Reaction Details |
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Target | Trypanothione reductase |
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Ligand | BDBM50259708 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_1691709 |
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Ki | 245000±n/a nM |
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Citation | Arias, DG; Herrera, FE; Garay, AS; Rodrigues, D; Forastieri, PS; Luna, LE; Bürgi, MD; Prieto, C; Iglesias, AA; Cravero, RM; Guerrero, SA Rational design of nitrofuran derivatives: Synthesis and valuation as inhibitors of Trypanosoma cruzi trypanothione reductase. Eur J Med Chem125:1088-1097 (2017) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Trypanothione reductase |
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Name: | Trypanothione reductase |
Synonyms: | N(1),N(8)-bis(glutathionyl)spermidine reductase | TR |
Type: | Homodimer; oxidoreductase |
Mol. Mass.: | 53868.26 |
Organism: | Trypanosoma cruzi |
Description: | n/a |
Residue: | 492 |
Sequence: | MMSKIFDLVVIGAGSGGLEAAWNAATLYKKRVAVIDVQMVHGPPFFSALGGTCVNVGCVP
KKLMVTGAQYMEHLRESAGFGWEFDRTTLRAEWKKLIAVKDEAVLNINKSYEEMFRDTEG
LEFFLGWGSLESKNVVNVRESADPASAVKERLETENILLASGSWPHMPNIPGIEHCISSN
EAFYLPEPPRRVLTVGGGFISVEFAGIFNAYKPKDGQVTLCYRGEMILRGFDHTLREELT
KQLTANGIQILTKENPAKVELNADGSKSVTFESGKKMDFDLVMMAIGRSPRTKDLQLQNA
GVMIKNGGVQVDEYSRTNVSNIYAIGDVTNRVMLTPVAINEAAALVDTVFGTNPRKTDHT
RVASAVFSIPPIGTCGLIEEVASKRYEVVAVYLSSFTPLMHNISGSKYKTFVAKIITNHS
DGTVLGVHLLGDNAPEIIQGVGICLKLNAKISDFYNTIGVHPTSAEELCSMRTPSYYYVK
GEKMEKPSEASL
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BDBM50259708 |
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Name | BDBM50259708 |
Synonyms: | BAY-2502 | BAY-A2502 | BAYER-2502 | CHEBI:7566 | DNDI1613515 | Lampit | NIFURTIMOX | Nifurtimox |
Type | Small organic molecule |
Emp. Form. | C10H13N3O5S |
Mol. Mass. | 287.292 |
SMILES | CC1CS(=O)(=O)CCN1\N=C\c1ccc(o1)[N+]([O-])=O |
Structure |  |
n/a |
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