NP-MRD: Showing NP-Card for (3s,3ar,4s,5s,6ar,10s,17as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3h,3ah,4h,5h,6ah,9h,10h,15h,16h-cyclotrideca[d]isoindole-6,13,14,17-tetrone (NP0194214)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 11:50:28 UTC

Updated at

2022-09-04 11:50:28 UTC

NP-MRD ID

NP0194214

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,3ar,4s,5s,6ar,10s,17as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3h,3ah,4h,5h,6ah,9h,10h,15h,16h-cyclotrideca[d]isoindole-6,13,14,17-tetrone

Description

Chaetomadrasin A belongs to the class of organic compounds known as isoindolones. These are aromatic polycyclic compounds that an isoindole bearing a ketone. (3s,3ar,4s,5s,6ar,10s,17as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3h,3ah,4h,5h,6ah,9h,10h,15h,16h-cyclotrideca[d]isoindole-6,13,14,17-tetrone is found in Chaetomium madrasense. Based on a literature review very few articles have been published on Chaetomadrasin A.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309042213502D          

 39 43  0  0  1  0            999 V2000
    7.2777    2.0777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4497    1.8245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3950    1.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6030    0.5680    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9696    1.0489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2965   -0.1980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4733   -0.1432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2711    0.6566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5434    1.1910    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8031    0.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6203   -0.0131    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1176    1.2858    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3479    0.9065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1724    2.1090    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4070    2.4950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9126    2.4732    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1374    3.2670    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5637    3.9275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9337    4.6813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5481    5.4107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1227    6.0028    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8633    5.6393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6290    5.9465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2778    5.4370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1610    4.6203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3954    4.3131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7465    4.8226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9617    3.2986    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0257    2.5995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8624    3.1432    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5982    2.0142    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3384    2.3783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0411    1.6655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3932    3.2015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1335    3.5657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8190    3.1067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5623    3.5461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7642    2.2835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8684    2.0802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 19 27  1  0  0  0  0
 22 27  1  0  0  0  0
 17 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 31 29  1  1  0  0  0
  9 31  1  0  0  0  0
 16 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
  2 38  1  0  0  0  0
 38 39  2  0  0  0  0
M  END


  Mrv1652309042213502D          

 39 43  0  0  1  0            999 V2000
    7.2777    2.0777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4497    1.8245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3950    1.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6030    0.5680    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9696    1.0489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2965   -0.1980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4733   -0.1432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2711    0.6566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5434    1.1910    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8031    0.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6203   -0.0131    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1176    1.2858    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3479    0.9065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1724    2.1090    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4070    2.4950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9126    2.4732    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1374    3.2670    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5637    3.9275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9337    4.6813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5481    5.4107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1227    6.0028    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8633    5.6393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6290    5.9465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2778    5.4370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1610    4.6203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3954    4.3131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7465    4.8226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9617    3.2986    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0257    2.5995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8624    3.1432    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5982    2.0142    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3384    2.3783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0411    1.6655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3932    3.2015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1335    3.5657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8190    3.1067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5623    3.5461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7642    2.2835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8684    2.0802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  6  1  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 19 27  1  0  0  0  0
 22 27  1  0  0  0  0
 17 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 31 29  1  1  0  0  0
  9 31  1  0  0  0  0
 16 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
  2 38  1  0  0  0  0
 38 39  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0194214

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1[C@H]2[C@H](CC3=CNC4=CC=CC=C34)N=C(O)[C@@]22[C@@H](C=CC[C@H](C)C=C(C)C(=O)C(=O)CCC2=O)C(=O)[C@H]1C

> <INCHI_IDENTIFIER>
InChI=1S/C32H36N2O5/c1-17-8-7-10-23-30(38)20(4)19(3)28-25(15-21-16-33-24-11-6-5-9-22(21)24)34-31(39)32(23,28)27(36)13-12-26(35)29(37)18(2)14-17/h5-7,9-11,14,16-17,19-20,23,25,28,33H,8,12-13,15H2,1-4H3,(H,34,39)/t17-,19+,20-,23-,25-,28-,32+/m0/s1

> <INCHI_KEY>
ZVGDMFNGQGPHGS-BLKGCJBVSA-N

> <FORMULA>
C32H36N2O5

> <MOLECULAR_WEIGHT>
528.649

> <EXACT_MASS>
528.262422267

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
57.32733474464394

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,4S,5S,6aR,10S,17aS,17bR)-1-hydroxy-3-[(1H-indol-3-yl)methyl]-4,5,10,12-tetramethyl-3H,4H,5H,6H,6aH,9H,10H,13H,14H,15H,16H,17H,17bH-cyclotrideca[e]isoindole-6,13,14,17-tetrone

> <JCHEM_LOGP>
5.159377217597155

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.630550352377728

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.6947229976570686

> <JCHEM_PKA_STRONGEST_BASIC>
5.406622599530048

> <JCHEM_POLAR_SURFACE_AREA>
116.66000000000001

> <JCHEM_REFRACTIVITY>
150.9918

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4S,5S,6aR,10S,17aS,17bR)-1-hydroxy-3-(1H-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3H,4H,5H,6aH,9H,10H,15H,16H,17bH-cyclotrideca[e]isoindole-6,13,14,17-tetrone

