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H-GLY-PRO-ARG-PRO-NH2. 25mg The inhibitory effect of GPRP amide, H-1998, on fibrinogen/thrombin clotting is 3.52 times higher than that of GPRP, H-2935. CAS: 126047-75-4 C18H32N8O4 FW: 424.5 . fibrin

H-ASP-ALA-HIS-LYS-OH. 100mg The tetrapeptide DAHK corresponding to the N-terminal sequence of human serum albumin forms a tight binding site for Cu(II) ions. DAHK inhibits Cu(II)-induced oxidative DNA double strand breaks.The tetrapeptide is as effective as HSA in preventing neuronal death induced by CuClG/ascorbic acid. DAHK may be an effective, small-molecular-weight alternative to HSA as a therapeutic agent for stroke. CAS: 111543-77-2 C19H31N7O7 FW: 469.5 . Synonym: DAHK

B-MSH (MONKEY). 1mg CAS: 17750-75-3 C98H138N28O29S FW: 2204.41 . Synonym: b-MSH (5-22) (human), beta-Melanocyte-Stimulating Hormone (monkey)

B-MSH (MONKEY). 5mg CAS: 17750-75-3 C98H138N28O29S FW: 2204.41 . Synonym: b-MSH (5-22) (human), beta-Melanocyte-Stimulating Hormone (monkey)

NEUROKININ B. 1mg CAS: 86933-75-7 C55H79N13O14S2 FW: 1210.44 . Synonym: NKB

NEUROKININ B. 5mg CAS: 86933-75-7 C55H79N13O14S2 FW: 1210.44 . Synonym: NKB

C-PROCALCITONIN (HUMAN). 0.5mg This potent plasma calcium-lowering peptide, also called C-procalcitonin, katacalcin or PDN-21, flanks calcitonin on the C-terminal side within the human calcitonin precursor. CAS: 85916-47-8 C97H154N34O36S2 FW: 2436.63 . Synonym: C-Procalcitonin (human), Katacalcin, PDN-21

VIP (6-28) (HUMAN, MOUSE, RAT), 0.5mg This carboxy-terminal VIP fragment was found to be twofold more potent than any previously described VIP receptor antagonists. CAS: 69698-54-0 C126H207N37O34S FW: 2816.32. Synonym: Aviptadil (6-28).

VIP (6-28) (HUMAN, MOUSE, RAT), 1mg This carboxy-terminal VIP fragment was found to be twofold more potent than any previously described VIP receptor antagonists. CAS: 69698-54-0 C126H207N37O34S FW: 2816.32. Synonym: Aviptadil (6-28).

CCK OCTAPEPTIDE SULFATED. 1mg CCK-8 exhibits various gastrointestinal effects as contraction of the gallbladder and stimulation of pancreatic secretion and gastrointestinal transit. In rats, CCK-8 facilitated the uptake of leptin from peripheral circulation to cerebrospinal fluid and its access to the hypothalamus. CAS: 25126-32-3 C49H62N10O16S3 FW: 1143.29 . Synonym: CCK-8 (sulfated), Cholecystokinin (26-33) (sulfated), Sincalide

CCK OCTAPEPTIDE SULFATED. 5mg CCK-8 exhibits various gastrointestinal effects as contraction of the gallbladder and stimulation of pancreatic secretion and gastrointestinal transit. In rats, CCK-8 facilitated the uptake of leptin from peripheral circulation to cerebrospinal fluid and its access to the hypothalamus. CAS: 25126-32-3 C49H62N10O16S3 FW: 1143.29 . Synonym: CCK-8 (sulfated), Cholecystokinin (26-33) (sulfated), Sincalide

CCK OCTAPEPTIDE DESULFATED. 1mg CAS: 25679-24-7 C49H62N10O13S2 FW: 1063.22 . Synonym: CCK-8 (desulfated), Sincalide (desulfated)

CCK OCTAPEPTIDE DESULFATED. 5mg CAS: 25679-24-7 C49H62N10O13S2 FW: 1063.22 . Synonym: CCK-8 (desulfated), Sincalide (desulfated)

ATRIAL NATRIURETIC FACTOR (1-28) . 0.5mg (Disulfide bond) CAS: 88898-17-3 C128H205N45O39S2 FW: 3062.45 . Synonym: rANF (1-28)

ATRIAL NATRIURETIC FACTOR (1-28) . 1mg (Disulfide bond) CAS: 88898-17-3 C128H205N45O39S2 FW: 3062.45 . Synonym: rANF (1-28)

