69923262 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 8 8 7 7 7 7 7 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 6 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 2 3 3 3 4 4 4 5 5 6 6 6 7 7 7 8 8 8 9 9 9 10 10 10 11 11 11 12 12 13 13 14 16 16 17 18 18 19 20 20 21 21 22 22 23 23 23 24 24 24 25 25 26 27 28 28 29 29 30 30 31 32 32 32 33 33 33 15 27 32 8 14 44 9 15 45 14 18 15 20 47 17 23 24 10 11 34 12 13 35 12 36 37 13 38 39 40 41 42 43 16 17 46 19 19 21 22 27 28 25 48 26 49 50 51 52 53 54 55 26 56 57 29 30 58 31 59 31 60 61 33 62 63 64 65 66 2 1 1 1 1 1 1 1 1 2 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 1 1 1 2 2 1 2 1 1 1 1 1 1 1 1 1 1 2 1 1 2 1 1 1 1 2 1 1 1 1 1 1 1 1 1 5 255 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 10.7282 13.3263 6.3981 9.8622 4.666 11.5942 4.666 7.2641 8.9962 7.2641 8.1301 8.1301 8.9962 5.5321 10.7282 5.5321 4.666 3.8 3.8 12.4603 2.9061 2.9061 5.5321 3.8 2 2 13.3263 12.4603 14.1923 13.3263 14.1923 14.1923 14.1923 6.7272 9.5331 7.0521 6.6535 7.7316 8.5287 8.5287 7.7316 9.2082 9.6067 6.3981 9.8622 6.069 11.5942 2.9132 2.9132 5.8421 6.069 5.2221 4.11 3.2631 3.49 1.4643 1.4643 11.9233 14.7292 13.3263 14.7292 14.4044 14.8029 14.8123 14.1923 13.5723 -1.44 1.06 -1.94 0.06 -1.94 0.06 1.06 -1.44 -0.44 -0.44 -1.94 0.06 -1.44 -1.44 -0.44 -0.44 0.06 -1.44 -0.44 -0.44 -1.9747 0.0947 1.56 1.56 -1.4608 -0.4192 0.06 -1.44 -0.44 -1.94 -1.44 1.56 2.56 -1.13 -0.75 0.1426 -0.5477 -2.415 -2.415 0.5349 0.5349 -2.0226 -1.3323 -2.56 0.68 -0.13 0.68 -2.5946 0.7146 1.0231 1.87 2.0969 2.0969 1.87 1.0231 -1.7729 -0.1071 -1.75 -0.13 -2.56 -1.75 0.9774 1.6677 2.56 3.18 2.56 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 5 5 14 16 17 18 18 19 20 20 21 22 25 27 28 29 30 14 18 16 17 19 19 21 22 27 28 25 26 26 29 30 31 31 0 Compound Canonicalized 5 2019.01.04 1 Compound Complexity 7 E_COMPLEXITY 3.4.6.11 Cactvs xemistry.com 2019.06.18 610 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.6.11 Cactvs xemistry.com 2019.06.18 5 Count Hydrogen Bond Donor 5 E_NHDONORS 3.4.6.11 Cactvs xemistry.com 2019.06.18 3 Count Rotatable Bond 5 E_NROTBONDS 3.4.6.11 Cactvs xemistry.com 2019.06.18 7 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.6.11 Cactvs xemistry.com 2019.06.18 00000371F07BB0000000000000000000000000000000000000003C60C1000000000000B1F400001E00100000000C2CE19E0633F6F3C81400A803266274008288292122200998A03F6C988E26E2C4F9DB873C28ECD613D8E82790C0800E00000000000210000001000000042000000000000000 IUPAC Name Allowed 1 2.6.6 LexiChem openeye.com 2019.06.18 1-[4-[[4-(dimethylamino)-2-quinolyl]amino]cyclohexyl]-3-(2-ethoxyphenyl)urea IUPAC Name CAS-like Style 1 2.6.6 LexiChem openeye.com 2019.06.18 1-[4-[[4-(dimethylamino)-2-quinolinyl]amino]cyclohexyl]-3-(2-ethoxyphenyl)urea IUPAC Name Markup 1 2.6.6 LexiChem openeye.com 2019.06.18 1-[4-[[4-(dimethylamino)quinolin-2-yl]amino]cyclohexyl]-3-(2-ethoxyphenyl)urea IUPAC Name Preferred 1 2.6.6 LexiChem openeye.com 2019.06.18 1-[4-[[4-(dimethylamino)quinolin-2-yl]amino]cyclohexyl]-3-(2-ethoxyphenyl)urea IUPAC Name Systematic 1 2.6.6 LexiChem openeye.com 2019.06.18 1-[4-[[4-(dimethylamino)quinolin-2-yl]amino]cyclohexyl]-3-(2-ethoxyphenyl)urea IUPAC Name Traditional 1 2.6.6 LexiChem openeye.com 2019.06.18 1-[4-[[4-(dimethylamino)-2-quinolyl]amino]cyclohexyl]-3-o-phenetyl-urea InChI Standard 1 1.0.5 InChI iupac.org 2019.06.18 InChI=1S/C26H33N5O2/c1-4-33-24-12-8-7-11-22(24)30-26(32)28-19-15-13-18(14-16-19)27-25-17-23(31(2)3)20-9-5-6-10-21(20)29-25/h5-12,17-19H,4,13-16H2,1-3H3,(H,27,29)(H2,28,30,32) InChIKey Standard 1 1.0.5 InChI iupac.org 2019.06.18 LAGPEDKRRNPWCN-UHFFFAOYSA-N Log P XLogP3-AA 7 3.0 sioc-ccbg.ac.cn 2019.06.18 5 Mass Exact 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 447.26342531 Molecular Formula 1 2.1 PubChem ncbi.nlm.nih.gov 2019.06.18 C26H33N5O2 Molecular Weight 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 447.6 SMILES Canonical 1 2.1.5 OEChem openeye.com 2019.06.18 CCOC1=CC=CC=C1NC(=O)NC2CCC(CC2)NC3=NC4=CC=CC=C4C(=C3)N(C)C SMILES Isomeric 1 2.1.5 OEChem openeye.com 2019.06.18 CCOC1=CC=CC=C1NC(=O)NC2CCC(CC2)NC3=NC4=CC=CC=C4C(=C3)N(C)C Topological Polar Surface Area 7 E_TPSA 3.4.6.11 Cactvs xemistry.com 2019.06.18 78.5 Weight MonoIsotopic 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 447.26342531 33 0 0 0 0 0 0 0 1 -1