Receptor opioide
Os receptores opioides são um grupo de receptores acoplados à proteína G que mediam os efeitos dos opioides endógenos e exógenos. Estes receptores desempenham um papel central na modulação da dor, regulação do humor e comportamentos aditivos. Agonistas e antagonistas dos receptores opioides são amplamente utilizados no manejo da dor e tratamento de dependências, bem como em pesquisas sobre distúrbios neurológicos e psiquiátricos. Na CymitQuimica, oferecemos uma seleção abrangente de moduladores de receptores opioides de alta qualidade para apoiar sua pesquisa em neurobiologia, manejo da dor e terapia de dependência.
Foram encontrados 298 produtos de "Receptor opioide"
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Viminol
CAS:<p>Viminol is an opioid analgesic. Viminol is based on the α-pyrryl-2-aminoethanol structure, unlike any other class of opioids.</p>Fórmula:C21H31ClN2OPureza:98%Cor e Forma:SolidPeso molecular:362.94PF-4455242 HCl
CAS:<p>PF-4455242 HCl is a selective and orally available κ-opioid receptor antagonist that exhibiting antidepressant effects.</p>Fórmula:C21H29ClN2O2SPureza:99.59%Cor e Forma:SolidPeso molecular:408.99Opioid receptor modulator 1
CAS:<p>Opioid receptor modulator 1 is a modulator of opioid receptor.</p>Fórmula:C18H23NO2Pureza:98%Cor e Forma:SolidPeso molecular:285.38LY2444296
CAS:<p>LY2444296 (FP3FBZ) is an orally active and selective antagonist of kappa opioid receptor(Ki = 1 nM).</p>Fórmula:C24H22F2N2O2Pureza:99.18%Cor e Forma:SolidPeso molecular:408.44LY2048978
CAS:<p>LY2048978: orally-active kappa antagonist, shows promise for mood and addiction in animal studies.</p>Fórmula:C19H24N2O2Pureza:98%Cor e Forma:SolidPeso molecular:312.41μ opioid receptor agonist 2
CAS:μ opioid receptor agonist 2 （Compound H-3）is a MOR receptor agonist. μ opioid receptor agonist 2 can be used for the research of pain and pain related diseases.Fórmula:C25H34N4OCor e Forma:SolidPeso molecular:406.56SCH 221510
CAS:<p>SCH 221510: oral NOP agonist, EC50=12 nM, Ki=0.3 nM, anxiolytic, for neurological research.</p>Fórmula:C28H31NOPureza:99.54%Cor e Forma:SolidPeso molecular:397.55JTC-801 free base
CAS:<p>JTC-801 is a selective antagonist of the opioid receptor-like1 receptor (Ki: 8.2 nM).</p>Fórmula:C26H25N3O2Pureza:98%Cor e Forma:SolidPeso molecular:411.5TIPP
CAS:<p>TIPP is an agent of delta opioid antagonist.</p>Fórmula:C37H38N4O6Pureza:98%Cor e Forma:SolidPeso molecular:634.72ICI 154,129
CAS:<p>Selective δ opioid antagonist</p>Fórmula:C34H46N4O6SPureza:98%Cor e Forma:SolidPeso molecular:638.82AT-076
CAS:<p>AT-076: κ-opioid (Ki=1.14 nM) & nociceptin (Ki=1.75 nM) noncompetitive antagonist; μ-opioid (Ki=1.67 nM) & δ-opioid (Ki=19.6 nM) competitive antagonist.</p>Fórmula:C26H35N3O3Cor e Forma:SolidPeso molecular:437.57AZD7268
CAS:<p>AZD7268 is a potent, selective, reversible, and orally bioavailable agonist of δ-opioid receptor with CNS penetration.</p>Fórmula:C29H30N4O2SCor e Forma:SolidPeso molecular:498.64ORL1 antagonist 1
