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(208 products)
- Annexin A(11 products)
- Aromatase(20 products)
- Estrogen/progestogen Receptor(48 products)
- GPR(1 products)
- Glucocorticoid Receptor(153 products)
- LHRH(1 products)
- Opioid Receptor(297 products)
- Prostaglandin Receptor(119 products)
- RAAS(86 products)
- Reductase(52 products)
- Somatostatin(46 products)
- Thyroid hormone receptor(THR)(26 products)
- Vasopressin Receptor(44 products)
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Found 3180 products of "Endocrinology/Hormones"
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GPR81 agonist 1
CAS:<p>GPR81 agonist 1 is a GPR81 agonist that improves glycaemic control in insulin-resistant mouse models for the study of diabetes and obesity.</p>Formula:C22H30N4O2S2Purity:99.68%Color and Shape:SolidMolecular weight:446.63EM-800
CAS:<p>EM-800, an ERα ligand & prodrug of EM-652, inhibits E1-stimulated ZR-75-1 tumor growth in mice.</p>Formula:C39H47NO6Color and Shape:SolidMolecular weight:625.79JTC-801 free base
CAS:<p>JTC-801 is a selective antagonist of the opioid receptor-like1 receptor (Ki: 8.2 nM).</p>Formula:C26H25N3O2Purity:98%Color and Shape:SolidMolecular weight:411.5ML138
CAS:<p>ML138 is a probe for MLPCN, an agonist of the κ opioid receptor.</p>Formula:C19H14Cl2N4OSColor and Shape:SolidMolecular weight:417.31Estrogen receptor antagonist 2
CAS:<p>ER antagonist 2 selectively suppresses ERα, a key breast cancer driver, with research potential in the disease.</p>Formula:C26H31F4N5Color and Shape:SolidMolecular weight:489.55LY88074 Methyl ether
CAS:<p>LY88074 Methyl ether combats estrogen deficit, targeting osteoporosis and hyperlipidemia.</p>Formula:C22H16O4SPurity:98%Color and Shape:SolidMolecular weight:376.42(R)-Bicalutamide
CAS:<p>(R)-Bicalutamide, an AR antagonist with antitumor properties, is crucial in prostate cancer research.</p>Formula:C18H14F4N2O4SColor and Shape:SolidMolecular weight:430.37Cancer-Targeting Compound 1
CAS:<p>Cancer-Targeting Compound 1 can be used in the study of hormone-related cancers, including the treatment or prevention of fibroids, uterine leiomyomas,</p>Formula:C15H13N3O2SPurity:99.83%Color and Shape:SolidMolecular weight:299.35Xelaglifam
CAS:<p>Xelaglifam is a potent agonist of G protein-coupled receptor 40 (GPR40) and exhibits hypoglycemic effects.</p>Formula:C30H28FNO5Color and Shape:SolidMolecular weight:501.55GSK1521498 free base
CAS:<p>GSK1521498 free base is an effective and selective μ-opioid receptor antagonist with potential applications in obesity, alcoholism, and drug addiction.</p>Formula:C24H20F2N4Purity:99.85%Color and Shape:SolidMolecular weight:402.44Norethisterone enanthate
CAS:<p>Norethisterone enanthate (NSC-9564) is a long-acting parenteral progestogen with antigonadotropic effects.</p>Formula:C27H38O3Purity:99.23%Color and Shape:SolidMolecular weight:410.59BMS 183920
CAS:<p>BMS 183920 is a potent Angiotensin II Receptor antagonist that improves improves Caco-2 cell permeability in vivo.</p>Formula:C26H19N5O3Purity:98.92%Color and Shape:SolidMolecular weight:449.46GSK1521498 free base (hydrochloride)
CAS:<p>GSK1521498 free base (hydrochloride) is a selective antagonist of the μ-opioid receptor (MOR).</p>Formula:C24H21ClF2N4Purity:98%Color and Shape:SolidMolecular weight:438.9TAK-875 Hemihydrate
