GPCR/Proteína-G
Os inibidores de GPCR/proteínas G são compostos que têm como alvo os receptores acoplados a proteínas G (GPCRs) e as proteínas G associadas, que desempenham papéis críticos na transmissão de sinais do exterior para o interior das células. Esses inibidores são essenciais para estudar as vias de sinalização mediadas por GPCRs, que estão envolvidas em numerosos processos fisiológicos, incluindo percepção sensorial, resposta imunológica e neurotransmissão. Os inibidores de GPCR também são importantes no desenvolvimento de medicamentos, pois muitos agentes terapêuticos têm como alvo esses receptores. Na CymitQuimica, oferecemos uma ampla gama de inibidores de GPCR/proteínas G de alta qualidade para apoiar sua pesquisa em farmacologia, biologia celular e áreas afins.
Subcategorias de "GPCR/Proteína-G"
- Receptor 5-HT(939 produtos)
- Receptor de adenosina(242 produtos)
- Receptor adrenérgico(2.945 produtos)
- Receptor de Bombesina(30 produtos)
- Receptor de Bradicinina(59 produtos)
- CXCR(148 produtos)
- CaSR(32 produtos)
- Receptor de Canabinóides(195 produtos)
- Receptor de Dopamina(407 produtos)
- Receptor Endotelina(76 produtos)
- Receptor GNRH(73 produtos)
- GPCR19(31 produtos)
- GRK(31 produtos)
- GTPase(21 produtos)
- Receptor Glucagon(165 produtos)
- Hedgehog/Smoothened(44 produtos)
- Receptor de Histamina(358 produtos)
- Receptor LPA(21 produtos)
- Receptor de Melatonina(24 produtos)
- Receptor OX(40 produtos)
- Receptor opioide(297 produtos)
- PAFR(11 produtos)
- PKA(48 produtos)
- Receptor S1P(17 produtos)
- SGLT(30 produtos)
- Receptor Sigma(46 produtos)
Exibir 18 mais subcategorias
Foram encontrados 5352 produtos de "GPCR/Proteína-G"
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5-HT2A receptor agonist-2
CAS:<p>Potent 5-HT2A receptor agonist-2 targets 5-HT2A/B/C with EC50 1.7, 0.58, 0.50 nM.</p>Fórmula:C20H21ClN2O3Cor e Forma:SolidPeso molecular:372.85BGC201531
CAS:<p>BGC201531 (AP-1531) is a EP4 antagonist for the treatment of acute migraine.</p>Fórmula:C26H28N2O6SPureza:98.51% - 99.33%Cor e Forma:SolidPeso molecular:496.58MAT2A-IN-3
CAS:<p>MAT2A-IN-3: potent MAT2A inhibitor, hinders MTAP-deficient cancer cell growth, potential for cancer research.</p>Fórmula:C24H16F5N5O3Cor e Forma:SolidPeso molecular:517.41VUF 5574
CAS:<p>VUF 5574 is a selective antagonist of adenosine A3 receptor with a Ki of 4.03 nM for the recombinant human receptor.</p>Fórmula:C21H17N5O2Pureza:99.53%Cor e Forma:SolidPeso molecular:371.39CJ 033466
CAS:<p>CJ 033466 is a selective partial agonist of 5-HT4 receptor (EC50 = 9 nM) with gastroprokinetic effect.</p>Fórmula:C19H28ClN5OPureza:99.72%Cor e Forma:SolidPeso molecular:377.91Darbufelone
CAS:<p>Darbufelone (CI-1004) is a non-competitive dual inhibitor of PGF2α and LTB4.</p>Fórmula:C18H24N2O2SPureza:99.72%Cor e Forma:SolidPeso molecular:332.46Adatanserin
CAS:<p>Adatanserin (WY 50324) is a mixed 5-HT1A receptor partial agonist and a 5-HT2A and 5-HT2C receptor antagonist.</p>Fórmula:C21H31N5OPureza:99.33%Cor e Forma:SolidPeso molecular:369.5Dihydroalprenolol, (S)-
