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PTH (1-84) (HUMAN). 0.1mg CAS: 68893-82-3 C408H674N126O126S2 FW: 9424.74 . Synonym: Parathyroid hormone (1-84) (human)

PTH (1-84) (HUMAN). 0.5mg CAS: 68893-82-3 C408H674N126O126S2 FW: 9424.74 . Synonym: Parathyroid hormone (1-84) (human)

PTH (1-84) (HUMAN). 1mg CAS: 68893-82-3 C408H674N126O126S2 FW: 9424.74 . Synonym: Parathyroid hormone (1-84) (human)

ENDOTOXIN INHIBITOR. 1mg The cyclic peptide KTKCKFLKKC has ben shown to form a strong complex with lipid A, the toxic component of the endotoxin lipopolysaccharide (LPS) with Ka = 0.56 -+ 107 M-1. It detoxifies LPS in vitro and prevents LPS-induced cytokine release and lethality in vivo. Furthermore, it shows neither antibiotic activity nor toxicity and might therefore be useful in the prophylaxis and treatment of LPS-mediated diseases.

ENDOTOXIN INHIBITOR. 5mg The cyclic peptide KTKCKFLKKC has ben shown to form a strong complex with lipid A, the toxic component of the endotoxin lipopolysaccharide (LPS) with Ka = 0.56 -+ 107 M-1. It detoxifies LPS in vitro and prevents LPS-induced cytokine release and lethality in vivo. Furthermore, it shows neither antibiotic activity nor toxicity and might therefore be useful in the prophylaxis and treatment of LPS-mediated diseases.

AMYLOID B-PROTEIN (10-20). 1mg The amyloid precursor protein (APP) is cleaved within the amyloid +-protein region by a putative APP secretase to release its extracellular portion. Gelatinase A, the matrix metalloproteinase MMP-2, possesses such APP secretase-like activity, effectively hydrolyzing also the synthetic amyloid +-protein fragment (10-20) YEVHHQKLVFF at the normal processing site, the Lys16-Leu17 bond (Km approx. 0.13 mM). CAS: 152286-31-2 C71H99N17O16 FW: 1446.67 . amyloid

IL-6 (88-121) (HUMAN). 0.5mg IL-6 (88-121) competitively inhibits the binding of human IL-6 to its receptor by interacting with the IL-6 receptor to a significant degree. It is sug gested that this peptide comprises a part of the receptor-binding region of IL-6. CAS: 145990-81-4 C179H281N45O58S FW: 4023.53 . Synonym: Interleukin-6 (88-121) (human)

IL-6 (88-121) (HUMAN). 1mg IL-6 (88-121) competitively inhibits the binding of human IL-6 to its receptor by interacting with the IL-6 receptor to a significant degree. It is sug gested that this peptide comprises a part of the receptor-binding region of IL-6. CAS: 145990-81-4 C179H281N45O58S FW: 4023.53 . Synonym: Interleukin-6 (88-121) (human)

GLUTEN EXORPHIN C. 5mg This peptide, isolated from the pepsin-trypsin-chymo-trypsin digest of wheat gluten, was considered as a +-opioid receptor-selective ligand. The hydrophobicity of Ile- seems to be important for the expression of the opioid activity of gluten exorphin C. Moreover, this peptide appears to be quite different from any of the endogenous and exogenous opioid peptides ever reported as the N-terminal Tyr is the only aromatic amino acid in the structure. CAS: 142479-62-7 C29H45N5O8 FW: 591.71 . gluten

GLUTEN EXORPHIN C. 25mg This peptide, isolated from the pepsin-trypsin-chymo-trypsin digest of wheat gluten, was considered as a +-opioid receptor-selective ligand. The hydrophobicity of Ile- seems to be important for the expression of the opioid activity of gluten exorphin C. Moreover, this peptide appears to be quite different from any of the endogenous and exogenous opioid peptides ever reported as the N-terminal Tyr is the only aromatic amino acid in the structure. CAS: 142479-62-7 C29H45N5O8 FW: 591.71 . gluten

