GPCR/G-Protein
GPCR/G-Protein inhibitors are compounds that target G-protein coupled receptors (GPCRs) and associated G-proteins, which play critical roles in transmitting signals from the outside to the inside of cells. These inhibitors are essential for studying the signaling pathways mediated by GPCRs, which are involved in numerous physiological processes, including sensory perception, immune response, and neurotransmission. GPCR inhibitors are also important in drug development, as many therapeutic agents target these receptors. At CymitQuimica, we offer a wide range of high-quality GPCR/G-Protein inhibitors to support your research in pharmacology, cell biology, and related fields.
Subcategories of "GPCR/G-Protein"
- 5-HT Receptor(1,025 products)
- Adenosine Receptor(248 products)
- Adrenergic Receptor(3,031 products)
- Bombesin Receptor(35 products)
- Bradykinin Receptor(61 products)
- CXCR(154 products)
- CaSR(34 products)
- Cannabinoid Receptor(216 products)
- Cholecystokinin(1 products)
- Dopamine Receptor(445 products)
- Endothelin Receptor(86 products)
- GNRH Receptor(84 products)
- GPCR19(33 products)
- GRK(33 products)
- GTPase(22 products)
- Glucagon Receptor(191 products)
- Hedgehog/Smoothened(49 products)
- Histamine Receptor(385 products)
- LPA Receptor(21 products)
- Melatonin Receptor(26 products)
- OX Receptor(41 products)
- Opioid Receptor(325 products)
- PAFR(14 products)
- PKA(59 products)
- S1P Receptor(17 products)
- SGLT(31 products)
- Sigma receptor(46 products)
Show 19 more subcategories
Found 5963 products of "GPCR/G-Protein"
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KY 234
CAS:KY 234 is a thromboxane synthetase antagonist.Formula:C33H35N5O2Color and Shape:SolidMolecular weight:533.676GR 196429
CAS:GR 196429: MT1-selective melatonin receptor agonist; induces sleep, alters circadian rhythm, stimulates melatonin in mice.Formula:C14H18N2O2Purity:98%Color and Shape:SolidMolecular weight:246.3CID1792197
CAS:CID1792197 is a selective agonist of GPR55.Formula:C24H23N3O4S2Purity:98%Color and Shape:SolidMolecular weight:481.59Setastine HCl
CAS:Setastine HCl is a potent antagonist of histamine H1-receptor mediated responses.Formula:C22H29Cl2NOColor and Shape:SolidMolecular weight:394.38PM226
CAS:CB2 agonist with Ki of 12.8 nM; EC50 of 38.67 nM. Negligible CB1 affinity, no GPR55 activity. Anti-inflammatory, neuroprotective, crosses BBB.Formula:C22H31NO3Color and Shape:SolidMolecular weight:357.49L-817,818
CAS:somatostatin sst5 receptor agonistFormula:C33H36N4O3Purity:98%Color and Shape:SolidMolecular weight:536.66threo Ifenprodil hemitartrate
CAS:σ receptor agonist and NR2B subunit-selective NMDA receptor antagonistFormula:C21H27NO2C4H6O6Purity:98%Color and Shape:SolidMolecular weight:400.49Vasopressin V2 receptor antagonist 1
CAS:Vasopressin V2 receptor antagonist 1 (Compound 4g) is a vasopressin V2receptor (V2R) antagonist (Ki: 3.8 nM). dominant polycystic kidney disease (ADPKD).Formula:C33H37ClN4O4Color and Shape:SolidMolecular weight:589.12PA-9
CAS:PA-9 is the first small-molecule PAC1 receptor antagonist.Formula:C17H18N6O2Purity:98%Color and Shape:SolidMolecular weight:338.36MRS1177
CAS:MRS1177 is an effective and selective antagonist of the human Adenosine A3 receptor (hA3AR) (Ki: 0.3 nM).Formula:C20H12ClN5O2Purity:98%Color and Shape:SolidMolecular weight:389.79(R)-PF-06256142
