.89LGD-2226
CAS:<p>LGD-2226: selective oral androgen receptor modulator, EC50: 0.2nM, Ki: 1.5nM. Treats muscle loss, osteoporosis, sexual issues.</p>Fórmula:C14H9F9N2OPureza:98%Forma y color:SolidPeso molecular:392.22S-40503
CAS:<p>S-40503 is an investigational selective androgen receptor modulator (SARM).</p>Fórmula:C15H23N3O3Forma y color:SolidPeso molecular:293.36Cyprodinil
CAS:<p>Cyprodinil is a fungicide blocking methionine synthesis in fungi and hinders B. cinerea, P. herpotrichoides, H. oryzae growth; it's also an AR agonist.</p>Fórmula:C14H15N3Forma y color:SolidPeso molecular:225.29BMS-641988
CAS:<p>BMS-641988 is a novel nonsteroidal androgen receptor antagonist for the treatment of prostate cancer.</p>Fórmula:C20H20F3N3O5SPureza:99.57% - 99.92%Forma y color:SoildPeso molecular:471.45GLPG0492
CAS:<p>GLPG0492 is a novel selective androgen receptor modulator.</p>Fórmula:C19H14F3N3O3Pureza:99.58%Forma y color:SolidPeso molecular:389.33ONC1-13B
CAS:<p>ONC1-13B, an androgen receptor antagonist, is used potentially for the treatment of prostate cancer.</p>Fórmula:C22H16F4N4O3SPureza:99.36% - 99.85%Forma y color:SolidPeso molecular:492.45Ralaniten triacetate
CAS:<p>Ralaniten triacetate (EPI-506) is a precursor of Ralaniten, an AR-NTD inhibitor, which can be used in the study of prostate and breast cancer.</p>Fórmula:C27H33ClO8Pureza:98.69%Forma y color:SolidPeso molecular:521.00Androgen receptor-IN-5
CAS:<p>Androgen receptor-IN-5 is a potent inhibitor of the androgen receptor with anticancer properties.</p>Fórmula:C22H10Cl2F4N4OSPureza:98%Forma y color:SolidPeso molecular:525.31(rel)-BMS-641988
CAS:<p>(rel)-BMS-641988, a relative configuration of the potent nonsteroidal androgen receptor antagonist BMS-641988, holds potential for prostate cancer research.</p>Fórmula:C20H20F3N3O5SPureza:98%Forma y color:SolidPeso molecular:471.45LGD-2941
CAS:<p>LGD-2941 is an androgen receptor modulator. LGD-2941 is used for the treatment of hypogonadism, female sexual dysfunction and menopausal syndrome.</p>Fórmula:C17H16F6N2O2Forma y color:SolidPeso molecular:394.31Androgen receptor degrader-1
CAS:<p>Androgen Receptor Degrader-1 (Compound 18) is a potent agent for androgen receptor degradation, applicable in cancer research [1].</p>Fórmula:C15H14ClN3O4Pureza:98%Forma y color:SolidPeso molecular:335.74Androgen receptor degrader-2
CAS:<p>Androgen Receptor Degrader-2 (Compound 9) is a potent degrader of androgen receptors, with potential application in cancer research [1].</p>Fórmula:C16H16ClN3O4Pureza:98%Forma y color:SolidPeso molecular:349.77N-Nitrosodicyclohexylamine
CAS:<p>N-Nitrosodicyclohexylamine (NDCHA), an N-nitrosocompound, exhibits anti-androgenic activity by competitively binding to the androgen receptor (AR) in opposition</p>Fórmula:C12H22N2OPureza:98%Forma y color:SolidPeso molecular:210.32Celiprolol hydrochloride
CAS:<p>Celiprolol hydrochloride (Selectrol) is a cardioselective beta-1 adrenergic antagonist that has intrinsic sympathomimetic activity.</p>Fórmula:C20H33N3O4·HClForma y color:White Crystalline SolidPeso molecular:415.96Androgen receptor antagonist 5
CAS:<p>AR antagonist 5 blocks AR (IC50: 6.17 μM), hinders LNCaP cell growth, and has anti-tumor effects in mouse models.</p>Fórmula:C21H15F4N5O3SForma y color:SolidPeso molecular:493.43Trimegestone
CAS:<p>Trimegestone, a highly effective oral progestogen, is used for endometrial protection, all doses inducing secretory endometrial transformation.</p>Fórmula:C22H30O3Pureza:98%Forma y color:SolidPeso molecular:342.47JJH260
CAS:<p>JJH260, a N-hydroxy hydantoin carbamate, inhibits AIG1 and ADTRP with IC50 values of 0.57 μM and 8.5 μM, respectively, and targets ABHD6, LYPLA1/2.</p>Fórmula:C29H34ClN5O5Forma y color:SolidPeso molecular:568.06JNJ-26146900