CAS:<p>Dihydroalprenolol, (S)- is a hydrogenated alprenolol derivative. It acts as a beta-adrenergic blocker.</p>Fórmula:C15H25NO2Pureza:98%Cor e Forma:SolidPeso molecular:251.36Napitane
CAS:<p>napitane (A 75200) is a novel catecholamine uptake inhibitor with inhibitory effects on α-adrenergic receptors and potential antidepressant activity for the</p>Fórmula:C22H25NO2Pureza:99.77% - 99.89%Cor e Forma:SolidPeso molecular:335.44DA 4643
CAS:<p>DA 4643, a histamine H2-receptor antagonist, binds similarly to mifentidine at the receptor.</p>Fórmula:C12H16Cl2N6SPureza:98%Cor e Forma:SolidPeso molecular:347.26SMANT hydrochloride
CAS:<p>SMANT hydrochloride (N-(4-bromophenyl)-3-(3,5-dimethylpiperidin-1-yl)propanamide hydrochloride) is an antagonist of Smoothened accumulation.</p>Fórmula:C16H24BrClN2OPureza:99.81%Cor e Forma:SolidPeso molecular:375.73RS-601
CAS:<p>RS-601 is a potent dual leukotriene D4/thromboxane A2 inhibitor that inhibits antigen-induced airway hyperresponsiveness (AHR) and shows asthmatic effects in a</p>Fórmula:C22H23F6NO4SPureza:99.31%Cor e Forma:SolidPeso molecular:511.48LUF5981
CAS:<p>LUF5981 is a selective agonist of human adenosine A1 receptor.</p>Fórmula:C24H23N3Cor e Forma:SolidPeso molecular:353.46SK1-IN-1
CAS:<p>SK1-IN-1 is a SPHK1 inhibitor (IC50: 58 nM), with potential anticancer activity, and can be used to study cancer and neurodegenerative diseases.</p>Fórmula:C22H30N4O3Pureza:98.72%Cor e Forma:SolidPeso molecular:398.5Flerobuterol
CAS:<p>Flerobuterol is a potential antidepressant agent related to beta-adrenergic agonists.</p>Fórmula:C12H18FNOPureza:98%Cor e Forma:SolidPeso molecular:211.28CCX354
CAS:<p>CCX354 (CCR1 antagonist 1) is a potent small molecule CCR1 antagonist with anti-inflammatory activity for the treatment of rheumatoid arthritis.</p>Fórmula:C22H22ClN7O2Pureza:99.82% - 99.82%Cor e Forma:SolidPeso molecular:451.91Licogliflozin
CAS:<p>Licogliflozin (LIK066) is an inhibitor of sodium-glucose cotransporter (SGLT1 and SGLT2).</p>Fórmula:C23H28O7Pureza:98%Cor e Forma:SolidPeso molecular:416.46L-692429
CAS:<p>L-692429 (MK-0751) is a GHS agonist with high affinity for G protein-coupled receptors and can be used to study acromegaly and obesity.</p>Fórmula:C29H31N7O2Pureza:98.64% - 99.90%Cor e Forma:SolidPeso molecular:509.614Arvanil
CAS:<p>Arvanil (N-Vanillylarachidonamide) is a synthetic capsaicin-amphetamine hybrid that acts as a ligand for VR1 and CB1, offering neuroprotective effects.</p>Fórmula:C28H41NO3Pureza:99.49%Cor e Forma:SolidPeso molecular:439.63CJB-090 2HCl
CAS:<p>CJB-090 2HCl is a partial agonist of the dopamine D3 receptor.</p>Fórmula:C26H30Cl4N4OCor e Forma:SolidPeso molecular:556.35Nα-Methylhistamine dihydrochloride
CAS:<p>Nα-Methylhistamine dihydrochloride is a histamine H3 receptor agonist.</p>Fórmula:C6H13Cl2N3Pureza:98%Cor e Forma:SolidPeso molecular:198.094Azelastine
CAS:<p>Azelastine (Azelastinum) is a phthalazine derivative, and is an histamine antagonist and mast cell stabilizer.</p>Fórmula:C22H24ClN3OPureza:99.35%Cor e Forma:White Crystal PowderPeso molecular:381.90MRS2567