BAM-12P. 1mg Bovine adrenomedullary Met-enkephalin precursor. CAS: 75513-71-2 C62H97N21O16S FW: 1424.65 . BAM

BAM-12P. 5mg Bovine adrenomedullary Met-enkephalin precursor. CAS: 75513-71-2 C62H97N21O16S FW: 1424.65 . BAM

BIM-23042. 1mg This peptide functions as neuromedin B receptor antagonist (IC50 = 885 - 98 nM). It displays a 100-fold higher selectivity for neuromedin B versus gastrin-releasing peptide receptors. (Disulfide bond) CAS: 111857-96-6 C63H73N11O9S2 FW: 1192.47 . Synonym: BIM-23042, DC-13-217

BIM-23042. 5mg This peptide functions as neuromedin B receptor antagonist (IC50 = 885 - 98 nM). It displays a 100-fold higher selectivity for neuromedin B versus gastrin-releasing peptide receptors. (Disulfide bond) CAS: 111857-96-6 C63H73N11O9S2 FW: 1192.47 . Synonym: BIM-23042, DC-13-217

BAM-22P. 0.5mg Bovine adrenomedullary Met-enkephalin precursor. CAS: 76622-26-9 C130H184N38O31S2 FW: 2839.26 . BAM

BAM-22P. 1mg Bovine adrenomedullary Met-enkephalin precursor. CAS: 76622-26-9 C130H184N38O31S2 FW: 2839.26 . BAM

BEAUVERICIN. 5mg Beauvericin is a member of the enniatin family of antibiotics. Activity against Gram-positive bacteria and mycobacteria has been demonstrated. The cyclic depsipeptide forms complexes with alkali metal and alkaline earth metal ions. Additionally, beauvericin was reported to be toxic to brine shrimps and mosquito larvae. CAS: 26048-05-5 C45H57N3O9 FW: 783.96 . beauvericin

BEAUVERICIN. 25mg Beauvericin is a member of the enniatin family of antibiotics. Activity against Gram-positive bacteria and mycobacteria has been demonstrated. The cyclic depsipeptide forms complexes with alkali metal and alkaline earth metal ions. Additionally, beauvericin was reported to be toxic to brine shrimps and mosquito larvae. CAS: 26048-05-5 C45H57N3O9 FW: 783.96 . beauvericin

BIOTINYL-PTH (1-34) (HUMAN). 0.5mg C191H305N57O53S3 FW: 4344.07 . Synonym: Biotinyl-Parathyroid Hormone (1-34) (human)

BIOTINYL-PTH (1-34) (HUMAN). 1mg C191H305N57O53S3 FW: 4344.07 . Synonym: Biotinyl-Parathyroid Hormone (1-34) (human)

BOMBESIN. 5mg A tetradecapeptide isolated from amphibian skin, which is biologically active in both the central nervous system and gastrointestinal tract. It was also shown that bombesin suppresses feeding in rats. Bombesin-like peptides have been biochemically characterized in rat brain. CAS: 31362-50-2 C71H110N24O18S FW: 1619.87 . bombesin

BOMBESIN. 25mg A tetradecapeptide isolated from amphibian skin, which is biologically active in both the central nervous system and gastrointestinal tract. It was also shown that bombesin suppresses feeding in rats. Bombesin-like peptides have been biochemically characterized in rat brain. CAS: 31362-50-2 C71H110N24O18S FW: 1619.87 . bombesin

(TYR4)-BOMBESIN. 5mg CAS: 67338-70-9 C74H108N24O19S FW: 1669.89 . bombesin

(TYR4)-BOMBESIN. 25mg CAS: 67338-70-9 C74H108N24O19S FW: 1669.89 . bombesin

UROGUANYLIN (HUMAN). 0.5mg Uroguanylin belongs to the guanylin family of cyclic guanosine monophosphate (cGMP) regulating peptides. This family of peptides shows homology to the heat stable enterotoxins produced by strains of Escherichia coli and other enteric bacteria that cause a secretory form of diarrhea. Along with the isolation of uroguanylin from urine and the subsequent demonstration of its natriuretic activity by direct effects on the kidney, uroguanylin has been sug gested to play a role in the physiological maintenance of sodium balance in vivo. (Disulfide bonds between Cys4 and Cys12/Cys7 and Cys15) CAS: 154525-25-4 C64H102N18O26S4 FW: 1667.88 . Synonym: ug N (human)

