• 0
Shop Products $

H-GLY-PHE-GLY-OH. 5G CAS: 14656-09-8 C13H17N3O4 FW: 279.3

H-GLY-PRO-ALA-OH. 1G Cleavage product of the collagenase substrate Z-GPGGPA (M-1260).

H-GLY-PRO-HYP-OH. 250mg CAS: 2239-67-0 C12H19N3O5 FW: 285.3

H-GLY-PRO-HYP-OH. 1G CAS: 2239-67-0 C12H19N3O5 FW: 285.3

H-GLY-TRP-GLY-OH. 250mg CAS: 23067-32-5 C15H18N4O4 FW: 318.33

H-GLY-TRP-GLY-OH. 1G CAS: 23067-32-5 C15H18N4O4 FW: 318.33

H-GLY-TYR-GLY-OH. 1G GYG was used as a model peptide in a study on the UV-absorption behavior of Tyr-containing proteins. CAS: 6099-08-7 C13H17N3O5 FW: 295.3

H-D-PHE-CYS-TYR-D-TRP-ARG-THR-PEN-. 1mg CTAP, an analog of CTOP, is a selective --opioid receptor antagonist. (Disulfide bond between Cys2 and Pen7) CAS: 103429-32-9 C51H69N13O11S2 FW: 1104.32 . Synonym: CTAP

H-D-PHE-CYS-TYR-D-TRP-ARG-THR-PEN-. 5mg CTAP, an analog of CTOP, is a selective --opioid receptor antagonist. (Disulfide bond between Cys2 and Pen7) CAS: 103429-32-9 C51H69N13O11S2 FW: 1104.32 . Synonym: CTAP

(D-ALA2)-GRF (1-29) AMIDE (HUMAN). 0.5mg This peptide was approximately 50 times more potent than GRF (1-29) in eliciting GH secretion in the rat. CAS: 89453-59-8 C149H246N44O42S FW: 3357.93 . Synonym: (D-Ala2)-Sermorelin

HIPPURYL-PHE-ARG-OH. 250mg Hip-Phe-Arg is used as substrate for angiotensin I-converting enzyme and for dipeptidyl carboxypeptidase. CAS: 73167-83-6 C24H30N6O5 FW: 482.54 . Synonym: Bz-Gly-Phe-Arg-OH

PHI-27 (PORCINE). 1mg Porcine intestinal peptide which belongs to the glucagon-secretin family. It exhibits biological activities similar to vasoactive intestinal peptide (VIP) and secretin. CAS: 80458-29-3 C136H216N36O40 FW: 2995.43 . VIP

CHARACTERISTIC MSH-TETRAPEPTIDE. 25mg C32H40N10O5 FW: 644.73 . MSH

MTII. 1mg This cyclic MSH analog is a potent full agonist of the melanocortin-3 and melanocortin-4 receptors (MC3-R and MC4-R). Intracerebroventricular administration of MTII inhibited feeding in four different mouse models of hyperphagia. MTII is a valuable tool for the study of the agouti obesity syndrome and of the role of melanocortinergic neurons in feeding. CAS: 121062-08-6 C50H69N15O9 FW: 1024.19 . Synonym: MTII, Melanotan II, Bremelanotide amide

MTII. 5mg This cyclic MSH analog is a potent full agonist of the melanocortin-3 and melanocortin-4 receptors (MC3-R and MC4-R). Intracerebroventricular administration of MTII inhibited feeding in four different mouse models of hyperphagia. MTII is a valuable tool for the study of the agouti obesity syndrome and of the role of melanocortinergic neurons in feeding. CAS: 121062-08-6 C50H69N15O9 FW: 1024.19 . Synonym: MTII, Melanotan II, Bremelanotide amide

H-LEU-LEU-ALA-OH. 1G CAS: 20274-80-0 C15H29N3O4 FW: 315.41

H-LEU-LEU-LEU-OH. 1G The tripeptide trileucine, found in casein and soy protein, was shown to increase the endothelial release of TXB2, a stable marker of TXA2.

H-LEU-LEU-LEU-OH. 5G The tripeptide trileucine, found in casein and soy protein, was shown to increase the endothelial release of TXB2, a stable marker of TXA2.

