Peptides - BioCrick

Cat.No. Product Name Information

BCC5899 TCS 184 TCS 184

BCC1246 Scrambled 10Panx Scrambled version of 10Panx, Panx-1 mimetic inhibitory peptide

BCC5883 PDZ1 Domain inhibitor peptide

BCC2395 Bax inhibitor peptide, negative control Negative control peptide for Bax inhibitor peptide V5

BCC5785 pep2-SVKE

BCC5887 Rac1 Inhibitor F56, control peptide

BCC1027 Amyloid Beta-peptide (25-35) (human) Amyloid beta-peptide(25-35) is the fragment Aβ(25-35) of the Alzheimer's amyloid β-peptide, has shown neurotoxic activities in cultured cells.

BCC5722 [Leu31,Pro34]-Neuropeptide Y (human, rat)

BCC5945 BIM 23052 sst5 agonist

BCC5801 GR 73632 GR-73632 is a novel tachykinin neurokinin 1 (NK-1) receptor agonist. GR-73632 acts directly on the peripheral terminals of primary sensory neurons through NK1 receptor which convey itch signals.

BCC7257 Exendin-3 (9-39) amide Avexitide (Exendin (9-39)) is a specific and competitive GLP-1 receptor antagonist.

BCC4271 HG-10-102-01 HG-10-102-01 is a potent and selective inhibitor of wild-type LRRK2(IC50=23.3 nM) and the G2019S mutant(IC50=3.2 nM) IC50 Value: 23.3 nM (WT LRRK2); 3.2 nM (LRRK2 G2019S) [1] Target: LRRK2 HG-10-102-01 maintains the ability to potently inhibit the biochemical activity of wild-type and G2019S mutant LRRK2.

BCC7133 MEN 10376 Men 10376 is a selective tachykinin NK-2 receptor antagonist, with a Ki of 4.4 μM for rat small intestine NK-2 receptor.

BCC5392 HG-14-10-04 HG-14-10-04 is a potent and specific ALK inhibitor with IC50 of 20 nM.

BCC5729 MDL 29,913

BCC1031 Angiotensin III (human, mouse) Angiotensin III, human, mouse is a heptapeptide, acts as an endogenous angiotensin type 2 receptor (AT2R) agonist, with IC50s of 0.648 nM and 21.1 nM for AT2R and AT1R, respectively.

BCC5850 [D-Lys3]-GHRP-6

BCC6295 TAT 14 TAT 14

BCC6963 BQ-123 BQ-123 is a selective endothelin A receptors (ETAR) antagonist with an IC50 value of 7.3 nM and a Ki vaule of 25 nM. BQ-123

BCC1022 [Ser25] Protein Kinase C (19-31)

BCC6962 PACAP 1-38 PACAP (1-38), human, ovine, rat is a neuropeptide with 38 amino acid residues. PACAP (1-38) binds to PACAP type I receptor, PACAP type II receptor VIP1, and PACAP type II receptor VIP2 with IC50s of 4 nM, 2 nM, and 1 nM, respectively.

BCC2349 Spinorphin Enkephalin-degrading and ACE inhibitor

BCC3950 Thrombin Receptor Agonist Peptide Sfllrnpndkyepf is a synthetic thrombin receptor agonist peptide.

BCC5399 VT-464 racemate Seviteronel racemate (VT-464 racemate) is the racemate form of Seviteronel (VT-464), which is a potent CYP17 lyase inhibitor(h-Lyase IC50=nM)inhibition.

BCC5994 [Lys5,MeLeu9,Nle10]-NKA(4-10)

BCC5800 GR 64349

BCC5933 BIM 187 BIM 187

BCC5863 JMV 449 JMV 449

BCC6333 Purotoxin 1

BCC5856 PR 39 (porcine)

BCC1086 7-Methoxycoumarin-4-acetyl-P-L-G-L-β-(2,4-dinitrophenylamino)A-R amide

BCC4632 Bacitracin Bacitracin is a polypeptide antibiotic used for staphylococcal infections. Bacitracin functions as an inhibitor of cell wall biosynthesis through its binding to the undecaprenyl pyrophosphate. The combination of bacitracin with other antibiotics has been efficient to be used as a topical agent.

BCC4633 Bacitracin Zinc Bacitracin Zinc is a dephosphorylation of the C55-isoprenyl pyrophosphate interference for inhibition of cleavage of Tyr from Met-enkephalin with IC50 of 10 μM.

