1. Antibody-drug Conjugate/ADC Related Cytoskeleton Cell Cycle/DNA Damage
  2. Antibody-Drug Conjugates (ADCs) Microtubule/Tubulin
  3. Cofetuzumab pelidotin

Cofetuzumab pelidotin  (Synonyms: PF-06647020; ABBV-647; h6M24-vc0101)

Cat. No.: HY-P99829 Purity: 99.67%
COA

Cofetuzumab pelidotin (PF-06647020) is a PTK7-targeting ADC comprising a humanized anti-PTK7 mAb (hu6M024, IgG1) joined to an auristatin microtubule inhibitor payload, auristatin-0101 (Aur0101; HY-12522), by a cleavable valine-citrulline (vc)-based linker. Cofetuzumab pelidotin has a DAR of 4. Cofetuzumab pelidotin binds to cell-surface PTK7 with an EC50 of 1153 pM by flow cytometry. Cofetuzumab pelidotin has the potential for solid tumors research.

For research use only. We do not sell to patients.

Cofetuzumab pelidotin Chemical Structure

Cofetuzumab pelidotin Chemical Structure

CAS No. : 1869937-48-3

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Based on 1 publication(s) in Google Scholar

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Description

Cofetuzumab pelidotin (PF-06647020) is a PTK7-targeting ADC comprising a humanized anti-PTK7 mAb (hu6M024, IgG1) joined to an auristatin microtubule inhibitor payload, auristatin-0101 (Aur0101; HY-12522), by a cleavable valine-citrulline (vc)-based linker. Cofetuzumab pelidotin has a DAR of 4. Cofetuzumab pelidotin binds to cell-surface PTK7 with an EC50 of 1153 pM by flow cytometry. Cofetuzumab pelidotin has the potential for solid tumors research[1][2][3].

In Vitro

Cofetuzumab pelidotin (PF-06647020) shows in vitro cytotoxic effects on PTK7 expressing cancer cell lines H446, H661 and OVCAR3 with EC50 values of 7.6, 27.5 and 105 ng/mL, respectively[1].
Cofetuzumab pelidotin (PF-06647020) (for 6 days) shows high potency and PTK7-specific cytotoxicity in a panel of cancer cell lines (A549, MDA-MB-468, KYSE-150, SKOV-3, PC9, NCI-H1975 cells) with IC50s of 0-1100 nM[2].
Cofetuzumab pelidotin is less stable with a much shorter T1/2 of less than 3 days[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Cofetuzumab pelidotin (PF-06647020; 3 mg/kg; Intraperitoneal injection twice a week for four cycles) induces striking in vivo anti-tumor effects on a subset of PDXs derived from NSCLC, OVCA and TNBC[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: 6- to 10-week-old NOD scid mice with NSCLC, OVCA and TNBC cells[1]
Dosage: 3 mg/kg
Administration: Intraperitoneal injection twice a week for four cycles
Result: Induced striking in vivo anti-tumor effects on a subset of patient–derived xenografts (PDXs) derived from NSCLC, OVCA and TNBC.
CAS No.
Appearance

Liquid

Color

Colorless to light yellow

SMILES

[Cofetuzumab pelidotin]

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Purity & Documentation
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