NP-MRD: Showing NP-Card for Spirodihydrobenzofuranlactam V (NP0023153)

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Record Information

Version

2.0

Created at

2021-01-06 08:16:17 UTC

Updated at

2021-07-15 17:40:58 UTC

NP-MRD ID

NP0023153

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Spirodihydrobenzofuranlactam V

Provided By

NPAtlas

Description

Spirodihydrobenzofuranlactam V belongs to the class of organic compounds known as phthalimides. These are aromatic heterocyclic compounds containing a 1,3-dioxoisoindoline moiety. They are imide derivatives of phthalic anhydrides. Spirodihydrobenzofuranlactam V is found in Stachybotrys sp. Based on a literature review very few articles have been published on Spirodihydrobenzofuranlactam V.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242105393D          

 58 62  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652306242105393D          

 58 62  0  0  0  0            999 V2000
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   -0.2216   -3.7018    0.4080 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9036   -4.1497   -0.8761 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8752   -2.1454   -1.8825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6352   -3.3613   -0.9704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1689   -2.7642   -2.5494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8316   -1.2849   -2.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0456   -1.6484   -0.5879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2893    0.4379   -1.8631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5184   -0.4436   -1.5289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7672    1.3614   -1.6991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5049    0.6007   -2.6800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4359    2.8301   -1.4329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4058    2.8452    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7489    2.3380   -1.6538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5668    1.7269    1.1777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3892    1.0579    0.2282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6542    0.2929    2.6410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5548   -1.0749    1.9925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8561   -0.9709    2.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7518   -1.9474    0.9581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2150    1.4713    1.5676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1808    1.9600    0.1225 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4729    0.9754    1.4415 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6898    0.9807   -1.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5339   -0.4487   -2.0328 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5011   -0.8960    2.5606 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7616    1.8456   -2.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5479    2.1003    1.4594 H   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  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  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  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 18 29  1  0  0  0  0
 15  2  1  0  0  0  0
 22 17  1  0  0  0  0
 13  5  1  0  0  0  0
 15 29  1  1  0  0  0
 27 20  1  0  0  0  0
  1 30  1  0  0  0  0
  1 31  1  0  0  0  0
  1 32  1  0  0  0  0
  2 33  1  6  0  0  0
  3 34  1  0  0  0  0
  3 35  1  0  0  0  0
  4 36  1  0  0  0  0
  4 37  1  0  0  0  0
  5 38  1  6  0  0  0
  7 39  1  0  0  0  0
  7 40  1  0  0  0  0
  7 41  1  0  0  0  0
  8 42  1  0  0  0  0
  8 43  1  0  0  0  0
  8 44  1  0  0  0  0
  9 45  1  1  0  0  0
 10 46  1  0  0  0  0
 11 47  1  0  0  0  0
 11 48  1  0  0  0  0
 12 49  1  0  0  0  0
 12 50  1  0  0  0  0
 14 51  1  0  0  0  0
 14 52  1  0  0  0  0
 14 53  1  0  0  0  0
 16 54  1  0  0  0  0
 16 55  1  0  0  0  0
 19 56  1  0  0  0  0
 23 57  1  0  0  0  0
 26 58  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0023153

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C2C(=O)N([H])C(=O)C2=C([H])C2=C1C([H])([H])[C@]1(O2)[C@@]([H])(C([H])([H])[H])C([H])([H])C([H])([H])[C@@]2([H])C(C([H])([H])[H])(C([H])([H])[H])[C@@]([H])(O[H])C([H])([H])C([H])([H])[C@@]12C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C23H29NO5/c1-11-5-6-15-21(2,3)16(25)7-8-22(15,4)23(11)10-13-14(29-23)9-12-17(18(13)26)20(28)24-19(12)27/h9,11,15-16,25-26H,5-8,10H2,1-4H3,(H,24,27,28)/t11-,15-,16-,22+,23-/m0/s1