CAS:<p>ORL1 antagonist 1 is an o antagonist of pioid receptor-like 1 (ORL1) (IC50 of 61 nM).</p>Fórmula:C20H22ClN5Pureza:98.92%Cor e Forma:SolidPeso molecular:367.88Norbinaltorphimine
CAS:<p>nor-Binaltorphimine dihydrochloride is a long-acting potent and highly selective kappa opioid receptor antagonist.</p>Fórmula:C40H43N3O6Cor e Forma:SolidPeso molecular:661.79Dup 747
CAS:<p>Dup 747 is an analgesic that binds with high affinity and selectivity to the kappa-opioid receptor.</p>Fórmula:C24H28Cl2N2O2Pureza:98%Cor e Forma:SolidPeso molecular:447.4CR-665 Acetate
CAS:<p>CR-665, a kappa-opioid agonist, is used potentially for the treatment of postoperative pain.</p>Fórmula:C38H53N9O6Cor e Forma:SolidPeso molecular:731.899Loperamide oxide
CAS:<p>Loperamide oxide (R 58425) is a secreted antidiarrheal agent that increases peristalsis and inhibits intestinal absorption of water and ions.</p>Fórmula:C29H33ClN2O3Cor e Forma:SolidPeso molecular:493.04Diallyl G
CAS:<p>Diallyl G is a delta-opioid receptor antagonist agent.</p>Fórmula:C38H53N5O8Cor e Forma:SolidPeso molecular:707.86DIPPA hydrochloride
CAS:<p>κ receptor antagonist</p>Fórmula:C22H24Cl3N3OSPureza:98%Cor e Forma:SolidPeso molecular:484.87σ1 Receptor/μ Opioid receptor modulator 1
CAS:<p>σ 1 Receptor/ μ Opioid receiver modulator 1 (Compound 44) is an effective σ 1 receptor antagonist (Ki=1.86 nM) and μ Opioid receptor agonists (Ki=2.1 nM).</p>Fórmula:C24H31FN2O2Cor e Forma:SolidPeso molecular:398.51ML138
CAS:<p>ML138 is a probe for MLPCN, an agonist of the κ opioid receptor.</p>Fórmula:C19H14Cl2N4OSCor e Forma:SolidPeso molecular:417.31Axomadol
CAS:<p>Axomadol (EN3324) is a centrally active analgesic compound. It has opioid agonistic properties and inhibitory effects on the reuptake of monoamines.</p>Fórmula:C16H25NO3Pureza:98%Cor e Forma:SolidPeso molecular:279.37Ici 174865
CAS:<p>Ici 174865 is a delta opioid receptor antagonist agent.</p>Fórmula:C38H53N5O7Cor e Forma:SolidPeso molecular:691.86Trimebutine CTB salt
CAS:<p>Trimebutine CTB salt (GIC-1001) is an opioid receptor agonist used in the study of pain.</p>Fórmula:C29H36N2O8S2Pureza:99.85% - >99.99%Cor e Forma:SolidPeso molecular:604.74AT-121
CAS:<p>AT-121 is a dual μ-opioid and neuropeptide receptor partial agonist (Kis 16.49 and 3.67 nM, respectively).</p>Fórmula:C24H38N4O3SPureza:98.49% - 99.73%Cor e Forma:SolidPeso molecular:462.65ADL-5747
CAS:<p>ADL-5747 (ADL-5747 (free base)) (free base) is a delta opioid receptor agonist used in the treatment of neurological disorders, skin and musculoskeletal</p>Fórmula:C24H28N2O3Pureza:98.94% - 99.74%Cor e Forma:SolidPeso molecular:392.49ICI 199,441 hydrochloride
CAS:<p>ICI 199,441 hydrochloride is a potent, selective agonist of κ-opioid receptor.</p>Fórmula:C21H25Cl3N2OPureza:99.57%Cor e Forma:SolidPeso molecular:427.8JNJ-20788560
