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TargetSepiapterin reductase
LigandBDBM660088
Substrate/Competitorn/a
Meas. Tech.Measurement of Human SPR Inhibitory Activity Assay
IC50 0.650±n/a nM
Citation KAMAURA, MINABA, YSHINTANI, YKUWANO, YNAKAO, MNAGAI, HKUROSE, NTAKAYA, KNAKAJIMA, M CONDENSED HETEROCYCLIC COMPOUND US Patent US20240092784 Publication Date 3/21/2024
More Info.:Get all data from this article,  Assay Method
 
Sepiapterin reductase
Name:Sepiapterin reductase
Synonyms:SPR | SPRE_HUMAN | Sepiapterin reductase (SPR)
Type:Enzyme
Mol. Mass.:28050.66
Organism:Homo sapiens (Human)
Description:P35270
Residue:261
Sequence:
MEGGLGRAVCLLTGASRGFGRTLAPLLASLLSPGSVLVLSARNDEALRQLEAELGAERSG
LRVVRVPADLGAEAGLQQLLGALRELPRPKGLQRLLLINNAGSLGDVSKGFVDLSDSTQV
NNYWALNLTSMLCLTSSVLKAFPDSPGLNRTVVNISSLCALQPFKGWALYCAGKAARDML
FQVLALEEPNVRVLNYAPGPLDTDMQQLARETSVDPDMRKGLQELKAKGKLVDCKVSAQK
LLSLLEKDEFKSGAHVDFYDK
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  Blast E-value cutoff:
BDBM660088
n/a
NameBDBM660088
Synonyms:(S,E)-N-Cyclopropyl-7-hydroxy-3-(3-(3-(hydroxymethyl)morpholino)-3-oxoprop-1-en-1-yl)-4-isobutyl-5-oxo-4,5-dihydropyrazolo[1,5-a]pyrimidine-6-carboxamide | US20240092784, Example 525
TypeSmall organic molecule
Emp. Form.C22H29N5O6
Mol. Mass.459.4956
SMILESCC(C)Cn1c2c(\C=C\C(=O)N3CCOC[C@@H]3CO)cnn2c(O)c(C(=O)NC2CC2)c1=O
Structure
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