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Adenosine+5'-monophosphate+monohydrate
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Adenosine+5'-monophosphate+monohydrate
Supplier:
MP Biomedicals
Description:
Ribavarin is an antiviral compound reported to be active against RSV, HIV, HCV and other infectious agents. Its metabolite, ribavirin 5'-phosphate, inhibits inosine monophosphate dehydrogenase (IMP). It is also an analog of the imidazole nucleotide intermediates in purine nucleotide biosynthesis.
Ribavirin is active against a number of DNA and RNA viruses. It is a member of the nucleoside antimetabolite drugs that interfere with duplication of viral genetic material. Antiviral agent used against a wide variety of human viral infections, in particular, chronic hepatitis C, HIV, and adenovirus. Its metabolite, ribavirin 5′-phosphate, is an inhibitor of inosine monophosphate (IMP) dehydrogenase, but many other mechanisms of action are also supported with experimental evidence. Antiviral agent whose metabolite, ribavirin 5′-phosphate, is an inhibitor of inosine monophosphate (IMP) dehydrogenase. Used to inhibit purine (GTP pools) biosynthesis at the level of inosine monophosphate (IMP) dehydrogenase and as a precursor to the di- and tri-phosphates which inhibit viral RNA-dependent RNA polymerases. Store at +4 °C.
Catalog Number:
(10665-770)
Supplier:
Bioss
Description:
The protein encoded by this gene is a transferase, which catalyzes conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate via transfer of the 5-phosphoribosyl group from 5-phosphoribosyl 1-pyrophosphate. This enzyme plays a central role in the generation of purine nucleotides through the purine salvage pathway. Mutations in this gene result in Lesch-Nyhan syndrome or gout.[provided by RefSeq, Jun 2009].
Supplier:
TCI America
Description:
CAS Number: 58-61-7
MDL Number: MFCD00005752 Molecular Formula: C10H13N5O4 Molecular Weight: 267.25 Purity/Analysis Method: >99.0% (HPLC,T) Form: Crystal Melting point (°C): 235 Specific rotation [a]20/D: -70 deg (C=2, NaOH sol.(5%))
Catalog Number:
(77985-755)
Supplier:
LGC STANDARDS
Description:
Guanosine 3',5'-Cyclic-13C,15N2 Monophosphate, TRC, LGC Standards
Catalog Number:
(ALA192087250MG)
Supplier:
ALADDIN SCIENTIFIC
Description:
5'-Amino-5'-deoxy-2',3'-O-(1-methylethylidene)-adenosine ≥98%
Catalog Number:
(80050-134)
Supplier:
MilliporeSigma
Description:
A relatively stable, slowly hydrolyzable ATP analog that can substitute for ATP in various kinase reactions. Used as a substrate and as an inhibitor of ATP-dependent enzyme systems.
Catalog Number:
(77981-001)
Supplier:
LGC STANDARDS
Description:
Cytidine 5’-Monophosphate Methyl Ester Sodium Salt, TRC, LGC Standards
Supplier:
TCI America
Description:
S-Benzoylthiamine O-Monophosphate, Purity: >98.0%(HPLC)(T), Cas no. 22457-89-2, Molecular formula: C19H23N4O6PS, Form: Crystal- Powder, Colour: White - Almost white, Synonyms: Benfotiamine, Size: 25G
Supplier:
AMBEED, INC
Description:
Adenosine-5'-diphosphoric acid (ADP) 95%
Catalog Number:
(77694-468)
Supplier:
LGC STANDARDS
Description:
Guanosine 3’,5’-Cyclic-13C,15N2 Monophosphate, TRC, LGC Standards
Catalog Number:
(10665-768)
Supplier:
Bioss
Description:
The protein encoded by this gene is a transferase, which catalyzes conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate via transfer of the 5-phosphoribosyl group from 5-phosphoribosyl 1-pyrophosphate. This enzyme plays a central role in the generation of purine nucleotides through the purine salvage pathway. Mutations in this gene result in Lesch-Nyhan syndrome or gout.[provided by RefSeq, Jun 2009].
Catalog Number:
(10665-772)
Supplier:
Bioss
Description:
The protein encoded by this gene is a transferase, which catalyzes conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate via transfer of the 5-phosphoribosyl group from 5-phosphoribosyl 1-pyrophosphate. This enzyme plays a central role in the generation of purine nucleotides through the purine salvage pathway. Mutations in this gene result in Lesch-Nyhan syndrome or gout.[provided by RefSeq, Jun 2009].
Supplier:
AMBEED, INC
Description:
N6-(3-Methyl-2-butenyl)adenosine 98%
Catalog Number:
(10105-084)
Supplier:
Prosci
Description:
Pyrimidine 5-prime-nucleotidase (P5N), also called uridine 5-prime monophosphate hydrolase (UMPH), catalyzes the dephosphorylation of the pyrimidine 5-prime monophosphates UMP and CMP to the corresponding nucleosides. There are 2 isozymes of pyrimidine 5-prime nucleotidase in red blood cells, referred to as type I (UMPH1) and type II (UMPH2). The 2 enzymes are not separable by electrophoresis in humans but have distinct kinetic properties, and the proteins show no homology. Pyrimidine 5-prime-nucleotidase (P5N; EC 3.1.3.5), also called uridine 5-prime monophosphate hydrolase (UMPH), catalyzes the dephosphorylation of the pyrimidine 5-prime monophosphates UMP and CMP to the corresponding nucleosides. There are 2 isozymes of pyrimidine 5-prime nucleotidase in red blood cells, referred to as type I (UMPH1) and type II (UMPH2; MIM 191720). The 2 enzymes are not separable by electrophoresis in humans but have distinct kinetic properties, and the proteins show no homology.
Supplier:
AMBEED, INC
Description:
5'-Uridylic acid disodium salt xhydrate, Purity: 97%, CAS Number: 681435-27-8, Appearance: Solid, Storage: Inert atmosphere, 2-8 C, Size: 500g
Supplier:
Matrix Scientific
Description:
((2R, 3S, 4R, 5R)-5-(4-Amino-2-Oxopyrimidin-1(2H)-Yl)-3, 4-Dihydroxytetrahydrofuran-2-Yl)Methyl Dihydrogen Phosphate, purity: 95+%, CAS number: 63-37-6, Molecular formula: C9H14N3O8P, Molecular weight: 323.2, Size: 100G
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