Tiazofurin
CAS No. 60084-10-8
Tiazofurin ( NSC 286193; Riboxamide )
Catalog No. M28325 CAS No. 60084-10-8
Tiazofurin is a synthetic nucleoside analogue with antineoplastic activity. Tiazofurin is anabolized intracellularly to tiazole-4-carboxamide adenine dinucleotide (TAD), a potent inhibitor of IMP dehydrogenase (IMPDH) .
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 479 | Get Quote |
|
10MG | 692 | Get Quote |
|
25MG | 1071 | Get Quote |
|
50MG | 1422 | Get Quote |
|
100MG | 1944 | Get Quote |
|
200MG | Get Quote | Get Quote |
|
500MG | Get Quote | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameTiazofurin
-
NoteResearch use only, not for human use.
-
Brief DescriptionTiazofurin is a synthetic nucleoside analogue with antineoplastic activity. Tiazofurin is anabolized intracellularly to tiazole-4-carboxamide adenine dinucleotide (TAD), a potent inhibitor of IMP dehydrogenase (IMPDH) .
-
DescriptionTiazofurin is a synthetic nucleoside analogue with antineoplastic activity. Tiazofurin is anabolized intracellularly to tiazole-4-carboxamide adenine dinucleotide (TAD), a potent inhibitor of IMP dehydrogenase (IMPDH) .
-
SynonymsNSC 286193; Riboxamide
-
PathwayMetabolic Enzyme/Protease
-
TargetDehydrogenase
-
RecptorAntifungal
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number60084-10-8
-
Formula Weight260.3
-
Molecular FormulaC9H12N2O5S
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESNC(=O)c1csc(n1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Moraes DC, et al. β-lapachone and α-nor-lapachone modulate Candida albicans viability and virulence factors. J Mycol Med. 2018 Mar 26. pii: S1156-5233(17)30379-7.
molnova catalog
related products
-
Qc1
Qc1 is an inhibitor of threonine dehydrogenase (TDH) inhibitor and can be used in studies about metabolic diseases.
-
Bipenquinate
Bipenquinate is a potent and selective inhibitor of dihydroorotate dehydrogenase (DHODH) with IC50 of 20 nM,?blocking de novo pyrimidine biosynthesis.
-
CM 10
CM 10 is an aldehyde dehydrogenase 1A family(ALDH1A) inhibitor.