CAS:(R)-PF-06256142: low-activity R enantiomer of a potent, selective D1 agonist reducing receptor desensitization.Formula:C21H16N4O2Color and Shape:SolidMolecular weight:356.38Vicagrel
CAS:Vicagrel, an oral antiplatelet, boosts aspirin's effect, targeting P2Y12 and fights clots in heart and vessel diseases.Formula:C18H18ClNO4SPurity:98%Color and Shape:SolidMolecular weight:379.86Ibodutant
CAS:Ibodutant is an effective and selective tachykinin NK2 receptor antagonist (pKi: 10.1).Formula:C37H48N4O4SPurity:98%Color and Shape:SolidMolecular weight:644.87APC-3316 tosylate
CAS:APC-3316 tosylate is a vinyl sulfone cysteine protease inhibitor and selective CCR4 antagonist.Formula:C39H46N4O7S2Color and Shape:SolidMolecular weight:746.94Benzoctamine
CAS:Benzoctamine: oral psychoactive with tranquillizing effects; boosts catecholamine turnover; enhances rat heart [3H]noradrenaline uptake.Formula:C18H19NColor and Shape:SolidMolecular weight:249.35S20928
CAS:S20928 is an antagonist of melatonin receptor.Formula:C17H19NOColor and Shape:SolidMolecular weight:253.34DV 7028 hydrochloride
CAS:DV 7028 hydrochloride is a 5-HT2A receptor antagonist.Formula:C21H26ClFN4O3Purity:98%Color and Shape:SolidMolecular weight:436.91hA2A/hCA XII modulator 1
CAS:Potent hA2AAR antagonist & hCA XII inhibitor; Ki: hA2AAR 6.4 nM, hCA XII 6.2 nM. Possible cancer research use.Formula:C24H19N7O4SColor and Shape:SolidMolecular weight:501.52Efpeglenatide
CAS:Efpeglenatide is a long-acting GLP-1 receptor agonist that improves insulin sensitivity, lowers blood glucose, delays weight gain, and supports metabolic disease research.Purity:100% - 100%Color and Shape:SolidVPC12249
CAS:VPC12249, a lysophosphatidic acid receptor type 1 (LPA1) antagonist, plays a functional role in osteoclast differentiation and bone resorption activity.Formula:C34H52NO6PColor and Shape:SolidMolecular weight:601.75A2AAR antagonist 1
CAS:Compound 21a, A2AAR antagonist with 20 nM Ki, useful in neurodegenerative disease study.Formula:C12H8BrN3OColor and Shape:SolidMolecular weight:290.12Carbinoxamine
CAS:Carbinoxamine: antihistamine for hay fever, angioedema, rhinitis, mild urticaria, dermatographism, allergic conjunctivitis; an H1-antagonist.Formula:C16H19ClN2OPurity:98%Color and Shape:LiquidMolecular weight:290.79EGIS-7625
CAS:EGIS-7625 is a selective and competitive antagonist of 5-HT2B receptor.Formula:C18H24Cl2N4O2Purity:98%Color and Shape:SolidMolecular weight:399.32Alprenolol hydrochloride, (S)-
CAS:Alprenolol hydrochloride, (S)- is a nonselective β-blocker. It is also a serotonin 5HT1A receptor antagonist.Formula:C15H24ClNO2Color and Shape:SolidMolecular weight:285.81GR-203040 HCl
CAS:GR203040 inhibits cyclophosphamide-induced damage in the rat and ferret bladder. GR-203040 is a selective NK1 receptor antagonist.Formula:C20H26Cl2N6OColor and Shape:SolidMolecular weight:437.37HEMADO
CAS:HEMADO is a potent and selective agonist of adenosine A3 receptor (Ki: 1.1 nM at the human A3 subtype).Formula:C17H23N5O4Purity:98%Color and Shape:SolidMolecular weight:361.4PF-592379
CAS:PF-592379 is a potent agonist of dopamine D3 receptor (EC50: 21 nM).Formula:C13H21N3OPurity:98%Color and Shape:SolidMolecular weight:235.33Centanafadine
CAS:Centanafadine inhibits NE/DA transporters and serotonin transporter (IC50: NE=6 nM, DA=38 nM, 5-HT=83 nM).Formula:C15H15NPurity:98%Color and Shape:SolidMolecular weight:209.29Clonidine