> <INCHI_KEY>
MOKUWDUXHMMMFK-UHFFFAOYSA-N

> <FORMULA>
C23H29NO5

> <MOLECULAR_WEIGHT>
399.487

> <EXACT_MASS>
399.204573038

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
43.09170721598758

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,2'S,4'aS,6'S,8'aR)-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-3,3',4',4'a,5,5',6,6',7,7',8',8'a-dodecahydro-2'H-spiro[furo[2,3-f]isoindole-2,1'-naphthalene]-5,7-dione

> <ALOGPS_LOGP>
3.73

> <JCHEM_LOGP>
3.8217463783333327

> <ALOGPS_LOGS>
-4.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.809599496102605

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.5052510263050936

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8351357121061601

> <JCHEM_POLAR_SURFACE_AREA>
95.86

> <JCHEM_REFRACTIVITY>
107.80119999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.42e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,2'S,4'aS,6'S,8'aR)-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-3,3',4',4'a,6,6',7',8'-octahydro-2'H-spiro[furo[2,3-f]isoindole-2,1'-naphthalene]-5,7-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 58 62  0  0  0  0  0  0  0  0999 V2000
    0.6338   -3.3190   -0.1591 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1454   -2.1381   -1.0145 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2208   -2.4284   -1.4665 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.7698   -0.0118   -0.9725 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9690    0.8301   -0.6333 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0259    0.5076   -1.7063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5917    2.2872   -0.9578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4980    0.6839    0.7388 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8659    0.3198    0.6201 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8568   -0.2442    1.6626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5878   -0.8967    1.2709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8268   -0.1476    0.1914 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4364    1.1626    0.8074 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3872   -0.8683   -0.2720 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2185    0.0946   -1.0952 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4683    0.3426   -0.3522 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3875   -0.4216    0.7928 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4898   -0.3334    1.6534 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5710    0.4688    1.3565 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5998    1.2132    0.1960 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5356    1.1406   -0.6550 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5233    1.8795   -1.8442 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8461    1.9729    0.1168 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1725    2.7451   -0.8177 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6067    1.6772    1.2791 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8409    0.7649    2.0380 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2049    0.2835    3.1362 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2133   -1.1304    0.8567 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5047   -3.0413    0.4468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2216   -3.7018    0.4080 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9036   -4.1497   -0.8761 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8752   -2.1454   -1.8825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6352   -3.3613   -0.9704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1689   -2.7642   -2.5494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8316   -1.2849   -2.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0456   -1.6484   -0.5879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2893    0.4379   -1.8631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5184   -0.4436   -1.5289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7672    1.3614   -1.6991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5049    0.6007   -2.6800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4359    2.8301   -1.4329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4058    2.8452    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7489    2.3380   -1.6538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5668    1.7269    1.1777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3892    1.0579    0.2282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6542    0.2929    2.6410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5548   -1.0749    1.9925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8561   -0.9709    2.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7518   -1.9474    0.9581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2150    1.4713    1.5676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1808    1.9600    0.1225 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4729    0.9754    1.4415 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6898    0.9807   -1.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5339   -0.4487   -2.0328 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5011   -0.8960    2.5606 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7616    1.8456   -2.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5479    2.1003    1.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  6  8  1  0
  6  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 21 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  0
 27 28  2  0
 18 29  1  0
 15  2  1  0
 22 17  1  0
 13  5  1  0
 15 29  1  1
 27 20  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  6
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  6
  7 39  1  0
  7 40  1  0
  7 41  1  0
  8 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  1
 10 46  1  0
 11 47  1  0
 11 48  1  0
 12 49  1  0
 12 50  1  0
 14 51  1  0
 14 52  1  0
 14 53  1  0
 16 54  1  0
 16 55  1  0
 19 56  1  0
 23 57  1  0
 26 58  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       0.634  -3.319  -0.159  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.145  -2.138  -1.014  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.221  -2.428  -1.466  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.244  -1.380  -1.341  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.770  -0.012  -0.973  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.969   0.830  -0.633  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.026   0.508  -1.706  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.592   2.287  -0.958  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.498   0.684   0.739  0.00  0.00           C+0
HETATM   10  O   UNK     0      -4.866   0.320   0.620  0.00  0.00           O+0
HETATM   11  C   UNK     0      -2.857  -0.244   1.663  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.588  -0.897   1.271  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.827  -0.148   0.191  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.436   1.163   0.807  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.387  -0.868  -0.272  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.218   0.095  -1.095  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.468   0.343  -0.352  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.388  -0.422   0.793  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.490  -0.333   1.653  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.571   0.469   1.357  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.600   1.213   0.196  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.536   1.141  -0.655  0.00  0.00           C+0