CAS:<p>JNJ-20788560 is a delta opioid receptor (DOR) agonist with analgesic activity. It is more selective for DOR than for mu opioid receptors (MOR).</p>Fórmula:C25H28N2O2Pureza:98.02%Cor e Forma:SolidPeso molecular:388.5GR 89696 fumarate
CAS:<p>GR 89696 fumarate is a highly selective κ2 opioid receptor agonist (IC50 = 0.04nM) with anti-pruritchy, anti-injury and neuroprotective effects.</p>Fórmula:C23H29Cl2N3O7Pureza:99.84%Cor e Forma:SolidPeso molecular:530.4IPAG
CAS:<p>IPAG is a potent σ-receptor antagonist (pKi=4.3). IPAG can induce cell apoptosis.</p>Fórmula:C17H22IN3Pureza:99.65%Cor e Forma:SolidPeso molecular:395.28ML-335
CAS:<p>ML-335, a μ-δ targeted agonist and MOR/DOR ligand, may lead to isomer-biased drugs with pain-relief properties.</p>Fórmula:C25H32N2O3Pureza:98.52%Cor e Forma:SolidPeso molecular:408.53ICI 204,448
CAS:<p>ICI 204,448 is a potent κ-opioid agonist with potential analgesic activity for the study of neurological diseases.</p>Fórmula:C23H27Cl3N2O4Pureza:>99.99%Cor e Forma:SolidPeso molecular:501.83SCH-486757
CAS:<p>SCH-486757 is an agonist of nociceptin-1 (NOP1) and orphanin FQ peptide receptors and is used in the study of cough.</p>Fórmula:C24H23Cl2N3OPureza:99.53% - >99.99%Cor e Forma:SolidPeso molecular:440.37NNC 63-0532
CAS:<p>NNC 63-0532 is a potentnociceptin receptor agonist, Ki=7.3 nM, EC50=305 nM.</p>Fórmula:C27H29N3O3Pureza:99.53%Cor e Forma:SolidPeso molecular:443.54Bevenopran
CAS:<p>Bevenopran (CB-5945) is a peripheral antagonist of μ-opioid receptor and can be used in studies about the treatment of opioid-induced bowel dysfunction.</p>Fórmula:C20H26N4O4Pureza:98.69% - 98.9%Cor e Forma:SolidPeso molecular:386.44Naloxonazine dihydrochloride
CAS:<p>μ1 receptor antagonist</p>Fórmula:C38H43ClN4O6Pureza:98%Cor e Forma:SolidPeso molecular:687.22Prodilidine hydrochloride
CAS:Prodilidine hydrochloride is an opioid analgesic.Fórmula:C15H22ClNO2Cor e Forma:SolidPeso molecular:283.79μ opioid receptor agonist 1
CAS:<p>μ opioid receptor agonist 1 (Compound H-1a) is an optically pure oxyheterocyclic substituted pyrroloxypyrazole derivative and an MOR receptor agonist that can</p>Fórmula:C26H38N4OCor e Forma:SolidPeso molecular:422.61SNC 162
CAS:<p>SNC 162 is a potent and selective delta-opioid receptor (δ-opioid) agonist with analgesic, antidepressant and antiarrhythmic effects.</p>Fórmula:C27H37N3OPureza:98%Cor e Forma:SolidPeso molecular:419.6DPI-3290
CAS:<p>DPI-3290 is a specific agonist of opioid receptors (Ki: 0.18 nM, 0.46 nM, and 0.62 nM for δ-, μ-, and κ-opioid receptors, respectively) with potent</p>Fórmula:C30H34FN3O2Pureza:98%Cor e Forma:SolidPeso molecular:487.61Trap-101 hydrochloride
CAS:<p>nociceptin/orphanin FQ (NOP) receptor antagonist</p>Fórmula:C24H36ClN3O2Pureza:98%Cor e Forma:SolidPeso molecular:434.02Frakefamide
CAS:<p>Frakefamide: potent analgesic, μ-selective agonist, non-CNS penetrating.</p>Fórmula:C30H34FN5O5Pureza:98%Cor e Forma:SolidPeso molecular:563.62Naloxonazine