THROMBOSPONDIN-1 (1016-1023) (HUM. 5mg The octapeptide RFYVVMWK constitutes the active sequence within the 30-mer peptide named C4 as it is essential for the cell attachment activity of the TS1 CBD. It supports the attachment of G361 melanoma cells and inhibits their adhesion to the rec CBD of TS1. Moreover, this peptide appears to be highly conserved in all TS1 isoforms, and a related sequence is also present in the fragment F9 of laminin. H-1414 (4N1) has been used as CD47 agonist (see also H-6414). CAS: 149234-04-8 C56H81N13O10S FW: 1128.41 . Synonym: TS1 (1016-1023) (human, bovine, mouse)

FIBRINOPEPTIDE A (HUMAN). 1mg CAS: 25422-31-5 C63H97N19O26 FW: 1536.58 . fibrinopeptide

FIBRINOPEPTIDE A (HUMAN). 5mg CAS: 25422-31-5 C63H97N19O26 FW: 1536.58 . fibrinopeptide

A-CGRP (HUMAN). 0.5mg (Disulfide bond) CAS: 90954-53-3 C163H267N51O49S2 FW: 3789.36 . Synonym: CGRP-I (human)

A-CGRP (HUMAN). 1mg (Disulfide bond) CAS: 90954-53-3 C163H267N51O49S2 FW: 3789.36 . Synonym: CGRP-I (human)

B-MSH (HUMAN). 1mg CAS: 17908-57-5 C118H174N34O35S FW: 2660.95 . MSH

B-MSH (HUMAN). 5mg CAS: 17908-57-5 C118H174N34O35S FW: 2660.95 . MSH

H-ALA-GLY-ALA-OH. 1G CAS: 37460-22-3 C8H15N3O4 FW: 217.23

MCH (HUMAN, MOUSE, RAT), 0.5mg (Disulfide bond) CAS: 128315-56-0 C105H160N30O26S4 FW: 2386.88. Synonym: Melanin-Concentrating Hormone (human, mouse, rat).

MCH (HUMAN, MOUSE, RAT), 1mg (Disulfide bond) CAS: 128315-56-0 C105H160N30O26S4 FW: 2386.88. Synonym: Melanin-Concentrating Hormone (human, mouse, rat).

SOMATOSTATIN-14. 5mg Somatostatin-14 (SRIF) was originally isolated from ovine hypothalamic extracts on the basis of its ability to inhibit the secretion of radioimmunoassayable growth hormone by primary cultures of enzymatically dispersed rat anterior pituitary cells. SRIF is a small cyclic neuropeptide hormone with broad inhibitory effects on endocrine secretions such as the production of GH, glucagon, and insulin. (Disulfide bond) CAS: 38916-34-6 C76H104N18O19S2 FW: 1637.9 . Synonym: Somatotropin Release-Inhibiting Factor, SRIF, SRIF-14

SOMATOSTATIN-14. 25mg Somatostatin-14 (SRIF) was originally isolated from ovine hypothalamic extracts on the basis of its ability to inhibit the secretion of radioimmunoassayable growth hormone by primary cultures of enzymatically dispersed rat anterior pituitary cells. SRIF is a small cyclic neuropeptide hormone with broad inhibitory effects on endocrine secretions such as the production of GH, glucagon, and insulin. (Disulfide bond) CAS: 38916-34-6 C76H104N18O19S2 FW: 1637.9 . Synonym: Somatotropin Release-Inhibiting Factor, SRIF, SRIF-14

(TYR11)-SOMATOSTATIN-14. 1mg (Disulfide bond) CAS: 59481-27-5 C76H104N18O20S2 FW: 1653.9 . somatostatin

(TYR11)-SOMATOSTATIN-14. 5mg (Disulfide bond) CAS: 59481-27-5 C76H104N18O20S2 FW: 1653.9 . somatostatin

