5-Aza-2'-deoxycytidine

Indications and Usage Mechanisms of Action Side Effects Category Toxicity grading Acute toxicity Flammability Hazardous characteristics Storage characteristics Fire extinguishing agent

Product Name: 5-Aza-2'-deoxycytidine
CAS No.: 2353-33-5
Chemical Name: 5-Aza-2'-deoxycytidine
Synonyms: DECITABINE;Dacogen;5-AZA-CDR;5-AZA-DC;CS-1979;Decitabin;NSC 127716;Aza deoxycytidine;5-azadeoxycytidine;Ornidazole 2353-33-5
CBNumber: CB6284800
Molecular Formula: C8H12N4O4
Formula Weight: 228.21
MOL File: 2353-33-5.mol

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5-Aza-2'-deoxycytidine Property

Melting point:: ~200 °C (dec.)
alpha: D22 +68.5° (30 min) +57.8° (6 hr) (c = 0.5 in water)
Boiling point:: 370.01°C (rough estimate)
Density: 1.3771 (rough estimate)
refractive index: 1.6590 (estimate)
storage temp.: Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
solubility: acetic acid/water (1:1): 50 mg/mL
form: Powder
pka: 14.02±0.60(Predicted)
color: White to Off-white
Merck: 14,2853
BRN: 617982
Stability:: Stable. May be light or air sensitive. Incompatible with strong oxidizing agents.
InChIKey: XAUDJQYHKZQPEU-KVQBGUIXSA-N
CAS DataBase Reference: 2353-33-5(CAS DataBase Reference)
EPA Substance Registry System: 5-Aza-2'-deoxycytidine (2353-33-5)

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Safety

Hazard Codes: Xn,Xi,T
Risk Statements: 22-36/37/38-68-61
Safety Statements: 26-36-36/37
WGK Germany: 3
RTECS: XZ3012000
F: 10-34
HS Code: 29349990
Toxicity: LD50 in mice (mg/kg): 190 i.p. (Momparler, 1985)

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

H341Suspected of causing genetic defects

H360May damage fertility or the unborn child

Precautionary statements

P201Obtain special instructions before use.

P202Do not handle until all safety precautions have been read and understood.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P308+P313IF exposed or concerned: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: A3656
Product name: 5-Aza-2′-deoxycytidine
Purity: ≥97%
Packaging: 5mg
Price: $94.6
Updated: 2024/03/01

Sigma-Aldrich

Product number: 189826
Product name: InSolution? 5-Aza-2?-Deoxycytidine
Packaging: 10mg
Price: $159
Updated: 2024/03/01

TCI Chemical

Product number: A2232
Product name: 5-Aza-2'-deoxycytidine
Packaging: 20mg
Price: $75
Updated: 2024/03/01

TCI Chemical

Product number: A2232
Product name: 5-Aza-2'-deoxycytidine
Packaging: 100mg
Price: $255
Updated: 2024/03/01

Alfa Aesar

Product number: J65513
Product name: 5-Aza-2'-deoxycytidine, 98%
Packaging: 100mg
Price: $279
Updated: 2024/03/01

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5-Aza-2'-deoxycytidine Chemical Properties,Usage,Production

Indications and Usage

5-Aza-2’-deoxycytidine, also known as decitabine or 2'-deoxy-5-azacytidine, is a cell cycle S phase-specific drug used to treat myelodysplastic syndromes (MDS.)

Mechanisms of Action

Demethylating agents can regulate gene expression by activating tumor suppressor genes and enhancing the differentiation of genes, which help treat MDS. 5-Aza-2’-deoxycytidine is a natural andenosine analogue of 2′-deoxycytidine, known to the be strongest methylation specific inhibitor of DNA. After phosphorylation it can inhibit DNA methyltransferase, reducing DNA methylation, leading to demethylation of tumor cells, which can restore the normal functioning of genes, thus inhibiting tumor cell proliferation and preventing the occurrence of drug resistance. 5-Aza-2’-deoxycytidine inhibits DNA methylation in vitro, but does not affect its synthesis. Moreover, non-proliferating cells are not sensitive to it. 5-Aza-2’-deoxycytidine has anti-tumor activity and is characterized by a dual mechanism based on dose differences. At high concentrations it is cytoxic, while at low concentrations it is demethlyating.

Side Effects

Neutropenia, thrombocytopenia, anemia, vomiting, fatigue, fever, cough, nausea, constipation, diarrhea, hyperglycemia, and heat induced neutrophil.
Large doses may cause neurotoxicity, manifested as lethargy, aphasia, hemiplegia, etc., which disappears after stopping.

Toxicity grading

high

Acute toxicity

Intravenous – mouse LD50: 22 mg/kg; peritoneal – mouse LD50: 190 mg/kg

Flammability Hazardous characteristics

Combustible; produces toxic nitrogen oxide fumes.

Storage characteristics

Ventilated, cold, and dry; store away from raw food materials.

Fire extinguishing agent

dry powder, foam, sand, carbon dioxide, water mist.

