Peptides (3)

[Glp5,(Me)Phe8,Sar9] Substance P (5-11)

Reference: HY-P3801

€0.00 (tax incl.)

[Glp5,(Me)Phe8,Sar9] Substance P (5-11) (DiMe-C7) is a Substance P (HY-P0201) analogue that has approximately the same effects as Substance P (HY-P0201) on neurokinin 1 receptor (NK1R) in rat brain, but with a much...

[Glp1]-FGL peptide acetate

Reference: HY-P3532

€0.00 (tax incl.)

[Glp1]-FGL peptide acetate is a neural cell adhesion molecule (NCAM) derived motif and can be used for the research of neurogenesis.

[Gln8]-C517 (LH-RH), chicken

Reference: HY-P1905

€0.00 (tax incl.)

[Gln8]-C517 (LH-RH), chicken is an avian hypothalamic peptide, which stimulates release of gonadotropins from anterior pituitary, thus regulating reproductive functions.

[DPro5] Corticotropin Releasing Factor, human, rat

Reference: HY-P3684

€0.00 (tax incl.)

[DPro5] Corticotropin Releasing Factor, human, rat is a selective R2 agonist of corticotropin releasing factor/hormone. Corticotropin releasing factor (CRF) is a hypothalamic hormone, stimulates the release of...

[DPro10] Dynorphin A (1-11), porcine

Reference: HY-P3647

€0.00 (tax incl.)

[DPro10] Dynorphin A (1-11), porcine, a N-Alkylated derivative, is a potent κ-opioid receptor agonist with a Ki value of 0.13 nM. [DPro10] Dynorphin A (1-11), porcine has analgesic property.

[DPen2, Pen5] Enkephalin

Reference: HY-P3546

€0.00 (tax incl.)

[DPen2, Pen5] Enkephalin is a δ-opioid receptor selective analog of [Leu5]-Enkephalin (HY-P0288).

[Des-Tyr1]-Met-Enkephalin

Reference: HY-P2658

€0.00 (tax incl.)

[Des-Tyr1]-Met-Enkephalin, a tetrapeptide, is a degradationproduct of enkephalins.

[Des-His1,Glu9]-Glucagon amide TFA

Reference: HY-P1143A

€0.00 (tax incl.)

[Des-His1,Glu9]-Glucagon amide TFA is a potent and peptide antagonist of the glucagon receptor, with a pA2 of 7.2. [Des-His1,Glu9]-Glucagon amide TFA is potentially useful in the study of the pathogenesis of diabetes.

[Des-His1,Glu9]-Glucagon amide

Reference: HY-P1143

€0.00 (tax incl.)

[Des-His1,Glu9]-Glucagon amide is a potent and peptide antagonist of the glucagon receptor, with a pA2 of 7.2. [Des-His1,Glu9]-Glucagon amide is potentially useful in the study of the pathogenesis of diabetes.

[Des-His1,Glu9] Glucagon

Reference: HY-P3608

€0.00 (tax incl.)

[Des-His1,Glu9] Glucagon is a potent glucagon receptor system peptide antagonist. [Des-His1,Glu9] Glucagon enhances the glucose-stimulated release of insulin from pancreatic islet cells. [Des-His1,Glu9] Glucagon can...

[Des-Arg9]-Bradykinin acetate

Reference: HY-P0298A

€0.00 (tax incl.)

[Des-Arg9]-Bradykinin acetate is a Bradykinin B1 receptor agonist that displays selectivity for B1 over B2 receptors.

[Des-Arg9]-Bradykinin

Reference: HY-P0298

€0.00 (tax incl.)

[Des-Arg9]-Bradykinin is a Bradykinin (B1) receptor agonist that displays selectivity for B1 over B2 receptors.

[Dehydro-Pro4] Substance P (4-11)

Reference: HY-P3820

€0.00 (tax incl.)

[Dehydro-Pro4] Substance P (4-11) is a peptide fragment of Substance P. Substance P is a peptide mainly secreted by neurons. Substance P takes part in many biological processes, including nociception, inflammation and...

