(S)-4-Amino-9-ethyl-9-hydroxy-2,3,12,15-tetrahydrobenzo[de]pyrano[3',4':6,7]indolizino[1,2-b]quinoline-10,13(1H,9H)-dione

95%

Reagent Code: #233354
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CAS Number 2495742-21-5

science Other reagents with same CAS 2495742-21-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 403.43 g/mol
Formula C₂₃H₂₁N₃O₄
thermostat Physical Properties
Boiling Point 856.1±65.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.53±0.1 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used in research as a fluorescent probe for DNA detection due to its strong binding affinity to nucleic acids, particularly in identifying G-quadruplex structures. Exhibits high selectivity and sensitivity in cellular imaging, making it valuable in studying cancer cell proliferation and gene regulation. As a camptothecin derivative, it is investigated for its potential as a chemotherapeutic agent owing to its ability to intercalate into DNA and inhibit topoisomerase I activity. Shows promise in photodynamic therapy applications due to its light-induced cytotoxic effects.

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inventory 1mg
10-20 days ฿9,800.00

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(S)-4-Amino-9-ethyl-9-hydroxy-2,3,12,15-tetrahydrobenzo[de]pyrano[3',4':6,7]indolizino[1,2-b]quinoline-10,13(1H,9H)-dione
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Used in research as a fluorescent probe for DNA detection due to its strong binding affinity to nucleic acids, particularly in identifying G-quadruplex structures. Exhibits high selectivity and sensitivity in cellular imaging, making it valuable in studying cancer cell proliferation and gene regulation. As a camptothecin derivative, it is investigated for its potential as a chemotherapeutic agent owing to its ability to intercalate into DNA and inhibit topoisomerase I activity. Shows promise in photodyna

Used in research as a fluorescent probe for DNA detection due to its strong binding affinity to nucleic acids, particularly in identifying G-quadruplex structures. Exhibits high selectivity and sensitivity in cellular imaging, making it valuable in studying cancer cell proliferation and gene regulation. As a camptothecin derivative, it is investigated for its potential as a chemotherapeutic agent owing to its ability to intercalate into DNA and inhibit topoisomerase I activity. Shows promise in photodynamic therapy applications due to its light-induced cytotoxic effects.

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