General Information of the Compound
Compound ID
CP0290513
Compound Name
[1-[4-(2,2-diphenylethylamino)-3-(morpholine-4-carbonyl)phenyl]sulfonylpiperidin-4-yl]-(4-methylpiperazin-1-yl)methanone
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Synonyms
Bradykinin B1 receptor antagonists (inflammatory pain)
Bradykinin B1 receptor antagonists (inflammatory pain), Novartis
NVP-SAA164
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Structure
Formula
C36H45N5O5S
Molecular Weight
659.853
Canonical SMILES
CN1CCN(CC1)C(=O)C1CCN(CC1)S(=O)(=O)c1ccc(NCC(c2ccccc2)c2ccccc2)c(c1)C(=O)N1CCOCC1
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InChI
InChI=1S/C36H45N5O5S/c1-38-18-20-39(21-19-38)35(42)30-14-16-41(17-15-30)47(44,45)31-12-13-34(32(26-31)36(43)40-22-24-46-25-23-40)37-27-33(28-8-4-2-5-9-28)29-10-6-3-7-11-29/h2-13,26,30,33,37H,14-25,27H2,1H3
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InChIKey
VODUCDWVPSEMSZ-UHFFFAOYSA-N
Physicochemical Property
logP
3.5777
Rotatable Bonds
9
Heavy Atom Count
47
Polar Areas
102.5
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
7
Complexity
47

"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: 9831083
SID: 14790258
ChEMBL ID
CHEMBL273869
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: PT01032, B1 bradykinin receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000790 MR-5 Homo sapiens (Human)  1
1
IC50 = 33 nM
   TI
   LI
   LO
   TS
CL000006 HEK293 Homo sapiens (Human)  2
1
Ki = 8 nM
   TI
   LI
   LO
   TS
2
Ki = 10 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( NVP-SAA164 )
Drug Name NVP-SAA164
Company Novartis AG
Indication
Pain
Investigative
Target(s)
B1 bradykinin receptor (BDKRB1)
Antagonist