[Deamino-4-valine, 8-D-arginine]-Vasopressin

Reference: HY-P4008

€0.00 (tax incl.)

[Deamino-4-valine, 8-D-arginine]-Vasopressin (dVDAVP) is a highly potent and specific antidiuretic agent possessing protracted effects.

[DAla4] Substance P (4-11)

Reference: HY-P3883

€0.00 (tax incl.)

[DAla4] Substance P (4-11) is an analog of Substance P (Substance P (HY-P0201)) that inhibits the binding of 125I-Bolton Hunter-conjugated Eledoisin (Eledoisin (HY-P0006)) (IC50 of 0.5 μM) and 125I-Bolton...

[DAla2] Dynorphin A (1-9) (porcine)

Reference: HY-P3646

€0.00 (tax incl.)

[DAla2] Dynorphin A (1-9) (porcine) is a dynorphin, which can be used in studies of analgesic, addiction, and depression.

[DAla2] Dynorphin A (1-13), amide (porcine)

Reference: HY-P3634

€0.00 (tax incl.)

[DAla2] Dynorphin A (1-13), amide (porcine) is a petide. [DAla2] Dynorphin A (1-13), amide (porcine) might have the κ opioid receptor agonist effect. [DAla2] Dynorphin A (1-13), amide (porcine) can be used for the...

[DAla2, DArg6] Dynorphin A, (1-13) (porcine)

Reference: HY-P3632

€0.00 (tax incl.)

[DAla2, DArg6] Dynorphin A, (1-13) (porcine) (DADAD) is an opioid peptide (dynorphinl-13, DYN) derivative found in porcine pituitary extracts. DYN is highly potent at the peripheral opioid receptors GPI and MVD, but...

[D-Val22, Phe33] Big Endothelin-1 (16-38), human

Reference: HY-P3569

€0.00 (tax incl.)

[D-Val22, Phe33] Big Endothelin-1 (16-38), human is a polypeptide.

[D-Trp8]-γ-MSH TFA

Reference: HY-P1217A

€0.00 (tax incl.)

[D-Trp8]-γ-MSH TFA is a potent and selective agonist of melanocortin 3 (MC3) receptor, with IC50s of 6.7 nM, 600 nM and 340 nM for hMC3, hMC4 and hMC5, respectively in CHO cells. [D-Trp8]-γ-MSH TFA could provide...

[D-Trp8]-γ-MSH

Reference: HY-P1217

€0.00 (tax incl.)

[D-Trp8]-γ-MSH is a potent and selective agonist of melanocortin 3 (MC3) receptor, with IC50s of 6.7 nM, 600 nM and 340 nM for hMC3, hMC4 and hMC5, respectively in CHO cells. [D-Trp8]-γ-MSH could provide protection...

[D-Trp8] Somatostatin-14

Reference: HY-P3902

€0.00 (tax incl.)

[D-Trp8] Somatostatin-14, a tetradecapeptide, is an analog of Somatostatin more potent than the native Somatostatin.

[D-Trp8,Tyr11] Somatostatin

Reference: HY-P3903

€0.00 (tax incl.)

[D-Trp8,Tyr11] Somatostatin is an analogue of somatostatin. Somatostatin is a hormone that regulates a variety of bodily functions. DTrp8 residue can increase stability.

[D-Trp7,9,10]-Substance P TFA

Reference: HY-P1375A

€0.00 (tax incl.)

[D-Trp7,9,10]-Substance P TFA is a substance P analogue. Substance P stimulates substance P receptors but also inhibits ion conductance through nicotinic acetylcholine receptors.

[D-Trp7,9,10]-Substance P

Reference: HY-P1375

€0.00 (tax incl.)

[D-Trp7,9,10]-Substance P is a substance P analogue. Substance P stimulates substance P receptors but also inhibits ion conductance through nicotinic acetylcholine receptors.

[D-Trp34]-Neuropeptide Y TFA

Reference: HY-P1322A

€0.00 (tax incl.)