O-AGATOXIN IVA. 1mg --Agatoxin IVa is a peptide isolated from the venom of the American funnel web spider, Agelenopsis aperta. --Aga IVa is a selective and potent blocker of the mammalian P-type voltage-dependent calcium channel. (Disulfide bonds between Cys4 and Cys20/Cys12 and Cys25/Cys19 and Cys36/Cys27 and Cys34) CAS: 145017-83-0 C217H360N68O60S10 FW: 5202.33 . agatoxin

H-GLY-CYS-GLY-OH. 250mg CAS: 88440-55-5 C7H13N3O4S FW: 235.26

H-ALA-HIS-LYS-OH. 250mg This GHK analog also forms complexes with Cu(II). CAS: 126828-32-8 C15H26N6O4 FW: 354.41 . GHK

H-ALA-HIS-LYS-OH. 1G This GHK analog also forms complexes with Cu(II). CAS: 126828-32-8 C15H26N6O4 FW: 354.41 . GHK

S-(1,2-DICARBOXYETHYL)GLUTATHIONE, 250mg This intrinsic tripeptide is found in considerable amounts in rat liver, heart, and lens. It shows anti-inflammatory and anti-anaphylactic effects in vivo and inhibits histamine release from rat mast cells in vitro. CAS: 1115-52-2 C14H21N3O10S FW: 423.4. glutathione.

HYDRIN 1'. 1mg This Xenopus peptide hydrin 1' shows equivalent aldosterone-releasing activity compared to hydrin 1 and is also effective in stimulating water flux from the isolated toad bladder. (Disulfide bond) CAS: 148440-73-7 C51H81N17O15S2 FW: 1236.44 . Synonym: (Arg8,Gly10,Lys11)-Vasotocin

SUBSTANCE P (1-7). 5mg This amino-terminal fragment of substance P exerts depressor and bradycardic effects when applied to the nucleus tractus solitarius. It was also shown that this fragment, contrary to substance P, may reduce signs of opioid withdrawal in mice. CAS: 68060-49-1 C41H65N13O10 FW: 900.05 . substance P

SUBSTANCE P (1-7). 25mg This amino-terminal fragment of substance P exerts depressor and bradycardic effects when applied to the nucleus tractus solitarius. It was also shown that this fragment, contrary to substance P, may reduce signs of opioid withdrawal in mice. CAS: 68060-49-1 C41H65N13O10 FW: 900.05 . substance P

AMYLOID B-PROTEIN (1-43). 0.5mg The amyloid +-protein is a 39- to 43-amino acid polypeptide that is the primary constituent of senile plaques and cerebrovascular deposits in Alzheimer's disease and Down's syndrome. Additionally it acts as an inhibitor of the ubiquitin-dependent protein degradation in vitro. CAS: 134500-80-4 C207H318N56O62S FW: 4615.21 . amyloid

AMYLOID B-PROTEIN (1-43). 1mg The amyloid +-protein is a 39- to 43-amino acid polypeptide that is the primary constituent of senile plaques and cerebrovascular deposits in Alzheimer's disease and Down's syndrome. Additionally it acts as an inhibitor of the ubiquitin-dependent protein degradation in vitro. CAS: 134500-80-4 C207H318N56O62S FW: 4615.21 . amyloid

PROCOLLAGEN TYPE I (212-216). 5mg A subfragment of the carboxy-terminal propeptide of type I collagen (residues 197-241) was shown to stimulate extracellular matrix biosynthesis in fibroblasts. The pentapeptide KTTKS has been found to be the minimum sequence necessary for this potent stimulation of collagen and fibronectin production in a variety of mesenchymal cells. The palmitoylated peptide is marketed as a cosmetic ingredient under the trade name palmitoyl pentapeptide-3 or Matrixyl -. CAS: 149128-48-3 C23H45N7O9 FW: 563.65 . Synonym: KTTKS

