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Full Catalog (page 27)
Product Number Product Name Molecular Formula Cas. No.

PY 7598

Cytidine-5-carboxylic acid, sodium
salt

C10H12N3NaO7 

64623-37-6 (parent acid) 

PY 7599

5-Formylcytidine

C10H13N3O6 

148608-53-1 

PY 7600

5-(2-Hydroxyethyl)-2'-deoxyuridine

C11H16N2O6 

90301-60-3 

PY 7604

5-Acetoxymethyl-2'-deoxyuridine

C12H16N2O7 

148380-55-6 

PY 7605

5-Hydroxymethyl-2'-deoxyuridine

C10H14N2O6 

5116-24-5 

PY 7607

5-Iodo-2'-deoxycytidine

C9H12IN3O4 

611-53-0 

PY 7609

5-Iodocytidine

C9H12IN3O5 

1147-23-5 

PY 7610

5'-Iodo-5'-deoxythymidine

C10H13IN2O4 

25953-14-4 

PY 7612

2'-Fluoro-5'-iodo deoxyuridine

C9H10FIN2O4 

211694-25-6 

PY 7615

5-Iodo-2'-deoxyuridine

C9H11IN2O5 

54-42-2 

PY 7620

5-Iodo-2'-O-
methylcytidine

C10H14IN3O5 

847650-69-5 

PY 7630

5-Iodo-2'-O-methyluridine

C10H13IN2O6 

34218-84-3 

PY 7632

5-Iodouridine

C9H11IN2O6 

1024-99-3 

PY 7635

5-Methyl-2'-deoxycytidine
Hydrochloride

C10H15N3O4·HCl 

838-07-3 (Free Base) 5241-10-1 (HCl Salt) 

PY 7637

5-Methylcytidine

C10H15N3O5 

2140-61-6 

PY 7640

5-Methyl-2'-O-
methylcytidine

C11H17N3O5 

113886-70-7 

PY 7650

5-Methyl-2'-O-
methyluridine

C11H16N2O6 

55486-09-4 

PY 7660

5-(1-Propynyl)-2'-O-
methylcytidine

C13H17N3O5 

179817-96-0 

PY 7670

5-(1-Propynyl)-2'-O-
methyluridine

C13H16N2O6 

179817-95-9 

PY 7680

5'-O-Methylthymidine

C11H16N2O5 

14504-60-0 

Description

The 5'-O-methyl ether of thymidine is not cleaved by uridine deoxyuridine phosphorylase (EC 2.4.2.3) or thymidine phosphorylase (EC 2.4.2.4) and does not inhibit cleavage of thymidine by the enzyme.

PY 7690

2'-O-Methyluridine

C10H14N2O6 

2140-76-3 

PY 7694

3-Methyluridine

C10H14N2O6 

2140-69-4 

Alternate Name(s):

N-Methyluridine

PY 7695

5-Methyluridine

C10H14N2O6 

1463-10-1 

PY 7700

5-(1-Propynyl)-2'-deoxycytidine

C12H15N3O4 

117693-24-0 

PY 7710

5-(1-Propynyl)-2'-deoxyuridine

C12H14N2O5 

84558-94-1 

PY 7712

5-(Propargyloxy)-2'-deoxyuridine

C12H14N2O6 

65367-85-3 

Description

The purchase of these products for use in applications relating to copper catalyzed azide-alkyne cycloaddition chemistry (“Click Chemistry”) includes a limited, nontransferable license to intellectual property owned by TSRI to use this product solely for internal non-commercial research activities and specifically excludes clinical, therapeutic, or diagnostic use in humans or animals. Information regarding a license for commercial use in Click Chemistry may be obtained directly from The Scripps Research Institute, 10550 N. Torrey Pines Rd., La Jolla, CA 92037, or by contacting 858-784-8140 or click@scripps.edu.



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