[D-Trp34]-Neuropeptide Y TFA is a potent and selective neuropeptide Y (NPY) Y5 receptor agonist. [D-Trp34]-Neuropeptide Y TFA is a significantly less potent agonist at the NPY Y1, Y2, Y4, and y6 receptors....

[D-Trp34]-Neuropeptide Y

Reference: HY-P1322

€0.00 (tax incl.)

[D-Trp34]-Neuropeptide Y is a potent and selective neuropeptide Y (NPY) Y5 receptor agonist. [D-Trp34]-Neuropeptide Y is a significantly less potent agonist at the NPY Y1, Y2, Y4, and y6 receptors....

[D-Trp2,7,9] Substance P

Reference: HY-P3802

€0.00 (tax incl.)

[D-Trp2,7,9] Substance P is a tachykinin (Neurokinin Receptor) antagonist with Ki values of 1 μM, 1.3 μM, and ~9 μM for NK-1, NK-2,and NK-3 receptor, respectively.

[D-Trp11]-Neurotensin

Reference: HY-P3057

€0.00 (tax incl.)

[D-Trp11]-Neurotensin, an analogue of Neurotensin (NT), is a selective antagonist of NT in perfused rat hearts but behaves as a full agonist in guinea pig atria and rat stomach strips. [D-Trp11]-Neurotensin can...

[D-Pro4,D-Trp7,9] Substance P (4-11)

Reference: HY-P3803

€0.00 (tax incl.)

[D-Pro4,D-Trp7,9] Substance P (4-11) is a potent antagonist of Substance P (HY-P0201). [D-Pro4,D-Trp7,9] Substance P (4-11) decreases plasma aldosterone (ALDO) concentration.

[D-Pro4,D-Trp7,9,Nle11] Substance P (4-11)

Reference: HY-P3805

€0.00 (tax incl.)

[D-Pro4,D-Trp7,9,Nle11] Substance P (4-11) is a potent neurokinin NK1 antagonist. [D-Pro4,D-Trp7,9,Nle11] Substance P (4-11) inhibits the effects of gold-protein-substance P (GPSP) and substance P (SP).

[D-Pro4,D-Trp7,9,10] Substance P (4-11)

Reference: HY-P3806

€0.00 (tax incl.)

[D-Pro4,D-Trp7,9,10] Substance P (4-11) is a potent tachykinin antagonist.

[D-Pro2,D-Trp7,9] Substance P

Reference: HY-P3808

€0.00 (tax incl.)

[D-Pro2,D-Trp7,9] Substance P, a Substance P (HY-P0201) analogue, is a weak agonist and a potent, specific, competitive Substance P antagonist.

[D-Pro2,D-Phe7,D-Trp9] Substance P

Reference: HY-P3809

€0.00 (tax incl.)

[D-Pro2,D-Phe7,D-Trp9] Substance P is a Substance P (HY-P0201) analogue. [D-Pro2,D-Phe7,D-Trp9] Substance P is an inhibitor of Substance P. [D-Pro2,D-Phe7,D-Trp9] Substance P contracts guinea-pig ileum (GPI) indirectly.

[D-Phe2,D-Ala6]-LH-RH

Reference: HY-P3664

€0.00 (tax incl.)

[D-Phe2,D-Ala6]-LH-RH is a potent LH-RH antagonist. [D-Phe2,D-Ala6]-LH-RH shows anti-LH/FSH-RH and antiovulatory activities.

[D-Phe2,6, Pro3]-LH-RH

Reference: HY-P3666

€0.00 (tax incl.)

[D-Phe2,6, Pro3]-LH-RH is a potent luteinizing hormone releasing hormone (LHRH) antagonist.

[D-p-Cl-Phe6,Leu17]-VIP TFA

Reference: HY-P1159A

€0.00 (tax incl.)

[D-p-Cl-Phe6,Leu17]-VIP TFA is a competitive and selective antagonist of vasoactive intestinal peptide (VIP) receptor, with the IC50 of 125.8 nM. [D-p-Cl-Phe6,Leu17]-VIP TFA has no activity on glucagon, secretin or...

