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home » Chemicals » Peptide Receptor Ligands
 

Peptide Receptor Ligands

  • (1R,1'S,3'R/1R,1'R,3'S)-L-054,264
    Potent and selective somatostatin sst2 receptor agonist (Ki values are 4, 537, 2480, 3614 and 5017 nM for cloned human sst2, sst1, sst4, sst3 and sst5 receptors respectively).
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203766208706-12-1C33H41N5O2•xH2O1 mg/10 mg
  • 2-Furoyl-LIGRLO-amide trifluoroacetate salt
    A potent, selective protease-activated receptor 2 (PAR2) agonist where PAR-2 activation is associated with increases in cAMP and intracellular Ca(2+).
    Catalog #CAS NumberMolecular FormulaUnit
    sc-213814729589-58-6 (non-salt)C36H63N11O8 ·xC2HF3O21 mg
  • A-71623
    A robust and selective CCL28 (cholecystokinin 1; CCK1) receptor agonist. In comparison to other CCL28 agonists the compound does not have a tyrosine residue in which sulfation is necessary for strong CCL28 agonist activity in larger peptides.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203487130408-77-4C44H56N8O91 mg
  • AC 55541
    Potent and selective protease-activated receptor 2 (PAR2) agonist (pEC50 = 6.7) that displays no activity at other PAR subtypes or at over 30 other receptors involved in inflammation and nociception. Stimulates cell proliferation, PI hydrolysis andCa2+ mobilization in vitro (pEC50 values are 6.7, 5.9 and 6.6 respectively) and exhibits pronociceptive activity in vivo.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203799916170-19-9C25H20BrN5O310 mg/50 mg
  • (±)-AC 7954 hydrochloride
    Highly selective, non-peptide urotensin II (UT) receptor agonist that displays potent activity at human and rat UT receptors (pEC50 values are 6.5 and 6.7 respectively).
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203491477313-09-0C19H20ClNO2 ·HCl10 mg/50 mg
  • AG 045572
    Selective gonadotropin-releasing hormone (GnRH) receptor antagonist (Ki values are 2.2, 3.8 and 6.0 nM for mouse, rat and human receptors respectively). Suppresses testosterone and luteinising hormone (LH) levels in vivo.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203499263847-55-8C30H37NO51 mg/10 mg
  • Antalarmin hydrochloride
    A non-peptide CRF-RI receptor antagonist. Blocks ACTH release stimulated by CRH, and inflammation induced by carageenin in studies.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203820220953-69-5C24H34N4.HCl10 mg/50 mg
  • APC 366
    Selective inhibitor of the mast cell tryptase (Ki= 7.1 μM).
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203516178925-65-0C22H28N6O45 mg
  • BIBO 3304 trifluoroacetate
    High affinity NPY Y1 receptor antagonist (IC50 values are 0.38 and 0.72 nM at human and rat receptors respectively) that displays > 2600-fold selectivity over Y2, Y4 and Y5 receptors. Inhibits NPY- and fasting-induced feeding in vivo following central administration. Also antagonizes anxiolytic-like effects of NPY.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203841191868-14-1C29H35N7O3 ·2CF3CO2H10 mg/50 mg
  • BIBP 3226 trifluoroacetate
    Mixed non-peptide neuropeptide Y Y1 (NPY Y1) and neuropeptide FF (NPFF) receptor antagonist (Ki values are 1.1, 79, 108, > 1000, > 1000 and >1000 for rNPY Y1, hNPFF2, rNPFF, rNPY Y2, rNPY Y4 and rNPY Y5 respectively) Produces an anxiogenic-like effect in rats following i.c.v. administration.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203842159013-54-4 (non-salt)C27H31N5O3 ·CF3CO2H1 mg/10 mg
  • BIIE 0246
    A selective non-peptide antagonist which binds to the neuropeptide NPY Y2RY2 receptor in a competitive manner. In addition, BIIE 0246 suppresses another neuropeptide, [ahx5-24]NPY.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203530246146-55-4C49H57N11O6•xH2O1 mg/10 mg