PROCOLLAGEN TYPE I (212-216). 25mg A subfragment of the carboxy-terminal propeptide of type I collagen (residues 197-241) was shown to stimulate extracellular matrix biosynthesis in fibroblasts. The pentapeptide KTTKS has been found to be the minimum sequence necessary for this potent stimulation of collagen and fibronectin production in a variety of mesenchymal cells. The palmitoylated peptide is marketed as a cosmetic ingredient under the trade name palmitoyl pentapeptide-3 or Matrixyl -. CAS: 149128-48-3 C23H45N7O9 FW: 563.65 . Synonym: KTTKS

FIBRONECTIN ADHESION-PROMOTING PEPT. 1mg The octapeptide Peptide V, WQPPRARI, constitutes one of the heparin-binding amino acid sequences found in the carboxy-terminal heparin-binding domain of fibronectin. The ovalbumin-coupled peptide is able to support cell attachment, and both the ovalbumin-coupled and the free peptides are potent inducers of focal adhesion formation. CAS: 125720-21-0 C47H74N16O10 FW: 1023.21 . Synonym: Peptide V

FIBRONECTIN ADHESION-PROMOTING PEPT. 5mg The octapeptide Peptide V, WQPPRARI, constitutes one of the heparin-binding amino acid sequences found in the carboxy-terminal heparin-binding domain of fibronectin. The ovalbumin-coupled peptide is able to support cell attachment, and both the ovalbumin-coupled and the free peptides are potent inducers of focal adhesion formation. CAS: 125720-21-0 C47H74N16O10 FW: 1023.21 . Synonym: Peptide V

COLLAGEN TYPE II FRAGMENT. 1mg PTGPLGPKGQTGELGAGNKGEQGPK, a peptide analog of an antigenic determinant of type II collagen, prevents the onset of collagen-induced arthritis in vivo. CAS: 144703-90-2 C106H174N32O37 FW: 2488.74 . Synonym: (Ala260,Hyp261,Asn263)-Collagen Type II (245-270)

PANCREATIC POLYPEPTIDE (HUMAN). 0.5mg CAS: 75976-10-2 C185H287N53O54S2 FW: 4181.77 . pancreatic polypeptide

PANCREATIC POLYPEPTIDE (HUMAN). 1mg CAS: 75976-10-2 C185H287N53O54S2 FW: 4181.77 . pancreatic polypeptide

PTH (1-34) (BOVINE). 0.5mg CAS: 12583-68-5 C183H288N54O50S2 FW: 4108.77 . Synonym: Parathyroid Hormone (1-34) (bovine)

PTH (1-34) (BOVINE). 1mg CAS: 12583-68-5 C183H288N54O50S2 FW: 4108.77 . Synonym: Parathyroid Hormone (1-34) (bovine)

GLUTEN EXORPHIN B5. 25mg Among all exogenous opioid peptides reported to date and especially among the gluten exorphins A, B and C, gluten exorphin B5 shows the most potent activity. Its IC50 values were 0.05 -M and 0.017 -M in the GPI and MVD assays, respectively. CAS: 68382-18-3 C30H38N6O7 FW: 594.67 . Synonym: (Trp4)-Leu-Enkephalin

GLUTEN EXORPHIN B5. 100mg Among all exogenous opioid peptides reported to date and especially among the gluten exorphins A, B and C, gluten exorphin B5 shows the most potent activity. Its IC50 values were 0.05 -M and 0.017 -M in the GPI and MVD assays, respectively. CAS: 68382-18-3 C30H38N6O7 FW: 594.67 . Synonym: (Trp4)-Leu-Enkephalin

GLUTEN EXORPHIN A5. 25mg The sequence of this opioid peptide was found at 15 sites in the primary structure of the high molecular weight glutenin. Gluten exorphin A5 is highly specific for +-receptors and displays opioid activity in the MVD assay. The N-terminal Gly increases its activity - thus the structure-activity relationships of gluten exorphins A are quite different from those of the endogenous opioid peptides. CAS: 142155-24-6 C29H37N5O9 FW: 599.64 . gluten