CAS:<p>MRS2567 is a potent P2Y6 nucleotide receptors antagonists.</p>Fórmula:C16H12N2S2Cor e Forma:SolidPeso molecular:296.41Ono 6240
CAS:<p>Ono 6240 is an antagonist of platelet-activating factor. Ono 6240 prevents airway eosinophilia by inhibiting production of IL-2 and IL-5.</p>Fórmula:C32H63NO6S2Pureza:98%Cor e Forma:SolidPeso molecular:621.98Indanidine
CAS:<p>Indanidine is a highly selective and potent α-adrenergic agonist with antihypertensive activity.Indanidine is an α-adrenergic antagonist that can be used in the</p>Fórmula:C11H13N5Pureza:>99.99%Cor e Forma:SolidPeso molecular:215.25CP-66948
CAS:<p>CP-66948 is a potent histamine H2 receptor antagonist with inhibitory effect on gastric acid secretion and can be used to protect gastric and intestinal mucosa.</p>Fórmula:C13H20N6SPureza:99.14%Cor e Forma:SolidPeso molecular:292.4CCR1 antagonist 9
CAS:<p>CCR1 antagonist 9 (compound 19e) is a selective CCR1 antagonist based on aziridine. CCR1 inhibition in calcium flux assays.</p>Fórmula:C20H16FN5O3SPureza:99.13%Cor e Forma:SolidPeso molecular:425.44Dipiproverine hydrochloride
CAS:<p>Dipiproverine hydrochloride is an antispasmodic alpha-amino acid ester used as an anticholinergic.</p>Fórmula:C20H32Cl2N2O2Pureza:98%Cor e Forma:SolidPeso molecular:403.39Etoperidone hydrochloride
CAS:<p>Etoperidone hydrochloride is an antidepressant agent.</p>Fórmula:C19H29Cl2N5OCor e Forma:SolidPeso molecular:414.37GPR183 antagonist-2
CAS:<p>GPR183 antagonist-2 (compound 32), a selective antagonist of GPR183, exhibits excellent water solubility and pharmacokinetic properties. This compound effectively diminishes paw and joint swelling, and reduces gene expression of pro-inflammatory cytokines (MCP-1, MMPs, and VEGF) in a dose-dependent manner within a collagen-induced arthritis (CIA) mouse model. GPR183 antagonist-2 is applicable in researching autoimmune diseases [1].</p>Fórmula:C20H18F2N4O5Cor e Forma:SolidPeso molecular:432.38Lusaperidone
CAS:<p>Kaerophyllin ( (-)-Kaerophylin) inhibits hepatic stellate cell activation and inhibits HSC activation to protect against liver cell damage and fibrosis in rats.</p>Fórmula:C22H21N3O2Pureza:99.75%Cor e Forma:SolidPeso molecular:359.42Latanoprost ethyl amide
CAS:<p>Lat-NEt, a latanoprost analog, is an ocular hypotensive prodrug with slower hydrolysis, converting to free acids in corneal tissue.</p>Fórmula:C25H39NO4Cor e Forma:SolidPeso molecular:417.58E55888
CAS:<p>E55888 is a potent and selective full agonist of the 5HT7 serotonin receptor.</p>Fórmula:C16H23N3Cor e Forma:SolidPeso molecular:257.37F13714 fumarate
CAS:<p>F13714 fumarate is a 5-HT1A receptor-biased agonist.</p>Fórmula:C25H29ClF2N4O5Pureza:98.86%Cor e Forma:SolidPeso molecular:538.97LRH-1 Inhibitor-3
CAS:<p>LRH-1 Inhibitor-3 is an antagonist that inhibits LRH-1 transcriptional activity, reducing SHP, cyclin E1 (CCNE1), and G0S2,antiproliferation anticancer.</p>Fórmula:C23H25N3O2Pureza:98%Cor e Forma:SolidPeso molecular:375.46Clonidine
