General Information of the Compound
Compound ID
CP0075373
Compound Name
2-{[2-({[1-(propan-2-yl)piperidin-4-yl]methyl}amino)benzene]sulfonamido}-5,6,7,8-tetrahydronaphthalene-1-carboxylic acid
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Structure
Formula
C26H35N3O4S
Molecular Weight
485.65
Canonical SMILES
CC(C)N1CCC(CNc2ccccc2S(=O)(=O)Nc2ccc3CCCCc3c2C(O)=O)CC1
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InChI
InChI=1S/C26H35N3O4S/c1-18(2)29-15-13-19(14-16-29)17-27-22-9-5-6-10-24(22)34(32,33)28-23-12-11-20-7-3-4-8-21(20)25(23)26(30)31/h5-6,9-12,18-19,27-28H,3-4,7-8,13-17H2,1-2H3,(H,30,31)
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InChIKey
QJADDKYVLQKIJJ-UHFFFAOYSA-N
Physicochemical Property
logP
4.5967
Rotatable Bonds
8
Heavy Atom Count
34
Polar Areas
98.74
Hydrogen Bond Donor Count
3
Hydrogen Bond Acceptor Count
5
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: 11684506
SID: 16788684
ChEMBL ID
CHEMBL212407
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: PT00973, Methionine aminopeptidase 2
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000156 HT-1080 Homo sapiens (Human)  1
1
EC50 = 1000 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 45.71 nM
2 IC50 = 46 nM
3 IC50 = 3600 nM
Cell Viability or Cytotoxicity Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000156 HT-1080 Homo sapiens (Human)  1
1
EC50 = 950 nM
   TI
   LI
   LO
   TS