General Information of the Compound
Compound ID
CP0343798
Compound Name
2-[(3R)-4-[(4-chlorophenyl)methyl]-7-fluoro-5-methylsulfonyl-2,3-dihydro-1H-cyclopenta[b]indol-3-yl]acetic acid
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Synonyms
2-[(3R)-4-[(4-chlorophenyl)methyl]-7-fluoro-5-methanesulfonyl-1H,2H,3H,4H-cyclopenta[b]indol-3-yl]acetic acid
2-[(3R)-4-[(4-chlorophenyl)methyl]-7-fluoro-5-methylsulfonyl-2,3-dihydro-1H-cyclopenta[b]indol-3-yl]acetic acid
571170-77-9
AMOT0189
CHEMBL426559
CTK8F0660
Cardaptive
G7N11T8O78
GTPL3356
KS-00000XIE
LAROPIPRANT
Laropiprant
Laropiprant (INN/USAN)
Laropiprant (MK-0524)
Laropiprant [USAN:INN:BAN]
Laropiprant/MK-0524
MK 0524
MK-0524
MK-0524B
SCHEMBL991107
Tedaptive
UNII-G7N11T8O78
[14C]-Laropiprant
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Structure
Formula
C21H19ClFNO4S
Molecular Weight
435.904
Canonical SMILES
CS(=O)(=O)c1cc(F)cc2c3CC[C@H](CC(O)=O)c3n(Cc3ccc(Cl)cc3)c12
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InChI
InChI=1S/C21H19ClFNO4S/c1-29(27,28)18-10-15(23)9-17-16-7-4-13(8-19(25)26)20(16)24(21(17)18)11-12-2-5-14(22)6-3-12/h2-3,5-6,9-10,13H,4,7-8,11H2,1H3,(H,25,26)/t13-/m1/s1
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InChIKey
NXFFJDQHYLNEJK-CYBMUJFWSA-N
CAS
571170-77-9
Physicochemical Property
logP
4.3901
Rotatable Bonds
5
Heavy Atom Count
29
Polar Areas
76.37
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
4
Complexity
29

"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: 9867642
SID: 16319858
ChEMBL ID
CHEMBL426559
DrugBank ID
DB11629
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: PT02279, Prostacyclin receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
Ki = 6628 nM
   TI
   LI
   LO
   TS
Protein ID: PT01054, Prostaglandin D2 receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  2
1
Kd = 0.03 nM
   TI
   LI
   LO
   TS
2
Ki = 0.57 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 1.4 nM
Protein ID: PT01205, Prostaglandin E2 receptor EP1 subtype
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
Ki = 1160 nM
   TI
   LI
   LO
   TS
Protein ID: PT00948, Prostaglandin E2 receptor EP2 subtype
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
Ki = 136 nM
   TI
   LI
   LO
   TS
Protein ID: PT01367, Prostaglandin E2 receptor EP3 subtype
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
Ki = 892 nM
   TI
   LI
   LO
   TS
Protein ID: PT01534, Prostaglandin E2 receptor EP4 subtype
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
Ki > 15200 nM
   TI
   LI
   LO
   TS
Protein ID: PT01823, Prostaglandin F2-alpha receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
Ki = 9991 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)  2
1
Kd = 10.9 nM
   TI
   LI
   LO
   TS
2
Ki = 2.95 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( LAROPIPRANT )
Drug Name LAROPIPRANT
Indication
Coronary heart disease
Phase 4
Arteriosclerosis
Discontinued in Phase 3
Target(s)
Thromboxane A2 receptor (TBXA2R)
Inhibitor
Prostaglandin D2 receptor (PTGDR)
Inhibitor
Prostacyclin receptor (PTGIR)
Inhibitor
Prostaglandin D2 receptor 2 (PTGDR2)
Inhibitor
Prostaglandin F2-alpha receptor (PTGFR)
Inhibitor
Prostaglandin E2 receptor EP2 (PTGER2)
Inhibitor
HMG-CoA reductase (HMGCR)
Inhibitor