CAS:<p>TAK-875 Hemihydrate (Fasiglifam) is a selective GPR40 agonist with EC50 of 14 nM, 400-fold more potent than oleic acid.</p>Formula:C29H32O7SH2OPurity:98%Color and Shape:SolidMolecular weight:533.63OT antagonist 3
CAS:<p>OT antagonist 3 is an antagonist of oxytocin (OT).</p>Formula:C21H20N6O2Purity:98%Color and Shape:SolidMolecular weight:388.42LY191704
CAS:<p>LY 191704 is a 5α-reductase type 1 inhibitor.</p>Formula:C14H16ClNOColor and Shape:SolidMolecular weight:249.74TUG-905
CAS:<p>TUG-905 is an agonist for free fatty acid receptor 4 (FFA4/GPR120), and TUG-905 has the potential to treat agitation.</p>Formula:C27H30FNO5SColor and Shape:SolidMolecular weight:499.59AT2R antagonist 1
CAS:<p>AT2R antagonist 1: potent, selective ligand, Ki 29 nM, inhibits CYP enzymes, stable in liver microsomes.</p>Formula:C23H30N4O4S2Color and Shape:SolidMolecular weight:490.64GSK1521498
CAS:<p>GSK1521498 is a selective antagonist of the μ-opioid receptor (MOR).</p>Formula:C24H23F2N4O4PPurity:98%Color and Shape:SolidMolecular weight:500.43Org30958
CAS:<p>Org30958 is a potent inhibitor of aromatase in vivo.</p>Formula:C21H30O2S2Purity:98%Color and Shape:SolidMolecular weight:378.59Estrogen receptor antagonist 1
CAS:<p>"Potent estrogen receptor blocker with promise for breast cancer treatment per WO2021249533A1."</p>Formula:C28H33F4N5Color and Shape:SolidMolecular weight:515.59(R)-DPN
CAS:<p>estrogen receptor (ER) β agonist</p>Formula:C15H13NO2Purity:98%Color and Shape:SolidMolecular weight:239.27MK181
CAS:<p>MK181 is an inhibitor of AKR1B10, a tumor marker and promising antineoplastic target.</p>Formula:C16H13BrClNO4Purity:98%Color and Shape:SolidMolecular weight:398.64GSK1104252A
CAS:<p>GSK1104252A is a potent and selective agonist of GPR119.</p>Formula:C22H27FN4O5SPurity:98%Color and Shape:SolidMolecular weight:478.54DIPPA hydrochloride
CAS:<p>κ receptor antagonist</p>Formula:C22H24Cl3N3OSPurity:98%Color and Shape:SolidMolecular weight:484.87Gumelutamide
CAS:<p>Gumelutamide, a tetrahydropyridopyrimidine compound, functions as both an antiandrogen and an antineoplastic agent by acting as an androgen antagonist.</p>Formula:C22H21ClN6OColor and Shape:SolidMolecular weight:420.89Methylprednisolone Aceponate
CAS:<p>Methylprednisolone Aceponate (SH 440), a non-halogenated corticosteroid, is a potent anti-inflammatory agent.</p>Formula:C27H36O7Purity:99.00% - 99.61%Color and Shape:SolidMolecular weight:472.57DDD028
CAS:<p>DDD-028 is a potential non-opioid and non-cannabinoid analgesic. It was used for treating neuropathic and inflammatory pain.</p>Formula:C20H20N2Purity:98%Color and Shape:SolidMolecular weight:288.39MK-3984
CAS:<p>MK-3984 is a selective androgen receptor modulator, used in the study of conditions caused by androgen deficiency.</p>Formula:C17H12F7NO2Purity:99.91%Color and Shape:SolidMolecular weight:395.27LY117018
CAS:<p>LY117018 shows antiproliferative effects on breast cancer cell lines. LY117018 is a Raloxifene analog and is a selective estrogen receptor modulator.</p>Formula:C27H25NO4SPurity:98%Color and Shape:SolidMolecular weight:459.56Aldose reductase-IN-5
CAS:<p>Aldose reductase-IN-5 inhibits ALR2, boosts inhibitory response and antioxidants, slowing diabetes complications.</p>Formula:C18H15NO5Color and Shape:SolidMolecular weight:325.32ALR2-IN-2
