NP-MRD: Showing NP-Card for 1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione (NP0225633)

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Record Information

Version

2.0

Created at

2022-09-06 04:24:57 UTC

Updated at

2022-09-06 04:24:57 UTC

NP-MRD ID

NP0225633

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione

Description

1-Hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3H,4H,6aH,9H,10H,11H,12H,13H,14H,15H,15bH-cycloundeca[e]isoindole-12,15-dione belongs to the class of organic compounds known as aspochalasins. These are cytochalasans with a structure in which the hydrogenated isoindole bears a 2-methylpropyl group. Based on a literature review very few articles have been published on 1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3H,4H,6aH,9H,10H,11H,12H,13H,14H,15H,15bH-cycloundeca[e]isoindole-12,15-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062206242D          

 30 32  0  0  0  0            999 V2000
    2.5369    0.4641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2172   -0.3727    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.4366   -1.3481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8351   -0.6257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6453   -0.7816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3535   -0.2828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7474   -1.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4036   -2.2203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2478   -3.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4682   -3.3005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5130   -4.1687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8446   -2.7605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0650   -3.0306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9092   -3.8408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1297   -4.1109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9849   -4.9558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5060   -3.5709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2543   -3.9636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6618   -2.7607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1640   -2.1028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7135   -2.1348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3800   -1.6061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1472   -1.9095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2592   -0.7900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6359   -1.4261    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3204   -1.6148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9163   -1.0641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4413   -2.4906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5972   -1.6804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1171   -0.8557    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  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
 10 12  2  0  0  0  0
 12 13  1  4  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 20 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 13 28  1  0  0  0  0
 19 28  1  0  0  0  0
 28 29  1  0  0  0  0
  3 29  1  0  0  0  0
 29 30  2  0  0  0  0
M  END

     RDKit          3D

 67 69  0  0  0  0  0  0  0  0999 V2000
   -2.3723    3.7859    2.5080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1768    2.0360    2.1789 S   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4167    1.7497    0.5162 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4384    2.2344   -0.4847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8056    1.7452   -0.2675 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5944    2.5148    0.3038 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3026    0.4142   -0.6771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8996   -0.0518   -2.0252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2297   -1.3853   -2.1116 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8458   -2.0064   -0.8460 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0322   -2.6510   -0.1040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6727   -2.1225   -0.2799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3171   -1.6908   -0.6811 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5893   -2.5818    0.1189 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4524   -2.2841    1.0334 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2699   -3.2690    1.7397 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6686   -0.8219    1.3475 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9232   -0.3268    2.5243 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4774   -0.1931    0.0382 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9308    1.1301   -0.2996 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3370    1.3761   -0.7252 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5189    1.0937    0.0837 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7009    1.6743   -0.8117 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9120   -0.3858    0.0912 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2218    1.2711   -1.6130 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2087    0.5234   -1.7153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6236    0.4693   -2.8799 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0278   -0.2575   -0.4618 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9893    0.3666    0.4044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5840   -0.4317    1.1674 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3843    3.9970    2.9338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6497    4.0653    3.3137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1658    4.4229    1.6393 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.4037    3.3773   -0.3489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0735   -0.2660    0.1668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4437    0.4483   -0.6496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2671    0.7430   -2.4850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8134   -0.0413   -2.7112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4670   -1.3865   -2.9022 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0225   -2.0832   -2.5624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9797   -2.3422   -0.5139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8778   -3.7374   -0.2911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9163   -2.4984    0.9666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7446   -2.6682    0.7120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1074   -1.9577   -1.7603 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4494   -3.6571   -0.1650 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2524   -3.3405    1.1933 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5365   -2.9696    2.7759 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8511   -4.3021    1.7048 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7608   -0.7174    1.6277 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6363   -0.1696    3.4182 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2378   -1.1049    2.9520 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4673    0.6774    2.4320 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9787   -0.9179   -0.7184 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5950    1.9478    0.3980 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3941    2.4494   -1.1507 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4359    0.7882   -1.7237 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6191    1.5750    1.0472 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6350    1.2582   -0.4070 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6504    2.7598   -0.8001 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5541    1.2589   -1.8268 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9415   -0.5146   -0.3317 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2243   -1.0288   -0.4612 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.1476    0.1291   -3.7008 H   0  0  0  0  0  0  0  0  0  0  0  0
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 28 26  1  6
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 29 30  2  0
 29  3  1  0
 28 13  1  0
 28 19  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  1
  4 35  1  0
  4 36  1  0
  7 37  1  0
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  8 39  1  0
  8 40  1  0
  9 41  1  0
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 11 43  1  0
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 23 61  1  0
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 23 63  1  0
 24 64  1  0
 24 65  1  0
 24 66  1  0
 27 67  1  0
M  END


  Mrv1652309062206242D          

 30 32  0  0  0  0            999 V2000
    2.5369    0.4641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2172   -0.3727    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.4366   -1.3481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8351   -0.6257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6453   -0.7816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3535   -0.2828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7474   -1.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4036   -2.2203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2478   -3.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4682   -3.3005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5130   -4.1687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9849   -4.9558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5060   -3.5709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2543   -3.9636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6618   -2.7607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1640   -2.1028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7135   -2.1348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3800   -1.6061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1472   -1.9095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2592   -0.7900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6359   -1.4261    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3204   -1.6148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9163   -1.0641    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4413   -2.4906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5972   -1.6804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1171   -0.8557    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
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  8  9  1  0  0  0  0
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 29 30  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0225633

