SavePeptidesCompound
Re-checked hourly
All peptides
OtherResearch-onlyVendors pending
Research-onlyVendors pendingFacts verified · 2026-05-25

PNC-27

Also known as pnc27

PNC-27 is a synthetic 32-amino-acid chimeric anticancer research peptide that fuses a p53 MDM-2/HDM-2-binding sequence (residues 12-26) with a membrane-residency leader peptide. In preclinical cell-culture and rodent xenograft models, it has been reported to selectively bind HDM-2 aberrantly displayed on the plasma membrane of many cancer cells, form transmembrane pores, and cause rapid colloid-osmotic necrosis while sparing normal cells that lack surface HDM-2 (Sarafraz-Yazdi et al., 2010). All published evidence is preclinical: there are no registered human clinical trials. Vendor sale to consumers seeking cancer treatment is a serious safety and regulatory concern.

best

price

per

mg

vendors

tracked

Research-only

stage

Vendor data

Coming soon.

Per-vendor pricing and verification tiers populate as the SavePeptides crawler comes online. Until then, browse all approved vendors directly.

Browse all vendors

Mechanism of action

PNC-27 combines the p53 transactivation-domain residues 12-26 (HDM-2/MDM-2-binding motif) with a membrane-penetrating leader sequence. In cancer cells that aberrantly display HDM-2 on the outer plasma membrane, PNC-27 docks onto membrane HDM-2 and assembles into transmembrane pores, triggering loss of ionic gradients and colloid-osmotic necrosis rather than classical caspase-mediated apoptosis (Sarafraz-Yazdi et al.

PNC-27 combines the p53 transactivation-domain residues 12-26 (HDM-2/MDM-2-binding motif) with a membrane-penetrating leader sequence. In cancer cells that aberrantly display HDM-2 on the outer plasma membrane, PNC-27 docks onto membrane HDM-2 and assembles into transmembrane pores, triggering loss of ionic gradients and colloid-osmotic necrosis rather than classical caspase-mediated apoptosis (Sarafraz-Yazdi et al., Proc Natl Acad Sci USA 2010; Davitt et al., Frontiers in Oncology 2022). Internalised peptide has also been reported to disrupt mitochondrial membranes in cancer cells, amplifying lethality (Bowne et al., 2024). Normal cells, which do not present HDM-2 on the outer leaflet, are largely spared in vitro. Selectivity in vivo and across human tumour types has not been clinically demonstrated.

Pharmacokinetic properties

Half-life

Not characterized in humans; preclinical IV/IP studies suggest minutes-to-hours plasma residence

Routes

intravenous · intraperitoneal · subcutaneous

Bioavailability

Not orally bioavailable. Original preclinical work used IV and IP administration. Subcutaneous self-administration is unsupported by data.

Amino-acid sequence

MPRFMDYWEGLNQRSRKRALSR

Use & research dosing

No human clinical dose has ever been established for PNC-27. Preclinical murine xenograft studies have used roughly 10-30 mg/kg/day intraperitoneally or intravenously for short courses (Sarafraz-Yazdi et al., 2010). Gray-market self-experimentation reports of subcutaneous injection exist online but are not supported by any safety, pharmacokinetic, or dose-finding evidence in humans. Allometric scaling from rodent IP dosing to a human SC protocol is not validated. There is no FDA-approved label, no Investigational New Drug filing publicly registered, and no validated formulation.

Research-use framing only. SavePeptides sells nothing for human consumption. Doses above reflect reported research / self-experimentation ranges, not clinical recommendations.

Editorial perspective

PNC-27 was originated by Pincus, Michl and colleagues at NYMC and remains a preclinical experimental anticancer peptide despite roughly two decades of work. There is no IND-stage or registered clinical trial. The serious red flag is vendor sale of PNC-27 to retail buyers, some of whom self-administer it as DIY oncology in lieu of standard care. Any cancer-treatment claim attached to a research-chemical sale is a regulatory and patient-safety violation. Knowledge-base copy should consistently flag this.

— SavePeptides editorial desk · last updated 2026-05-25

Cautions & contraindications

Before researching this compound, note:

  • Zero human clinical trial data; no validated safety profile
  • Membrane-lytic mechanism with unknown systemic toxicity in humans
  • Selectivity is based on in vitro surface HDM-2 expression; not confirmed across human tumour types in vivo
  • Marketing to cancer patients as a treatment is irresponsible and may constitute illegal drug claims
  • Cancer patients should NOT substitute PNC-27 for evidence-based oncologic care
  • Vendor purity, sterility, sequence verification, and endotoxin content are not assured
  • Theoretical risk of off-target lysis of any cell expressing surface HDM-2 (poorly characterised)
  • Pregnancy, lactation, paediatric use: contraindicated (no data)
  • No data on immunogenicity, infusion reactions, or anaphylaxis risk

Facts verified

2026-05-25

Confidence

low

What this means

  • preclinical only - no human clinical trials
  • vendor marketing to cancer patients is a serious safety concern
  • membrane-lytic mechanism with no human safety data
  • low traffic / floor-tier evidence base

How we check →

Vendor data coming soon

All vendors

001 — Independent

We don't list what we wouldn't research.

SavePeptides lists vendors after an initial review and distinguishes verified vendors where additional checks have been completed. We may earn commissions from referral links, and sponsored placements will be clearly disclosed.

002 — Vendor-funded

Free to browse. Supported by referrals.

SavePeptides is free for buyers. We may earn a commission when you order through our links, but we do not lock deals behind a paywall, require an email to view codes, or inflate comparison prices.

003 — Research use

Research-use disclaimer.

SavePeptides surfaces vendor, pricing, and coupon information for research compounds. These products are not intended, approved, or recommended for human consumption. Our content is informational only and does not constitute medical advice.