CAS:<p>Clonidine (Kapvay): central alpha-adrenergic agonist, antihypertensive, often combined, not tied to liver issues.</p>Fórmula:C9H9Cl2N3Pureza:99.42% - 99.44%Cor e Forma:Crystals SolidPeso molecular:230.09CP94253 hydrochloride
CAS:<p>CP94253 hydrochloride: selective 5-HT1B agonist, Ki=2 nM; less active on 5-HT1A/D/C/2 (Ki=89/49/860/1600 nM).</p>Fórmula:C15H20ClN3OPureza:99.78%Cor e Forma:SolidPeso molecular:293.79LEK 8841
CAS:<p>LEK 8841 is an ergoline derivative that is a potential antipsychotic.</p>Fórmula:C21H24BrN3O4SPureza:98%Cor e Forma:SolidPeso molecular:494.4Falintolol
CAS:<p>Falintolol is a novel beta-adrenergic antagonist with antihypertensive effects and can be used to study glaucoma.</p>Fórmula:C12H24N2O2Pureza:>99.99% - >99.99%Cor e Forma:SolidPeso molecular:228.33Donitriptan
CAS:<p>Donitriptan 是一种 5-HT 受体激动剂，对 5-HT1B 和 5-HT1D 的 pKi 分别为 9.4 和 9.3。</p>Fórmula:C23H25N5O2Pureza:98.76%Cor e Forma:SolidPeso molecular:403.48L748337
CAS:<p>L748337 is a β3-adrenoceptor antagonist that inhibits β3-, β2-, and β1-adrenoceptors and inhibits the protective effects of CL316243.</p>Fórmula:C26H31N3O5SPureza:99.67% - >99.99%Cor e Forma:SolidPeso molecular:497.61CI-943
CAS:<p>CI-943 is a novel potential antipsychotic drug that does not bind to dopamine (DA) receptors and has some developmental neurotoxicity.</p>Fórmula:C12H17N5Pureza:98%Cor e Forma:SolidPeso molecular:231.3ML230
CAS:<p>ML230 is a selective ATP-binding cassette (ABC) transporter ABCG2 inhibitor.</p>Fórmula:C25H21N5O3Pureza:98%Cor e Forma:SolidPeso molecular:439.47Ipramidil
CAS:<p>Ipramidil (C80-1324) reveals marked dilator activity in the coronary circulation of isolated working hearts.</p>Fórmula:C10H16N4O4Pureza:98%Cor e Forma:SolidPeso molecular:256.26RG-12915
CAS:<p>RG-12915 is a selective antagonist of 5-HT3(IC50 value of 0.16 nM).</p>Fórmula:C20H25ClN2O2Pureza:98%Cor e Forma:SolidPeso molecular:360.88Nelonicline
CAS:<p>Nelonicline is a selective agonist of neuronal nicotinic receptors.</p>Fórmula:C17H19N3OSPureza:98%Cor e Forma:SolidPeso molecular:313.42Dipiproverine
CAS:<p>Dipiproverine is an alpha-amino acid ester, an antispasmodic compound. It is used as an anticholinergic drug.</p>Fórmula:C20H30N2O2Cor e Forma:SolidPeso molecular:330.46SB 258585 hydrochloride
CAS:SB 258585 hydrochloride is a 5-HT6 receptor antagonist.Fórmula:C18H23ClIN3O3SPureza:98%Cor e Forma:SolidPeso molecular:523.82L 368935
CAS:<p>L 368935 is an antagonist of the cholecystokinin receptor.</p>Fórmula:C27H26N8O2Pureza:98%Cor e Forma:SolidPeso molecular:494.55Aplysamine-1
CAS:Aplysamine-1 is an antagonist of histamine H3 receptor.Fórmula:C15H24Br2N2OPureza:98%Cor e Forma:SolidPeso molecular:408.17BW-A 575C
CAS:<p>BW-A 575C is an inhibitor of ACE.</p>Fórmula:C29H43N5O8Pureza:98%Cor e Forma:SolidPeso molecular:589.68AK-IN-1
CAS:<p>AK-IN-1: competitive adenosine inhibitor, not ATP; inhibits AK 86-89% at 2-10 µM; promising for ischaemia, inflammation, seizure research.</p>Fórmula:C22H21N3O4Cor e Forma:SolidPeso molecular:391.42PF-04781340
CAS:<p>PF-04781340 is an effective, selective, and CNS penetrant agonist of 5-HT2C receptor.</p>Fórmula:C17H21N3Pureza:98%Cor e Forma:SolidPeso molecular:267.37AP-521 (Free base)