[D-p-Cl-Phe6,Leu17]-VIP

Reference: HY-P1159

€0.00 (tax incl.)

[D-p-Cl-Phe6,Leu17]-VIP is a competitive and selective antagonist of vasoactive intestinal peptide (VIP) receptor, with the IC50 of 125.8 nM. [D-p-Cl-Phe6,Leu17]-VIP has no activity on glucagon, secretin or GRF...

[D-Lys6]-LH-RH

Reference: HY-P3668

€0.00 (tax incl.)

[D-Lys6]-LH-RH is a Luteinizing-hormone-releasing hormone (LHRH) analogue. [D-Lys6]-LH-RH acts as a GnRH receptor agonist.

[D-Leu6, Val7]-LH-RH (1-9) Ethyl Amide

Reference: HY-P3670

€0.00 (tax incl.)

[D-Leu6, Val7]-LH-RH (1-9) Ethyl Amide is a LHRH peptide analogue.

[D-Leu-4]-OB3

Reference: HY-P3342

€0.00 (tax incl.)

[D-Leu-4]-OB3 inhibits expressions of pro-inflammatory, proliferative and metastatic genes and PD-L1 expression. [D-Leu-4]-OB3 stimulates expression of pro-apoptotic genes.

[D-Glp1,D-Phe2,D-Trp3,6]-LH-RH

Reference: HY-P3671

€0.00 (tax incl.)

[D-Glp1,D-Phe2,D-Trp3,6]-LH-RH is a Luteinizing-hormone-releasing hormone (LHRH) analogue. [D-Glp1,D-Phe2,D-Trp3,6]-LH-RH acts as a GnRH receptor antagonist.

[D-Asp3]-Microcystin-LR

Reference: HY-P3090

€0.00 (tax incl.)

Microcystin-[D-Asp3]-LR/Microcystin A is a cyanotoxin. Microcystin-[D-Asp3]-LR/Microcystin A can activate Nrf2 and promote oxidative stress response. Microcystin-[D-Asp3]-LR/Microcystin A can also be used in...

[D-Asn5]-Oxytocin

Reference: HY-P3220

€0.00 (tax incl.)

[D-Asn5]-Oxytocin possesses very low specific oxytocic and vasodepressor activities. By cumulative dose-response studies for oxytocic activity, [D-Asn5]-Oxytocin has similar intrinsic activity to oxytocin.

[D-Arg2]Dermorphin-(1-4) amide

Reference: HY-P3869

€0.00 (tax incl.)

[D-Arg2]Dermorphin-(1-4) amide is a N-terminal shorter peptide amide of [D-Arg2]dermorphin with the hypothermic effect. [D-Arg2]Dermorphin-(1-4) amide shows analgesic activity and degradation in soluble mouse liver...

[D-Arg25]-Neuropeptide Y (human)

Reference: HY-P0198B

€0.00 (tax incl.)

[D-Arg25]-Neuropeptide Y (human) ([D-Arg25] NPY) is a Y1 receptor selective agonist. Neuropeptide Y (human) is involved in Alzheimer's disease (AD) and protects rat cortical neurons against β-Amyloid toxicity.

[D-Ala6]-LH-RH

Reference: HY-P3672

€0.00 (tax incl.)

[D-Ala6]-LH-RH is a Luteinizing-hormone-releasing hormone (LHRH) analogue. [D-Ala6]-LH-RH acts as a GnRH receptor agonist.

[D-Ala2]leucine-enkephalin

Reference: HY-P0098

€0.00 (tax incl.)

[D-Ala2]leucine-enkephalin, a delta opioid agonist, is a degradation resistant long-acting Leu-enkephalin.

[D-Ala2]-Met-Enkephalinamide

Reference: HY-P3548

€0.00 (tax incl.)

[D-Ala2]-Met-Enkephalinamide, an opioid peptide, is a potent opioid agonist. [D-Ala2]-Met-Enkephalinamide decreases bile flow by a central mechanism. [D-Ala2]-Met-Enkephalinamide has analgesic properties.

