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ForumsOther Peptides & Research CompoundsDSIP (Delta Sleep Inducing Peptide) — need advice Page 2

DSIP (Delta Sleep Inducing Peptide) — need advice

AussieAnna Mon, Nov 11, 2024 at 10:49 PM 12 replies 1,816 viewsPage 2 of 3
DataDave
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Nov 12, 2024 at 3:12 AM#6
amsterdam_pete said:
I want to add the drug interaction perspective on the pharmacology.

Semaglutide structural biology relevant to the pharmacology: semaglutide is a 31-amino acid peptide with 94% homology to native GLP-1(7-36). Three key modifications enable its pharmacokinetic profile:

  1. Aib8 substitution: DPP-4 resistance (prevents enzymatic degradation)
  2. Arg34 substitution: improved chemical stability
  3. C18 fatty diacid at Lys26: albumin binding → long half-life

These three modifications transform a peptide with a 2-minute half-life (native GLP-1) into one with a 168-hour half-life (semaglutide). A masterclass in peptide engineering.

41 11VendorMark, COA_Karl, MikeFit_NJ and 38 others
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dave_SLC
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Nov 12, 2024 at 4:55 AM#7
AussieAnna said:
I went looking for why the dosing schedule is what it is and found that almost every practical question on this board has a pharmacokinetic answer…

PK/PD modeling for the pharmacology: understanding the pharmacokinetics helps optimize dosing. Semaglutide:

  • Tmax: 24-72 hours post-injection
  • T½: ~168 hours (7 days) — enables weekly dosing
  • Steady state: reached at 4-5 weeks
  • Bioavailability (SubQ): ~89%
  • Volume of distribution: ~12.5L (primarily plasma)

The albumin binding (>99%) is the key pharmacological innovation — creating a sustained-release effect from a single injection. Previous GLP-1 agonists (exenatide) required BID dosing due to rapid clearance.

Last edited: Nov 12, 2024 at 8:55 AM
40 10NicoleRaleigh, james_edin, FranDenver and 37 others
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TrialTracker_MD
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Maryland
Nov 12, 2024 at 6:38 AM#8
DataDave said:
Semaglutide structural biology relevant to the pharmacology: semaglutide is a 31-amino acid peptide with 94% homology to native GLP-1(7-36).

Amycretin (AMY/GLP-1 dual agonist) emerging data relevant to the pharmacology: Phase 1 showed -13.1% body weight at only 12 weeks, the fastest trajectory ever seen for an anti-obesity agent[1].

Amylin receptor agonism enhances satiety signaling through the area postrema and reduces glucagon secretion. Combined with GLP-1R agonism, this dual mechanism may produce even greater efficacy than current agents.

Early-stage data — interpret with caution. But the trajectory is extraordinary.

References:
[1] Novo Nordisk investor presentation, September 2023.
Last edited: Nov 12, 2024 at 11:38 AM
39 9maya_sedona, stefan_berlin, Dr.EM_Chicago and 36 others
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Dr.DermMIA
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Nov 12, 2024 at 8:21 AM#9

One thing that is still open after JenPlateau’s answer:

How long did you give it before you decided it was working?

38 8PeptideChemSF, A1cHero_PHX, Dr.RenalNash and 35 others
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AussieAnna
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Nov 12, 2024 at 4:35 PM#10

OP back with an update, since a thread like this is useless without one.

Closing this out: the trough rather than the peak explains the pattern I was seeing on day six, which I had been blaming on the vial.

28 1pete_manc_UK, anna.melb_AU, mark_tokyo and 25 others
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