22 Results for "

ddC

" in MedChemExpress (MCE) Product Catalog:
Products (22)

22 Results for "ddC" in MCE Product Catalog:

17
17 Cited Publications
Cat. No.: HY-17392
CAS No.: 7481-89-2
Synonyms: 2',3'-Dideoxycytidine; ddC; Dideoxycytidine
Research Areas:  

Infection

Zalcitabine is a potent nucleoside analogue reverse transcriptase inhibitor used in the treatment of HIV infection.
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Cat. No.: HY-118594
CAS No.: 632-93-9
Purity:  99.79%
Target:  

Ferrochelatase

Research Areas:  

Metabolic Disease

Diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate is an orally active porphyrin inducer and ferrochelatase inhibitor. Diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate can induce small bile duct obstruction in mice, resulting in blocked bile excretion and causing cholestasis. Long-term use of Diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate can cause damage to bile duct epithelial cells, inflammatory responses, and liver fibrosis. Diethyl 2,4,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate can be used to simulate the pathological features of cholestatic liver diseases such as sclerosing cholangitis (PSC) .
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Cat. No.: HY-139997
CAS No.: 2140806-84-2
Target:  

PROTACs EGFR

Research Areas:  

Cancer

DDC-01-163 is an allosteric PROTAC degrader targeting EGFR. DDC-01-163 is dependent on the ubiquitin–proteasome system. DDC-01-163 can selectively inhibit the proliferation of L858R/T790M (L/T) mutant Ba/F3 cells. DDC-01-163 is effective against Osimertinib (HY-15772)-resistant cells with L/T/C797S and L/T/L718Q EGFR mutations. DDC-01-163 exhibits enhanced anti-proliferative activity against L858R/T790M EGFR-Ba/F3 cells when combined with the ATP-site EGFR inhibitor Osimertinib. DDC-01-163 can be used for the study of non-small cell lung cancer .
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Cat. No.: HY-17392R
CAS No.: 7481-89-2
Synonyms: 2',3'-Dideoxycytidine (Standard); ddC (Standard); Dideoxycytidine (Standard)
Research Areas:  

Infection

Zalcitabine (Standard) is the analytical standard of Zalcitabine. This product is intended for research and analytical applications. Zalcitabine is a potent nucleoside analogue reverse transcriptase inhibitor used in the treatment of HIV infection.
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Cat. No.: HY-151048
CAS No.: 2140807-58-3
Target:  

EGFR

Research Areas:  

Cancer

JBJ-07-149 is an inhibitor for EGFRL858R/T790M with an IC50 of 1.1 nM. JBJ-07-149 inhibits the proliferation of cell Ba/F3 with IC50 of 4.9 μM and 0.148 μM, without and with presence of Cetuximab (HY-P9905). JBJ-07-149 can be used as ligand for target protein in synthesis of DDC-01-163 (HY-139997) .
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Cat. No.: HY-163203
CAS No.: 1402224-73-0
Target:  

Bacterial

Research Areas:  

Infection

DDC18-8A is an amphiphilic dendrimer that exhibits high antibacterial and antibiofilm efficacy .
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Cat. No.: HY-163461
Target:  

PARP

Research Areas:  

Cancer

4F-DDC is a novel PARP1 inhibitor with an IC50 value of 82 nM. 4F-DDC induces DNA damage and activates the cGAS–STING pathway. 4F-DDC inhibits the growth of HCC-1937-derived tumor xenografts .
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Cat. No.: HY-156179
Target:  

Amyloid-β

Research Areas:  

Neurological Disease

DDC 2′,3′-O-disulfate (compound 4) prevents the fibrillization and oligomerization of Aβ42. DDC 2′,3′-O-disulfate has the potential for Alzheimer's disease (AD) research .
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Cat. No.: HY-RS03608
Research Areas:  

Others

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

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Cat. No.: HY-156180
Target:  

Drug Metabolite

Research Areas:  

Neurological Disease

DDC 3′-O-β-D glucuronide (compound 5) is a drug metabolite that can prevent the fibrillization and oligomerization of Aβ42. DDC 3′-O-β-D glucuronide has potential for the research of Alzheimer's disease .
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Cat. No.: HY-W784611
CAS No.: 195375-65-6
Target:  

DNA/RNA Synthesis

Research Areas:  

Others

3'-NH-Tr-2',3'-ddC(Bz)-5'-CE-Phosphoramidite is a phosphoramidite monomer used in nucleic acid synthesis, such as oligonucleotides.
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Cat. No.: HY-170351
Target:  

PROTAC Linkers

Research Areas:  

Cancer

NH2-PEG2-OMs is the linker, that could be used for synthesis of PROTAC degrader DDC-01-163 (HY-139997) .
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Cat. No.: HY-170350
CAS No.: 2140807-37-8
Research Areas:  

Cancer

Pomalidomide-PEG2-Oms (CRBN ligand Pomalidomide (HY-10984)) is an E3 Ligase Ligand-Linker Conjugate for EGFR PROTAC DDC-01-163 (HY-139997) .
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Cat. No.: HY-W393396
CAS No.: 84472-90-2
Research Areas:  

Metabolic Disease

3'-NH2-ddC is a monomeric raw material that can be used for nucleic acid synthesis.
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Cat. No.: HY-P701909
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: ddC; Aromatic-L-amino-acid decarboxylase; AADC; DOPA decarboxylase; ddC
Species:  
Source:  
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Cat. No.: HY-180325
CAS No.: 2375048-04-5
Target:  

EGFR

Research Areas:  

Others

DDC4002 is a selective EGFR inhibitor. DDC4002 has inhibitory activity against the L858R/T790M mutant EGFR subtype (IC50 = 39 nM) .
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Cat. No.: HY-P701910
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: ddC; Aromatic-L-amino-acid decarboxylase; AADC; DOPA decarboxylase; ddC
Species:  
Source:  
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Cat. No.: HY-P704655
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: ddC; Aromatic-L-amino-acid decarboxylase; AADC; DOPA decarboxylase; ddC
Species:  
Source:  
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Cat. No.: HY-RS16935
Research Areas:  

Others

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

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Cat. No.: HY-RS23378
Research Areas:  

Others

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

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