Dayang Chem (Hangzhou) Co., Ltd.
China
Product Name: 1-(4-Azido-5-trityloxymethyl-tetrahdyro-furan-2-yl)-5-methyl-1H-pyrimidine-2,4-dione
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Purity: 98.0%
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29706-84-1

29706-84-1 structure

Name: 5'-O-Trt-Zidovudine
Chemical Name: 1-[(2R,4S,5S)-4-azido-5-(trityloxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione
CAS Number: 29706-84-1
Molecular Formula: C₂₉H₂₇N₅O₄
Molecular Weight: 509.56
Catalog: Signaling Pathways Cell Cycle/DNA Damage Nucleoside Antimetabolite/Analog
Create Date: 2016-12-05 11:57:46
Modify Date: 2026-07-01 19:31:05
3′-Azido-3′-deoxy-5′-O-(triphenylmethyl)thymidine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].

Name	1-[(2R,4S,5S)-4-azido-5-(trityloxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione
Synonyms	3-Azido-3-deoxy-5-O-triphe THYMIDINE,3'-AZIDO-3'-DEOXY-5'-O-(TRIPHENYLMETHYL) 3''-AZIDO-3''-DEOXY-5''-O-TRITYLTHYMIDINE 1-(4-azido-5-((trityloxy)methyl)tetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione 5'-Trt-Zidovudine Zidovudine Impurity 2 Trityl protected Zidovudine 5 '- O-triphenylmethyl zidovudine 3'-Azido-5'-O-trityl-2',3'-dideoxy-5-methyluridine 3'-Azido-3'-deoxy-5'-O-tritylthymidine 1-((2R,4S,5S)-4-azido-5-((trityloxy)Methyl)tetrahydrofuran-2-yl)-5-MethylpyriMidine-2,4(1H,3H)-dione 3'-Azido-3'-deoxy-5'-O-triphenylMethylthyMidine 3-Azido-3-deoxy-5-O-triphenylmethylthymidine Zidovudine Impurity J Trityl Azido Thymidine 1-(4-azido-5-trityloxymethyl-tetrahdyro-furan-2-yl)-5-methyl-1H-pyrimidine-2,4-dione Thymidine,3'-azido-3'-deoxy-5'-O-(triphenylmethyl) Zidovudine Impurity 10(Zidovudine Impurity J) Zidovudine impurity Q 3’-Azido-5’-O-trityl-2’,3’-dideoxy-5-methyluridine Thymidine,3'-azido-3'-deoxy-5'-O-trityl-(8CI) 3'-Azido-5'-O-tritylthymidine

Description	3′-Azido-3′-deoxy-5′-O-(triphenylmethyl)thymidine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].
Related Catalog	Research Areas >> Cancer Signaling Pathways >> Cell Cycle/DNA Damage >> Nucleoside Antimetabolite/Analog
References	[1]. Robak T, Robak P. Purine nucleoside analogs in the treatment of rarer chronic lymphoid leukemias. Curr Pharm Des. 2012;18(23):3373-88.

Precursor 0
DownStream 4
108895-46-1 141039-00-1 52450-18-7 30516-87-1