NP-MRD: Showing NP-Card for 11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0⁴,¹²]dodecane]-1'(12'),4',6',8',10'-pentaen-3-one (NP0237574)

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Record Information

Version

2.0

Created at

2022-09-06 20:45:10 UTC

Updated at

2022-09-06 20:45:11 UTC

NP-MRD ID

NP0237574

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0⁴,¹²]dodecane]-1'(12'),4',6',8',10'-pentaen-3-one

Description

11'-Hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-2,3-dihydro-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0⁴,¹²]Dodecane]-1'(11'),4',6',8'(12'),9'-pentaen-3-one belongs to the class of organic compounds known as naphthols and derivatives. These are naphthalene derivatives carrying one or more hydroxyl (-OH) groups at any ring position. Based on a literature review very few articles have been published on 11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-2,3-dihydro-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0⁴,¹²]Dodecane]-1'(11'),4',6',8'(12'),9'-pentaen-3-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062222452D          

 28 32  0  0  0  0            999 V2000
    2.3519   -0.2330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2145    0.5805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8503    1.1062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6234    0.8185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2592    1.3442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1218    2.1577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3486    2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7129    1.9197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0164    2.3619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8110    1.5629    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9877    1.5113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4751    0.8648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3411    0.9855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8537    0.3391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6446    1.7527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320    2.3991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2265    3.3796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4093    3.9054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1825    3.6176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6247    4.3141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3199    2.8041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6841    2.2784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2217    3.1610    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6960    3.7968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9837    4.5699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4580    5.2057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0451    3.2126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4873    3.9091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
  9 21  1  0  0  0  0
 21 22  1  0  0  0  0
 11 22  2  0  0  0  0
 16 22  1  0  0  0  0
  9 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 23 27  1  0  0  0  0
  7 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END

     RDKit          3D

 47 51  0  0  0  0  0  0  0  0999 V2000
   -0.1560   -3.6447    1.7485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4020   -2.3939    1.1760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6920   -1.9448    0.8565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7809   -2.7614    1.1118 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0266   -2.2814    0.7829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1999   -1.0460    0.2240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0885   -0.2577   -0.0167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8368   -0.6973    0.2950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8681    0.3572   -0.0761 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1578    0.8460    1.0461 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1838    0.6782    0.8434 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3466    0.9570    1.5708 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5950    0.6519    1.0652 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8463    0.9453    1.8338 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7352    0.0598   -0.1789 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5861   -0.2200   -0.9068 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6376   -0.8097   -2.1562 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4509   -1.0551   -2.8150 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2207   -0.7233   -2.2505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9821   -0.9599   -2.8927 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1704   -0.1354   -1.0049 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3716    0.0943   -0.3777 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6153    1.4455   -0.6249 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0458    2.6818   -1.1139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9487    3.7228   -0.0151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1872    4.0343    0.5247 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9732    1.0954   -0.5999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9167    1.8037   -1.0004 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0615   -4.4575    0.9859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8622   -3.9539    2.5197 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8484   -3.5704    2.2590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6465   -3.7401    1.5542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8876   -2.9247    0.9837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1823   -0.6559   -0.0404 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2383    1.4140    2.5309 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4409    0.0384    2.0175 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6259    1.5396    2.7198 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4643    1.6010    1.1562 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6872   -0.1825   -0.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6022   -1.0501   -2.5567 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4464   -1.5143   -3.7930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9411   -1.3949   -3.8137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0259    2.5361   -1.5165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6605    3.1414   -1.9203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4711    4.6408   -0.3871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3237    3.2817    0.7822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5579    4.8085    0.0546 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  1
 10 11  1  0
 11 22  1  0
 22 21  2  0
 21 19  1  0
 19 20  1  0
 19 18  2  0
 18 17  1  0
 17 16  2  0
 16 15  1  0
 15 13  2  0
 13 14  1  0
 13 12  1  0
  9 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 23 27  1  0
 27 28  2  0
  8  3  1  0
 21  9  1  0
 27  7  1  0
 12 11  2  0
 16 22  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  4 32  1  0
  5 33  1  0
  6 34  1  0
 20 42  1  0
 18 41  1  0
 17 40  1  0
 15 39  1  0
 14 36  1  0
 14 37  1  0
 14 38  1  0
 12 35  1  0
 24 43  1  0
 24 44  1  0
 25 45  1  0
 25 46  1  0
 26 47  1  0
M  END


  Mrv1652309062222452D          

 28 32  0  0  0  0            999 V2000
    2.3519   -0.2330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2145    0.5805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8503    1.1062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6234    0.8185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2592    1.3442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1218    2.1577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3486    2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7129    1.9197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0164    2.3619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8110    1.5629    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9877    1.5113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4751    0.8648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3411    0.9855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8537    0.3391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6446    1.7527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320    2.3991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2265    3.3796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4093    3.9054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1825    3.6176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6247    4.3141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3199    2.8041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6841    2.2784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2217    3.1610    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6960    3.7968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9837    4.5699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4580    5.2057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0451    3.2126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4873    3.9091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
  9 21  1  0  0  0  0
 21 22  1  0  0  0  0
 11 22  2  0  0  0  0
 16 22  1  0  0  0  0
  9 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 23 27  1  0  0  0  0
  7 27  1  0  0  0  0
 27 28  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0237574