  • BMS 182874 hydrochloride
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361123153042-42-3C17H19N3O3S.HCl10 mg/50 mg
  • BMS 193885
    Potent, competitive neuropeptide (NPY) Y1 antagonist (Ki = 3.3 nM, IC50 = 5.9 nM) that displays > 47, > 100, > 160, > 160 and > 160-fold selectivity over σ1, α1, Y2, Y4 and Y5 receptors respectively. Reduces food intake and body weight via central Y1 inhibition and is brain penetrant.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203848186185-03-5C33H42N4O6 ·C3H6O310 mg/50 mg
  • Boc-MLF
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361128N/AC25H39N3O6S1 mg
  • BQ 788 sodium salt
    Selective ETB antagonist
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203534156161-89-6C34H50N5O7•Na1 mg
  • BQ-610
    A highly selective ETA receptor antagonist (IC50= 20 nM) which attenuates ET-induced reduction in cardiac output. It also inhibits ET-1- and ET-3-induced activation of adenylate cyclase (IC50= 28.2 nM). BQ-610 is 30-fold more potent than BQ-123, in porcine aortic smooth muscle membrane assay.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-221380141595-53-1C36H44N6O6500 µg
  • CGP 71683 hydrochloride hydrate
    Selective and potent non-peptide NPY Y5 receptor antagonist.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203881192322-50-2C26H29N5O2S ·HCl ·1/4 ·H2O10 mg/50 mg
  • CI 988
    A selective and effective antagonist of CCKBR (CCK2, CCK-B) receptors. Described to block the elevated levels of cytosolic Ca2+ induced by CCK-8.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-205244130332-27-3C35H42N4O610 mg/50 mg
  • CP 96345
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361160132746-60-2C28H32N2O10 mg/50 mg
  • CP 99994 dihydrochloride
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361161136982-36-0C19H24N2O.2HCl10 mg/50 mg
  • CP 154526
    A compound described to act as a selective and potent non-peptide CRF-RI and ACTH antagonist.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-205268157286-86-7C23H32N4 ·HCl10 mg/50 mg
  • CP 376395 hydrochloride
    CRF1 receptor antagonist which is potent and selective. CRF-induced activation of the HPA axis is weakened in in vivo studies following oral activation.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-205271175140-00-8C21H30N2 ·HCl10 mg/50 mg
  • Cyclosomatostatin
    Non-selective somatostatin (sst) receptor antagonist. Effects of sst are blocked on release of growth hormone, insulin and glucagon, airway β-adrenergic function, modulation of ACh release and CRF-induced suppression of gastric empyting. Potentially acts as an sst receptor agonist in SH-SY5Y, the human neuroblastoma cell line.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-20528084211-54-1C44H57N7O61 mg
  • [D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P
    Catalog #CAS NumberMolecular FormulaUnit
    sc-36116696736-12-8C79H109N19O121 mg
  • Devazepide
    A non-peptide CCL28 (cholecystokinin 1; CCK1) receptor antagonist. Shown to induce apoptosis and inhibit cell proliferation.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203562103420-77-5C25H20N4O210 mg/50 mg
  • EMD 66684
    Potent, selective non-peptide AT1 receptor antagonist.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203941187683-79-0C28H30N8O2 ·HCl10 mg/50 mg
  • FK 888
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361178138449-07-7C36H36N4O410 mg
  • FPR A14
    Formyl peptide receptor (FPR) agonist that potently activates neutrophils in vitro (EC50 values are 42 and 630 nM for neutrophil chemotaxis and Ca2+ mobilization respectively).