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      13.585   3.878   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.040   3.406   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.937   1.869   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.459   1.060   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.277   1.958   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.887  -0.370   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.350  -0.267   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.973   1.226   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.614   2.223   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.232   1.543   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.891  -0.025   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.953   2.400   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.516   1.692   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.055   3.937   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.626   4.657   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.437   4.617   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.856   6.098   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.786   7.331   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.476   8.739   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.757  10.100   0.000  0.00  0.00           C+0
HETATM   21  N   UNK     0       5.829  11.205   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       7.211  10.527   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.641  11.100   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.852  10.149   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.634   8.625   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.205   8.051   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.993   9.002   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0       7.395   6.157   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0       7.515   4.852   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       9.077   5.867   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       6.717   3.760   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.098   4.440   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       9.410   3.109   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       8.201   5.976   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.582   6.656   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      10.862   5.799   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      12.250   6.619   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      10.760   4.263   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       9.088   3.883   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   38                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   31                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   31                                                  
CONECT   17   16   18   28                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   27                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   19   22                                                  
CONECT   28   17   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29    9   16   32                                             
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36    2   39                                                  
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₃₆N₂O₅

Average Mass

528.6490 Da

Monoisotopic Mass

528.26242 Da

IUPAC Name

(3S,4S,5S,6aR,10S,17aS,17bR)-1-hydroxy-3-[(1H-indol-3-yl)methyl]-4,5,10,12-tetramethyl-3H,4H,5H,6H,6aH,9H,10H,13H,14H,15H,16H,17H,17bH-cyclotrideca[e]isoindole-6,13,14,17-tetrone

Traditional Name

(3S,4S,5S,6aR,10S,17aS,17bR)-1-hydroxy-3-(1H-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3H,4H,5H,6aH,9H,10H,15H,16H,17bH-cyclotrideca[e]isoindole-6,13,14,17-tetrone

CAS Registry Number

Not Available

SMILES

C[C@H]1[C@H]2[C@H](CC3=CNC4=CC=CC=C34)N=C(O)[C@@]22[C@@H](C=CC[C@H](C)C=C(C)C(=O)C(=O)CCC2=O)C(=O)[C@H]1C

InChI Identifier

InChI=1S/C32H36N2O5/c1-17-8-7-10-23-30(38)20(4)19(3)28-25(15-21-16-33-24-11-6-5-9-22(21)24)34-31(39)32(23,28)27(36)13-12-26(35)29(37)18(2)14-17/h5-7,9-11,14,16-17,19-20,23,25,28,33H,8,12-13,15H2,1-4H3,(H,34,39)/t17-,19+,20-,23-,25-,28-,32+/m0/s1

InChI Key

ZVGDMFNGQGPHGS-BLKGCJBVSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Chaetomium madrasense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoindolones. These are aromatic polycyclic compounds that an isoindole bearing a ketone.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoindoles and derivatives

Sub Class

Isoindolines

Direct Parent

Isoindolones

Alternative Parents

Substituents

3-alkylindole
Isoindolone
Isoindole
Indole or derivatives
Indole
Benzenoid
Substituted pyrrole
2-pyrrolidone
Pyrrolidone
Heteroaromatic compound
Pyrrolidine
Pyrrole
Cyclic ketone
Secondary carboxylic acid amide
Lactam
Ketone
Carboxamide group
Azacycle
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
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	5.16	ChemAxon
pKa (Strongest Acidic)	2.69	ChemAxon
pKa (Strongest Basic)	5.41	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	116.66 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	150.99 m³·mol⁻¹	ChemAxon
Polarizability	57.33 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

146682644

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,3ar,4s,5s,6ar,10s,17as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3h,3ah,4h,5h,6ah,9h,10h,15h,16h-cyclotrideca[d]isoindole-6,13,14,17-tetrone (NP0194214)

MOL for NP0194214 ((3s,3ar,4s,5s,6ar,10s,17as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3h,3ah,4h,5h,6ah,9h,10h,15h,16h-cyclotrideca[d]isoindole-6,13,14,17-tetrone)

3D MOL for NP0194214 ((3s,3ar,4s,5s,6ar,10s,17as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3h,3ah,4h,5h,6ah,9h,10h,15h,16h-cyclotrideca[d]isoindole-6,13,14,17-tetrone)

3D SDF for NP0194214 ((3s,3ar,4s,5s,6ar,10s,17as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3h,3ah,4h,5h,6ah,9h,10h,15h,16h-cyclotrideca[d]isoindole-6,13,14,17-tetrone)

3D-SDF for NP0194214 ((3s,3ar,4s,5s,6ar,10s,17as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3h,3ah,4h,5h,6ah,9h,10h,15h,16h-cyclotrideca[d]isoindole-6,13,14,17-tetrone)

PDB for NP0194214 ((3s,3ar,4s,5s,6ar,10s,17as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3h,3ah,4h,5h,6ah,9h,10h,15h,16h-cyclotrideca[d]isoindole-6,13,14,17-tetrone)

3D PDB for NP0194214 ((3s,3ar,4s,5s,6ar,10s,17as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3h,3ah,4h,5h,6ah,9h,10h,15h,16h-cyclotrideca[d]isoindole-6,13,14,17-tetrone)

SMILES for NP0194214 ((3s,3ar,4s,5s,6ar,10s,17as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3h,3ah,4h,5h,6ah,9h,10h,15h,16h-cyclotrideca[d]isoindole-6,13,14,17-tetrone)

INCHI for NP0194214 ((3s,3ar,4s,5s,6ar,10s,17as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3h,3ah,4h,5h,6ah,9h,10h,15h,16h-cyclotrideca[d]isoindole-6,13,14,17-tetrone)

Structure for NP0194214 ((3s,3ar,4s,5s,6ar,10s,17as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3h,3ah,4h,5h,6ah,9h,10h,15h,16h-cyclotrideca[d]isoindole-6,13,14,17-tetrone)

3D Structure for NP0194214 ((3s,3ar,4s,5s,6ar,10s,17as)-1-hydroxy-3-(1h-indol-3-ylmethyl)-4,5,10,12-tetramethyl-3h,3ah,4h,5h,6ah,9h,10h,15h,16h-cyclotrideca[d]isoindole-6,13,14,17-tetrone)