BDBM525969 US11185100, TABLE 6.6

SMILES C[C@]1(COP([O-])([O-])=S)O[C@@](C)(n2cnc3c(N)ncnc23)C(C)(O)[C@@]1(C)O

InChI Key InChIKey=DNHPGWUHPZPLIB-UHFFFAOYSA-L

Data  4 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 525969   

TargetTaste receptor type 1 member 1/3(Human)
Mars

US Patent
LigandPNGBDBM525969(US11185100, TABLE 6.6)
Affinity DataEC50:  6.00E+4nMAssay Description:The concentration of alanine is 20 mM.More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/9/2022
Entry Details
US Patent

TargetTaste receptor type 1 member 1/3(Human)
Mars

US Patent
LigandPNGBDBM525969(US11185100, TABLE 6.6)
Affinity DataEC50: >1.00E+6nMAssay Description:HEK293 cells that stably express T1R3 and inducibly express T1R1 were exposed to nucleotide derivatives alone to activate the umami receptor. Activat...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/9/2022
Entry Details
US Patent

TargetTaste receptor type 1 member 1/3(Human)
Mars

US Patent
LigandPNGBDBM525969(US11185100, TABLE 6.6)
Affinity DataEC50: >1.00E+6nMAssay Description:The concentration of IMP is 0.2 mM.More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/9/2022
Entry Details
US Patent

TargetTaste receptor type 1 member 1/3(Human)
Mars

US Patent
LigandPNGBDBM525969(US11185100, TABLE 6.6)
Affinity DataEC50: >1.00E+6nMAssay Description:The concentration of alanine is 20 mM, and the concentration of IMP is 0.2 mM.More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/9/2022
Entry Details
US Patent