HOMOGLUTATHIONE. 50mg Homoglutathione is a taste-modifying peptide responsible (in combination with +-glutamyl peptides as +-Glu-Leu (G-1950) and +-Glu-Val (G-2015)) for the GCkokumiGCY flavor.ePesticides containing electrophilic centers can be metabolized in legumes via conjug ation to homoglutathione (H-3944) or glutathione. CAS: 18710-27-5 C11H19N3O6S FW: 321.35 . glutathione

HOMOGLUTATHIONE. 250mg Homoglutathione is a taste-modifying peptide responsible (in combination with +-glutamyl peptides as +-Glu-Leu (G-1950) and +-Glu-Val (G-2015)) for the GCkokumiGCY flavor.ePesticides containing electrophilic centers can be metabolized in legumes via conjug ation to homoglutathione (H-3944) or glutathione. CAS: 18710-27-5 C11H19N3O6S FW: 321.35 . glutathione

ACETYL-(NLE4,ASP5,D-2-NAL7,LYS10), 1mg Screening analogs of the cyclic lactam melanocortin agonist MTII led to the identification of the agoutimimetic SHU9119. The cyclopeptide SHU9119 shares pharmacological properties with the agouti peptide in that it is a potent antagonist of the melanocortin-4 receptor and a less potent antagonist of the melanocortin-3 receptor. CAS: 168482-23-3 C54H71N15O9 FW: 1074.25. Synonym: SHU9119.

ACETYL-(NLE4,ASP5,D-2-NAL7,LYS10), 5mg Screening analogs of the cyclic lactam melanocortin agonist MTII led to the identification of the agoutimimetic SHU9119. The cyclopeptide SHU9119 shares pharmacological properties with the agouti peptide in that it is a potent antagonist of the melanocortin-4 receptor and a less potent antagonist of the melanocortin-3 receptor. CAS: 168482-23-3 C54H71N15O9 FW: 1074.25. Synonym: SHU9119.

H-LEU-SER-PHE-OH. 1G CAS: 40290-77-5 C18H27N3O5 FW: 365.43

H-GLY-PEN-GLY-ARG-GLY-ASP-SER-PRO-. 1mg GPenGRGDSPCA (cRGD), a cyclic RGD peptide has been used in the study of vascular wound response. GPenGRGDSPCA caused vasodilation when applied to isolated rat cremaster arterioles. The vasodilation is dependent on interaction of the soluble cRGD sequence with the +v+3 integrin expressed by smooth muscle cells in the arteriolar wall. (Disulfide bond between Pen2 and Cys9) CAS: 126716-28-7 C35H57N13O14S2 FW: 948.05 . fibronectin

H-GLY-PEN-GLY-ARG-GLY-ASP-SER-PRO-. 5mg GPenGRGDSPCA (cRGD), a cyclic RGD peptide has been used in the study of vascular wound response. GPenGRGDSPCA caused vasodilation when applied to isolated rat cremaster arterioles. The vasodilation is dependent on interaction of the soluble cRGD sequence with the +v+3 integrin expressed by smooth muscle cells in the arteriolar wall. (Disulfide bond between Pen2 and Cys9) CAS: 126716-28-7 C35H57N13O14S2 FW: 948.05 . fibronectin

H-LEU-TRP-MET-ARG-OH. 250mg LWMR. CAS: 67368-23-4 C28H44N8O5S FW: 604.77

(D-LEU6,PRO-NHET9)-LHRH (4-9), 5mg CAS: 202333-85-5 C37H62N10O8 FW: 774.96. Synonym: Leuprolide (4-9), Leuprorelin (4-9).

(D-LEU6,PRO-NHET9)-LHRH (4-9), 25mg CAS: 202333-85-5 C37H62N10O8 FW: 774.96. Synonym: Leuprolide (4-9), Leuprorelin (4-9).

