10 Results for "

CuI

" in MedChemExpress (MCE) Product Catalog:
Products (10)

10 Results for "CuI" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-Y0032
CAS No.: 79-19-6
Target:  

Orthopoxvirus

Research Areas:  

Infection Others Cancer

Thiosemicarbazide is a vitamin B6 antagonist with anti-acne activity. Thiosemicarbazide is also a well-known source in the synthesis of heterocycles, and its derivatives have potential anticancer activity. Thiosemicarbazide (TSC: HL1) reacts with metal salts, urea (U), to prepare Co(II) and Cu(I) metal complexes. Thiosemicarbazide is also used in the fields of media communications and optical storage, and in the spectrophotometric detection of metals .
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Cat. No.: HY-153419
CAS No.: 1334179-86-0
Research Areas:  

Others

BTTES is a tris(triazolylmethyl)amine-based ligand for Cu(I) without apparent toxicity. BTTES IMPROVES the cycloaddition reaction rapidly in living systems .
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Cat. No.: HY-161181
CAS No.: 2223032-74-2
Research Areas:  

Others

BTTES-acid is an analog of BTTES. BTTES is a tris(triazolylmethyl)amine-based ligand for Cu(I) without apparent toxicity. BTTES improves the cycloaddition reaction rapidly in living systems .
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Cat. No.: HY-163200
CAS No.: 3034768-68-5
Target:  

Cuproptosis

Research Areas:  

Neurological Disease

Cu(I) chelator 1 (Compound LH2) is a chelator which targets the Cu(I) redox state. Cu(I) chelator 1 prevents ROS production .
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Cat. No.: HY-Y0032R
CAS No.: 79-19-6
Research Areas:  

Infection Others Cancer

Thiosemicarbazide is a vitamin B6 antagonist with anti-acne activity. Thiosemicarbazide is also a well-known source in the synthesis of heterocycles, and its derivatives have potential anticancer activity. Thiosemicarbazide (TSC: HL1) reacts with metal salts, urea (U), to prepare Co(II) and Cu(I) metal complexes. Thiosemicarbazide is also used in the fields of media communications and optical storage, and in the spectrophotometric detection of metals .
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Cat. No.: HY-161436
Research Areas:  

Others

TPA-dT is a thymidine analog with a tris[(2-pyridyl)methyl]amine (TPA) group. TPA-dT can be used to modify siRNAs. The TPA-modified siRNAs remain functionally inactive and is incapable of silencing gene expression until the TPA moiety is removed upon exposure to Cu(I) .
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Cat. No.: HY-W800697
CAS No.: 2644752-87-2
BP Fluor 430 Picolyl Azide is an advanced fluorescent probe that incorporatess a copper-chelating motif to raise the effective concentration of Cu(I) at the reaction site. The rate of the CuAAC reaction depends on the concentrations of all reagents, including copper, therefore raising the effective copper concentration at the reaction site will dramatically increase the rate of CuAAC reaction without the need to increase concentration of azide reagent or copper. In addition, the use of BP Fluor 430 Picolyl Azide instead of conventional BP Fluor 430 Azide allows for at least a tenfold reduction in the concentration of the copper catalyst without sacrificing the efficiency of labeling. In summary, the introduction of a picolyl moiety into an azide probe leads to a substantial increase in the sensitivity of alkyne detection. This is of special value for the detection of low abundance targets or where significant increase in signal intensity is desired.
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Cat. No.: HY-W1049767
CAS No.: 2088834-55-1
Target:  

MOFs

Research Areas:  

Others

TIFSIX-2-Cu-i is a metal-organic framework (MOF).
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Cat. No.: HY-W1049774
CAS No.: 2119615-01-7
Target:  

MOFs

Research Areas:  

Others

SIFSIX-14-Cu-i is a metal-organic framework (MOF).
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Cat. No.: HY-W800693
CAS No.: 2841143-99-3
BP Fluor 405 Picolyl Azide is an advanced fluorescent probe that incorporatess a copper-chelating motif to raise the effective concentration of Cu(I) at the reaction site. The rate of the CuAAC reaction depends on the concentrations of all reagents, including copper, therefore raising the effective copper concentration at the reaction site dramatically increases the rate of CuAAC reaction without increasing the concentrations of azide reagent or copper. In addition, the use of picolyl azide instead of conventional azides allows for at least a tenfold reduction in the concentration of the copper catalyst without sacrificing the efficiency of labeling. In summary, the introduction of a picolyl moiety into an azide probe leads to a substantial increase in the sensitivity of alkyne detection. This is of special value for the detection of low abundance targets or where significant increase in signal intensity is desired.
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