BCC3957 TRAP-6 TRAP-6 (PAR-1 agonist peptide) is a protease-activated receptor 1 (PAR1) agonist. TRAP-6

BCC5799 GR 94800

BCC1025 Thrombin Receptor Activator for Peptide 5 (TRAP-5) Thrombin Receptor Activator for Peptide 5 (TRAP-5) is also called Coagulation Factor II Receptor (1-5) or Proteinase Activated Receptor 1 (1-5), used in the research of coronary heart disease (CHD).

BCC5763 Galanin (2-29) (rat)

BCC1568 Exendin-4 Exendin-4 (Exenatide), a 39 amino acid peptide, is a long-acting glucagon-like peptide-1 receptor agonist with an IC50 of 3.22 nM.

BCC5697 Endomorphin-2 Endomorphin 2, a high affinity, highly selective agonist of the μ-opioid receptor, displays reasonable affinities for kappa3 binding sites, with Ki value between 20 and 30 nM.

BCC5934 BIM 189 BIM 189

BCC5935 Catestatin

BCC5728 BQ-3020 Selective ETB agonist BQ-3020

BCC1294 (S)-Tedizolid (S)-Tedizolid is the S-enantiomer of Tedizolid. Tedizolid is a novel oxazolidinone with activity against Gram-positive pathogens. (S)-Tedizolid is the less active isomer.

BCC5336 (Arg)9 peptide (Arg)9 (Nona-L-arginine;Peptide R9) is a cell-penetrating peptide; exhibits neuroprotective activity with an IC50 of 0.78 μM in the glutamic acid model.

BCC7206 G-Protein antagonist peptide

BCC7611 PACAP 6-38 PACAP (6-38), human, ovine, rat is a potent PACAP receptor antagonist with IC50s of 30, 600, and 40 nM for PACAP type I receptor, PACAP type II receptor VIP1, and PACAP type II receptor VIP2, respectively.

BCC7686 M40 M40 is a potent, non-selective galanin receptor antagonist. M40

BCC5730 IRL-1038

BCC7488 ω-Agatoxin IVA

BCC7710 Kaliotoxin

BCC4071 HG-9-91-01 HG-9-91-01 is a potent and highly selective salt-inducible kinase (SIK) inhibitor with IC50s of 0.92 nM, 6.6 nM and 9.6 nM for SIK1, SIK2 and SIK3 respectively.

BCC7709 Margatoxin Margatoxin, an alpha-KTx scorpion toxin, is a high affinity inhibitor of Kv1.3 (Kd=11.7 pM). Margatoxin inhibits the Kv1.2 (Kd=6.4 pM) and Kv1.1 (Kd=4.2 nM). Margatoxin, a 39 amino-acid-long peptide, is isolated from the venom of the scorpion Centruroides margaritatus and widely used in ion channel research.

BCC6248 TT 232 TT 232

BCC5699 ω-Conotoxin MVIIC

BCC3649 CA-074 Me CA-074 methyl ester is a specific inhibitor of Cathepsin B, which has potent bioactivities such as neuroprotective, anti-cancer, and anti-inflamatory effects.

BCC2456 Calcineurin Autoinhibitory Peptide Selective calcineurin inhibitor

BCC6027 Prion Protein 106-126 (human)

BCC5922 JMV 390-1

BCC6048 GRK2i GRK2i

BCC5851 pp60 c-src (521-533) (phosphorylated)

BCC3670 MOG (35-55) Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat is a minor component of CNS myelin. Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat produces a relapsing-remitting neurological disease with extensive plaque-like demyelination. Myelin Oligodendrocyte Glycoprotein Peptide (35-55), mouse, rat induces strong T and B cell responses and is highly encephalitogenic. MOG (35-55)

BCC6030 Decanoyl-RVKR-CMK

BCC5824 BIM 23056 sst receptor ligand

BCC5599 Gap19 Gap19, a peptide derived from nine amino acids of the Cx43 cytoplasmic loop (CL), is a potent and selective connexin 43 (Cx43) hemichannel blocker. Gap19 inhibits hemichannels caused by preventing intramolecular interactions of the C-terminus (CT) with the CL. Gap19 is not blocking GJ channels or Cx40/pannexin-1 hemichannels. Gap19 has protective effects against myocardial. Gap19

BCC6018 AC 187 Potent and selective amylin receptor antagonist AC 187

BCC5825 Ac2-26 Ac2-26, an active N-terminal peptide of annexin A1 (AnxA1), attenuates ischemia-reperfusion-induced acute lung injury. Ac2-26 also decreases AnxA1 protein expression, inhibits the activation of NF-κB and MAPK pathways in the injured lung tissue. Ac2-26

BCC1026 Amyloid β-Peptide (10-20) (human) Amyloid β-Protein (10-20) is a fragment of Amyloid-β peptide, maybe used in the research of neurological disease.