CYCLOLINOPEPTIDE B. 1mg Cyclolinopeptide B has been isolated from the seeds of Linum usitatissimum. It showed potent immunosuppressive activity comparable with that of cyclosporin A. CAS: 193139-41-2 C56H83N9O9S FW: 1058.4 . cyclolinopeptide

CYCLOLINOPEPTIDE B. 5mg Cyclolinopeptide B has been isolated from the seeds of Linum usitatissimum. It showed potent immunosuppressive activity comparable with that of cyclosporin A. CAS: 193139-41-2 C56H83N9O9S FW: 1058.4 . cyclolinopeptide

AC-CALPASTATIN (184-210) (HUMAN). 0.5mg Ac-DPMSSTYIEELGKREVTIPPKYRELLA-amide, a calpain inhibitor homologous to the minimal inhibitory domain I of human calpastatin, was shown to modulate the amyloid +-protein 42 secretion ratio. This finding might point to the possibility of exploring compounds that inhibit A+42 secretion. CAS: 123714-50-1 C142H230N36O44S FW: 3177.67 . Synonym: Acetyl-Calpain Inhibitor Fragment (184-210) (human), Acetyl-Sperm BS-17 Component (184-210) (human)

AC-CALPASTATIN (184-210) (HUMAN). 1mg Ac-DPMSSTYIEELGKREVTIPPKYRELLA-amide, a calpain inhibitor homologous to the minimal inhibitory domain I of human calpastatin, was shown to modulate the amyloid +-protein 42 secretion ratio. This finding might point to the possibility of exploring compounds that inhibit A+42 secretion. CAS: 123714-50-1 C142H230N36O44S FW: 3177.67 . Synonym: Acetyl-Calpain Inhibitor Fragment (184-210) (human), Acetyl-Sperm BS-17 Component (184-210) (human)

KALA AMPHIPATHIC PEPTIDE. 0.5mg WEAKLAKALAKALAKHLAKALAKALKACEA, a low-molecular weight cationic amphipathic peptide was able to bind to DNA, to destabilize membranes and to mediate transfection of plasmid DNA in various cell lines. Thus, KALA provides a starting point for a family of peptides that incorporate other functions to improve DNA delivery systems. C144H248N40O35S FW: 3131.87 . amphipathic peptide

KALA AMPHIPATHIC PEPTIDE. 1mg WEAKLAKALAKALAKHLAKALAKALKACEA, a low-molecular weight cationic amphipathic peptide was able to bind to DNA, to destabilize membranes and to mediate transfection of plasmid DNA in various cell lines. Thus, KALA provides a starting point for a family of peptides that incorporate other functions to improve DNA delivery systems. C144H248N40O35S FW: 3131.87 . amphipathic peptide

MELANOCYTE PROTEIN PMEL 17 (185-193. 1mg This peptide is as H-3958 and H-2174 a gp100 epitope that is recognized in the context of HLA-A2 by tumorinfiltrating lymphocytes (TIL) in vivo. PMEL 17 could be a melanogenic enzyme. CAS: 162558-10-3 C46H72N10O15 FW: 1005.14 . Synonym: Melanocyte Lineage-Specific Antigen GP100 (185-193) (human, bovine, mouse), Melanoma-Associated ME20 Antigen (185-193) (human, bovine, mouse), ME20M/ME20S (130-138) (human), ME20-M/ME20-S (130-138) (human), 95 kDa Melanocyte-Specific Secreted Glycoprotein (130-138) (human)

MELANOCYTE PROTEIN PMEL 17 (185-193. 5mg This peptide is as H-3958 and H-2174 a gp100 epitope that is recognized in the context of HLA-A2 by tumorinfiltrating lymphocytes (TIL) in vivo. PMEL 17 could be a melanogenic enzyme. CAS: 162558-10-3 C46H72N10O15 FW: 1005.14 . Synonym: Melanocyte Lineage-Specific Antigen GP100 (185-193) (human, bovine, mouse), Melanoma-Associated ME20 Antigen (185-193) (human, bovine, mouse), ME20M/ME20S (130-138) (human), ME20-M/ME20-S (130-138) (human), 95 kDa Melanocyte-Specific Secreted Glycoprotein (130-138) (human)

OREXIN A (HUMAN, BOVINE, CANINE) 0.5mg Orexin A is a hypothalamic neuropeptide regulating the feeding behavior. Central administration of this peptide to rats stimulated food consumption in a dose-dependent manner. The effect persisted at 4 h after injection, as orexin A seems to be resistant to peptidases. Orexin A specifically binds a G protein-coupled receptor, OX1R (IC50 = 20 nM to displace 50 % of radiolabeled orexin A bound to this receptor). (Disulfide bonds between Cys6 and Cys12/Cys7 and Cys14) CAS: 205640-90-0 C152H243N47O44S4 FW: 3561.16. Synonym: Hypocretin-1 (human, bovine, canine, mouse, ovine, porcine, rat).

