47 Results for "

CDA

" in MedChemExpress (MCE) Product Catalog:
Products (47)

47 Results for "CDA" in MCE Product Catalog:

91
91 Publications Verification
Cat. No.: HY-12885
CAS No.: 1638241-89-0
Purity:  99.40%
Synonyms: ADU-S100; MIW815; ML RR-S2 CDA
Target:  

STING

Research Areas:  

Inflammation/Immunology Cancer

2’3’-c-di-AM(PS)2 (Rp,Rp) (ADU-S100), an activator of stimulator of interferon genes (STING), leads to potent and systemic tumor regression and immunity .
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91
91 Publications Verification
Cat. No.: HY-12885A
CAS No.: 1638750-95-4
Purity:  99.43%
Synonyms: ADU-S100 disodium salt; MIW815 disodium salt; ML RR-S2 CDA disodium salt
Target:  

STING

Research Areas:  

Inflammation/Immunology Cancer

2’3’-c-di-AM(PS)2 (Rp,Rp) disodium salt (ADU-S100 disodium salt) is an activator of stimulator of interferon genes (STING).
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91
91 Publications Verification
Cat. No.: HY-12885B
CAS No.: 1638750-96-5
Purity:  99.60%
Synonyms: ADU-S100 ammonium salt; MIW815 ammonium salt; ML RR-S2 CDA ammonium salt
Target:  

STING

Research Areas:  

Inflammation/Immunology Cancer

2’3’-c-di-AM(PS)2 (Rp,Rp) ammonium salt (ADU-S100 ammonium salt), an activator of stimulator of interferon genes (STING), leads to potent and systemic tumor regression and immunity .
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10
10 Cited Publications
Cat. No.: HY-13599
CAS No.: 4291-63-8
Purity:  99.97%
Synonyms: 2-Chloro-2′-deoxyadenosine; CldAdo; 2CDA
Cladribine (2-Chloro-2′-deoxyadenosine), a purine nucleoside analog, is an orally active adenosine deaminase inhibitor. Cladribine functions as an inhibitor of DNA synthesis to block the repair of the damaged DNA. Cladribine can inhibit DNA methylation. Cladribine has anti-lymphoma activity. Cladribine can be used for the research of several hematologic malignancies and multiple sclerosis .
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3
3 Cited Publications
Cat. No.: HY-15345A
CAS No.: 18771-50-1
Purity:  99.89%
Synonyms: THU; NSC-112907
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

Tetrahydrouridine dihydrate is potent inhibitor of cytidine deaminase (CDA), which competitively blocks the enzyme's active site more effectively than intrinsic cytidine .
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3
3 Cited Publications
Cat. No.: HY-15345
Purity:  99.79%
Synonyms: THU dihydrate; NSC-112907 dihydrate
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

Tetrahydrouridine dihydrate (THU dihydrate) is potent inhibitor of cytidine deaminase (CDA), which competitively blocks the enzyme's active site more effectively than intrinsic cytidine.
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1
1 Cited Publications
Cat. No.: HY-109081
CAS No.: 1141397-80-9
Purity:  ≥98.0%
Synonyms: E7727
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

Cedazuridine (E7727) (Compound 7a) is an orally active cytidine deaminase (CDA) inhibitor with an IC50 value of 0.4 μM. Cedazuridine can be used for cancer research .
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Cat. No.: HY-Y1058
CAS No.: 495-18-1
Synonyms: BHA
Target:  

Fungal

Research Areas:  

Infection

Benzohydroxamic acid (BHA) is a chitin deacetylase (CDA) inhibitor with significant antifungal activity. The Ki values of BHA against the CDAs of Verticillium dahliae and Puccinia striiformis f. sp. tritici are 8.31 μM and 9.83 μM, respectively. Benzohydroxamic acid can restore the defense responses of infected host plants, upregulate the expression of defense-related genes, and reduce the growth and reproduction of fungi in plants. Benzohydroxamic acid can be used in the research of the field of controlling agricultural fungal diseases, such as various plant fungal diseases caused by Verticillium dahliae, Puccinia striiformis and other fungi, like cotton wilt and wheat stripe rust .
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Cat. No.: HY-12885C
Purity:  98.94%
Synonyms: ADU-S100 enantiomer ammonium salt; MIW815 enantiomer ammonium salt; ML RR-S2 CDA enantiomer ammonium salt
Target:  

IFNAR

Research Areas:  