<p>ALR2-IN-2 inhibits ALR2 (27 nM IC50) & ALR1 (228 nM IC50), used in diabetes complication research.</p>Formula:C17H11FN2O2S2Color and Shape:SolidMolecular weight:358.41AT1R antagonist 1
CAS:<p>AT1R Antagonist 1 (compound 10) serves as a potent, selective ligand for AT1R with considerable affinity, demonstrated by a K i value of 8.5 nM [1].</p>Formula:C28H32F3N5O4S2Color and Shape:SolidMolecular weight:623.71SB 611812
CAS:<p>SB 611812 is an antagonist of urotensin-II (UT) and can be used in studies about the treatment of cardiovascular disease.</p>Formula:C17H16Cl3F3N2O3SPurity:99.34%Color and Shape:SolidMolecular weight:491.74Glucocorticoid receptor-IN-2
CAS:<p>Glucocorticoid receptor-IN-2 selectively targets GR with anti-inflammatory effects (IC50: 0.171 nM) and activates MMTV (EC50: 0.94 nM).</p>Formula:C25H20F4N6O2Color and Shape:SolidMolecular weight:512.46D-Methionine sulfoxide
CAS:<p>D-Methionine sulfoxide inhibits peptide methionine sulfoxide reductase and can be used to inhibit ochre mites.D-Methionine sulfoxide can be added to chicken</p>Formula:C5H11NO3SPurity:99.54%Color and Shape:SolidMolecular weight:165.21OP-1074
CAS:<p>OP-1074 is a pure antiestrogen and a selective degrader of ER, shows specific antiestrogenic activity for ERα and ERβ.</p>Formula:C29H31NO4Purity:98%Color and Shape:SolidMolecular weight:457.56Levormeloxifene
CAS:<p>Levormeloxifene is a selective modulator of the estrogen receptor. It inhibits the production of vaginal tropoelastin and transforming growth factor-beta 1.</p>Formula:C30H35NO3Purity:98%Color and Shape:SolidMolecular weight:457.6L 158809
CAS:<p>L 158809 is an antagonist of the angiotensin II type 1 receptor.</p>Formula:C24H23N7Color and Shape:SolidMolecular weight:409.49OBHS
CAS:<p>OBHS is an inhibitor of estrogen receptor alpha (ERα).</p>Formula:C24H20O6SColor and Shape:SolidMolecular weight:436.48Nitromifene
CAS:<p>Nitromifene is the estrogen receptor antagonist.</p>Formula:C27H28N2O4Purity:98%Color and Shape:SolidMolecular weight:444.52A 81282
CAS:<p>A 81282 is a selective antagonist of angiotensin receptors. It has the activity of lowering blood pressure.</p>Formula:C23H23N7O2Purity:98%Color and Shape:SolidMolecular weight:429.47(±)-AC 7954 hydrochloride
CAS:<p>(±)-AC 7954 hydrochloride is a urotensin-II (UT) receptor activator.</p>Formula:C19H21Cl2NO2Purity:99.42%Color and Shape:White SolidMolecular weight:366.28DK3
CAS:<p>DK3 is a potent and selective agonist of estrogen-related receptor alpha (ERRα). ERRα is a potential drug target for cancer and metabolic diseases [1].</p>Formula:C16H14N2O2Color and Shape:SolidMolecular weight:266.29SHR1653
CAS:<p>SHR1653 is a highly potent, selective and brain penetrated antagonist of oxytocin receptor (OTR)(IC50 of 15 nM for hOTR).</p>Formula:C21H21ClFN5O2Purity:98%Color and Shape:SolidMolecular weight:429.88Capesaris
CAS:<p>Capesaris (GTX-758) is an oral estrogen receptor α agonist, used in prostate cancer research.</p>Formula:C19H13F2NO3Purity:99.65%Color and Shape:SolidMolecular weight:341.31Androgen 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>Formula:C21H25ClN4O3Purity:99.054%Color and Shape:SolidMolecular weight:416.9PF-4455242 HCl