HETATM   23  O   UNK     0       3.523   1.880  -1.844  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.846   1.973   0.117  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.173   2.745  -0.818  0.00  0.00           O+0
HETATM   26  N   UNK     0       6.607   1.677   1.279  0.00  0.00           N+0
HETATM   27  C   UNK     0       5.841   0.765   2.038  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.205   0.284   3.136  0.00  0.00           O+0
HETATM   29  O   UNK     0       1.213  -1.130   0.857  0.00  0.00           O+0
HETATM   30  H   UNK     0       1.505  -3.041   0.447  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.222  -3.702   0.408  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.904  -4.150  -0.876  0.00  0.00           H+0
HETATM   33  H   UNK     0       0.875  -2.145  -1.883  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.635  -3.361  -0.970  0.00  0.00           H+0
HETATM   35  H   UNK     0      -1.169  -2.764  -2.549  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.832  -1.285  -2.302  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.046  -1.648  -0.588  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.289   0.438  -1.863  0.00  0.00           H+0
HETATM   39  H   UNK     0      -4.518  -0.444  -1.529  0.00  0.00           H+0
HETATM   40  H   UNK     0      -4.767   1.361  -1.699  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.505   0.601  -2.680  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.436   2.830  -1.433  0.00  0.00           H+0
HETATM   43  H   UNK     0      -2.406   2.845   0.003  0.00  0.00           H+0
HETATM   44  H   UNK     0      -1.749   2.338  -1.654  0.00  0.00           H+0
HETATM   45  H   UNK     0      -3.567   1.727   1.178  0.00  0.00           H+0
HETATM   46  H   UNK     0      -5.389   1.058   0.228  0.00  0.00           H+0
HETATM   47  H   UNK     0      -2.654   0.293   2.641  0.00  0.00           H+0
HETATM   48  H   UNK     0      -3.555  -1.075   1.992  0.00  0.00           H+0
HETATM   49  H   UNK     0      -0.856  -0.971   2.129  0.00  0.00           H+0
HETATM   50  H   UNK     0      -1.752  -1.947   0.958  0.00  0.00           H+0
HETATM   51  H   UNK     0      -1.215   1.471   1.568  0.00  0.00           H+0
HETATM   52  H   UNK     0      -0.181   1.960   0.123  0.00  0.00           H+0
HETATM   53  H   UNK     0       0.473   0.975   1.442  0.00  0.00           H+0
HETATM   54  H   UNK     0       0.690   0.981  -1.426  0.00  0.00           H+0
HETATM   55  H   UNK     0       1.534  -0.449  -2.033  0.00  0.00           H+0
HETATM   56  H   UNK     0       3.501  -0.896   2.561  0.00  0.00           H+0
HETATM   57  H   UNK     0       2.762   1.846  -2.482  0.00  0.00           H+0
HETATM   58  H   UNK     0       7.548   2.100   1.459  0.00  0.00           H+0
CONECT    1    2   30   31   32                                             
CONECT    2    1    3   15   33                                             
CONECT    3    2    4   34   35                                             
CONECT    4    3    5   36   37                                             
CONECT    5    4    6   13   38                                             
CONECT    6    5    7    8    9                                             
CONECT    7    6   39   40   41                                             
CONECT    8    6   42   43   44                                             
CONECT    9    6   10   11   45                                             
CONECT   10    9   46                                                       
CONECT   11    9   12   47   48                                             
CONECT   12   11   13   49   50                                             
CONECT   13   12   14   15    5                                             
CONECT   14   13   51   52   53                                             
CONECT   15   13   16    2   29                                             
CONECT   16   15   17   54   55                                             
CONECT   17   16   18   22                                                  
CONECT   18   17   19   29                                                  
CONECT   19   18   20   56                                                  
CONECT   20   19   21   27                                                  
CONECT   21   20   22   24                                                  
CONECT   22   21   23   17                                                  
CONECT   23   22   57                                                       
CONECT   24   21   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   58                                                  
CONECT   27   26   28   20                                                  
CONECT   28   27                                                            
CONECT   29   18   15                                                       
CONECT   30    1                                                            
CONECT   31    1                                                            
CONECT   32    1                                                            
CONECT   33    2                                                            
CONECT   34    3                                                            
CONECT   35    3                                                            
CONECT   36    4                                                            
CONECT   37    4                                                            
CONECT   38    5                                                            
CONECT   39    7                                                            
CONECT   40    7                                                            
CONECT   41    7                                                            
CONECT   42    8                                                            
CONECT   43    8                                                            
CONECT   44    8                                                            
CONECT   45    9                                                            
CONECT   46   10                                                            
CONECT   47   11                                                            
CONECT   48   11                                                            
CONECT   49   12                                                            
CONECT   50   12                                                            
CONECT   51   14                                                            
CONECT   52   14                                                            
CONECT   53   14                                                            
CONECT   54   16                                                            
CONECT   55   16                                                            
CONECT   56   19                                                            
CONECT   57   23                                                            
CONECT   58   26                                                            
MASTER        0    0    0    0    0    0    0    0   58    0  124    0
END

