D5782

2′,3′-Dideoxycytidine

≥98% (HPLC)

Manufacturer: Sigma Aldrich

CAS Number: 7481-89-2

Synonym(S): ddC

Select a Size

Pack Size SKU Availability Price
100 MG D5782-100-MG In Stock ₹ 21,022.15
250 MG D5782-250-MG In Stock ₹ 45,908.83
500 MG D5782-500-MG In Stock ₹ 76,056.45

D5782 - 100 MG

₹ 21,022.15

In Stock

Quantity

1

Base Price: ₹ 21,022.15

GST (18%): ₹ 3,783.987

Total Price: ₹ 24,806.137

biological source

synthetic (organic)

Quality Level

200

Assay

≥98% (HPLC)

form

powder

color

colorless

mp

217-218 °C (lit.)

solubility

water: 50 mg/mL, clear, colorless to faintly yellow

storage temp.

−20°C

SMILES string

NC1=NC(=O)N(C=C1)[C@H]2CC[C@@H](CO)O2

InChI

1S/C9H13N3O3/c10-7-3-4-12(9(14)11-7)8-2-1-6(5-13)15-8/h3-4,6,8,13H,1-2,5H2,(H2,10,11,14)/t6-,8+/m0/s1

Other Options

Image Product Name Manufacturer Price Range
50-180-5942
Sigma Aldrich Fine Chemicals Biosciences 2',3'-Dideoxycytidine >=98% (HPLC) | 7481-89-2 | MFCD00012188 | 100MG
Sigma Aldrich Fine Chemicals Biosciences ₹ 19,914.09
50-180-5943
Sigma Aldrich Fine Chemicals Biosciences 2',3'-Dideoxycytidine >=98% (HPLC) | 7481-89-2 | MFCD00012188 | 250MG
Sigma Aldrich Fine Chemicals Biosciences ₹ 42,711.55
50-101-3386
Apexbio Technology LLC Zalcitabine is a nucleoside analog reverse transcriptase inhibitor (NRTI). 7481-89-2. MFCD09837879
Apexbio Technology LLC ₹ 5,989.20
PHR3266
Zalcitabine
Supelco ₹ 18,987.05
CS-1110
Zalcitabine
ChemScene ₹ 2,823.48 - ₹ 1,27,056.60
AC44601
7481-89-2 | Dideoxycytidine
A2B Chem ₹ 342.24 - ₹ 41,411.04

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Description

  • Application: 2′,3′-Dideoxycytidine is used:as a DNA chain-terminating nucleotide for DNA sequencing methods based on the Sanger chain-termination methodas a nucleoside reverse transcriptase inhibitor (NRTI) to study its effects on the development of mechanical allodynia in aging mice[1]as a mitochondrial DNA (mtDNA) replication inhibitor to inhibit the activation of cGAS-STING pathway and study its effects on signaling protein-stimulator of interferon genes (STING), cyclic GMP-AMP synthase (cGAS), and phospho-interferon regulator factor 3 (p-IRF3) expression in mouse hippocampal and microglial cells[2]as an NRTI inhibitor to study its effects on the drug induced-mitochondrial toxicity in Caenorhabditis elegans[3]
  • Biochem/physiol Actions: 2′,3′-Dideoxycytidine (ddC), is an ionic compound and a nucleoside analog.[4] [5]It acts as a nucleoside reverse transcriptase inhibitor and exhibits therapeutic effects against human immunodeficiency virus (HIV) infection.[5] 2′,3′-Dideoxycytidine possesses anti-adenovirus activity and inhibits the adenovirus polymerase.[6]

SAFETY INFORMATION

Pictograms

GHS08

Signal Word

Warning

Hazard Statements

H351

Precautionary Statements

P281

Hazard Classifications

Carc. 2

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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synthetic (organic)

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200

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mp:
217-218 °C (lit.)

solubility:
water: 50 mg/mL, clear, colorless to faintly yellow

storage temp.:
−20°C

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NC1=NC(=O)N(C=C1)[C@H]2CC[C@@H](CO)O2

InChI:
1S/C9H13N3O3/c10-7-3-4-12(9(14)11-7)8-2-1-6(5-13)15-8/h3-4,6,8,13H,1-2,5H2,(H2,10,11,14)/t6-,8+/m0/s1

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