OREXIN A (HUMAN, BOVINE, CANINE) 1mg Orexin A is a hypothalamic neuropeptide regulating the feeding behavior. Central administration of this peptide to rats stimulated food consumption in a dose-dependent manner. The effect persisted at 4 h after injection, as orexin A seems to be resistant to peptidases. Orexin A specifically binds a G protein-coupled receptor, OX1R (IC50 = 20 nM to displace 50 % of radiolabeled orexin A bound to this receptor). (Disulfide bonds between Cys6 and Cys12/Cys7 and Cys14) CAS: 205640-90-0 C152H243N47O44S4 FW: 3561.16. Synonym: Hypocretin-1 (human, bovine, canine, mouse, ovine, porcine, rat).

OREXIN A (HUMAN, BOVINE, CANINE) 5mg Orexin A is a hypothalamic neuropeptide regulating the feeding behavior. Central administration of this peptide to rats stimulated food consumption in a dose-dependent manner. The effect persisted at 4 h after injection, as orexin A seems to be resistant to peptidases. Orexin A specifically binds a G protein-coupled receptor, OX1R (IC50 = 20 nM to displace 50 % of radiolabeled orexin A bound to this receptor). (Disulfide bonds between Cys6 and Cys12/Cys7 and Cys14) CAS: 205640-90-0 C152H243N47O44S4 FW: 3561.16. Synonym: Hypocretin-1 (human, bovine, canine, mouse, ovine, porcine, rat).

OREXIN B (HUMAN). 0.5mg Like orexin A, orexin B is a hypothalamic neuropeptide regulating the feeding behavior. Central administration of this peptide to rats stimulated food consumption in a similar manner to orexin A, but the effect did not last as long as that of orexin A. The affinity of orexin B for the OX1 receptor is significantly lower (IC50 = 240 nM) than that of orexin A. Binding affinities for the OX2 receptor are similar for orexin A and B (IC50 = 38 nM and 36 nM, respectively, for displacement of radiolabeled orexin A bound to the receptor). CAS: 205640-91-1 C123H212N44O35S FW: 2899.38 . Synonym: Hypocretin-2 (human)

OREXIN B (HUMAN). 1mg Like orexin A, orexin B is a hypothalamic neuropeptide regulating the feeding behavior. Central administration of this peptide to rats stimulated food consumption in a similar manner to orexin A, but the effect did not last as long as that of orexin A. The affinity of orexin B for the OX1 receptor is significantly lower (IC50 = 240 nM) than that of orexin A. Binding affinities for the OX2 receptor are similar for orexin A and B (IC50 = 38 nM and 36 nM, respectively, for displacement of radiolabeled orexin A bound to the receptor). CAS: 205640-91-1 C123H212N44O35S FW: 2899.38 . Synonym: Hypocretin-2 (human)

OREXIN B (HUMAN). 5mg Like orexin A, orexin B is a hypothalamic neuropeptide regulating the feeding behavior. Central administration of this peptide to rats stimulated food consumption in a similar manner to orexin A, but the effect did not last as long as that of orexin A. The affinity of orexin B for the OX1 receptor is significantly lower (IC50 = 240 nM) than that of orexin A. Binding affinities for the OX2 receptor are similar for orexin A and B (IC50 = 38 nM and 36 nM, respectively, for displacement of radiolabeled orexin A bound to the receptor). CAS: 205640-91-1 C123H212N44O35S FW: 2899.38 . Synonym: Hypocretin-2 (human)

H-LYS-LYS-LYS-OH. 50mg Trilysine. CAS: 13184-14-0 C18H38N6O4 FW: 402.54

H-LYS-LYS-LYS-OH. 250mg Trilysine. CAS: 13184-14-0 C18H38N6O4 FW: 402.54

OREXIN B (MOUSE, RAT), 0.5mg CAS: 202801-92-1 C126H215N45O34S FW: 2936.44. Synonym: Hypocretin-2 (mouse, rat).