UROGUANYLIN (HUMAN). 1mg Uroguanylin belongs to the guanylin family of cyclic guanosine monophosphate (cGMP) regulating peptides. This family of peptides shows homology to the heat stable enterotoxins produced by strains of Escherichia coli and other enteric bacteria that cause a secretory form of diarrhea. Along with the isolation of uroguanylin from urine and the subsequent demonstration of its natriuretic activity by direct effects on the kidney, uroguanylin has been sug gested to play a role in the physiological maintenance of sodium balance in vivo. (Disulfide bonds between Cys4 and Cys12/Cys7 and Cys15) CAS: 154525-25-4 C64H102N18O26S4 FW: 1667.88 . Synonym: ug N (human)

LYS-BRADYKININ. 25mg Kallidin is the precursor of the vasodilator bradykinin. CAS: 342-10-9 C56H85N17O12 FW: 1188.4 . Synonym: Kallidin

LYS-BRADYKININ. 100mg Kallidin is the precursor of the vasodilator bradykinin. CAS: 342-10-9 C56H85N17O12 FW: 1188.4 . Synonym: Kallidin

H-D-PHE-CYS-TYR-D-TRP-ORN-THR-PEN. 1mg The somatostatin analog CTOP is a very potent and highly selective ligand for --opioid receptors. It shows only little interaction with other opioid receptor systems. (Disulfide bond between Cys2 and Pen7) CAS: 103429-31-8 C50H67N11O11S2 FW: 1062.28 . Synonym: (Tyr3,Orn5,Pen7)-Octreotate amide, CTOP

H-D-PHE-CYS-TYR-D-TRP-ORN-THR-PEN. 5mg The somatostatin analog CTOP is a very potent and highly selective ligand for --opioid receptors. It shows only little interaction with other opioid receptor systems. (Disulfide bond between Cys2 and Pen7) CAS: 103429-31-8 C50H67N11O11S2 FW: 1062.28 . Synonym: (Tyr3,Orn5,Pen7)-Octreotate amide, CTOP

BRADYKININ (2-9). 5mg CAS: 16875-11-9 C44H61N11O10 FW: 904.04 . Synonym: (Des-Arg1)-Bradykinin

ELCATONIN. 1mg Elcatonin, also known as carbocalcitonin, is the aminosuberic acid analog of eel calcitonin. It has all the biological properties of the corresponding natural calcitonin (H-2255). The substitution of the disulfide bond of natural calcitonins with an ethylene bridge in 1-7 N-terminal position gives elcatonin greater stability and excellent tolerability when used in vivo. CAS: 60731-46-6 C148H244N42O47 FW: 3363.82 . Synonym: (Asu1-+7)-Calcitonin (eel), Elcatonin

ELCATONIN. 5mg Elcatonin, also known as carbocalcitonin, is the aminosuberic acid analog of eel calcitonin. It has all the biological properties of the corresponding natural calcitonin (H-2255). The substitution of the disulfide bond of natural calcitonins with an ethylene bridge in 1-7 N-terminal position gives elcatonin greater stability and excellent tolerability when used in vivo. CAS: 60731-46-6 C148H244N42O47 FW: 3363.82 . Synonym: (Asu1-+7)-Calcitonin (eel), Elcatonin

BPP 9A. 5mg A nonapeptide originally isolated from the venom of the Brazilian pit viper Bothrops jararaca. Teprotide inhibits angiotensin-converting enzyme (ACE) in vitro and in vivo. CAS: 35115-60-7 C53H76N14O12 FW: 1101.27 . Synonym: Teprotide, SQ20881

BPP 9A. 25mg A nonapeptide originally isolated from the venom of the Brazilian pit viper Bothrops jararaca. Teprotide inhibits angiotensin-converting enzyme (ACE) in vitro and in vivo. CAS: 35115-60-7 C53H76N14O12 FW: 1101.27 . Synonym: Teprotide, SQ20881

(GLU2)-TRH. 50mg This TRH analog, also called fertilization-promoting peptide (FPP), was previously purified and characterized from both rabbit prostate and human semen. Nanomolar concentrations of this peptide have been shown to enhance capacitation of mouse epididymal spermatozoa with a concomitant increase in fertilizing ability. It was also detected in the thyroid gland.eAccording to a study of Nguyen et al. Pyr-Glu-Pro-NHG opposes the cholinergic effect of TRH in the mammalian CNS: Co-perfusion with an equivalent of TRH in the rat hippocampus resulted in a significant attenuation of TRH-induced acetylcholine release. CAS: 85541-78-2 C15H22N4O6 FW: 354.36 . Synonym: FPP, Fertilization-Promoting Peptide