[D-Ala2]-Met-Enkephalin

Reference: HY-P2626

€0.00 (tax incl.)

[D-Ala2]-Met-Enkephalin, an opioid peptide, is a potent opioid agonist. [D-Ala2]-Met-Enkephalin inhibits ACh-induced and suckling-induced oxytocin (OT) release.

[D-Ala2] Leu-Enkephalinamide

Reference: HY-P3549

€0.00 (tax incl.)

[D-Ala2] Leu-Enkephalinamide is an enkephalin analog. [D-Ala2] Leu-Enkephalinamide has great corneal permeability and analgesic effect. [D-Ala2] Leu-Enkephalinamide can be used for the research of ocular diseases.

[Cys(Bzl)84] CD (81-92)

Reference: HY-P3983

€0.00 (tax incl.)

[Cys(Bzl)84] CD (81-92) is an acidic peptide. [Cys(Bzl)84] CD (81-92) can be sequencing by negative ion postsource decay (PSD) spectra.

[cPP1-7,NPY19-23,Ala31,Aib32,Gln34]-hPancreatic polypeptide TFA

Reference: HY-P1324A

€0.00 (tax incl.)

[cPP1-7,NPY19-23,Ala31,Aib32,Gln34]-hPancreatic Polypeptide is a potent and selective neuropeptide Y Y5 receptor agonist with an IC50 of 0.24 nM for binding to the hY5 receptor....

[cPP1-7,NPY19-23,Ala31,Aib32,Gln34]-hPancreatic Polypeptide

Reference: HY-P1324

€0.00 (tax incl.)

[cPP1-7,NPY19-23,Ala31,Aib32,Gln34]-hPancreatic Polypeptide is a potent and selective neuropeptide Y Y5 receptor agonist with an IC50 of 0.24 nM for binding to the hY5 receptor....

[bAla8]-Neurokinin A(4-10)

Reference: HY-P1031

€0.00 (tax incl.)

[bAla8]-Neurokinin A(4-10) is a neurokinin 2 (NK2) receptor agonist.

[Asu1,6]-Oxytocin

Reference: HY-P3866

€0.00 (tax incl.)

[Asu1,6]-Oxytocin is an analog of oxytocin. [Asu1,6]-Oxytocin reverses insulin resistance and glucose intolerance prior to reduction of obesity. [Asu1,6]-Oxytocin has the potential for the research of obesity and...

[Asu1,6-Arg8]Vasopressin

Reference: HY-P4012

€0.00 (tax incl.)

[Asu1,6-Arg8]Vasopressin is an vasopressin agonist which potentiates cyclic AMP accumulation and ACTH release induced by corticotropin-releasing factor (CRF) in rat anterior pituitary cells in culture.

[Asp5]-Oxytocin acetate

Reference: HY-P3217A

€0.00 (tax incl.)

[Asp5]-Oxytocin acetate is the first 5-position neurohypophyseal hormone analogue possessing significant biological activity. [Asp5]-Oxytocin acetate causes uterine contractions in vitro, enhanced by Mg2+....

[Asp5]-Oxytocin

Reference: HY-P3217

€0.00 (tax incl.)

[Asp5]-Oxytocin is the first 5-position neurohypophyseal hormone analogue possessing significant biological activity. [Asp5]-Oxytocin causes uterine contractions in vitro, enhanced by Mg2+. [Asp5]-Oxytocin has the...

[Asp371]-Tyrosinase (369-377), human

Reference: HY-P1919

€0.00 (tax incl.)

Tyrosinase 369-377, human is a HLA-A2.1-restricted epitope derived from tyrosinase, has been used to develop tumor-targeted vaccines with mixed efficacy.

[Asn18] Endothelin-1, human

Reference: HY-P3615

€0.00 (tax incl.)

[Asn18] Endothelin-1, human is a peptide. Endothelin-1 is a major isoform of Endothelin and plays an important role for regulation of vascular function.

[Arg8]-Vasotocin TFA

Reference: HY-P1574A

€0.00 (tax incl.)