CAS:<p>PF-4455242 HCl is a selective and orally available κ-opioid receptor antagonist that exhibiting antidepressant effects.</p>Formula:C21H29ClN2O2SPurity:99.59%Color and Shape:SolidMolecular weight:408.99SB-568849
CAS:<p>SB-568849 is a melanin-concentrating hormone receptor 1 antagonist (pKi: 7.7).</p>Formula:C28H31F3N2O3Purity:98%Color and Shape:SolidMolecular weight:500.55Dimethomorph
CAS:<p>Dimethomorph is a fungicide and sterol biosynthesis inhibitor that inhibits fungal cell wall formation,. inhibits androgen receptor (AR) .</p>Formula:C21H22ClNO4Purity:99.2%Color and Shape:Solid CrystallineMolecular weight:387.86FSHR agonist 1
CAS:<p>FSHR agonist 1: high-affinity, allosteric FSHR activator, pEC50 of 7.72, interacts with TMD.</p>Formula:C26H33N3O3SColor and Shape:SolidMolecular weight:467.62MCH-1 antagonist 1
CAS:<p>MCH-1 antagonist 1 also inhibits CYP3A4 (IC50: 10μM).MCH-1 antagonist 1 is a potent melanin concentrating hormone (MCH-1) antagonist (Ki: 2.6 nM).</p>Formula:C25H26N4O2Purity:98%Color and Shape:SolidMolecular weight:414.5CP-866087
CAS:<p>CP-866087 is a novel, potent and selective mu-opioid receptor antagonist for the study of female sexual dysfunction.</p>Formula:C24H28N2O2Purity:99.56% - >99.99%Color and Shape:SoildMolecular weight:376.49SB 706375
CAS:<p>urotensin-II (UT) receptor antagonist</p>Formula:C20H22BrF3N2O5SPurity:98%Color and Shape:SolidMolecular weight:539.36ATC0065 HCl
CAS:<p>ATC0065 dihydrochloride is a novel nonpeptidic and potent melanin-concentrating hormone receptor 1 (MCHR1) selective antagonist.</p>Formula:C25H31BrCl2F3N5OColor and Shape:SolidMolecular weight:625.35GPR84 antagonist 8
CAS:<p>GPR84 antagonist 8 is a selective GPR84 antagonist applicable for investigating inflammatory and fibrotic diseases.</p>Formula:C23H23N3O5Purity:99.45%Color and Shape:SolidMolecular weight:421.45J9
CAS:<p>J9 is an inhibitor of Glucocorticoid resistance. J9 reverses Dexamethasone Resistance in T-cell Acute Lymphoblastic Leukemia.</p>Formula:C12H12N4Color and Shape:SolidMolecular weight:212.25Camizestrant
CAS:<p>Camizestrant (Estrogen receptor antagonist 2) is an antagonist of the estrogen receptor and can be used in studies about ER+ HER2-advanced breast cancer[1].</p>Formula:C24H28F4N6Purity:97.25% - 99.57%Color and Shape:SolidMolecular weight:476.51L 366682
CAS:<p>L 366682 is an oxytocin antagonist.</p>Formula:C40H53N9O6Purity:98%Color and Shape:SolidMolecular weight:755.91OT antagonist 1
CAS:<p>OT antagonist 1 is a potent and selective antagonist of Oxytocin(Ki of 50 nM)</p>Formula:C22H22N4O3Purity:98%Color and Shape:SolidMolecular weight:390.44VPC-13789
CAS:<p>VPC-13789: potent, selective oral antiandrogen for CRPC with 0.19 μM IC50 in LNCaP cells.</p>Formula:C21H16F3N3OColor and Shape:SolidMolecular weight:383.37Axomadol
CAS:<p>Axomadol (EN3324) is a centrally active analgesic compound. It has opioid agonistic properties and inhibitory effects on the reuptake of monoamines.</p>Formula:C16H25NO3Purity:98%Color and Shape:SolidMolecular weight:279.37(R,R)-THC
CAS:<p>agonist at ERα receptor and antagonist at ERβ receptor</p>Formula:C22H24O2Purity:98%Color and Shape:SolidMolecular weight:320.42LY285434
CAS:<p>LY285434 is a suitable angiotensin II receptor antagonist.</p>Formula:C23H25N5O2Purity:98%Color and Shape:SolidMolecular weight:403.48Chlorothalonil