(GLU2)-TRH. 250mg This TRH analog, also called fertilization-promoting peptide (FPP), was previously purified and characterized from both rabbit prostate and human semen. Nanomolar concentrations of this peptide have been shown to enhance capacitation of mouse epididymal spermatozoa with a concomitant increase in fertilizing ability. It was also detected in the thyroid gland.eAccording to a study of Nguyen et al. Pyr-Glu-Pro-NHG opposes the cholinergic effect of TRH in the mammalian CNS: Co-perfusion with an equivalent of TRH in the rat hippocampus resulted in a significant attenuation of TRH-induced acetylcholine release. CAS: 85541-78-2 C15H22N4O6 FW: 354.36 . Synonym: FPP, Fertilization-Promoting Peptide

(DES-ALA3)-GHRP-2. 5mg CAS: 290312-22-0 C42H50N8O5 FW: 746.91 . Synonym: (Des-Ala3)-Pralmorelin, (Des-Ala3)-KP-102, (Des-Ala3,D-Ala1,D-2-Nal2)-GHRP-6, (Des-Ala8,D-Ala6,D-2-Nal7,D-Phe10)-a-MSH (6-11) amide

(DES-ALA3)-GHRP-2. 25mg CAS: 290312-22-0 C42H50N8O5 FW: 746.91 . Synonym: (Des-Ala3)-Pralmorelin, (Des-Ala3)-KP-102, (Des-Ala3,D-Ala1,D-2-Nal2)-GHRP-6, (Des-Ala8,D-Ala6,D-2-Nal7,D-Phe10)-a-MSH (6-11) amide

(LYS8)-VASOPRESSIN. 5mg A compound with reduced vasopressor and antidiuretic activity, as compared to AVP. (Disulfide bond) CAS: 50-57-7 C46H65N13O12S2 FW: 1056.23 . Synonym: Terlipressin (4-12), Lypressin, LVP

(LYS8)-VASOPRESSIN. 25mg A compound with reduced vasopressor and antidiuretic activity, as compared to AVP. (Disulfide bond) CAS: 50-57-7 C46H65N13O12S2 FW: 1056.23 . Synonym: Terlipressin (4-12), Lypressin, LVP

DAGO. 25mg --Receptor-specific enkephalin analog. CAS: 100929-53-1 C26H35N5O6 FW: 513.59 . Synonym: DAGO, DAmg O

DAGO. 100mg --Receptor-specific enkephalin analog. CAS: 100929-53-1 C26H35N5O6 FW: 513.59 . Synonym: DAGO, DAmg O

D-SLEEP INDUCING PEPTIDE. 5mg CAS: 62568-57-4 C35H48N10O15 FW: 848.82 . Synonym: DSIP, Emideltide

D-SLEEP INDUCING PEPTIDE. 25mg CAS: 62568-57-4 C35H48N10O15 FW: 848.82 . Synonym: DSIP, Emideltide

(B-ASP5)-D-SLEEP INDUCING PEP. 5mg This DSIP analog serves as a good substrate for protein L-isoaspartyl methyltransferase, a n enzyme occuring in the brain involved in the repair of age-damaged proteins containing atypical iosaspartyl peptide bonds. CAS: 82602-88-8 C35H48N10O15 FW: 848.82 . Synonym: (b-Asp5)-Delta-Sleep Inducing Peptide (rabbit), (b-Asp5)-DSIP (rabbit)

(B-ASP5)-D-SLEEP INDUCING PEP. 25mg This DSIP analog serves as a good substrate for protein L-isoaspartyl methyltransferase, a n enzyme occuring in the brain involved in the repair of age-damaged proteins containing atypical iosaspartyl peptide bonds. CAS: 82602-88-8 C35H48N10O15 FW: 848.82 . Synonym: (b-Asp5)-Delta-Sleep Inducing Peptide (rabbit), (b-Asp5)-DSIP (rabbit)

