General Information of the Compound
Compound ID
CP0424120
Compound Name
N-[(2R)-1-[acetyl-[(2-methoxyphenyl)methyl]amino]-3-(1H-indol-3-yl)propan-2-yl]-2-(4-piperidin-1-ylpiperidin-1-yl)acetamide
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Synonyms
LANEPITANT
LY-302654 (racemate)
LY-303870
Lanepitant
N-[1(R)-(1H-Indol-3-ylmethyl)-2-[N-(2-methoxybenzyl)acetamido]ethyl]-2-[4-(1-piperidinyl)piperidin-1-yl]acetamide
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Structure
Formula
C33H45N5O3
Molecular Weight
559.755
Canonical SMILES
COc1ccccc1CN(C[C@@H](Cc1c[nH]c2ccccc12)NC(=O)CN1CCC(CC1)N1CCCCC1)C(C)=O
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InChI
InChI=1S/C33H45N5O3/c1-25(39)38(22-26-10-4-7-13-32(26)41-2)23-28(20-27-21-34-31-12-6-5-11-30(27)31)35-33(40)24-36-18-14-29(15-19-36)37-16-8-3-9-17-37/h4-7,10-13,21,28-29,34H,3,8-9,14-20,22-24H2,1-2H3,(H,35,40)/t28-/m1/s1
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InChIKey
CVXJAPZTZWLRBP-MUUNZHRXSA-N
CAS
170566-84-4
Physicochemical Property
logP
4.2028
Rotatable Bonds
11
Heavy Atom Count
41
Polar Areas
80.91
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
5
Complexity
41

"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: 3086681
SID: 14764005
ChEMBL ID
CHEMBL42407
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: PT01410, Substance-P receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000228 IM-9 Homo sapiens (Human)  2
1
IC50 = 0.15 nM
   TI
   LI
   LO
   TS
2
IC50 = 0.23 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( LANEPITANT )
Drug Name LANEPITANT
Indication
Pain
Phase 2
Target(s)
Substance-P receptor (TACR1)
Antagonist