CAS:Clonidine (Kapvay): central alpha-adrenergic agonist, antihypertensive, often combined, not tied to liver issues.Formula:C9H9Cl2N3Purity:99.42% - 99.44%Color and Shape:Crystals SolidMolecular weight:230.09UCSF678
CAS:UCSF678: selective 42 nM partial agonist at 5-HT5AR, fewer off-target effects, and lower assay risks than SB-699551.Formula:C15H18N2O2SColor and Shape:SolidMolecular weight:290.38S(-)-Bisoprolol
CAS:S(-)-Bisoprolol, a β1-blocker, may aid in researching hypertension and heart diseases.Formula:C18H31NO4Color and Shape:SolidMolecular weight:325.44Spirendolol
CAS:Spirendolol is an antagonist of β adrenergic receptor.Formula:C21H31NO3Purity:98%Color and Shape:SolidMolecular weight:345.48UP202-56
CAS:UP202-56 is an adenosinergic agonist and is an adenosine analog.Formula:C33H37N7O4Purity:98%Color and Shape:SolidMolecular weight:595.69A331440
CAS:A331440 is an modulator of L-histidine and histamine H3 receptor.Formula:C22H27N3OColor and Shape:SolidMolecular weight:349.47TCS-OX2-29 HCl
CAS:TCS-OX2-29 is a selective orexin-2 receptor antagonist (IC50 = 40 nM), which plays an important role in pain modulation.Formula:C23H32ClN3O3Purity:98%Color and Shape:SolidMolecular weight:433.97(R,R)-Reboxetine mesylate
CAS:(R,R)-Reboxetine mesylate: Antidepressant, high bioavailability, (R,R) enantiomer, selective for noradrenaline, low toxicity.Formula:C20H27NO6SColor and Shape:SolidMolecular weight:409.5AZD5213
CAS:AZD5213: selective human H3 receptor antagonist, pKi 9.3, for sleep/cognition research.Formula:C19H25N3O2Color and Shape:SolidMolecular weight:327.42PF-06256142
CAS:PF-06256142 is a potent and selective orthosteric D1 receptor agonist(D1 EC50=30 nM ).Formula:C21H16N4O2Purity:98%Color and Shape:SolidMolecular weight:356.38MRS 1334
CAS:antagonist for the human adenosine A3 receptorFormula:C31H26N2O6Purity:98%Color and Shape:SolidMolecular weight:522.55SB357134
CAS:SB357134 is a potent, selective and orally active antagonist of 5-HT6 receptor and shows nootropic effects in animal studies.Formula:C17H18Br2FN3O3SPurity:98%Color and Shape:SolidMolecular weight:523.21AChE-IN-14
CAS:AChE-IN-14 inhibits eeAChE, hAChE, eqBuChE (IC50: 0.46-0.48 μM) and binds to H3R (Ki: 159.8 nM), useful for Alzheimer's research.Formula:C28H35NO3Color and Shape:SolidMolecular weight:433.58CP94253 hydrochloride
CAS:CP94253 hydrochloride: selective 5-HT1B agonist, Ki=2 nM; less active on 5-HT1A/D/C/2 (Ki=89/49/860/1600 nM).Formula:C15H20ClN3OPurity:99.78%Color and Shape:SolidMolecular weight:293.79Ref: TM-T22689
5mg66.00€10mg90.00€25mg205.00€50mg334.00€100mg537.00€200mg745.00€1mL*10mM (DMSO)66.00€YQA14
CAS:YQA14 is a selective, high-affinity dopamine D3 receptor antagonist that inhibits cocaine self-administration in rats and mice, opioid addiction research.Formula:C23H27ClN4O3Purity:99.52%Color and Shape:SolidMolecular weight:442.94(R)-(-)-α-Methylhistamine dihydrobromide
CAS:(R)-(-)-α-Methylhistamine dihydrobromide is a potent and selective agonist of H3 histamine receptor( Kd of 50.3 nM).Formula:C6H13Br2N3Purity:98%Color and Shape:SolidMolecular weight:287WIN 62,577
CAS:WIN 62,577 is a allosteric antagonist of mAChR.Formula:C29H31N3OPurity:98%Color and Shape:SolidMolecular weight:437.58JNJ-39220675
CAS:JNJ-39220675, a selective histamine H3 receptor antagonist, reduces the abuse-related effects of alcohol in rats.Formula:C21H24FN3O2Purity:98.13% - 99.89%Color and Shape:SolidMolecular weight:369.43LUF6000
