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Peptides

Chemical Structure Cat. No. Product Name CAS No.
Amylin, Human Chemical Structure
 BCP30745 Amylin, Human 122384-88-7
Amylin, islet Amyloid Polypeptide (IAPP), is a 37-residue peptide hormone secreted by pancreatic β-cells.
Protirelin Chemical Structure
 BCP12450 Protirelin 24305-27-9
Protirelin is a highly conserved neuropeptide that exerts the hormonal control of thyroid-stimulating hormone (TSH) levels as well as neuromodulatory functions.
[D-Ala2]leucine-enkephalin Chemical Structure
 BCP25053 [D-Ala2]leucine-enkephalin 64963-01-5
[D-Ala2]leucine-enkephalin, a delta opioid agonist, is a degradation resistant long-acting Leu-enkephalin.
Chlorotoxin Chemical Structure
 BCP30217 Chlorotoxin 163515-35-3
Chlorotoxin is a 36 amino-acid peptide from the venom of the Israeli scorpion Leiurus quinquestriatus with anticancer activity.
Lecirelin Acetate Chemical Structure
 BCP01995 Lecirelin Acetate 61012-19-9
Lecirelin (Dalmarelin) Acetate is a synthetic hypothalamic gonadotropin releasing hormone (GnRH) analogue. Lecirelin is a nonapeptide, while the natural compound is a decapeptide; moreover the glycine aminoacid in the 6th position has been substituted by leucine.
AC-DEVD-AFC Chemical Structure
 BCP18218 AC-DEVD-AFC 201608-14-2
Ac-DEVD-AFC is a fluorogenic substrate (λex=400 nm, λem=530 nm).
Dolastatin 10 Chemical Structure
 BCP12967 Dolastatin 10 110417-88-4
Dolastatin 10 is a potent antimitotic peptide from a marine animal, strongly inhibits microtubule assembly. Dolastatin and Dolastatin's analogs are the cytotoxic components in Antibody-drug conjugates design.
Met-Enkephalin Chemical Structure
 BCP25058 Met-Enkephalin 58569-55-4
Met-Enkephalin is synthetic opioid peptides that has opioid effects of a relatively short duration.
Thymalfasin Chemical Structure
 BCP24721 Thymalfasin 62304-98-7
Thymalfasin is an immunomodulating agent able to enhance the Thl immune response.
Angiotensin Acetate Chemical Structure
 BCP27671 Angiotensin Acetate 58-49-1
Angiotensin II 5-valine is an angiotensin II analog which is an agonist at angiotensin receptors.
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