CAS:<p>JNJ-26146900 is a nonsteroidal androgen receptor (AR) ligand with tissue-selective activity in rats. JNJ-26146900 binds to the rat AR with a K(i) of 400nM.</p>Fórmula:C15H15F3N2O3SPureza:98%Forma y color:SolidPeso molecular:360.35VPC-14228
CAS:<p>VPC-14228 is a specific AR-DBD inhibitor that acts by inhibiting both Y594A and Q592A mutants.</p>Fórmula:C13H14N2OSPureza:99.96%Forma y color:SolidPeso molecular:246.33PLK1/BRD4-IN-1
CAS:<p>PLK1/BRD4-IN-1 (9b) is an orally active dual inhibitor of PLK1 (IC50: 22 nM) and BRD4 (IC50: 109 nM).</p>Fórmula:C31H43N9O2Forma y color:SolidPeso molecular:573.73RU 59063
CAS:<p>RU 59063 is a prototype of a new class of high-affinity nonsteroidal androgen receptor (AR) ligands.</p>Fórmula:C17H18F3N3O2SPureza:99.09%Forma y color:SolidPeso molecular:385.4YXG-158
CAS:<p>YXG-158 (Compound 23-h), an orally active androgen receptor (AR) degrader and cytochrome P450 17A1 (CYP17A1) inhibitor, exhibits AR degradation with a DC50 of 1</p>Fórmula:C30H36FN3OPureza:98%Forma y color:SolidPeso molecular:473.62Androgen receptor degrader-3
CAS:<p>Androgen Receptor Degrader-3 (ARD-3) is a compound that inhibits androgen receptor signaling and promotes the degradation of the receptor, with potential</p>Fórmula:C45H51ClN8O5Pureza:98%Forma y color:SolidPeso molecular:819.39EPI-7170
CAS:<p>EPI-7170: Ralaniten analogue, blocks androgen receptor, inhibits transcription in AR & variants, fights enzalutamide-resistant prostate cancer.</p>Fórmula:C22H28Cl3NO6SForma y color:SolidPeso molecular:540.88ID11916
CAS:<p>ID11916 is an orally active compound functioning as both an androgen receptor (AR) antagonist and a phosphodiesterase 5 (PDE5) inhibitor. It disrupts androgen binding to AR, impedes nuclear translocation, and blocks androgen-dependent transcriptional activity of AR, while simultaneously elevating intracellular cGMP levels by inhibiting PKG activation. Moreover, ID11916 exhibits potent anticancer effects in prostate cancer cell lines VCaP and 22Rv1, as well as in AR-positive breast cancer cell line SK-BR-3.</p>Fórmula:C29H27F3N8O3SForma y color:SolidPeso molecular:624.637Androstatrione
CAS:<p>Androstatrione is an androgenic compound.</p>Fórmula:C19H26O3Forma y color:SolidPeso molecular:302.41Androgen receptor antagonist 12
CAS:<p>Compound EF2 (Androgen receptor antagonist 12) is an orally active antagonist of the androgen receptor (AR) with an IC50 of 0.30 µM. It inhibits the transcriptional activity of mutant AR and the proliferation of AR-positive PCa (prostate cancer) cell lines. Additionally, Compound EF2 blocks the nuclear translocation of AR and suppresses tumor growth in the C4-2B xenograft mouse model. This compound is used for research in prostate cancer.</p>Fórmula:C12H8F3N3O2Forma y color:SolidPeso molecular:283.21SJ1008066
CAS:<p>SJ1008066 is a MAGE-A11 inhibitor with an IC50 of 0.13 μM. It binds to the MAGE homology domain (MHD) and disrupts the MAGE-A11:PCF11 interaction.</p>Fórmula:C21H22N4Forma y color:SolidPeso molecular:330.43Androgen receptor antagonist 11
CAS:<p>Androgen receptor antagonist 11 (compound N29) is a selective, orally available antagonist.</p>Fórmula:C20H19F3N4O3SForma y color:SolidPeso molecular:452.45AR/BET protein degrader-1
CAS:<p>AR/BET protein degrader-1 (Compound 149) is a dual-targeting protein degrader of Androgen Receptor and BET (bromodomain and extra-terminal domain), suitable for cancer research.</p>Fórmula:C43H44N6O5Peso molecular:724.85GLPG0492 (R enantiomer)
CAS:<p>GLPG0492 R enantiomer is the R enantiomer of GLPG-0492, a novel selective androgen receptor modulator.</p>Fórmula:C19H14F3N3O3Forma y color:SolidPeso molecular:389.33VNPP433-3β
