Abaloparatide
Tymlos
A PTHrP analog that stimulates bone formation with potentially fewer side effects than teriparatide. Represents a newer anabolic option for osteoporosis management.
Comprehensive profiles for 105+ peptides — dosing protocols, mechanisms of action, clinical research, and safety data.
105
Peptides
9
Categories
32 peptides match your filters · page 1 of 2
Tymlos
A PTHrP analog that stimulates bone formation with potentially fewer side effects than teriparatide. Represents a newer anabolic option for osteoporosis management.
Angiomax
A synthetic direct thrombin inhibitor derived from hirudin used as an anticoagulant during percutaneous coronary intervention procedures.
Miacalcin
A thyroid hormone that inhibits bone resorption. Salmon calcitonin demonstrates 40-50x greater potency than human forms.
Cortrosyn
A synthetic fragment of ACTH used to diagnose adrenal insufficiency. The standard test for evaluating adrenal function. Contains the first 24 amino acids of ACTH.
DDAVP
Synthetic vasopressin analog that selectively activates V2 receptors in kidneys, promoting water reabsorption.
Trulicity
An FDA-approved weekly GLP-1 receptor agonist for type 2 diabetes. Fused to an Fc antibody fragment for extended duration (~5 day half-life).
Fuzeon
A 36-amino acid peptide functioning as an HIV fusion inhibitor that prevents viral entry into cells. The first approved drug in its class.
Integrilin
A cyclic peptide that inhibits platelet aggregation. Used during coronary interventions to prevent clot formation. Derived from a protein in pygmy rattlesnake venom.
Byetta
The first GLP-1 receptor agonist approved for diabetes. Derived from Gila monster saliva. 53% homology with human GLP-1.
GlucaGen
Life-saving treatment for severe hypoglycemia since the 1960s. Newer formulations include nasal spray (Baqsimi) and stable liquid (Gvoke).
GnRH
A synthetic version of gonadotropin-releasing hormone used diagnostically and therapeutically for reproductive conditions.
Regular Insulin
The essential peptide hormone for glucose metabolism. Multiple formulations from rapid to long-acting available for diabetes management.
Somatuline
A somatostatin analog that binds preferentially to SST2 and SST5 receptors for treatment of acromegaly and gastroenteropancreatic neuroendocrine tumors.
Lupron
A GnRH agonist suppressing testosterone and estrogen production, approved for prostate cancer, endometriosis, uterine fibroids, and precocious puberty.
Linzess
A peptide activator of guanylate cyclase-C for irritable bowel syndrome with constipation and chronic idiopathic constipation, with localized gut action and minimal systemic uptake.
Victoza
An FDA-approved GLP-1 receptor agonist for type 2 diabetes and chronic weight management. The predecessor to semaglutide with daily dosing. 97% homology to native GLP-1.
Macrilen
An oral ghrelin mimetic for diagnosing adult growth hormone deficiency. The first FDA-approved oral GH stimulation test. 92% concordance with insulin tolerance testing.
Afamelanotide
A 13-amino acid synthetic analog of α-MSH that stimulates melanin production. FDA approved for erythropoietic protoporphyria. Unlike MT-II, minimal affinity for MC3R and MC4R.
Sandostatin
A somatostatin analog that binds to SST2 and SST5 receptors, suppressing GH, glucagon, insulin, and gastrointestinal hormones.
Pitocin
A naturally occurring peptide hormone essential for social bonding, childbirth, and lactation. Under investigation for autism, anxiety, and social disorders.
Bremelanotide
An FDA-approved melanocortin receptor agonist for treating hypoactive sexual desire disorder (HSDD) in premenopausal women.
Signifor
A somatostatin analog with broader receptor binding than octreotide, particularly effective for Cushing's disease due to SST5 receptor activity.
Somavert
A GH receptor antagonist that blocks growth hormone action. Used for acromegaly when surgery and somatostatin analogs fail to normalize IGF-1. ~90% achieve normal IGF-1.
Trulance
A uroguanylin analog for chronic constipation and IBS-C, engineered to mimic a naturally occurring peptide. pH-sensitive activation may provide more targeted action in the small intestine.