- Oligonucléotides
- Nucleoside Analogs
- Thymidine
Thymidine
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Thymidine (36)
- 1
- 2
- Formule: C5H6N2O2
- Masse moléculaire: 126.11
Thymine, one of the four bases of DNA, is a substrate for rat liver dihydropyrimidine dehydrogenase (DPD), with a Km value of 2.2 μM, Ki of 24 μM (using 5-FU as the DPD substrate), and a specific activity of 0.68 nmol/min/mg.
August 31
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August 31
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- Formule: C10H14N2O4S
- Masse moléculaire: 258.29
4-Thiothymidine 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.
August 31
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August 31
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- Formule: C10H13FN2O5
- Masse moléculaire: 260.22
Clevudine (L-FMAU), a nucleoside analog of the unnatural L-configuration, has potent anti-HBV activity with long half-life, low toxicity. Clevudine is a non-competitive inhibitor that is not incorporated into the viral DNA but rather binds to the polymerase. Clevudine is active against cowpox virus respiratory infection in mice.
August 31
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August 31
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- Formule: C16H28N2O5Si
- Masse moléculaire: 356.49
5'-O-TBDMS-dT is a nucleoside with protective and modification effects.
August 31
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August 31
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- Formule: C10H14N2O5
- Masse moléculaire: 242.23
Pseudothymidine is a C-nucleoside analog of thymidine.
August 31
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August 31
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- Formule: C10H14N2O5
- Masse moléculaire: 242.23
1-(2-Deoxy-β-D-threo-pentofuranosyl)thymine is a thymidine analog. Analogs of this series have insertional activity towards replicated DNA. They can be used to label cells and track DNA synthesis.
August 31
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August 31
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- Formule: C29H29N3O4
- Masse moléculaire: 483.56
7’-OH-N-trityl morpholinothymine (PMO Thymidine Precusor) 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.
August 31
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August 31
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- Formule: C11H16N2O5
- Masse moléculaire: 256.26
4’-Methylthymidine 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.
August 31
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August 31
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- Formule: C31H30N2O7
- Masse moléculaire: 542.58
5'-DMTr-2,2'-anhydrothymidine 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.
August 31
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August 31
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- Formule: C17H18N2O6
- Masse moléculaire: 346.33
5’-O-Benzoylthymidine is a thymidine analog. Analogs of this series have insertional activity towards replicated DNA. They can be used to label cells and track DNA synthesis.
August 31
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August 31
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- Formule: C10H13N5O4
- Masse moléculaire: 267.24
3-epi-Azido-3-deoxythymidine 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.
August 31
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August 31
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- Formule: C10H13ClN2O4
- Masse moléculaire: 260.67
3′-Chloro-3′-deoxythymidine 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.
August 31
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August 31
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- Formule: C29H27N5O4
- Masse moléculaire: 509.56
1-(3-β-Azido-2,3-dideoxy-5-O-trityl-D-threopenta-furanosyl)thymine 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.
August 31
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August 31
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- Formule: C10H15N3O4
- Masse moléculaire: 241.24
1-(3-Beta-amino-2,3-dideoxy-beta-d-threopenta-furanosyl)thymine 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.
August 31
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August 31
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- Formule: C24H22N2O7
- Masse moléculaire: 450.44
3’,5’-Di-O-benzoyl 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.
August 31
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August 31
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- Formule: C10H12N2O4
- Masse moléculaire: 224.21
2,3’-Anhydrothymidine; 2’-Deoxy-3’,2-anhydro-5-methyluridine 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.
August 31
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August 31
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- Formule: C29H27ClN2O4
- Masse moléculaire: 502.99
3′-Chloro-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.
August 31
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August 31
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- Formule: C14H23N3O4
- Masse moléculaire: 297.35
5’-Deoxy-5’-N,N-diethylamino 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.
August 31
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August 31
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- Formule: C10H13IN2O4
- Masse moléculaire: 352.13
5′-Deoxy-5′-iodothymidine 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.
August 31
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August 31
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- Formule: C11H14BrNO4
- Masse moléculaire: 304.14
3′-Bromo-3′-deoxythymidine 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.
August 31
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August 31
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