CAS:<p>AP-521, a 5-HT1A receptor antagonist, is used potentially for the treatment of anxiety.</p>Fórmula:C20H18N2O3SCor e Forma:SolidPeso molecular:366.43A-77636
CAS:<p>A-77636 is a potent, selective, and long-acting oral dopamine D1 receptor agonist with an effective concentration (EC50) of 1.1 nM and a corresponding pEC50</p>Fórmula:C20H27NO3Pureza:98%Cor e Forma:SolidPeso molecular:329.43Undecylenoyl phenylalanine
CAS:<p>Undecylenoyl phenylalanine (Sepiwhite msh QD) is a novel depigmenting agent, which possibly acts as an alpha-melanocyte-stimulating hormone antagonist, thus</p>Fórmula:C20H29NO3Pureza:≥98%Cor e Forma:White To Pinkish Solid PowderPeso molecular:331.45AMX12006
CAS:<p>AMX12006, a potent and selective EP4 antagonist, exhibits cytotoxic and antitumor activity, demonstrating oral activity with an IC50 of 4.3 nM [1].</p>Fórmula:C26H22F3N3O3Pureza:98%Cor e Forma:SolidPeso molecular:481.47Palonosetron
CAS:<p>Palonosetron, a 5-HT3 antagonist with Ki of 0.17 nM, is used in the prevention and treatment of chemotherapy-induced nausea and vomiting (CINV).</p>Fórmula:C19H24N2OPureza:98%Cor e Forma:SolidPeso molecular:296.41A 68930 hydrochloride
CAS:<p>A68930 hydrochloride is a dopamine D1 receptor agonist which can be used for the research of bronchiectasis [1].</p>Fórmula:C16H18ClNO3Cor e Forma:Off-White SolidPeso molecular:307.77Romifidine
CAS:<p>Romifidine is used as a sedative in veterinary medicine mainly in large animals such as horses. It acts as an agonist at the α2 adrenergic receptor subtype.</p>Fórmula:C9H9BrFN3Cor e Forma:SolidPeso molecular:258.09Pridefine
CAS:<p>Pridefine: antidepressant, balances serotonin, dopamine, norepinephrine reuptake, weakly releases them.</p>Fórmula:C19H21NPureza:99.15% - 99.66%Cor e Forma:SolidPeso molecular:263.38WAY 629 hydrochloride
CAS:<p>5-HT2C agonist</p>Fórmula:C15H19ClN2Pureza:98%Cor e Forma:SolidPeso molecular:262.78Impromidine
CAS:<p>Impromidine is a highly potent and specific agonist of the histamine H2 receptor.</p>Fórmula:C14H23N7SPureza:98%Cor e Forma:SolidPeso molecular:321.44(4-Acetamidocyclohexyl) nitrate
CAS:<p>(4-Acetamidocyclohexyl) nitrate (BM121307) is an activator of guanylate cyclase.</p>Fórmula:C8H14N2O4Pureza:98%Cor e Forma:SolidPeso molecular:202.21JHW 007 hydrochloride
CAS:<p>JHW 007 hydrochloride is a Dopamine uptake inhibitor.</p>Fórmula:C24H30ClF2NOPureza:98%Cor e Forma:SolidPeso molecular:421.95BRD5814
CAS:<p>BRD5814 is a highly brain penetrant β-arrestin biased D2R antagonist.</p>Fórmula:C21H23ClF3NO2Cor e Forma:SolidPeso molecular:413.86Alosetron ((Z)-2-butenedioate)
CAS:<p>Alosetron (GR 68755) (Z)-2-butenedioate is a Serotonin 5HT3-receptor antagonist that is used in the treatment of irritable bowel syndrome.</p>Fórmula:C21H22N4O5Pureza:98%Cor e Forma:SolidPeso molecular:410.42(S)-Carvedilol
CAS:<p>(S)-Carvedilol is a non-selective β/α-1 blocker.It exerts protection against the vascular or cardiac toxicity of Doxorubicin (DOX).</p>Fórmula:C24H26N2O4Pureza:98%Cor e Forma:Less Crystalline Solid Colourless Crystalline SolidPeso molecular:406.47Adenosine receptor inhibitor 1