CAS:<p>Naloxonazine, a potent, selective opiate mu-1 (μ1) antagonist, also influences leishmania through the modulation of host coding function.</p>Fórmula:C38H42N4O6Cor e Forma:SolidPeso molecular:650.76Deltakephalin
CAS:<p>Deltakephalin is a synthetic, potent specific opiate delta receptors agonist.</p>Fórmula:C34H48N6O10Pureza:98%Cor e Forma:SolidPeso molecular:700.78N-Benzylnaltrindole hydrochloride
CAS:δ2 opioid receptor antagonistFórmula:C33H33ClN2O3Pureza:98%Cor e Forma:SolidPeso molecular:541.08Mu opioid receptor antagonist 7
CAS:<p>Compound 24, also known as Mu opioid receptor antagonist 7, is a potent, centrally-acting µ-opioid receptor (µOR) antagonist with an inhibitory concentration (</p>Fórmula:C22H27ClN2O2Pureza:98%Cor e Forma:SolidPeso molecular:386.91μ opioid receptor agonist 3
CAS:<p>Compound 20, identified as μ opioid receptor agonist 3, is a potent µOR agonist that exhibits an EC50 value of 0.87 nM.</p>Fórmula:C22H28N2O2Pureza:98%Cor e Forma:SolidPeso molecular:352.47ADL-08-0011
CAS:<p>ADL-08-0011 is an metabolite of alvimopan.</p>Fórmula:C23H29NO3Cor e Forma:SolidPeso molecular:367.49CYT-1010
CAS:<p>CYT-1010, a mu-opioid receptor agonist; EC50: β-arrestin, 13.1 nM; cAMP, 0.0053 nM. Extracted from patent WO2013173730A2.</p>Fórmula:C35H40N6O5Pureza:98%Cor e Forma:SolidPeso molecular:624.73ICI 204448
CAS:<p>ICI 204448 is a potent and peripherally selective κ-opioid agonist.</p>Fórmula:C23H26Cl2N2O4Cor e Forma:SolidPeso molecular:465.37Icalcaprant
CAS:<p>Icalcaprant is a kappa-opioid receptor antagonist [1].</p>Fórmula:C23H26N4O3Pureza:98%Cor e Forma:SolidPeso molecular:406.48FK 33-824
CAS:<p>FK 33-824, a stable synthetic analog of methionine enkephalin, reversible with naloxone.</p>Fórmula:C29H41N5O7SPureza:98%Cor e Forma:SolidPeso molecular:603.73R-84760 hydrochloride
CAS:<p>R-84760, a potent κ-opioid receptor agonist, relieves tonic pain via supraspinal/spinal pathways, activating noradrenergic descent.</p>Fórmula:C19H25Cl3N2OSCor e Forma:SolidPeso molecular:435.84Norbinaltorphimine dihydrochloride
CAS:<p>Norbinaltorphimine dihydrochloride is a selective and potent κ opioid receptor antagonist that induces itch-associated responses in mice.</p>Fórmula:C40H45Cl2N3O6Pureza:98.17% - 99.88%Cor e Forma:SolidPeso molecular:734.71Isotodesnitazene
CAS:<p>Isotodesnitazene is an opioid compound that primarily targets the μ-opioid receptor (MOR). It exhibits EC50 values of 34.8 nM and 142 nM for MOR-βarr2 and MOR-mini-Gi, respectively. Isotodesnitazene can be utilized for research in opioid drugs.</p>Fórmula:C23H31N3OCor e Forma:SolidPeso molecular:365.51Riminkefon
CAS:<p>Riminkefon is a kappa opioid receptor agonist .</p>Fórmula:C38H57N7O6Cor e Forma:SolidPeso molecular:707.9Mu opioid receptor antagonist 8