GLUTEN EXORPHIN A5. 100mg The sequence of this opioid peptide was found at 15 sites in the primary structure of the high molecular weight glutenin. Gluten exorphin A5 is highly specific for +-receptors and displays opioid activity in the MVD assay. The N-terminal Gly increases its activity - thus the structure-activity relationships of gluten exorphins A are quite different from those of the endogenous opioid peptides. CAS: 142155-24-6 C29H37N5O9 FW: 599.64 . gluten

ANGIOTENSIN I. 25mg Angiotensin I, DRVYIHPFHL, is cleaved by angiotensin-converting enzyme (ACE) yielding Ang II (H-1705) and His-Leu (G-2310). Ang I is also converted to Ang II by chymase, especially in the human heart. Hence, this mast cell protease is also involved in blood pressure regulation. The chymase pathway gains importance in inflammatory conditions. CAS: 484-42-4 C62H89N17O14 FW: 1296.5 . Synonym: Ang I, Angiotensinogen (1-10)

ANGIOTENSIN I. 100mg Angiotensin I, DRVYIHPFHL, is cleaved by angiotensin-converting enzyme (ACE) yielding Ang II (H-1705) and His-Leu (G-2310). Ang I is also converted to Ang II by chymase, especially in the human heart. Hence, this mast cell protease is also involved in blood pressure regulation. The chymase pathway gains importance in inflammatory conditions. CAS: 484-42-4 C62H89N17O14 FW: 1296.5 . Synonym: Ang I, Angiotensinogen (1-10)

(DES-ASP1)-ANGIOTENSIN I. 25mg CAS: 56317-01-2 C58H84N16O11 FW: 1181.41 . angiotensin

(DES-ASP1)-ANGIOTENSIN I. 100mg CAS: 56317-01-2 C58H84N16O11 FW: 1181.41 . angiotensin

ANGIOTENSIN II. 25mg Angiotensin II, DRVYIHPF, is the major biologically active component of the renin-angiotensin system. Its activities include the regulation of blood pressure, salt and water balance, and vascular tonus. Ang II stimulates various enzymes as NADPH oxidase.eAng II is often used as a model compound in the development and evaluation of analytical methods for peptides and proteins (e.g. MS). CAS: 4474-91-3 C50H71N13O12 FW: 1046.19 . Synonym: Ang II

ANGIOTENSIN I/II (1-7). 25mg Angiotensin (1-7), DRVYIHP, an enzymatically produced peptide of the renin-angiotensin system, shows pharmacologically distinct, tissue-specific actions that differ from those of angiotensin II. Angiotensin (1-7) shows considerable cardiovascular and antiangiogenic activity. Iusuf et al. reviewed its phamacological properties and pharmacotherapeutic perspectives.

ANGIOTENSIN I/II (1-7). 100mg Angiotensin (1-7), DRVYIHP, an enzymatically produced peptide of the renin-angiotensin system, shows pharmacologically distinct, tissue-specific actions that differ from those of angiotensin II. Angiotensin (1-7) shows considerable cardiovascular and antiangiogenic activity. Iusuf et al. reviewed its phamacological properties and pharmacotherapeutic perspectives.

(SAR1,ILE8)-ANGIOTENSIN II, 25mg Angiotensin II antagonist. CAS: 37827-06-8 C46H73N13O10 FW: 968.17. Synonym: Sarilesin.

(SAR1)-ANGIOTENSIN II. 25mg The substitution with Sar at position 1 of angiotensin II resulted in a partial agonistic activity. CAS: 51833-69-3 C49H71N13O10 FW: 1002.18 . angiotensin

(SAR1)-ANGIOTENSIN II. 100mg The substitution with Sar at position 1 of angiotensin II resulted in a partial agonistic activity. CAS: 51833-69-3 C49H71N13O10 FW: 1002.18 . angiotensin