CAS:<p>Potent, selective adenosine receptor blocker with strong affinity, especially A2A (Ki 68.5 nM). Promising for cancer, neurodegeneration study.</p>Fórmula:C17H19ClFN5O3Cor e Forma:SolidPeso molecular:395.82BGC-20-1531 free base
CAS:<p>BGC-20-1531 (PGN 1531) free base is a selective and potent prostaglandin EP4 receptor antagonist (pKB: 7.6) that exhibits potential for migraine research.</p>Fórmula:C26H24N2O6SCor e Forma:SolidPeso molecular:492.54Orexin receptor antagonist 2
CAS:<p>Compound 30, potent orexin antagonist with pKis of 7.69/9.78, potential for insomnia research.</p>Fórmula:C25H31N5O2Cor e Forma:SolidPeso molecular:433.55CGS-12066 maleate salt
CAS:<p>CGS-12066 maleate salt is an agonist of 5-HT1B serotonin receptor.</p>Fórmula:C21H21F3N4O4Cor e Forma:SolidPeso molecular:450.41CGP 35949
CAS:<p>CGP 35949 is an LTD4 antagonist with phospholipase inhibitory activity.</p>Fórmula:C23H25ClN5NaO5Pureza:99.62%Cor e Forma:SolidPeso molecular:509.92JNJ-39220675
CAS:<p>JNJ-39220675, a selective histamine H3 receptor antagonist, reduces the abuse-related effects of alcohol in rats.</p>Fórmula:C21H24FN3O2Pureza:98.13% - 99.89%Cor e Forma:SolidPeso molecular:369.43PF 03654746 FA
<p>PF 03654746 FA is a human histamine receptor H(3) antagonist that can be used to study cognitive impairment and Alzheimer's disease.</p>Fórmula:C19H26F2N2O3Pureza:99.44%Cor e Forma:SoildPeso molecular:368.42Wy 49051
CAS:<p>Wy 49051 is an orally active antagonist of H1 receptor(IC50 of 44 nM).</p>Fórmula:C28H33N5O3Pureza:99.89%Cor e Forma:SolidPeso molecular:487.59Methylcarbamyl PAF C-16
CAS:<p>Methylcarbamyl PAF C-16 (Carbamyl-PAF) is a PAF analog with PAF agonistic properties, activating inflammation in pregnancy tissues and promoting preterm birth.</p>Fórmula:C26H55N2O7PCor e Forma:SolidPeso molecular:538.7PF-03654746
CAS:<p>PF-03654746: selective H3 antagonist, boosts cognition in Alzheimer's, may treat allergic rhinitis.</p>Fórmula:C18H24F2N2OPureza:98.85% - 99.57%Cor e Forma:SolidPeso molecular:322.39Oxetorone fumarate
CAS:<p>Oxetorone fumarate is a non-selective, orally active antagonist of serotonin and 5-HT receptors,used for migraine treatment.</p>Fórmula:C25H25NO6Pureza:99.809%Cor e Forma:SolidPeso molecular:435.48CB1/2 agonist 4
CAS:<p>CB1/2 agonist 4 is a potent CB1 full agonist (EC50: 15.09 nM) and CB2 partial agonist (EC50: 1.16 nM), with anti-pain and TRPV1 activation properties.</p>Fórmula:C27H45NO3Cor e Forma:SolidPeso molecular:431.65LUF 6283
CAS:<p>partial agonist of hydroxycarboxylic acid receptor 2 (HCA2)</p>Fórmula:C8H12N2O2Cor e Forma:SolidPeso molecular:168.19Arbutamine
CAS:<p>Arbutamine (GP 21213) is a β-adrenoceptor agonist with alpha-1-sympathomimetic activity that can be used to study cardiac stress.</p>Fórmula:C18H23NO4Pureza:95.06%Cor e Forma:SolidPeso molecular:317.38GSK 894281
CAS:<p>GSK 894281 is a ghrelin receptor agonist. It may produces myocardial degeneration/necrosis in rats.</p>Fórmula:C24H28FN3O4SPureza:98%Cor e Forma:SolidPeso molecular:473.56Bavisant dihydrochloride