    Catalog #CAS NumberMolecular FormulaUnit
    sc-294992N/AC23H20N2O510 mg/50 mg
  • GR 159897
    A compound that acts as an effective and selective NK2 receptor antagonist.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361193158848-32-9C23H27FN2O2S10 mg/50 mg
  • GR 231118
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361194158859-98-4C110H170N34O24500 µg
  • GW 803430
    Catalog #CAS NumberMolecular FormulaUnit
    sc-363281515141-51-2C25H24ClN3O3S10 mg/50 mg
  • ICI 216,140
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361211124001-41-8C45H65N13O81 mg
  • IRL-2500
    Potent, selective ET(B) antagonist.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204018169545-27-1C36H35N3O410 mg
  • JNJ 5207787
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361218683746-68-1C32H38N4O210 mg/50 mg
  • L 760735
    Catalog #CAS NumberMolecular FormulaUnit
    sc-362760171242-11-8C26H28F7N5O2.HCl10 mg/50 mg
  • L-152,804
    Potent, selective non-peptide neuropeptide Y Y5 receptor antagonist (Ki = 26 nM for hY5). Displays > 300-fold selectivity over hY1, hY2, and hY4 receptors. Causes weight loss in diet-induced obese mice by modulating food intake and energy expenditure. Centrally active upon oral administration in vivo.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-2036186508-43-6C23H26O410 mg/50 mg
  • L-168,049
    Potent, orally active non-peptidyl human glucagon receptor antagonist.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204034191034-25-0C24H20BrClN2O10 mg/50 mg
  • L-368,899 hydrochloride
    Potent, non-peptide spiroindenylpiperidine camphor-sulfonamide oxytocin receptor antagonist.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204037148927-60-0C26H42N4O5S2•HCl1 mg/10 mg
  • L-371,257
    Orally active potent and selective oxytocin (OT) receptor antagonist.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204038162042-44-6C28H33N3O610 mg
  • L-692,585
    Potent, non-peptidyl growth hormone (GH) secretagogue. Will increase growth hormone levels in vivo.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204043145455-35-2C32H37N7O3•xH2O10 mg
  • L-732,138
    A selective nonpepetide tachykinin NK-1R antagonist with 1000 fold more potency towards the NK-1R receptor over NK-2R and NK-3R receptors with an IC50 = 2.3 nM.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203437148451-96-1C22H18F6N2O310 mg/50 mg
  • L-733,060 hydrochloride
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361226148700-85-0C20H19F6NO.HCl10 mg/50 mg
  • L-803,087 trifluoroacetate
    Potent and selective sst4 agonist Potent and selective somatostatin sst4 receptor agonist. Ki values are 0.7, 199, 4720, 1280 and 3880 nM for cloned human sst4, sst1, sst2, sst3 and sst5 receptors respectively. Facilitates AMPA-mediated hippocampal synaptic responses in vitro and increases kainate-induced seizures in mice in vivo.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203619217480-26-7C25H29F2N5O3 ·CF3CO2H10 mg
  • LRGILS-NH2
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361979245329-01-5C29H56N10O71 mg
  • L-817,818
    Potent and selective non-peptide somatostatin subtype-5 receptor agonist. Inhibits growth hormone release from rat pituitary cells and insulin release from mouse pancreatic islets in vitro.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204048217480-27-8C33H36N4O310 mg
  • LU AA33810
    A potent neuropeptide Y (NPY) Y5 receptor antagonist. Displays ≥ 3300-fold affinity for Y5 over Y1, Y2 and Y4 receptors. Also binds human 5-HT2B and 5-HT1A receptors (Ki values are 247 and 478 nM respectively). Exerts anxiolytic- and antidepressant-like effects in rat models of stress sensitivity.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-295367304008-29-5C19H25N3O2S310 mg/50 mg
  • LY 225910
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361237133040-77-4C27H24BrN3O25 mg/25 mg
  • LY 288513
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361242147523-65-7C22H18BrN3O210 mg/50 mg
  • NBI 27914 hydrochloride
    A selective corticotropin-releasing factor 1 inhibitor.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204119184241-44-9C18H20Cl4N4•HCl10 mg/50 mg
  • NBI-31772
    A non-peptide ligand. Exhibits high-affinity towards all six human insulin-like growth factor-I binding proteins (IGFBPs). Displaces insulin-like growth factor-I (IGF-I) from the IGF-I:IGFBP complex in 3T3 fibroblasts, but does not interact with the IGF receptors.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-222047N/AC17H11NO75 mg
  • NNC 26-9100
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361276199522-35-5C22H25N6Cl2SBr10 mg
  • NTNCB hydrochloride
    Potent, selective, competitive non-peptidic Y5 antagonist. Ki values are 8.0 and 16032 nM at human recombinant Y5 and Y1 receptors respectively. Potently antagonizes NPY inhibition of forskolin-stimulated cAMP. Some affinity for cloned human D2 and α2C receptors (Ki values are 63 and 100 nM respectively).