H-ALA-ALA-GLN-OH. 250mg CAS: 290312-62-8 C11H20N4O5 FW: 288.3

H-ALA-ALA-GLN-OH. 1G CAS: 290312-62-8 C11H20N4O5 FW: 288.3

CYCLO(-ARG-GLY-ASP-D-PHE-VAL). 1mg c(RGDfV) is a potent inhibitor of cell adhesion. It inhibited tumor cell adhesion to laminin and vitronectin substrates. In vivo investigations in rats provided the first evidence of its utility in the amelioration of ischemic acute renal failure. c(RGDfV) inhibited tubular obstruction by preventing cell-cell adhesion. Hammes et al. showed that the cyclopeptide can also be used to prevent retinal neovascularization. c(RGDfV) binds to +v+3 receptors. CAS: 137813-35-5 C26H38N8O7 FW: 574.64 . Synonym: EMD 66203, c(RGDfV)

CYCLO(-ARG-GLY-ASP-D-PHE-VAL). 5mg c(RGDfV) is a potent inhibitor of cell adhesion. It inhibited tumor cell adhesion to laminin and vitronectin substrates. In vivo investigations in rats provided the first evidence of its utility in the amelioration of ischemic acute renal failure. c(RGDfV) inhibited tubular obstruction by preventing cell-cell adhesion. Hammes et al. showed that the cyclopeptide can also be used to prevent retinal neovascularization. c(RGDfV) binds to +v+3 receptors. CAS: 137813-35-5 C26H38N8O7 FW: 574.64 . Synonym: EMD 66203, c(RGDfV)

(3,5-DIIODO-TYR1)-DAGO, 5mg. --Receptor-specific enkephalin analog. For tritiation. CAS: 103213-42-9 C26H33I2N5O6 FW: 765.39. Synonym: (3,5-Diiodo-Tyr1)-DAGO.

NON-AB COMPONENT OF ALZHEIMER'S. 0.5mg This 35 amino acid peptide has originally been isolated from the insoluble core of Alzheimer's disease (AD) amyloid plaque. The sequence EQVTNVGGAVVTGVTAVAQKTVEGAGSIAAATGFV corresponds to the fragment (61-95) of a 140 amino acid precursor known as NACP or +-synuclein and was found to form amyloid fibrils via a nucleation-dependent polymerization mechanism. Accumulation of NAC aggregates in the synapse might be responsible for the neurodegeneration in AD and in the prion diseases. CAS: 154040-19-4 C141H235N39O49 FW: 3260.65 . Synonym: NAC

NON-AB COMPONENT OF ALZHEIMER'S. 1mg This 35 amino acid peptide has originally been isolated from the insoluble core of Alzheimer's disease (AD) amyloid plaque. The sequence EQVTNVGGAVVTGVTAVAQKTVEGAGSIAAATGFV corresponds to the fragment (61-95) of a 140 amino acid precursor known as NACP or +-synuclein and was found to form amyloid fibrils via a nucleation-dependent polymerization mechanism. Accumulation of NAC aggregates in the synapse might be responsible for the neurodegeneration in AD and in the prion diseases. CAS: 154040-19-4 C141H235N39O49 FW: 3260.65 . Synonym: NAC

H-CYS-ARG-GLY-ASP-PHE-PRO-ALA-SER-. 1mg CRGDFPASSC is a cyclic RGD-containing decapeptide which binds to the fibrinogen receptor on the platelet surface. This analog with Phe substituted for Ser at position 5 was found to be 3 times more active (IC50 = 2.5 -M) as a platelet aggregation inhibitor than CRGDSPASSC. (Disulfide bond) C41H61N13O15S2 FW: 1040.15 . Synonym: CRGDFPASSC

(MET5,PRO6,D-PHE7,D-TRP9,PHE10)-A-M, 1mg Potent +-MSH antagonist (ICGG = 11 - 7 nM). CAS: 158563-45-2 C61H87N15O9S FW: 1206.52. MSH.

PACAP-38 (6-38) (HUMAN, CHICKEN) 0.5mg The PACAP selective antagonist, PACAP (6-38), is a much more potent and selective inhibitor of PACAP-27-stimulated pituitary adenylate cyclase than PACAP (6-27) (H-8435). Ki values for the inhibition of the enzyme were 7 nM and 150 nM respectively. CAS: 143748-18-9 C182H300N56O45S FW: 4024.8. Synonym: Pituitary Adenylate Cyclase Activating Polypeptide-38 (6-38) (human, chicken, mouse, ovine, porcine, rat).

PACAP-38 (6-38) (HUMAN, CHICKEN) 1mg The PACAP selective antagonist, PACAP (6-38), is a much more potent and selective inhibitor of PACAP-27-stimulated pituitary adenylate cyclase than PACAP (6-27) (H-8435). Ki values for the inhibition of the enzyme were 7 nM and 150 nM respectively. CAS: 143748-18-9 C182H300N56O45S FW: 4024.8. Synonym: Pituitary Adenylate Cyclase Activating Polypeptide-38 (6-38) (human, chicken, mouse, ovine, porcine, rat).

