أبحاث تكوين الجسم
Adipotide
أبحاث تكوين الجسم | 5mg
Adipotide is a prohibitin-targeting peptidomimetic studied for adipose vasculature signaling in metabolic research, including preclinical and primate obesity literature.
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Get catalog updatesFor laboratory research use only. Not for human or veterinary use. Not intended to diagnose, treat, cure, mitigate, or prevent disease.
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سياق البحث
ملف بحث Adipotide
Adipotide is a targeted peptidomimetic investigated in preclinical metabolic research. Its design links a prohibitin-binding sequence associated with white-adipose vasculature to a pro-apoptotic peptide cargo, allowing researchers to examine targeted vascular disruption, adipose-tissue changes, metabolic markers, and safety observations. Published work includes animal and nonhuman-primate models, with renal findings forming an important part of the experimental record. This material is most relevant to projects studying targeted adipose-vasculature biology rather than incretin receptors, AMPK signaling, or conventional appetite pathways. There is no established human therapeutic evidence, and results should not be generalized beyond the cited models.
Molecular class
Bifunctional targeted peptidomimetic
Sequence / composition
A prohibitin-binding homing motif linked to a D-amino-acid pro-apoptotic cargo; it is not a native signaling peptide.
Research design note
Studies distinguish target binding, cellular uptake, vascular localization, and cargo-driven effects with separate controls.
الآلية المقترحة
A targeted peptidomimetic that combines a prohibitin-binding motif associated with white-adipose vasculature and a pro-apoptotic D-peptide cargo. The proposed mechanism is selective damage to supporting blood vessels in white fat, followed by loss of adipose tissue.
التأثيرات المذكورة في الدراسات
- Rodent and obese-primate studies reported reduced food intake, loss of body mass and fat mass, and improved insulin-sensitivity markers.
- Histologic studies reported apoptosis and vascular disruption in targeted white-adipose tissue.
- Renal tubular changes and other kidney-related safety findings were important adverse observations in primate research.
نقاط القياس البحثية الشائعة
Prohibitin binding, vascular targeting, apoptosis, adipose mass, food intake, body mass, insulin sensitivity, renal chemistry, urinalysis, and kidney histology.
الأدلة والقيود
Evidence is preclinical, including nonhuman primate work. There is no established human therapeutic evidence, and renal findings are a material limitation.
External reading
الأدبيات للسياق، وليست إثباتًا للمنتج.
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