Inflammation/Immunology

2’3’-c-di-AM(PS)2 (Rp,Rp) enantiomer ammonium salt (ADU-S100 enantiomer ammonium salt) is the less active enantiomer of 2’3’-c-di-AM(PS)2 (Rp,Rp). 2’3’-c-di-AM(PS)2 (Rp,Rp) is an activator of stimulator of interferon genes (STING) .
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Cat. No.: HY-13599R
CAS No.: 4291-63-8
Synonyms: 2-Chloro-2′-deoxyadenosine (Standard); CldAdo (Standard); 2CDA (Standard)
Cladribine (Standard) is the analytical standard of Cladribine. This product is intended for research and analytical applications. Cladribine (2-Chloro-2′-deoxyadenosine), a purine nucleoside analog, is an orally active adenosine deaminase inhibitor. Cladribine functions as an inhibitor of DNA synthesis to block the repair of the damaged DNA. Cladribine can inhibit DNA methylation. Cladribine has anti-lymphoma activity. Cladribine can be used for the research of several hematologic malignancies and multiple sclerosis .
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Cat. No.: HY-172523
CAS No.: 932889-57-1
Research Areas:  

Infection

CDA-IN-3 (NCDI) is an inhibitor of chitin deacetylase (CDA) with anti-parasitic activity. CDA-IN-3 disrupts the chitin metabolism of nematodes, leading to an increase in the level of ROS in nematodes and causing cell damage. CDA-IN-3 has a significant inhibitory effect on all developmental stages of Caenorhabditis elegans. CDA-IN-3 can be used in the research of the anti-infection field .
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Cat. No.: HY-173448
CAS No.: 466656-34-8
Target:  

Fungal

Research Areas:  

Infection

CDA-IN-4 (compound VS-24) is a chitin deacetylase (CDA) inhibitor. CDA-IN-4 shows a 61.2% protective effect against rice blast at a concentration of 100 μg/mL .
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Cat. No.: HY-171541
CAS No.: 354562-11-1
Target:  

Fungal

Research Areas:  

Infection

CDA-IN-1 (Compound vs#2-1) is an inhibitor of chitin deacetylase (CDA). CDA-IN-1 exhibits antifungal activity. It can inhibit fungal growth by suppressing the activity of fungal CDA, activating the plant immune response, and accumulating reactive oxygen species (ROS). At a concentration of 100 μM, CDA-IN-1 can achieve inhibition rates of 86.9% and 74.5% against PxCDA1 and PxCDA2 of P. xanthii, respectively. CDA-IN-1 can be applied to the research in the field of controlling plant fungal diseases, such as the research on diseases like cucurbit powdery mildew and tomato gray mold .
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Cat. No.: HY-171542
CAS No.: 2559404-67-8
Target:  

Fungal

Research Areas:  

Infection

CDA-IN-2 (Compound VS#2-3) is a chitin deacetylase (Chitin Deacetylase, CDA) inhibitor with antifungal activity. At a concentration of 100 μM, it can inhibit the CDA PxCDA1 and PxCDA2 of P. xanthii by 83.7% and 74.5% respectively. CDA-IN-2 can be applied to the research in the field of controlling agricultural fungal diseases, such as dealing with resistant powdery mildew and Botrytis cinerea .
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Cat. No.: HY-RS02282
Research Areas:  

Others

CDA Human Pre-designed siRNA Set A contains three designed siRNAs for CDA gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS17118
Research Areas:  

Others

Cda Mouse Pre-designed siRNA Set A contains three designed siRNAs for Cda gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS23563
Research Areas:  

Others

Cda Rat Pre-designed siRNA Set A contains three designed siRNAs for Cda gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-109081A
Synonyms: E7727 hydrochloride
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

Cedazuridine (E7727) (Compound 7a) hydrochloride is an orally active cytidine deaminase (CDA) inhibitor with an IC50 value of 0.4 μM. Cedazuridine hydrochloride can be used for cancer research .
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Cat. No.: HY-109081R
CAS No.: 1141397-80-9
Synonyms: E7727 (Standard)
Research Areas:  

Cancer

Cedazuridine (Standard) is the analytical standard of Cedazuridine. This product is intended for research and analytical applications. Cedazuridine (E7727) (Compound 7a) is an orally active cytidine deaminase (CDA) inhibitor with an IC50 value of 0.4 μM. Cedazuridine can be used for cancer research .
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Cat. No.: HY-15345AS
Synonyms: THU-d3; NSC-112907-d3
Tetrahydrouridine-d3 is the deuterium labeled Tetrahydrouridine . Tetrahydrouridine dihydrate is potent inhibitor of cytidine deaminase (CDA), which competitively blocks the enzyme's active site more effectively than intrinsic cytidine .
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