(VAL5)-ANGIOTENSIN II. 25mg CAS: 58-49-1 C49H69N13O12 FW: 1032.17 . angiotensin

(VAL5)-ANGIOTENSIN II. 100mg CAS: 58-49-1 C49H69N13O12 FW: 1032.17 . angiotensin

ANTIPAIN. 50mg A reversible inhibitor of Ser and Cys proteases with an activity spectrum comparable to leupeptin (N-1000). H-1765 inhibited transformation of NIH3T3 cells after transfection with an activated H-ras oncogene (Cox et al.). Vaccari et al. used antipain for evaluating the role of proteases in the process of malignant transformation of BALB/c 3T3 cells. CAS: 37691-11-5 C27H44N10O6 FW: 604.71 . antipain

(ARG8)-VASOPRESSIN (FREE ACID). 5mg Compared to AVP, AVP (free acid) shows markedly reduced antidiuretic activity and almost no vasopressor activity in vivo. (Disulfide bond) CAS: 25255-33-8 C46H64N14O13S2 FW: 1085.23 . Synonym: (Arg8)-Vasopressinoic acid, (Arg8,Gly-OH9)-Vasopressin, AVP (free acid), Argipressin (free acid), (Phe3,Arg8)-Oxytocin (free acid), Pitressin (free acid), Leiormone (free acid), Arginine Antidiuretic Hormone (free acid)

(ARG8)-VASOPRESSIN (FREE ACID). 25mg Compared to AVP, AVP (free acid) shows markedly reduced antidiuretic activity and almost no vasopressor activity in vivo. (Disulfide bond) CAS: 25255-33-8 C46H64N14O13S2 FW: 1085.23 . Synonym: (Arg8)-Vasopressinoic acid, (Arg8,Gly-OH9)-Vasopressin, AVP (free acid), Argipressin (free acid), (Phe3,Arg8)-Oxytocin (free acid), Pitressin (free acid), Leiormone (free acid), Arginine Antidiuretic Hormone (free acid)

(ArgG+)-Vasopressin H-Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NHG (Disulfide bond) Trifluoroacetate salt. (ArgG+)-Vasopressin H-Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NHG (Disulfide bond) Trifluoroacetate salt 1mg, Cas number: 113-79-1, Source: Synthetic, Synonym: AVP, Argipressin.

(ARG8)-VASOPRESSIN. 5mg The major physiological roles of AVP are regulation of water balance in animals (antidiuretic action) and contraction of arterioles (vasopressor action). (Disulfide bond) CAS: 113-79-1 C46H65N15O12S2 FW: 1084.25 . Synonym: AVP, Argipressin, (Phe3,Arg8)-Oxytocin, Pitressin, Leiormone, Arginine Antidiuretic Hormone

(ARG8)-VASOTOCIN. 5mg Vasotocin (argiprestocin) is the vasopressin/oxytocin analog produced in birds, amphibians and fish. The peptide shows antidiuretic as well as reproductive activities. (Disulfide bond) CAS: 113-80-4 C43H67N15O12S2 FW: 1050.23 . Synonym: Argiprestocin

(ARG8)-VASOTOCIN. 25mg Vasotocin (argiprestocin) is the vasopressin/oxytocin analog produced in birds, amphibians and fish. The peptide shows antidiuretic as well as reproductive activities. (Disulfide bond) CAS: 113-80-4 C43H67N15O12S2 FW: 1050.23 . Synonym: Argiprestocin

H-ARG-ARG-ARG-OH. 250mg Triarginine. CAS: 6418-87-7 C18H38N12O4 FW: 486.58

H-ARG-ARG-ARG-OH. 1G Triarginine. CAS: 6418-87-7 C18H38N12O4 FW: 486.58

PROINSULIN C-PEPTIDE (55-89) (HU). 0.5mg CAS: 11097-48-6 C153H259N49O52 FW: 3617.04 . c-peptide

PROINSULIN C-PEPTIDE (55-89) (HU). 1mg CAS: 11097-48-6 C153H259N49O52 FW: 3617.04 . c-peptide

NEUROTENSIN (8-13). 5mg CAS: 60482-95-3 C38H64N12O8 FW: 817 . neurotensin

NEUROTENSIN (8-13). 25mg CAS: 60482-95-3 C38H64N12O8 FW: 817 . neurotensin

PTH (44-68) (HUMAN). 0.5mg CAS: 64421-69-8 C117H199N41O41 FW: 2836.12 . Synonym: Parathyroid hormone (44-68) (human)