[Arg8]-Vasotocin (TFA) is a vertebrate neurohypophyseal peptide of the vasopressin/oxytocin hormone family.

[Arg8]-Vasotocin

Reference: HY-P1574

€0.00 (tax incl.)

[Arg8]-Vasotocin is a vertebrate neurohypophyseal peptide of the vasopressin/oxytocin hormone family.

[Arg15,20,21, Leu17] VIP-Gly-Lys-Arg-NH2

Reference: HY-P4013

€0.00 (tax incl.)

[Arg15,20,21, Leu17] VIP-Gly-Lys-Arg-NH2 is a vasoactive intestinal polypeptide (VIP) analog with relaxant effects.

[Arg14,Lys15]Nociceptin TFA

Reference: HY-P1301A

€0.00 (tax incl.)

[Arg14,Lys15]Nociceptin TFA is a highly potent and selective NOP receptor (ORL1; OP4) agonist, with an EC50 of 1 nM. [Arg14,Lys15]Nociceptin TFA displays high selectivity over opioid receptors, with IC50s of 0.32,...

[Arg14,Lys15]Nociceptin

Reference: HY-P1301

€0.00 (tax incl.)

[Arg14,Lys15]Nociceptin is a highly potent and selective NOP receptor (ORL1; OP4) agonist, with an EC50 of 1 nM. [Arg14,Lys15]Nociceptin displays high selectivity over opioid receptors, with IC50s of 0.32, 280, >10000...

[Arg-15,20,21,Leu17]-PACAP-Gly-Lys-Arg-NH2

Reference: HY-P3875

€0.00 (tax incl.)

[Arg-15,-20,-21,Leu17]-PACAP-Gly-Lys-Arg-NH2 (BM-PACAP) is a synthetic PACAP 1-27 (HY-P0176) analogue with relaxant effect.

[Ala9,10, Lys11,12] Glycogen Synthase (1-12)

Reference: HY-P3741

€0.00 (tax incl.)

[Ala9,10, Lys11,12] Glycogen Synthase (1-12) is a selective substrate for phosphorylation by protein kinase C (PKC). [Ala9,10, Lys11,12] Glycogen Synthase (1-12) can be used to determine the activity of protein kinase C.

[Ala3,11,18, Nle7] Endothelin-1, human

Reference: HY-P3614

€0.00 (tax incl.)

[Ala3,11,18, Nle7] Endothelin-1, human is a synthetic peptide.

[Ala2] Met-Enkephalinamide

Reference: HY-P3551

€0.00 (tax incl.)

[Ala2] Met-Enkephalinamide is an active peptide. [Ala2] Met-Enkephalinamide can be used for the research of various biochemical studies.

[Ala2] Endothelin-3, human

Reference: HY-P3571

€0.00 (tax incl.)

[Ala2] Endothelin-3, human is a linear analog of endothelin-3 (ET-3) where substitution of Ala for Cys residues. TE-3 is a vasoactive peptide, produced by human rhabdomyosarcoma cell lines, whereas it is not expressed...

[Ala18] Endothelin-1, human

Reference: HY-P3610

€0.00 (tax incl.)

[Ala18] Endothelin-1, human is a biologically active peptide. [Ala18] Endothelin-1, human can be used for the research of various biochemical studies.

[Ala17]-MCH TFA

Reference: HY-P1204A

€0.00 (tax incl.)

[Ala17]-MCH TFA, a MCH analogue (HY-P1525A), is a selective ligand for MCHR1 (Ki=0.16 nM) over MCHR2 (Ki=34 nM). [Eu3+ chelate-labeled [Ala17]-MCH shows high affnity for MCHR1 (Kd=0.37 nM) while has little...

[Ala17]-MCH

Reference: HY-P1204

€0.00 (tax incl.)

[Ala17]-MCH, a MCH analogue (HY-P1525A), is a selective ligand for MCHR1 (Ki=0.16 nM) over MCHR2 (Ki=34 nM). [Eu3+ chelate-labeled [Ala17]-MCH shows high affnity for MCHR1 (Kd=0.37 nM) while has little demonstrable...

