113 Results for "

DT

" in MedChemExpress (MCE) Product Catalog:
Products (113)

113 Results for "DT" in MCE Product Catalog:

19
19 Publications Verification
Cat. No.: HY-112929
CAS No.: 1809427-19-7
Purity:  99.83%
Target:  

Phosphatase

Research Areas:  

Cancer

DT-061 is an orally bioavailable activator of protein phosphatase 2A (PP2A) and could be applied in the therapy of KRAS-mutant and MYC-driven tumorigenesis .
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8
8 Cited Publications
Cat. No.: HY-132591
CAS No.: 1639324-58-5
Purity:  99.80%
Synonyms: ALN-PCSsc
Inclisiran is a double-stranded small interfering RNA (siRNA) molecule. Inclisiran inhibits the transcription of PCSK9. Inclisiran inhibits Pyroptosis, activates PPARγ, and reduces NLRP3, cleaved caspase-1, IL-1β, and IL-18. Inclisiran has anti-inflammatory, lipid-regulating and anti-atherosclerotic activities. Inclisiran can be used in researches of hyperlipidemia and cardiovascular disease (CVD) .
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6
6 Cited Publications
Cat. No.: HY-138646
CAS No.: 86828-69-5
Synonyms: Poly(dA:DT) sodium
Research Areas:  

Inflammation/Immunology

Poly(deoxyadenylic-thymidylic) acid (Poly(dA:dT)) sodium is a double-stranded DNA stimulant. Poly(deoxyadenylic-thymidylic) acid sodium is recognized by the intracellular DNA sensor DDX41 and activates the innate immune pathway via the adaptor protein STING, inducing the production of cytokines such as type I interferons. Poly(deoxyadenylic-thymidylic) acid sodium also serves as an in vitro transcription template for free RNA polymerase .
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2
2 Cited Publications
Cat. No.: HY-130604
CAS No.: 2365172-42-3
Purity:  99.61%
Research Areas:  

Inflammation/Immunology Cancer

DT2216 is a potent and selective BCL-XL (Bcl-2 family member) degrader based on PROTAC technology. DT2216 causes effective degradation of BCL-XL protein by recruiting Von Hippel-Lindau (VHL) E3 ubiquitin ligase. DT2216 inhibits various BCL-XL-dependent leukemia and cancer cells but considerably less toxic to platelets .
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2
2 Cited Publications
Cat. No.: HY-P2692B
Target:  

PKG

Research Areas:  

Cancer

DT-2 is a potent and selective inhibitor of the cGMP-dependent protein kinase (PKG). DT-2 inhibits PKG catalyzed phosphorylation (Ki: 12.5 nM) .
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1
1 Cited Publications
Cat. No.: HY-132609
CAS No.: 1386913-72-9
Purity:  99.09%
Patisiran sodium is a double-stranded small interfering RNA that targets a sequence within the transthyretin (TTR) messenger RNA. Patisiran sodium specifically inhibits hepatic synthesis of mutant and wild-type TTR. Patisiran sodium can be used for the research of hereditary TTR amyloidosis .
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1
1 Cited Publications
Cat. No.: HY-120272
CAS No.: 1809068-70-9
Purity:  99.53%
Synonyms: DT-1154
Target:  

Phosphatase

Research Areas:  

Cancer

SMAP-2 (DT-1154) is an orally active protein phosphatase 2A (PP2A) activator, with anti-cancer activity .
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1
1 Cited Publications
Cat. No.: HY-132581
CAS No.: 2170507-65-8
Synonyms: BIIB078; IONIS-C9Rx
Target:  

Ras Others

Research Areas:  

Neurological Disease

Tadnersen (BIIB078), an antisense oligonucleotide (ASO), selectively targets C9ORF72 transcript variants 1 and 3 that carry the expansion .
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1
1 Cited Publications
Cat. No.: HY-124801
CAS No.: 332108-65-3
Purity:  98.68%
Research Areas:  

Infection

ABMA is a broad-spectrum inhibitor of intracellular toxins and pathogens. ABMA efficiently protects cells against various toxins and pathogens including viruses, intracellular bacteria and parasite. ABMA selectively acts at host cell late endosomes rather than targeting toxin or pathogen itself. ABMA has broad-spectrum anti-infection activity .
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1
1 Cited Publications
Cat. No.: HY-112929B
CAS No.: 1809427-20-0
Purity:  99.77%
Target:  

Phosphatase

Research Areas:  

Cancer

(1S,2S,3R)-DT-061 is an enantiomer of DT-061 (HY-112929). DT-061 is an orally active activator of protein phosphatase 2A (PP2A). (1S,2S,3R)-DT-061 can be used as a negative control in the research of KRAS-mutant and MYC-driven lung cancer tumorigenesis .
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1
1 Cited Publications
Cat. No.: HY-K0228

MCE Oligo (dT)30 Magnetic Beads are designed for the rapid isolation of highly purified, intact mRNA from eukaryotic total RNA or directly from crude extracts of cells, plant and animal tissues. The 1 mL volume is defined as the base specification. All larger sizes correspond to incremental volumes of this base.