PTH (44-68) (HUMAN). 1mg CAS: 64421-69-8 C117H199N41O41 FW: 2836.12 . Synonym: Parathyroid hormone (44-68) (human)

H-ARG-GLY-ASP-OH. 25mg The target epitope of several integrin receptors is the RGD sequence, a cell adhesion motif shared by several matrix-associated adhesive glycoproteins, such as fibronectin, vitronectin, fibrinogen, collagen type I, laminin, and von Willebrand factor. CAS: 99896-85-2 C12H22N6O6 FW: 346.34 . Synonym: RGD

H-ARG-GLY-ASP-OH. 100mg The target epitope of several integrin receptors is the RGD sequence, a cell adhesion motif shared by several matrix-associated adhesive glycoproteins, such as fibronectin, vitronectin, fibrinogen, collagen type I, laminin, and von Willebrand factor. CAS: 99896-85-2 C12H22N6O6 FW: 346.34 . Synonym: RGD

SUBSTANCE P (FREE ACID). 5mg CAS: 71977-09-8 C63H97N17O14S FW: 1348.64 . substance P

SUBSTANCE P (FREE ACID). 25mg CAS: 71977-09-8 C63H97N17O14S FW: 1348.64 . substance P

SUBSTANCE P. 5mg CAS: 33507-63-0 C63H98N18O13S FW: 1347.65 . substance P

SUBSTANCE P. 25mg CAS: 33507-63-0 C63H98N18O13S FW: 1347.65 . substance P

GRF (1-29) AMIDE (RAT). 0.5mg CAS: 91826-20-9 C155H251N49O40S FW: 3473.07 . Synonym: Growth Hormone-Releasing Factors (1-29) amide (rat)

GRF (1-29) AMIDE (RAT). 1mg CAS: 91826-20-9 C155H251N49O40S FW: 3473.07 . Synonym: Growth Hormone-Releasing Factors (1-29) amide (rat)

H-GLU-GLU-LEU-OH. 250mg CAS: 189080-99-7 C16H27N3O8 FW: 389.41

(D-ARG1,D-TRP7-+9,LEU11)-SUBSTANCE P, 1mg A high potency substance P antagonist with a weak spasmogenic and a poor histamine releasing effect. CAS: 91224-37-2 C75H108N20O13 FW: 1497.81. Synonym: Spantide I.

(D-ARG1,D-TRP7-+9,LEU11)-SUBSTANCE P, 5mg A high potency substance P antagonist with a weak spasmogenic and a poor histamine releasing effect. CAS: 91224-37-2 C75H108N20O13 FW: 1497.81. Synonym: Spantide I.

(D-ARG1,D-TRP7-+9,LEU11)-SUBSTANCE P, 25mg A high potency substance P antagonist with a weak spasmogenic and a poor histamine releasing effect. CAS: 91224-37-2 C75H108N20O13 FW: 1497.81. Synonym: Spantide I.

(D-ARG1,D-PRO2,D-TRP7-+9,LEU11)-SU, 1mg A potent antagonist for substance P and bombesin. CAS: 84676-91-5 C75H108N20O13 FW: 1497.81. substance P.

(DL-ISOSER1)-TRAP-6. 1mg This racemic isoserine analog of SFLLRN (H-8365) has only 15-20% of the platelet aggregating activity of SFLLRN. In compensation iso-SFLLRN significantly resists degradation by aminopeptidase M and is much more stable in plasma and serum. CAS: 150242-29-8 C34H56N10O9 FW: 748.88 . Synonym: iso-TRAP, (DL-Isoser1)-Thrombin Receptor Activator Peptide 6, (DL-Isoser1)-PAR-1 (1-6) (human), (DL-Isoser1)-Proteinase Activated Receptor 1 (1-6) (human), (DL-Isoser1)-Thrombin Receptor 1 (1-6) (human)