CAS:<p>Chlorothalonil (DAC 2787): Broad-spectrum, efficient, low-toxicity fungicide for fruits, vegetables, rice, wheat, cotton.</p>Formula:C8Cl4N2Purity:98.01% - 98.71%Color and Shape:Colorless Crystals SolidMolecular weight:265.91D36
CAS:<p>D36 is an androgen receptor allosteric antagonist. It also has inverse agonist properties.</p>Formula:C21H24N2O2Purity:98%Color and Shape:SolidMolecular weight:336.43FERb 033
CAS:<p>ERβ receptor agonist</p>Formula:C13H9ClFNO3Purity:98%Color and Shape:SolidMolecular weight:281.67BTI-A-404
CAS:<p>BTI-A-404 is a potent and selective competitive inverse agonist of human GPR43.</p>Formula:C22H26N4O2Color and Shape:SolidMolecular weight:378.47CPSA
CAS:<p>CPSA is an effective and selective AKR1C1 inhibitor.</p>Formula:C13H9ClO3Color and Shape:SolidMolecular weight:248.66MK-4541
CAS:<p>MK-4541: oral, selective AR modulator, blocks 5α-reductase, curbs AR+ prostate cancer growth, effective in mouse model.</p>Formula:C22H31F3N2O3Color and Shape:SolidMolecular weight:428.49SCH 221510
CAS:<p>SCH 221510: oral NOP agonist, EC50=12 nM, Ki=0.3 nM, anxiolytic, for neurological research.</p>Formula:C28H31NOPurity:99.54%Color and Shape:SolidMolecular weight:397.55VPC-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>Formula:C21H14O2Purity:98%Color and Shape:SolidMolecular weight:298.33CR-665 Acetate
CAS:<p>CR-665, a kappa-opioid agonist, is used potentially for the treatment of postoperative pain.</p>Formula:C38H53N9O6Color and Shape:SolidMolecular weight:731.899Dehydro Olmesartan
CAS:<p>Dehydro Olmesartan, from Olmesartan, is an AT1R blocker for researching hypertension.</p>Formula:C24H24N6O2Color and Shape:SolidMolecular weight:428.49KB-130015
CAS:<p>KB-130015, a activator of hERG1 potassium channels, blocks native and recombinant hERG1 channels at high voltages.</p>Formula:C18H14I2O4Purity:98%Color and Shape:SolidMolecular weight:548.11RU 43044
CAS:<p>RU 43044 is a selective glucocorticoid receptor antagonist that has exhibited an antidepressant-like effect.</p>Formula:C29H34O2Purity:98%Color and Shape:SolidMolecular weight:414.58LY 281217
CAS:<p>LY 281217, an organic opioid agonist, can produce analgesic effects in mice.</p>Formula:C32H42N4O6Purity:98%Color and Shape:SolidMolecular weight:578.7Idoxifene
CAS:<p>Idoxifene is a tissue-specific selective estrogen receptor modulator.</p>Formula:C28H30INOColor and Shape:SolidMolecular weight:523.45L-366509
CAS:<p>L-366,509 is an antagonist of oxytocin.</p>Formula:C25H33NO5SPurity:98%Color and Shape:SolidMolecular weight:459.6Cyprodinil
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>Formula:C14H15N3Color and Shape:SolidMolecular weight:225.29Dup 747
CAS:<p>Dup 747 is an analgesic that binds with high affinity and selectivity to the kappa-opioid receptor.</p>Formula:C24H28Cl2N2O2Purity:98%Color and Shape:SolidMolecular weight:447.4Androgen 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>Formula:C22H18ClNColor and Shape:SolidMolecular weight:331.84BMS-986124
CAS:<p>BMS-986124 is an allosteric modulator of the μ-Opioid Receptor.</p>Formula:C16H15BrClNO3S2Color and Shape:SolidMolecular weight:448.78Aldose reductase-IN-4
CAS:<p>Aldose reductase-IN-4 (compund IIc) is an inhibitor of aldose reductase with IC50s of 11.70 μM and 0.98 μM for ALR1 and ALR2, respectively [1].</p>Formula:C14H10FNO3SColor and Shape:SolidMolecular weight:291.3Aldose reductase-IN-6
