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DBI33-50

pharmaceutical compound

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General referenceInterpretive dossier study · Crown Archives visual atlas
Record originEnglish Wikipedia
Text licenseCC BY-SA 4.0
Source revisionMay 9, 2026
Entity authorityQ136419216 ↗
Source-derived summary

DBI33-50 (Octadecaneuropeptide, ODN) is an endogenous polypeptide with the amino acid sequence QATVGDINTERPGMLDFT. It consists of residues 33–50 of the diazepam binding inhibitor (DBI), generated by proteolytic cleavage of the parent protein. A related fragment, DBI17-50 (triakontatetraneuropeptide, TTN), shares similar biological effects but is expressed in different tissues.

DBI itself is highly expressed in the gastrointestinal tract, where it inhibits the secretion of hormones such as insulin and cholecystokinin. ODN (but not TTN) also suppresses insulin release. However, both peptides are more widely studied as neuropeptides in the brain, where they are secreted by astrocytes and act as endogenous allosteric modulators of benzodiazepine receptors (endozepines). ODN primarily acts at the central benzodiazepine receptor, while TTN preferentially targets the so-called peripheral benzodiazepine receptor (TSPO), which is also present in the brain.

In addition to its benzodiazepine site activity, ODN binds to a distinct metabotropic receptor. At benzodiazepine receptors it displays a biphasic action: at low concentrations it acts as a positive allosteric modulator, mainly at α5-containing GABAA receptor subtypes, whereas at higher concentrations it acts as a negative allosteric modulator, particularly at α3-containing GABAA receptors.

Pathologically elevated ODN levels can therefore produce effects opposite to those of benzodiazepines, and have been linked to anxiety and epilepsy. At normal physiological concentrations, by contrast, ODN is neuroprotective, promotes neurogenesis, and regulates immune responses by modulating interleukin production.

Editorial summary

Begin with the source’s own compact description: “DBI33-50” is pharmaceutical compound. The dossier treats that line as a proposition to test through DBI33-50, pharmaceutical and compound, not as a finished interpretation.

Editorial reviewA dependable orientation record for establishing vocabulary, names and a first evidence trail. The current 224-word lead offers orientation but no explicit four-digit date, so chronology should not be assumed. The selected authority fields contribute no independent date. For this dossier, DBI33-50, pharmaceutical and compound is the immediate research focus.
Editorial analysis

Why this record matters

The phrase “pharmaceutical compound” supplies a clear boundary for inquiry. It also exposes the unanswered questions: who defined that boundary, when it became stable and which sources sit outside it.

Evidence profile

Named sources, stable identifiers and responsible institutions provide the strongest route from overview to verifiable evidence. The source revision retrieved here is dated May 9, 2026. The linked authority identifier is Q136419216. None of the 0 selected statements returned an explicit reference.

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Overview language is designed for orientation and should not be treated as a substitute for the evidence cited beneath it. The source lead contains qualifying language; that uncertainty should survive quotation, summary and reuse. Authority statements aid reconciliation but still require their own references, qualifiers and ranks to be checked.

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Source & attribution

This entry incorporates text from “DBI33-50” on English Wikipedia. Contributors are listed in the page history. Text is available under the Creative Commons Attribution-ShareAlike 4.0 License. Selected authority identifiers and statements are retrieved from Wikidata under CC0; their references and qualifiers remain part of the verification path.