RDKit          3D

58 62  0  0  0  0  0  0  0  0999 V2000
    0.6338   -3.3190   -0.1591 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1454   -2.1381   -1.0145 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2208   -2.4284   -1.4665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2444   -1.3800   -1.3407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7698   -0.0118   -0.9725 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9690    0.8301   -0.6333 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0259    0.5076   -1.7063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5917    2.2872   -0.9578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4980    0.6839    0.7388 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8659    0.3198    0.6201 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8568   -0.2442    1.6626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5878   -0.8967    1.2709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8268   -0.1476    0.1914 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4364    1.1626    0.8074 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3872   -0.8683   -0.2720 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2185    0.0946   -1.0952 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4683    0.3426   -0.3522 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3875   -0.4216    0.7928 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4898   -0.3334    1.6534 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5710    0.4688    1.3565 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5998    1.2132    0.1960 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5356    1.1406   -0.6550 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5233    1.8795   -1.8442 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8461    1.9729    0.1168 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1725    2.7451   -0.8177 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6067    1.6772    1.2791 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8409    0.7649    2.0380 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2049    0.2835    3.1362 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2133   -1.1304    0.8567 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5047   -3.0413    0.4468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2216   -3.7018    0.4080 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9036   -4.1497   -0.8761 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8752   -2.1454   -1.8825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6352   -3.3613   -0.9704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1689   -2.7642   -2.5494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8316   -1.2849   -2.3021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0456   -1.6484   -0.5879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2893    0.4379   -1.8631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5184   -0.4436   -1.5289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7672    1.3614   -1.6991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5049    0.6007   -2.6800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4359    2.8301   -1.4329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4058    2.8452    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7489    2.3380   -1.6538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5668    1.7269    1.1777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3892    1.0579    0.2282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6542    0.2929    2.6410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5548   -1.0749    1.9925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8561   -0.9709    2.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7518   -1.9474    0.9581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2150    1.4713    1.5676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1808    1.9600    0.1225 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4729    0.9754    1.4415 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6898    0.9807   -1.4260 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5339   -0.4487   -2.0328 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5011   -0.8960    2.5606 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7616    1.8456   -2.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5479    2.1003    1.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  6
  6  8  1  0
  6  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 21 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  0
 27 28  2  0
 18 29  1  0
 15  2  1  0
 22 17  1  0
 13  5  1  0
 15 29  1  1
 27 20  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  6
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  5 38  1  6
  7 39  1  0
  7 40  1  0
  7 41  1  0
  8 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  1
 10 46  1  0
 11 47  1  0
 11 48  1  0
 12 49  1  0
 12 50  1  0
 14 51  1  0
 14 52  1  0
 14 53  1  0
 16 54  1  0
 16 55  1  0
 19 56  1  0
 23 57  1  0
 26 58  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₃H₂₉NO₅