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1
1 Cited Publications
Cat. No.: HY-P72487
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Proheparin-binding EGF-like growth factor; HB-EGF; DT-R; DTS; HEGFL
Species:  
Source:  
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Cat. No.: HY-147080
CAS No.: 1491144-00-3
Purity:  98.53%
Synonyms: ARC1905
Target:  

Complement System

Research Areas:  

Others

Avacincaptad pegol (ARC1905) sodium is a 40KDa PEG-conjugated aptamer. Avacincaptad pegol sodium targets complement factor 5 (C5), inhibits the cleavage of C5 into C5a and C5b, limits inflammatory stimulation and complement membrane attack complex (MAC), and is used to study age-related macular degeneration (AMD). Avacincaptad pegol sodium limits irregular cell apoptosis by targeting downstream factors in the complement cascade while preserving the early steps of the complement system .
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Cat. No.: HY-20140
CAS No.: 40615-39-2
Synonyms: 5'-O-(4,4'-Dimethoxytrityl)thymidine
5'-O-DMT-dT (5'-O-(4,4'-Dimethoxytrityl)thymidine) is a nucleoside derivative which can be used in the preparation of oligonucleotides .
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Cat. No.: HY-W013068
CAS No.: 98796-51-1
DMT-dT Phosphoramidite is typically used in the synthesis of DNA .
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Cat. No.: HY-44432
CAS No.: 2143096-93-7
Synonyms: ABT-263-piperazine
Navitoclax-piperazine (ABT-263-piperazine) is a Navitoclax (HY-10087) analog and BCL-XL inhibitor. Navitoclax-piperazine is the ligand for target protein of PROTAC DT2216 (HY-130604). Navitodax-pperaie and E3 ubiquitin ligase VHL ligand can be used to synthesize PROTAC DT2216 (HY-130604) .
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Cat. No.: HY-145720
CAS No.: 1639264-46-2
Synonyms: ALN-CC5
Cemdisiran (ALN-CC5) is an N-acetylgalactosamine-conjugated RNAi agent and also a complement component C5 inhibitor. Cemdisiran targets C5 mRNA, cleaves C5 mRNA via the endogenous RNA interference pathway, and inhibits the production of C5 protein in the liver. Cemdisiran exerts a dose-dependent inhibitory effect on total C5 concentrations in cynomolgus monkeys. When used in combination with Pozelimab (HY-P99786) in cynomolgus monkeys, Cemdisiran achieves a more sustained and complete inhibitory effect on complement activity. Cemdisiran can be used in the research of paroxysmal nocturnal hemoglobinuria and other complement-mediated diseases .
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Cat. No.: HY-148457
CAS No.: 1613641-69-2
Synonyms: Izervay
Avacincaptad pegol (Izervay) is a selective inhibitor targeting complement component C5, and is a pegylated ribonucleic acid aptamer. Avacincaptad pegol inhibits the cleavage of C5 into pro-inflammatory C5a and C5b, which forms the membrane attack complex (C5b-9), thereby reducing inflammatory cell recruitment and retinal cell damage. Avacincaptad pegol can slow the growth of geographic atrophy (GA) lesions and reduce the risk of persistent vision loss. Avacincaptad pegol can be used in research of geographic atrophy associated with age-related macular degeneration (AMD) and has been approved by the FDA .
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Cat. No.: HY-A0152
CAS No.: 51-49-0
Synonyms: D-T4
D-Thyroxine (D-T4) is an orally active thyroid hormone that inhibits the secretion of TSH. D-Thyroxine can inhibit goiter, promote metamorphosis of tadpoles and influence cholesterol metabolism. D-Thyroxine can be used for the study of hypercholesterolemia .
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Cat. No.: HY-109561
CAS No.: 222716-86-1
Purity:  98.09%
Synonyms: EYE001; NX1838
Target:  

VEGFR

Pegaptanib sodium is an RNA aptamer with polyethylene glycol modifications, which is directed against vascular endothelial growth factor (VEGF)-165. Pegaptanib could be used for the study of neovascular age-related macular degeneration (AMD) .
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