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=CC2=C1C1(OC3=C4C1=C(O)C=CC4=CC(C)=C3)N(CCO)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H19NO5/c1-12-10-13-6-7-15(25)20-18(13)17(11-12)28-22(20)19-14(4-3-5-16(19)27-2)21(26)23(22)8-9-24/h3-7,10-11,24-25H,8-9H2,1-2H3

> <INCHI_KEY>
TXNICMSEHSRCQN-UHFFFAOYSA-N

> <FORMULA>
C22H19NO5

> <MOLECULAR_WEIGHT>
377.396

> <EXACT_MASS>
377.126322716

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
39.16405155482721

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-2,3-dihydro-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0^{4,12}]dodecane]-1'(11'),4'(12'),5',7',9'-pentaen-3-one

> <JCHEM_LOGP>
3.3294870383333337

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.567045338987779

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.507846834915826

> <JCHEM_PKA_STRONGEST_BASIC>
-2.5507755336685296

> <JCHEM_POLAR_SURFACE_AREA>
79.22999999999999

> <JCHEM_REFRACTIVITY>
103.66419999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0^{4,12}]dodecane]-1'(11'),4'(12'),5',7',9'-pentaen-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       4.390  -0.435   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.134   1.084   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.320   2.065   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.764   1.528   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.951   2.509   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.694   4.028   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.251   4.565   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.064   3.583   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.764   4.409   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       3.381   2.917   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.844   2.821   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.887   1.614   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.637   1.840   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.593   0.633   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.203   3.272   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.246   4.478   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.423   6.309   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.764   7.290   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.207   6.753   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       3.033   8.053   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.464   5.234   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.277   4.253   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       4.147   5.900   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       3.166   7.087   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.703   8.531   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.722   9.717   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       5.684   5.997   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.510   7.297   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   27                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8   10   21   23                                             
CONECT   10    9   11                                                       
CONECT   11   10   12   22                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    9   22                                                  
CONECT   22   21   11   16                                                  
CONECT   23    9   24   27                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   23    7   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₁₉NO₅

Average Mass

377.3960 Da

Monoisotopic Mass

377.12632 Da

IUPAC Name

11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-2,3-dihydro-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0^{4,12}]dodecane]-1'(11'),4'(12'),5',7',9'-pentaen-3-one

Traditional Name

11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0^{4,12}]dodecane]-1'(11'),4'(12'),5',7',9'-pentaen-3-one

CAS Registry Number

Not Available

SMILES

COC1=CC=CC2=C1C1(OC3=C4C1=C(O)C=CC4=CC(C)=C3)N(CCO)C2=O

InChI Identifier

InChI=1S/C22H19NO5/c1-12-10-13-6-7-15(25)20-18(13)17(11-12)28-22(20)19-14(4-3-5-16(19)27-2)21(26)23(22)8-9-24/h3-7,10-11,24-25H,8-9H2,1-2H3

InChI Key

TXNICMSEHSRCQN-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthols and derivatives. These are naphthalene derivatives carrying one or more hydroxyl (-OH) groups at any ring position.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Naphthalenes

Sub Class

Naphthols and derivatives

Direct Parent

Naphthols and derivatives

Alternative Parents

Substituents

2-naphthol
Isoindolone
Isoindole or derivatives
Isoindole
Isoindoline
Anisole
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Tertiary carboxylic acid amide
Lactam
Carboxamide group
Oxacycle
Azacycle
Organoheterocyclic compound
Ether
Carboxylic acid derivative
Alkanolamine
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organonitrogen compound
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.33	ChemAxon
pKa (Strongest Acidic)	8.51	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	79.23 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	103.66 m³·mol⁻¹	ChemAxon
Polarizability	39.16 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163113804

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0⁴,¹²]dodecane]-1'(12'),4',6',8',10'-pentaen-3-one (NP0237574)

MOL for NP0237574 (11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0⁴,¹²]dodecane]-1'(12'),4',6',8',10'-pentaen-3-one)

3D MOL for NP0237574 (11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0⁴,¹²]dodecane]-1'(12'),4',6',8',10'-pentaen-3-one)

3D SDF for NP0237574 (11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0⁴,¹²]dodecane]-1'(12'),4',6',8',10'-pentaen-3-one)

3D-SDF for NP0237574 (11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0⁴,¹²]dodecane]-1'(12'),4',6',8',10'-pentaen-3-one)

PDB for NP0237574 (11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0⁴,¹²]dodecane]-1'(12'),4',6',8',10'-pentaen-3-one)

3D PDB for NP0237574 (11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0⁴,¹²]dodecane]-1'(12'),4',6',8',10'-pentaen-3-one)

SMILES for NP0237574 (11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0⁴,¹²]dodecane]-1'(12'),4',6',8',10'-pentaen-3-one)

INCHI for NP0237574 (11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0⁴,¹²]dodecane]-1'(12'),4',6',8',10'-pentaen-3-one)

Structure for NP0237574 (11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0⁴,¹²]dodecane]-1'(12'),4',6',8',10'-pentaen-3-one)

3D Structure for NP0237574 (11'-hydroxy-2-(2-hydroxyethyl)-7-methoxy-6'-methyl-3'-oxaspiro[isoindole-1,2'-tricyclo[6.3.1.0⁴,¹²]dodecane]-1'(12'),4',6',8',10'-pentaen-3-one)