Description

Decitabine, 5-aza-2’-deoxycytidine, has been launched for the treatment of myelodysplastic syndromes (MDS). MDS are a set of hematologic disorders affecting the bone marrow that result in ineffective formation and development of blood cells. Furthermore, patients with MDS have a high risk of progressing to acute myeloid leukemia (AML). Traditional treatments include blood transfusions, hematopoietic growth factors, and prophylactic antibiotics, but these measures merely improve the quality of life with questionable effects on disease modification. While stem-cell transplantation is an aggressive, potentially curative approach, the advanced age or the other complicating health issues of most patients preclude them from considering this option. Recent advances in the underlying etiology of MDS, however, have led to the development of a new class of compounds known as ‘‘demethylating agents’’. Decitabine follows the successful introduction of the first DNA methyltransferase inhibitor azacitidine.

Chemical Properties

white crystalline powder

Originator

Pharmachemie (Netherlands)

Uses

Used as cancer treatment, in particular to inhibit the growth of pancreatic endocrine tumor cell lines.

Uses

Decitabine is a potent inhibitor of DNA methylation with IC50 of 438 nM and 4.38 nM in HL-60 and KG1a cells, respectively

Uses

5-Aza-2′-deoxycytidine has been used as a demethylating agent in breast cancer cell line, chromatin, DNA and promoter region of p16 gene.

Definition

ChEBI: 5-aza-2'-deoxycytidine is a 2'-deoxyribonucleoside.

brand name

Dacogen (Millot Laboratories, France).

General Description

Fine white crystalline powder. Used as a drug.

Air & Water Reactions

Probably light and air sensitive. Water soluble. Decomposes in aqueous solution at a rate that depends on pH: at pH 7 the drug is more stable than at pH 9, but is less stable than at pH 6. At pH 7 and 99°F, approximately 7% conversion occurs in 1 hour .

Reactivity Profile

5-Aza-2'-deoxycytidine is an aminoalcohol. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.

Fire Hazard

Flash point data for 5-Aza-2'-deoxycytidine are not available. 5-Aza-2'-deoxycytidine is probably combustible.

Biological Activity

Cytosine analog that once incorporated into DNA acts as a suicide substrate for DNA methyltransferase. Inhibits DNA methyltransferase and results in DNA hypomethylation and activation of silent genes. Chemotherapeutic agent; suppresses growth of human tumor cell lines. Demethylates differentiation-related genes; reverses embryonic stem cell differentiation.

Biochem/physiol Actions

Primary TargetDNA methyltransferase inhibitor

Clinical Use

Antineoplastic antimetabolite agent:
Treatment of acute myeloid leukaemia

Safety Profile

Poison by intravenous route.Human mutation data reported. When heated todecomposition it emits toxic fumes of NOx.

Synthesis

Silylated 5-aza-cytosine (28) was condensed with 9- fluorenylmethoxycarbonyl (Fmoc) protected 2-deoxy-1-chlororibose (27) with tin chloride (IV) in dichloroethane (Scheme 4). The coupled product 29 was de-protected with excess triethylamine in dry pyridine to give decitabine (IV) in 36% yield after separation from its corresponding |áisomer.

target

Telomerase | DNA Methyltransferase | p21

Drug interactions

Potentially hazardous interactions with other drugs
Antipsychotics: avoid with clozapine, increased risk of agranulocytosis.

Metabolism

The exact route of metabolism and elimination is unknown but thought to be through deamination by cytidine deaminase in the liver, kidney, intestinal epithelium and blood to form inactive metabolites.

storage

+4°C

References

1) Bender et al. (1998), Inhibition of DNA methylation by 5-aza-2′-deoxycytidine suppresses the growth of human tumor cell lines; Cancer Res., 58 95 2) El-Serafi et al. (2011), Epigenetic modifiers influence lineage commitment of human bone marrow stromal cells: Differential effects of 5-aza-deoxycytidine and trichostatin A; Differentiation, 81 35

5-Aza-2'-deoxycytidine Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from 5-Aza-2'-deoxycytidine manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD

Product: Decitabine 2353-33-5
Price: US $0.00/KG
Min. Order: 10g
Purity: 98%min
Supply Ability: 10kg
Release date: 2021-10-21

Hebei Mujin Biotechnology Co.,Ltd

Product: 5-Aza-2'-deoxycytidine 2353-33-5
Price: US $0.00/KG
Min. Order: 1KG
Purity: 99%
Supply Ability: 50000KG/month
Release date: 2023-10-13

Hebei Chuanghai Biotechnology Co., Ltd

Product: 5-Aza-2'-deoxycytidine 2353-33-5
Price: US $30.00-10.00/KG
Min. Order: 50KG
Purity: 99%
Supply Ability: 500000kg
Release date: 2024-11-05

2353-33-5, 5-Aza-2'-deoxycytidineRelated Search:

Cytidine-5'-triphosphate disodium salt dihydrate Floxuridine Glycine 3-Aminophenol 5-Azacytidine ALTRENOGEST 6-Aminocaproic acid Cytarabine 5-Azacytosine Cytosine 5-Fluorocytidine Tris(hydroxymethyl)aminomethane Fluorocytosine Cytidine Cytidine 5’-monophosphate 2'-Deoxycytidine monohydrate α-Decitabine Fazarabine

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CS-1979

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