[Ala127] Hepatitis B Virus Pre-S Region (120-131)

Reference: HY-P4041

€0.00 (tax incl.)

[Ala127] Hepatitis B Virus Pre-S Region (120-131) is a peptide with the sequence of MQWNSTAFHQT. [Ala127] Hepatitis B Virus Pre-S Region (120-131) can be used in the activity enhancement study.

[Ala113]MBP(104-118) TFA

Reference: HY-P1289C

€0.00 (tax incl.)

[Ala113]MBP(104-118) TFA is an noncompetitive peptide inhibitors of protein kinase C (PKC), with IC50s ranging from 28-62 μM.

[Ala113]MBP(104-118)

Reference: HY-P1289

€0.00 (tax incl.)

[Ala113]MBP(104-118) is an noncompetitive peptide inhibitors of protein kinase C (PKC), with IC50s ranging from 28-62 μM.

[Ala11,D-Leu15]-Orexin B(human) TFA

Reference: HY-P1340A

€0.00 (tax incl.)

[Ala11,D-Leu15]-Orexin B(human) TFA is a potent and selective orexin-2 receptor (OX2) agonist. [Ala11,D-Leu15]-Orexin B(human) TFA shows a 400-fold selectivity for the OX2 (EC50=0.13 nM) over OX1 (52 nM).

[Ala11,D-Leu15]-Orexin B(human)

Reference: HY-P1340

€0.00 (tax incl.)

[Ala11,D-Leu15]-Orexin B(human) is a potent and selective orexin-2 receptor (OX2) agonist. [Ala11,D-Leu15]-Orexin B(human) shows a 400-fold selectivity for the OX2 (EC50=0.13 nM) over OX1 (52 nM).

[Ala107]MBP(104-118) TFA

Reference: HY-P1289B

€0.00 (tax incl.)

[Ala107]MBP(104-118) TFA is an noncompetitive peptide inhibitors of protein kinase C (PKC), with IC50s ranging from 46-145 μM.

[Ala107]MBP(104-118)

Reference: HY-P1289A

€0.00 (tax incl.)

[Ala107]MBP(104-118) is an noncompetitive peptide inhibitors of protein kinase C (PKC), with IC50s ranging from 46-145 μM.

[Ala1,3,11,15]-Endothelin (53-63) (TFA)

Reference: HY-P1019A

€0.00 (tax incl.)

[Ala1,3,11,15]-Endothelin (53-63) (TFA) is an ETB agonist. [Ala1,3,11,15]-Endothelin (53-63) (TFA) has selectivity for ETB with IC50 values range from 0.33 nM to 0.61 nM. [Ala1,3,11,15]-Endothelin (53-63) (TFA) can be...

[Ala1,3,11,15]-Endothelin (53-63)

Reference: HY-P1019

€0.00 (tax incl.)

[Ala1,3,11,15]-Endothelin (53-63) is an ETB agonist. [Ala1,3,11,15]-Endothelin (53-63) has selectivity for ETB with IC50 values range from 0.33 nM to 0.61 nM. [Ala1,3,11,15]-Endothelin (53-63) can be used for the...

[Ala 353, 367]Presenilin 1 (349-361)

Reference: HY-P3701

€0.00 (tax incl.)

[Ala 353, 367]Presenilin 1 (349-361) is a peptide.

[Ac-Tyr1,D-Phe2]GRF 1-29, amide (human)

Reference: HY-P0211

€0.00 (tax incl.)

[Ac-Tyr1,D-Phe2]GRF 1-29, amide (human), a growth hormone releasing factor (GRF) analogue, is a vasoactive intestinal peptide (VIP) antagonist.

[3,5 Diiodo-Tyr7] Peptide T

Reference: HY-P3994

€0.00 (tax incl.)

[3,5 Diiodo-Tyr7] Peptide T is a threonine derivative.

[1,6-Aminosuberic acid]-arginine-Vasotocin

Reference: HY-P4011

€0.00 (tax incl.)

