Name | 5'-O-(4,4'-Dimethoxytrityl)-2'-deoxyuridine |
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Synonyms |
5'-O-[Bis(4-methoxyphenyl)benzyl]-2'-deoxyuridine
5'-O-Dimethylterephthale-2'-deoxyuridine 5'-(4,4'-dimethoxytrityl)-2'-deoxyuridine 5'-O-DMT-2'-DEOXYURIDINE 2'-deoxy-5'-O-dimethoxytrityluridine DMT-DEOXYURIDINE 2'-deoxy-5'-(4,4'-dimethoxytrityl)uridine 5'-O-[Bis(4-methoxyphenyl)phenylmethyl]-2'-deoxyuridine dmt-du 2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-uridine 5'-O-(4,4'-dimetoxytrityl)-2'-deoxyuridine 2'-Deoxy-5'-O-DMT-uridine |
Description | 5'-O-(4,4'-Dimethoxytrityl)-2'-deoxyuridine (5'-O-DMT-dU) is a competitive inhibitor of E. coli dUTP nucleotidohydrolase (dUTPase), with the Ki higher than 1000 μM. 5'-O-(4,4'-Dimethoxytrityl)-2'-deoxyuridine can be used in machine-assisted DNA synthesis by synthesizing nucleosidic phosphoramidite blocks[1][2]. |
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Related Catalog | |
Target |
Ki: >1000 μM (E. coli dUTPase)[1] |
References |
Density | 1.294 g/cm3 |
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Molecular Formula | C30H30N2O7 |
Molecular Weight | 530.56800 |
Exact Mass | 530.20500 |
PSA | 112.01000 |
LogP | 3.21090 |
Appearance | Powder | White to Off-white |
Index of Refraction | 1.61 |
Storage condition | −20°C |
Water Solubility | Soluble in acetonitrile at 20mg/ml |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H315-H319-H332-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xn: Harmful; |
Risk Phrases | R20/22;R36/37/38 |
Safety Phrases | S22-S26-S36 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
~10% 23669-79-6 |
Literature: Avino, Anna; Garcia, Ramon Gueimil; Albericio, Fernando; Mann, Matthias; Wilm, Matthias; Neubauer, Gitte; Eritja, Ramon Bioorganic and Medicinal Chemistry, 1996 , vol. 4, # 10 p. 1649 - 1658 |
~% 23669-79-6 |
Literature: Bioorganic and Medicinal Chemistry Letters, , vol. 21, # 4 p. 1181 - 1184 |
~% 23669-79-6 |
Literature: Bioorganic and Medicinal Chemistry Letters, , vol. 21, # 4 p. 1181 - 1184 |
~% 23669-79-6 |
Literature: Bioorganic and Medicinal Chemistry Letters, , vol. 21, # 4 p. 1181 - 1184 |
Precursor 3 | |
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DownStream 1 | |