OREXIN B (MOUSE, RAT), 1mg CAS: 202801-92-1 C126H215N45O34S FW: 2936.44. Synonym: Hypocretin-2 (mouse, rat).

H-LYS-LYS-LYS-LYS-OH. 50mg Tetralysine. CAS: 997-20-6 C24H50N8O5 FW: 530.71

H-LYS-LYS-LYS-LYS-OH. 250mg Tetralysine. CAS: 997-20-6 C24H50N8O5 FW: 530.71

H-LYS-LYS-LYS-LYS-LYS-OH. 50mg Pentalysine. KKKKK corresponds to the N-terminal sequence of the MARCKS peptide. CAS: 19431-21-1 C30H62N10O6 FW: 658.89 . pentalysine

H-LYS-LYS-LYS-LYS-LYS-OH. 250mg Pentalysine. KKKKK corresponds to the N-terminal sequence of the MARCKS peptide. CAS: 19431-21-1 C30H62N10O6 FW: 658.89 . pentalysine

ACV. 5mg ACV is the key intermediate in the biosynthesis of all penicillins and cephalosporins by eukaryotic and prokaryotic microorganisms. CAS: 32467-88-2 C14H25N3O6S FW: 363.44 . Synonym: d-(L-a-Aminoadipyl)-L-cysteinyl-D-valine

ACV. 25mg ACV is the key intermediate in the biosynthesis of all penicillins and cephalosporins by eukaryotic and prokaryotic microorganisms. CAS: 32467-88-2 C14H25N3O6S FW: 363.44 . Synonym: d-(L-a-Aminoadipyl)-L-cysteinyl-D-valine

(DES-GLY10,D-SER(TBU)6,PRO-NHET9)- 5mg Buserelin is a longer acting synthetic peptide analog of the naturally occurring gonadotropin-releasing hormone (GnRH/LHRH). Substitution of glycine in position 6 by D-serine and that of glycinamide in position 10 by ethylamide, leads to a nonapeptide with a significantly enhanced LHRH effect. The effects of buserelin on follicle-stimulating hormone (FSH) and luteinizing hormone (LH) release are approximately 20 to 170 times higher than those of natural LHRH. CAS: 57982-77-1 C60H86N16O13 FW: 1239.44. Synonym: Buserelin.

([D8]VAL7-+10)-C-PEPTIDE (HUMAN). 0.5mg C129H195D16N35O48 FW: 3036.43 . c-peptide

([D8]VAL7-+10)-C-PEPTIDE (HUMAN). 1mg C129H195D16N35O48 FW: 3036.43 . c-peptide

H-LYS-TYR-LYS-OH. 250mg This tripeptide is able to nick supercoiled or relaxed DNAs at apurinic/apyrimidinic sites. See also H-Lys-Trp-Lys-OH (H-4265). CAS: 35193-18-1 C21H35N5O5 FW: 437.54 . DNA binding

H-LYS-TYR-LYS-OH. 1G This tripeptide is able to nick supercoiled or relaxed DNAs at apurinic/apyrimidinic sites. See also H-Lys-Trp-Lys-OH (H-4265). CAS: 35193-18-1 C21H35N5O5 FW: 437.54 . DNA binding

MIF-I. 1G MIF-I, the C-terminal tripeptide of oxytocin, has been shown to be active in numerous behavioral tests and clinical situations. For further information on its pharmacological application see: CAS: 2002-44-0 C13H24N4O3 FW: 284.36 . Synonym: MIF-I, Melanostatin, Melanotropin Release-Inhibiting Factor

MIF-I. 5G MIF-I, the C-terminal tripeptide of oxytocin, has been shown to be active in numerous behavioral tests and clinical situations. For further information on its pharmacological application see: CAS: 2002-44-0 C13H24N4O3 FW: 284.36 . Synonym: MIF-I, Melanostatin, Melanotropin Release-Inhibiting Factor

MELITTIN. 1mg Synthetic melittin, the main component of the honeybee venom. The amphiphilic nature of this antimicrobial peptide makes it a excellent model compound for monitoring lipid-protein interactions in membranes. CAS: 20449-79-0 C131H229N39O31 FW: 2846.5 . melittin

