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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
42 Results for "
Deoxyribose
" in MedChemExpress (MCE) Product Catalog:
Products (42)
42 Results for "Deoxyribose" in MCE Product Catalog:
16
Target:
Research Areas:
Cardiovascular Disease Inflammation/Immunology Endocrinology Cancer
9
9 Cited Publications
Synonyms: Deoxycytidine; Cytosine deoxyriboside; Deoxyribose cytidine
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2'-Deoxycytidine, a deoxyribonucleoside, can inhibit biological effects of Bromodeoxyuridine (Brdu). 2'-Deoxycytidine is essential for the synthesis of nucleic acids, that can be used for the research of cancer .
6
6 Cited Publications
Cat. No.: HY-D0185
CAS No.: 312693-72-4
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Research Areas:
2'-Deoxyguanosine monohydrate is a nucleoside composed of guanine and 2'-deoxyribose, and it is one of the basic structural units of DNA. The oxidation products of 2'-Deoxyguanosine monohydrate may participate in DNA damage, which in turn may affect gene expression or induce cancer .
1
Research Areas:
Bacitracin Zinc is a complex formed by the binding of Bacitracin (HY-107193) with zinc ions. Bacitracin Zinc is an orally active polypeptide antibiotic with bactericidal properties. Bacitracin Zinc can cause DNA and deoxyribose damage, as well as improve the gut microbiota of broiler and beef cattle .
Category:
Human Gut Microbiota Metabolites Microorganisms Metabolic Disease Endogenous metabolite Disease Research Fields Saccharides
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Target:
Synonyms: Deoxycytidine (Standard); Cytosine deoxyriboside (Standard); Deoxyribose cytidine (Standard)
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Research Areas:
Purine nucleoside phosphorylase, Microorganism (PNP) is a key enzyme in purine metabolism, which is involved in the purine rescue pathway. The deficiency of Purine nucleoside phosphorylase resulted in impaired T cell function. In the presence of inorganic orthophosphate as the second substrate, Purine nucleoside phosphorylase catalyzes the breaking of the glycosidic bond between ribose and deoxyribonucleoside to generate purine base and ribose (deoxyribose) -1-phosphate .
Cat. No.: HY-D0184S2
Synonyms: Deoxycytidine-15N3; Cytosine deoxyriboside-15N3; Deoxyribose cytidine-15N3
Cat. No.: HY-W541025
CAS No.: 9007-49-2
Cat. No.: HY-W338294S3
CAS No.: 478511-25-0
Synonyms: Deoxycytidine-d2 monohydrate; Cytosine deoxyriboside-d2 monohydrate; Deoxyribose cytidine-d2 monohydrate
Cat. No.: HY-P5443
CAS No.: 224569-84-0
Cat. No.: HY-D0184S3
CAS No.: 1987883-22-6
Synonyms: Deoxycytidine-13C9,15N3; Cytosine deoxyriboside-13C9,15N3; Deoxyribose cytidine-13C9,15N3
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Research Areas:
Purine nucleoside phosphorylase, Bacillus sp. is a key enzyme in purine metabolism, involved in the purine salvage pathway. A deficiency in Purine nucleoside phosphorylase, Bacillus sp. can lead to impaired T-cell function. In the presence of inorganic phosphate as a second substrate, Purine nucleoside phosphorylase, Bacillus sp. catalyzes the cleavage of the glycosidic bond of ribonucleosides and deoxyribonucleosides, producing purine bases and ribose (or deoxyribose)-1-phosphate. Purine nucleoside phosphorylase, Bacillus sp. can be used for the determination of inorganic phosphate .
Cat. No.: HY-126877
CAS No.: 78582-17-9
3-Deaza-2 '-deoxyadenosine is a nucleoside analog synthesized from 2' -deoxyadenosine. 3-Deaza-2 '-deoxyadenosine inhibits RNA synthesis by binding to ribose fragments of ribonucleotides, thereby preventing the formation of enzyme-substrate complexes, thereby preventing chain elongation, It can also inhibit DNA synthesis by binding deoxyribose fragments of DNA and preventing DNA polymerase from adding nucleotides to the growth chain. 3-Deaza-2 '-deoxyadenosine has antiviral activity .
Cat. No.: HY-D0184S4
Synonyms: Deoxycytidine-d13; Cytosine deoxyriboside-d13; Deoxyribose cytidine-d13
Cat. No.: HY-D0184S5
Synonyms: Deoxycytidine-13C9; Cytosine deoxyriboside-13C9; Deoxyribose cytidine-13C9
Cat. No.: HY-W1008609
CAS No.: 182625-87-2
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Research Areas:
(R)-GNA-A(Bz) phosphoramidite is a monophosphate nucleoside similar to DNA or RNA but differing in the composition of its sugar-phosphodiester backbone, using propylene glycol in place of ribose or deoxyribose.
Cat. No.: HY-N2214
CAS No.: 329361-25-3
Category:
Liliaceae Monophenols Simple Phenylpropanols Aloe vera (L.) Burm. f. Phenols Phenylpropanoids Plants Disease Research Fields Inflammation/Immunology
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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