[1,6-Aminosuberic acid]-arginine-Vasotocin is a synthetic peptide analogue to neurohypophyseaI hormones. [1,6-Aminosuberic acid]-arginine-Vasotocin has excitatory effect on the periodically oxcillating neuron (PON) of...

[(tert-butoxycarbonyl)amino](3-chlorophenyl)acetic acid

Reference: HY-78105

€0.00 (tax incl.)

[(tert-butoxycarbonyl)amino](3-chlorophenyl)acetic acid is a Glycine (HY-Y0966) derivative.

[(pF)Phe4]Nociceptin(1-13)NH2 TFA

Reference: HY-P1300A

€0.00 (tax incl.)

[(pF)Phe4]Nociceptin(1-13)NH2 TFA is a highly potent and selective NOP receptor (OP4) agonist, with a pKi of 10.68 and a pEC50 of 9.31. [(pF)Phe4]Nociceptin(1-13)NH2 TFA displays high selectivity over δ, κ, and μ...

[(pF)Phe4]Nociceptin(1-13)NH2

Reference: HY-P1300

€0.00 (tax incl.)

[(pF)Phe4]Nociceptin(1-13)NH2 is a highly potent and selective NOP receptor (OP4) agonist, with a pKi of 10.68 and a pEC50 of 9.31. [(pF)Phe4]Nociceptin(1-13)NH2 displays high selectivity over δ, κ, and μ opioid...

ZP 120C

Reference: HY-106234

€0.00 (tax incl.)

ZP 120C is a potent and partial ORL1 receptor agonist. ZP 120C inhibits electrically induced contraction. ZP 120C can be used in the research of hyponatremia/hypokalemia.

Zoptarelin doxorubicin

Reference: HY-16532

€0.00 (tax incl.)

Zoptarelin doxorubicin (AEZS-108; AN-152) is a hybrid anticancer agent, containing Zoptarelin and Doxorubicin. Zoptarelin doxorubicin has been used to research targeting tumors expressing LHRH receptors. Zoptarelin...

ZIP(Scrambled) TFA

Reference: HY-P1391A

€0.00 (tax incl.)

ZIP(Scrambled) TFA is a scrambled control peptide for zeta inhibitory peptide (ZIP).

ZIP(Scrambled)

Reference: HY-P1391

€0.00 (tax incl.)

ZIP(Scrambled) is a scrambled control peptide for zeta inhibitory peptide (ZIP).

ZIP TFA

Reference: HY-P1284A

€0.00 (tax incl.)

ZIP TFA is a selective peptide inhibitor of PKMζ. ZIP TFA injections can block the impairment in morphine conditioned place preference induced.

ZIP

Reference: HY-P1284

€0.00 (tax incl.)

ZIP is a selective peptide inhibitor of PKMζ. ZIP injections can block the impairment in morphine conditioned place preference induced.

Zilucoplan

Reference: HY-P3502

€0.00 (tax incl.)

Zilucoplan (RA101495), a 15-amino acid macrocyclic peptide, is a potent complement component 5 (C5) inhibitor. Zilucoplan can be used in research of immune-mediated necrotising myopathy (IMNM).

Ziconotide TFA

Reference: HY-P0062A

€0.00 (tax incl.)

Ziconotide TFA (SNX-111 TFA), a peptide, is a potent and selective block of N-type calcium channels antagonist. Ziconotide TFA reduces synaptic transmission, and can be used for chronic pain research.

Ziconotide acetate

Reference: HY-P0062B

€0.00 (tax incl.)

Ziconotide acetate (SNX-111 acetate), a peptide, is a potent and selective block of N-type calcium channels antagonist. Ziconotide acetate reduces synaptic transmission, and can be used for chronic pain research.

Ziconotide

Reference: HY-P0062

€0.00 (tax incl.)

Ziconotide (SNX-111), a peptide, is a potent and selective block of N-type calcium channels antagonist. Ziconotide reduces synaptic transmission, and can be used for chronic pain research.

Category: Peptides

Menu

Settings