CAS:<p>Muopioid Receptor Antagonist 8 (368) serves as an antagonist to the μ-opioid receptor, significantly inhibiting the activation of Gi induced by met-enkephalin at the µOR.</p>Fórmula:C36H35N3O4SCor e Forma:SolidPeso molecular:605.75Mu opioid receptor antagonist 3
<p>Potent, selective MOR antagonist (compound 26); crosses blood-brain barrier. Ki: 0.24 nM, EC50: 0.54 nM; for studying OUD.</p>Fórmula:C25H28N2O4SCor e Forma:SolidPeso molecular:452.57BU09059
CAS:<p>BU09059 is a potent, selective, short-acting antagonist of the κ-opioid receptor (KOR).</p>Fórmula:C28H37N3O5Pureza:98%Cor e Forma:SolidPeso molecular:495.616β-Naltrexol
CAS:<p>6β-Naltrexol is a peripherally selective opioid antagonist that reduces constipation from opioids while minimizing central nervous system effects.</p>Fórmula:C20H25NO4Pureza:99.933%Cor e Forma:SolidPeso molecular:343.42BU72
CAS:<p>BU72 is a potent, long-lasting agonist for μ and κ opioid receptors, with partial agonistic activity at the δ opioid receptor (EC50 values of 0.054, 0.033, and 0.58 nM, respectively). It provides strong, enduring analgesic effects primarily mediated through μ opioid receptors. BU72 also exhibits a prolonged duration of activity and can partially reverse morphine-induced analgesia. It is applicable in studies of opioid dependence.</p>Fórmula:C28H32N2O2Cor e Forma:SolidPeso molecular:428.57SC13
CAS:<p>SC13, a novel mitragynine analog, exhibits low-efficacy agonism at Mu opioid receptors and provides antinociception while minimizing adverse effects.</p>Fórmula:C26H30N2O5Cor e Forma:SolidPeso molecular:450.53RX 809055AX
CAS:<p>RX 809055AX is a long lasting opioid antagonist at mu and delta receptors.</p>Fórmula:C29H29ClN2O4Cor e Forma:SolidPeso molecular:505Anilopam
CAS:<p>Anilopam is an opioid analgesic belonging to the benzazepine class and acts as an agonist at opioid receptors.</p>Fórmula:C20H26N2OCor e Forma:SolidPeso molecular:310.43GNTI dihydrochloride
CAS:<p>κ opioid receptor antagonist</p>Fórmula:C27H30ClN5O3Pureza:98%Cor e Forma:SolidPeso molecular:508.0122-Thiocyanatosalvinorin A
CAS:<p>22-Thiocyanatosalvinorin A (RB-64) is a potent selective agonist for the kappa-opioid receptor, exhibiting an EC50 value of 0.077 nM.</p>Fórmula:C24H27NO8SCor e Forma:SolidPeso molecular:489.54CCG258747
CAS:CCG258747 is a novel, selective inhibitor of the GRK2 subfamily.Fórmula:C28H27FN4O4Cor e Forma:SolidPeso molecular:502.54BNTX
CAS:<p>BNTX (7-Benzylidenenaltrexone) is a selective δ1-opioid receptor antagonist. It competitively counteracts the antisecretory effects of DPDPE, Deltorphin 2, and DAMGO. BNTX is applicable in research focused on antinociceptive effects.</p>Fórmula:C27H27NO4Cor e Forma:SolidPeso molecular:429.508rel-SB-612111 hydrochloride
CAS:<p>NOP receptor antagonist</p>Fórmula:C24H30Cl3NOPureza:98%Cor e Forma:SolidPeso molecular:454.86JDTic Dihydrochloride
CAS:JDTic Dihydrochloride is a high-affinity and selective κ-opioid receptor (KOR) antagonist that blocks dynorphin-KOR signalling,antidepressant.Fórmula:C28H41Cl2N3O3Pureza:98%Cor e Forma:SolidPeso molecular:538.55Naldemedine tosylate