CAS:LUF6000 is an allosteric modulator of the human A3 adenosine receptor (AR).Formula:C22H20Cl2N4Color and Shape:SolidMolecular weight:411.33Tacitin
CAS:Tacitin (Benzoctamine Hydrochloride) shows sedative and anti-anxiety properties. Tacitin blocks the central postsynaptic serotonin receptors.Formula:C18H20ClNPurity:98%Color and Shape:SolidMolecular weight:285.81Melatonin receptor agonist 1
CAS:Melatonin receptor agonist 1 (compound 20c) is a potent agonist of melatonin receptor (MT) with Ki values of 108 nM for MT2 and 1140 nM for MT 1 [1].Formula:C15H19N3O2Color and Shape:SolidMolecular weight:273.33MAT2A-IN-2
CAS:MAT2A-IN-2 is a potent inhibitor of MAT2A. MAT2A-IN-2 has potential for cancer disease research.Formula:C23H17F3N6O2Color and Shape:SolidMolecular weight:466.42Fosnetupitant
CAS:Fosnetupitant is a methylene phosphate prodrug of Netupitant. It has a pKi of 9.5 for the human NK1 receptor.Formula:C31H35F6N4O5PPurity:98%Color and Shape:SolidMolecular weight:688.6Proglumide sodium
CAS:Non-selective cholecystokinin (CCK) antagonistFormula:C18H26N2NaO4Purity:98%Color and Shape:SolidMolecular weight:357.4Epanolol
CAS:Epanolol is a potent β-adrenoceptor partial agonist with a greater affinity for β1- than β2-adrenoceptors.Formula:C20H23N3O4Purity:98%Color and Shape:SolidMolecular weight:369.41OPC-14523 hydrochloride
CAS:OPC-14523 hydrochloride, an oral sigma/5-HT1A agonist, shows potent antidepressant activity with strong receptor affinity.Formula:C23H29Cl2N3O2Purity:99.60%Color and Shape:SolidMolecular weight:450.4A2A/A1 AR antagonist-1
CAS:A2A/A1 AR antagonist-1 is a potent dual antagonist for ischemic stroke research with Ki values of 5.58 nM (A2A) and 24.2 nM (A1).Formula:C15H12N6O2Color and Shape:SolidMolecular weight:308.29GPR55 agonist 3
CAS:Compound 26, a GPR55 agonist, exhibits potent activity with EC50 values of 0.239 nM for hGPR55 and 1.76 nM for rGPR55.Formula:C19H16F4N4Color and Shape:SolidMolecular weight:376.35LY 306669
CAS:LY 306669 is an antagonist of leukotriene B4 receptor.Formula:C23H29FN4NaO2Color and Shape:SolidMolecular weight:435.499Adriforant
CAS:Adriforant (PF-3893787,ZPL-3893797) is a competitive histamine receptor 4 h4 antagonist that antagonizes histamine-induced phosphorylation of ERK, inflammation.Formula:C13H22N6Purity:99.84%Color and Shape:SolidMolecular weight:262.35SNT-207858
CAS:SNT-207858: selective, BBB-penetrating, oral MC-4 receptor antagonist with 22 nM IC50 (binding), 11 nM (function).Formula:C32H45Cl4N5O3Purity:98%Color and Shape:SolidMolecular weight:689.54Palmitoyl serinol
CAS:Anticancer agent 110 is an anticancer compound with cytotoxic, antitumor and antileukemic activities.Formula:C19H39NO3Color and Shape:SolidMolecular weight:329.52Orexin receptor antagonist 3
CAS:Orexin receptor antagonist 3 (example 216) is an orexin receptor antagonist.Formula:C21H22N8O3Color and Shape:SolidMolecular weight:434.45AGI-41998
CAS:AGI-41998: a potent MAT2A inhibitor that crosses the blood-brain barrier, targeting SAM enzymes for cancer therapy and CNS research.Formula:C22H16BrF3N4O2Color and Shape:SolidMolecular weight:505.29LY 393558
CAS:Dual 5-HT1B/1D receptor antagonistFormula:C26H31FN4O4S2Purity:98%Color and Shape:SolidMolecular weight:546.68SF 11
