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CAS RN: 119413-54-6 | Product Number: T2795

Topotecan Hydrocholoride


Purity: >95.0%(T)(HPLC)
Synonyms:
  • Nogitecan Hydrocholoride
  • (4S)-10-[(Dimethylamino)methyl]-4-ethyl-4,9-dihydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione Hydrochloride
Product Documents:
250MG
€95.00
1   39  

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Product Number T2795
Purity / Analysis Method >95.0%(T)(HPLC)
Molecular Formula / Molecular Weight C__2__3H__2__3N__3O__5·HCl = 457.91 
Physical State (20 deg.C) Solid
Storage Temperature Room Temperature (Recommended in a cool and dark place, <15°C)
Store Under Inert Gas Store under inert gas
Condition to Avoid Hygroscopic
Packaging and Container 250MG-Glass Bottle with Plastic Insert (View image)
CAS RN 119413-54-6
Reaxys Registry Number 5470704
PubChem Substance ID 468592816
Merck Index (14) 9548
MDL Number

MFCD00866235

Specifications
Appearance Light yellow to Yellow powder to crystal
Purity(HPLC) min. 95.0 area%
Purity(Nonaqueous Titration) min. 95.0% (calcd. on anh. substance)
Specific rotation 100 to 105 deg(C=0.5, water, calcd.on anh.substance)
Water max. 12.0 %
NMR confirm to structure
Properties (reference)
Melting Point 215 °C(dec.)
Maximum Absorption Wavelength 414(Phosphate buffer sol.) nm
GHS
Pictogram Pictogram
Signal Word Danger
Hazard Statements H361 : Suspected of damaging fertility or the unborn child.
H340 : May cause genetic defects.
H351 : Suspected of causing cancer.
Precautionary Statements P501 : Dispose of contents/ container to an approved waste disposal plant.
P202 : Do not handle until all safety precautions have been read and understood.
P201 : Obtain special instructions before use.
P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection.
P308 + P313 : IF exposed or concerned: Get medical advice/ attention.
P405 : Store locked up.
Related Laws:
RTECS# UQ0491400
Transport Information:
HS Number 2939799090
Application
Topotecan Hydrocholoride: A Water-Soluble Topoisomerase I Inhibitor

Topotecan hydrocholoride is a topoisomerase I inhibitor that is a semi-synthetic water-soluble derivative of camptothecin [C1495].1) During the course of its normal cell cycle, topoisomerase I relieves torsional strain in DNA by inducing reversible single strand breaks, and transiently forms a covalent bond with DNA. Topotecan prevents the re-ligation of these single-strand breaks by binding to and stabilizing the complex of topoisomerase I and DNA. This process leads to breaks in the DNA strand resulting in apoptosis and cell death.1-3) Recently, lipid nanoencapsulation of topotecan has attracted much attention in order to reduce the loss of efficacy of topotecan due to its hydrolysis in vivo4). (The product is for research purpose only.)

References


Product Documents (Note: Some products will not have analytical charts available.)
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