CAS:<p>Naldemedine (S-297995) tosylate, a PAMORA, targets μ-, δ-, κ-opioid receptors, aiding OIC research, may bind to SARS-CoV2's 3CL pro.</p>Fórmula:C39H42N4O9SCor e Forma:SolidPeso molecular:742.84J-113397
CAS:<p>J-113397 is a potent and selective NOP receptor antagonist (IC50 = 2.3 nM).</p>Fórmula:C24H37N3O2Pureza:98%Cor e Forma:SolidPeso molecular:399.57Allyphenyline oxalate
CAS:<p>The pKi values of Allyphenyline oxalate (compound 9) for the α2-adrenergic receptor subtypes α2A, α2B, and α2C are 7.24, 6.47, and 7.07, respectively.</p>Fórmula:C16H20N2O5Cor e Forma:SolidPeso molecular:320.34σ1 Receptor/μ Opioid receptor modulator 2
CAS:<p>Compound 4x, also known as σ1 Receptor/μOpioid receptormodulator 2, acts as a μOR agonist and a σ1R antagonist, exhibiting a potent μOR EC50 of 0.6 nM and strong σ1R inhibitory activity (Ki: 363.7 nM). It demonstrates significant analgesic effects in various pain models.</p>Fórmula:C23H31N3OPeso molecular:365.51DS34942424
<p>DS34942424 is an orally potent analgesic which did not exhibit mu opioid receptor agonist activity.</p>Fórmula:C15H17FN2OCor e Forma:SolidPeso molecular:260.315′-Guanidinonaltrindole
CAS:<p>5′-Guanidinonaltrindole (GNTI) is a selective antagonist of the kappa opioid receptor.</p>Fórmula:C27H29N5O3Cor e Forma:SolidPeso molecular:471.551(±)-J 113397
CAS:<p>(±)-J-113397 is a potent and selective non-peptidyl ORL1 receptor antagonist (K(i): cloned human ORL1=1.8 nM).</p>Fórmula:C24H37N3O2Cor e Forma:SolidPeso molecular:399.57SB-612111 hydrochloride
<p>SB-612111 is a potent ORL-1 antagonist, with high affinity (Ki: 0.33 nM) and µ-receptor activity (Ki: 57.6 nM), blocking Nociceptin-induced pain.</p>Fórmula:C24H30Cl3NOCor e Forma:SolidPeso molecular:454.86KNT-127
CAS:<p>KNT-127 is an agonist of δ-Opioid receptor.</p>Fórmula:C24H24N2O2Pureza:98%Cor e Forma:SolidPeso molecular:372.46Mu opioid receptor antagonist 5
<p>Compound NAP: MOR antagonist, crosses blood-brain barrier, EC50: 1.14 nM, Ki: 0.37 nM, useful for OUD research.</p>Fórmula:C26H29N3O4Cor e Forma:SolidPeso molecular:447.53Daeatal
CAS:<p>Dynorphin A ethylamide (1-9), the opioid activities were examined in the bioassays.</p>Fórmula:C56H93N19O10Pureza:98%Cor e Forma:SolidPeso molecular:1192.46Mu opioid receptor antagonist 4
<p>Compound 31: Potent, selective MOR antagonist; crosses blood-brain barrier; Ki & EC50: 0.38 nM; useful for OUD research.</p>Fórmula:C25H28N2O4SCor e Forma:SolidPeso molecular:452.57SB-612111
CAS:<p>SB-612111: potent ORL-1 antagonist, Ki=0.33 nM; μ-, κ-, δ-receptor Ki=57.6, 160.5, 2109 nM; blocks nociceptin's pain effect.</p>Fórmula:C24H29Cl2NOCor e Forma:SolidPeso molecular:418.40BNTX maleate
CAS:<p>δ1 opioid receptor antagonist</p>Fórmula:C31H31NO8Pureza:98%Cor e Forma:SolidPeso molecular:545.58BW 443C
