General Information of the Compound
Compound ID
CP0410061
Compound Name
(R)-2-(8-(1-(4-fluorophenyl)-N-methylcyclopropanecarboxamido)-6,7,8,9-tetrahydropyrido[3,2-b]indolizin-5-yl)acetic acid
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Structure
Formula
C24H24FN3O3
Molecular Weight
421.472
Canonical SMILES
CN([C@@H]1CCc2c(CC(O)=O)c3cccnc3n2C1)C(=O)C1(CC1)c1ccc(F)cc1
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InChI
InChI=1S/C24H24FN3O3/c1-27(23(31)24(10-11-24)15-4-6-16(25)7-5-15)17-8-9-20-19(13-21(29)30)18-3-2-12-26-22(18)28(20)14-17/h2-7,12,17H,8-11,13-14H2,1H3,(H,29,30)/t17-/m1/s1
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InChIKey
WEVBYBXURYFREE-QGZVFWFLSA-N
Physicochemical Property
logP
3.3075
Rotatable Bonds
5
Heavy Atom Count
31
Polar Areas
75.43
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
4
Complexity
31

"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: 53317854
ChEMBL ID
CHEMBL1641814
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: PT01054, Prostaglandin D2 receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
Ki > 3700 nM
   TI
   LI
   LO
   TS
Protein ID: PT01171, Prostaglandin D2 receptor 2
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  2
1
IC50 = 7.5 nM
   TI
   LI
   LO
   TS
2
Ki = 3.6 nM
   TI
   LI
   LO
   TS
Protein ID: PT01819, Thromboxane A2 receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
Ki > 6800 nM
   TI
   LI
   LO
   TS