Responsive image

Common name


(3R,4S)-1,4-diethyl-3-phenyl-pyrrolidin-2-one

IUPAC name


(3R,4S)-1,4-diethyl-3-phenyl-pyrrolidin-2-one

SMILES


O=C1N(CC(C1c2ccccc2)CC)CC

Common name


(3R,4S)-1,4-diethyl-3-phenyl-pyrrolidin-2-one

IUPAC name


(3R,4S)-1,4-diethyl-3-phenyl-pyrrolidin-2-one

SMILES


O=C1N(CC(C1c2ccccc2)CC)CC

INCHI


InChI=1S/C14H19NO/c1-3-11-10-15(4-2)14(16)13(11)12-8-6-5-7-9-12/h5-9,11,13H,3-4,10H2,1-2H3/t11-,13-/m1/s1

FORMULA


C14H19NO

Responsive image

Common name


(3R,4S)-1,4-diethyl-3-phenyl-pyrrolidin-2-one

IUPAC name


(3R,4S)-1,4-diethyl-3-phenyl-pyrrolidin-2-one





Molecular weight


217.307

clogP


2.812

clogS


-3.105

Frequency


0.0003





HBond Acceptor


1

HBond Donor


0

Total Polar
Surface Area


20.31

Number of Rings


2

Rotatable Bond


3

Drug ID Common name Structure CAS Compound class Therapeutic area
FDBD00428 Doxapram Responsive image Central Nervous System Stimulants; Respiratory System Agents; Respiratory System; Respiratory Stimulants; For use as a temporary measure in hospitalized patients with acute respiratory insufficiency superimposed on chronic obstructive pulmonary disease.
1 , 1
FRAGNAME PDBID SIMILIRITY XSCORE SMILE HAC
2fv5_ligand_2_13.mol2 2fv5 0.887097 -7.42 c1ccc(cc1)[C@@]1(CCN(CC)C1=O)C 15
2fv5_ligand_1_3.mol2 2fv5 0.854839 -7.14 c1ccc(cc1)[C@@]1(CCNC1=O)C 13
1mzc_ligand_1_0.mol2 1mzc 0.835821 -7.09 c1(ccccc1)[C@H]1C(=O)N(CCCC1)C 15
2fv5_ligand_3_17.mol2 2fv5 0.797101 -7.47 Oc1ccc(cc1)[C@@]1(CCN(CC)C1=O)C 16
4tw7_ligand_2_122.mol2 4tw7 0.777778 -7.35 c1(ccccc1)CC(=O)N1CCCCC1 15
4tw8_ligand_2_139.mol2 4tw8 0.777778 -7.19 C(C(=O)N1CCCCC1)c1ccccc1 15
1eb2_ligand_2_6.mol2 1eb2 0.777778 -6.02 c1c(cccc1)CC(=O)N1CCCCC1 15
2fv5_ligand_2_9.mol2 2fv5 0.768116 -7.19 Oc1ccc(cc1)[C@@]1(CCNC1=O)C 14
4zxx_ligand_2_8.mol2 4zxx 0.758065 -6.27 C(c1ccccc1)C(=O)N1CCCC1 14
4x8v_ligand_2_1.mol2 4x8v 0.758065 -6.14 c1ccccc1CC(=O)N1CCCC1 14
109 , 11