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203655486453-65-0C25H33N3O4S.HCl10 mg/50 mg
  • Oxytocin acetate salt hydrate
    Involved in uterine contraction and lactation. Cys-Tyr-Ile-Gln-Asn-Cys-Pro-Leu-Gly-NH2 [Disulfide Bridge: 1-6]
    Catalog #CAS NumberMolecular FormulaUnit
    sc-27993850-56-6C43H66N12O12S21 mg/5 mg
  • PD 135158
    A specific and effective CCK-BR antagonist. Reported to show limited affinity for substance P, benzodiazepine, GABAA, neurotensin, bradykinin, and 5-HT3 binding sites.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204163130325-35-8C35H44N4O6•1/2H2010 mg/50 mg
  • PD 160170
    Potent, selective non-peptide NPY Y1 antagonist; ; selective over Y2 and Y5 receptors. Antagonizes NPY-mediated inhibition of cAMP accumulation in SK-N-MC cells.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204836181468-88-2C18H17N3O4S10 mg/50 mg
  • PD 168368
    Neuromedin B antagonist displaying ~40-fold selectivity over GRP-R, BB2 and >300-fold selectivity over BRS-R. Antagonizes neuromedin B-stimulated Ca2+ release and inhibits proliferation of rat glioma cells.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204166204066-82-0C31H34N6O41 mg/10 mg
  • PD 176252
    Gastrin-releasing peptide and Neuromedin B antagonist. Inhibits proliferation of C6 glioma cells as well as NCI-H1299 xenograft proliferation in nude mice.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204171204067-01-6C32H36N6O510 mg
  • [PYR1]-APELIN-13
    The pyro-glutamine form of Apelin-13 (sc-351718) that has shown high activity.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-359030217082-60-5C69H108N22O16S1 mg
  • RO 90-7501
    Inhibitor of amyloid β42 (Aβ42) fibril assembly; reduces Aβ42-induced toxicity (EC50 = 2 μM).
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204891293762-45-5C20H16N610 mg/50 mg
  • RP 67580
    Potent and selective tachykinin NK1 receptor antagonist. Displays higher affinity at rat and mouse than human receptors. Antinociceptive in vivo, possibly partly via inhibition of calcium channels.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204894135911-02-3C29H30N2O2•xH2O10 mg/50 mg
  • S 25585
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361325263-849-50-9C22H23F3N4O6S10 mg/50 mg
  • SB 218795
    Potent, selective non-peptide NK3 antagonist
    Catalog #CAS NumberMolecular FormulaUnit
    sc-224280174635-53-1C25H20N2O310 mg/50 mg
  • SB 222200
    Potent, selective non-peptide NK3 antagonist. Brain penetrant
    Catalog #CAS NumberMolecular FormulaUnit
    sc-224282174635-69-9C26H24N2O10 mg/50 mg
  • SB 268262
    Catalog #CAS NumberMolecular FormulaUnit
    sc-362793217438-17-0C18H15N3O4S210 mg/50 mg
  • SB 334867
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361344249889-64-3C17H13N5O21 mg/10 mg
  • SB 408124
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361345288150-92-5C19H18F2N4O10 mg
  • SB-366791
    A new, potent and selective vanilloid receptor (TRPV1) antagonist. An effective antagonist of hTRPV1 when stimulated by capsaicin, acid, or noxious heat.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-222293N/AC16H14NO2Cl5 mg/25 mg
  • SCH 79797
    A selective PAR1 antagonist that has been shown to inhibit binding of a high-affinity thrombin receptor-activating peptide.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203693245520-69-8C23H25N5 ·2HCl10 mg/50 mg
  • SDZ NKT 343
    Highly selective human tachykinin NK1 antagonist receptor(IC50 values are 0.62 and 451 nM for human and rat receptors respectively) that displays > 130-fold selectivity over human NK2 and NK3 receptors. Potently antagonizes SP-induced Ca2+ efflux in vitro and inhibits mechanical hyperalgesia in vivo.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204274180046-99-5C33H33N5O510 mg
  • SLIGRL-NH2
    Catalog #CAS NumberMolecular FormulaUnit
    sc-359903171436-38-7C29H56N10O71 mg
  • SN 003
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361361197801-88-0C19H25N5O210 mg
  • SR 142948
    Highly potent non-peptide neurotensin (NT) receptor antagonist that binds with high affinity (IC50 = 0.32 - 3.96 nM). Attenuates amphetamine-induced hyperactivity and is orally active in vivo.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204297184162-64-9C39H51N5O61 mg/10 mg
  • SR 27897
    An effective non-peptide antagonist of CCL28 (cholecystokinin 1; CCK1) receptors. Described to act as selective and robust ligand for CCL28 binding sites.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204298136381-85-6C20H14ClN3O3S10 mg/50 mg
  • SR 49059
    Potent, selective, non-peptide, orally active vasopressin V1a receptor antagonist; devoid of agonist activity. Shows high affinity and efficacy at both rat (Ki = 1.6 nM) and human (Ki = 1.1-6.3 nM) V1a receptors. Potently antagonizes arginine vasopressin-induced effects in vitro (IC50 = 3.7 nM for inhibition of human platelet aggregation) and is orally active in vivo.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204300150375-75-0C28H27Cl2N3O7S10 mg
  • SSR 146977 hydrochloride
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361366264618-44-2C35H42Cl2N4O2.HCl10 mg/50 mg
  • Sulfisoxazole
    Selective ETA endothelin antagonist receptor (IC50 values are 600 and 2200 nM for ETA and ETB receptors respectively).