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CSC1CC(=O)CCCC(C)=CC2C=C(C)C(C)C3C(CC(C)C)N=C(O)C23C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H37NO3S/c1-14(2)10-20-22-17(5)16(4)12-18-11-15(3)8-7-9-19(27)13-21(30-6)23(28)25(18,22)24(29)26-20/h11-12,14,17-18,20-22H,7-10,13H2,1-6H3,(H,26,29)

> <INCHI_KEY>
SKBNNAZECLMWGM-UHFFFAOYSA-N

> <FORMULA>
C25H37NO3S

> <MOLECULAR_WEIGHT>
431.64

> <EXACT_MASS>
431.249415229

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
48.868723681867664

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3H,4H,6aH,9H,10H,11H,12H,13H,14H,15H,15bH-cycloundeca[e]isoindole-12,15-dione

> <JCHEM_LOGP>
4.3666865908031935

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.578352162848237

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.9208682450385632

> <JCHEM_PKA_STRONGEST_BASIC>
5.707493351201315

> <JCHEM_POLAR_SURFACE_AREA>
66.72999999999999

> <JCHEM_REFRACTIVITY>
125.56889999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3H,4H,6aH,9H,10H,11H,13H,14H,15bH-cycloundeca[e]isoindole-12,15-dione

> <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       4.736   0.866   0.000  0.00  0.00           C+0
HETATM    2  S   UNK     0       4.139  -0.696   0.000  0.00  0.00           S+0
HETATM    3  C   UNK     0       4.548  -2.516   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.292  -1.168   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.804  -1.459   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       8.127  -0.528   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       6.995  -2.987   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.220  -4.144   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.929  -5.657   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.474  -6.161   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.558  -7.782   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.310  -5.153   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.855  -5.657   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.564  -7.169   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.109  -7.674   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.839  -9.251   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.944  -6.666   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.475  -7.399   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.235  -5.153   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.306  -3.925   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.332  -3.985   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.576  -2.998   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.008  -3.564   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.350  -1.475   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       1.187  -2.662   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       2.465  -3.014   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       3.577  -1.986   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.690  -4.649   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.981  -3.137   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.085  -1.597   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   29                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   28                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   28                                                  
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   20   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   13   19   29                                             
CONECT   29   28    3   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Value	Source
1-Hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulphanyl)-3H,4H,6ah,9H,10H,11H,12H,13H,14H,15H,15BH-cycloundeca[e]isoindole-12,15-dione	Generator

Chemical Formula

C₂₅H₃₇NO₃S

Average Mass

431.6400 Da

Monoisotopic Mass

431.24942 Da

IUPAC Name

1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3H,4H,6aH,9H,10H,11H,12H,13H,14H,15H,15bH-cycloundeca[e]isoindole-12,15-dione

Traditional Name

1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3H,4H,6aH,9H,10H,11H,13H,14H,15bH-cycloundeca[e]isoindole-12,15-dione

CAS Registry Number

Not Available

SMILES

CSC1CC(=O)CCCC(C)=CC2C=C(C)C(C)C3C(CC(C)C)N=C(O)C23C1=O

InChI Identifier

InChI=1S/C25H37NO3S/c1-14(2)10-20-22-17(5)16(4)12-18-11-15(3)8-7-9-19(27)13-21(30-6)23(28)25(18,22)24(29)26-20/h11-12,14,17-18,20-22H,7-10,13H2,1-6H3,(H,26,29)

InChI Key

SKBNNAZECLMWGM-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 aspochalasins. These are cytochalasans with a structure in which the hydrogenated isoindole bears a 2-methylpropyl group.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Cytochalasans

Sub Class

Aspochalasins

Direct Parent

Aspochalasins

Alternative Parents

Substituents

Carbocyclic aspochalasin skeleton
Aspochalasin skeleton
Isoindolone
Isoindole or derivatives
Isoindole
Isoindoline
2-pyrrolidone
Pyrrolidone
Pyrrolidine
Cyclic ketone
Secondary carboxylic acid amide
Lactam
Ketone
Carboxamide group
Azacycle
Organoheterocyclic compound
Dialkylthioether
Sulfenyl compound
Thioether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	4.37	ChemAxon
pKa (Strongest Acidic)	2.92	ChemAxon
pKa (Strongest Basic)	5.71	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	66.73 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	125.57 m³·mol⁻¹	ChemAxon
Polarizability	48.87 Å³	ChemAxon
Number of Rings	3	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

162878707

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione (NP0225633)

MOL for NP0225633 (1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

3D MOL for NP0225633 (1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

3D SDF for NP0225633 (1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

3D-SDF for NP0225633 (1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

PDB for NP0225633 (1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

3D PDB for NP0225633 (1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

SMILES for NP0225633 (1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

INCHI for NP0225633 (1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

Structure for NP0225633 (1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

3D Structure for NP0225633 (1-hydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-14-(methylsulfanyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)