MELITTIN. 5mg Synthetic melittin, the main component of the honeybee venom. The amphiphilic nature of this antimicrobial peptide makes it a excellent model compound for monitoring lipid-protein interactions in membranes. CAS: 20449-79-0 C131H229N39O31 FW: 2846.5 . melittin

H-MET-ALA-SER-OH. 250mg Substrate for human methionine aminopeptidases 1D and 2. For the latter enzyme, Yang et al. determined the kinetic parameters Km 0.38 - 0.03 mM and kcat 210 - 5 min-1 at pH 7.5 and 30-C for the tripeptide MAS. CAS: 17351-33-6 C11H21N3O5S FW: 307.37 . methionine aminopeptidase substrate

H-MET-ALA-SER-OH. 1G Substrate for human methionine aminopeptidases 1D and 2. For the latter enzyme, Yang et al. determined the kinetic parameters Km 0.38 - 0.03 mM and kcat 210 - 5 min-1 at pH 7.5 and 30-C for the tripeptide MAS. CAS: 17351-33-6 C11H21N3O5S FW: 307.37 . methionine aminopeptidase substrate

(D-HIS2)-LEUPROLIDE. 1mg Impurity B of the Leuprorelin Ph. Eur. monograph. CAS: 112642-11-2 C59H84N16O12 FW: 1209.42 . Synonym: (D-His2)-Leuprolide, (D-His2)-Leuprorelin

(D-HIS2)-LEUPROLIDE. 5mg Impurity B of the Leuprorelin Ph. Eur. monograph. CAS: 112642-11-2 C59H84N16O12 FW: 1209.42 . Synonym: (D-His2)-Leuprolide, (D-His2)-Leuprorelin

H-MET-ARG-PHE-ALA-OH. 50mg MRFA is used as a calibration standard in mass spectrometry (ESI). Miao et al. studied Pt(II) complexes of the tetrapeptide by mass spectrometric methods.

H-MET-ARG-PHE-ALA-OH. 250mg MRFA is used as a calibration standard in mass spectrometry (ESI). Miao et al. studied Pt(II) complexes of the tetrapeptide by mass spectrometric methods.

PAR-4 (1-6) (HUMAN). 5mg This hexapeptide corresponding to the amino terminus of the fourth protease-activated receptor (PAR4) after the cleavage at Arg47/Gly48 was tested for its ability to stimulate COS cells expressing PAR4. This peptide readily activated both wild-type and mutant PAR4 (R47A) at 500 -M, whereas thrombin and trypsin only activate the wild-type PAR4. CAS: 225779-44-2 C28H41N7O9 FW: 619.68 . Synonym: Proteinase Activated Receptor 4 (1-6) (human), Thrombin Receptor-Like 3 (1-6) (human), Coagulation Factor II Receptor-Like 3 (1-6) (human), GYPGQV

PAR-4 (1-6) (HUMAN). 25mg This hexapeptide corresponding to the amino terminus of the fourth protease-activated receptor (PAR4) after the cleavage at Arg47/Gly48 was tested for its ability to stimulate COS cells expressing PAR4. This peptide readily activated both wild-type and mutant PAR4 (R47A) at 500 -M, whereas thrombin and trypsin only activate the wild-type PAR4. CAS: 225779-44-2 C28H41N7O9 FW: 619.68 . Synonym: Proteinase Activated Receptor 4 (1-6) (human), Thrombin Receptor-Like 3 (1-6) (human), Coagulation Factor II Receptor-Like 3 (1-6) (human), GYPGQV

PREPROLACTIN (23-53) (HUMAN). 0.5mg CAS: 215510-22-8 C160H252N56O42S FW: 3664.18 . Synonym: PrRP31 (human), Preprolactin (23-53) (human)

PREPROLACTIN (23-53) (HUMAN). 1mg CAS: 215510-22-8 C160H252N56O42S FW: 3664.18 . Synonym: PrRP31 (human), Preprolactin (23-53) (human)

PREPROLACTIN (23-53) (RAT). 0.5mg CAS: 215510-06-8 C156H242N54O43S FW: 3594.04 . Synonym: PrRP31 (rat), Preprolactin (23-53) (rat)

PREPROLACTIN (23-53) (RAT). 1mg CAS: 215510-06-8 C156H242N54O43S FW: 3594.04 . Synonym: PrRP31 (rat), Preprolactin (23-53) (rat)

MOTILIN (HUMAN, PORCINE), 0.5mg Althoug h the nucleic acid sequence for human motilin shows 7 differences compared to the cDNA of the pig, the amino acid sequence deduced from both sequences is identical. CAS: 9072-41-7 C120H188N34O35S FW: 2699.09. motilin.