BCC7690 [D-Trp34]-Neuropeptide Y

BCC6359 ANQ 11125 Selective motilin receptor antagonist

BCC5988 Echistatin, α1 isoform

BCC8027 LL 37 LL-37, Human is a 37-residue, amphipathic, cathelicidin-derived antimicrobial peptide, which exhibits a broad spectrum of antimicrobial activity. LL-37, Human could help protect the cornea from infection and modulates wound healing. LL 37

BCC6049 Lys-γ3-MSH

BCC5974 α-Conotoxin ImI

BCC7489 ω-Agatoxin TK

BCC7085 GR 231118

BCC7392 APC 366 Tryptase inhibitor APC 366

BCC5853 N-Acetyl-O-phosphono-Tyr-Glu-Glu-Ile-Glu

BCC5641 Enfuvirtide Enfuvirtide is an anti-HIV-1 fusion inhibitor peptide.

BCC8041 Huwentoxin XVI Potent and reversible N-type Ca2+ channel blocker

BCC5398 VT-464 Seviteronel (VT-464) is a potent CYP17 lyase inhibitor(h-Lyase IC50=69 nM) that demonstrated both exceptional in vitro lyase/hydroxylase selectivity (~10-fold) and oral activity in a hamster model of androgen biosynthesis inhibition. VT-464

BCC3590 Cyclo (-RGDfK) Cyclo(-RGDfK) is a potent and selective inhibitor of the αvβ3 integrin, with an IC50 of 0.94 nM.

BCC6001 GLP-1 (9-36) amide

BCC1525 Desmopressin Synthetic vasopressin analog; V1B and V2 agonist,Desmopressin(DDAVP) is the synthetic analogue of the antidiuretic hormone arginine vasopressin.

BCC7153 Autocamtide-2-related inhibitory peptide Selective CaM kinase II inhibitor

BCC8026 Agitoxin 2

BCC6019 SHU 9119 SHU 9119 is a potent human melanocortin 3 and 4 receptors (MC3/4R) antagonist and a partial MC5R agonist; with IC50 values of 0.23, 0.06, and 0.09 nM for human MC3R, MC4R and MC5R, respectively.

BCC5979 α-Conotoxin EI

BCC5686 Nociceptin Nociceptin, a heptadecapeptide, is the endogenous ligand of the nociceptin receptor, acting as a potent anti-analgesic.

BCC5790 Astressin Astressin is a potent corticotropin releasing factor (CRF) antagonist.

BCC1103 Posaconazole Posaconazole is a broad-spectrum, second generation, triazole compound with antifungal activity.

BCC3947 SLIGRL-NH2 Protease-Activated Receptor-2 Activating Peptide is an agonist of Protease-Activated Receptor-2 (PAR-2).

BCC5789 Urocortin (rat) Urocortin, rat (Urocortin (Rattus norvegicus)) is a neuropeptide and a potent endogenous CRFR agonist with Kis of 13 nM, 1.5 nM, and 0.97 nM for human CRF1, rat CRF2α and mouse CRF2β, respectively.

BCC5811 PKC β pseudosubstrate PKC β pseudosubstrate

BCC5865 BWX 46 Highly selective NPY Y5 agonist BWX 46

BCC7945 Phalloidin Phalloidin is a mushroom-derived toxin which can be used to label F-actin of the cytoskeleton with fluorochrome (λex=495 nm, λem=520 nm).

BCC5913 CH 275 CH 275

BCC5743 α-Conotoxin MII

BCC5788 Urocortin (human) Urocortin, human, a 40-aa neuropeptide, acts as a selective agonist of endogenous CRF2 receptor, with Kis of 0.4, 0.3, and 0.5 nM for hCRF1, rCRF2α and mCRF2β, respectively.

BCC5749 Nociceptin (1-13)NH2 Nociceptin (1-13), amide is a potent ORL1 (OP4) receptor agonist with a pEC50 of 7.9 for mouse vas deferens and a Ki of 0.75 nM for binding to rat forebrain membranes.

BCC6085 Orphanin FQ (1-11)

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