CAS:<p>VNPP433-3β acts as a molecular glue degrader, targeting the androgen receptor (AR) and its splice variants (AR-Vs) as well as MAP kinase-interacting serine/threonine protein kinase Mnk1/2. It effectively inhibits the proliferation of cancer cells LNCaP, C4-2B, and CWR22Rv1, with GI50 values of 0.2, 0.3, and 0.31 μM, respectively. Additionally, VNPP433-3β shows favorable pharmacokinetics in CD-1 mice and suppresses tumor growth in the CWR22Rv1 xenograft mouse model.</p>Fórmula:C29H34N4Forma y color:SolidPeso molecular:438.61AR antagonist 4
<p>AR antagonist 4 (Compound 67-b) is an orally active androgen receptor (AR) antagonist that acts on wild-type AR (IC50: 246.6 nM).</p>Fórmula:C29H36N4OForma y color:SolidPeso molecular:456.62AR antagonist 10
CAS:<p>AR antagonist 10 (Compound Y5) is a potent, orally active androgen receptor (AR) antagonist with an IC50 value of 0.04 μM. It demonstrates a dual mechanism of action: antagonizing AR by disrupting AR dimerization and inducing AR degradation through the ubiquitin-proteasome pathway. This compound shows excellent activity against various resistant AR mutants and effectively inhibits the growth of LNCaP xenograft tumors. AR antagonist 10 is applicable for research in resistant prostate cancer.</p>Fórmula:C18H17ClN4O3SForma y color:SolidPeso molecular:404.871FL442
CAS:<p>FL442 is an Androgen Receptor (AR) modulator. This compound exhibits potent inhibitory effects in AR-dependent prostate cancer cells, showing similar suppression efficiency to the traditional antiandrogen drugs Bicalutamide and Enzalutamide. It also maintains antiandrogen activity against the Enzalutamide-resistant AR mutant F876L. The pharmacokinetic properties of FL442 in mice reveal a longer half-life (8 hours), excellent targeting (prostate tissue), and metabolic stability. Additionally, it is effective at inhibiting LNCaP tumor growth at low plasma concentrations (30 ng/mL).</p>Fórmula:C15H13F3N2OForma y color:SolidPeso molecular:294.27(+)-JJ-74-138
CAS:<p>(+)-JJ-74-138 is a novel non-competitive androgen receptor (AR) antagonist capable of inhibiting enzalutamide-resistant castration-resistant prostate cancer (CRPC).</p>Fórmula:C22H22F8N2OSForma y color:SolidPeso molecular:514.48LX1
CAS:<p>LX1, an anti-prostate cancer compound, specifically targets the androgen receptor (AR), AR variants, and the steroidogenic enzyme AKR1C3. It inhibits AKR1C3's enzymatic function, decreases the conversion of androstenedione to testosterone, and reduces the expression of both AR and AR-V7, subsequently downregulating their target genes. Additionally, LX1 is effective in overcoming tumor cell resistance to Enzalutamide, and when combined with Enzalutamide, it further suppresses tumor growth.</p>Fórmula:C22H15F6NO2Forma y color:SolidPeso molecular:439.35Androgen receptor degrader-5
CAS:<p>Androgen receptor degrader-5 (compound 14k) demonstrates superior capabilities, specifically in androgen receptor degradation and antiproliferative activity, showcasing its promising properties.</p>Fórmula:C29H25F4N5O2Forma y color:SolidPeso molecular:551.53Androgen receptor ligand 1
CAS:<p>Androgen receptorligand 1 is a ligand for the androgen receptor (AR). It interacts with the CRBN E3 ligase via a linker to form an AR-PROTAC degrader. This compound is useful in prostate cancer research.</p>Fórmula:C19H16F4N2OForma y color:SolidPeso molecular:364.34A4B17
<p>A4B17 is an inhibitor of androgen receptor N-terminal with potential for androgen-responsive prostate cancer treatment.</p>Fórmula:C14H7F4NSForma y color:SolidPeso molecular:297.27
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