General Information of the Compound
Compound ID
CP0335634
Compound Name
N,N-dimethyl-2-[9-[2-methyl-1-oxo-1-(1,3,4-thiadiazol-2-ylamino)propan-2-yl]-9H-xanthen-3-yl]pyrimidine-5-carboxamide
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Structure
Formula
C26H24N6O3S
Molecular Weight
500.584
Canonical SMILES
CN(C)C(=O)c1cnc(nc1)-c1ccc2C(c3ccccc3Oc2c1)C(C)(C)C(=O)Nc1nncs1
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InChI
InChI=1S/C26H24N6O3S/c1-26(2,24(34)30-25-31-29-14-36-25)21-17-7-5-6-8-19(17)35-20-11-15(9-10-18(20)21)22-27-12-16(13-28-22)23(33)32(3)4/h5-14,21H,1-4H3,(H,30,31,34)
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InChIKey
OEVVOPPIVBWDRC-UHFFFAOYSA-N
Physicochemical Property
logP
4.5994
Rotatable Bonds
5
Heavy Atom Count
36
Polar Areas
110.2
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
8
Complexity
36

"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: 56594518
SID: 134226322
ChEMBL ID
CHEMBL1911285
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)  1
1
EC50 = 183 nM
   TI
   LI
   LO
   TS
CL000017 HeLa Homo sapiens (Human)  2
1
EC50 = 592 nM
   TI
   LI
   LO
   TS
2
EC50 = 596 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 Ki = 4.2 nM