CAS:<p>AR inhibitor Aldose reductase-IN-6: IC50 3.164 μM, Ki 0.018 μM, non-toxic to normal cells.</p>Formula:C20H16N4O2SColor and Shape:SolidMolecular weight:376.43BMS-819881
CAS:<p>BMS-819881 is a melaninconcentrating hormone receptor 1 (MCHR1) antagonist, which binds rat MCHR1 with a Ki of 7 nM and it also is selective and potent for</p>Formula:C24H21ClN2O4SPurity:98%Color and Shape:SolidMolecular weight:468.95Olmesartan methyl ester
CAS:<p>Olmesartan methyl ester: an intermediate for synthesizing Olmesartan medoxomil, a strong AT1 receptor blocker.</p>Formula:C25H28N6O3Color and Shape:SolidMolecular weight:460.53Fenhexamid
CAS:<p>Fenhexamid (Elevate), a sterol biosynthesis inhibitor, shows antifungal activity against the plant pathogenic fungus.</p>Formula:C14H17Cl2NO2Purity:99.56%Color and Shape:SolidMolecular weight:302.20DK1
CAS:<p>DK1: potent ERRα modulator, lowers blood glucose, promising for diabetes research.</p>Formula:C16H13ClN2O2Color and Shape:SolidMolecular weight:300.74GPR40 agonist 1
CAS:<p>GPR40 agonist 1 is an effective new GPR40 agonist (EC50s: 17 nM and 2 nM for rGPR40 and hGPR40).</p>Formula:C27H30FN3O4Purity:98%Color and Shape:SolidMolecular weight:479.54Endomorphin 1 acetate
CAS:<p>Endomorphin 1 acetate is a μ-opioid receptor agonist with antinociceptive and analgesic effects and can be used to study neurological diseases.</p>Formula:C36H42N6O7Color and Shape:SolidMolecular weight:670.75SIM-688
CAS:<p>SIM-688 is a selective and orally active estrogen receptor inhibitor of NF-κB transcriptional activity (IC50 = 122 nM in HAECT-1 cells).</p>Formula:C34H31F3N2O2Purity:99.56%Color and Shape:SolidMolecular weight:556.62ORL1 antagonist 1
CAS:<p>ORL1 antagonist 1 is an o antagonist of pioid receptor-like 1 (ORL1) (IC50 of 61 nM).</p>Formula:C20H22ClN5Purity:98.92%Color and Shape:SolidMolecular weight:367.88Opioid receptor modulator 1
CAS:<p>Opioid receptor modulator 1 is a modulator of opioid receptor.</p>Formula:C18H23NO2Purity:98%Color and Shape:SolidMolecular weight:285.38L-159282
CAS:<p>L-159282 is an orally active and nonpeptide angiotensin II receptor antagonist. It also has anti-hypertensive activity.</p>Formula:C30H28N4O3SPurity:98%Color and Shape:SolidMolecular weight:524.63Estrogen receptor-IN-1
CAS:<p>Estrogen receptor-IN-1 (compound 16) is an effective estrogen receptor (ER) inhibitor with IC 50 s of 13, 5μM for ERα and Erβ, respectively [1].</p>Formula:C14H16OSiColor and Shape:SolidMolecular weight:228.36Tolonidine
CAS:<p>Tolonidine is orally active and has been shown to possess hypotensive. Tolonidine is a derivative of imidazoline.</p>Formula:C10H12ClN3Purity:98%Color and Shape:SolidMolecular weight:209.68LY2048978
CAS:<p>LY2048978: orally-active kappa antagonist, shows promise for mood and addiction in animal studies.</p>Formula:C19H24N2O2Purity:98%Color and Shape:SolidMolecular weight:312.41RU 45144
CAS:<p>RU 45144 is an estradiol derivative with antiestrogenic activity.</p>Formula:C28H37NO3Purity:98%Color and Shape:SolidMolecular weight:435.6AZD7268
CAS:<p>AZD7268 is a potent, selective, reversible, and orally bioavailable agonist of δ-opioid receptor with CNS penetration.</p>Formula:C29H30N4O2SColor and Shape:SolidMolecular weight:498.64