CAS:<p>BW 443C is a selective agonist of mu-opioid receptor.</p>Fórmula:C33H46N10O10Cor e Forma:SolidPeso molecular:742.791Bromadoline
CAS:<p>Bromadoline is an opioid compound that exhibits anti-nociceptive properties in rodents.</p>Fórmula:C15H21BrN2OCor e Forma:SolidPeso molecular:325.244Naltrindole 5′-isothiocyanate
CAS:<p>Naltrindole 5′-isothiocyanate (5'-NTII) is an irreversible delta opioid receptor antagonist that counters the analgesic effects induced by DSLET without altering the effects caused by DPDPE.</p>Fórmula:C27H25N3O3SCor e Forma:SolidPeso molecular:471.571Opioid receptor antagonist 1
CAS:<p>Opioid receptor antagonist 1 (Compound 10) is an Orvinol-based antagonist of opioid receptors. It exhibits activity as an antagonist against the analgesic properties of morphine.</p>Fórmula:C24H29ClF3NO4Cor e Forma:SolidPeso molecular:487.94Mu opioid receptor antagonist 2
<p>Compound 25: potent, selective MOR antagonist, crosses blood-brain barrier (Ki: 0.37 nM, EC50: 0.44 nM), for OUD research.</p>Fórmula:C25H28N2O4SCor e Forma:SolidPeso molecular:452.57(S)-MCOPPB
CAS:<p>(S)-MCOPPB is the S-enantiomer of MCOPPB, an orally active selective agonist for the Nociceptin/Orphanin FQ-Receptor. It inhibits signal transduction in mouse brain NOP receptors and is utilized in anxiety disorder research.</p>Fórmula:C26H40N4Cor e Forma:SolidPeso molecular:408.623Sunobinop
CAS:<p>Sunobinop (S 117957) is an opioid receptor-like orphan receptor (ORL1) modulator.</p>Fórmula:C26H33N3O3Cor e Forma:SolidPeso molecular:435.56Nalmefene
CAS:<p>Nalmefene (ORF 11676) is a μ-opioid antagonist and partial κ agonist used in the study of opioid overdose and alcohol dependence.</p>Fórmula:C21H25NO3Pureza:99.86%Cor e Forma:SolidPeso molecular:339.43Propiram fumarate HCl
CAS:<p>Propiram fumarate HClis an orally available Opioid receptors agonist with analgesic activity for the study of musculoskeletal pain.</p>Fórmula:C16H25N3O·xClHPureza:99.25%Cor e Forma:SoildSR17018
CAS:<p>SR17018 is an mu-opioid-receptor (MOR) agonist, binding with GTPγS, with an EC50 of 97 nM.</p>Fórmula:C19H18Cl3N3OPureza:99.89%Cor e Forma:SolidPeso molecular:410.72Cebranopadol
CAS:<p>Cebranopadol (GRT6005) is an analgesic NOP and opioid receptor agonist with Kis of 0.9 nM, 0.7 nM, 2.6 nM, 18 nM for human NOP, μ-opioid (MOP), κ-opioid (KOP)</p>Fórmula:C24H27FN2OPureza:98.32% - 99.78%Cor e Forma:SolidPeso molecular:378.48Bromadoline maleate
CAS:<p>Bromadoline is an opioid analgesic selective for the μ-opioid receptor.</p>Fórmula:C19H25BrN2O5Pureza:98%Cor e Forma:SolidPeso molecular:441.322SR14150
CAS:<p>SR14150 is a partial agonist of high-affinity NOP receptor.</p>Fórmula:C21H30N2OPureza:98%Cor e Forma:SolidPeso molecular:326.48MOR agonist-1
CAS:<p>MOR Agonist-1 is a μ-opioid receptor (MOR) agonist noted for its potent analgesic properties and is utilized in research concerning pain and associated</p>Fórmula:C22H26ClFN2O2Pureza:98%Cor e Forma:SolidPeso molecular:404.91