CAS:SF 11 is a potent and brain penetrant neuropeptide Y Y2 receptor antagonist with IC50 of 199 nM. Antidepressant-like activityFormula:C27H30N2O2SPurity:99.51%Color and Shape:SolidMolecular weight:446.6LUF 5834
CAS:A2A and A2B adenosine receptor partial agonistFormula:C17H12N6OSPurity:98%Color and Shape:SolidMolecular weight:348.38Anatibant
CAS:Anatibant: a strong non-peptide, inhibits bradykinin B2; lowers brain swelling and damage post-trauma.Formula:C34H36Cl2N6O5SPurity:98%Color and Shape:SolidMolecular weight:711.66PROTAC(H-PGDS)-7
CAS:PROTAC(H-PGDS)-7, a potent H-PGDS degrader, inhibits PGD2 in KU812 cells; DC50 is 17.3 pM. Potential DMD treatment.Formula:C40H38N8O7Color and Shape:SolidMolecular weight:742.78Adrenaline sulfate
CAS:Adrenaline sulfate: orally active, α/β-adrenergic agonist, treats anaphylaxis, researched for cardiac arrest.Formula:C9H15NO7SColor and Shape:SolidMolecular weight:281.279SDZ 21009
CAS:β-adrenoceptor and 5-HT1A/1B receptor antagonistFormula:C19H28N2O4Purity:98%Color and Shape:SolidMolecular weight:348.44Midodrine (hydrochloride)
CAS:Midodrine hydrochloride ((±)-Midodrine hydrochloride) is an α1-receptor agonist used in the treatment of dysautonomia and orthostatic hypotension.Formula:C12H19ClN2O4Molecular weight:290.74ROS 234
CAS:ROS 234 is a potent H3 antagonist with pKB 9.46 for Guinea-pig ileum and pKi 8.90 for Rat cortex; ED50 of 19.12 mg/kg in rats, but with limited central access.Formula:C13H15N5Color and Shape:SolidMolecular weight:241.295'-(N-Cyclopropyl)carboxamidoadenosine
CAS:adenosine A2 receptor agonistFormula:C13H16N6O4Purity:98%Color and Shape:SolidMolecular weight:320.3SM-130686
CAS:SM-130,686: orally-active GHSR agonist, 50% as potent as ghrelin in stimulating growth hormone.Formula:C22H24Cl2F3N3O3Color and Shape:SolidMolecular weight:506.35SKF83959
CAS:SKF83959: dopamine D1 partial agonist, Ki: D1(1.18 nM), D5(7.56 nM), D2(920 nM), D3(399 nM); improves cognitive function in depression, Alzheimer's.
Formula:C18H20ClNO2Purity:98.68%Color and Shape:SolidMolecular weight:317.81DW-1350
CAS:DW-1350 is an antagonist of LTB4 receptor.Formula:C25H31N3O3SPurity:98%Color and Shape:SolidMolecular weight:453.6Substance P Receptor Antagonist 1
CAS:Substance P Receptor Antagonist 1 may aid in treating GI, inflammatory, respiratory, and CNS disorders.Formula:C24H29F3N2O2Purity:98%Color and Shape:SolidMolecular weight:434.49JNJ 10181457 dihydrochloride
CAS:JNJ 10181457 dihydrochloride is a Histamine H3 receptor antagonist.Formula:C20H28N2OPurity:98%Color and Shape:SolidMolecular weight:312.45CFM 1571 hydrochloride
CAS:CFM 1571 hydrochloride stimulates sGC with EC50 of 5.49 μM; potential for cardiovascular research.Formula:C23H29ClN4O3Color and Shape:SolidMolecular weight:444.96BMY-25271
CAS:BMY-25271 is an antagonist of histamine H2 receptor.Formula:C12H19N5O2S2Purity:98%Color and Shape:SolidMolecular weight:329.44Broxaterol
CAS:Broxaterol is a β2 adrenoreceptor agonist. It is part of a class of drugs that affect the smooth muscle receptors in the body.Formula:C9H15BrN2O2Purity:98%Color and Shape:SolidMolecular weight:263.13B-HT 933 dihydrochloride
CAS:Azepexole (B-HT 933) dihydrochloride is an α2-adrenoceptor agonist, pKi: 8.3/α2A, 7.6/α2B, 7.5/α2C; IC50: 78.72 nM for peristalsis inhibition.Formula:C9H17Cl2N3OColor and Shape:SolidMolecular weight:254.16Levobunolol
CAS:Levobunolol is a nonselective beta-blocker. It is used topically to treat glaucoma.Formula:C17H25NO3Color and Shape:White To Pink PowderMolecular weight:291.39BMS-665053