Average Mass

399.4870 Da

Monoisotopic Mass

399.20457 Da

IUPAC Name

(2S,2'S,4'aS,6'S,8'aR)-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-3,3',4',4'a,5,5',6,6',7,7',8',8'a-dodecahydro-2'H-spiro[furo[2,3-f]isoindole-2,1'-naphthalene]-5,7-dione

Traditional Name

(2S,2'S,4'aS,6'S,8'aR)-4,6'-dihydroxy-2',5',5',8'a-tetramethyl-3,3',4',4'a,6,6',7',8'-octahydro-2'H-spiro[furo[2,3-f]isoindole-2,1'-naphthalene]-5,7-dione

CAS Registry Number

Not Available

SMILES

CC1CCC2C(C)(C)C(O)CCC2(C)C11CC2=C(O1)C=C1C(=O)NC(=O)C1=C2O

InChI Identifier

InChI=1S/C23H29NO5/c1-11-5-6-15-21(2,3)16(25)7-8-22(15,4)23(11)10-13-14(29-23)9-12-17(18(13)26)20(28)24-19(12)27/h9,11,15-16,25-26H,5-8,10H2,1-4H3,(H,24,27,28)

InChI Key

MOKUWDUXHMMMFK-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Stachybotrys sp.	NPAtlas	8642001

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phthalimides. These are aromatic heterocyclic compounds containing a 1,3-dioxoisoindoline moiety. They are imide derivatives of phthalic anhydrides.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoindoles and derivatives

Sub Class

Isoindolines

Direct Parent

Phthalimides

Alternative Parents

Substituents

Phthalimide
Isoindole
Coumaran
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Benzenoid
Carboxylic acid imide
Cyclic alcohol
Carboxylic acid imide, n-unsubstituted
Vinylogous acid
Secondary alcohol
Carboxylic acid derivative
Ether
Oxacycle
Azacycle
Hydrocarbon derivative
Organic oxide
Organic nitrogen compound
Organopnictogen compound
Organic oxygen compound
Organonitrogen compound
Organooxygen 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	3.73	ALOGPS
logP	3.82	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	7.51	ChemAxon
pKa (Strongest Basic)	-0.84	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	95.86 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	107.8 m³·mol⁻¹	ChemAxon
Polarizability	43.09 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

NPAtlas ID

NPA009304

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

412726

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

469819

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Spirodihydrobenzofuranlactam V (NP0023153)

MOL for NP0023153 (Spirodihydrobenzofuranlactam V)

3D MOL for NP0023153 (Spirodihydrobenzofuranlactam V)

3D SDF for NP0023153 (Spirodihydrobenzofuranlactam V)

3D-SDF for NP0023153 (Spirodihydrobenzofuranlactam V)

PDB for NP0023153 (Spirodihydrobenzofuranlactam V)

3D PDB for NP0023153 (Spirodihydrobenzofuranlactam V)

SMILES for NP0023153 (Spirodihydrobenzofuranlactam V)

INCHI for NP0023153 (Spirodihydrobenzofuranlactam V)

Structure for NP0023153 (Spirodihydrobenzofuranlactam V)

3D Structure for NP0023153 (Spirodihydrobenzofuranlactam V)