Tri Acetyl Azacitidine

Chemical Name Tri Acetyl Azacitidine
Alternate Names Azacitidine Impurities, Impurities of Azacitidine
CAT No. CS-EO-00143
CAS Registry# 10302-78-0
Category Impurities
Stock IN-Stock
Mol. Wt. 370.31 g/mol
Mol. For. C₁₄H₁₈N₄O₈
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Azacitidine
Therapeutic Anti-Cancer / Oncology
Smileys CC(O[C@H]1[C@H](N(C=NC(N)=N2)C2=O)O[C@H](COC(C)=O)[C@H]1OC(C)=O)=O
Canonical Smiles CC(=O)OCC1C(C(C(O1)N2C=NC(=NC2=O)N)OC(=O)C)OC(=O)C
InchIKey OTQJVHISAFFLMA-DDHJBXDOSA-N
Inchl InChI=1S/C14H18N4O8/c1-6(19)23-4-9-10(24-7(2)20)11(25-8(3)21)12(26-9)18-5-16-13(15)17-14(18)22/h5,9-12H,4H2,1-3H3,(H2,15,17,22)/t9-,10-,11-,12-/m1/s1
IUPAC [(2R,3R,4R,5R)-3,4-diacetyloxy-5-(4-amino-2-oxo-1,3,5-triazin-1-yl)oxolan-2-yl]methyl acetate
Controlled No
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Tri Acetyl Azacitidine, also known as TAAC, is a synthetic compound and a derivative of the chemotherapy drug Azacitidine. TAAC is used as an anti-cancer agent and is specifically used in the treatment of acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). The chemical structure of TAAC is similar to Azacitidine, but with three acetyl groups added to the nitrogen atoms. This modification helps to increase the stability of the compound and also improves its bioavailability. TAAC works by inhibiting the activity of DNA methyltransferase enzymes, which causes the re-expression of silenced tumor suppressor genes and the suppression of cancer cell growth. TAAC is administered via injection into the bloodstream and is typically given as a 30-minute infusion once a day for five consecutive days in a 28-day cycle. The dosage is determined by the patient's body weight and other factors such as kidney function. In clinical trials, TAAC has shown promising results in the treatment of AML and MDS, with some patients achieving complete remission or significant improvement in their condition. However, like most chemotherapy drugs, TAAC can cause side effects such as low white blood cell count, fatigue, and increased risk of infection. In conclusion, TAAC is a potent anti-cancer agent that shows great potential in the treatment of AML and MDS. Its chemical structure and mechanism of action make it a valuable addition to the arsenal of chemotherapy drugs available for these diseases. However, further research is needed to fully understand its effectiveness and potential side effects.

Related Compounds

Azacitidine Impurity C isomers 2 | Azacitidine Related compound C(Isomer-1) | Azacitidine Impurity 6 | Azacitidine Impurity C isomers | Azacitidine Impurity 16 | Azacitidine Impurity C isomers 2(Free Base) | Azacitidine Impurity 4 | Azacitidine Impurity 9 | Azacitidine impurity 48 | Beta-L-Ribofuranose | Azacitidine Impurity 7 | Azacitidine Related Compound B | Azacitidine Impurity 14 | Azacitidine N- Formyl Impurity | Azacitidine Impurity 23 | Azacitidine Impurity 1 | Azacitidine Impurity C isomers 3 | N-(Diaminoethylene)-N'-(β-D-ribofuranosyl)-carbamimidic Acid | Azacitidine Amine Isomer-4 | Azacitidine Related Compound -C Isomer -3 | Monoacyl Azacitidine | Azacitidine Impurity 24 | Azacitidine Impurity | Azacitidine Impurity C isomers 4 | Azacitidine Impurity 12 | Azacitidine Amine Impurity | Azacitidine Impurity 15 |

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