(DL-ISOSER1)-TRAP-6. 5mg This racemic isoserine analog of SFLLRN (H-8365) has only 15-20% of the platelet aggregating activity of SFLLRN. In compensation iso-SFLLRN significantly resists degradation by aminopeptidase M and is much more stable in plasma and serum. CAS: 150242-29-8 C34H56N10O9 FW: 748.88 . Synonym: iso-TRAP, (DL-Isoser1)-Thrombin Receptor Activator Peptide 6, (DL-Isoser1)-PAR-1 (1-6) (human), (DL-Isoser1)-Proteinase Activated Receptor 1 (1-6) (human), (DL-Isoser1)-Thrombin Receptor 1 (1-6) (human)

BRADYKININ (1-5). 5mg The fragment RPPGF and the two dipeptides SP (G-2865) and FR (G-3230) are obtained by action of angiotensin-converting enzyme (ACE) on bradykinin. RPPGF inhibits thrombin-induced platelet activation, in high concentration, the pentapeptide inhibits thrombin-induced coagulant activity. CAS: 23815-89-6 C27H40N8O6 FW: 572.66 . bradykinin

BRADYKININ (1-5). 25mg The fragment RPPGF and the two dipeptides SP (G-2865) and FR (G-3230) are obtained by action of angiotensin-converting enzyme (ACE) on bradykinin. RPPGF inhibits thrombin-induced platelet activation, in high concentration, the pentapeptide inhibits thrombin-induced coagulant activity. CAS: 23815-89-6 C27H40N8O6 FW: 572.66 . bradykinin

BRADYKININ (1-7). 5mg CAS: 23815-87-4 C35H52N10O9 FW: 756.86 . bradykinin

MYELIN BASIC PROTEIN (87-99) (HUM. 1mg This peptide has been shown to induce the proliferation of an encephalitogenic, myelin basic protein-specific T cell line. Active immunization of rats with this peptide induced acute experimental autoimmune encephalomyelitis. This protein region is highly conserved among mammalian species. CAS: 118506-26-6 C74H114N20O17 FW: 1555.84 . MBP

(DES-ARG9)-BRADYKININ. 25mg CAS: 15958-92-6 C44H61N11O10 FW: 904.04 . bradykinin

(DES-ARG9)-BRADYKININ. 100mg CAS: 15958-92-6 C44H61N11O10 FW: 904.04 . bradykinin

HIRULLIN. 1mg This peptide, originally isolated from the leech Hirudinaria manillensis, is a hirudin-based fibrinogen recognition peptide inhibitor, which binds efficiently to thrombin (IC50= 4.2 -M, in bovine). CAS: 131147-81-4 C68H96N14O29 FW: 1573.59 . hirullin

HIRULLIN. 5mg This peptide, originally isolated from the leech Hirudinaria manillensis, is a hirudin-based fibrinogen recognition peptide inhibitor, which binds efficiently to thrombin (IC50= 4.2 -M, in bovine). CAS: 131147-81-4 C68H96N14O29 FW: 1573.59 . hirullin

BRADYKININ. 100mg The pharmacological properties of bradykinin include smooth muscle contraction, vasodilation and hypotension. Bradykinin increases capillary permeability together with edema formation and induction of pain. Bradykinin induces bronchoconstriction in asthmatic subjects and symptoms of rhinitis in nasal provocation. CAS: 6846-03-3 C50H73N15O11 FW: 1060.22 . Synonym: BK, Kallidin I, Kallidin-9, BRS-640

BRADYKININ. 500mg The pharmacological properties of bradykinin include smooth muscle contraction, vasodilation and hypotension. Bradykinin increases capillary permeability together with edema formation and induction of pain. Bradykinin induces bronchoconstriction in asthmatic subjects and symptoms of rhinitis in nasal provocation. CAS: 6846-03-3 C50H73N15O11 FW: 1060.22 . Synonym: BK, Kallidin I, Kallidin-9, BRS-640

H-GLY-PRO-ARG-PRO-NH2. 5mg 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

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