CAS:BMS-665053: CRF1 receptor antagonist, IC50 = 1.0 nM; inhibits cAMP in Y-79 cells, IC50 = 4.9 nM; anti-anxiety in rats, Cl = 17 mL/min/kg, t½ = 7.8 h.Formula:C16H14Cl3F2N3O2Purity:98%Color and Shape:SolidMolecular weight:424.66SNT-207858 free base
CAS:SNT-207858: selective MC-4 receptor antagonist, passes blood-brain barrier, orally active, IC50: 22 nM (binding), 11 nM (function).Formula:C32H43Cl2N5O3Purity:98%Color and Shape:SolidMolecular weight:616.62Mosapramine
CAS:Mosapramine is a dopamine D2-receptor antagonist.Formula:C28H35ClN4OPurity:98%Color and Shape:SolidMolecular weight:479.06Kadsurenone
CAS:Kadsurenone, from haifenteng, blocks PAF/PTAFR pathway, promising for breast cancer bone metastases treatment.Formula:C21H24O5Color and Shape:SolidMolecular weight:356.41Bufetolol
CAS:Bufetolol is an antagonist of beta-adrenoceptor.Formula:C18H29NO4Purity:98%Color and Shape:SolidMolecular weight:323.43MK-2894
CAS:MK-2894 is a highly potent and selective antagonist of second generation EP4 .Formula:C25H22F3NO3SPurity:99.22%Color and Shape:SolidMolecular weight:473.51Ref: TM-T12061
1mg57.00€5mg120.00€10mg205.00€25mg497.00€50mg879.00€100mg1,161.00€500mg2,367.00€1mL*10mM (DMSO)128.00€(Rac)-WAY-161503
CAS:(Rac)-WAY-161503 is a selective and high-affinity agonist of the 5-HT2C receptor (Ki: 4 nM; EC50: 12 nM), with anti-obesity and antidepressant effects.Formula:C11H11Cl2N3OPurity:99.51%Color and Shape:SolidMolecular weight:272.13Sultopride
CAS:Sultopride is a compound that an amino on the sulfamide group of sulpiride is replaced by an ethyl group.Formula:C17H26N2O4SColor and Shape:SolidMolecular weight:354.46Alprenolol tartrate, (S)-
CAS:Alprenolol tartrate, (S)- is an 5-HT1A antagonist.Formula:C19H29NO8Purity:98%Color and Shape:SolidMolecular weight:399.44Guanoxabenz hydrochloride
CAS:Guanoxabenz hydrochloride, α2 adrenergic receptor agonist; Ki: 4000 nM, α2A form Ki: 40 nM.Formula:C8H9Cl3N4OColor and Shape:SolidMolecular weight:283.54PD 119819
CAS:PD 119819 is a heterocyclic piperazine. PD 119819 is an extremely selective DA autoreceptor agonist.Formula:C21H25Cl2N3O3Purity:98%Color and Shape:SolidMolecular weight:438.35BI-L 239
CAS:BI-L 239 is an inhibition of 5-lipoxygenase products that cause bronchoconstriction.Formula:C16H15FOColor and Shape:SolidMolecular weight:242.29Bifeprunox Mesylate
CAS:Bifeprunox: partial dopamine/serotonin agonist for schizophrenia; suppresses VTA neurons via D2; affects rat nicotine-seeking.Formula:C25H27N3O5SPurity:98%Color and Shape:SolidMolecular weight:481.56Penbutolol
CAS:Penbutolol is a nonselective beta-blocker utilized as an antihypertensive and an antianginal.Formula:C18H29NO2Purity:98%Color and Shape:SolidMolecular weight:291.43DMP 696
CAS:DMP 696 is a selective antagonist of corticotropin-releasing hormone receptor 1. It is used for the treatment of anxiety and depression.Formula:C18H21Cl2N5O2Purity:98%Color and Shape:SolidMolecular weight:410.3IMTPPE
CAS:IMTPPE inhibits transcriptional activity and protein level of AR in C4-2 prostate cancer cells. It also inhibits AR-target gene expression.Formula:C20H27N3O2SColor and Shape:SolidMolecular weight:373.51JMV3002
CAS:JMV3002, a ghrelin receptor foe, blocks hexarelin-induced eating in rats by up to 98% without affecting growth hormone release.Formula:C35H34N6O3Color and Shape:SolidMolecular weight:586.68