MOTILIN (HUMAN, PORCINE), 1mg Althoug h the nucleic acid sequence for human motilin shows 7 differences compared to the cDNA of the pig, the amino acid sequence deduced from both sequences is identical. CAS: 9072-41-7 C120H188N34O35S FW: 2699.09. motilin.

(DES-ACETYL)-A-MSH. 1mg CAS: 53697-27-1 C75H107N21O18S FW: 1622.87 . Synonym: ACTH (1-13) amide

(DES-ACETYL)-A-MSH. 5mg CAS: 53697-27-1 C75H107N21O18S FW: 1622.87 . Synonym: ACTH (1-13) amide

PREPROLACTIN (34-53) (HUMAN). 0.5mg CAS: 235433-36-0 C104H158N32O26 FW: 2272.6 . Synonym: PrRP20 (human), Preprolactin (34-53) (human)

PREPROLACTIN (34-53) (HUMAN). 1mg CAS: 235433-36-0 C104H158N32O26 FW: 2272.6 . Synonym: PrRP20 (human), Preprolactin (34-53) (human)

G1-MSH. 1mg This fragment has been located in the cryptic region of the ACTH/+-lipotropin precursor protein from the intermediate lobe of bovine pituitary. CAS: 72629-65-3 C72H97N21O14S FW: 1512.76 . MSH

G1-MSH. 5mg This fragment has been located in the cryptic region of the ACTH/+-lipotropin precursor protein from the intermediate lobe of bovine pituitary. CAS: 72629-65-3 C72H97N21O14S FW: 1512.76 . MSH

G2-MSH. 1mg This fragment has been located in the cryptic region of the ACTH/+-lipotropin precursor protein from the intermediate lobe of bovine pituitary. CAS: 72711-43-4 C74H99N21O16S FW: 1570.8 . MSH

G2-MSH. 5mg This fragment has been located in the cryptic region of the ACTH/+-lipotropin precursor protein from the intermediate lobe of bovine pituitary. CAS: 72711-43-4 C74H99N21O16S FW: 1570.8 . MSH

CART (55-102) (HUMAN). 0.5mg CART peptides, especially CART (55-102) appear to have an important function in the regulation of energy homeostasis. Intracerebroventricular administration of CART (55-102) reduces appetite and stimulates energy expenditure, whereas injection of the peptide into specific hypothalamic nuclei increases food intake . (Disulfide bonds between Cys68 and Cys86/Cys74 and Cys94/Cys88 and Cys101) CAS: 214050-22-3 C225H365N65O65S7 FW: 5245.23 . CART

CART (55-102) (HUMAN). 1mg CART peptides, especially CART (55-102) appear to have an important function in the regulation of energy homeostasis. Intracerebroventricular administration of CART (55-102) reduces appetite and stimulates energy expenditure, whereas injection of the peptide into specific hypothalamic nuclei increases food intake . (Disulfide bonds between Cys68 and Cys86/Cys74 and Cys94/Cys88 and Cys101) CAS: 214050-22-3 C225H365N65O65S7 FW: 5245.23 . CART

CART (55-102) (RAT). 1mg (Disulfide bonds between Cys68 and Cys86/Cys74 and Cys94/Cys88 and Cys101) CAS: 209615-79-2 C226H367N65O65S7 FW: 5259.26 . CART

CART (61-102) (HUMAN, RAT), 0.5mg (Disulfide bonds between Cys68 and Cys86/Cys74 and Cys94/Cys88 and Cys101) CAS: 209615-75-8 C189H310N58O56S7 FW: 4515.36. CART.

CART (61-102) (HUMAN, RAT), 1mg (Disulfide bonds between Cys68 and Cys86/Cys74 and Cys94/Cys88 and Cys101) CAS: 209615-75-8 C189H310N58O56S7 FW: 4515.36. CART.

