67380128 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 8 7 7 7 7 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 2 2 2 3 3 4 4 4 5 6 6 6 7 7 7 8 8 8 9 9 10 10 11 12 12 13 13 14 14 15 16 16 17 18 19 19 20 20 21 21 22 9 10 6 11 32 11 12 5 15 20 18 7 8 23 9 24 25 10 26 27 28 29 30 31 13 14 16 17 33 15 18 19 17 34 35 36 21 37 22 38 22 39 40 1 1 1 1 1 1 2 1 1 1 2 1 1 1 1 1 1 1 1 1 1 1 1 1 2 1 1 1 1 2 1 1 2 1 1 1 2 1 2 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 8.1886 7.2566 5.9674 3.732 4.6783 7.5673 6.8994 8.5458 7.2101 8.8564 6.2781 4.9889 5.6103 4.6783 3.732 4.3211 4.6318 5.2619 2.866 2.866 2 2 6.9606 6.3525 6.5169 8.5663 9.1596 7.1895 6.5963 9.4034 9.239 7.6707 5.8029 3.7144 4.2177 5.8819 2.866 2.866 1.4631 1.4631 3.4849 0.6333 -0.5234 -2.9849 -3.2896 1.5838 2.3282 1.7901 3.2787 2.7406 0.4271 -0.7296 1.1714 -1.6802 -1.9849 0.0147 0.9652 -2.4849 -1.4849 -3.4849 -1.9849 -2.9849 1.456 2.6202 1.8402 1.1704 1.7027 3.8983 3.366 2.4486 3.2285 0.1719 1.7607 -0.1132 1.4267 -2.4849 -0.8649 -4.1049 -1.6749 -3.2949 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 8 3 3 4 4 4 5 11 12 13 14 14 15 16 19 20 21 11 12 5 15 20 18 13 16 17 15 18 19 17 21 22 22 0 Compound Canonicalized 5 2019.01.04 1 Compound Complexity 7 E_COMPLEXITY 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 361 Count Hydrogen Bond Acceptor 5 E_NHACCEPTORS 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 4 Count Hydrogen Bond Donor 5 E_NHDONORS 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 1 Count Rotatable Bond 5 E_NROTBONDS 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 3 Fingerprint SubStructure Keys 16 extended 2 E_SCREEN 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 00000371E07BA0000000000000000000000000000001600000002C589000000000005801F800001E00180000000C28E19E063DF0B2C81400A2033667640092842931822019D8A03864988820E2C0D9D186A4086E9802C8C8279080C00E00000000000000000000000000000000000000000000 IUPAC Name Allowed 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 6-pyrazolo[1,5-a]pyridin-3-yl-N-tetrahydropyran-4-yl-pyridin-2-amine IUPAC Name CAS-like Style 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 N-(4-oxanyl)-6-(3-pyrazolo[1,5-a]pyridinyl)-2-pyridinamine IUPAC Name Markup 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 <I>N</I>-(oxan-4-yl)-6-pyrazolo[1,5-a]pyridin-3-ylpyridin-2-amine IUPAC Name Preferred 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 N-(oxan-4-yl)-6-pyrazolo[1,5-a]pyridin-3-ylpyridin-2-amine IUPAC Name Systematic 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 N-(oxan-4-yl)-6-pyrazolo[1,5-a]pyridin-3-yl-pyridin-2-amine IUPAC Name Traditional 1 2.7.0 Lexichem TK OpenEye Scientific Software 2021.05.07 (6-pyrazolo[1,5-a]pyridin-3-yl-2-pyridyl)-tetrahydropyran-4-yl-amine InChI Standard 1 1.0.6 InChI iupac.org 2021.05.07 InChI=1S/C17H18N4O/c1-2-9-21-16(5-1)14(12-18-21)15-4-3-6-17(20-15)19-13-7-10-22-11-8-13/h1-6,9,12-13H,7-8,10-11H2,(H,19,20) InChIKey Standard 1 1.0.6 InChI iupac.org 2021.05.07 JHKBQGGJJNHMON-UHFFFAOYSA-N Log P XLogP3-AA 7 3.0 sioc-ccbg.ac.cn 2021.05.07 2.4 Mass Exact 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 294.14806121 Molecular Formula 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 C17H18N4O Molecular Weight 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 294.35 SMILES Canonical 1 2.3.0 OEChem OpenEye Scientific Software 2021.05.07 C1COCCC1NC2=CC=CC(=N2)C3=C4C=CC=CN4N=C3 SMILES Isomeric 1 2.3.0 OEChem OpenEye Scientific Software 2021.05.07 C1COCCC1NC2=CC=CC(=N2)C3=C4C=CC=CN4N=C3 Topological Polar Surface Area 7 E_TPSA 3.4.8.18 Cactvs Xemistry GmbH 2021.05.07 51.4 Weight MonoIsotopic 1 2.1 PubChem ncbi.nlm.nih.gov 2021.05.07 294.14806121 22 0 0 0 0 0 0 0 1 -1