GASTRIN TETRAPEPTIDE. 500mg Tetragastrin seems to be a potent releaser of insulin and other islet hormones. CAS: 1947-37-1 C29H36N6O6S FW: 596.71 . Synonym: Gastrin (14-17) (human), Cholecystokinin Tetrapeptide, CCK-4, Cholecystokinin Octapeptide (5-8), Tetragastrin

H-GLY-GLY-ALA-OH. 1G CAS: 19729-30-7 C7H13N3O4 FW: 203.2

H-GLY-GLY-ALA-OH. 5G CAS: 19729-30-7 C7H13N3O4 FW: 203.2

H-GLY-GLY-ARG-OH. 250mg Mimic of mussel pheromones, induces the aggregation of various mussel species as Mytilis edulis. GGR also stimulates planktonic larvae to settle. CAS: 54944-27-3 C10H20N6O4 FW: 288.31

H-GLY-GLY-ARG-OH. 1G Mimic of mussel pheromones, induces the aggregation of various mussel species as Mytilis edulis. GGR also stimulates planktonic larvae to settle. CAS: 54944-27-3 C10H20N6O4 FW: 288.31

(LEU31,PRO34)-NEUROPEPTIDE Y (HUM) 0.5mg Specific Y1 receptor agonist. CAS: 132699-73-1 C189H284N54O56S FW: 4240.73. neuropeptide Y.

(LEU31,PRO34)-NEUROPEPTIDE Y (HUM) 1mg Specific Y1 receptor agonist. CAS: 132699-73-1 C189H284N54O56S FW: 4240.73. neuropeptide Y.

NEUROPEPTIDE Y (FREE ACID) (HUMAN. 0.5mg Desamidation of neuropeptide Y suppresses almost all of NPY effects. CAS: 99575-89-0 C189H284N54O58S FW: 4272.73 . Synonym: NPY (free acid) (human, rat)

NEUROPEPTIDE Y (FREE ACID) (HUMAN. 1mg Desamidation of neuropeptide Y suppresses almost all of NPY effects. CAS: 99575-89-0 C189H284N54O58S FW: 4272.73 . Synonym: NPY (free acid) (human, rat)

NEUROPEPTIDE Y (3-36) (HUMAN, RAT) 0.5mg CAS: 150138-78-6 C175H269N53O54S FW: 4011.45. neuropeptide Y.

NEUROPEPTIDE Y (3-36) (HUMAN, RAT) 1mg CAS: 150138-78-6 C175H269N53O54S FW: 4011.45. neuropeptide Y.

PAR-2 (1-6) AMIDE (MOUSE, RAT), 1mg SLIGRL-amide, protease-activated receptor-2 (PAR2) selective agonist. For an inactive control see H-6508. CAS: 171436-38-7 C29H56N10O7 FW: 656.83. Synonym: Proteinase Activated Receptor 2 (1-6) amide (mouse, rat), Thrombin Receptor-Like 1 (1-6) amide (mouse, rat), Coagulation Factor II Receptor-Like 1 (1-6) amide (mouse, rat), SLIGRLamide.

H-TYR-TYR-TYR-OH. 50mg The bitter taste of tri-tyrosine, YYY, is due to its marked hydrophobicity.

H-Thr-Phe-Leu-Leu-Arg-NHG Trifluoroacetate salt 1mg, Synonym: TFLLRamide, (Thr1)-TRAP-5 amide, (Thr1)-PAR-1 (1-5) amide (human), Molecular Formula: CGGHGGNGOG, Cas number: 197794-83-5. Source: Synthetic.

H-Thr-Phe-Leu-Leu-Arg-NHG Trifluoroacetate salt 5mg, Synonym: TFLLRamide, (Thr1)-TRAP-5 amide, (Thr1)-PAR-1 (1-5) amide (human), Molecular Formula: CGGHGGNGOG, Cas number: 197794-83-5. Source: Synthetic.

(Ala1)-PAR-4 (1-6) amide (mouse) H-Ala-Tyr-Pro-Gly-Lys-Phe-NHG Trifluoroacetate salt 1mg. (Ala1)-PAR-4 (1-6) amide (mouse) H-Ala-Tyr-Pro-Gly-Lys-Phe-NHG Trifluoroacetate salt 1mg, Molecular Formula: CGGHGGNGOG, Cas number: 352017-71-1, Storage Condition: -20 +/- 5 degree C.

