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Deruxtecan
[CAS# 1599440-13-7]

List of Suppliers
Shanghai Min-biotech Co., Ltd. China Inquire
www.min-biotech.com
+86 15190045345
sales@min-biotech.com
Chemical manufacturer since 2017
chemBlink Standard supplier since 2024

Identification
NameDeruxtecan
Synonyms6-(2,5-dioxopyrrol-1-yl)-N-[2-[[2-[[(2S)-1-[[2-[[2-[[(10S,23S)-10-ethyl-18-fluoro-10-hydroxy-19-methyl-5,9-dioxo-8-oxa-4,15-diazahexacyclo[14.7.1.02,14.04,13.06,11.020,24]tetracosa-1,6(11),12,14,16,18,20(24)-heptaen-23-yl]amino]-2-oxoethoxy]methylamino]-2-oxoethyl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-2-oxoethyl]amino]-2-oxoethyl]hexanamide
Molecular StructureCAS # 1599440-13-7, Deruxtecan
Molecular FormulaC52H56FN9O13
Molecular Weight1034.05
Protein SequenceGGFG
CAS Registry Number1599440-13-7
SMILESCC[C@@]1(C2=C(COC1=O)C(=O)N3CC4=C5[C@H](CCC6=C5C(=CC(=C6C)F)N=C4C3=C2)NC(=O)COCNC(=O)CNC(=O)[C@H](CC7=CC=CC=C7)NC(=O)CNC(=O)CNC(=O)CCCCCN8C(=O)C=CC8=O)O
Properties
Density1.5±0.1 g/cm3, Calc.*
Index of Refraction1.682, Calc.*
Boiling Point1491.1±65.0 °C (760 mmHg), Calc.*
Flash Point855.6±34.3 °C, Calc.*
*Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbolssymbol   GHS06 Danger  Details
Risk StatementsH301  Details
Safety StatementsP501-P270-P264-P301+P310+P330-P405  Details
SDSAvailable
up Discovery and Applications
Deruxtecan, also known as DS-8201, represents a breakthrough advancement in oncology. The discovery of Deruxtecan began with the identification of trastuzumab, a monoclonal antibody that targets human epidermal growth factor receptor 2 (HER2), a drug that is implicated in some types of cancer, including breast cancer. ) overexpressed proteins. Trastuzumab has revolutionized the treatment of HER2-positive breast cancer, significantly improving patient outcomes.

Deruxtecan utilizes a complex mechanism of action to selectively target cancer cells while sparing healthy tissue. The monoclonal antibody component of Deruxtecan binds to the HER2 receptor on the surface of cancer cells, promoting internalization of the ADC into the cell. Once inside the cancer cell, Deruxtecan undergoes enzymatic cleavage, releasing its cytotoxic payload, a topoisomerase I inhibitor. This potent cytotoxic agent disrupts DNA replication and induces apoptosis, effectively killing cancer cells and inhibiting tumor growth. Deruxtecan has shown significant efficacy in clinical trials across multiple cancer types, including HER2-positive breast cancer, gastric cancer, and non-small cell lung cancer. Its ability to induce durable responses and overcome resistance to existing therapies makes it a promising treatment option for patients with advanced or metastatic disease. In HER2-positive breast cancer, Deruxtecan demonstrated unprecedented response rates and durable clinical benefit in patients who had progressed on prior HER2-targeted therapies, including trastuzumab and pertuzumab.

References

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Market Analysis Reports
List of Reports Available for Deruxtecan
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