General Information of the Compound
Compound ID
CP0093346
Compound Name
2-methyl-2-[(5R)-2-(4-propylphenyl)-5H-chromeno[2,3-b]pyridin-5-yl]-N-(1,3,4-thiadiazol-2-yl)propanamide
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Structure
Formula
C27H26N4O2S
Molecular Weight
470.598
Canonical SMILES
CCCc1ccc(cc1)-c1ccc2[C@@H](c3ccccc3Oc2n1)C(C)(C)C(=O)Nc1nncs1
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InChI
InChI=1S/C27H26N4O2S/c1-4-7-17-10-12-18(13-11-17)21-15-14-20-23(19-8-5-6-9-22(19)33-24(20)29-21)27(2,3)25(32)30-26-31-28-16-34-26/h5-6,8-16,23H,4,7H2,1-3H3,(H,30,31,32)/t23-/m1/s1
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InChIKey
QWKSNMYGEFJJIU-HSZRJFAPSA-N
Physicochemical Property
logP
6.4551
Rotatable Bonds
6
Heavy Atom Count
34
Polar Areas
77
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
6
Complexity
34

"RO5" indicates the cutoff set by lipinski's rule of five:

(1) Molecular weight less than 500 Dalton;

(2) xlogp less than 5;

(3) No more than 5 hbonddonor (Hydrogen Bond Donor Count);

(4) No more than 10 hbondacc (Hydrogen Bond Acceptor Count);

(5) No more than 10 rotbonds (Rotatable Bond Count).

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PubChem ID
CID: 57399054
ChEMBL ID
CHEMBL1911151
Map of Molecular Bioactivity Related to the Compound
Map of Molecular Bioactivity Related to the Compound

Compound
Cell Line
Protein

Bioactivity Value:

<= 0.1 μM
> 0.1 μM and <= 10 μM
> 10 μM
Imprecise Activity
Table of Molecular Bioactivities Related to the Compound
Protein ID: PT00967, Glucocorticoid receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000068 A-549 Homo sapiens (Human)  2
1
EC50 = 15.1 nM
   TI
   LI
   LO
   TS
2
EC50 = 29.7 nM
   TI
   LI
   LO
   TS
CL000017 HeLa Homo sapiens (Human)  2
1
EC50 = 36 nM
   TI
   LI
   LO
   TS
2
EC50 = 126 nM
   TI
   LI
   LO
   TS
CL000148 Huh-7 Homo sapiens (Human)  1
1
EC50 = 823 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 Ki = 2.4 nM