PAR-3 (1-6) (HUMAN). 25mg Mimicks the putative tethered ligand of human PAR-3 (protease activated receptor 3). CAS: 320347-28-2 C29H45N9O8 FW: 647.73 . Synonym: Proteinase Activated Receptor 3 (1-6) (human), Thrombin Receptor-Like 2 (1-6) (human), Coagulation Factor II Receptor-Like 2 (1-6) (human), TFRGAP

PEPTIDE YY (CANINE, MOUSE, PORCIN) 0.5mg CAS: 81858-94-8 C190H288N54O57 FW: 4240.71. Synonym: PYY (canine, mouse, porcine, rat).

PEPTIDE YY (CANINE, MOUSE, PORCIN) 1mg CAS: 81858-94-8 C190H288N54O57 FW: 4240.71. Synonym: PYY (canine, mouse, porcine, rat).

H-PHE-GLY-HIS-P-NITRO-PHE-PHE-ALA. 100mg A good substrate for pepsin which is also cleaved by cathepsin D. CAS: 50572-79-7 C48H54N10O10 FW: 931.02 . pepsin substrate

PARASIN I. 0.5mg The 19 amino acid peptide KGRGKQGGKVRAKAKTRSS was isolated from the epithelial mucosal layer of the injured catfish, Parasilurus asotus. Parasin I showed strong antimicrobial activity, about 12-100 times more potent than magainin II (H-6570), against a wide spectrum of microorganisms, without any hemolytic activity. CAS: 219552-69-9 C82H154N34O24 FW: 2000.34 . parasin

PARASIN I. 1mg The 19 amino acid peptide KGRGKQGGKVRAKAKTRSS was isolated from the epithelial mucosal layer of the injured catfish, Parasilurus asotus. Parasin I showed strong antimicrobial activity, about 12-100 times more potent than magainin II (H-6570), against a wide spectrum of microorganisms, without any hemolytic activity. CAS: 219552-69-9 C82H154N34O24 FW: 2000.34 . parasin

H-PHE-PHE-PHE-OH. 250mg FFF is a bitter-tasting peptide due to its hydrophobicity. As diphenylalanine, triphenylalanine forms ordered nanostructures. CAS: 2578-81-6 C27H29N3O4 FW: 459.55 . Synonym: triphenylalanine

H-PHE-PHE-PHE-OH. 1G FFF is a bitter-tasting peptide due to its hydrophobicity. As diphenylalanine, triphenylalanine forms ordered nanostructures. CAS: 2578-81-6 C27H29N3O4 FW: 459.55 . Synonym: triphenylalanine

H-PHE-PHE-PHE-PHE-OH. 250mg Tetraphenylalanine, FFFF. CAS: 2667-02-9 C36H38N4O5 FW: 606.72 . tetraphenylalanine

APELIN-13 (HUMAN, BOVINE, MOUSE) 1mg Endogenous peptide ligand for the human APJ receptor, a putative receptor protein related to the angiotensin receptor (AT1). This peptide exerted an acidification-rate-promoting activity in the CHO cells expressing the APJ receptor with a median effective concentration (EC50) value of 0.37 nM. In a study of Valle et al. chronic central administration of apelin-13 over 10 days increased food intake, body weight, locomotor activity and body temperature in C57BL/6 mice. CAS: 217082-58-1 C69H111N23O16S FW: 1550.85. apelin.

APELIN-13 (HUMAN, BOVINE, MOUSE) 5mg Endogenous peptide ligand for the human APJ receptor, a putative receptor protein related to the angiotensin receptor (AT1). This peptide exerted an acidification-rate-promoting activity in the CHO cells expressing the APJ receptor with a median effective concentration (EC50) value of 0.37 nM. In a study of Valle et al. chronic central administration of apelin-13 over 10 days increased food intake, body weight, locomotor activity and body temperature in C57BL/6 mice. CAS: 217082-58-1 C69H111N23O16S FW: 1550.85. apelin.

(PYR1)-APELIN-13 (HUMAN, BOVINE) 1mg The pyroglutamyl form of apelin-13 exhibited a high activity with an EC50 value of 0.30 nM. pERPRLSHKGPMPF is probably the final product of the post-translational modification of apelin and the biologically active endogenous ligand. (Pyr1)-Apelin-13 has been identified as the predominant apelin isoform in the human heart..

Category