PAR-4 (1-6) AMIDE (MOUSE). 5mg Protease-activated receptor-4 activating peptide derived from murine PAR-4. GYPGKFamide was able to cause rat platelet aggregation with an EC50 value of 40 -M. Its effect on leucocyte rolling and adherence points at a role of PAR-4 in mediating proinflammatory processes. CAS: 245443-52-1 C33H46N8O7 FW: 666.78 . Synonym: Proteinase Activated Receptor 4 (1-6) amide (mouse), Thrombin Receptor-Like 3 (1-6) amide (mouse), Coagulation Factor II Receptor-Like 3 (1-6) amide (mouse), GYPGKFamide

PAR-4 (1-6) AMIDE (MOUSE). 25mg Protease-activated receptor-4 activating peptide derived from murine PAR-4. GYPGKFamide was able to cause rat platelet aggregation with an EC50 value of 40 -M. Its effect on leucocyte rolling and adherence points at a role of PAR-4 in mediating proinflammatory processes. CAS: 245443-52-1 C33H46N8O7 FW: 666.78 . Synonym: Proteinase Activated Receptor 4 (1-6) amide (mouse), Thrombin Receptor-Like 3 (1-6) amide (mouse), Coagulation Factor II Receptor-Like 3 (1-6) amide (mouse), GYPGKFamide

UROTENSIN II-RELATED PEPTIDE (HUMAN. 1mg This peptide showed high affinity to urotensin II receptors in human and rat (Kd = 170 pM and 91 pM). Furthermore, it produced a long lasting, hypotensive effect in anesthetized rats at 10 nmol/kg. (Disulfide bond) CAS: 342878-90-4 C49H64N10O10S2 FW: 1017.24 . Synonym: URP (human, mouse, rat), Urotensin IIB (human, mouse, rat), UIIB (human, mouse, rat)

UROTENSIN II-RELATED PEPTIDE (HUMAN. 5mg This peptide showed high affinity to urotensin II receptors in human and rat (Kd = 170 pM and 91 pM). Furthermore, it produced a long lasting, hypotensive effect in anesthetized rats at 10 nmol/kg. (Disulfide bond) CAS: 342878-90-4 C49H64N10O10S2 FW: 1017.24 . Synonym: URP (human, mouse, rat), Urotensin IIB (human, mouse, rat), UIIB (human, mouse, rat)

(Ala1)-PAR-4 (1-6) (mouse) H-Ala-Tyr-Pro-Gly-Lys-Phe-OH Trifluoroacetate salt 1mg. (Ala1)-PAR-4 (1-6) (mouse) H-Ala-Tyr-Pro-Gly-Lys-Phe-OH Trifluoroacetate salt 1mg, Molecular Formula: CGGHGGNGOG, Cas number: 380900-00-5, Storage Condition: -20 +/- 5 degree C.

NEUROPEPTIDE S (RAT). 0.5mg CAS: 412938-75-1 C95H160N34O27 FW: 2210.53 . Synonym: NPS (rat)

NEUROPEPTIDE S (RAT). 1mg CAS: 412938-75-1 C95H160N34O27 FW: 2210.53 . Synonym: NPS (rat)

(DES-PYR1)-LEUPROLIDE. 5mg C54H79N15O10 FW: 1098.32 . Synonym: (Des-Pyr1)-Leuprolide, (Des-Pyr1)-Leuprorelin

HUMAN CMV PP65 (495-503). 1mg Immunodominant epitope derived from the human cytomegalovirus (HCMV) matrix protein pp65. It represents a useful tool for studying cell-mediated immunity against HCMV and might be used for the generation of HCMV-specific cytotoxic T-cells for adoptive immunotherapy. CAS: 153045-21-7 C42H74N10O12S FW: 943.18 . Synonym: pp65 (495-503) (human cytomegalovirus), 65 kDa Lower Matrix Phosphoprotein (495-503) (human cytomegalovirus)

HUMAN CMV PP65 (495-503). 5mg Immunodominant epitope derived from the human cytomegalovirus (HCMV) matrix protein pp65. It represents a useful tool for studying cell-mediated immunity against HCMV and might be used for the generation of HCMV-specific cytotoxic T-cells for adoptive immunotherapy. CAS: 153045-21-7 C42H74N10O12S FW: 943.18 . Synonym: pp65 (495-503) (human cytomegalovirus), 65 kDa Lower Matrix Phosphoprotein (495-503) (human cytomegalovirus)

