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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
9 Results for "
charge-transfer complex
" in MedChemExpress (MCE) Product Catalog:
Products (9)
9 Results for "charge-transfer complex" in MCE Product Catalog:
1
1 Cited Publications
Cat. No.: HY-W127832
CAS No.: 123148-15-2
Synonyms: Solvent Orange 3 hydrochloride; Basic Orange 2; Chrysoidine Y
Research Areas:
Chrysoidine G (Solvent Orange 3 hydrochloride; Basic Orange 2) is an industrial azo dye. Chrysoidine G is used in most textile dyeing, absorption fluorescent probes, and colorimetric sensors. Chrysoidine G can chemically complex with Co 2+, or bind with Cs + to inhibit the intramolecular charge transfer process, thereby triggering a red shift in the absorption spectrum and producing a significant color change. Chrysoidine G can induce DNA damage, and has moderate toxicity and carcinogenicity .
Cat. No.: HY-124357
CAS No.: 127685-30-7
Synonyms: S-Norfluoxetine hydrochloride; LY 215229 hydrochloride
Target:
Research Areas:
Seproxetine (S-Norfluoxetine) hydrochloride is a selective serotonin reuptake inhibitor (SSRI) that enhances serotonin levels in the brain by specifically inhibiting the serotonin uptake carrier. Seproxetine hydrochloride exhibits strong charge transfer interactions with π-electron acceptors, forming stable complexes that enhance its binding affinity to multiple receptors, including serotonin and dopamine receptors. Seproxetine hydrochloride demonstrates improved biological activity when interacting with charge transfer complexes, leading to increased stability and efficacy in therapeutic applications.
Synonyms: Solvent Orange 3; Basic Orange 2 free base; Chrysoidine Y free base
Research Areas:
Chrysoidine G free base (Solvent Orange 3; Basic Orange 2 free base) is an industrial azo dye. Chrysoidine G free base is used in most textile dyeing, absorption fluorescent probes, and colorimetric sensors. Chrysoidine G free base can chemically complex with Co 2+, or bind with Cs + to inhibit the intramolecular charge transfer process, thereby triggering a red shift in the absorption spectrum and producing a significant color change. Chrysoidine G free base can induce DNA damage, and has moderate toxicity and carcinogenicity .
Cat. No.: HY-D0303AR
CAS No.: 532-82-1
Synonyms: Solvent Orange 3 hydrochloride (Standard); Basic Orange 2 (Standard); Chrysoidine Y (Standard)
Research Areas:
Chrysoidine G (Solvent Orange 3 hydrochloride; Basic Orange 2) Standard is the analytical standard of Chrysoidine G (HY-D0303A). This product is intended for research and analytical applications. Chrysoidine G (Solvent Orange 3 hydrochloride; Basic Orange 2) is an industrial azo dye. Chrysoidine G is used in most textile dyeing, absorption fluorescent probes, and colorimetric sensors. Chrysoidine G can chemically complex with Co 2+, or bind with Cs + to inhibit the intramolecular charge transfer process, thereby triggering a red shift in the absorption spectrum and producing a significant color change. Chrysoidine G can induce DNA damage, and has moderate toxicity and carcinogenicity .
Target:
Cat. No.: HY-D0303AS
CAS No.: 1450729-16-4
Synonyms: Solvent Orange 3-d5 hydrochloride; Basic Orange 2-d5 hydrochloride; Chrysoidine Y-d5 hydrochloride
Research Areas:
Chrysoidine G-d5 (Solvent Orange 3-d5 hydrochloride; Basic Orange 2-d5) is the deuterated-labeled Chrysoidine G (HY-D0303A). Chrysoidine G (Solvent Orange 3 hydrochloride; Basic Orange 2) is an industrial azo dye. Chrysoidine G is used in most textile dyeing, absorption fluorescent probes, and colorimetric sensors. Chrysoidine G can chemically complex with Co 2+, or bind with Cs + to inhibit the intramolecular charge transfer process, thereby triggering a red shift in the absorption spectrum and producing a significant color change. Chrysoidine G can induce DNA damage, and has moderate toxicity and carcinogenicity .
Cat. No.: HY-D3125
Target:
Research Areas:
NtHzBtd is a fluorescent probe for detecting Fe 3+. NtHzBtd is applicable to the selective fluorescent detection of Fe 3+ ions and live cell imaging studies. NtHzBtd can selectively coordinate with Fe 3+ to form a 1:1 complex, triggering chelation enhanced quenching (CHEQ) and intramolecular charge transfer (ICT) processes, which result in fluorescence turn-off, thereby enabling sensitive detection of Fe 3+ and live cell fluorescence imaging. After binding to Fe 3+, NtHzBtd reduces fluorescence intensity, exhibits a rapid response property, with a limit of detection of 0.036 μM and a response time of approximately 55 s. The detection wavelengths are Ex/Em = 334/401 nm (solution system) .
Cat. No.: HY-D3127
CAS No.: 455251-97-5
Target:
Research Areas:
DCA-Mln is a Fluorescent probe for ferric iron (Fe³⁺) detection. The probe works via an internal charge transfer (ICT) process from its diethylamino group to its dicyano group, which produces bright pink fluorescence in its unbound state; when Fe³⁺ is present, two molecules of DCA-Mln chelate with one Fe³⁺ ion, with one cyano group of each DCA-Mln participating in the complexation, and this binding triggers a photoinduced electron transfer (PET) process that provides a nonradiative deactivation pathway, resulting in fluorescence quenching; additionally, the probe exhibits a visible color change from purple to peach pink upon Fe³⁺ binding, enabling dual-channel detection. The probe has an excitation wavelength of 570 nm and an emission wavelength of 670 nm, and it shows a rapid response, with fluorescence stabilizing within 15 seconds of Fe³⁺ addition. DCA-Mln is cell-membrane-permeable, nontoxic at the imaging concentration of 10 μM, and can be used for Fe³⁺ detection in actual water samples, Fe³⁺ imaging in living cells, and as an anti-counterfeiting ink[1].
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
