Peptide Database

Jardiance (Empagliflozin) is a selective SGLT2 inhibitor studied in metabolic, renal, and cardiovascular research. It is investigated for its effects on renal glucose reabsorption, urinary glucose excretion, sodium handling, energy metabolism, and pathways connecting kidney and cardiovascular function.

Klomen (Clomiphene Citrate) is a selective estrogen receptor modulator studied in reproductive endocrinology and hormone-signaling research. It is investigated for its effects on estrogen receptor activity, HPG-axis regulation, gonadotropin signaling, and reproductive endocrine pathways.

Lioresal (Baclofen) is a centrally acting muscle relaxant and GABA-B receptor agonist studied in neurology and neuromuscular research. It is investigated for its effects on inhibitory neurotransmission, spinal reflex activity, motor-neuron signaling, and regulation of skeletal muscle tone.

Lipitor (atorvastatin) is a statin medication researched for its role in regulating cholesterol and lipid metabolism. It works primarily by reducing hepatic cholesterol synthesis, making it an important compound for research involving LDL cholesterol, cardiovascular risk factors, and lipid homeostasis.

Muscoril (Thiocolchicoside) is a centrally acting muscle relaxant studied in neuromuscular and musculoskeletal research. It is investigated for its effects on inhibitory neurotransmitter pathways, muscle-tone regulation, spinal reflex activity, and mechanisms associated with muscle-spasm signaling.

Micardis Plus 80 is a combination formulation containing telmisartan and hydrochlorothiazide, studied in cardiovascular and renal research. It provides a useful model for investigating angiotensin II receptor signaling, vascular regulation, renal sodium and fluid balance, and electrolyte homeostasis.

Muscoflex (Thiocolchicoside) is a centrally acting muscle relaxant studied in neuromuscular and musculoskeletal research. It is investigated for its interaction with inhibitory neurotransmitter pathways, muscle-tone regulation, spinal reflex activity, and mechanisms associated with muscle-spasm signaling in controlled research models.

Arimidex (Anastrozole) is a non-steroidal aromatase inhibitor studied in oncology and endocrine research for its ability to reduce estrogen biosynthesis. It is used to investigate aromatase activity, estrogen-dependent signaling, steroid metabolism, hormonal regulation, and hormone-responsive cellular pathways in controlled research models.

Dodex (Vitamin B12) is a vitamin B12 preparation studied in nutritional, metabolic, hematological, and neurological research. It is investigated for its role in DNA synthesis, red blood cell formation, methylation pathways, cellular metabolism, and neurological function in controlled laboratory and research models.

Letu/Letrozol (Letrozole) is an aromatase inhibitor primarily studied for its ability to reduce estrogen production by inhibiting the aromatase enzyme. It is widely researched in hormone-sensitive conditions and endocrine pathways, particularly those involving estrogen-dependent signaling. Suitable for laboratory and research applications, Letrozole is valued for its selective mechanism and established pharmacological profile.

Aromasin (Exemestane) is a steroidal aromatase inhibitor used in endocrine and oncology research to study estrogen biosynthesis, aromatase activity, hormone signaling, and estrogen-dependent cellular pathways. It provides a useful research model for investigating steroid metabolism, breast cancer biology, and hormonal regulation.

Tamoxifen is a selective estrogen receptor modulator (SERM) widely studied in oncology, endocrinology, and molecular biology research. It is investigated for estrogen receptor signaling, hormone-responsive cell growth, gene transcription, endocrine regulation, and pharmacokinetic mechanisms in controlled laboratory models.