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Orforglipron

Oral Small-Molecule GLP-1 Receptor Agonist | Weight Loss & Diabetes

First oral non-peptide GLP-1 completing Phase 3 trials. Achieves substantial weight loss without injections, refrigeration, or dietary restrictions, with clinical evidence of 12.4% weight reduction at 72 weeks.

Yarı ömür
25-68 hours
Sıklık
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Döngü
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Doz
Start 3-6mg daily, titrate up to 12-36mg based on response
Orforglipron 2D chemical structure

M.W.: 882.974 Da

PubChem 2D yapı diyagramı

DEEP ARCHIVESUPPLEMENTOrforglipronOral Small-Molecule GLP-1 …PURITY: 99% HPLCRUO: Research Use OnlyREF ORF-483-DSAM.W. 882.974 DaNOT FOR HUMAN OR VETERINARY USE

Referans illüstrasyonu — ürün listesi değildir

Etki Mekanizması

Small-molecule GLP-1 receptor agonist with biased signaling preferentially activating G protein/cAMP pathways, enhancing insulin secretion, suppressing glucagon, delaying gastric emptying, and reducing appetite while minimizing receptor desensitization. 79.1% oral bioavailability with 29-49 hour half-life.

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First oral non-peptide GLP-1 completing Phase 3 trials. Achieves substantial weight loss without injections, refrigeration, or dietary restrictions, with clinical evidence of 12.4% weight reduction at 72 weeks.

Moleküler Veri

Tür
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Moleküler ağırlık
882.974 Da

1000 mcg = 1 mg

1 = her gün · 7 = haftalık

Süre (gün)

Araştırma Endikasyonları

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most effective

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most effective

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effective

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most effective

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most effective

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effective

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Doz Protokolleri

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HedefDozSıklıkYol
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Etkileşimler

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Semaglutide
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~
Insulin
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Metformin
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