CAS:139570-93-7:Zoptarelin Doxorubicin

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CAS:139570-93-7:Zoptarelin Doxorubicin
Details
CAS: 139570-93-7
Core structure: LHRH agonist peptide (gonadotropin-releasing hormone analog) covalently conjugated with doxorubicin via cleavable linker, LHRH receptor-targeted peptide-drug conjugate
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Related documents
COA/MS/HPLC Report
Peptide Dissolution and Storage Guide
Category
Targeted Drug Conjugate / LHRH Receptor Targeted Antitumor Conjugate
Category
Pharmaceutical Peptides
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Description

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Product Name CAS:139570-93-7:Zoptarelin doxorubicin
Description Zoptarelin doxorubicin is a peptide-drug conjugate (PDC). It uses a high-affinity LHRH agonist peptide as the targeting carrier to directionally deliver the cytotoxic drug doxorubicin to tumor cells with high LHRH receptor expression (prostate cancer, breast cancer, endometrial cancer), and releases the drug inside the tumor to exert killing effect, significantly reducing the systemic toxic side effects of chemotherapeutic drugs. Applied in targeted antitumor research, peptide drug conjugation technology, and reproductive system tumor targeted therapy research.
Peptide Purity (HPLC, %) 90%/95%/98%
Theoretical molecular weight (Da) ~1700 (subject to actual batch)
Structure type Peptide-small molecule conjugate, cleavable linker

 

Product Basic Information Table

 

Product Standard English Name Product Abbreviation / Alias Function Tags (comma-separated) Core Structure Molecular Formula Exact Mass (Da) Average MW (Da) Structure Type Target Receptor
Zoptarelin doxorubicin Zoptarelin doxorubicin; LHRH-targeted doxorubicin conjugate; AN-152 Targeted antitumor,Peptide-drug conjugate,LHRH receptor targeting,Prostate cancer research,Reduced chemotherapy toxicity,Reproductive system tumors LHRH agonist decapeptide + cleavable linker + doxorubicin anthracycline pharmacophore Large conjugate, no precise small-molecule formula; subject to actual batch MS - ~1700 (theoretical) Peptide-small molecule conjugate LHRH receptor (GnRHR)

Physicochemical Solubility & Storage Parameters

 

Product Code Appearance Long-term Storage Conditions Short-term Storage Conditions Liquid Stability Solid Powder Stability
PEP-ZOP001 Orange-red powder Store at -20℃, strictly protected from light, sealed and dry, aliquoted. **Cytotoxic, handle with protection** Solid powder stable for 1 year at 2-8℃ sealed in dark; prepare aqueous solutions freshly before use Stable for 48 h at 4℃ in dark; stable for 2 weeks at -20℃ in aliquots. **Moderate water solubility, freely soluble in aqueous organic solvents and acidic buffers**. Anthracycline structure highly sensitive to light and prone to oxidative degradation. Linker easily cleaved under acid/base and enzymatic conditions to release drug Stable for 2 years at -20℃ under dry & dark conditions

Functional Description

 

Product Code Frontend Short Summary (for search list display) Detailed Biological Function Description Applicable Research Areas (comma-separated) Targets / Pathways
PEP-ZOP001 LHRH-targeted peptide-drug conjugate that directionally delivers doxorubicin to kill tumors and reduces systemic chemotherapy toxicity Zoptarelin doxorubicin is a classic targeted peptide-drug conjugate, formed by conjugating LHRH agonist peptide with doxorubicin via a cleavable linker. Its targeting carrier peptide binds with high specificity to LHRH receptors highly expressed on the surface of tumor cells, mediates endocytosis of the conjugate into cells, and the linker is cleaved under the action of intracellular acidic environment and enzymes, releasing active doxorubicin, which intercalates into DNA and inhibits topoisomerase II, blocking nucleic acid synthesis and inducing tumor cell apoptosis. Compared with free doxorubicin, it significantly increases the drug concentration at the tumor site, reduces drug exposure to normal tissues such as heart and bone marrow, and significantly reduces toxic side effects. This molecule serves as a core tool for peptide drug conjugation technology research, reproductive system tumor targeted therapy, and chemotherapy toxicity reduction protocol optimization. Prostate cancer research,Breast cancer research,Peptide drug conjugation technology,Targeted antitumor research,Chemotherapy toxicity reduction,Reproductive endocrine tumors Gonadotropin-Releasing Hormone Receptor (GnRHR/LHRHR); Topoisomerase II inhibition; DNA damage and tumor cell apoptosis pathway

 

 

 

 

 

 

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