CAS:<p>Bavisant (JNJ-310010740) is an oral, selective H3 receptor antagonist enhancing wakefulness and cognition.</p>Fórmula:C19H29Cl2N3O2Pureza:98%Cor e Forma:SolidPeso molecular:402.36Fonazine
CAS:<p>Forazine (dimethiazide) is a phenothiazine drug used in the treatment of migraine and is a serotonin antagonist and a histamine antagonist.</p>Fórmula:C19H25N3O2S2Cor e Forma:SolidPeso molecular:391.55MRS2768 tetrasodium salt
CAS:<p>MRS2768 tetrasodium: a P2Y2 agonist; offers cardioprotection against ischemia.</p>Fórmula:C15H16N2Na4O18P4Cor e Forma:SolidPeso molecular:728.14Guanoxabenz
CAS:<p>Guanoxabenz is an α2 adrenergic receptor agonist.</p>Fórmula:C8H8Cl2N4OPureza:98%Cor e Forma:SolidPeso molecular:247.08Acetylaszonalenin
CAS:<p>Acetylaszonalenin, from A. flavipes, is an NK1 receptor antagonist with a Ki of 170 μM, blocking substance P.</p>Fórmula:C25H25N3O3Cor e Forma:SolidPeso molecular:415.48PF-3246799
CAS:<p>PF-3246799 is an effective and selective agonist of the 5-HT2C receptor.</p>Fórmula:C15H17N3Pureza:98%Cor e Forma:SolidPeso molecular:239.32Pancopride
CAS:<p>Pancopride（LAS 30451） is a novel, orally available, long-acting, selective 5-HT3 receptor antagonist that blocks nitrogen mustard and dacarbazine-induced</p>Fórmula:C18H24ClN3O2Pureza:93.64%Cor e Forma:SolidPeso molecular:349.86L 641953
CAS:<p>L 641953 is an antagonist of the thromboxane receptor.</p>Fórmula:C15H9FO3SCor e Forma:SolidPeso molecular:288.29GP531
CAS:<p>GP531, a second-gen adenosine regulator, is inactive at rest but boosts adenosine in ischemia.</p>Fórmula:C16H21N5O4Cor e Forma:SolidPeso molecular:347.37CCR1 antagonist 7
CAS:<p>CCR1 antagonist 7 (compound 16r) is an antagonist of chemokine receptor 1 (CCR1) with an IC 50 of 4 nM [1].</p>Fórmula:C21H24ClN5O3SPureza:98%Cor e Forma:SolidPeso molecular:461.96MS47134
<p>MS47134: potent MRGPRX4 agonist, EC50 = 149 nM, for pain/itch/hypersensitivity research.</p>Fórmula:C22H29NO3Cor e Forma:SolidPeso molecular:355.47NPC 17731
CAS:<p>NPC 17731 is a bradykinin receptor antagonist.</p>Fórmula:C59H95N19O14Cor e Forma:SolidPeso molecular:1294.5SB-221284
CAS:<p>5-HT2C/2B receptor antagonist</p>Fórmula:C16H14F3N3OSPureza:98%Cor e Forma:SolidPeso molecular:353.36Levobunolol hydrochloride
CAS:<p>Levobunolol hydrochloride 是一种非选择性的 β-肾上腺素受体阻滞剂，可用于治疗青光眼和上斜肌肌障碍的研究。</p>Fórmula:C17H26ClNO3Pureza:98.49% - >99.99%Cor e Forma:SolidPeso molecular:327.85Sequifenadine
CAS:<p>Sequifenadine has the potential in researching of inflammatory eye disease with allergic symptoms that is a H1-antihistamine [1] [2].</p>Fórmula:C22H27NOCor e Forma:SolidPeso molecular:321.46A412997
CAS:<p>A412997 is a selective agonist of dopamine D4 receptor.</p>Fórmula:C19H23N3OPureza:98%Cor e Forma:SolidPeso molecular:309.41Iodophenpropit dihydrobromide
CAS:<p>Iodophenpropit dihydrobromide: selective histamine H3 antagonist, reversible binding, high affinity (KD: 0.32 nM).</p>Fórmula:C15H20BrIN4SPureza:98%Cor e Forma:SolidPeso molecular:495.22
