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Assay Detail

CHEMBL840050

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition of [3H]U-69593 binding to Opioid receptor kappa 1
12
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Design, chemical synthesis, and biological evaluation of thiosaccharide analogues of morphine- and codeine-6-glucuronide.
MacDougall JM, Zhang XD, Polgar WE, Khroyan TV, Toll L, Cashman JR.
J Med Chem (2004) 47 : 5809 -5815
PubMed 15509180 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 12 4.65 4.96

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL363976 1 4.96
CHEMBL70 MORPHINE 4.0 1 4.33
CHEMBL1330 MORPHINE GLUCURONIDE 2.0 1 -
CHEMBL434900 1 -
CHEMBL438373 1 -
CHEMBL264244 1 -
CHEMBL361491 2 -
CHEMBL361921 1 -
CHEMBL187225 1 -
CHEMBL365900 1 -
CHEMBL434723 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL363976 Ki = 11000.0 nM 4.96
CHEMBL70 MORPHINE Ki = 47000.0 nM 4.33
CHEMBL1330 MORPHINE GLUCURONIDE Ki = 4060000.0 nM -
CHEMBL434900 Ki = 189000.0 nM -
CHEMBL438373 Ki = 499000.0 nM -
CHEMBL264244 Ki = 1390000.0 nM -
CHEMBL361491 Ki = 2970000.0 nM -
CHEMBL361491 Ki = 2190000.0 nM -
CHEMBL361921 Ki = 288000.0 nM -
CHEMBL187225 Ki > 10000000.0 nM -
CHEMBL365900 Ki = 136000.0 nM -
CHEMBL434723 Ki = 2480000.0 nM -