H-LEU-PRO-PRO-OH. 250mg The proline-rich tripeptide LPP showed ACE-inhibiting activity as IPP (H-4632) and VPP (H-4634), IC50 9.6 -M. CAS: 121305-26-8 C16H27N3O4 FW: 325.41 . Synonym: LPP

H-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-. 5mg Nonaarginine is one of the most efficient protein transduction domains and a cell-penetrating peptide. CAS: 143413-47-2 C54H110N36O10 FW: 1423.7 . Synonym: Nonaarginine, H(-Arg)9-OH

H-ARG-ARG-ARG-ARG-ARG-ARG-ARG-ARG-. 25mg Nonaarginine is one of the most efficient protein transduction domains and a cell-penetrating peptide. CAS: 143413-47-2 C54H110N36O10 FW: 1423.7 . Synonym: Nonaarginine, H(-Arg)9-OH

FLAG EPITOPE PEPTIDE. 5mg The FLAG Epitope Peptide consists of eight amino acids (DYKDDDDK) and represents a versatile fusion tag for the purification of recombinant proteins. It can be enzymatically removed with enterokinase which cleaves C-terminally to the tag sequence. The peptide is commonly used for the elution of immunoaffinity chromatography-purified recombinant proteins. CAS: 98849-88-8 C41H60N10O20 FW: 1012.98 . FLAG

FLAG EPITOPE PEPTIDE. 25mg The FLAG Epitope Peptide consists of eight amino acids (DYKDDDDK) and represents a versatile fusion tag for the purification of recombinant proteins. It can be enzymatically removed with enterokinase which cleaves C-terminally to the tag sequence. The peptide is commonly used for the elution of immunoaffinity chromatography-purified recombinant proteins. CAS: 98849-88-8 C41H60N10O20 FW: 1012.98 . FLAG

(PHE1,SER2,TYR6)-PAR-1 (1-6) AMIDE, 5mg PAR-2 antagonist. FSLLRY-amide inhibited activation of PAR-2 by trypsin in PAR-2 receptor expressing KNRK cells. Half-maximal inhibition of calcium signaling was observed at about 50 -M. In contrast, the activation of PAR-2 by SLIGRL-amide (PAR-2 (1-6) amide (mouse, rat) (H-5078)) was not inhibited by FSLLRY-amide.. CAS: 245329-02-6 C39H60N10O8 FW: 796.97. Synonym: FSLLRYamide, (Phe1,Ser2,Tyr6)-Proteinase Activated Receptor 1 (1-6) amide (human), (Phe1,Ser2,Tyr6)-Thrombin Receptor (1-6) amide (human), (Phe1,Ser2,Tyr6)-Coagulation Factor II Receptor (1-6) amide (mouse).

PAR-4 (1-6) AMIDE (HUMAN). 5mg Tethered ligand sequence of human PAR-4. CAS: 245443-51-0 C28H42N8O8 FW: 618.69 . Synonym: Proteinase Activated Receptor 4 (1-6) amide (human), Coagulation Factor II Receptor-Like 3 (1-6) amide (human), Thrombin Receptor-Like 3 (1-6) amide (human), GYPGQVamide

PAR-4 (1-6) AMIDE (HUMAN). 25mg Tethered ligand sequence of human PAR-4. CAS: 245443-51-0 C28H42N8O8 FW: 618.69 . Synonym: Proteinase Activated Receptor 4 (1-6) amide (human), Coagulation Factor II Receptor-Like 3 (1-6) amide (human), Thrombin Receptor-Like 3 (1-6) amide (human), GYPGQVamide

PAR-1 (1-6) (MOUSE, RAT), 5mg PAR-1 agonist. CAS: 140436-67-5 C37H54N10O9 FW: 782.9. Synonym: Proteinase Activated Receptor 1 (1-6) (mouse, rat), Thrombin Receptor (1-6) (mouse, rat), SFFLRN.

PAR-1 (1-6) (MOUSE, RAT), 25mg PAR-1 agonist. CAS: 140436-67-5 C37H54N10O9 FW: 782.9. Synonym: Proteinase Activated Receptor 1 (1-6) (mouse, rat), Thrombin Receptor (1-6) (mouse, rat), SFFLRN.

EXENDIN-4 (1-8). 1mg C35H51N11O13 FW: 833.86 . exendin

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