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204313127-69-5C11H13N3O3S50 mg
  • SUN-B 8155
    In CHO/hCTR cells, non-peptide calcitonin (CT) receptor agonist fully stimulates cAMP production. Following i.p. administration, it also causes a significant reduction in serum calcium concentrations in vivo.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-203704345893-91-6C14H15N3O310 mg/50 mg
  • T 98475
    Potent, non-peptide, and orally active gonadotropin-releasing hormone (GnRH, LHRH) receptor antagonist (IC50 values are 0.2, 4.0 and 60 nM for human, monkey, and rat GnRH receptors respectively). Inhibits LH release in vitro (IC50 = 100 nM) and reduces plasma LH concentration in castrated male cynomolgus monkeys.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204318192887-28-8C37H37F2N3O4S1 mg
  • Taltirelin
    Synthetic thyrotropin-releasing hormone (TRH) analog. Displays ~ 30-100-fold more potent CNS activity and ~ 50-fold weaker endocrine activity than TRH. Both antinociceptive and neuroprotective.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204319103300-74-9C17H23N7O51 mg/10 mg
  • TCS 1102
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361375916141-36-1C27H26N4O2S10 mg/50 mg
  • TCS OX2 29
    Potent orexin 2 receptor (OX2) antagonist (IC50 = 40 nM) that displays > 250 fold selectivity over OX1 and over 50 other ion channels, receptors and transporters.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204329372523-75-6C23H31N3O3•HCl•xH2O10 mg/50 mg
  • THIQ
    Selective and potent melanocortin 4 (MC4) receptor agonist (IC50 values are 1.2, 761 and 2067 nM for human MC4, MC3 and MC1 receptors respectively). Following systemic administration, enhances intracavernosal pressure and stimulates erectile activity in rats ex copula.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204343312637-48-2C33H41ClN6O21 mg
  • TNF-α Antagonist
    Also designated WP9QY, an cyclic peptide which mimics the most critical recognition loop on TNF receptor I.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-358755199999-60-5C58H71N11O15S21 mg
  • Tramiprosate
    Sulfated glycosaminoglycan (sGAG) mimetic that targets soluble amyloid β (Aβ) and maintains Aβ in a non-fibrillar form. Decreases brain amyloid plaque load by 30%, increases tau polymerization and is brain penetrant. Decreases Aβ42-induced neuronal death and inhibits amyloid deposition in vitro. Also a GABA analog that protects against the convulsant and cytotoxic activity of kainic acid in vivo.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-2043533687-18-1C3H9NO3S50 mg
  • Wang resin
    Useful resin in the synthesis of peptide acids using Fmoc synthesis strategy. Cleavage can be affected by 95% TFA.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-286858201058-08-4N/A5 g/25 g
  • WIN 64338 hydrochloride
    The first potent, non-peptide, competitive bradykinin B2 receptor antagonist. In organ bath studies, WIN 64338 inhibits [3H]-bradykinin binding on guinea pig trachea with nanomolar affinity but not active in the rabbit aorta (the classical bradykinin B1 preparation).
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204398151039-63-3C45H68ClN4OP.HCl10 mg/50 mg
  • YIL 781
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361410875258-85-8C24H28FN3O2.HCl10 mg/50 mg
  • YM 022
    Highly potent and selective non-peptide CCK2 silent antagonist (Ki values are 68 pM and 63 nM at CCK2 and CCK1 receptors respectively). Acts in vivo to potently inhibit gastrin-induced gastric acid secretion and histidine decarboxylase activation with a long duration of action.
    Catalog #CAS NumberMolecular FormulaUnit
    sc-204409145084-28-2C32H28N4O310 mg/50 mg
  • ZD 7155 hydrochloride
    Catalog #CAS NumberMolecular FormulaUnit
    sc-361418146709-78-6C26H26N6O.HCl10 mg/50 mg